geneid | 5663 |
---|---|
ensemblid | ENSG00000080815.20 |
hgncid | 9508 |
symbol | PSEN1 |
name | presenilin 1 |
refseq_nuc | NM_000021.4 |
refseq_prot | NP_000012.1 |
ensembl_nuc | ENST00000324501.10 |
ensembl_prot | ENSP00000326366.5 |
mane_status | MANE Select |
chr | chr14 |
start | 73136507 |
end | 73223691 |
strand | + |
ver | v1.2 |
region | chr14:73136507-73223691 |
region5000 | chr14:73131507-73228691 |
regionname0 | PSEN1_chr14_73136507_73223691 |
regionname5000 | PSEN1_chr14_73131507_73228691 |
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 | 467 | 376 | 87 | 74 | 167 | 10 | 36 | 123 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0002 | 0/0 | 467 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0003 | 0/0 | 467 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
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 | 1404 | 372 | 85 | 74 | 165 | 10 | 36 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
c0002 | 0/0 | 1404 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
c0003 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
c0004 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
c0005 | 0/0 | 1404 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
c0006 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
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 | 4615 | 117 | 30 | 23 | 55 | 2 | 7 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0002 | 1/0 | 4615 | 66 | 12 | 21 | 23 | 4 | 5 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0003 | 0/0 | 4615 | 47 | 8 | 3 | 31 | 1 | 4 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0004 | 0/0 | 4615 | 36 | 9 | 12 | 6 | 1 | 8 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0005 | 0/0 | 4615 | 34 | 1 | 6 | 27 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0006 | 0/0 | 4615 | 17 | 1 | 1 | 12 | 0 | 3 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0007 | 0/0 | 4615 | 10 | 9 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0008 | 0/0 | 4615 | 6 | 0 | 1 | 1 | 2 | 2 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0009 | 0/1 | 4615 | 6 | 0 | 3 | 0 | 0 | 2 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0010 | 0/0 | 4615 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0011 | 0/0 | 4615 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0012 | 0/0 | 4603 | 4 | 0 | 0 | 4 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0013 | 0/0 | 4615 | 3 | 0 | 0 | 0 | 0 | 3 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0014 | 0/0 | 4615 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0015 | 0/0 | 4615 | 2 | 1 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0016 | 0/0 | 4615 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0017 | 0/0 | 4615 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0018 | 0/0 | 4615 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0019 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0020 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0021 | 0/0 | 4572 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0022 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0023 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0024 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0025 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0026 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0027 | 0/0 | 4615 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0028 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0029 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0030 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
t0031 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
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 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0325 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
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 | 1404 | 372 | 85 | 74 | 165 | 10 | 36 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0002 | 0/0 | 1404 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0004 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0006 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0002c0005 | 0/0 | 1404 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0003c0003 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6018 | 117 | 30 | 23 | 55 | 2 | 7 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0002 | 1/0 | 6018 | 66 | 12 | 21 | 23 | 4 | 5 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0003 | 0/0 | 6018 | 46 | 7 | 3 | 31 | 1 | 4 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0004 | 0/0 | 6018 | 36 | 9 | 12 | 6 | 1 | 8 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0005 | 0/0 | 6018 | 32 | 1 | 6 | 25 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0006 | 0/0 | 6018 | 15 | 0 | 1 | 11 | 0 | 3 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0007 | 0/0 | 6018 | 10 | 9 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0008 | 0/0 | 6018 | 6 | 0 | 1 | 1 | 2 | 2 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0009 | 0/1 | 6018 | 6 | 0 | 3 | 0 | 0 | 2 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0010 | 0/0 | 6018 | 5 | 0 | 0 | 5 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0011 | 0/0 | 6018 | 4 | 4 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0012 | 0/0 | 6006 | 4 | 0 | 0 | 4 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0013 | 0/0 | 6018 | 3 | 0 | 0 | 0 | 0 | 3 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0014 | 0/0 | 6018 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0015 | 0/0 | 6018 | 2 | 1 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0016 | 0/0 | 6018 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0017 | 0/0 | 6018 | 2 | 2 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0018 | 0/0 | 6018 | 2 | 0 | 0 | 0 | 0 | 2 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0019 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0021 | 0/0 | 5975 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0022 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0023 | 0/0 | 6018 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0024 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0025 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0026 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0027 | 0/0 | 6018 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0028 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0029 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0030 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0001t0031 | 0/0 | 6018 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0002t0005 | 0/0 | 6018 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0004t0020 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0001c0006t0006 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0002c0005t0006 | 0/0 | 6018 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
a0003c0003t0003 | 0/0 | 6018 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | copy fasta | chr14 | 73131507 | 73228691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0325 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0007g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0008g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0009g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0009g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0009g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0009g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0009g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0011g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0011g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0012g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0013g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0013g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0013g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0014g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0015g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0016g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0016g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0017g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0017g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0018g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0018g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0019g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0021g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0022g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0023g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0024g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0025g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0026g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0027g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0028g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0029g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0030g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0001t0031g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0002t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0002t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0004t0020g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0001c0006t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0002c0005t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
a0003c0003t0003g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0330 | EUR | GBR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0240 | EUR | GBR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0298 | EUR | GBR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0327 | EUR | FIN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0106 | EUR | FIN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00423 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0128 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00621 | hp1 | a0001 | c0002 | t0005 | g0118 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | CHS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0215 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0355 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0181 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01070 | hp1 | a0001 | c0001 | t0009 | g0198 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0182 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01074 | hp2 | a0001 | c0001 | t0027 | g0307 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0241 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01081 | hp2 | a0001 | c0001 | t0015 | g0302 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01099 | hp1 | a0001 | c0001 | t0021 | g0342 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0324 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01192 | hp1 | a0001 | c0001 | t0009 | g0225 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0348 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0328 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0326 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01261 | hp2 | a0001 | c0001 | t0008 | g0191 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0352 | EUR | IBS | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01884 | hp2 | a0001 | c0001 | t0016 | g0267 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0369 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0239 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0264 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01975 | hp1 | a0001 | c0001 | t0006 | g0273 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0356 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02040 | hp1 | a0001 | c0001 | t0031 | g0222 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02055 | hp1 | a0001 | c0001 | t0022 | g0144 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0285 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0278 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0301 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0121 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CDX | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | CDX | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0164 | EAS | CDX | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02257 | hp1 | a0001 | c0001 | t0024 | g0242 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02257 | hp2 | a0001 | c0001 | t0030 | g0168 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02293 | hp2 | a0001 | c0001 | t0004 | g0255 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0335 | AMR | PEL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0265 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02615 | hp2 | a0001 | c0001 | t0026 | g0289 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02683 | hp1 | a0001 | c0001 | t0018 | g0344 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02698 | hp2 | a0001 | c0001 | t0018 | g0337 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0370 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02723 | hp2 | a0001 | c0001 | t0017 | g0195 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02735 | hp2 | a0001 | c0001 | t0008 | g0107 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0271 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0308 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02818 | hp1 | a0001 | c0001 | t0028 | g0293 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0294 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03098 | hp1 | a0001 | c0001 | t0029 | g0133 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03098 | hp2 | a0001 | c0001 | t0016 | g0279 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0303 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0288 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0291 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0268 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03491 | hp1 | a0001 | c0001 | t0009 | g0201 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03491 | hp2 | a0001 | c0001 | t0013 | g0353 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03492 | hp1 | a0001 | c0001 | t0013 | g0349 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03579 | hp2 | a0001 | c0006 | t0006 | g0153 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03654 | hp2 | a0001 | c0001 | t0013 | g0336 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03688 | hp1 | a0001 | c0001 | t0009 | g0367 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0295 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0343 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0257 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03831 | hp1 | a0001 | c0001 | t0008 | g0192 | SAS | BEB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | BEB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0140 | SAS | BEB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0297 | SAS | BEB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0120 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0234 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | STU | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | YRI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | YRI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18612 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | CHB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18747 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | CHB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0309 | AFR | YRI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18942 | hp1 | a0001 | c0002 | t0005 | g0119 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18944 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18944 | hp2 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18947 | hp2 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18950 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0178 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18969 | hp2 | a0001 | c0001 | t0023 | g0321 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0372 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0073 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18974 | hp1 | a0001 | c0001 | t0014 | g0177 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0374 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18980 | hp2 | a0001 | c0001 | t0012 | g0179 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0160 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18986 | hp2 | a0001 | c0001 | t0012 | g0184 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0345 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18991 | hp2 | a0001 | c0001 | t0010 | g0053 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18992 | hp2 | a0002 | c0005 | t0006 | g0274 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0346 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18999 | hp1 | a0001 | c0001 | t0010 | g0094 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0310 | AFR | LWK | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19030 | hp2 | a0001 | c0004 | t0020 | g0312 | AFR | LWK | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0371 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19063 | hp1 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0186 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19064 | hp2 | a0001 | c0001 | t0012 | g0188 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19072 | hp1 | a0001 | c0001 | t0005 | g0159 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19072 | hp2 | a0001 | c0001 | t0006 | g0284 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19085 | hp1 | a0001 | c0001 | t0005 | g0176 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0376 | AFR | YRI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | ASW | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0329 | EUR | TSI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA20805 | hp2 | a0001 | c0001 | t0008 | g0193 | EUR | TSI | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02486 | hp1 | a0001 | c0001 | t0019 | g0311 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0157 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0306 | AFR | MSL | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0269 | AFR | USA | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA18955 | hp2 | a0001 | c0001 | t0014 | g0171 | EAS | JPT | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | USA | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0368 | AFR | USA | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
NA21309 | hp2 | a0003 | c0003 | t0003 | g0366 | AFR | LWK | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0009 | g0197 | REF | REF | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0325 | REF | REF | PSEN1_chr14_73131507_73228691 | PSEN1 | chr14 | 73131507 | 73228691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73198103
|
C | T | 1 | a0002 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.842C>T | p.Thr281Met | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/12 | 1054/6018 | 842/1404 | 281/467 | chr14 | 73198103 | ||
chr14:73211803
|
G | C | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.990G>C | p.Glu330Asp | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/12 | 1202/6018 | 990/1404 | 330/467 | chr14 | 73211803 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73170847
|
C | T | 1 | a0001c0002 | 2 | HG00621.hp1 NA18942.hp1 |
synonymous_variant | LOW | c.138C>T | p.His46His | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/12 | 350/6018 | 138/1404 | 46/467 | chr14 | 73170847 | ||
chr14:73171030
|
C | G | 1 | a0001c0006 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.321C>G | p.Thr107Thr | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/12 | 533/6018 | 321/1404 | 107/467 | chr14 | 73171030 | ||
chr14:73211815
|
C | T | 1 | a0001c0004 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1002C>T | p.Gly334Gly | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/12 | 1214/6018 | 1002/1404 | 334/467 | chr14 | 73211815 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73219519
|
G | T | 1 | a0001c0001t0018 | 2 | HG02683.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*230G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 230 | chr14 | 73219519 | |||||
chr14:73219602
|
C | A | 3 | a0001c0001t0008a0001c0001t0011a0001c0001t0019 | 11 | HG00323.hp2 HG01261.hp2 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*313C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 313 | chr14 | 73219602 | |||||
chr14:73219653
|
T | C | 1 | a0001c0001t0009 | 6 | HG00642.hp1 HG01070.hp1 HG01192.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*364T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 364 | chr14 | 73219653 | |||||
chr14:73219785
|
G | A | 1 | a0001c0004t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 496 | chr14 | 73219785 | |||||
chr14:73219960
|
C | T | 1 | a0001c0001t0031 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 671 | chr14 | 73219960 | |||||
chr14:73220236
|
G | A | 4 | a0001c0001t0003a0001c0001t0009a0001c0001t0031others(1): Show | 54 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*947G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 947 | chr14 | 73220236 | |||||
chr14:73220306
|
GTGCTGTC others(5): Show |
G | 1 | a0001c0001t0012 | 4 | NA18964.hp1 NA18980.hp2 NA18986.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1027_*1038delCCCT others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1027 | INFO_REALIGN_3_PRIME | chr14 | 73220306 | ||||
chr14:73220436
|
C | T | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
3_prime_UTR_variant | MODIFIER | c.*1147C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1147 | chr14 | 73220436 | |||||
chr14:73220670
|
G | A | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG02257.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1381G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1381 | chr14 | 73220670 | |||||
chr14:73220773
|
A | C | 1 | a0001c0001t0023 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1484 | chr14 | 73220773 | |||||
chr14:73220821
|
C | T | 1 | a0001c0004t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1532C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1532 | chr14 | 73220821 | |||||
chr14:73220886
|
ACAGAGAG others(36): Show |
A | 1 | a0001c0001t0021 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1598_*1640delCAGA others(39): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1598 | chr14 | 73220886 | |||||
chr14:73220979
|
T | C | 2 | a0001c0001t0007a0001c0001t0026 | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1690T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1690 | chr14 | 73220979 | |||||
chr14:73221080
|
A | T | 1 | a0001c0001t0030 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1791A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 1791 | chr14 | 73221080 | |||||
chr14:73221397
|
G | A | 1 | a0001c0001t0022 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2108G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2108 | chr14 | 73221397 | |||||
chr14:73221685
|
G | A | 1 | a0001c0001t0027 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2396G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2396 | chr14 | 73221685 | |||||
chr14:73221719
|
T | C | 2 | a0001c0001t0007a0001c0001t0026 | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2430T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2430 | chr14 | 73221719 | |||||
chr14:73221733
|
C | T | 1 | a0001c0001t0019 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2444C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2444 | chr14 | 73221733 | |||||
chr14:73221832
|
C | T | 1 | a0001c0001t0010 | 5 | NA18944.hp2 NA18971.hp2 NA18991.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2543C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2543 | chr14 | 73221832 | |||||
chr14:73221922
|
G | C | 1 | a0001c0001t0028 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2633G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2633 | chr14 | 73221922 | |||||
chr14:73222153
|
A | C | 4 | a0001c0001t0005a0001c0001t0012a0001c0001t0014others(1): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2864A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 2864 | chr14 | 73222153 | |||||
chr14:73222647
|
A | G | 2 | a0001c0001t0017a0001c0001t0027 | 3 | HG01074.hp2 HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3358A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3358 | chr14 | 73222647 | |||||
chr14:73222649
|
A | G | 2 | a0001c0001t0007a0001c0001t0026 | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3360A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3360 | chr14 | 73222649 | |||||
chr14:73222669
|
T | C | 1 | a0001c0001t0014 | 2 | NA18955.hp2 NA18974.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3380T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3380 | chr14 | 73222669 | |||||
chr14:73222684
|
T | C | 1 | a0001c0001t0024 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3395T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3395 | chr14 | 73222684 | |||||
chr14:73222814
|
A | G | 2 | a0001c0001t0007a0001c0001t0026 | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3525A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3525 | chr14 | 73222814 | |||||
chr14:73222827
|
C | G | 2 | a0001c0001t0016a0001c0001t0025 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3538C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3538 | chr14 | 73222827 | |||||
chr14:73222855
|
A | G | 2 | a0001c0001t0017a0001c0001t0027 | 3 | HG01074.hp2 HG02723.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3566A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3566 | chr14 | 73222855 | |||||
chr14:73222921
|
G | A | 6 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(3): Show | 23 | HG00323.hp2 HG01243.hp2 HG01261.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3632G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3632 | chr14 | 73222921 | |||||
chr14:73222926
|
C | T | 2 | a0001c0001t0007a0001c0001t0026 | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3637C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3637 | chr14 | 73222926 | |||||
chr14:73223011
|
C | T | 2 | a0001c0001t0001a0001c0001t0010 | 122 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*3722C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3722 | chr14 | 73223011 | |||||
chr14:73223112
|
G | A | 2 | a0001c0001t0007a0001c0001t0026 | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3823G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3823 | chr14 | 73223112 | |||||
chr14:73223120
|
C | T | 1 | a0001c0001t0015 | 2 | HG01081.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3831C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3831 | chr14 | 73223120 | |||||
chr14:73223121
|
G | A | 1 | a0001c0001t0027 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3832G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3832 | chr14 | 73223121 | |||||
chr14:73223178
|
G | A | 2 | a0001c0001t0011a0001c0001t0019 | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3889G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3889 | chr14 | 73223178 | |||||
chr14:73223230
|
C | A | 1 | a0001c0004t0020 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3941C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 3941 | chr14 | 73223230 | |||||
chr14:73223319
|
A | G | 2 | a0001c0001t0013a0001c0001t0018 | 5 | HG02683.hp1 HG02698.hp2 HG03491.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4030A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 4030 | chr14 | 73223319 | |||||
chr14:73223436
|
T | G | 4 | a0001c0001t0006a0001c0001t0015a0001c0006t0006others(1): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4147T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 4147 | chr14 | 73223436 | |||||
chr14:73223630
|
A | G | 1 | a0001c0001t0029 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4341A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 4341 | chr14 | 73223630 | |||||
chr14:73223662
|
T | C | 1 | a0001c0001t0026 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4373T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 12/12 | 4373 | chr14 | 73223662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73136715
|
G | A | 4 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(1): Show | 4 | HG01169.hp2 HG01943.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+132G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73136715 | ||||||
chr14:73136745
|
C | T | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-136+162C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73136745 | ||||||
chr14:73136878
|
C | G | 5 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0002g0373others(2): Show | 5 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-136+295C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73136878 | ||||||
chr14:73136928
|
C | T | 1 | a0001c0001t0007g0370 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-136+345C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73136928 | ||||||
chr14:73136992
|
G | C | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-136+409G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73136992 | ||||||
chr14:73137265
|
C | G | 1 | a0001c0001t0002g0369 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-136+682C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73137265 | ||||||
chr14:73137324
|
A | G | 1 | a0001c0001t0002g0368 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-136+741A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73137324 | ||||||
chr14:73137533
|
G | T | 1 | a0001c0001t0009g0367 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-136+950G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73137533 | ||||||
chr14:73137784
|
A | G | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-136+1201A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73137784 | ||||||
chr14:73137870
|
G | C | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.-136+1287G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73137870 | ||||||
chr14:73137904
|
C | T | 2 | a0001c0001t0003g0313a0001c0001t0003g0314 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-136+1321C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73137904 | ||||||
chr14:73138069
|
C | CA | 13 | a0001c0001t0001g0007a0001c0001t0001g0099a0001c0001t0001g0100others(10): Show | 13 | HG00323.hp2 HG01123.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-136+1500dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138069 | |||||
chr14:73138069
|
CA | C | 12 | a0001c0001t0001g0098a0001c0001t0003g0303a0001c0001t0003g0305others(9): Show | 12 | HG01074.hp2 HG02486.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.-136+1500delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138069 | |||||
chr14:73138159
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-136+1576A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138159 | ||||||
chr14:73138159
|
A | T | 2 | a0001c0001t0015g0301a0001c0001t0015g0302 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-136+1576A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138159 | ||||||
chr14:73138161
|
C | T | 3 | a0001c0001t0003g0298a0001c0001t0003g0299a0001c0001t0003g0300 | 3 | HG00140.hp2 HG01433.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-136+1578C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138161 | ||||||
chr14:73138191
|
A | ATTAT | 14 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0099others(11): Show | 14 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-136+1647_-136+165 others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138191 | |||||
chr14:73138191
|
ATTAT | A | 229 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(226): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.-136+1647_-136+165 others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138191 | |||||
chr14:73138191
|
ATTATTTA others(1): Show |
A | 25 | a0001c0001t0001g0095a0001c0001t0002g0266a0001c0001t0002g0270others(22): Show | 25 | HG00408.hp1 HG01074.hp2 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136+1643_-136+165 others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138191 | |||||
chr14:73138191
|
ATTATTTA others(5): Show |
A | 14 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(11): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.-136+1639_-136+165 others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138191 | |||||
chr14:73138191
|
ATTATTTA others(9): Show |
A | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0004g0295others(2): Show | 5 | HG00140.hp1 HG01496.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.-136+1635_-136+165 others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138191 | |||||
chr14:73138380
|
G | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-136+1797G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138380 | ||||||
chr14:73138385
|
A | AT | 9 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0149others(6): Show | 9 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-136+1809dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138385 | |||||
chr14:73138402
|
G | T | 1 | a0001c0001t0001g0093 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-136+1819G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138402 | ||||||
chr14:73138405
|
G | A | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-136+1822G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138405 | ||||||
chr14:73138407
|
C | G | 1 | a0001c0001t0005g0265 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-136+1824C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138407 | ||||||
chr14:73138452
|
C | T | 1 | a0001c0001t0004g0264 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-136+1869C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138452 | ||||||
chr14:73138597
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+2014C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138597 | ||||||
chr14:73138696
|
C | T | 9 | a0001c0001t0002g0357a0001c0001t0002g0358a0001c0001t0002g0359others(6): Show | 9 | HG00558.hp2 HG02015.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+2113C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138696 | ||||||
chr14:73138709
|
C | T | 3 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284 | 3 | HG00408.hp1 NA18747.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.-136+2126C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138709 | ||||||
chr14:73138787
|
A | G | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.-136+2204A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138787 | ||||||
chr14:73138795
|
T | C | 2 | a0001c0001t0004g0101a0001c0001t0004g0116 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-136+2212T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138795 | ||||||
chr14:73138804
|
C | CA | 19 | a0001c0001t0002g0319a0001c0001t0002g0368a0001c0001t0004g0120others(16): Show | 19 | HG00423.hp2 HG00621.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.-136+2234dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73138804 | |||||
chr14:73138823
|
C | A | 39 | a0001c0001t0002g0185a0001c0001t0005g0001a0001c0001t0005g0102others(36): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-136+2240C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138823 | ||||||
chr14:73138825
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-136+2242G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138825 | ||||||
chr14:73138915
|
G | A | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-136+2332G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138915 | ||||||
chr14:73138972
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-136+2389A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138972 | ||||||
chr14:73138975
|
G | A | 25 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(22): Show | 25 | HG00323.hp2 HG01074.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.-136+2392G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73138975 | ||||||
chr14:73139080
|
G | C | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+2497G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139080 | ||||||
chr14:73139082
|
G | A | 2 | a0001c0001t0008g0106a0001c0001t0008g0107 | 2 | HG00323.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-136+2499G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139082 | ||||||
chr14:73139117
|
A | T | 1 | a0001c0001t0007g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-136+2534A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139117 | ||||||
chr14:73139123
|
A | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+2540A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139123 | ||||||
chr14:73139124
|
G | A | 6 | a0001c0001t0002g0327a0001c0001t0002g0328a0001c0001t0002g0329others(3): Show | 6 | HG00099.hp1 HG00323.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+2541G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139124 | ||||||
chr14:73139192
|
A | T | 4 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-136+2609A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139192 | ||||||
chr14:73139203
|
A | G | 1 | a0001c0001t0007g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-136+2620A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139203 | ||||||
chr14:73139287
|
T | A | 7 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(4): Show | 7 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+2704T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139287 | ||||||
chr14:73139288
|
T | A | 15 | a0001c0001t0003g0194a0001c0001t0003g0298a0001c0001t0003g0299others(12): Show | 15 | HG00140.hp2 HG00323.hp2 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.-136+2705T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139288 | ||||||
chr14:73139327
|
G | A | 1 | a0001c0001t0017g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-136+2744G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139327 | ||||||
chr14:73139378
|
G | A | 48 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(45): Show | 49 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-136+2795G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139378 | ||||||
chr14:73139529
|
G | A | 1 | a0001c0001t0006g0128 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-136+2946G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139529 | ||||||
chr14:73139567
|
G | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-136+2984G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139567 | ||||||
chr14:73139591
|
A | G | 1 | a0001c0001t0005g0190 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-136+3008A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139591 | ||||||
chr14:73139890
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-136+3307G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73139890 | ||||||
chr14:73140063
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+3480A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140063 | ||||||
chr14:73140140
|
C | T | 1 | a0001c0001t0003g0127 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-136+3557C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140140 | ||||||
chr14:73140202
|
C | CT | 21 | a0001c0001t0002g0266a0001c0001t0002g0315a0001c0001t0002g0316others(18): Show | 21 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-136+3645dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73140202 | |||||
chr14:73140202
|
C | CTT | 6 | a0001c0001t0002g0319a0001c0001t0008g0106a0001c0001t0008g0107others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+3644_-136+364 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73140202 | |||||
chr14:73140202
|
CT | C | 193 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.-136+3645delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73140202 | |||||
chr14:73140202
|
CTT | C | 7 | a0001c0001t0001g0041a0001c0001t0003g0196a0001c0001t0011g0306others(4): Show | 7 | HG01074.hp2 HG02155.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-136+3644_-136+364 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73140202 | |||||
chr14:73140202
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-136+3634_-136+364 others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73140202 | |||||
chr14:73140296
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-136+3713C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140296 | ||||||
chr14:73140332
|
TC | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0152 | 3 | HG02258.hp1 HG02258.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-136+3752delC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73140332 | |||||
chr14:73140662
|
A | G | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+4079A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140662 | ||||||
chr14:73140739
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-136+4156C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140739 | ||||||
chr14:73140780
|
G | A | 2 | a0001c0001t0008g0191a0001c0001t0008g0192 | 2 | HG01261.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-136+4197G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140780 | ||||||
chr14:73140897
|
G | T | 1 | a0001c0001t0006g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-136+4314G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140897 | ||||||
chr14:73140921
|
G | C | 8 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-136+4338G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73140921 | ||||||
chr14:73141035
|
G | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-136+4452G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141035 | ||||||
chr14:73141056
|
A | G | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-136+4473A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141056 | ||||||
chr14:73141135
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-136+4552T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141135 | ||||||
chr14:73141316
|
G | GA | 26 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0266others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.-136+4745dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73141316 | |||||
chr14:73141419
|
C | T | 6 | a0001c0001t0003g0108a0001c0001t0003g0123a0001c0001t0003g0124others(3): Show | 6 | HG00423.hp1 HG02155.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+4836C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141419 | ||||||
chr14:73141562
|
C | G | 6 | a0001c0001t0004g0251a0001c0001t0004g0252a0001c0001t0004g0253others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.-136+4979C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141562 | ||||||
chr14:73141619
|
T | A | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-136+5036T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141619 | ||||||
chr14:73141658
|
G | A | 1 | a0001c0001t0001g0010 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-136+5075G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141658 | ||||||
chr14:73141692
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-136+5109G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141692 | ||||||
chr14:73141717
|
G | A | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-136+5134G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141717 | ||||||
chr14:73141761
|
G | A | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+5178G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141761 | ||||||
chr14:73141806
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-136+5223G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141806 | ||||||
chr14:73141839
|
T | G | 32 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0266others(29): Show | 32 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-136+5256T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141839 | ||||||
chr14:73141851
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+5268A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141851 | ||||||
chr14:73141895
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-136+5312G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73141895 | ||||||
chr14:73142045
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+5462C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142045 | ||||||
chr14:73142053
|
G | C | 1 | a0001c0001t0002g0371 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-136+5470G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142053 | ||||||
chr14:73142061
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-136+5478C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142061 | ||||||
chr14:73142066
|
C | CA | 9 | a0001c0001t0001g0010a0001c0001t0002g0261a0001c0001t0002g0262others(6): Show | 9 | HG01891.hp1 HG01943.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-136+5497dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73142066 | |||||
chr14:73142079
|
A | G | 7 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(4): Show | 7 | HG02055.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-136+5496A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142079 | ||||||
chr14:73142248
|
A | G | 1 | a0001c0001t0005g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-135-5547A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142248 | ||||||
chr14:73142299
|
A | G | 25 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0266others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.-135-5496A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142299 | ||||||
chr14:73142404
|
T | C | 3 | a0001c0001t0009g0197a0001c0001t0009g0198a0001c0001t0009g0225 | 3 | HG01070.hp1 HG01192.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-135-5391T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142404 | ||||||
chr14:73142423
|
C | A | 3 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0190 | 3 | NA18612.hp2 NA18959.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-135-5372C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142423 | ||||||
chr14:73142530
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-135-5265G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142530 | ||||||
chr14:73142861
|
G | C | 1 | a0001c0001t0005g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-135-4934G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142861 | ||||||
chr14:73142904
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-135-4891T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142904 | ||||||
chr14:73142943
|
G | A | 375 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(372): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-135-4852G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142943 | ||||||
chr14:73142974
|
C | T | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-135-4821C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73142974 | ||||||
chr14:73143063
|
A | C | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-135-4732A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143063 | ||||||
chr14:73143102
|
G | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-135-4693G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143102 | ||||||
chr14:73143121
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-135-4674C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143121 | ||||||
chr14:73143130
|
A | G | 2 | a0001c0001t0003g0313a0001c0001t0003g0314 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-135-4665A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143130 | ||||||
chr14:73143161
|
G | A | 8 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-4634G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143161 | ||||||
chr14:73143436
|
A | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-135-4359A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143436 | ||||||
chr14:73143456
|
T | G | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-135-4339T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143456 | ||||||
chr14:73143529
|
T | G | 1 | a0001c0001t0002g0320 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-135-4266T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143529 | ||||||
chr14:73143556
|
G | C | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-135-4239G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143556 | ||||||
chr14:73143676
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-135-4119C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143676 | ||||||
chr14:73143702
|
A | G | 2 | a0001c0001t0008g0191a0001c0001t0008g0192 | 2 | HG01261.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-135-4093A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143702 | ||||||
chr14:73143707
|
G | A | 1 | a0001c0001t0009g0201 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-135-4088G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143707 | ||||||
chr14:73143803
|
A | C | 2 | a0001c0001t0002g0320a0001c0001t0002g0324 | 2 | HG01069.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.-135-3992A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73143803 | ||||||
chr14:73143988
|
T | TA | 9 | a0001c0001t0002g0315a0001c0001t0003g0126a0001c0001t0003g0202others(6): Show | 9 | HG01192.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-135-3780dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73143988 | |||||
chr14:73143988
|
TA | T | 191 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(188): Show | 192 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-135-3780delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73143988 | |||||
chr14:73143988
|
TAA | T | 18 | a0001c0001t0001g0035a0001c0001t0001g0084a0001c0001t0001g0098others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-135-3781_-135-378 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73143988 | |||||
chr14:73143988
|
TAAAA | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-3783_-135-378 others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73143988 | |||||
chr14:73144035
|
C | CT | 52 | a0001c0001t0001g0054a0001c0001t0001g0114a0001c0001t0001g0250others(49): Show | 52 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.-135-3737dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73144035 | |||||
chr14:73144035
|
C | CTT | 8 | a0001c0001t0004g0006a0001c0001t0004g0116a0001c0001t0004g0236others(5): Show | 8 | HG00741.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-3738_-135-373 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73144035 | |||||
chr14:73144035
|
CT | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(126): Show | 130 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-135-3737delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73144035 | |||||
chr14:73144035
|
CTT | C | 18 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(15): Show | 18 | HG00323.hp2 HG00735.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.-135-3738_-135-373 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73144035 | |||||
chr14:73144035
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0003g0298a0001c0001t0003g0299a0001c0001t0003g0300 | 3 | HG00140.hp2 HG01433.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-135-3747_-135-373 others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73144035 | |||||
chr14:73144063
|
T | TG | 3 | a0001c0001t0003g0151a0001c0001t0003g0303a0001c0001t0004g0304 | 3 | HG02976.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-135-3730dupG | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73144063 | |||||
chr14:73144477
|
A | G | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-135-3318A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73144477 | ||||||
chr14:73144528
|
C | A | 1 | a0001c0001t0003g0305 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-135-3267C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73144528 | ||||||
chr14:73144544
|
G | A | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-135-3251G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73144544 | ||||||
chr14:73144546
|
A | C | 3 | a0001c0001t0004g0143a0001c0001t0029g0133a0001c0001t0030g0168 | 3 | HG02257.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-135-3249A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73144546 | ||||||
chr14:73144664
|
G | A | 1 | a0001c0001t0006g0273 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-135-3131G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73144664 | ||||||
chr14:73145048
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-2747A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145048 | ||||||
chr14:73145134
|
C | T | 35 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(32): Show | 35 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.-135-2661C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145134 | ||||||
chr14:73145185
|
G | A | 47 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(44): Show | 48 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-135-2610G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145185 | ||||||
chr14:73145189
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-135-2606G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145189 | ||||||
chr14:73145324
|
A | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-135-2471A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145324 | ||||||
chr14:73145360
|
G | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-135-2435G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145360 | ||||||
chr14:73145460
|
G | A | 2 | a0001c0001t0005g0175a0001c0001t0005g0176 | 2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-135-2335G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145460 | ||||||
chr14:73145724
|
T | G | 1 | a0001c0001t0012g0188 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-135-2071T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145724 | ||||||
chr14:73145804
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-135-1991A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145804 | ||||||
chr14:73145880
|
G | A | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-135-1915G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73145880 | ||||||
chr14:73146060
|
C | T | 30 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(27): Show | 30 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-135-1735C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146060 | ||||||
chr14:73146184
|
C | CT | 97 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(94): Show | 97 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-135-1590dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73146184 | |||||
chr14:73146184
|
CT | C | 27 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0002g0259others(24): Show | 27 | HG00408.hp1 HG00544.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-135-1590delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73146184 | |||||
chr14:73146184
|
CTT | C | 8 | a0001c0001t0006g0257a0001c0001t0006g0284a0001c0001t0011g0306others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-135-1591_-135-159 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73146184 | |||||
chr14:73146206
|
A | T | 1 | a0001c0001t0005g0121 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-135-1589A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146206 | ||||||
chr14:73146231
|
C | T | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-135-1564C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146231 | ||||||
chr14:73146286
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-135-1509C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146286 | ||||||
chr14:73146296
|
C | T | 1 | a0001c0001t0003g0194 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-135-1499C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146296 | ||||||
chr14:73146334
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-1461C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146334 | ||||||
chr14:73146433
|
T | C | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-1362T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146433 | ||||||
chr14:73146844
|
T | A | 4 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-135-951T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146844 | ||||||
chr14:73146946
|
T | C | 26 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-135-849T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146946 | ||||||
chr14:73146969
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-135-826A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73146969 | ||||||
chr14:73147044
|
C | CT | 44 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(41): Show | 45 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-135-735dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73147044 | |||||
chr14:73147060
|
T | TC | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-135-734dupC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73147060 | |||||
chr14:73147104
|
G | A | 16 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(13): Show | 16 | HG00408.hp1 HG00544.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-135-691G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147104 | ||||||
chr14:73147201
|
G | A | 2 | a0001c0001t0004g0234a0001c0001t0004g0246 | 2 | HG04199.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-135-594G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147201 | ||||||
chr14:73147250
|
C | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-135-545C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147250 | ||||||
chr14:73147338
|
T | G | 1 | a0001c0001t0003g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-135-457T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147338 | ||||||
chr14:73147454
|
G | A | 2 | a0001c0001t0004g0237a0001c0001t0004g0238 | 2 | HG00544.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-135-341G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147454 | ||||||
chr14:73147509
|
G | C | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-135-286G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147509 | ||||||
chr14:73147616
|
T | G | 1 | a0001c0001t0002g0354 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-135-179T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147616 | ||||||
chr14:73147638
|
C | CTACCTTG others(4): Show |
3 | a0001c0001t0012g0178a0001c0001t0012g0179a0001c0001t0012g0184 | 3 | NA18964.hp1 NA18980.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-135-154_-135-144d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr14 | 73147638 | |||||
chr14:73147679
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-135-116C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 1/11 | chr14 | 73147679 | ||||||
chr14:73148192
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.87+86A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148192 | ||||||
chr14:73148358
|
G | A | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.87+252G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148358 | ||||||
chr14:73148412
|
G | A | 1 | a0001c0001t0002g0355 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.87+306G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148412 | ||||||
chr14:73148548
|
C | T | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+442C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148548 | ||||||
chr14:73148561
|
G | T | 1 | a0001c0001t0007g0370 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.87+455G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148561 | ||||||
chr14:73148641
|
T | A | 1 | a0001c0001t0004g0239 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.87+535T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148641 | ||||||
chr14:73148687
|
C | G | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.87+581C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148687 | ||||||
chr14:73148902
|
C | G | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.87+796C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148902 | ||||||
chr14:73148911
|
C | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+805C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148911 | ||||||
chr14:73148914
|
C | T | 2 | a0001c0002t0005g0118a0001c0002t0005g0119 | 2 | HG00621.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.87+808C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148914 | ||||||
chr14:73148945
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.87+839T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73148945 | ||||||
chr14:73149020
|
T | C | 69 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(66): Show | 69 | HG00408.hp1 HG00544.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.87+914T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149020 | ||||||
chr14:73149199
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.87+1093C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149199 | ||||||
chr14:73149323
|
T | G | 2 | a0001c0001t0004g0143a0001c0001t0029g0133 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.87+1217T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149323 | ||||||
chr14:73149353
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.87+1247G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149353 | ||||||
chr14:73149387
|
A | T | 73 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(70): Show | 73 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.87+1281A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149387 | ||||||
chr14:73149416
|
A | G | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.87+1310A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149416 | ||||||
chr14:73149521
|
A | G | 1 | a0001c0001t0001g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.87+1415A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149521 | ||||||
chr14:73149802
|
C | A | 1 | a0001c0001t0004g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.87+1696C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149802 | ||||||
chr14:73149840
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.87+1734A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149840 | ||||||
chr14:73149927
|
G | A | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+1821G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73149927 | ||||||
chr14:73150164
|
C | T | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.87+2058C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150164 | ||||||
chr14:73150440
|
G | A | 1 | a0001c0001t0006g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.87+2334G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150440 | ||||||
chr14:73150445
|
G | A | 7 | a0001c0001t0001g0059a0001c0001t0011g0306a0001c0001t0011g0308others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.87+2339G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150445 | ||||||
chr14:73150605
|
A | G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+2499A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150605 | ||||||
chr14:73150610
|
G | A | 43 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.87+2504G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150610 | ||||||
chr14:73150764
|
CA | C | 183 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0021others(180): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.87+2682delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73150764 | |||||
chr14:73150764
|
CAA | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.87+2681_87+2682del others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73150764 | |||||
chr14:73150798
|
G | A | 1 | a0001c0001t0002g0356 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.87+2692G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150798 | ||||||
chr14:73150808
|
G | A | 45 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(42): Show | 46 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.87+2702G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150808 | ||||||
chr14:73150839
|
G | A | 1 | a0001c0001t0003g0203 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.87+2733G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150839 | ||||||
chr14:73150938
|
C | T | 1 | a0001c0001t0004g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.87+2832C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73150938 | ||||||
chr14:73151046
|
C | T | 31 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(28): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.87+2940C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151046 | ||||||
chr14:73151077
|
A | G | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.87+2971A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151077 | ||||||
chr14:73151097
|
G | A | 1 | a0001c0001t0002g0357 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.87+2991G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151097 | ||||||
chr14:73151330
|
G | A | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.87+3224G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151330 | ||||||
chr14:73151372
|
A | C | 1 | a0001c0001t0005g0183 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.87+3266A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151372 | ||||||
chr14:73151372
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+3266A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151372 | ||||||
chr14:73151465
|
A | G | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.87+3359A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151465 | ||||||
chr14:73151490
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.87+3384G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151490 | ||||||
chr14:73151684
|
C | T | 15 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.87+3578C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151684 | ||||||
chr14:73151830
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.87+3724A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151830 | ||||||
chr14:73151860
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+3754C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151860 | ||||||
chr14:73151878
|
T | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.87+3772T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151878 | ||||||
chr14:73151878
|
T | TTATATAT others(3): Show |
1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.87+3780_87+3789dup others(10): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTATATAT others(7): Show |
1 | a0001c0001t0011g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.87+3776_87+3789dup others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTATATAT others(9): Show |
1 | a0001c0001t0006g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.87+3774_87+3789dup others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTATATAT others(21): Show |
1 | a0002c0005t0006g0274 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(28): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTATATAT others(23): Show |
1 | a0001c0001t0006g0272 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(30): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTATATAT others(25): Show |
1 | a0001c0001t0006g0281 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(32): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTATATAT others(37): Show |
1 | a0001c0001t0006g0128 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(44): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151878
|
T | TTTTATAT others(17): Show |
1 | a0001c0001t0015g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.87+3773_87+3774ins others(24): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151878 | |||||
chr14:73151880
|
A | T | 1 | a0001c0001t0015g0302 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.87+3774A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151880 | ||||||
chr14:73151882
|
A | T | 1 | a0001c0001t0005g0159 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.87+3776A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151882 | ||||||
chr14:73151892
|
ATATTTTT others(4): Show |
A | 1 | a0001c0001t0011g0309 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.87+3788_87+3798del others(11): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151892 | |||||
chr14:73151892
|
ATATTTTT others(6): Show |
A | 1 | a0001c0001t0002g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.87+3788_87+3800del others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151892 | |||||
chr14:73151892
|
ATATTTTT others(8): Show |
A | 1 | a0001c0001t0028g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.87+3788_87+3802del others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151892 | |||||
chr14:73151893
|
TA | T | 7 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0322others(4): Show | 7 | HG01106.hp1 HG01167.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.87+3788delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151893 | ||||||
chr14:73151894
|
A | G | 1 | a0001c0001t0006g0276 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.87+3788A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151894 | ||||||
chr14:73151894
|
A | T | 2 | a0001c0001t0002g0317a0001c0001t0002g0363 | 2 | HG02135.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.87+3788A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151894 | ||||||
chr14:73151894
|
AT | A | 15 | a0001c0001t0001g0012a0001c0001t0002g0331a0001c0001t0002g0333others(12): Show | 15 | HG01175.hp1 HG01192.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.87+3823delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151894
|
ATT | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(61): Show | 64 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.87+3822_87+3823del others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151894
|
ATTT | A | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.87+3821_87+3823del others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151894
|
ATTTT | A | 56 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0068others(53): Show | 57 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.87+3820_87+3823del others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151894
|
ATTTTT | A | 63 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0104others(60): Show | 63 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.87+3819_87+3823del others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151894
|
ATTTTTT | A | 26 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0110others(23): Show | 27 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.87+3818_87+3823del others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151894
|
ATTTTTTT | A | 6 | a0001c0001t0001g0111a0001c0001t0001g0135a0001c0001t0004g0143others(3): Show | 6 | HG02717.hp2 HG02922.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+3817_87+3823del others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73151894 | |||||
chr14:73151895
|
T | TATATATA others(8): Show |
1 | a0001c0001t0019g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(10): Show |
1 | a0001c0001t0011g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(12): Show |
1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(19): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(14): Show |
1 | a0001c0001t0011g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(21): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(16): Show |
1 | a0001c0001t0015g0302 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(23): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(20): Show |
3 | a0001c0001t0006g0273a0001c0001t0006g0283a0001c0001t0006g0284 | 3 | HG00408.hp1 HG01975.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.87+3789_87+3790ins others(27): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(22): Show |
1 | a0001c0001t0006g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(29): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(26): Show |
1 | a0001c0001t0006g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(33): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(28): Show |
4 | a0001c0001t0006g0257a0001c0001t0006g0275a0001c0001t0006g0277others(1): Show | 4 | HG03704.hp2 NA18747.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+3789_87+3790ins others(35): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(30): Show |
1 | a0001c0001t0006g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(37): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151895
|
T | TATATATA others(32): Show |
1 | a0001c0001t0006g0276 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.87+3789_87+3790ins others(39): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151895 | ||||||
chr14:73151896
|
T | A | 12 | a0001c0001t0001g0083a0001c0001t0002g0327a0001c0001t0006g0128others(9): Show | 12 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(9): Show |
intron_variant | MODIFIER | c.87+3790T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151896 | ||||||
chr14:73151897
|
T | A | 20 | a0001c0001t0001g0012a0001c0001t0002g0333a0001c0001t0003g0194others(17): Show | 20 | HG00408.hp1 HG01081.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.87+3791T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151897 | ||||||
chr14:73151898
|
T | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(49): Show | 52 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.87+3792T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151898 | ||||||
chr14:73151899
|
T | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 103 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.87+3793T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151899 | ||||||
chr14:73151900
|
T | A | 70 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0049others(67): Show | 71 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.87+3794T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151900 | ||||||
chr14:73151901
|
T | A | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 108 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.87+3795T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151901 | ||||||
chr14:73151902
|
T | A | 53 | a0001c0001t0001g0051a0001c0001t0001g0088a0001c0001t0001g0100others(50): Show | 54 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.87+3796T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151902 | ||||||
chr14:73151903
|
T | A | 75 | a0001c0001t0001g0061a0001c0001t0001g0111a0001c0001t0001g0129others(72): Show | 75 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.87+3797T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151903 | ||||||
chr14:73151904
|
T | A | 26 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113others(23): Show | 27 | HG00323.hp2 HG01074.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.87+3798T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151904 | ||||||
chr14:73151905
|
T | A | 40 | a0001c0001t0001g0111a0001c0001t0001g0135a0001c0001t0002g0185others(37): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.87+3799T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151905 | ||||||
chr14:73151906
|
T | A | 3 | a0001c0001t0005g0001a0001c0001t0016g0267a0001c0001t0027g0307 | 4 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.87+3800T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151906 | ||||||
chr14:73151907
|
T | A | 6 | a0001c0001t0001g0135a0001c0001t0005g0174a0001c0001t0006g0278others(3): Show | 6 | HG02027.hp1 HG02056.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+3801T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151907 | ||||||
chr14:73151908
|
T | A | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.87+3802T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151908 | ||||||
chr14:73151909
|
T | A | 1 | a0001c0001t0006g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.87+3803T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73151909 | ||||||
chr14:73152005
|
G | A | 9 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(6): Show | 9 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.87+3899G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152005 | ||||||
chr14:73152062
|
C | T | 6 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+3956C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152062 | ||||||
chr14:73152102
|
G | A | 1 | a0001c0001t0003g0207 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.87+3996G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152102 | ||||||
chr14:73152112
|
C | T | 1 | a0001c0001t0004g0003 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.87+4006C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152112 | ||||||
chr14:73152158
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0002g0369 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.87+4052C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152158 | ||||||
chr14:73152440
|
G | GA | 14 | a0001c0001t0005g0180a0001c0001t0005g0183a0001c0001t0007g0154others(11): Show | 14 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.87+4351dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73152440 | |||||
chr14:73152440
|
GA | G | 30 | a0001c0001t0001g0041a0001c0001t0003g0151a0001c0001t0003g0303others(27): Show | 30 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.87+4351delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73152440 | |||||
chr14:73152478
|
G | A | 1 | a0001c0001t0005g0176 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.87+4372G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152478 | ||||||
chr14:73152506
|
C | A | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4400C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152506 | ||||||
chr14:73152510
|
A | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4404A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152510 | ||||||
chr14:73152513
|
A | G | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4407A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152513 | ||||||
chr14:73152514
|
C | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4408C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152514 | ||||||
chr14:73152517
|
G | A | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4411G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152517 | ||||||
chr14:73152527
|
A | C | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4421A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152527 | ||||||
chr14:73152531
|
C | G | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4425C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152531 | ||||||
chr14:73152532
|
A | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4426A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152532 | ||||||
chr14:73152533
|
G | A | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4427G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152533 | ||||||
chr14:73152543
|
G | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4437G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152543 | ||||||
chr14:73152548
|
A | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4442A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152548 | ||||||
chr14:73152549
|
G | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4443G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152549 | ||||||
chr14:73152556
|
G | T | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4450G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152556 | ||||||
chr14:73152557
|
A | G | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4451A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152557 | ||||||
chr14:73152562
|
G | C | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4456G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152562 | ||||||
chr14:73152565
|
C | G | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4459C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152565 | ||||||
chr14:73152574
|
C | T | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.87+4468C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152574 | ||||||
chr14:73152575
|
C | G | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4469C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152575 | ||||||
chr14:73152598
|
G | A | 78 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(75): Show | 78 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.87+4492G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152598 | ||||||
chr14:73152627
|
A | C | 1 | a0001c0001t0003g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.87+4521A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152627 | ||||||
chr14:73152762
|
G | A | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+4656G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152762 | ||||||
chr14:73152769
|
A | C | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+4663A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152769 | ||||||
chr14:73152780
|
C | T | 3 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0230 | 3 | NA18955.hp1 NA18991.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.87+4674C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152780 | ||||||
chr14:73152946
|
A | G | 26 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.87+4840A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73152946 | ||||||
chr14:73153057
|
T | A | 1 | a0001c0001t0001g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.87+4951T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153057 | ||||||
chr14:73153313
|
A | G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+5207A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153313 | ||||||
chr14:73153352
|
A | G | 1 | a0001c0001t0003g0223 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.87+5246A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153352 | ||||||
chr14:73153528
|
T | G | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.87+5422T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153528 | ||||||
chr14:73153662
|
A | AT | 249 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(246): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.87+5570dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73153662 | |||||
chr14:73153662
|
A | ATT | 21 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0020others(18): Show | 21 | HG00408.hp2 HG01361.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.87+5569_87+5570dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73153662 | |||||
chr14:73153679
|
C | G | 1 | a0001c0001t0004g0245 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.87+5573C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153679 | ||||||
chr14:73153714
|
C | CT | 64 | a0001c0001t0001g0022a0001c0001t0001g0132a0001c0001t0002g0141others(61): Show | 64 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.87+5624dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73153714 | |||||
chr14:73153714
|
CT | C | 8 | a0001c0001t0001g0056a0001c0001t0002g0320a0001c0001t0002g0328others(5): Show | 8 | HG01069.hp1 HG01256.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.87+5624delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73153714 | |||||
chr14:73153751
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.87+5645C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153751 | ||||||
chr14:73153829
|
T | C | 15 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.87+5723T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153829 | ||||||
chr14:73153854
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+5748C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153854 | ||||||
chr14:73153945
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+5839C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153945 | ||||||
chr14:73153962
|
C | T | 41 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(38): Show | 41 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.87+5856C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153962 | ||||||
chr14:73153983
|
G | A | 1 | a0001c0001t0018g0344 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.87+5877G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73153983 | ||||||
chr14:73154050
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.87+5944G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154050 | ||||||
chr14:73154122
|
A | G | 1 | a0001c0001t0005g0001 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.87+6016A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154122 | ||||||
chr14:73154195
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+6089A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154195 | ||||||
chr14:73154203
|
G | T | 1 | a0001c0001t0012g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87+6097G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154203 | ||||||
chr14:73154207
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+6101A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154207 | ||||||
chr14:73154288
|
C | T | 2 | a0001c0001t0014g0171a0001c0001t0014g0177 | 2 | NA18955.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.87+6182C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154288 | ||||||
chr14:73154434
|
C | CA | 251 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(248): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.87+6338dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73154434 | |||||
chr14:73154434
|
C | CAA | 18 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.87+6337_87+6338dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73154434 | |||||
chr14:73154541
|
C | T | 2 | a0001c0001t0006g0140a0001c0001t0006g0257 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.87+6435C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154541 | ||||||
chr14:73154596
|
G | C | 1 | a0001c0001t0008g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.87+6490G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154596 | ||||||
chr14:73154677
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.87+6571A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154677 | ||||||
chr14:73154831
|
A | C | 1 | a0001c0001t0002g0146 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.87+6725A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154831 | ||||||
chr14:73154865
|
A | G | 2 | a0001c0001t0004g0143a0001c0001t0029g0133 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.87+6759A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154865 | ||||||
chr14:73154868
|
A | G | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.87+6762A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154868 | ||||||
chr14:73154909
|
A | G | 2 | a0001c0001t0004g0101a0001c0001t0004g0116 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.87+6803A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73154909 | ||||||
chr14:73155089
|
T | C | 11 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0020others(8): Show | 11 | HG00408.hp2 HG02080.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.87+6983T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73155089 | ||||||
chr14:73155770
|
C | T | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.87+7664C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73155770 | ||||||
chr14:73155875
|
A | G | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.87+7769A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73155875 | ||||||
chr14:73155954
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+7848G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73155954 | ||||||
chr14:73156000
|
T | C | 56 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.87+7894T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156000 | ||||||
chr14:73156031
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.87+7925C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156031 | ||||||
chr14:73156040
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.87+7934C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156040 | ||||||
chr14:73156055
|
T | A | 15 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.87+7949T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156055 | ||||||
chr14:73156105
|
C | T | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+7999C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156105 | ||||||
chr14:73156215
|
G | T | 5 | a0001c0001t0002g0371a0001c0001t0002g0372a0001c0001t0002g0373others(2): Show | 5 | NA18971.hp1 NA18975.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+8109G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156215 | ||||||
chr14:73156257
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0041 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.87+8151G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156257 | ||||||
chr14:73156466
|
C | T | 31 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(28): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.87+8360C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156466 | ||||||
chr14:73156559
|
A | C | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.87+8453A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156559 | ||||||
chr14:73156833
|
T | G | 1 | a0001c0001t0005g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.87+8727T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73156833 | ||||||
chr14:73157126
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(60): Show | 63 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.87+9020C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157126 | ||||||
chr14:73157127
|
C | CT | 6 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+9034dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73157127 | |||||
chr14:73157127
|
CT | C | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.87+9034delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73157127 | |||||
chr14:73157178
|
T | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0082 | 2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.87+9072T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157178 | ||||||
chr14:73157188
|
T | C | 8 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.87+9082T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157188 | ||||||
chr14:73157196
|
G | T | 17 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(14): Show | 17 | HG00323.hp2 HG01243.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.87+9090G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157196 | ||||||
chr14:73157382
|
G | A | 4 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0192others(1): Show | 4 | HG01261.hp2 HG03831.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+9276G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157382 | ||||||
chr14:73157430
|
C | T | 2 | a0001c0001t0016g0279a0001c0001t0025g0269 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.87+9324C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157430 | ||||||
chr14:73157486
|
G | A | 1 | a0001c0001t0002g0357 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.87+9380G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157486 | ||||||
chr14:73157497
|
A | G | 6 | a0001c0001t0004g0251a0001c0001t0004g0252a0001c0001t0004g0253others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.87+9391A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157497 | ||||||
chr14:73157500
|
C | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.87+9394C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157500 | ||||||
chr14:73157580
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.87+9474A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157580 | ||||||
chr14:73157587
|
C | T | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.87+9481C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157587 | ||||||
chr14:73157589
|
A | G | 1 | a0001c0001t0003g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.87+9483A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157589 | ||||||
chr14:73157917
|
C | T | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+9811C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73157917 | ||||||
chr14:73158056
|
A | C | 4 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0192others(1): Show | 4 | HG01261.hp2 HG03831.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.87+9950A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158056 | ||||||
chr14:73158254
|
A | G | 2 | a0001c0001t0007g0156a0001c0001t0007g0157 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.87+10148A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158254 | ||||||
chr14:73158282
|
T | TTCTA | 133 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.87+10226_87+10229d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
T | TTCTATCT others(1): Show |
44 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 44 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.87+10222_87+10229d others(10): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
T | TTCTATCT others(5): Show |
5 | a0001c0001t0001g0070a0001c0001t0001g0086a0001c0001t0003g0123others(2): Show | 5 | HG01952.hp1 HG02155.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.87+10218_87+10229d others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
T | TTCTATCT others(9): Show |
1 | a0001c0001t0004g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.87+10191_87+10192i others(18): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
TTCTA | T | 41 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0055others(38): Show | 41 | HG00408.hp2 HG01099.hp1 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.87+10226_87+10229d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
TTCTATCT others(1): Show |
T | 10 | a0001c0001t0001g0099a0001c0001t0001g0137a0001c0001t0002g0141others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.87+10222_87+10229d others(10): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
TTCTATCT others(5): Show |
T | 6 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0138others(3): Show | 6 | HG01106.hp2 HG02258.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+10218_87+10229d others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158282
|
TTCTATCT others(9): Show |
T | 1 | a0001c0001t0008g0106 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.87+10214_87+10229d others(18): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158282 | |||||
chr14:73158286
|
A | ATCTATCT others(5): Show |
2 | a0001c0001t0004g0292a0001c0001t0004g0294 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.87+10191_87+10192i others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73158286 | |||||
chr14:73158290
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.87+10184A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158290 | ||||||
chr14:73158345
|
G | A | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+10239G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158345 | ||||||
chr14:73158442
|
C | G | 2 | a0001c0001t0004g0101a0001c0001t0004g0116 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.87+10336C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158442 | ||||||
chr14:73158659
|
C | T | 78 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(75): Show | 78 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.87+10553C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158659 | ||||||
chr14:73158662
|
A | G | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.87+10556A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158662 | ||||||
chr14:73158720
|
C | A | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.87+10614C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158720 | ||||||
chr14:73158750
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.87+10644C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158750 | ||||||
chr14:73158790
|
A | G | 1 | a0001c0001t0002g0375 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.87+10684A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158790 | ||||||
chr14:73158834
|
A | C | 56 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.87+10728A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158834 | ||||||
chr14:73158961
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.87+10855G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73158961 | ||||||
chr14:73159017
|
G | T | 1 | a0001c0001t0002g0318 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.87+10911G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159017 | ||||||
chr14:73159179
|
A | AT | 24 | a0001c0001t0001g0092a0001c0001t0002g0322a0001c0001t0002g0323others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.87+11090dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73159179 | |||||
chr14:73159179
|
AT | A | 56 | a0001c0001t0002g0318a0001c0001t0003g0002a0001c0001t0003g0108others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.87+11090delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73159179 | |||||
chr14:73159352
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.87+11246C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159352 | ||||||
chr14:73159443
|
T | G | 1 | a0001c0001t0001g0020 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.87+11337T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159443 | ||||||
chr14:73159486
|
C | G | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.88-11311C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159486 | ||||||
chr14:73159512
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-11285G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159512 | ||||||
chr14:73159589
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-11208A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159589 | ||||||
chr14:73159900
|
G | C | 1 | a0001c0001t0002g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.88-10897G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73159900 | ||||||
chr14:73160035
|
G | A | 39 | a0001c0001t0002g0185a0001c0001t0005g0001a0001c0001t0005g0102others(36): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.88-10762G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160035 | ||||||
chr14:73160195
|
A | G | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.88-10602A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160195 | ||||||
chr14:73160197
|
T | A | 48 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(45): Show | 48 | HG00408.hp1 HG00544.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.88-10600T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160197 | ||||||
chr14:73160611
|
T | A | 4 | a0001c0001t0005g0169a0001c0001t0005g0170a0001c0001t0014g0171others(1): Show | 4 | HG00621.hp2 NA18955.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-10186T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160611 | ||||||
chr14:73160701
|
T | C | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.88-10096T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160701 | ||||||
chr14:73160803
|
C | CT | 310 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(307): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.88-9972dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73160803 | |||||
chr14:73160803
|
C | CTT | 38 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0039others(35): Show | 38 | HG00408.hp1 HG00544.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.88-9973_88-9972dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73160803 | |||||
chr14:73160900
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-9897C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160900 | ||||||
chr14:73160932
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.88-9865A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160932 | ||||||
chr14:73160936
|
T | C | 1 | a0001c0001t0017g0268 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.88-9861T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160936 | ||||||
chr14:73160969
|
C | CT | 43 | a0001c0001t0001g0030a0001c0001t0001g0063a0001c0001t0002g0266others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.88-9809dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73160969 | |||||
chr14:73160969
|
CT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0104others(4): Show | 7 | HG01169.hp1 HG01943.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.88-9809delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73160969 | |||||
chr14:73160990
|
G | A | 1 | a0001c0001t0007g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.88-9807G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73160990 | ||||||
chr14:73161141
|
A | G | 2 | a0001c0001t0003g0313a0001c0001t0003g0314 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88-9656A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161141 | ||||||
chr14:73161415
|
A | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-9382A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161415 | ||||||
chr14:73161416
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-9381G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161416 | ||||||
chr14:73161417
|
T | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-9380T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161417 | ||||||
chr14:73161418
|
T | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-9379T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161418 | ||||||
chr14:73161419
|
T | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-9378T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161419 | ||||||
chr14:73161420
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-9377C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161420 | ||||||
chr14:73161481
|
GACTCA | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-9310_88-9306del others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73161481 | |||||
chr14:73161596
|
G | A | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.88-9201G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161596 | ||||||
chr14:73161729
|
A | T | 1 | a0001c0001t0004g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.88-9068A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161729 | ||||||
chr14:73161731
|
A | G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-9066A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161731 | ||||||
chr14:73161798
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-8999C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161798 | ||||||
chr14:73161820
|
A | G | 1 | a0001c0001t0005g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.88-8977A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161820 | ||||||
chr14:73161892
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.88-8905C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73161892 | ||||||
chr14:73161992
|
T | TA | 127 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(124): Show | 127 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.88-8781dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73161992 | |||||
chr14:73161992
|
T | TAA | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0048others(8): Show | 11 | HG00642.hp2 HG00735.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.88-8782_88-8781dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73161992 | |||||
chr14:73161992
|
TA | T | 7 | a0001c0001t0006g0257a0001c0001t0006g0273a0001c0001t0011g0306others(4): Show | 7 | HG01074.hp2 HG01975.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-8781delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73161992 | |||||
chr14:73162017
|
T | A | 2 | a0001c0001t0007g0285a0001c0001t0007g0287 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.88-8780T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162017 | ||||||
chr14:73162021
|
A | G | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.88-8776A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162021 | ||||||
chr14:73162097
|
C | T | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-8700C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162097 | ||||||
chr14:73162098
|
T | G | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.88-8699T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162098 | ||||||
chr14:73162175
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-8622A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162175 | ||||||
chr14:73162179
|
C | CA | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-8604dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73162179 | |||||
chr14:73162286
|
C | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0080 | 2 | NA18980.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.88-8511C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162286 | ||||||
chr14:73162346
|
G | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88-8451G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162346 | ||||||
chr14:73162422
|
C | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0249others(1): Show | 4 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-8375C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162422 | ||||||
chr14:73162447
|
G | GCT | 64 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0003g0002others(61): Show | 65 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.88-8334_88-8333dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73162447 | |||||
chr14:73162450
|
C | G | 2 | a0001c0001t0002g0333a0001c0001t0023g0321 | 2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.88-8347C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162450 | ||||||
chr14:73162473
|
G | GGA | 4 | a0001c0001t0006g0140a0001c0001t0016g0267a0001c0001t0016g0279others(1): Show | 4 | HG01884.hp2 HG03098.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-8304_88-8303dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73162473 | |||||
chr14:73162473
|
GGA | G | 55 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(52): Show | 55 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.88-8304_88-8303del others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73162473 | |||||
chr14:73162498
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.88-8299G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162498 | ||||||
chr14:73162647
|
T | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0041 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.88-8150T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162647 | ||||||
chr14:73162654
|
C | G | 1 | a0001c0001t0002g0256 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.88-8143C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162654 | ||||||
chr14:73162920
|
T | C | 33 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(30): Show | 33 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.88-7877T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162920 | ||||||
chr14:73162996
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.88-7801A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73162996 | ||||||
chr14:73163024
|
A | G | 39 | a0001c0001t0002g0185a0001c0001t0005g0001a0001c0001t0005g0102others(36): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.88-7773A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163024 | ||||||
chr14:73163312
|
T | C | 1 | a0001c0001t0003g0209 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.88-7485T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163312 | ||||||
chr14:73163349
|
A | C | 1 | a0001c0001t0003g0194 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.88-7448A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163349 | ||||||
chr14:73163447
|
C | T | 8 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-7350C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163447 | ||||||
chr14:73163562
|
G | A | 263 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(260): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.88-7235G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163562 | ||||||
chr14:73163706
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-7091A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163706 | ||||||
chr14:73163734
|
G | T | 1 | a0001c0001t0028g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88-7063G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163734 | ||||||
chr14:73163850
|
G | C | 3 | a0001c0001t0004g0143a0001c0001t0029g0133a0001c0001t0030g0168 | 3 | HG02257.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.88-6947G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73163850 | ||||||
chr14:73163930
|
T | TA | 8 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(5): Show | 8 | HG01074.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.88-6855dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73163930 | |||||
chr14:73164254
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-6543A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164254 | ||||||
chr14:73164352
|
T | C | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88-6445T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164352 | ||||||
chr14:73164384
|
A | G | 31 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(28): Show | 31 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.88-6413A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164384 | ||||||
chr14:73164503
|
G | A | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-6294G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164503 | ||||||
chr14:73164532
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-6265A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164532 | ||||||
chr14:73164658
|
C | CT | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.88-6138dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73164658 | |||||
chr14:73164768
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.88-6029A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164768 | ||||||
chr14:73164863
|
C | CAT | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-5923_88-5922dup others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73164863 | |||||
chr14:73164900
|
C | A | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.88-5897C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164900 | ||||||
chr14:73164985
|
C | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88-5812C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73164985 | ||||||
chr14:73165049
|
C | T | 2 | a0001c0001t0005g0102a0001c0001t0005g0121 | 2 | HG01261.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.88-5748C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165049 | ||||||
chr14:73165081
|
C | T | 4 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0192others(1): Show | 4 | HG01261.hp2 HG03831.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-5716C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165081 | ||||||
chr14:73165202
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-5595C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165202 | ||||||
chr14:73165247
|
C | T | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.88-5550C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165247 | ||||||
chr14:73165270
|
T | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88-5527T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165270 | ||||||
chr14:73165312
|
G | C | 1 | a0001c0001t0002g0354 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.88-5485G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165312 | ||||||
chr14:73165353
|
A | G | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88-5444A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165353 | ||||||
chr14:73165520
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-5277C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165520 | ||||||
chr14:73165727
|
A | G | 1 | a0001c0001t0005g0001 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.88-5070A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165727 | ||||||
chr14:73165744
|
G | A | 35 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(32): Show | 35 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.88-5053G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165744 | ||||||
chr14:73165748
|
T | TA | 24 | a0001c0001t0001g0040a0001c0001t0002g0356a0001c0001t0004g0101others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-5032dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73165748 | |||||
chr14:73165748
|
TA | T | 6 | a0001c0001t0003g0200a0001c0001t0003g0213a0001c0001t0004g0251others(3): Show | 7 | HG00639.hp2 HG01070.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.88-5032delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73165748 | |||||
chr14:73165780
|
G | A | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00408.hp2 HG00609.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.88-5017G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165780 | ||||||
chr14:73165784
|
G | A | 3 | a0001c0001t0003g0298a0001c0001t0003g0299a0001c0001t0003g0300 | 3 | HG00140.hp2 HG01433.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.88-5013G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165784 | ||||||
chr14:73165786
|
G | T | 1 | a0001c0001t0013g0336 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.88-5011G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165786 | ||||||
chr14:73165949
|
G | C | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.88-4848G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165949 | ||||||
chr14:73165962
|
G | A | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.88-4835G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73165962 | ||||||
chr14:73166049
|
A | AAAT | 112 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(109): Show | 113 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.88-4727_88-4725dup others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73166049 | |||||
chr14:73166183
|
G | A | 4 | a0001c0001t0005g0102a0001c0001t0005g0121a0001c0001t0005g0181others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.88-4614G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73166183 | ||||||
chr14:73166789
|
A | G | 2 | a0001c0001t0008g0106a0001c0001t0008g0107 | 2 | HG00323.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.88-4008A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73166789 | ||||||
chr14:73166914
|
C | T | 3 | a0001c0001t0004g0143a0001c0001t0029g0133a0001c0001t0030g0168 | 3 | HG02257.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.88-3883C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73166914 | ||||||
chr14:73166993
|
G | GATTT | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.88-3787_88-3784dup others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73166993 | |||||
chr14:73167147
|
CCAG | C | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.88-3644_88-3642del others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73167147 | |||||
chr14:73167619
|
C | T | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88-3178C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73167619 | ||||||
chr14:73167742
|
G | GT | 33 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(30): Show | 33 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.88-3044dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73167742 | |||||
chr14:73167742
|
GT | G | 39 | a0001c0001t0003g0002a0001c0001t0003g0196a0001c0001t0003g0202others(36): Show | 40 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.88-3044delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73167742 | |||||
chr14:73167758
|
T | G | 52 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.88-3039T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73167758 | ||||||
chr14:73167828
|
C | CT | 24 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0043others(21): Show | 24 | HG01243.hp2 HG01358.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.88-2951dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73167828 | |||||
chr14:73167828
|
CT | C | 28 | a0001c0001t0003g0210a0001c0001t0004g0003a0001c0001t0004g0004others(25): Show | 28 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.88-2951delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73167828 | |||||
chr14:73167828
|
CTTT | C | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.88-2953_88-2951del others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73167828 | |||||
chr14:73168032
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.88-2765C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168032 | ||||||
chr14:73168090
|
T | TC | 5 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0068others(2): Show | 5 | HG00140.hp1 HG01496.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.88-2706dupC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr14 | 73168090 | |||||
chr14:73168122
|
G | A | 2 | a0001c0001t0013g0349a0001c0001t0013g0353 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.88-2675G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168122 | ||||||
chr14:73168337
|
C | A | 26 | a0001c0001t0004g0376a0001c0001t0007g0154a0001c0001t0007g0155others(23): Show | 26 | HG00323.hp2 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.88-2460C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168337 | ||||||
chr14:73168422
|
G | A | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.88-2375G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168422 | ||||||
chr14:73168500
|
G | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-2297G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168500 | ||||||
chr14:73168513
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-2284G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168513 | ||||||
chr14:73168556
|
G | T | 2 | a0001c0001t0002g0103a0001c0001t0002g0146 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.88-2241G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168556 | ||||||
chr14:73168697
|
C | T | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.88-2100C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168697 | ||||||
chr14:73168791
|
T | A | 52 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.88-2006T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168791 | ||||||
chr14:73168897
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.88-1900T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168897 | ||||||
chr14:73168916
|
A | T | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.88-1881A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168916 | ||||||
chr14:73168938
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-1859C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73168938 | ||||||
chr14:73169083
|
C | T | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.88-1714C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169083 | ||||||
chr14:73169256
|
T | A | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88-1541T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169256 | ||||||
chr14:73169309
|
G | T | 1 | a0001c0001t0004g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.88-1488G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169309 | ||||||
chr14:73169336
|
T | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88-1461T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169336 | ||||||
chr14:73169384
|
G | A | 4 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.88-1413G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169384 | ||||||
chr14:73169403
|
T | G | 2 | a0001c0001t0005g0158a0001c0001t0005g0161 | 2 | NA18941.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.88-1394T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169403 | ||||||
chr14:73169438
|
C | T | 1 | a0001c0001t0006g0128 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.88-1359C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169438 | ||||||
chr14:73169525
|
C | T | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88-1272C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169525 | ||||||
chr14:73169598
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.88-1199C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169598 | ||||||
chr14:73169735
|
A | T | 44 | a0001c0001t0004g0376a0001c0001t0006g0128a0001c0001t0006g0140others(41): Show | 44 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.88-1062A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169735 | ||||||
chr14:73169807
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.88-990G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169807 | ||||||
chr14:73169835
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.88-962G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73169835 | ||||||
chr14:73170197
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0041 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.88-600C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73170197 | ||||||
chr14:73170372
|
C | T | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.88-425C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73170372 | ||||||
chr14:73170402
|
T | C | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.88-395T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73170402 | ||||||
chr14:73170486
|
A | G | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.88-311A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73170486 | ||||||
chr14:73170511
|
C | G | 1 | a0001c0001t0002g0141 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.88-286C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 3/11 | chr14 | 73170511 | ||||||
chr14:73171253
|
T | C | 44 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0110others(41): Show | 44 | HG00408.hp1 HG00544.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.338+206T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171253 | ||||||
chr14:73171334
|
G | A | 1 | a0001c0001t0024g0242 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.338+287G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171334 | ||||||
chr14:73171433
|
G | A | 1 | a0001c0001t0005g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.338+386G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171433 | ||||||
chr14:73171502
|
A | G | 1 | a0001c0001t0003g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.338+455A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171502 | ||||||
chr14:73171619
|
T | C | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.338+572T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171619 | ||||||
chr14:73171770
|
G | A | 1 | a0001c0001t0005g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.338+723G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171770 | ||||||
chr14:73171921
|
G | C | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.338+874G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171921 | ||||||
chr14:73171994
|
T | C | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.338+947T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73171994 | ||||||
chr14:73172135
|
G | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.338+1088G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172135 | ||||||
chr14:73172243
|
G | A | 11 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0020others(8): Show | 11 | HG00408.hp2 HG02080.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.338+1196G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172243 | ||||||
chr14:73172360
|
G | A | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.339-1206G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172360 | ||||||
chr14:73172399
|
T | C | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.339-1167T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172399 | ||||||
chr14:73172430
|
A | G | 45 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(42): Show | 46 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.339-1136A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172430 | ||||||
chr14:73172432
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.339-1134G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172432 | ||||||
chr14:73172486
|
C | T | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.339-1080C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172486 | ||||||
chr14:73172512
|
G | C | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.339-1054G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172512 | ||||||
chr14:73172573
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.339-993A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172573 | ||||||
chr14:73172609
|
T | C | 3 | a0001c0001t0002g0317a0001c0001t0002g0318a0001c0001t0002g0338 | 3 | HG02165.hp1 NA18951.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.339-957T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172609 | ||||||
chr14:73172792
|
G | T | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.339-774G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172792 | ||||||
chr14:73172969
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.339-597C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73172969 | ||||||
chr14:73173118
|
T | C | 1 | a0001c0001t0003g0125 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.339-448T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73173118 | ||||||
chr14:73173321
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0072 | 2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.339-245A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 4/11 | chr14 | 73173321 | ||||||
chr14:73173851
|
C | T | 5 | a0001c0001t0002g0319a0001c0001t0002g0322a0001c0001t0002g0323others(2): Show | 5 | HG01106.hp1 HG01257.hp1 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+144C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73173851 | ||||||
chr14:73173929
|
C | T | 1 | a0001c0001t0004g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.480+222C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73173929 | ||||||
chr14:73173930
|
A | G | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.480+223A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73173930 | ||||||
chr14:73174283
|
A | G | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.480+576A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73174283 | ||||||
chr14:73174337
|
G | A | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+630G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73174337 | ||||||
chr14:73174416
|
T | A | 1 | a0001c0001t0005g0189 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480+709T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73174416 | ||||||
chr14:73174500
|
C | CTGGGA | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+795_480+799dup others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73174500 | |||||
chr14:73174750
|
A | T | 45 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(42): Show | 45 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.480+1043A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73174750 | ||||||
chr14:73175208
|
G | A | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.480+1501G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175208 | ||||||
chr14:73175213
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.480+1506G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175213 | ||||||
chr14:73175314
|
A | AC | 63 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(60): Show | 63 | HG00408.hp1 HG00544.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.480+1608dupC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73175314 | |||||
chr14:73175468
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.480+1761C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175468 | ||||||
chr14:73175511
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.480+1804G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175511 | ||||||
chr14:73175602
|
G | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.480+1895G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175602 | ||||||
chr14:73175676
|
AAT | A | 3 | a0001c0001t0006g0272a0001c0001t0006g0281a0002c0005t0006g0274 | 3 | NA18947.hp2 NA18965.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.480+1970_480+1971d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175676 | ||||||
chr14:73175839
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.480+2132A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175839 | ||||||
chr14:73175859
|
A | G | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.480+2152A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175859 | ||||||
chr14:73175877
|
A | G | 1 | a0001c0001t0005g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.480+2170A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175877 | ||||||
chr14:73175937
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+2230C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73175937 | ||||||
chr14:73176251
|
A | G | 1 | a0001c0001t0030g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.480+2544A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176251 | ||||||
chr14:73176351
|
G | A | 26 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.480+2644G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176351 | ||||||
chr14:73176490
|
C | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.480+2783C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176490 | ||||||
chr14:73176666
|
A | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.480+2959A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176666 | ||||||
chr14:73176726
|
C | T | 1 | a0001c0001t0004g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.480+3019C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176726 | ||||||
chr14:73176780
|
T | C | 2 | a0001c0001t0015g0301a0001c0001t0015g0302 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.480+3073T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176780 | ||||||
chr14:73176911
|
C | G | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.480+3204C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176911 | ||||||
chr14:73176960
|
T | C | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+3253T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73176960 | ||||||
chr14:73177010
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+3303A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73177010 | ||||||
chr14:73177011
|
AT | A | 25 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(22): Show | 25 | HG00323.hp2 HG01074.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.480+3310delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73177011 | |||||
chr14:73177030
|
G | A | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+3323G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73177030 | ||||||
chr14:73177055
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.480+3348C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73177055 | ||||||
chr14:73177288
|
CTCT | C | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+3585_480+3587d others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73177288 | |||||
chr14:73177391
|
G | GTGTTTT | 36 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(33): Show | 36 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.480+3709_480+3714d others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73177391 | |||||
chr14:73177755
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.480+4048C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73177755 | ||||||
chr14:73177830
|
T | C | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.480+4123T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73177830 | ||||||
chr14:73177966
|
CTT | C | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+4269_480+4270d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73177966 | |||||
chr14:73178027
|
T | A | 39 | a0001c0001t0002g0185a0001c0001t0005g0001a0001c0001t0005g0102others(36): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.480+4320T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178027 | ||||||
chr14:73178219
|
C | CT | 14 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0040others(11): Show | 14 | HG00642.hp2 HG00735.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.480+4530dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73178219 | |||||
chr14:73178219
|
C | CTT | 31 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(28): Show | 31 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.480+4529_480+4530d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73178219 | |||||
chr14:73178219
|
CT | C | 12 | a0001c0001t0005g0174a0001c0001t0007g0154a0001c0001t0007g0155others(9): Show | 12 | HG01243.hp2 HG02027.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.480+4530delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73178219 | |||||
chr14:73178220
|
T | C | 1 | a0001c0001t0002g0361 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.480+4513T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178220 | ||||||
chr14:73178221
|
T | C | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+4514T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178221 | ||||||
chr14:73178244
|
G | C | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.480+4537G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178244 | ||||||
chr14:73178354
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.480+4647A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178354 | ||||||
chr14:73178699
|
A | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.480+4992A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178699 | ||||||
chr14:73178975
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.480+5268T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73178975 | ||||||
chr14:73179043
|
T | G | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.480+5336T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179043 | ||||||
chr14:73179230
|
A | G | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.480+5523A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179230 | ||||||
chr14:73179264
|
C | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.480+5557C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179264 | ||||||
chr14:73179397
|
G | A | 2 | a0001c0001t0016g0279a0001c0001t0025g0269 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.480+5690G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179397 | ||||||
chr14:73179447
|
T | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+5740T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179447 | ||||||
chr14:73179477
|
C | CA | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+5771dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73179477 | |||||
chr14:73179664
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.480+5957G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179664 | ||||||
chr14:73179690
|
A | G | 1 | a0001c0001t0002g0355 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.480+5983A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179690 | ||||||
chr14:73179789
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.480+6082T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179789 | ||||||
chr14:73179968
|
T | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0071 | 3 | HG01256.hp1 HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.480+6261T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179968 | ||||||
chr14:73179991
|
A | AT | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+6295dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73179991 | |||||
chr14:73179996
|
T | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(122): Show | 125 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.480+6289T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73179996 | ||||||
chr14:73180015
|
C | CA | 38 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(35): Show | 38 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.480+6309dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73180015 | |||||
chr14:73180142
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.480+6435G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73180142 | ||||||
chr14:73180283
|
C | A | 1 | a0001c0001t0002g0319 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.481-6570C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73180283 | ||||||
chr14:73180445
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.481-6408G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73180445 | ||||||
chr14:73180466
|
G | C | 81 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.481-6387G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73180466 | ||||||
chr14:73180525
|
G | A | 47 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(44): Show | 48 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.481-6328G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73180525 | ||||||
chr14:73180622
|
A | T | 1 | a0001c0001t0006g0128 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.481-6231A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73180622 | ||||||
chr14:73181059
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.481-5794A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181059 | ||||||
chr14:73181115
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-5738G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181115 | ||||||
chr14:73181262
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.481-5591A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181262 | ||||||
chr14:73181271
|
C | G | 2 | a0001c0001t0015g0301a0001c0001t0015g0302 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.481-5582C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181271 | ||||||
chr14:73181441
|
A | G | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.481-5412A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181441 | ||||||
chr14:73181493
|
A | C | 15 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-5360A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181493 | ||||||
chr14:73181724
|
G | C | 3 | a0001c0001t0003g0151a0001c0001t0003g0303a0001c0001t0004g0304 | 3 | HG02976.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.481-5129G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181724 | ||||||
chr14:73181782
|
A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0032others(1): Show | 4 | NA19003.hp1 NA19007.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-5071A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181782 | ||||||
chr14:73181794
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.481-5059G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181794 | ||||||
chr14:73181798
|
A | G | 1 | a0001c0001t0003g0300 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.481-5055A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181798 | ||||||
chr14:73181878
|
A | G | 1 | a0001c0001t0003g0194 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.481-4975A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181878 | ||||||
chr14:73181907
|
G | A | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-4946G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181907 | ||||||
chr14:73181919
|
A | G | 24 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(21): Show | 24 | HG00323.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.481-4934A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73181919 | ||||||
chr14:73182105
|
G | A | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.481-4748G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73182105 | ||||||
chr14:73182507
|
T | A | 1 | a0001c0001t0005g0346 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.481-4346T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73182507 | ||||||
chr14:73182775
|
G | T | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.481-4078G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73182775 | ||||||
chr14:73182861
|
A | T | 1 | a0001c0001t0004g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.481-3992A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73182861 | ||||||
chr14:73183080
|
T | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-3773T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183080 | ||||||
chr14:73183158
|
C | T | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.481-3695C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183158 | ||||||
chr14:73183223
|
T | G | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.481-3630T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183223 | ||||||
chr14:73183292
|
AT | A | 201 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(198): Show | 202 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.481-3549delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73183292 | |||||
chr14:73183304
|
T | A | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.481-3549T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183304 | ||||||
chr14:73183335
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.481-3518T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183335 | ||||||
chr14:73183391
|
T | C | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.481-3462T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183391 | ||||||
chr14:73183752
|
C | T | 1 | a0001c0001t0004g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.481-3101C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183752 | ||||||
chr14:73183753
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.481-3100G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183753 | ||||||
chr14:73183802
|
G | C | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-3051G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183802 | ||||||
chr14:73183838
|
C | G | 1 | a0001c0001t0003g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.481-3015C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183838 | ||||||
chr14:73183869
|
GGCGGCCG others(120): Show |
G | 1 | a0001c0001t0002g0348 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.481-2968_481-2842d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73183869 | |||||
chr14:73183893
|
ACCTCCCG others(269): Show |
A | 12 | a0001c0001t0006g0128a0001c0001t0006g0272a0001c0001t0006g0273others(9): Show | 12 | HG00408.hp1 HG00544.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.481-2951_481-2676d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73183893 | |||||
chr14:73183899
|
C | T | 3 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0004g0235 | 3 | HG02109.hp1 HG03139.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.481-2954C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183899 | ||||||
chr14:73183902
|
G | A | 13 | a0001c0001t0006g0140a0001c0001t0006g0148a0001c0001t0006g0257others(10): Show | 13 | HG01074.hp2 HG01081.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.481-2951G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183902 | ||||||
chr14:73183919
|
GCGGGGGG others(220): Show |
G | 5 | a0001c0001t0006g0140a0001c0001t0006g0148a0001c0001t0015g0301others(2): Show | 5 | HG01081.hp2 HG02145.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2883_481-2657d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73183919 | |||||
chr14:73183921
|
GGGGGGCT others(268): Show |
G | 1 | a0001c0001t0006g0271 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.481-2926_481-2652d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73183921 | |||||
chr14:73183931
|
C | T | 8 | a0001c0001t0002g0358a0001c0001t0003g0210a0001c0001t0011g0306others(5): Show | 8 | HG01074.hp2 HG02071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-2922C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183931 | ||||||
chr14:73183949
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2904G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183949 | ||||||
chr14:73183965
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.481-2888C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183965 | ||||||
chr14:73183966
|
GGGCAGAG others(71): Show |
G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-2883_481-2806d others(80): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73183966 | |||||
chr14:73183969
|
CAGAGGGG others(219): Show |
C | 1 | a0001c0001t0006g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.481-2883_481-2658d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183969 | ||||||
chr14:73183972
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2881A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183972 | ||||||
chr14:73183978
|
T | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-2875T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183978 | ||||||
chr14:73183979
|
C | A | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-2874C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183979 | ||||||
chr14:73183979
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.481-2874C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183979 | ||||||
chr14:73183981
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2872T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183981 | ||||||
chr14:73183985
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2868T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183985 | ||||||
chr14:73183990
|
A | T | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2863A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183990 | ||||||
chr14:73183991
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2862G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183991 | ||||||
chr14:73183992
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2861T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183992 | ||||||
chr14:73183993
|
A | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2860A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183993 | ||||||
chr14:73183996
|
A | G | 238 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(235): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.481-2857A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73183996 | ||||||
chr14:73184003
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2850G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184003 | ||||||
chr14:73184007
|
A | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2846A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184007 | ||||||
chr14:73184009
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2844A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184009 | ||||||
chr14:73184012
|
C | G | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2841C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184012 | ||||||
chr14:73184017
|
C | G | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.481-2836C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184017 | ||||||
chr14:73184018
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2835T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184018 | ||||||
chr14:73184020
|
ACCTCCCG others(42): Show |
A | 1 | a0001c0001t0001g0030 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.481-2826_481-2778d others(51): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184020 | |||||
chr14:73184021
|
C | G | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.481-2832C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184021 | ||||||
chr14:73184044
|
A | G | 13 | a0001c0001t0002g0358a0001c0001t0003g0226a0001c0001t0007g0154others(10): Show | 13 | HG01243.hp2 HG02055.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-2809A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184044 | ||||||
chr14:73184047
|
C | T | 2 | a0001c0001t0005g0181a0001c0001t0005g0182 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.481-2806C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184047 | ||||||
chr14:73184057
|
A | AC | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-2796_481-2795i others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184057 | ||||||
chr14:73184058
|
T | C | 7 | a0001c0001t0002g0358a0001c0001t0011g0306a0001c0001t0011g0308others(4): Show | 7 | HG01074.hp2 HG02071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2795T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184058 | ||||||
chr14:73184076
|
A | G | 7 | a0001c0001t0002g0358a0001c0001t0011g0306a0001c0001t0011g0308others(4): Show | 7 | HG01074.hp2 HG02071.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2777A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184076 | ||||||
chr14:73184079
|
C | T | 1 | a0001c0001t0003g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.481-2774C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184079 | ||||||
chr14:73184092
|
C | T | 2 | a0001c0001t0005g0175a0001c0001t0005g0176 | 2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.481-2761C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184092 | ||||||
chr14:73184098
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2755G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184098 | ||||||
chr14:73184105
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2748G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184105 | ||||||
chr14:73184106
|
A | AC | 22 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0017others(19): Show | 22 | HG01167.hp1 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.481-2738dupC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184106 | |||||
chr14:73184106
|
A | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2747A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184106 | ||||||
chr14:73184107
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2746C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184107 | ||||||
chr14:73184108
|
C | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2745C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184108 | ||||||
chr14:73184108
|
C | CCCCCCCA others(41): Show |
28 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(25): Show | 28 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.481-2739_481-2738i others(50): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184108 | |||||
chr14:73184108
|
CCCCCCCC others(42): Show |
C | 4 | a0001c0001t0003g0151a0001c0001t0003g0305a0001c0001t0004g0304others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2722_481-2674d others(51): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184108 | |||||
chr14:73184109
|
C | A | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2744C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184109 | ||||||
chr14:73184109
|
CCCCCCCA others(41): Show |
C | 7 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0202others(4): Show | 7 | HG02129.hp1 HG02280.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2737_481-2690d others(50): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184109 | |||||
chr14:73184109
|
CCCCCCCA others(90): Show |
C | 1 | a0001c0001t0003g0229 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.481-2737_481-2641d others(99): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184109 | |||||
chr14:73184111
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2742C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184111 | ||||||
chr14:73184112
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2741C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184112 | ||||||
chr14:73184116
|
A | AGTAGGAG others(18): Show |
1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2737_481-2736i others(27): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184116 | ||||||
chr14:73184131
|
A | G | 89 | a0001c0001t0001g0043a0001c0001t0001g0099a0001c0001t0001g0100others(86): Show | 89 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.481-2722A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184131 | ||||||
chr14:73184131
|
AGGGCGGC others(42): Show |
A | 1 | a0001c0001t0002g0266 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.481-2707_481-2659d others(51): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184131 | |||||
chr14:73184143
|
C | T | 2 | a0001c0001t0008g0193a0001c0001t0010g0053 | 2 | NA18991.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.481-2710C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184143 | ||||||
chr14:73184144
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2709G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184144 | ||||||
chr14:73184146
|
C | G | 36 | a0001c0001t0002g0358a0001c0001t0004g0003a0001c0001t0004g0004others(33): Show | 36 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.481-2707C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184146 | ||||||
chr14:73184146
|
CCGGGGGG others(42): Show |
C | 48 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(45): Show | 49 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.481-2558_481-2510d others(51): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184146 | |||||
chr14:73184158
|
C | T | 2 | a0001c0001t0002g0358a0001c0006t0006g0153 | 2 | HG02071.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.481-2695C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184158 | ||||||
chr14:73184176
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2677G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184176 | ||||||
chr14:73184180
|
G | A | 6 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0202others(3): Show | 6 | HG02129.hp1 HG02280.hp2 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-2673G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184180 | ||||||
chr14:73184195
|
G | C | 11 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0151others(8): Show | 11 | HG02129.hp1 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-2658G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184195 | ||||||
chr14:73184195
|
G | GCGGGGGG others(91): Show |
1 | a0001c0001t0016g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-2625_481-2624i others(100): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184195 | |||||
chr14:73184196
|
C | G | 1 | a0001c0001t0006g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.481-2657C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184196 | ||||||
chr14:73184206
|
A | AC | 11 | a0001c0001t0001g0013a0001c0001t0001g0047a0001c0001t0001g0069others(8): Show | 11 | HG01074.hp2 HG02056.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.481-2640dupC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184206 | |||||
chr14:73184207
|
CCCCCCCA others(41): Show |
C | 1 | a0001c0001t0009g0215 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.481-2639_481-2592d others(50): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184207 | |||||
chr14:73184209
|
C | A | 6 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-2644C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184209 | ||||||
chr14:73184228
|
C | T | 7 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(4): Show | 7 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-2625C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184228 | ||||||
chr14:73184229
|
G | A | 2 | a0001c0001t0002g0358a0001c0001t0003g0229 | 2 | HG02071.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.481-2624G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184229 | ||||||
chr14:73184241
|
C | A | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.481-2612C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184241 | ||||||
chr14:73184241
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-2612C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184241 | ||||||
chr14:73184244
|
G | C | 2 | a0001c0001t0002g0358a0001c0001t0003g0229 | 2 | HG02071.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.481-2609G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184244 | ||||||
chr14:73184246
|
GGGGGGCT others(41): Show |
G | 1 | a0001c0001t0009g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.481-2601_481-2554d others(50): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184246 | |||||
chr14:73184261
|
C | G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-2592C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184261 | ||||||
chr14:73184267
|
CCCTCCCG others(83): Show |
C | 17 | a0001c0001t0002g0339a0001c0001t0002g0345a0001c0001t0002g0350others(14): Show | 17 | HG00558.hp2 HG02015.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.481-2532_481-2443d others(92): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184267 | |||||
chr14:73184275
|
G | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-2578G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184275 | ||||||
chr14:73184286
|
TGGCCGGG others(169): Show |
T | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.481-2558_481-2383d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184286 | |||||
chr14:73184294
|
C | CA | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2559_481-2558i others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184294 | ||||||
chr14:73184296
|
G | A | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2557G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184296 | ||||||
chr14:73184302
|
TGACCC | T | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2550_481-2546d others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184302 | ||||||
chr14:73184304
|
A | ACCCCCCC others(43): Show |
1 | a0001c0001t0004g0238 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.481-2510_481-2509i others(52): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184304 | |||||
chr14:73184305
|
CCCCCCCA others(82): Show |
C | 1 | a0001c0001t0002g0363 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.481-2541_481-2453d others(91): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184305 | |||||
chr14:73184306
|
C | CCCCCCAC others(42): Show |
4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2510_481-2509i others(51): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184306 | |||||
chr14:73184310
|
C | G | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.481-2543C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184310 | ||||||
chr14:73184310
|
C | T | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2543C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184310 | ||||||
chr14:73184312
|
ACCTC | A | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2534_481-2531d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184312 | |||||
chr14:73184316
|
CCCTCCCG others(34): Show |
C | 3 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0072 | 3 | HG00738.hp1 HG01433.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.481-2509_481-2469d others(43): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184316 | |||||
chr14:73184318
|
C | T | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2535C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184318 | ||||||
chr14:73184323
|
G | A | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2530G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184323 | ||||||
chr14:73184325
|
A | T | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2528A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184325 | ||||||
chr14:73184326
|
C | A | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2527C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184326 | ||||||
chr14:73184331
|
CGGCT | C | 10 | a0001c0001t0007g0156a0001c0001t0007g0157a0001c0001t0008g0193others(7): Show | 10 | HG01074.hp2 HG01243.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-2518_481-2515d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184331 | |||||
chr14:73184335
|
T | TGGCCGGG others(30): Show |
44 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(41): Show | 44 | HG00323.hp2 HG00733.hp1 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.481-2505_481-2504i others(39): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184335 | |||||
chr14:73184335
|
TGGCCGGG others(120): Show |
T | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(81): Show | 84 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.481-2440_481-2314d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184335 | |||||
chr14:73184340
|
GGGCAGAG others(83): Show |
G | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.481-2504_481-2415d others(92): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184340 | |||||
chr14:73184344
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2509A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184344 | ||||||
chr14:73184346
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2507A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184346 | ||||||
chr14:73184350
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2503G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184350 | ||||||
chr14:73184355
|
T | A | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2498T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184355 | ||||||
chr14:73184357
|
A | C | 1 | a0001c0001t0002g0358 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.481-2496A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184357 | ||||||
chr14:73184375
|
CTGGCCGG others(119): Show |
C | 1 | a0001c0001t0001g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.481-2477_481-2352d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184375 | ||||||
chr14:73184381
|
G | A | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481-2472G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184381 | ||||||
chr14:73184383
|
G | T | 1 | a0001c0001t0007g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.481-2470G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184383 | ||||||
chr14:73184384
|
C | G | 1 | a0001c0001t0003g0202 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.481-2469C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184384 | ||||||
chr14:73184384
|
C | T | 55 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(52): Show | 56 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.481-2469C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184384 | ||||||
chr14:73184385
|
GGGGGGCT others(119): Show |
G | 1 | a0001c0001t0001g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.481-2462_481-2337d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184385 | |||||
chr14:73184388
|
G | A | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2465G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184388 | ||||||
chr14:73184395
|
CCCCCCCA others(119): Show |
C | 1 | a0001c0001t0001g0047 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.481-2451_481-2326d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184395 | |||||
chr14:73184411
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0072 | 3 | HG00738.hp1 HG01433.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.481-2442T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184411 | ||||||
chr14:73184413
|
C | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0063others(1): Show | 4 | HG00738.hp1 HG01433.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2440C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184413 | ||||||
chr14:73184417
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.481-2436G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184417 | ||||||
chr14:73184425
|
TGGCCTGG others(30): Show |
T | 3 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0072 | 3 | HG00738.hp1 HG01433.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.481-2423_481-2387d others(39): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184425 | |||||
chr14:73184491
|
G | A | 3 | a0001c0001t0002g0185a0001c0001t0005g0186a0001c0001t0005g0265 | 3 | HG02523.hp1 NA18998.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.481-2362G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184491 | ||||||
chr14:73184495
|
G | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.481-2358G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184495 | ||||||
chr14:73184502
|
C | T | 56 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.481-2351C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184502 | ||||||
chr14:73184507
|
CGGGCGGG others(169): Show |
C | 1 | a0001c0001t0001g0029 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.481-2315_481-2140d others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184507 | |||||
chr14:73184511
|
C | G | 3 | a0001c0001t0003g0151a0001c0001t0003g0303a0001c0001t0004g0304 | 3 | HG02976.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.481-2342C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184511 | ||||||
chr14:73184537
|
C | G | 1 | a0001c0001t0004g0297 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.481-2316C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184537 | ||||||
chr14:73184540
|
G | C | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-2313G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184540 | ||||||
chr14:73184541
|
G | A | 1 | a0001c0001t0004g0241 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.481-2312G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184541 | ||||||
chr14:73184543
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.481-2310C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184543 | ||||||
chr14:73184544
|
A | G | 26 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.481-2309A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184544 | ||||||
chr14:73184589
|
C | T | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2264C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184589 | ||||||
chr14:73184597
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.481-2256C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184597 | ||||||
chr14:73184603
|
C | T | 4 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(1): Show | 4 | HG01243.hp2 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-2250C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184603 | ||||||
chr14:73184617
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-2236C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184617 | ||||||
chr14:73184670
|
C | T | 2 | a0001c0001t0003g0126a0001c0001t0003g0216 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.481-2183C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184670 | ||||||
chr14:73184697
|
AC | A | 34 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(31): Show | 34 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.481-2149delC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184697 | |||||
chr14:73184718
|
A | G | 1 | a0001c0001t0004g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.481-2135A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184718 | ||||||
chr14:73184741
|
G | T | 13 | a0001c0001t0002g0185a0001c0001t0005g0169a0001c0001t0005g0170others(10): Show | 13 | HG00621.hp2 HG02027.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-2112G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184741 | ||||||
chr14:73184764
|
C | T | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-2089C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184764 | ||||||
chr14:73184773
|
G | T | 1 | a0001c0001t0002g0316 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.481-2080G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184773 | ||||||
chr14:73184781
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-2072C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184781 | ||||||
chr14:73184791
|
C | CGCTCCTC others(33): Show |
1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481-2009_481-1970d others(42): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184791 | |||||
chr14:73184791
|
CGCTCCTC others(33): Show |
C | 1 | a0001c0001t0028g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.481-2009_481-1970d others(42): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73184791 | |||||
chr14:73184809
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-2044C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184809 | ||||||
chr14:73184814
|
C | T | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.481-2039C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184814 | ||||||
chr14:73184835
|
C | G | 1 | a0001c0001t0004g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.481-2018C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184835 | ||||||
chr14:73184852
|
G | GC | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.481-2001_481-2000i others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184852 | ||||||
chr14:73184871
|
G | A | 1 | a0001c0001t0002g0351 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.481-1982G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184871 | ||||||
chr14:73184926
|
C | T | 52 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(49): Show | 53 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.481-1927C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184926 | ||||||
chr14:73184929
|
G | C | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1924G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184929 | ||||||
chr14:73184938
|
C | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1915C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73184938 | ||||||
chr14:73185015
|
G | A | 4 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0192others(1): Show | 4 | HG01261.hp2 HG03831.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1838G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185015 | ||||||
chr14:73185028
|
C | T | 5 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(2): Show | 5 | HG01169.hp2 HG01943.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-1825C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185028 | ||||||
chr14:73185041
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.481-1812A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185041 | ||||||
chr14:73185045
|
G | T | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.481-1808G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185045 | ||||||
chr14:73185072
|
A | G | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.481-1781A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185072 | ||||||
chr14:73185095
|
G | A | 1 | a0001c0001t0005g0187 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.481-1758G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185095 | ||||||
chr14:73185156
|
A | G | 1 | a0001c0001t0005g0163 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.481-1697A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185156 | ||||||
chr14:73185198
|
C | CG | 4 | a0001c0001t0001g0069a0001c0001t0002g0147a0001c0001t0005g0346others(1): Show | 4 | HG00738.hp2 HG02055.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1651dupG | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73185198 | |||||
chr14:73185207
|
G | C | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.481-1646G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185207 | ||||||
chr14:73185219
|
G | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-1634G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185219 | ||||||
chr14:73185222
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0152 | 3 | HG02258.hp1 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.481-1631A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185222 | ||||||
chr14:73185313
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.481-1540A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185313 | ||||||
chr14:73185321
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.481-1532G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185321 | ||||||
chr14:73185341
|
C | T | 1 | a0001c0001t0007g0154 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.481-1512C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185341 | ||||||
chr14:73185429
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1424C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185429 | ||||||
chr14:73185433
|
G | C | 1 | a0001c0001t0010g0053 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.481-1420G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185433 | ||||||
chr14:73185478
|
G | A | 1 | a0001c0001t0021g0342 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.481-1375G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185478 | ||||||
chr14:73185507
|
A | G | 2 | a0001c0001t0003g0208a0001c0001t0003g0214 | 2 | NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.481-1346A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185507 | ||||||
chr14:73185536
|
A | G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-1317A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185536 | ||||||
chr14:73185591
|
G | C | 6 | a0001c0001t0007g0285a0001c0001t0007g0286a0001c0001t0007g0287others(3): Show | 6 | HG02055.hp2 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-1262G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185591 | ||||||
chr14:73185607
|
G | A | 1 | a0001c0001t0012g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.481-1246G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185607 | ||||||
chr14:73185615
|
AGAGAGG | A | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-1220_481-1215d others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr14 | 73185615 | |||||
chr14:73185623
|
A | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.481-1230A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185623 | ||||||
chr14:73185659
|
A | G | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-1194A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185659 | ||||||
chr14:73185972
|
C | T | 1 | a0001c0001t0004g0297 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.481-881C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73185972 | ||||||
chr14:73186071
|
T | C | 2 | a0001c0001t0003g0313a0001c0001t0003g0314 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.481-782T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186071 | ||||||
chr14:73186207
|
G | C | 81 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.481-646G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186207 | ||||||
chr14:73186235
|
C | G | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.481-618C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186235 | ||||||
chr14:73186275
|
G | A | 43 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.481-578G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186275 | ||||||
chr14:73186311
|
G | A | 3 | a0001c0001t0003g0151a0001c0001t0003g0303a0001c0001t0004g0304 | 3 | HG02976.hp2 HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.481-542G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186311 | ||||||
chr14:73186335
|
C | T | 46 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(43): Show | 47 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.481-518C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186335 | ||||||
chr14:73186490
|
A | G | 4 | a0001c0001t0002g0185a0001c0001t0005g0186a0001c0001t0005g0187others(1): Show | 4 | HG02523.hp1 NA18947.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.481-363A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186490 | ||||||
chr14:73186548
|
G | A | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.481-305G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186548 | ||||||
chr14:73186648
|
G | A | 1 | a0001c0001t0018g0337 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.481-205G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 5/11 | chr14 | 73186648 | ||||||
chr14:73187132
|
A | T | 6 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.548+212A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187132 | ||||||
chr14:73187219
|
G | A | 1 | a0001c0001t0002g0319 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.548+299G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187219 | ||||||
chr14:73187281
|
A | G | 3 | a0001c0001t0004g0251a0001c0001t0004g0252a0001c0001t0004g0253 | 3 | HG00639.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.548+361A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187281 | ||||||
chr14:73187313
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.548+393T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187313 | ||||||
chr14:73187459
|
G | A | 1 | a0001c0001t0006g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.548+539G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187459 | ||||||
chr14:73187618
|
T | C | 6 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.548+698T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187618 | ||||||
chr14:73187619
|
C | A | 1 | a0001c0001t0007g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.548+699C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187619 | ||||||
chr14:73187980
|
G | A | 4 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(1): Show | 4 | HG01891.hp1 HG02145.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.548+1060G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187980 | ||||||
chr14:73187984
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.548+1064A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187984 | ||||||
chr14:73187987
|
G | C | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.548+1067G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187987 | ||||||
chr14:73187997
|
C | T | 1 | a0001c0001t0011g0310 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.548+1077C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187997 | ||||||
chr14:73187998
|
G | A | 1 | a0001c0001t0004g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.548+1078G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73187998 | ||||||
chr14:73188009
|
A | G | 1 | a0001c0001t0004g0120 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.548+1089A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73188009 | ||||||
chr14:73188016
|
C | T | 1 | a0001c0001t0005g0117 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.548+1096C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73188016 | ||||||
chr14:73188063
|
G | C | 1 | a0001c0001t0003g0194 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.548+1143G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73188063 | ||||||
chr14:73188176
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.548+1256C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73188176 | ||||||
chr14:73188200
|
TA | T | 47 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0263others(44): Show | 47 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.548+1282delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73188200 | |||||
chr14:73188295
|
GATC | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.548+1382_548+1384d others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73188295 | |||||
chr14:73188378
|
G | A | 14 | a0001c0001t0005g0117a0001c0001t0005g0158a0001c0001t0005g0159others(11): Show | 14 | HG00423.hp2 HG00621.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.548+1458G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73188378 | ||||||
chr14:73188765
|
TTTTC | T | 3 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0369 | 3 | HG01891.hp1 HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.548+1853_548+1856d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73188765 | |||||
chr14:73189036
|
C | G | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.548+2116C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189036 | ||||||
chr14:73189070
|
C | T | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.548+2150C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189070 | ||||||
chr14:73189360
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.548+2440C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189360 | ||||||
chr14:73189383
|
G | C | 2 | a0001c0001t0016g0279a0001c0001t0025g0269 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.548+2463G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189383 | ||||||
chr14:73189448
|
T | TAAAAATA others(169): Show |
9 | a0001c0001t0006g0272a0001c0001t0006g0273a0001c0001t0006g0275others(6): Show | 9 | HG00408.hp1 HG01975.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.548+2554_548+2555i others(178): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(174): Show |
1 | a0001c0001t0006g0148 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.548+2554_548+2555i others(183): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(183): Show |
2 | a0001c0001t0015g0302a0001c0006t0006g0153 | 2 | HG01081.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.548+2554_548+2555i others(192): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(184): Show |
1 | a0001c0001t0015g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.548+2554_548+2555i others(193): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(188): Show |
1 | a0001c0001t0006g0277 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.548+2554_548+2555i others(197): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(189): Show |
2 | a0001c0001t0006g0140a0001c0001t0006g0271 | 2 | HG02738.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.548+2554_548+2555i others(198): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(198): Show |
1 | a0001c0001t0006g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.548+2554_548+2555i others(207): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(201): Show |
1 | a0001c0001t0006g0128 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.548+2554_548+2555i others(210): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189448
|
T | TAAAAATA others(202): Show |
1 | a0001c0001t0006g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.548+2554_548+2555i others(211): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73189448 | |||||
chr14:73189469
|
G | A | 1 | a0001c0001t0005g0001 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.548+2549G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189469 | ||||||
chr14:73189495
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.548+2575C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189495 | ||||||
chr14:73189561
|
G | A | 2 | a0001c0001t0004g0246a0001c0004t0020g0312 | 2 | NA19030.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.548+2641G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189561 | ||||||
chr14:73189607
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.548+2687C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189607 | ||||||
chr14:73189895
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0019others(4): Show | 7 | HG00642.hp2 HG00735.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.549-2749C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189895 | ||||||
chr14:73189896
|
G | A | 6 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(3): Show | 6 | HG00735.hp1 HG00738.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.549-2748G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189896 | ||||||
chr14:73189997
|
GTGGCTCC others(21): Show |
G | 1 | a0001c0001t0001g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.549-2646_549-2619d others(30): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73189997 | ||||||
chr14:73190233
|
A | G | 4 | a0001c0001t0003g0151a0001c0001t0003g0303a0001c0001t0003g0305others(1): Show | 4 | HG02647.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-2411A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190233 | ||||||
chr14:73190281
|
G | T | 1 | a0001c0001t0023g0321 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.549-2363G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190281 | ||||||
chr14:73190460
|
G | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.549-2184G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190460 | ||||||
chr14:73190472
|
C | A | 39 | a0001c0001t0002g0185a0001c0001t0005g0001a0001c0001t0005g0102others(36): Show | 40 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.549-2172C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190472 | ||||||
chr14:73190485
|
TA | T | 73 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0052others(70): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.549-2139delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73190485 | |||||
chr14:73190485
|
TAA | T | 14 | a0001c0001t0001g0043a0001c0001t0004g0005a0001c0001t0007g0154others(11): Show | 14 | HG01169.hp2 HG01243.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.549-2140_549-2139d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73190485 | |||||
chr14:73190486
|
A | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG00609.hp1 HG02083.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.549-2158A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190486 | ||||||
chr14:73190487
|
A | T | 9 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(6): Show | 9 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.549-2157A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190487 | ||||||
chr14:73190488
|
A | T | 1 | a0001c0001t0008g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.549-2156A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190488 | ||||||
chr14:73190543
|
T | A | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.549-2101T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190543 | ||||||
chr14:73190634
|
T | G | 35 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(32): Show | 35 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.549-2010T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190634 | ||||||
chr14:73190912
|
A | G | 1 | a0001c0001t0011g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.549-1732A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73190912 | ||||||
chr14:73191153
|
A | T | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.549-1491A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73191153 | ||||||
chr14:73191398
|
A | AGT | 25 | a0001c0001t0003g0208a0001c0001t0003g0214a0001c0001t0003g0217others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.549-1233_549-1232d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr14 | 73191398 | |||||
chr14:73191429
|
C | T | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.549-1215C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73191429 | ||||||
chr14:73191533
|
C | T | 3 | a0001c0001t0004g0239a0001c0001t0004g0240a0001c0001t0024g0242 | 3 | HG00099.hp2 HG01928.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.549-1111C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73191533 | ||||||
chr14:73191557
|
TC | T | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.549-1086delC | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73191557 | ||||||
chr14:73192180
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.549-464G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73192180 | ||||||
chr14:73192267
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.549-377A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73192267 | ||||||
chr14:73192346
|
T | A | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.549-298T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73192346 | ||||||
chr14:73192359
|
T | G | 2 | a0001c0001t0013g0349a0001c0001t0013g0353 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.549-285T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73192359 | ||||||
chr14:73192366
|
C | T | 2 | a0001c0001t0004g0254a0001c0001t0005g0189 | 2 | HG01361.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.549-278C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73192366 | ||||||
chr14:73192446
|
C | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.549-198C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 6/11 | chr14 | 73192446 | ||||||
chr14:73193028
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.769+164C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193028 | ||||||
chr14:73193048
|
T | C | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.769+184T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193048 | ||||||
chr14:73193167
|
G | A | 4 | a0001c0001t0005g0169a0001c0001t0005g0170a0001c0001t0014g0171others(1): Show | 4 | HG00621.hp2 NA18955.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+303G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193167 | ||||||
chr14:73193199
|
A | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0061a0001c0001t0001g0062others(4): Show | 7 | HG00558.hp1 HG01943.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.769+335A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193199 | ||||||
chr14:73193390
|
C | T | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+526C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193390 | ||||||
chr14:73193404
|
G | C | 1 | a0001c0001t0003g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.769+540G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193404 | ||||||
chr14:73193491
|
A | G | 15 | a0001c0001t0001g0100a0001c0001t0001g0109a0001c0001t0001g0114others(12): Show | 15 | HG01891.hp2 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.769+627A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193491 | ||||||
chr14:73193536
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.769+672C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193536 | ||||||
chr14:73193549
|
CA | C | 235 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(232): Show | 236 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.769+700delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73193549 | |||||
chr14:73193549
|
CAA | C | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+699_769+700del others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73193549 | |||||
chr14:73193551
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0003g0298 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.769+700_769+714del others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73193551 | |||||
chr14:73193563
|
A | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.769+699A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193563 | ||||||
chr14:73193564
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0006g0277others(1): Show | 4 | HG01978.hp1 HG03688.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+700A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193564 | ||||||
chr14:73193565
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.769+701G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193565 | ||||||
chr14:73193565
|
G | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0006g0277others(1): Show | 4 | HG01978.hp1 HG03688.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+701G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193565 | ||||||
chr14:73193566
|
C | A | 5 | a0001c0001t0001g0037a0001c0001t0001g0078a0001c0001t0006g0277others(2): Show | 5 | HG01978.hp1 HG03688.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+702C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193566 | ||||||
chr14:73193584
|
A | G | 120 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 120 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.769+720A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193584 | ||||||
chr14:73193822
|
A | G | 1 | a0001c0001t0005g0001 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.769+958A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193822 | ||||||
chr14:73193859
|
A | G | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.769+995A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193859 | ||||||
chr14:73193872
|
G | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.769+1008G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193872 | ||||||
chr14:73193922
|
A | G | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.769+1058A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73193922 | ||||||
chr14:73194073
|
C | T | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1209C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194073 | ||||||
chr14:73194122
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.769+1258C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194122 | ||||||
chr14:73194239
|
C | CT | 40 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(37): Show | 40 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.769+1385dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73194239 | |||||
chr14:73194425
|
T | A | 39 | a0001c0001t0001g0098a0001c0001t0004g0003a0001c0001t0004g0004others(36): Show | 39 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.769+1561T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194425 | ||||||
chr14:73194426
|
A | T | 9 | a0001c0001t0002g0326a0001c0001t0003g0127a0001c0001t0004g0101others(6): Show | 9 | HG01257.hp1 HG02129.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+1562A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194426 | ||||||
chr14:73194435
|
T | A | 1 | a0001c0001t0001g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.769+1571T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194435 | ||||||
chr14:73194439
|
T | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.769+1575T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194439 | ||||||
chr14:73194499
|
G | T | 1 | a0001c0001t0010g0067 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.769+1635G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194499 | ||||||
chr14:73194528
|
TG | T | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.769+1667delG | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73194528 | |||||
chr14:73194566
|
C | CT | 20 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0055others(17): Show | 20 | HG01358.hp1 HG01496.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+1721dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73194566 | |||||
chr14:73194566
|
CT | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0092a0001c0001t0001g0111others(59): Show | 63 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.769+1721delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73194566 | |||||
chr14:73194629
|
C | T | 1 | a0001c0001t0005g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.769+1765C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194629 | ||||||
chr14:73194657
|
C | T | 1 | a0001c0001t0003g0207 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.769+1793C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194657 | ||||||
chr14:73194729
|
C | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.769+1865C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194729 | ||||||
chr14:73194819
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1955C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194819 | ||||||
chr14:73194820
|
G | A | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.769+1956G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194820 | ||||||
chr14:73194822
|
C | A | 1 | a0001c0001t0004g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.769+1958C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194822 | ||||||
chr14:73194995
|
T | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+2131T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73194995 | ||||||
chr14:73195139
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.769+2275C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195139 | ||||||
chr14:73195209
|
G | A | 1 | a0001c0001t0002g0326 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.769+2345G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195209 | ||||||
chr14:73195261
|
C | T | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+2397C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195261 | ||||||
chr14:73195457
|
A | G | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.770-2574A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195457 | ||||||
chr14:73195611
|
A | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0084others(1): Show | 4 | HG01934.hp1 HG01952.hp1 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-2420A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195611 | ||||||
chr14:73195651
|
G | A | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-2380G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195651 | ||||||
chr14:73195660
|
T | C | 26 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.770-2371T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195660 | ||||||
chr14:73195761
|
T | C | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.770-2270T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195761 | ||||||
chr14:73195921
|
C | T | 81 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(78): Show | 81 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.770-2110C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73195921 | ||||||
chr14:73196049
|
G | C | 32 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(29): Show | 32 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.770-1982G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196049 | ||||||
chr14:73196100
|
G | A | 6 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(3): Show | 6 | HG01074.hp2 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-1931G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196100 | ||||||
chr14:73196383
|
GTACTA | G | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0352 | 3 | HG01106.hp1 HG01516.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.770-1645_770-1641d others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196383 | |||||
chr14:73196413
|
CTATAT | C | 15 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-1611_770-1607d others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196413 | |||||
chr14:73196474
|
A | AT | 62 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0033others(59): Show | 62 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.770-1532dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196474 | |||||
chr14:73196474
|
A | ATT | 26 | a0001c0001t0004g0239a0001c0001t0006g0128a0001c0001t0006g0140others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.770-1533_770-1532d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196474 | |||||
chr14:73196474
|
AT | A | 57 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0087others(54): Show | 58 | HG00140.hp2 HG00423.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.770-1532delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196474 | |||||
chr14:73196535
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.770-1496G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196535 | ||||||
chr14:73196663
|
C | T | 51 | a0001c0001t0002g0103a0001c0001t0002g0141a0001c0001t0002g0145others(48): Show | 52 | HG00323.hp2 HG00423.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.770-1368C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196663 | ||||||
chr14:73196712
|
T | C | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.770-1319T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196712 | ||||||
chr14:73196767
|
G | A | 1 | a0001c0001t0003g0313 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.770-1264G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196767 | ||||||
chr14:73196802
|
A | G | 1 | a0001c0001t0006g0257 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.770-1229A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196802 | ||||||
chr14:73196928
|
CTTTCT | C | 18 | a0001c0001t0006g0128a0001c0001t0006g0148a0001c0001t0006g0257others(15): Show | 18 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.770-1099_770-1095d others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196928 | |||||
chr14:73196932
|
C | CT | 18 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0099others(15): Show | 18 | HG01169.hp2 HG01243.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.770-1081dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196932 | |||||
chr14:73196932
|
CT | C | 15 | a0001c0001t0001g0029a0001c0001t0001g0051a0001c0001t0001g0061others(12): Show | 15 | HG00558.hp1 HG01167.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-1081delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73196932 | |||||
chr14:73196936
|
T | C | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-1095T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73196936 | ||||||
chr14:73197005
|
G | T | 1 | a0001c0001t0008g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.770-1026G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197005 | ||||||
chr14:73197057
|
C | T | 1 | a0001c0001t0025g0269 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.770-974C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197057 | ||||||
chr14:73197058
|
G | A | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.770-973G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197058 | ||||||
chr14:73197135
|
G | A | 1 | a0001c0001t0011g0306 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.770-896G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197135 | ||||||
chr14:73197137
|
G | T | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.770-894G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197137 | ||||||
chr14:73197144
|
A | G | 9 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(6): Show | 9 | HG01496.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.770-887A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197144 | ||||||
chr14:73197154
|
T | C | 8 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0259others(5): Show | 8 | HG01496.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.770-877T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197154 | ||||||
chr14:73197175
|
C | T | 1 | a0001c0001t0004g0241 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.770-856C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197175 | ||||||
chr14:73197224
|
C | T | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.770-807C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197224 | ||||||
chr14:73197238
|
G | T | 43 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(40): Show | 43 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.770-793G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197238 | ||||||
chr14:73197277
|
T | C | 2 | a0001c0001t0008g0106a0001c0001t0008g0107 | 2 | HG00323.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.770-754T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197277 | ||||||
chr14:73197308
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.770-723A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197308 | ||||||
chr14:73197636
|
G | A | 6 | a0001c0001t0004g0251a0001c0001t0004g0252a0001c0001t0004g0253others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-395G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197636 | ||||||
chr14:73197703
|
CTA | C | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-326_770-325del others(2): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr14 | 73197703 | |||||
chr14:73197833
|
C | T | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.770-198C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73197833 | ||||||
chr14:73198010
|
T | C | 4 | a0001c0001t0005g0102a0001c0001t0005g0121a0001c0001t0005g0181others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-21T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 7/11 | chr14 | 73198010 | ||||||
chr14:73198145
|
G | T | 251 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(248): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.868+16G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198145 | ||||||
chr14:73198230
|
T | C | 1 | a0001c0001t0005g0167 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.868+101T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198230 | ||||||
chr14:73198349
|
T | C | 1 | a0001c0001t0004g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.868+220T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198349 | ||||||
chr14:73198544
|
T | C | 1 | a0001c0001t0003g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.868+415T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198544 | ||||||
chr14:73198646
|
G | A | 98 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(95): Show | 98 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.868+517G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198646 | ||||||
chr14:73198709
|
C | G | 42 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(39): Show | 42 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.868+580C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198709 | ||||||
chr14:73198725
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+596G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198725 | ||||||
chr14:73198833
|
G | C | 3 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0369 | 3 | HG01891.hp1 HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.868+704G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198833 | ||||||
chr14:73198859
|
G | A | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.868+730G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198859 | ||||||
chr14:73198914
|
C | T | 3 | a0001c0001t0003g0127a0001c0001t0003g0212a0001c0001t0003g0229 | 3 | HG02129.hp1 HG02280.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.868+785C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73198914 | ||||||
chr14:73199101
|
T | C | 1 | a0001c0001t0004g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.868+972T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199101 | ||||||
chr14:73199180
|
C | T | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.868+1051C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199180 | ||||||
chr14:73199228
|
T | C | 3 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0369 | 3 | HG01891.hp1 HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.868+1099T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199228 | ||||||
chr14:73199387
|
G | A | 1 | a0001c0001t0003g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.868+1258G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199387 | ||||||
chr14:73199777
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.868+1648G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199777 | ||||||
chr14:73199832
|
G | A | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.868+1703G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199832 | ||||||
chr14:73199967
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.868+1838G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73199967 | ||||||
chr14:73200196
|
A | G | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.868+2067A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200196 | ||||||
chr14:73200278
|
T | G | 1 | a0001c0001t0001g0076 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.868+2149T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200278 | ||||||
chr14:73200377
|
C | G | 24 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.868+2248C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200377 | ||||||
chr14:73200475
|
G | A | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+2346G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200475 | ||||||
chr14:73200513
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.868+2384C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200513 | ||||||
chr14:73200636
|
G | A | 2 | a0001c0001t0015g0301a0001c0001t0015g0302 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.868+2507G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200636 | ||||||
chr14:73200724
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.868+2595A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200724 | ||||||
chr14:73200729
|
T | C | 2 | a0001c0001t0015g0301a0001c0001t0015g0302 | 2 | HG01081.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.868+2600T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200729 | ||||||
chr14:73200747
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0058a0001c0001t0001g0071 | 3 | HG01256.hp1 HG01928.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.868+2618A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200747 | ||||||
chr14:73200825
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0041 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.868+2696C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200825 | ||||||
chr14:73200929
|
T | C | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.868+2800T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73200929 | ||||||
chr14:73201059
|
A | G | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.868+2930A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201059 | ||||||
chr14:73201075
|
T | TTTTG | 10 | a0001c0001t0002g0185a0001c0001t0002g0259a0001c0001t0002g0260others(7): Show | 10 | HG01192.hp2 HG02027.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.868+2976_868+2979d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73201075 | |||||
chr14:73201075
|
T | TTTTGTTT others(1): Show |
6 | a0001c0001t0002g0256a0001c0001t0002g0258a0001c0001t0002g0266others(3): Show | 6 | HG01496.hp2 HG01884.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.868+2972_868+2979d others(10): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73201075 | |||||
chr14:73201075
|
TTTTG | T | 50 | a0001c0001t0002g0343a0001c0001t0004g0291a0001c0001t0004g0292others(47): Show | 50 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.868+2976_868+2979d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73201075 | |||||
chr14:73201079
|
G | A | 56 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(53): Show | 57 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.868+2950G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201079 | ||||||
chr14:73201173
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.868+3044C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201173 | ||||||
chr14:73201240
|
G | A | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.868+3111G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201240 | ||||||
chr14:73201244
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.868+3115C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201244 | ||||||
chr14:73201248
|
C | T | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.868+3119C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201248 | ||||||
chr14:73201249
|
G | A | 2 | a0001c0001t0008g0106a0001c0001t0008g0107 | 2 | HG00323.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.868+3120G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201249 | ||||||
chr14:73201268
|
A | G | 3 | a0001c0001t0005g0172a0001c0001t0005g0173a0001c0001t0005g0190 | 3 | NA18612.hp2 NA18959.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.868+3139A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201268 | ||||||
chr14:73201375
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.868+3246C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201375 | ||||||
chr14:73201415
|
A | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.868+3286A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201415 | ||||||
chr14:73201588
|
T | C | 1 | a0001c0001t0002g0364 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.868+3459T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201588 | ||||||
chr14:73201760
|
T | A | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.868+3631T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73201760 | ||||||
chr14:73202016
|
G | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.868+3887G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202016 | ||||||
chr14:73202109
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.868+3980A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202109 | ||||||
chr14:73202131
|
A | G | 33 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(30): Show | 33 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.868+4002A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202131 | ||||||
chr14:73202191
|
T | C | 1 | a0001c0001t0003g0123 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.868+4062T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202191 | ||||||
chr14:73202211
|
A | AT | 244 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(241): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.868+4092dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202211 | |||||
chr14:73202224
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.868+4095A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202224 | ||||||
chr14:73202313
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.869-4073T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202313 | ||||||
chr14:73202366
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.869-4020A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202366 | ||||||
chr14:73202406
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.869-3980A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202406 | ||||||
chr14:73202417
|
ACTATATA others(3): Show |
A | 1 | a0001c0001t0015g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.869-3968_869-3959d others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202417 | ||||||
chr14:73202417
|
ACTATATA others(7): Show |
A | 4 | a0001c0001t0006g0140a0001c0001t0006g0148a0001c0001t0006g0271others(1): Show | 4 | HG02738.hp1 HG03942.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-3968_869-3955d others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202417 | ||||||
chr14:73202417
|
ACTATATA others(9): Show |
A | 1 | a0001c0001t0006g0284 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.869-3968_869-3953d others(18): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202417 | ||||||
chr14:73202417
|
ACTATATA others(11): Show |
A | 3 | a0001c0001t0007g0285a0001c0001t0007g0288a0001c0001t0007g0370 | 3 | HG02055.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.869-3968_869-3951d others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202417 | ||||||
chr14:73202417
|
ACTATATA others(13): Show |
A | 3 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0193 | 3 | HG01261.hp2 NA18944.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.869-3968_869-3949d others(22): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202417 | ||||||
chr14:73202418
|
C | CTA | 20 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0021others(17): Show | 20 | HG00558.hp2 HG01069.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.869-3924_869-3923d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATA | 10 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0028others(7): Show | 10 | HG00733.hp2 HG01167.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.869-3926_869-3923d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATATA | 4 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0070others(1): Show | 4 | HG00741.hp2 HG01952.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3928_869-3923d others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0001g0050a0001c0001t0001g0060a0001c0001t0002g0280others(1): Show | 4 | HG01123.hp1 HG01884.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3930_869-3923d others(10): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.869-3932_869-3923d others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0002g0266 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.869-3934_869-3923d others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATATAT others(7): Show |
1 | a0001c0001t0016g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.869-3936_869-3923d others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | CTATATAT others(9): Show |
1 | a0001c0001t0001g0038 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.869-3938_869-3923d others(18): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
C | T | 30 | a0001c0001t0006g0128a0001c0001t0006g0257a0001c0001t0006g0272others(27): Show | 30 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.869-3968C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202418 | ||||||
chr14:73202418
|
CTA | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(21): Show | 24 | HG00423.hp2 HG01433.hp1 HG02683.hp1 others(21): Show |
intron_variant | MODIFIER | c.869-3924_869-3923d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
CTATATA | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-3928_869-3923d others(8): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
CTATATAT others(3): Show |
C | 1 | a0001c0001t0030g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.869-3932_869-3923d others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
CTATATAT others(5): Show |
C | 1 | a0001c0001t0002g0141 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.869-3934_869-3923d others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
CTATATAT others(7): Show |
C | 2 | a0001c0001t0004g0143a0001c0001t0004g0237 | 2 | HG02132.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.869-3936_869-3923d others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202418
|
CTATATAT others(19): Show |
C | 4 | a0001c0001t0003g0196a0001c0001t0003g0203a0001c0001t0003g0313others(1): Show | 4 | HG03139.hp1 HG03453.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3948_869-3923d others(28): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202418 | |||||
chr14:73202420
|
A | T | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-3966A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202420 | ||||||
chr14:73202426
|
A | T | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.869-3960A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202426 | ||||||
chr14:73202428
|
A | T | 1 | a0001c0001t0015g0301 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.869-3958A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202428 | ||||||
chr14:73202432
|
A | T | 4 | a0001c0001t0006g0140a0001c0001t0006g0148a0001c0001t0006g0271others(1): Show | 4 | HG02738.hp1 HG03942.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-3954A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202432 | ||||||
chr14:73202432
|
ATATATAT others(28): Show |
A | 1 | a0001c0001t0004g0101 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.869-3952_869-3918d others(37): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202432 | |||||
chr14:73202434
|
A | T | 1 | a0001c0001t0006g0284 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.869-3952A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202434 | ||||||
chr14:73202434
|
ATATATAT others(28): Show |
A | 1 | a0001c0001t0004g0116 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.869-3950_869-3916d others(37): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202434 | |||||
chr14:73202435
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.869-3951T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202435 | ||||||
chr14:73202436
|
A | T | 3 | a0001c0001t0007g0285a0001c0001t0007g0288a0001c0001t0007g0370 | 3 | HG02055.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.869-3950A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202436 | ||||||
chr14:73202436
|
ATATATAT others(20): Show |
A | 3 | a0001c0001t0003g0126a0001c0001t0003g0199a0001c0001t0003g0216 | 3 | HG01346.hp2 HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.869-3948_869-3922d others(29): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202436 | |||||
chr14:73202436
|
ATATATAT others(21): Show |
A | 5 | a0001c0001t0003g0151a0001c0001t0003g0206a0001c0001t0003g0303others(2): Show | 5 | HG02109.hp1 HG02647.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-3948_869-3921d others(30): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202436 | |||||
chr14:73202436
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0004g0304 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.869-3948_869-3920d others(31): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202436 | |||||
chr14:73202437
|
TATATATA others(16): Show |
T | 1 | a0001c0001t0002g0348 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.869-3948_869-3926d others(25): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202437 | ||||||
chr14:73202438
|
A | T | 3 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0193 | 3 | HG01261.hp2 NA18944.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.869-3948A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202438 | ||||||
chr14:73202438
|
ATATATAT others(19): Show |
A | 15 | a0001c0001t0003g0002a0001c0001t0003g0202a0001c0001t0003g0205others(12): Show | 16 | HG02818.hp1 HG02922.hp2 HG03540.hp1 others(13): Show |
intron_variant | MODIFIER | c.869-3946_869-3921d others(28): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202438 | |||||
chr14:73202438
|
ATATATAT others(20): Show |
A | 16 | a0001c0001t0003g0108a0001c0001t0003g0194a0001c0001t0003g0208others(13): Show | 16 | HG00642.hp1 HG01433.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.869-3946_869-3920d others(29): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202438 | |||||
chr14:73202438
|
ATATATAT others(21): Show |
A | 3 | a0001c0001t0003g0200a0001c0001t0003g0221a0001c0001t0003g0298 | 3 | HG00140.hp2 HG00639.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.869-3946_869-3919d others(30): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202438 | |||||
chr14:73202438
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0017g0268 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.869-3946_869-3917d others(32): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202438 | |||||
chr14:73202438
|
ATATATAT others(34): Show |
A | 4 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0125others(1): Show | 4 | HG00423.hp1 HG02155.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-3946_869-3906d others(43): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202438 | |||||
chr14:73202439
|
TATATATA others(16): Show |
T | 1 | a0001c0001t0002g0354 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.869-3946_869-3924d others(25): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202439 | ||||||
chr14:73202440
|
ATATATAT others(19): Show |
A | 2 | a0001c0001t0003g0127a0003c0003t0003g0366 | 2 | HG02129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.869-3944_869-3919d others(28): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202440 | |||||
chr14:73202440
|
ATATATAT others(20): Show |
A | 4 | a0001c0001t0003g0204a0001c0001t0003g0224a0001c0001t0009g0198others(1): Show | 4 | HG01070.hp1 HG01192.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3944_869-3918d others(29): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202440 | |||||
chr14:73202440
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0017g0195 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.869-3944_869-3915d others(32): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202440 | |||||
chr14:73202441
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0006g0283 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.869-3944_869-3932d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202441 | ||||||
chr14:73202441
|
TATATATA others(8): Show |
T | 4 | a0001c0001t0006g0257a0001c0001t0006g0272a0001c0001t0006g0281others(1): Show | 4 | HG03704.hp2 NA18947.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-3944_869-3930d others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202441 | ||||||
chr14:73202441
|
TATATATA others(12): Show |
T | 1 | a0001c0001t0008g0192 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.869-3944_869-3926d others(21): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202441 | ||||||
chr14:73202442
|
ATATATAT others(16): Show |
A | 2 | a0001c0001t0027g0307a0001c0004t0020g0312 | 2 | HG01074.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.869-3942_869-3920d others(25): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202442 | |||||
chr14:73202442
|
ATATATAT others(20): Show |
A | 1 | a0001c0001t0009g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.869-3942_869-3916d others(29): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202442 | |||||
chr14:73202443
|
TATATATA others(6): Show |
T | 2 | a0001c0001t0006g0128a0001c0001t0006g0278 | 2 | HG00544.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.869-3942_869-3930d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202443 | ||||||
chr14:73202443
|
TATATATA others(8): Show |
T | 4 | a0001c0001t0006g0273a0001c0001t0006g0275a0001c0001t0006g0276others(1): Show | 4 | HG01975.hp1 NA18747.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.869-3942_869-3928d others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202443 | ||||||
chr14:73202444
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0007g0287 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.869-3940_869-3922d others(21): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202444 | |||||
chr14:73202444
|
ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0064 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.869-3940_869-3917d others(26): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202444 | |||||
chr14:73202445
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0022g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.869-3940_869-3928d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202445 | ||||||
chr14:73202445
|
TATATATA others(10): Show |
T | 1 | a0001c0001t0007g0155 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.869-3940_869-3924d others(19): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202445 | ||||||
chr14:73202446
|
A | C | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.869-3940A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202446 | ||||||
chr14:73202446
|
ATATATAT others(10): Show |
A | 2 | a0001c0001t0007g0156a0001c0001t0007g0157 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.869-3938_869-3922d others(19): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202446 | |||||
chr14:73202446
|
ATATATAT others(11): Show |
A | 4 | a0001c0001t0002g0328a0001c0001t0007g0286a0001c0001t0007g0290others(1): Show | 4 | HG01256.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.869-3938_869-3921d others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202446 | |||||
chr14:73202447
|
TATATATA others(4): Show |
T | 3 | a0001c0001t0011g0309a0001c0001t0011g0310a0001c0001t0019g0311 | 3 | HG02486.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.869-3938_869-3928d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202447 | ||||||
chr14:73202447
|
TATATATA others(8): Show |
T | 2 | a0001c0001t0007g0154a0001c0001t0029g0133 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.869-3938_869-3924d others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202447 | ||||||
chr14:73202448
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0001g0052 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.869-3936_869-3919d others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202448 | |||||
chr14:73202449
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0011g0306a0001c0001t0011g0308 | 2 | HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.869-3936_869-3926d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202449 | ||||||
chr14:73202449
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0002g0103 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.869-3936_869-3924d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202449 | ||||||
chr14:73202450
|
ATATATAT others(6): Show |
A | 2 | a0001c0001t0002g0145a0001c0001t0002g0146 | 2 | HG00735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.869-3934_869-3922d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202450 | |||||
chr14:73202451
|
TATATATA others(4): Show |
T | 2 | a0001c0001t0002g0147a0001c0001t0015g0302 | 2 | HG00738.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.869-3934_869-3924d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202451 | ||||||
chr14:73202452
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0250a0001c0001t0002g0361 | 2 | HG01891.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.869-3932_869-3922d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202452 | |||||
chr14:73202452
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0233 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.869-3932_869-3920d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202452 | |||||
chr14:73202454
|
A | T | 2 | a0001c0001t0002g0262a0001c0001t0004g0237 | 2 | HG02132.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.869-3932A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202454 | ||||||
chr14:73202454
|
ATATATAT others(3): Show |
A | 2 | a0001c0001t0001g0232a0001c0001t0001g0249 | 2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.869-3930_869-3921d others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202454 | |||||
chr14:73202454
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0001g0231 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.869-3930_869-3920d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202454 | |||||
chr14:73202454
|
ATATATAT others(8): Show |
A | 1 | a0001c0001t0005g0173 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.869-3930_869-3916d others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202454 | |||||
chr14:73202456
|
A | T | 6 | a0001c0001t0002g0262a0001c0001t0004g0237a0001c0001t0005g0160others(3): Show | 6 | HG00408.hp1 HG00423.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-3930A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202456 | ||||||
chr14:73202456
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0005g0001 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.869-3928_869-3912d others(19): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202456 | |||||
chr14:73202457
|
TA | T | 6 | a0001c0001t0001g0092a0001c0001t0002g0185a0001c0001t0005g0166others(3): Show | 6 | HG02132.hp1 HG02135.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-3928delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202457 | ||||||
chr14:73202458
|
A | T | 24 | a0001c0001t0001g0035a0001c0001t0002g0258a0001c0001t0002g0262others(21): Show | 24 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.869-3928A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202458 | ||||||
chr14:73202460
|
A | AT | 3 | a0001c0001t0001g0089a0001c0001t0002g0333a0001c0001t0005g0187 | 3 | HG02027.hp2 NA18947.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.869-3925dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202460 | |||||
chr14:73202460
|
A | ATT | 5 | a0001c0001t0001g0020a0001c0001t0001g0134a0001c0001t0005g0121others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-3925_869-3924i others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202460 | |||||
chr14:73202460
|
A | ATTT | 5 | a0001c0001t0002g0323a0001c0001t0004g0254a0001c0001t0004g0255others(2): Show | 5 | HG01106.hp1 HG01361.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-3925_869-3924i others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202460 | |||||
chr14:73202460
|
A | T | 54 | a0001c0001t0001g0035a0001c0001t0001g0092a0001c0001t0001g0105others(51): Show | 54 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.869-3926A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202460 | ||||||
chr14:73202462
|
A | ATAT | 6 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0034others(3): Show | 6 | HG00408.hp2 HG01928.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-3923_869-3922i others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0326 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.869-3923_869-3922i others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0295 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.869-3923_869-3922i others(22): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0004g0241 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.869-3923_869-3922i others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0004g0236 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.869-3923_869-3922i others(18): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0004g0243 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.869-3923_869-3922i others(19): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(3): Show |
2 | a0001c0001t0004g0235a0001c0001t0005g0176 | 2 | HG03710.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.869-3923_869-3922i others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0004g0246 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.869-3923_869-3922i others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0248 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.869-3923_869-3922i others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0113 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.869-3923_869-3922i others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0110a0001c0001t0004g0003a0001c0001t0004g0006 | 3 | HG01243.hp1 HG01943.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.869-3923_869-3922i others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0004g0244a0001c0001t0004g0297a0001c0001t0005g0174 | 3 | HG02027.hp1 HG03942.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.869-3923_869-3922i others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0004g0247 | 3 | HG00733.hp1 HG01106.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.869-3923_869-3922i others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0004g0005 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.869-3923_869-3922i others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0004g0004 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.869-3904_869-3894d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202462
|
A | T | 93 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0066others(90): Show | 93 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.869-3924A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202462 | ||||||
chr14:73202462
|
ATT | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0022others(5): Show | 8 | HG00738.hp1 HG02683.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.869-3895_869-3894d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73202462 | |||||
chr14:73202463
|
T | TA | 6 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0002g0358others(3): Show | 6 | HG00642.hp2 HG01099.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.869-3923_869-3922i others(3): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202463 | ||||||
chr14:73202463
|
T | TATA | 3 | a0001c0001t0001g0074a0001c0001t0001g0095a0001c0001t0005g0117 | 3 | HG00609.hp2 NA19077.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.869-3923_869-3922i others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202463 | ||||||
chr14:73202463
|
T | TATATA | 5 | a0001c0001t0001g0007a0001c0001t0001g0031a0001c0001t0001g0078others(2): Show | 5 | HG00323.hp1 HG01169.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.869-3923_869-3922i others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202463 | ||||||
chr14:73202464
|
T | A | 38 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0017others(35): Show | 38 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.869-3922T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202464 | ||||||
chr14:73202465
|
T | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0065others(5): Show | 8 | HG00642.hp2 HG01099.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.869-3921T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202465 | ||||||
chr14:73202466
|
T | A | 18 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0017others(15): Show | 18 | HG00558.hp2 HG00609.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.869-3920T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202466 | ||||||
chr14:73202467
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.869-3919T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202467 | ||||||
chr14:73202468
|
T | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0041others(2): Show | 5 | HG00558.hp2 HG02074.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-3918T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202468 | ||||||
chr14:73202469
|
T | A | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.869-3917T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202469 | ||||||
chr14:73202470
|
T | A | 3 | a0001c0001t0001g0041a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG02155.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.869-3916T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202470 | ||||||
chr14:73202471
|
T | A | 1 | a0001c0001t0016g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.869-3915T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202471 | ||||||
chr14:73202472
|
T | A | 1 | a0001c0001t0016g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.869-3914T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202472 | ||||||
chr14:73202498
|
A | C | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-3888A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202498 | ||||||
chr14:73202534
|
G | A | 1 | a0001c0001t0005g0167 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.869-3852G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202534 | ||||||
chr14:73202628
|
A | G | 3 | a0001c0001t0004g0143a0001c0001t0029g0133a0001c0001t0030g0168 | 3 | HG02257.hp2 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.869-3758A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202628 | ||||||
chr14:73202693
|
C | T | 8 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(5): Show | 8 | HG00733.hp1 HG01106.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.869-3693C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202693 | ||||||
chr14:73202804
|
T | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-3582T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202804 | ||||||
chr14:73202829
|
A | G | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.869-3557A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73202829 | ||||||
chr14:73203319
|
C | T | 8 | a0001c0001t0002g0357a0001c0001t0002g0358a0001c0001t0002g0359others(5): Show | 8 | HG00558.hp2 HG02015.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.869-3067C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73203319 | ||||||
chr14:73203419
|
T | TTTTTTCT others(4): Show |
1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.869-2950_869-2940d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73203419 | |||||
chr14:73203577
|
C | T | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.869-2809C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73203577 | ||||||
chr14:73203785
|
C | A | 1 | a0001c0001t0003g0203 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.869-2601C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73203785 | ||||||
chr14:73203899
|
A | G | 1 | a0001c0001t0004g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.869-2487A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73203899 | ||||||
chr14:73204061
|
C | T | 1 | a0001c0001t0003g0305 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.869-2325C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204061 | ||||||
chr14:73204084
|
C | T | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.869-2302C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204084 | ||||||
chr14:73204097
|
C | G | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-2289C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204097 | ||||||
chr14:73204111
|
G | C | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.869-2275G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204111 | ||||||
chr14:73204251
|
G | A | 34 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(31): Show | 34 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.869-2135G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204251 | ||||||
chr14:73204253
|
C | T | 1 | a0001c0001t0004g0304 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.869-2133C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204253 | ||||||
chr14:73204297
|
C | CT | 24 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.869-2074dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73204297 | |||||
chr14:73204321
|
C | T | 30 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(27): Show | 30 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.869-2065C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204321 | ||||||
chr14:73204382
|
T | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-2004T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204382 | ||||||
chr14:73204386
|
TA | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-1993delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73204386 | |||||
chr14:73204387
|
A | T | 1 | a0001c0001t0003g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.869-1999A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204387 | ||||||
chr14:73204471
|
A | G | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-1915A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204471 | ||||||
chr14:73204474
|
A | G | 27 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(24): Show | 27 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.869-1912A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204474 | ||||||
chr14:73204528
|
T | TAA | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.869-1844_869-1843d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73204528 | |||||
chr14:73204528
|
TA | T | 66 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0087others(63): Show | 67 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.869-1843delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73204528 | |||||
chr14:73204597
|
T | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-1789T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204597 | ||||||
chr14:73204794
|
T | C | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.869-1592T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204794 | ||||||
chr14:73204808
|
G | A | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-1578G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204808 | ||||||
chr14:73204847
|
G | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.869-1539G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204847 | ||||||
chr14:73204900
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.869-1486A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204900 | ||||||
chr14:73204937
|
T | G | 1 | a0001c0001t0012g0188 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.869-1449T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73204937 | ||||||
chr14:73205091
|
A | C | 1 | a0001c0001t0002g0260 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.869-1295A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205091 | ||||||
chr14:73205135
|
T | A | 26 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(23): Show | 26 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.869-1251T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205135 | ||||||
chr14:73205198
|
C | T | 1 | a0001c0001t0028g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.869-1188C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205198 | ||||||
chr14:73205203
|
G | A | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.869-1183G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205203 | ||||||
chr14:73205209
|
G | T | 2 | a0001c0001t0003g0313a0001c0001t0003g0314 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.869-1177G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205209 | ||||||
chr14:73205215
|
G | A | 15 | a0001c0001t0003g0002a0001c0001t0003g0196a0001c0001t0003g0202others(12): Show | 16 | HG02074.hp1 HG02723.hp2 HG03453.hp2 others(13): Show |
intron_variant | MODIFIER | c.869-1171G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205215 | ||||||
chr14:73205272
|
C | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-1114C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205272 | ||||||
chr14:73205285
|
G | T | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.869-1101G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205285 | ||||||
chr14:73205372
|
G | A | 1 | a0001c0001t0030g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.869-1014G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205372 | ||||||
chr14:73205407
|
A | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.869-979A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205407 | ||||||
chr14:73205411
|
G | A | 50 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(47): Show | 51 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.869-975G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205411 | ||||||
chr14:73205421
|
G | A | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 122 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.869-965G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205421 | ||||||
chr14:73205440
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.869-946C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205440 | ||||||
chr14:73205478
|
C | CA | 24 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0019others(21): Show | 24 | HG00735.hp2 HG01175.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.869-885dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73205478 | |||||
chr14:73205478
|
CA | C | 41 | a0001c0001t0001g0057a0001c0001t0001g0232a0001c0001t0002g0371others(38): Show | 41 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.869-885delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr14 | 73205478 | |||||
chr14:73205802
|
T | A | 2 | a0001c0001t0017g0195a0001c0001t0017g0268 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.869-584T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205802 | ||||||
chr14:73205815
|
C | G | 5 | a0001c0001t0013g0336a0001c0001t0013g0349a0001c0001t0013g0353others(2): Show | 5 | HG02683.hp1 HG02698.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-571C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205815 | ||||||
chr14:73205820
|
T | C | 2 | a0001c0001t0003g0151a0001c0001t0003g0303 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.869-566T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205820 | ||||||
chr14:73205873
|
T | C | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.869-513T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73205873 | ||||||
chr14:73206123
|
C | A | 262 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(259): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.869-263C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73206123 | ||||||
chr14:73206159
|
A | G | 2 | a0001c0001t0004g0143a0001c0001t0029g0133 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.869-227A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73206159 | ||||||
chr14:73206213
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.869-173C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73206213 | ||||||
chr14:73206322
|
T | G | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.869-64T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 8/11 | chr14 | 73206322 | ||||||
chr14:73206498
|
C | T | 1 | a0001c0001t0030g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.955+26C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73206498 | ||||||
chr14:73206658
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.955+186A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73206658 | ||||||
chr14:73206672
|
T | C | 24 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.955+200T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73206672 | ||||||
chr14:73206926
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0260 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.955+454C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73206926 | ||||||
chr14:73207116
|
G | A | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.955+644G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207116 | ||||||
chr14:73207128
|
G | T | 30 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(27): Show | 30 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.955+656G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207128 | ||||||
chr14:73207129
|
C | A | 1 | a0001c0001t0005g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.955+657C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207129 | ||||||
chr14:73207652
|
G | T | 14 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(11): Show | 14 | HG00323.hp2 HG01261.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.955+1180G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207652 | ||||||
chr14:73207669
|
A | G | 8 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(5): Show | 8 | HG00323.hp2 HG01261.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.955+1197A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207669 | ||||||
chr14:73207750
|
T | G | 66 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(63): Show | 66 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.955+1278T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207750 | ||||||
chr14:73207903
|
G | T | 1 | a0001c0001t0002g0363 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.955+1431G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73207903 | ||||||
chr14:73208045
|
TG | T | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.955+1577delG | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 73208045 | |||||
chr14:73208051
|
A | G | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+1579A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208051 | ||||||
chr14:73208133
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.955+1661C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208133 | ||||||
chr14:73208150
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.955+1678C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208150 | ||||||
chr14:73208191
|
G | A | 3 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0025g0269 | 3 | HG01884.hp2 HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.955+1719G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208191 | ||||||
chr14:73208202
|
C | T | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.955+1730C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208202 | ||||||
chr14:73208221
|
G | A | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.955+1749G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208221 | ||||||
chr14:73208242
|
C | T | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(119): Show | 122 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.955+1770C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208242 | ||||||
chr14:73208309
|
C | T | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.955+1837C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208309 | ||||||
chr14:73208519
|
A | G | 1 | a0001c0001t0028g0293 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.955+2047A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208519 | ||||||
chr14:73208718
|
A | G | 1 | a0001c0001t0004g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.955+2246A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208718 | ||||||
chr14:73208725
|
C | T | 1 | a0001c0001t0003g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.955+2253C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208725 | ||||||
chr14:73208914
|
C | T | 2 | a0001c0001t0013g0349a0001c0001t0013g0353 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.955+2442C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208914 | ||||||
chr14:73208995
|
G | A | 15 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 15 | HG00733.hp1 HG01106.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.955+2523G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73208995 | ||||||
chr14:73209008
|
C | T | 2 | a0001c0001t0008g0106a0001c0001t0008g0107 | 2 | HG00323.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.955+2536C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209008 | ||||||
chr14:73209040
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.955+2568A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209040 | ||||||
chr14:73209099
|
G | A | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.955+2627G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209099 | ||||||
chr14:73209208
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.956-2561G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209208 | ||||||
chr14:73209286
|
C | T | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.956-2483C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209286 | ||||||
chr14:73209334
|
G | A | 55 | a0001c0001t0003g0002a0001c0001t0003g0108a0001c0001t0003g0123others(52): Show | 56 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.956-2435G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209334 | ||||||
chr14:73209432
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.956-2337A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209432 | ||||||
chr14:73209439
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.956-2330G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209439 | ||||||
chr14:73209484
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.956-2285C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209484 | ||||||
chr14:73209558
|
C | A | 1 | a0001c0001t0008g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.956-2211C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209558 | ||||||
chr14:73209591
|
C | T | 1 | a0001c0001t0002g0362 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.956-2178C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209591 | ||||||
chr14:73209708
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.956-2061G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209708 | ||||||
chr14:73209992
|
C | A | 2 | a0001c0001t0004g0101a0001c0001t0004g0116 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.956-1777C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73209992 | ||||||
chr14:73210007
|
T | C | 20 | a0001c0001t0005g0186a0001c0001t0006g0128a0001c0001t0006g0140others(17): Show | 20 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.956-1762T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210007 | ||||||
chr14:73210230
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.956-1539G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210230 | ||||||
chr14:73210279
|
A | G | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.956-1490A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210279 | ||||||
chr14:73210284
|
A | G | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-1485A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210284 | ||||||
chr14:73210437
|
C | CT | 3 | a0001c0001t0002g0322a0001c0001t0002g0323a0001c0001t0002g0352 | 3 | HG01106.hp1 HG01516.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.956-1329dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 73210437 | |||||
chr14:73210502
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.956-1267G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210502 | ||||||
chr14:73210514
|
T | C | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.956-1255T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210514 | ||||||
chr14:73210514
|
T | G | 1 | a0001c0001t0006g0140 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.956-1255T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210514 | ||||||
chr14:73210796
|
G | A | 1 | a0001c0001t0004g0244 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.956-973G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210796 | ||||||
chr14:73210878
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.956-891T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210878 | ||||||
chr14:73210894
|
A | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-875A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210894 | ||||||
chr14:73210989
|
C | A | 1 | a0001c0001t0005g0174 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.956-780C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73210989 | ||||||
chr14:73211001
|
C | T | 5 | a0001c0001t0016g0267a0001c0001t0016g0279a0001c0001t0017g0195others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.956-768C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73211001 | ||||||
chr14:73211227
|
C | A | 2 | a0001c0001t0004g0291a0001c0001t0004g0292 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.956-542C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73211227 | ||||||
chr14:73211255
|
T | G | 263 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(260): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.956-514T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73211255 | ||||||
chr14:73211360
|
A | AT | 19 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(16): Show | 19 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.956-403dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr14 | 73211360 | |||||
chr14:73211461
|
A | G | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-308A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73211461 | ||||||
chr14:73211505
|
G | A | 21 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(18): Show | 21 | HG00323.hp2 HG01243.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.956-264G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73211505 | ||||||
chr14:73211552
|
G | GA | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.956-217_956-216ins others(1): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 9/11 | chr14 | 73211552 | ||||||
chr14:73212055
|
T | C | 3 | a0001c0001t0017g0195a0001c0001t0017g0268a0001c0001t0027g0307 | 3 | HG01074.hp2 HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1129+113T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212055 | ||||||
chr14:73212088
|
C | CT | 37 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0020others(34): Show | 37 | HG00738.hp1 HG00741.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.1129+187dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
C | CTT | 16 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0035others(13): Show | 16 | HG00609.hp1 HG00642.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1129+186_1129+187d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0137 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1129+176_1129+187d others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0111a0001c0001t0001g0135a0001c0001t0002g0145 | 3 | HG00735.hp1 HG02717.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1129+174_1129+187d others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
C | CTTTTTTT others(8): Show |
2 | a0001c0001t0002g0146a0001c0001t0029g0133 | 2 | HG03017.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1129+173_1129+187d others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0136a0001c0001t0002g0141 | 2 | HG01358.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1129+171_1129+187d others(19): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0138 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1129+170_1129+187d others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CT | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0016others(27): Show | 30 | HG00323.hp1 HG00558.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.1129+187delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTT | C | 19 | a0001c0001t0001g0036a0001c0001t0001g0098a0001c0001t0002g0339others(16): Show | 19 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1129+186_1129+187d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTT | C | 17 | a0001c0001t0002g0326a0001c0001t0003g0002a0001c0001t0003g0125others(14): Show | 18 | HG01070.hp1 HG01257.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1129+185_1129+187d others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTT | C | 15 | a0001c0001t0001g0149a0001c0001t0003g0123a0001c0001t0003g0126others(12): Show | 15 | HG00642.hp1 HG01192.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.1129+184_1129+187d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTT | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0150others(5): Show | 8 | HG02015.hp1 HG02630.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129+183_1129+187d others(7): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT | C | 6 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0142others(3): Show | 6 | HG02109.hp2 HG02559.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1129+181_1129+187d others(9): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(1): Show |
C | 28 | a0001c0001t0001g0070a0001c0001t0001g0100a0001c0001t0001g0109others(25): Show | 28 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1129+180_1129+187d others(10): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(2): Show |
C | 17 | a0001c0001t0001g0115a0001c0001t0001g0139a0001c0001t0003g0305others(14): Show | 17 | HG00741.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1129+179_1129+187d others(11): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0004g0003a0001c0001t0004g0143a0001c0001t0004g0251 | 3 | HG01070.hp2 HG01943.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1129+178_1129+187d others(12): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0002g0261a0001c0001t0002g0263a0001c0004t0020g0312 | 3 | HG02145.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1129+177_1129+187d others(13): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0369a0001c0001t0005g0181 | 2 | HG01069.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1129+176_1129+187d others(14): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(6): Show |
C | 19 | a0001c0001t0002g0185a0001c0001t0002g0256a0001c0001t0002g0258others(16): Show | 19 | HG00423.hp2 HG02056.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.1129+175_1129+187d others(15): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(7): Show |
C | 48 | a0001c0001t0002g0259a0001c0001t0002g0266a0001c0001t0002g0270others(45): Show | 49 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1129+174_1129+187d others(16): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(8): Show |
C | 10 | a0001c0001t0001g0062a0001c0001t0005g0186a0001c0001t0007g0156others(7): Show | 10 | HG01081.hp2 HG01243.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1129+173_1129+187d others(17): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(9): Show |
C | 7 | a0001c0001t0007g0287a0001c0001t0008g0106a0001c0001t0008g0107others(4): Show | 7 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129+172_1129+187d others(18): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0017g0268 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1129+170_1129+187d others(20): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0002g0319a0001c0001t0017g0195a0001c0001t0023g0321 | 3 | HG01361.hp1 HG02723.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.1129+169_1129+187d others(21): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(13): Show |
C | 2 | a0001c0001t0002g0317a0001c0001t0027g0307 | 2 | HG01074.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1129+168_1129+187d others(22): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(16): Show |
C | 3 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0086 | 3 | HG01934.hp1 NA18612.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1129+165_1129+187d others(25): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(18): Show |
C | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1129+163_1129+187d others(27): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212088
|
CTTTTTTT others(19): Show |
C | 2 | a0001c0001t0003g0313a0001c0001t0003g0314 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1129+162_1129+187d others(28): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73212088 | |||||
chr14:73212094
|
T | C | 1 | a0001c0001t0003g0299 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1129+152T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212094 | ||||||
chr14:73212095
|
T | C | 2 | a0001c0001t0003g0298a0001c0001t0003g0300 | 2 | HG00140.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1129+153T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212095 | ||||||
chr14:73212167
|
A | G | 40 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(37): Show | 40 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1129+225A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212167 | ||||||
chr14:73212184
|
C | T | 1 | a0001c0001t0008g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1129+242C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212184 | ||||||
chr14:73212302
|
G | C | 2 | a0001c0001t0003g0199a0001c0001t0003g0200 | 2 | HG00639.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1129+360G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212302 | ||||||
chr14:73212347
|
G | A | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129+405G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212347 | ||||||
chr14:73212466
|
T | C | 1 | a0001c0001t0002g0333 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1129+524T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212466 | ||||||
chr14:73212509
|
A | G | 1 | a0001c0001t0003g0221 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1129+567A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212509 | ||||||
chr14:73212512
|
G | C | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1129+570G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212512 | ||||||
chr14:73212690
|
T | G | 1 | a0001c0001t0002g0357 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1129+748T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212690 | ||||||
chr14:73212714
|
T | C | 1 | a0001c0001t0004g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1129+772T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212714 | ||||||
chr14:73212852
|
C | T | 40 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(37): Show | 40 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1129+910C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212852 | ||||||
chr14:73212885
|
G | A | 1 | a0001c0001t0004g0376 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1129+943G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212885 | ||||||
chr14:73212993
|
G | A | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129+1051G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73212993 | ||||||
chr14:73213081
|
A | G | 1 | a0001c0001t0003g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1129+1139A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213081 | ||||||
chr14:73213259
|
C | A | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1129+1317C>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213259 | ||||||
chr14:73213262
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1129+1320T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213262 | ||||||
chr14:73213398
|
C | G | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1129+1456C>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213398 | ||||||
chr14:73213412
|
A | T | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1129+1470A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213412 | ||||||
chr14:73213423
|
A | T | 1 | a0001c0001t0027g0307 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1129+1481A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213423 | ||||||
chr14:73213500
|
G | A | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1129+1558G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213500 | ||||||
chr14:73213746
|
A | C | 9 | a0001c0001t0006g0272a0001c0001t0006g0273a0001c0001t0006g0275others(6): Show | 9 | HG00408.hp1 HG01975.hp1 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1129+1804A>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73213746 | ||||||
chr14:73214389
|
T | G | 40 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(37): Show | 40 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1129+2447T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73214389 | ||||||
chr14:73214517
|
C | T | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1129+2575C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73214517 | ||||||
chr14:73214518
|
G | A | 10 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1129+2576G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73214518 | ||||||
chr14:73214530
|
CA | C | 11 | a0001c0001t0002g0333a0001c0001t0004g0291a0001c0001t0004g0292others(8): Show | 11 | HG01074.hp2 HG01884.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1130-2579delA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73214530 | |||||
chr14:73214530
|
CAA | C | 22 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(19): Show | 22 | HG00323.hp2 HG01243.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.1130-2580_1130-257 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73214530 | |||||
chr14:73214586
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1130-2540T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73214586 | ||||||
chr14:73214673
|
T | G | 41 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(38): Show | 41 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.1130-2453T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73214673 | ||||||
chr14:73215228
|
T | C | 1 | a0001c0001t0002g0356 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1130-1898T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215228 | ||||||
chr14:73215268
|
T | A | 3 | a0001c0001t0003g0203a0001c0001t0003g0207a0001c0001t0003g0220 | 3 | HG02074.hp1 NA18747.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1130-1858T>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215268 | ||||||
chr14:73215299
|
T | C | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1130-1827T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215299 | ||||||
chr14:73215476
|
G | A | 4 | a0001c0001t0008g0122a0001c0001t0008g0191a0001c0001t0008g0192others(1): Show | 4 | HG01261.hp2 HG03831.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1130-1650G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215476 | ||||||
chr14:73215518
|
G | A | 29 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(26): Show | 29 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1130-1608G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215518 | ||||||
chr14:73215541
|
T | TA | 24 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1130-1574dupA | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73215541 | |||||
chr14:73215541
|
T | TAA | 17 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(14): Show | 17 | HG00323.hp2 HG01243.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.1130-1575_1130-157 others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73215541 | |||||
chr14:73215559
|
T | C | 2 | a0001c0001t0005g0175a0001c0001t0005g0176 | 2 | NA19056.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1130-1567T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215559 | ||||||
chr14:73215660
|
A | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0152 | 3 | HG02258.hp1 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1130-1466A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215660 | ||||||
chr14:73215739
|
A | G | 1 | a0001c0001t0008g0193 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1130-1387A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215739 | ||||||
chr14:73215780
|
G | A | 1 | a0001c0001t0002g0362 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1130-1346G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215780 | ||||||
chr14:73215862
|
G | C | 1 | a0001c0001t0004g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1130-1264G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215862 | ||||||
chr14:73215957
|
A | G | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1130-1169A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73215957 | ||||||
chr14:73216068
|
A | AG | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130-1058_1130-105 others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216068 | ||||||
chr14:73216069
|
T | G | 5 | a0001c0001t0011g0306a0001c0001t0011g0308a0001c0001t0011g0309others(2): Show | 5 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1130-1057T>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216069 | ||||||
chr14:73216132
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1130-994C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216132 | ||||||
chr14:73216260
|
T | C | 1 | a0001c0001t0030g0168 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1130-866T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216260 | ||||||
chr14:73216302
|
G | T | 1 | a0001c0001t0002g0362 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1130-824G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216302 | ||||||
chr14:73216346
|
A | T | 1 | a0001c0001t0004g0235 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1130-780A>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216346 | ||||||
chr14:73216391
|
A | G | 1 | a0003c0003t0003g0366 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1130-735A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216391 | ||||||
chr14:73216418
|
G | C | 41 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(38): Show | 41 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.1130-708G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216418 | ||||||
chr14:73216486
|
T | C | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(317): Show | 322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1130-640T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216486 | ||||||
chr14:73216487
|
G | A | 1 | a0001c0006t0006g0153 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1130-639G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216487 | ||||||
chr14:73216542
|
T | C | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1130-584T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216542 | ||||||
chr14:73216688
|
G | A | 1 | a0001c0001t0004g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1130-438G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216688 | ||||||
chr14:73216688
|
G | T | 25 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(22): Show | 25 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.1130-438G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216688 | ||||||
chr14:73216758
|
C | CAA | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1130-355_1130-354d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr14 | 73216758 | |||||
chr14:73216803
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1130-323C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216803 | ||||||
chr14:73216815
|
G | T | 6 | a0001c0001t0008g0106a0001c0001t0008g0107a0001c0001t0008g0122others(3): Show | 6 | HG00323.hp2 HG01261.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1130-311G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216815 | ||||||
chr14:73216933
|
G | T | 42 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(39): Show | 42 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1130-193G>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 10/11 | chr14 | 73216933 | ||||||
chr14:73217252
|
T | C | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1248+8T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217252 | ||||||
chr14:73217272
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1248+28A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217272 | ||||||
chr14:73217387
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0025 | 3 | HG03017.hp2 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1248+143C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217387 | ||||||
chr14:73217714
|
G | C | 1 | a0001c0001t0002g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1248+470G>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217714 | ||||||
chr14:73217725
|
G | A | 4 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0004g0294others(1): Show | 4 | HG02818.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+481G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217725 | ||||||
chr14:73217741
|
C | T | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1248+497C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217741 | ||||||
chr14:73217795
|
A | AT | 58 | a0001c0001t0001g0017a0001c0001t0001g0048a0001c0001t0001g0054others(55): Show | 58 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1248+571dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73217795 | |||||
chr14:73217795
|
A | ATT | 75 | a0001c0001t0003g0002a0001c0001t0003g0123a0001c0001t0003g0124others(72): Show | 76 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1248+570_1248+571d others(4): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73217795 | |||||
chr14:73217795
|
A | ATTT | 9 | a0001c0001t0003g0108a0001c0001t0003g0203a0001c0001t0003g0206others(6): Show | 9 | HG02015.hp1 HG02074.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1248+569_1248+571d others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73217795 | |||||
chr14:73217795
|
A | ATTTT | 8 | a0001c0001t0007g0155a0001c0001t0007g0156a0001c0001t0007g0157others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1248+568_1248+571d others(6): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73217795 | |||||
chr14:73217833
|
A | G | 42 | a0001c0001t0006g0128a0001c0001t0006g0140a0001c0001t0006g0148others(39): Show | 42 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1248+589A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217833 | ||||||
chr14:73217864
|
T | C | 11 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(8): Show | 11 | HG01243.hp2 HG02055.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1248+620T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217864 | ||||||
chr14:73217928
|
C | T | 1 | a0001c0001t0007g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1248+684C>T | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73217928 | ||||||
chr14:73218086
|
C | CT | 46 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(43): Show | 46 | HG00423.hp2 HG00735.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1248+864dupT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73218086 | |||||
chr14:73218086
|
C | CTTT | 9 | a0001c0001t0007g0154a0001c0001t0007g0155a0001c0001t0007g0156others(6): Show | 9 | HG01243.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1248+862_1248+864d others(5): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73218086 | |||||
chr14:73218086
|
CT | C | 63 | a0001c0001t0004g0003a0001c0001t0004g0004a0001c0001t0004g0005others(60): Show | 63 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1248+864delT | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73218086 | |||||
chr14:73218131
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1248+887G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73218131 | ||||||
chr14:73218190
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0152 | 3 | HG02258.hp1 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1249-944G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73218190 | ||||||
chr14:73218473
|
T | C | 4 | a0001c0001t0012g0178a0001c0001t0012g0179a0001c0001t0012g0184others(1): Show | 4 | NA18964.hp1 NA18980.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-661T>C | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73218473 | ||||||
chr14:73218628
|
G | A | 5 | a0001c0001t0010g0053a0001c0001t0010g0067a0001c0001t0010g0073others(2): Show | 5 | NA18944.hp2 NA18971.hp2 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-506G>A | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73218628 | ||||||
chr14:73218643
|
ACACAGCA others(15): Show |
A | 1 | a0001c0001t0004g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1249-481_1249-460d others(24): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73218643 | |||||
chr14:73218653
|
AAGAATGC others(15): Show |
A | 3 | a0001c0001t0004g0291a0001c0001t0004g0292a0001c0001t0028g0293 | 3 | HG02818.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1249-473_1249-452d others(24): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73218653 | |||||
chr14:73218661
|
T | TCCCGCAC others(36): Show |
19 | a0001c0001t0002g0185a0001c0001t0002g0339a0001c0001t0002g0345others(16): Show | 19 | HG00558.hp2 HG02015.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1249-408_1249-366d others(45): Show |
PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr14 | 73218661 | |||||
chr14:73218923
|
A | G | 1 | a0001c0004t0020g0312 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1249-211A>G | PSEN1 | ENSG00000080815.20 | transcript | ENST00000324501.10 | protein_coding | 11/11 | chr14 | 73218923 |