geneid | 83464 |
---|---|
ensemblid | ENSG00000138613.14 |
hgncid | 24080 |
symbol | APH1B |
name | aph-1 homolog B, gamma-secretase subunit |
refseq_nuc | NM_031301.4 |
refseq_prot | NP_112591.2 |
ensembl_nuc | ENST00000261879.10 |
ensembl_prot | ENSP00000261879.5 |
mane_status | MANE Select |
chr | chr15 |
start | 63277605 |
end | 63309126 |
strand | + |
ver | v1.2 |
region | chr15:63277605-63309126 |
region5000 | chr15:63272605-63314126 |
regionname0 | APH1B_chr15_63277605_63309126 |
regionname5000 | APH1B_chr15_63272605_63314126 |
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 | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 257 | 341 | 96 | 57 | 144 | 8 | 35 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002 | 0/0 | 257 | 63 | 4 | 11 | 46 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0003 | 0/1 | 257 | 7 | 0 | 4 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0004 | 0/0 | 257 | 6 | 0 | 0 | 0 | 0 | 6 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0005 | 0/0 | 257 | 2 | 0 | 0 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0006 | 0/0 | 257 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0007 | 0/0 | 257 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0008 | 0/0 | 257 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 774 | 338 | 93 | 57 | 144 | 8 | 35 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0002 | 0/0 | 774 | 63 | 4 | 11 | 46 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0003 | 0/1 | 774 | 7 | 0 | 4 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0004 | 0/0 | 774 | 6 | 0 | 0 | 0 | 0 | 6 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0005 | 0/0 | 774 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0006 | 0/0 | 774 | 2 | 0 | 0 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0007 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0008 | 0/0 | 774 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0009 | 0/0 | 774 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
c0010 | 0/0 | 774 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3365 | 102 | 54 | 5 | 28 | 1 | 14 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0002 | 0/0 | 3365 | 80 | 1 | 17 | 56 | 2 | 4 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0003 | 0/0 | 3365 | 69 | 6 | 13 | 37 | 4 | 9 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0004 | 0/0 | 3365 | 60 | 7 | 11 | 41 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0005 | 0/0 | 3365 | 31 | 8 | 15 | 0 | 2 | 6 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0006 | 0/0 | 3365 | 14 | 0 | 0 | 12 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0007 | 0/0 | 3354 | 11 | 0 | 8 | 0 | 1 | 2 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0008 | 0/0 | 3365 | 8 | 8 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0009 | 0/0 | 3365 | 5 | 3 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0010 | 0/0 | 3365 | 4 | 4 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0011 | 0/0 | 3365 | 4 | 0 | 0 | 3 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0012 | 0/0 | 3365 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0013 | 0/0 | 3365 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0014 | 0/0 | 3365 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0015 | 0/0 | 3365 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0016 | 0/0 | 3365 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0017 | 0/0 | 3365 | 2 | 0 | 0 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0018 | 0/0 | 3365 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0019 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0020 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0021 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0022 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0023 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0024 | 0/1 | 3365 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0025 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0026 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0027 | 0/0 | 3365 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0028 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0029 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0030 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0031 | 1/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0032 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0033 | 0/0 | 3365 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0034 | 0/0 | 3365 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
t0035 | 0/0 | 3365 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
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 |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 24 | 0 | 3 | 21 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0002 | 0/0 | 22 | 0 | 6 | 15 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0003 | 0/0 | 18 | 1 | 4 | 11 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
g0004 | 0/0 | 14 | 1 | 2 | 9 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0006 | 0/0 | 8 | 0 | 4 | 0 | 1 | 3 | APH1B_chr15_63272605_63314126 | APH1B |
g0007 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0008 | 0/0 | 7 | 0 | 2 | 3 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0009 | 0/0 | 6 | 3 | 3 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0010 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0026 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0053 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/0 | 338 | 93 | 57 | 144 | 8 | 35 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0008 | a0001 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002 | a0002 | c0002 | 0/0 | 63 | 4 | 11 | 46 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0003c0003 | a0003 | c0003 | 0/1 | 7 | 0 | 4 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0004c0004 | a0004 | c0004 | 0/0 | 6 | 0 | 0 | 0 | 0 | 6 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0005c0006 | a0005 | c0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0006c0010 | a0006 | c0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0007c0009 | a0007 | c0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0008c0007 | a0008 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
acthapid | ahapid | chapid | thapid | 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 | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 96 | 54 | 5 | 28 | 1 | 8 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 77 | 1 | 15 | 55 | 2 | 4 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 61 | 6 | 11 | 34 | 1 | 9 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 31 | 8 | 15 | 0 | 2 | 6 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 14 | 0 | 0 | 12 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 11 | 0 | 8 | 0 | 1 | 2 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0031 | a0001 | c0001 | t0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0005t0008 | a0001 | c0005 | t0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0001c0008t0027 | a0001 | c0008 | t0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002t0003 | a0002 | c0002 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002t0004 | a0002 | c0002 | t0004 | 0/0 | 55 | 2 | 11 | 41 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002t0013 | a0002 | c0002 | t0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002t0014 | a0002 | c0002 | t0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0002c0002t0025 | a0002 | c0002 | t0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0003c0003t0002 | a0003 | c0003 | t0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0003c0003t0003 | a0003 | c0003 | t0003 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0003c0003t0024 | a0003 | c0003 | t0024 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0004c0004t0001 | a0004 | c0004 | t0001 | 0/0 | 6 | 0 | 0 | 0 | 0 | 6 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0005c0006t0017 | a0005 | c0006 | t0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0006c0010t0003 | a0006 | c0010 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0007c0009t0003 | a0007 | c0009 | t0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
a0008c0007t0003 | a0008 | c0007 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B | copy fasta |
actghapid | ahapid | chapid | thapid | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0222 | a0001 | c0001 | t0001 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0230 | a0001 | c0001 | t0001 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 21 | 0 | 6 | 14 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 18 | 1 | 4 | 11 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0020 | a0001 | c0001 | t0002 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0034 | a0001 | c0001 | t0002 | g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0036 | a0001 | c0001 | t0002 | g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0037 | a0001 | c0001 | t0002 | g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0102 | a0001 | c0001 | t0002 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0106 | a0001 | c0001 | t0002 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0108 | a0001 | c0001 | t0002 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0109 | a0001 | c0001 | t0002 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0112 | a0001 | c0001 | t0002 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0113 | a0001 | c0001 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0114 | a0001 | c0001 | t0002 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0119 | a0001 | c0001 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0002g0179 | a0001 | c0001 | t0002 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0004 | a0001 | c0001 | t0003 | g0004 | 0/0 | 12 | 1 | 2 | 7 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 6 | 0 | 2 | 2 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0044 | a0001 | c0001 | t0003 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0045 | a0001 | c0001 | t0003 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0046 | a0001 | c0001 | t0003 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0047 | a0001 | c0001 | t0003 | g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0048 | a0001 | c0001 | t0003 | g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0052 | a0001 | c0001 | t0003 | g0052 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0053 | a0001 | c0001 | t0003 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0096 | a0001 | c0001 | t0003 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0110 | a0001 | c0001 | t0003 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0139 | a0001 | c0001 | t0003 | g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0140 | a0001 | c0001 | t0003 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0144 | a0001 | c0001 | t0003 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0149 | a0001 | c0001 | t0003 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0152 | a0001 | c0001 | t0003 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0154 | a0001 | c0001 | t0003 | g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0155 | a0001 | c0001 | t0003 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0162 | a0001 | c0001 | t0003 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0167 | a0001 | c0001 | t0003 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0168 | a0001 | c0001 | t0003 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0171 | a0001 | c0001 | t0003 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0172 | a0001 | c0001 | t0003 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0173 | a0001 | c0001 | t0003 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0175 | a0001 | c0001 | t0003 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0176 | a0001 | c0001 | t0003 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0178 | a0001 | c0001 | t0003 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0181 | a0001 | c0001 | t0003 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0182 | a0001 | c0001 | t0003 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0185 | a0001 | c0001 | t0003 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0186 | a0001 | c0001 | t0003 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0187 | a0001 | c0001 | t0003 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0192 | a0001 | c0001 | t0003 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0200 | a0001 | c0001 | t0003 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0203 | a0001 | c0001 | t0003 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0205 | a0001 | c0001 | t0003 | g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0210 | a0001 | c0001 | t0003 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0214 | a0001 | c0001 | t0003 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0216 | a0001 | c0001 | t0003 | g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0217 | a0001 | c0001 | t0003 | g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0003g0218 | a0001 | c0001 | t0003 | g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0004g0013 | a0001 | c0001 | t0004 | g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0004g0190 | a0001 | c0001 | t0004 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0006 | a0001 | c0001 | t0005 | g0006 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0012 | a0001 | c0001 | t0005 | g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0026 | a0001 | c0001 | t0005 | g0026 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0027 | a0001 | c0001 | t0005 | g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0055 | a0001 | c0001 | t0005 | g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0056 | a0001 | c0001 | t0005 | g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0141 | a0001 | c0001 | t0005 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0223 | a0001 | c0001 | t0005 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0231 | a0001 | c0001 | t0005 | g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0233 | a0001 | c0001 | t0005 | g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0234 | a0001 | c0001 | t0005 | g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0236 | a0001 | c0001 | t0005 | g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0237 | a0001 | c0001 | t0005 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0238 | a0001 | c0001 | t0005 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0239 | a0001 | c0001 | t0005 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0005g0240 | a0001 | c0001 | t0005 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0004 | a0001 | c0001 | t0006 | g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0011 | a0001 | c0001 | t0006 | g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0035 | a0001 | c0001 | t0006 | g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0104 | a0001 | c0001 | t0006 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0117 | a0001 | c0001 | t0006 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0118 | a0001 | c0001 | t0006 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0153 | a0001 | c0001 | t0006 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0006g0184 | a0001 | c0001 | t0006 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0007g0007 | a0001 | c0001 | t0007 | g0007 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0007g0018 | a0001 | c0001 | t0007 | g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0007g0095 | a0001 | c0001 | t0007 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0008g0016 | a0001 | c0001 | t0008 | g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0008g0067 | a0001 | c0001 | t0008 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0008g0078 | a0001 | c0001 | t0008 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0008g0086 | a0001 | c0001 | t0008 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0009g0009 | a0001 | c0001 | t0009 | g0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0010g0049 | a0001 | c0001 | t0010 | g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0010g0057 | a0001 | c0001 | t0010 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0010g0189 | a0001 | c0001 | t0010 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0011g0090 | a0001 | c0001 | t0011 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0011g0092 | a0001 | c0001 | t0011 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0011g0093 | a0001 | c0001 | t0011 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0011g0094 | a0001 | c0001 | t0011 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0012g0193 | a0001 | c0001 | t0012 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0012g0194 | a0001 | c0001 | t0012 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0012g0195 | a0001 | c0001 | t0012 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0014g0202 | a0001 | c0001 | t0014 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0015g0043 | a0001 | c0001 | t0015 | g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0016g0165 | a0001 | c0001 | t0016 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0016g0166 | a0001 | c0001 | t0016 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0018g0042 | a0001 | c0001 | t0018 | g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0019g0061 | a0001 | c0001 | t0019 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0020g0006 | a0001 | c0001 | t0020 | g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0021g0170 | a0001 | c0001 | t0021 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0022g0180 | a0001 | c0001 | t0022 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0023g0235 | a0001 | c0001 | t0023 | g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0026g0169 | a0001 | c0001 | t0026 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0028g0120 | a0001 | c0001 | t0028 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0029g0002 | a0001 | c0001 | t0029 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0030g0111 | a0001 | c0001 | t0030 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0031g0157 | a0001 | c0001 | t0031 | g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0032g0006 | a0001 | c0001 | t0032 | g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0033g0107 | a0001 | c0001 | t0033 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0034g0008 | a0001 | c0001 | t0034 | g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0001t0035g0044 | a0001 | c0001 | t0035 | g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0005t0008g0029 | a0001 | c0005 | t0008 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0001c0008t0027g0075 | a0001 | c0008 | t0027 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0002g0132 | a0002 | c0002 | t0002 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0003g0183 | a0002 | c0002 | t0003 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0001 | a0002 | c0002 | t0004 | g0001 | 0/0 | 21 | 0 | 3 | 18 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0010 | a0002 | c0002 | t0004 | g0010 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0019 | a0002 | c0002 | t0004 | g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0021 | a0002 | c0002 | t0004 | g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0033 | a0002 | c0002 | t0004 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0038 | a0002 | c0002 | t0004 | g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0040 | a0002 | c0002 | t0004 | g0040 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0041 | a0002 | c0002 | t0004 | g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0062 | a0002 | c0002 | t0004 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0085 | a0002 | c0002 | t0004 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0105 | a0002 | c0002 | t0004 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0128 | a0002 | c0002 | t0004 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0129 | a0002 | c0002 | t0004 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0130 | a0002 | c0002 | t0004 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0131 | a0002 | c0002 | t0004 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0133 | a0002 | c0002 | t0004 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0135 | a0002 | c0002 | t0004 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0142 | a0002 | c0002 | t0004 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0143 | a0002 | c0002 | t0004 | g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0174 | a0002 | c0002 | t0004 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0191 | a0002 | c0002 | t0004 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0004g0201 | a0002 | c0002 | t0004 | g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0013g0001 | a0002 | c0002 | t0013 | g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0014g0050 | a0002 | c0002 | t0014 | g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0002c0002t0025g0137 | a0002 | c0002 | t0025 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0003c0003t0002g0051 | a0003 | c0003 | t0002 | g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0003c0003t0003g0024 | a0003 | c0003 | t0003 | g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0003c0003t0003g0213 | a0003 | c0003 | t0003 | g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0003c0003t0024g0147 | a0003 | c0003 | t0024 | g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0004c0004t0001g0145 | a0004 | c0004 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0004c0004t0001g0146 | a0004 | c0004 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0004c0004t0001g0196 | a0004 | c0004 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0004c0004t0001g0197 | a0004 | c0004 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0004c0004t0001g0198 | a0004 | c0004 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0004c0004t0001g0199 | a0004 | c0004 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APH1B_chr15_63272605_63314126 | APH1B |
a0005c0006t0017g0211 | a0005 | c0006 | t0017 | g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0005c0006t0017g0212 | a0005 | c0006 | t0017 | g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0006c0010t0003g0241 | a0006 | c0010 | t0003 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0007c0009t0003g0177 | a0007 | c0009 | t0003 | g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
a0008c0007t0003g0046 | a0008 | c0007 | t0003 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APH1B_chr15_63272605_63314126 | APH1B |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0007 | c0009 | t0003 | g0177 | EUR | GBR | APH1B_chr15_63272605_63314126 | APH1B |
HG00099 | hp2 | a0001 | c0001 | t0007 | g0007 | EUR | GBR | APH1B_chr15_63272605_63314126 | APH1B |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | GBR | APH1B_chr15_63272605_63314126 | APH1B |
HG00140 | hp2 | a0003 | c0003 | t0003 | g0024 | EUR | GBR | APH1B_chr15_63272605_63314126 | APH1B |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | APH1B_chr15_63272605_63314126 | APH1B |
HG00280 | hp2 | a0001 | c0001 | t0020 | g0006 | EUR | FIN | APH1B_chr15_63272605_63314126 | APH1B |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | FIN | APH1B_chr15_63272605_63314126 | APH1B |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0103 | EUR | FIN | APH1B_chr15_63272605_63314126 | APH1B |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00558 | hp1 | a0002 | c0002 | t0003 | g0183 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00609 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00639 | hp1 | a0003 | c0003 | t0002 | g0051 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00673 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0104 | EAS | CHS | APH1B_chr15_63272605_63314126 | APH1B |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00735 | hp2 | a0002 | c0002 | t0004 | g0010 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0236 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01099 | hp1 | a0003 | c0003 | t0003 | g0213 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0053 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0009 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01167 | hp2 | a0003 | c0003 | t0002 | g0051 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01169 | hp1 | a0001 | c0001 | t0009 | g0009 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0056 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | APH1B_chr15_63272605_63314126 | APH1B |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0096 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01256 | hp1 | a0003 | c0003 | t0003 | g0024 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0055 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01257 | hp2 | a0002 | c0002 | t0004 | g0001 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01258 | hp2 | a0001 | c0001 | t0005 | g0055 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01361 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0056 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01496 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01496 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01515 | hp1 | a0005 | c0006 | t0017 | g0211 | EUR | IBS | APH1B_chr15_63272605_63314126 | APH1B |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0026 | EUR | IBS | APH1B_chr15_63272605_63314126 | APH1B |
HG01517 | hp1 | a0003 | c0003 | t0003 | g0024 | EUR | IBS | APH1B_chr15_63272605_63314126 | APH1B |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0026 | EUR | IBS | APH1B_chr15_63272605_63314126 | APH1B |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG01934 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01934 | hp2 | a0002 | c0002 | t0004 | g0143 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01952 | hp2 | a0002 | c0002 | t0004 | g0001 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01975 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01978 | hp2 | a0001 | c0001 | t0035 | g0044 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0142 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02055 | hp2 | a0001 | c0001 | t0010 | g0057 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02080 | hp2 | a0002 | c0002 | t0004 | g0128 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02132 | hp2 | a0001 | c0001 | t0034 | g0008 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0012 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CDX | APH1B_chr15_63272605_63314126 | APH1B |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | APH1B_chr15_63272605_63314126 | APH1B |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0049 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02273 | hp1 | a0002 | c0002 | t0004 | g0010 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02280 | hp2 | a0001 | c0005 | t0008 | g0029 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02300 | hp2 | a0002 | c0002 | t0004 | g0001 | AMR | PEL | APH1B_chr15_63272605_63314126 | APH1B |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0117 | EAS | KHV | APH1B_chr15_63272605_63314126 | APH1B |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0043 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0007 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0043 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0237 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0049 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02895 | hp2 | a0001 | c0001 | t0018 | g0042 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02897 | hp2 | a0001 | c0001 | t0018 | g0042 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02922 | hp2 | a0002 | c0002 | t0004 | g0174 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03139 | hp2 | a0001 | c0001 | t0014 | g0202 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0067 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0189 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0078 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0035 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0035 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | APH1B_chr15_63272605_63314126 | APH1B |
HG03540 | hp1 | a0002 | c0002 | t0014 | g0050 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0086 | AFR | GWD | APH1B_chr15_63272605_63314126 | APH1B |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03688 | hp1 | a0002 | c0002 | t0025 | g0137 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0026 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG03704 | hp1 | a0004 | c0004 | t0001 | g0196 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0231 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03710 | hp1 | a0004 | c0004 | t0001 | g0199 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03710 | hp2 | a0001 | c0001 | t0033 | g0107 | SAS | PJL | APH1B_chr15_63272605_63314126 | APH1B |
HG03834 | hp1 | a0001 | c0001 | t0032 | g0006 | SAS | BEB | APH1B_chr15_63272605_63314126 | APH1B |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0095 | SAS | BEB | APH1B_chr15_63272605_63314126 | APH1B |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | BEB | APH1B_chr15_63272605_63314126 | APH1B |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0197 | SAS | BEB | APH1B_chr15_63272605_63314126 | APH1B |
HG04115 | hp1 | a0004 | c0004 | t0001 | g0198 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04115 | hp2 | a0004 | c0004 | t0001 | g0146 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0052 | SAS | BEB | APH1B_chr15_63272605_63314126 | APH1B |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | APH1B_chr15_63272605_63314126 | APH1B |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04204 | hp1 | a0004 | c0004 | t0001 | g0145 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04204 | hp2 | a0001 | c0001 | t0023 | g0235 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | APH1B_chr15_63272605_63314126 | APH1B |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | APH1B_chr15_63272605_63314126 | APH1B |
NA18522 | hp2 | a0002 | c0002 | t0014 | g0050 | AFR | YRI | APH1B_chr15_63272605_63314126 | APH1B |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHB | APH1B_chr15_63272605_63314126 | APH1B |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | CHB | APH1B_chr15_63272605_63314126 | APH1B |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CHB | APH1B_chr15_63272605_63314126 | APH1B |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | APH1B_chr15_63272605_63314126 | APH1B |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | APH1B_chr15_63272605_63314126 | APH1B |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | APH1B_chr15_63272605_63314126 | APH1B |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18940 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18942 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18944 | hp2 | a0001 | c0001 | t0026 | g0169 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18949 | hp1 | a0002 | c0002 | t0004 | g0129 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18949 | hp2 | a0001 | c0001 | t0022 | g0180 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18952 | hp2 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18953 | hp1 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18956 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18959 | hp1 | a0001 | c0001 | t0011 | g0094 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18959 | hp2 | a0002 | c0002 | t0004 | g0062 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18960 | hp2 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18961 | hp1 | a0002 | c0002 | t0004 | g0033 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18965 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18965 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18967 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18969 | hp1 | a0002 | c0002 | t0004 | g0135 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18972 | hp2 | a0002 | c0002 | t0004 | g0085 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18973 | hp2 | a0001 | c0001 | t0029 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18974 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18974 | hp2 | a0006 | c0010 | t0003 | g0241 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18975 | hp2 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18977 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18979 | hp2 | a0001 | c0001 | t0016 | g0166 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18982 | hp1 | a0001 | c0001 | t0028 | g0120 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18984 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18985 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18987 | hp1 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18988 | hp1 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18990 | hp1 | a0001 | c0001 | t0011 | g0092 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18990 | hp2 | a0002 | c0002 | t0004 | g0105 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18991 | hp1 | a0002 | c0002 | t0004 | g0041 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18991 | hp2 | a0001 | c0001 | t0021 | g0170 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18995 | hp1 | a0002 | c0002 | t0013 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18997 | hp2 | a0002 | c0002 | t0004 | g0041 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18999 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19001 | hp2 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19004 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19006 | hp2 | a0002 | c0002 | t0004 | g0038 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19009 | hp2 | a0002 | c0002 | t0004 | g0133 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19012 | hp2 | a0001 | c0001 | t0012 | g0195 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0009 | AFR | LWK | APH1B_chr15_63272605_63314126 | APH1B |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | APH1B_chr15_63272605_63314126 | APH1B |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | APH1B_chr15_63272605_63314126 | APH1B |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | APH1B_chr15_63272605_63314126 | APH1B |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19062 | hp2 | a0001 | c0001 | t0012 | g0194 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19063 | hp1 | a0002 | c0002 | t0004 | g0191 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19063 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19067 | hp1 | a0002 | c0002 | t0004 | g0033 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19068 | hp1 | a0002 | c0002 | t0004 | g0038 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19072 | hp2 | a0001 | c0001 | t0011 | g0093 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19074 | hp2 | a0001 | c0001 | t0012 | g0193 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19076 | hp1 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19077 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19079 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19080 | hp1 | a0002 | c0002 | t0004 | g0019 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19081 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19081 | hp2 | a0001 | c0001 | t0016 | g0165 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19084 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19084 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19087 | hp2 | a0002 | c0002 | t0004 | g0130 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19088 | hp2 | a0001 | c0001 | t0030 | g0111 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19090 | hp1 | a0008 | c0007 | t0003 | g0046 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA19240 | hp1 | a0001 | c0001 | t0019 | g0061 | AFR | YRI | APH1B_chr15_63272605_63314126 | APH1B |
NA19240 | hp2 | a0001 | c0005 | t0008 | g0029 | AFR | YRI | APH1B_chr15_63272605_63314126 | APH1B |
NA20129 | hp1 | a0001 | c0008 | t0027 | g0075 | AFR | ASW | APH1B_chr15_63272605_63314126 | APH1B |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ASW | APH1B_chr15_63272605_63314126 | APH1B |
NA20752 | hp1 | a0002 | c0002 | t0004 | g0040 | EUR | TSI | APH1B_chr15_63272605_63314126 | APH1B |
NA20752 | hp2 | a0005 | c0006 | t0017 | g0212 | EUR | TSI | APH1B_chr15_63272605_63314126 | APH1B |
NA20905 | hp1 | a0001 | c0001 | t0011 | g0090 | SAS | GIH | APH1B_chr15_63272605_63314126 | APH1B |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | GIH | APH1B_chr15_63272605_63314126 | APH1B |
HG01123 | hp1 | a0002 | c0002 | t0004 | g0201 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | APH1B_chr15_63272605_63314126 | APH1B |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02486 | hp2 | a0002 | c0002 | t0004 | g0040 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | APH1B_chr15_63272605_63314126 | APH1B |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | MSL | APH1B_chr15_63272605_63314126 | APH1B |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | USA | APH1B_chr15_63272605_63314126 | APH1B |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | USA | APH1B_chr15_63272605_63314126 | APH1B |
NA18955 | hp1 | a0002 | c0002 | t0004 | g0001 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | APH1B_chr15_63272605_63314126 | APH1B |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | APH1B_chr15_63272605_63314126 | APH1B |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | USA | APH1B_chr15_63272605_63314126 | APH1B |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | APH1B_chr15_63272605_63314126 | APH1B |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | LWK | APH1B_chr15_63272605_63314126 | APH1B |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0024 | g0147 | REF | REF | APH1B_chr15_63272605_63314126 | APH1B |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0031 | g0157 | REF | REF | APH1B_chr15_63272605_63314126 | APH1B |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:63277702
|
A | G | 1 | a0004 | 6 | HG03704.hp1 HG03710.hp1 HG03942.hp2 others(3): Show |
missense_variant | MODERATE | c.79A>G | p.Thr27Ala | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/6 | 98/4138 | 79/774 | 27/257 | chr15 | 63277702 | ||
chr15:63277703
|
C | T | 2 | a0003a0005 | 9 | HG00140.hp2 HG00639.hp1 HG01099.hp1 others(6): Show |
missense_variant | MODERATE | c.80C>T | p.Thr27Ile | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/6 | 99/4138 | 80/774 | 27/257 | chr15 | 63277703 | ||
chr15:63279300
|
A | T | 1 | a0006 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.253A>T | p.Met85Leu | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/6 | 272/4138 | 253/774 | 85/257 | chr15 | 63279300 | ||
chr15:63302461
|
G | T | 1 | a0007 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.595G>T | p.Val199Leu | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/6 | 614/4138 | 595/774 | 199/257 | chr15 | 63302461 | ||
chr15:63305658
|
T | G | 2 | a0002a0005 | 65 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(62): Show |
missense_variant | MODERATE | c.651T>G | p.Phe217Leu | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 670/4138 | 651/774 | 217/257 | chr15 | 63305658 | ||
chr15:63305714
|
G | A | 1 | a0008 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.707G>A | p.Arg236Gln | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 726/4138 | 707/774 | 236/257 | chr15 | 63305714 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:63279275
|
G | T | 1 | a0006c0010 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.228G>T | p.Ala76Ala | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/6 | 247/4138 | 228/774 | 76/257 | chr15 | 63279275 | ||
chr15:63305700
|
G | A | 1 | a0001c0005 | 2 | HG02280.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.693G>A | p.Ala231Ala | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 712/4138 | 693/774 | 231/257 | chr15 | 63305700 | ||
chr15:63305733
|
G | A | 1 | a0001c0008 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.726G>A | p.Leu242Leu | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 745/4138 | 726/774 | 242/257 | chr15 | 63305733 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:63277614
|
C | T | 2 | a0001c0001t0014a0002c0002t0014 | 3 | HG03139.hp2 HG03540.hp1 NA18522.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/6 | chr15 | 63277614 | ||||||
chr15:63305944
|
G | A | 1 | a0001c0001t0009 | 5 | HG01167.hp1 HG01169.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*163G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 163 | chr15 | 63305944 | |||||
chr15:63305997
|
A | G | 1 | a0001c0001t0035 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*216A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 216 | chr15 | 63305997 | |||||
chr15:63306103
|
C | T | 1 | a0001c0001t0034 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 322 | chr15 | 63306103 | |||||
chr15:63306189
|
G | A | 1 | a0001c0001t0019 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 408 | chr15 | 63306189 | |||||
chr15:63306231
|
T | G | 20 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(17): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*450T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 450 | chr15 | 63306231 | |||||
chr15:63306320
|
C | T | 1 | a0001c0001t0033 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*539C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 539 | chr15 | 63306320 | |||||
chr15:63306906
|
T | C | 1 | a0001c0001t0020 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1125T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1125 | chr15 | 63306906 | |||||
chr15:63307121
|
C | T | 1 | a0001c0001t0026 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1340 | chr15 | 63307121 | |||||
chr15:63307362
|
TTAGAGAT others(4): Show |
T | 1 | a0001c0001t0007 | 11 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1591_*1601delAATA others(7): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1591 | INFO_REALIGN_3_PRIME | chr15 | 63307362 | ||||
chr15:63307436
|
C | T | 1 | a0001c0001t0018 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1655C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1655 | chr15 | 63307436 | |||||
chr15:63307591
|
G | A | 1 | a0001c0001t0021 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1810G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1810 | chr15 | 63307591 | |||||
chr15:63307632
|
A | G | 1 | a0001c0001t0032 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1851A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1851 | chr15 | 63307632 | |||||
chr15:63307738
|
G | A | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
3_prime_UTR_variant | MODIFIER | c.*1957G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1957 | chr15 | 63307738 | |||||
chr15:63307753
|
C | G | 1 | a0001c0001t0016 | 2 | NA18979.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1972C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 1972 | chr15 | 63307753 | |||||
chr15:63307789
|
C | T | 7 | a0001c0001t0004a0001c0001t0014a0002c0002t0004others(4): Show | 69 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2008C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2008 | chr15 | 63307789 | |||||
chr15:63307792
|
C | T | 1 | a0001c0001t0030 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2011C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2011 | chr15 | 63307792 | |||||
chr15:63307901
|
A | T | 1 | a0001c0001t0029 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2120A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2120 | chr15 | 63307901 | |||||
chr15:63307961
|
G | C | 1 | a0001c0008t0027 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2180G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2180 | chr15 | 63307961 | |||||
chr15:63308067
|
T | G | 1 | a0002c0002t0013 | 3 | NA18952.hp2 NA18988.hp1 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2286T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2286 | chr15 | 63308067 | |||||
chr15:63308098
|
T | A | 1 | a0001c0001t0012 | 3 | NA19012.hp2 NA19062.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2317T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2317 | chr15 | 63308098 | |||||
chr15:63308229
|
G | T | 1 | a0001c0001t0015 | 2 | HG02572.hp2 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2448G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2448 | chr15 | 63308229 | |||||
chr15:63308303
|
T | G | 1 | a0001c0001t0022 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2522 | chr15 | 63308303 | |||||
chr15:63308325
|
C | T | 3 | a0001c0001t0007a0001c0001t0011a0001c0001t0033 | 16 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2544C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2544 | chr15 | 63308325 | |||||
chr15:63308404
|
G | A | 4 | a0001c0001t0005a0001c0001t0020a0001c0001t0023others(1): Show | 34 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2623G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2623 | chr15 | 63308404 | |||||
chr15:63308524
|
A | G | 1 | a0001c0001t0010 | 4 | HG02055.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2743A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2743 | chr15 | 63308524 | |||||
chr15:63308592
|
A | C | 2 | a0001c0001t0011a0001c0001t0033 | 5 | HG03710.hp2 NA18959.hp1 NA18990.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2811A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2811 | chr15 | 63308592 | |||||
chr15:63308662
|
G | C | 1 | a0001c0001t0028 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2881G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2881 | chr15 | 63308662 | |||||
chr15:63308677
|
T | C | 8 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(5): Show | 102 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2896T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2896 | chr15 | 63308677 | |||||
chr15:63308743
|
C | T | 1 | a0003c0003t0024 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2962C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2962 | chr15 | 63308743 | |||||
chr15:63308747
|
G | A | 1 | a0005c0006t0017 | 2 | HG01515.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2966G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 2966 | chr15 | 63308747 | |||||
chr15:63308827
|
A | T | 3 | a0001c0001t0007a0001c0001t0011a0001c0001t0033 | 16 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3046A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 3046 | chr15 | 63308827 | |||||
chr15:63308884
|
T | C | 2 | a0001c0001t0008a0001c0005t0008 | 8 | HG02280.hp2 HG02572.hp1 HG02896.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3103T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 6/6 | 3103 | chr15 | 63308884 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:63277864
|
G | C | 1 | a0001c0001t0010g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.113+128G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63277864 | ||||||
chr15:63278036
|
T | C | 2 | a0001c0001t0002g0058a0001c0001t0002g0059 | 2 | HG00408.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.113+300T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278036 | ||||||
chr15:63278141
|
T | A | 118 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 226 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.113+405T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278141 | ||||||
chr15:63278211
|
A | T | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.113+475A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278211 | ||||||
chr15:63278242
|
GA | G | 54 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0025others(51): Show | 81 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.113+521delA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr15 | 63278242 | |||||
chr15:63278242
|
GAA | G | 92 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0031others(89): Show | 191 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.113+520_113+521del others(2): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr15 | 63278242 | |||||
chr15:63278282
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.113+546G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278282 | ||||||
chr15:63278786
|
C | A | 2 | a0004c0004t0001g0145a0004c0004t0001g0146 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.114-375C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278786 | ||||||
chr15:63278917
|
G | A | 1 | a0003c0003t0024g0147 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.114-244G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278917 | ||||||
chr15:63278922
|
T | C | 90 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.114-239T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278922 | ||||||
chr15:63278982
|
G | A | 1 | a0001c0001t0002g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.114-179G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63278982 | ||||||
chr15:63279010
|
C | T | 18 | a0001c0001t0001g0232a0001c0001t0005g0006a0001c0001t0005g0012others(15): Show | 33 | HG00280.hp2 HG00741.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.114-151C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63279010 | ||||||
chr15:63279035
|
C | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(87): Show | 164 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.114-126C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | chr15 | 63279035 | ||||||
chr15:63279080
|
G | GT | 73 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0028others(70): Show | 134 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.114-68dupT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr15 | 63279080 | |||||
chr15:63279453
|
T | G | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+122T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279453 | ||||||
chr15:63279580
|
C | T | 34 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0001g0076others(31): Show | 54 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.284+249C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279580 | ||||||
chr15:63279610
|
G | A | 62 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0031others(59): Show | 119 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.284+279G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279610 | ||||||
chr15:63279621
|
C | T | 6 | a0003c0003t0002g0051a0003c0003t0003g0024a0003c0003t0003g0213others(3): Show | 9 | HG00140.hp2 HG00639.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+290C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279621 | ||||||
chr15:63279701
|
A | G | 4 | a0001c0001t0005g0027a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 6 | HG02886.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+370A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279701 | ||||||
chr15:63279764
|
A | G | 57 | a0001c0001t0001g0009a0001c0001t0001g0084a0001c0001t0001g0087others(54): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.284+433A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279764 | ||||||
chr15:63279796
|
C | CT | 38 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0076others(35): Show | 57 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.284+482dupT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63279796 | |||||
chr15:63279920
|
C | T | 3 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208 | 3 | HG02683.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.284+589C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279920 | ||||||
chr15:63279998
|
A | T | 1 | a0001c0001t0003g0205 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.284+667A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63279998 | ||||||
chr15:63280107
|
A | T | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+776A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63280107 | ||||||
chr15:63280418
|
A | T | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+1087A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63280418 | ||||||
chr15:63280451
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.284+1120G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63280451 | ||||||
chr15:63280482
|
CTT | C | 7 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(4): Show | 15 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.284+1154_284+1155d others(4): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63280482 | |||||
chr15:63280534
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284+1203A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63280534 | ||||||
chr15:63280672
|
C | A | 2 | a0005c0006t0017g0211a0005c0006t0017g0212 | 2 | HG01515.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.284+1341C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63280672 | ||||||
chr15:63280965
|
A | T | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+1634A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63280965 | ||||||
chr15:63281017
|
T | A | 1 | a0001c0001t0003g0214 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.284+1686T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281017 | ||||||
chr15:63281055
|
G | T | 1 | a0001c0001t0003g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.284+1724G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281055 | ||||||
chr15:63281235
|
C | G | 1 | a0001c0001t0002g0125 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.284+1904C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281235 | ||||||
chr15:63281343
|
G | T | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.284+2012G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281343 | ||||||
chr15:63281359
|
T | TCAGCGCC others(10): Show |
1 | a0001c0001t0001g0032 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.284+2030_284+2046d others(19): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63281359 | |||||
chr15:63281534
|
G | GA | 11 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(8): Show | 11 | HG00738.hp2 HG01515.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.284+2220dupA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63281534 | |||||
chr15:63281534
|
GA | G | 80 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0025others(77): Show | 138 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.284+2220delA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63281534 | |||||
chr15:63281534
|
GAA | G | 50 | a0001c0001t0001g0009a0001c0001t0001g0087a0001c0001t0001g0088others(47): Show | 101 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.284+2219_284+2220d others(4): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63281534 | |||||
chr15:63281543
|
A | C | 34 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0054others(31): Show | 55 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.284+2212A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281543 | ||||||
chr15:63281545
|
A | C | 4 | a0001c0001t0001g0124a0001c0001t0014g0202a0002c0002t0004g0201others(1): Show | 5 | HG01123.hp1 HG03139.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+2214A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281545 | ||||||
chr15:63281552
|
C | A | 1 | a0001c0001t0003g0149 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.284+2221C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281552 | ||||||
chr15:63281563
|
A | C | 1 | a0001c0001t0001g0014 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.284+2232A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281563 | ||||||
chr15:63281624
|
C | T | 30 | a0001c0001t0001g0039a0001c0001t0001g0134a0001c0001t0001g0136others(27): Show | 66 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.284+2293C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281624 | ||||||
chr15:63281725
|
A | G | 3 | a0002c0002t0004g0021a0002c0002t0004g0130a0002c0002t0004g0143 | 5 | HG01934.hp2 NA18941.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+2394A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281725 | ||||||
chr15:63281760
|
CT | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0222a0001c0001t0002g0100others(5): Show | 8 | HG01070.hp2 HG02976.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+2442delT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63281760 | |||||
chr15:63281903
|
A | G | 2 | a0001c0001t0014g0202a0002c0002t0014g0050 | 3 | HG03139.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.284+2572A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281903 | ||||||
chr15:63281944
|
G | T | 227 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.284+2613G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281944 | ||||||
chr15:63281974
|
G | A | 2 | a0001c0001t0016g0165a0001c0001t0016g0166 | 2 | NA18979.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.284+2643G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63281974 | ||||||
chr15:63282051
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0001g0065others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+2720A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282051 | ||||||
chr15:63282077
|
G | A | 1 | a0001c0001t0003g0167 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.284+2746G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282077 | ||||||
chr15:63282302
|
G | C | 4 | a0001c0001t0001g0014a0001c0001t0001g0063a0001c0001t0001g0065others(1): Show | 6 | HG02615.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+2971G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282302 | ||||||
chr15:63282373
|
T | C | 66 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0031others(63): Show | 129 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.284+3042T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282373 | ||||||
chr15:63282391
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.284+3060A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282391 | ||||||
chr15:63282428
|
A | G | 1 | a0002c0002t0004g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.284+3097A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282428 | ||||||
chr15:63282442
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0017others(67): Show | 135 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.284+3111G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282442 | ||||||
chr15:63282524
|
C | T | 1 | a0001c0001t0005g0240 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284+3193C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282524 | ||||||
chr15:63282537
|
A | T | 1 | a0001c0001t0019g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284+3206A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282537 | ||||||
chr15:63282564
|
T | A | 1 | a0001c0001t0003g0168 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.284+3233T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63282564 | ||||||
chr15:63283056
|
A | C | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-3502A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283056 | ||||||
chr15:63283092
|
A | G | 1 | a0001c0001t0004g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.285-3466A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283092 | ||||||
chr15:63283115
|
G | C | 227 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(224): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.285-3443G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283115 | ||||||
chr15:63283116
|
T | C | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-3442T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283116 | ||||||
chr15:63283184
|
A | G | 3 | a0001c0001t0010g0049a0001c0001t0010g0057a0001c0001t0010g0189 | 4 | HG02055.hp2 HG02258.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-3374A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283184 | ||||||
chr15:63283315
|
G | C | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-3243G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283315 | ||||||
chr15:63283397
|
C | CTG | 190 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(187): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.285-3160_285-3159i others(4): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63283397 | |||||
chr15:63283681
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0008g0086 | 3 | HG02723.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.285-2877G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283681 | ||||||
chr15:63283731
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0222a0001c0001t0005g0223 | 4 | HG02630.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2827T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283731 | ||||||
chr15:63283789
|
AC | A | 7 | a0001c0001t0001g0188a0004c0004t0001g0145a0004c0004t0001g0146others(4): Show | 7 | HG02055.hp1 HG03704.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-2767delC | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63283789 | |||||
chr15:63283793
|
A | G | 7 | a0001c0001t0005g0026a0001c0001t0005g0056a0001c0001t0005g0231others(4): Show | 10 | HG01071.hp1 HG01175.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.285-2765A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283793 | ||||||
chr15:63283882
|
T | C | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-2676T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283882 | ||||||
chr15:63283923
|
T | A | 1 | a0006c0010t0003g0241 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-2635T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283923 | ||||||
chr15:63283966
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.285-2592T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63283966 | ||||||
chr15:63284041
|
T | G | 2 | a0001c0001t0001g0124a0001c0001t0002g0102 | 2 | NA18966.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.285-2517T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284041 | ||||||
chr15:63284045
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.285-2513T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284045 | ||||||
chr15:63284169
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.285-2389T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284169 | ||||||
chr15:63284218
|
C | CT | 100 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(97): Show | 175 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.285-2325dupT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63284218 | |||||
chr15:63284375
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.285-2183G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284375 | ||||||
chr15:63284505
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285-2053C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284505 | ||||||
chr15:63284559
|
T | A | 17 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(14): Show | 23 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.285-1999T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284559 | ||||||
chr15:63284582
|
CG | C | 250 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(247): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.285-1970delG | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63284582 | |||||
chr15:63284584
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.285-1974G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63284584 | ||||||
chr15:63285088
|
G | T | 2 | a0001c0001t0016g0165a0001c0001t0016g0166 | 2 | NA18979.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.285-1470G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285088 | ||||||
chr15:63285270
|
C | T | 1 | a0001c0001t0007g0018 | 3 | HG01261.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.285-1288C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285270 | ||||||
chr15:63285389
|
T | A | 1 | a0001c0001t0002g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.285-1169T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285389 | ||||||
chr15:63285425
|
T | C | 7 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(4): Show | 15 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.285-1133T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285425 | ||||||
chr15:63285435
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0079a0001c0001t0008g0078 | 4 | HG02976.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-1123T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285435 | ||||||
chr15:63285672
|
G | C | 1 | a0001c0001t0026g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.285-886G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285672 | ||||||
chr15:63285721
|
C | G | 1 | a0002c0002t0004g0041 | 2 | NA18991.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.285-837C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285721 | ||||||
chr15:63285750
|
G | T | 7 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(4): Show | 15 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.285-808G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285750 | ||||||
chr15:63285802
|
G | C | 30 | a0001c0001t0001g0039a0001c0001t0001g0134a0001c0001t0001g0136others(27): Show | 66 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.285-756G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285802 | ||||||
chr15:63285852
|
A | G | 1 | a0001c0001t0003g0167 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.285-706A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285852 | ||||||
chr15:63285906
|
A | G | 1 | a0004c0004t0001g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.285-652A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63285906 | ||||||
chr15:63286061
|
T | C | 4 | a0004c0004t0001g0196a0004c0004t0001g0197a0004c0004t0001g0198others(1): Show | 4 | HG03704.hp1 HG03710.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-497T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286061 | ||||||
chr15:63286244
|
C | T | 1 | a0002c0002t0004g0129 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.285-314C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286244 | ||||||
chr15:63286338
|
G | A | 3 | a0001c0001t0011g0092a0001c0001t0011g0093a0001c0001t0011g0094 | 3 | NA18959.hp1 NA18990.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.285-220G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286338 | ||||||
chr15:63286339
|
G | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(214): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.285-219G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286339 | ||||||
chr15:63286341
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.285-217A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286341 | ||||||
chr15:63286369
|
A | G | 8 | a0001c0001t0001g0138a0001c0001t0003g0139a0001c0001t0003g0140others(5): Show | 14 | HG00323.hp1 HG00735.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.285-189A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286369 | ||||||
chr15:63286499
|
T | C | 1 | a0001c0001t0003g0205 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285-59T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | chr15 | 63286499 | ||||||
chr15:63286510
|
CT | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0028others(82): Show | 174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.285-32delT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63286510 | |||||
chr15:63286510
|
CTT | C | 8 | a0001c0001t0001g0074a0001c0001t0001g0124a0001c0001t0002g0020others(5): Show | 10 | HG00323.hp2 HG00558.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.285-33_285-32delTT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 63286510 | |||||
chr15:63286772
|
C | T | 1 | a0001c0001t0004g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.355+144C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | chr15 | 63286772 | ||||||
chr15:63286815
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.355+187C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | chr15 | 63286815 | ||||||
chr15:63286827
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.355+199T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | chr15 | 63286827 | ||||||
chr15:63286849
|
T | C | 1 | a0004c0004t0001g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.355+221T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | chr15 | 63286849 | ||||||
chr15:63287000
|
A | C | 1 | a0001c0001t0002g0121 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.355+372A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | chr15 | 63287000 | ||||||
chr15:63287182
|
C | T | 51 | a0001c0001t0001g0009a0001c0001t0001g0084a0001c0001t0001g0087others(48): Show | 102 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.356-242C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | chr15 | 63287182 | ||||||
chr15:63287352
|
T | TAACTAGT others(348): Show |
1 | a0001c0001t0002g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.356-58_356-57insGG others(353): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 63287352 | |||||
chr15:63287581
|
T | C | 4 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(1): Show | 12 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.478+35T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63287581 | ||||||
chr15:63287647
|
T | C | 1 | a0001c0001t0008g0086 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.478+101T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63287647 | ||||||
chr15:63287672
|
T | C | 1 | a0004c0004t0001g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.478+126T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63287672 | ||||||
chr15:63287755
|
G | A | 1 | a0001c0001t0019g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478+209G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63287755 | ||||||
chr15:63287828
|
T | A | 1 | a0001c0001t0010g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.478+282T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63287828 | ||||||
chr15:63287956
|
T | C | 71 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0079others(68): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.478+410T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63287956 | ||||||
chr15:63288130
|
CT | C | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG02258.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.478+588delT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63288130 | |||||
chr15:63288361
|
AT | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(10): Show | 17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.478+820delT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63288361 | |||||
chr15:63288397
|
T | C | 72 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0079others(69): Show | 102 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.478+851T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63288397 | ||||||
chr15:63288578
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.478+1032A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63288578 | ||||||
chr15:63288802
|
A | C | 2 | a0001c0001t0003g0185a0001c0001t0003g0186 | 2 | HG00438.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.478+1256A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63288802 | ||||||
chr15:63288879
|
T | C | 4 | a0001c0001t0003g0155a0001c0001t0003g0168a0001c0001t0003g0171others(1): Show | 4 | NA18968.hp1 NA18977.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+1333T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63288879 | ||||||
chr15:63289100
|
A | G | 1 | a0002c0002t0004g0131 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478+1554A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289100 | ||||||
chr15:63289102
|
G | A | 1 | a0002c0002t0004g0131 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478+1556G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289102 | ||||||
chr15:63289107
|
A | T | 1 | a0002c0002t0004g0131 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.478+1561A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289107 | ||||||
chr15:63289421
|
T | C | 225 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(222): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.478+1875T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289421 | ||||||
chr15:63289435
|
A | G | 2 | a0001c0001t0006g0153a0001c0001t0006g0184 | 2 | NA19006.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.478+1889A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289435 | ||||||
chr15:63289554
|
G | A | 1 | a0001c0001t0019g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478+2008G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289554 | ||||||
chr15:63289554
|
G | T | 55 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0081others(52): Show | 108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.478+2008G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289554 | ||||||
chr15:63289820
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.478+2274T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289820 | ||||||
chr15:63289876
|
C | T | 13 | a0001c0001t0002g0179a0001c0001t0003g0046a0001c0001t0003g0047others(10): Show | 14 | HG00558.hp1 NA18747.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.478+2330C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289876 | ||||||
chr15:63289896
|
C | T | 29 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0001g0221others(26): Show | 47 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.478+2350C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289896 | ||||||
chr15:63289905
|
G | A | 1 | a0001c0001t0018g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.478+2359G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289905 | ||||||
chr15:63289958
|
G | A | 7 | a0001c0001t0001g0188a0004c0004t0001g0145a0004c0004t0001g0146others(4): Show | 7 | HG02055.hp1 HG03704.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+2412G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63289958 | ||||||
chr15:63290000
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.478+2454T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290000 | ||||||
chr15:63290007
|
GA | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(13): Show | 31 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.478+2473delA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63290007 | |||||
chr15:63290065
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478+2519T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290065 | ||||||
chr15:63290082
|
C | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0031others(85): Show | 179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.478+2536C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290082 | ||||||
chr15:63290194
|
A | G | 7 | a0001c0001t0001g0188a0004c0004t0001g0145a0004c0004t0001g0146others(4): Show | 7 | HG02055.hp1 HG03704.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+2648A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290194 | ||||||
chr15:63290256
|
A | G | 1 | a0001c0001t0019g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.478+2710A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290256 | ||||||
chr15:63290265
|
T | C | 1 | a0001c0001t0003g0178 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.478+2719T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290265 | ||||||
chr15:63290358
|
G | T | 1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.478+2812G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290358 | ||||||
chr15:63290461
|
A | T | 7 | a0001c0001t0001g0188a0004c0004t0001g0145a0004c0004t0001g0146others(4): Show | 7 | HG02055.hp1 HG03704.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.478+2915A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290461 | ||||||
chr15:63290586
|
G | A | 57 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0031others(54): Show | 111 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.478+3040G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290586 | ||||||
chr15:63290930
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.478+3384A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290930 | ||||||
chr15:63290960
|
G | C | 189 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(186): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.478+3414G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63290960 | ||||||
chr15:63290965
|
A | AGAGGGAA others(53): Show |
1 | a0001c0001t0001g0063 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.478+3448_478+3449i others(62): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63290965 | |||||
chr15:63291456
|
A | G | 1 | a0001c0001t0001g0028 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.478+3910A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63291456 | ||||||
chr15:63291510
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0089 | 2 | HG02145.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.478+3964T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63291510 | ||||||
chr15:63291706
|
G | A | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(13): Show | 22 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.478+4160G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63291706 | ||||||
chr15:63291776
|
A | C | 1 | a0001c0001t0003g0205 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.478+4230A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63291776 | ||||||
chr15:63291844
|
G | C | 17 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(14): Show | 23 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.478+4298G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63291844 | ||||||
chr15:63291953
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0009g0009 | 6 | HG01167.hp1 HG01169.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+4407C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63291953 | ||||||
chr15:63292572
|
GGA | G | 21 | a0001c0001t0002g0002a0001c0001t0002g0036a0001c0001t0002g0037others(18): Show | 43 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.478+5029_478+5030d others(4): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63292572 | |||||
chr15:63292757
|
T | A | 1 | a0002c0002t0004g0133 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.478+5211T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63292757 | ||||||
chr15:63292929
|
C | T | 7 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(4): Show | 15 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.478+5383C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63292929 | ||||||
chr15:63292948
|
C | T | 3 | a0001c0001t0005g0141a0002c0002t0004g0010a0002c0002t0004g0142 | 8 | HG00735.hp2 HG01361.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+5402C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63292948 | ||||||
chr15:63293003
|
G | A | 1 | a0002c0002t0014g0050 | 2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.478+5457G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293003 | ||||||
chr15:63293031
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.478+5485C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293031 | ||||||
chr15:63293038
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0003g0045 | 3 | HG01109.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.478+5492C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293038 | ||||||
chr15:63293064
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 6 | HG02027.hp2 HG02135.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+5518A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293064 | ||||||
chr15:63293114
|
G | A | 1 | a0001c0001t0030g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.478+5568G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293114 | ||||||
chr15:63293321
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.478+5775C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293321 | ||||||
chr15:63293325
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066 | 6 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+5779T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293325 | ||||||
chr15:63293498
|
C | CT | 4 | a0001c0001t0001g0030a0001c0001t0001g0079a0002c0002t0004g0201others(1): Show | 6 | HG01123.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+5966dupT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63293498 | |||||
chr15:63293501
|
T | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(13): Show | 22 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.478+5955T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293501 | ||||||
chr15:63293508
|
T | G | 4 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(1): Show | 12 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.478+5962T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293508 | ||||||
chr15:63293537
|
G | T | 1 | a0003c0003t0003g0213 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.478+5991G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293537 | ||||||
chr15:63293657
|
G | A | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(13): Show | 22 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.478+6111G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293657 | ||||||
chr15:63293694
|
C | T | 2 | a0002c0002t0004g0201a0002c0002t0014g0050 | 3 | HG01123.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.478+6148C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293694 | ||||||
chr15:63293697
|
T | C | 186 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(183): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.478+6151T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293697 | ||||||
chr15:63293732
|
G | A | 1 | a0004c0004t0001g0145 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.478+6186G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293732 | ||||||
chr15:63293898
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.478+6352G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63293898 | ||||||
chr15:63294018
|
A | G | 4 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0008g0016others(1): Show | 6 | HG02572.hp1 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+6472A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294018 | ||||||
chr15:63294050
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.478+6504C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294050 | ||||||
chr15:63294069
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0079a0001c0001t0008g0078 | 4 | HG02976.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+6523T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294069 | ||||||
chr15:63294077
|
T | A | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.478+6531T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294077 | ||||||
chr15:63294109
|
A | AT | 57 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0081others(54): Show | 110 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.478+6574dupT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63294109 | |||||
chr15:63294109
|
AT | A | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(13): Show | 22 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.478+6574delT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63294109 | |||||
chr15:63294346
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0222 | 3 | HG02976.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.478+6800A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294346 | ||||||
chr15:63294382
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.478+6836T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294382 | ||||||
chr15:63294711
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.478+7165G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294711 | ||||||
chr15:63294785
|
C | T | 1 | a0001c0001t0003g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.478+7239C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63294785 | ||||||
chr15:63295034
|
C | G | 29 | a0001c0001t0001g0025a0001c0001t0001g0054a0001c0001t0001g0221others(26): Show | 47 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.479-7311C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295034 | ||||||
chr15:63295134
|
G | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479-7211G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295134 | ||||||
chr15:63295161
|
A | G | 1 | a0001c0001t0005g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.479-7184A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295161 | ||||||
chr15:63295307
|
T | G | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.479-7038T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295307 | ||||||
chr15:63295321
|
C | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066 | 6 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-7024C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295321 | ||||||
chr15:63295444
|
T | C | 249 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(246): Show | 419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.479-6901T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295444 | ||||||
chr15:63295472
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.479-6873A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295472 | ||||||
chr15:63295522
|
C | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(13): Show | 22 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.479-6823C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295522 | ||||||
chr15:63295605
|
T | C | 1 | a0001c0001t0005g0234 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.479-6740T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63295605 | ||||||
chr15:63296063
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479-6282C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296063 | ||||||
chr15:63296097
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066 | 6 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-6248G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296097 | ||||||
chr15:63296158
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.479-6187C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296158 | ||||||
chr15:63296250
|
T | C | 30 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0232others(27): Show | 65 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.479-6095T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296250 | ||||||
chr15:63296284
|
A | T | 1 | a0001c0001t0011g0094 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.479-6061A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296284 | ||||||
chr15:63296416
|
T | C | 246 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0015others(243): Show | 413 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(410): Show |
intron_variant | MODIFIER | c.479-5929T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296416 | ||||||
chr15:63296429
|
C | A | 1 | a0001c0001t0002g0112 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.479-5916C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296429 | ||||||
chr15:63296463
|
G | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0022others(89): Show | 138 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.479-5882G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296463 | ||||||
chr15:63296495
|
G | A | 1 | a0002c0002t0004g0105 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.479-5850G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296495 | ||||||
chr15:63296512
|
C | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(13): Show | 22 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.479-5833C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296512 | ||||||
chr15:63296658
|
C | A | 1 | a0001c0001t0002g0106 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.479-5687C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296658 | ||||||
chr15:63296658
|
C | CT | 58 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0161others(55): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.479-5670dupT | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63296658 | |||||
chr15:63296783
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066 | 6 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-5562G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296783 | ||||||
chr15:63296799
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.479-5546A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296799 | ||||||
chr15:63296938
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0002g0113 | 4 | HG00423.hp1 NA18948.hp2 NA19076.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-5407G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296938 | ||||||
chr15:63296960
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479-5385A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63296960 | ||||||
chr15:63297089
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066 | 6 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-5256T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297089 | ||||||
chr15:63297112
|
C | T | 1 | a0002c0002t0002g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.479-5233C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297112 | ||||||
chr15:63297485
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.479-4860G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297485 | ||||||
chr15:63297490
|
A | T | 10 | a0001c0001t0001g0138a0001c0001t0003g0139a0001c0001t0003g0140others(7): Show | 16 | HG00323.hp1 HG00735.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.479-4855A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297490 | ||||||
chr15:63297510
|
A | G | 1 | a0007c0009t0003g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.479-4835A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297510 | ||||||
chr15:63297523
|
C | T | 1 | a0001c0001t0006g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.479-4822C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297523 | ||||||
chr15:63297773
|
T | C | 67 | a0001c0001t0001g0053a0001c0001t0003g0004a0001c0001t0003g0008others(64): Show | 97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.479-4572T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297773 | ||||||
chr15:63297853
|
G | A | 1 | a0001c0001t0002g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.479-4492G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297853 | ||||||
chr15:63297907
|
A | G | 187 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0022others(184): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.479-4438A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297907 | ||||||
chr15:63297965
|
T | A | 29 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0232others(26): Show | 64 | HG00323.hp1 HG00544.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.479-4380T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63297965 | ||||||
chr15:63298168
|
G | A | 1 | a0001c0001t0005g0055 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.479-4177G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63298168 | ||||||
chr15:63298378
|
T | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0084a0001c0001t0001g0087others(49): Show | 102 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.479-3967T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63298378 | ||||||
chr15:63298440
|
G | A | 1 | a0001c0001t0018g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.479-3905G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63298440 | ||||||
chr15:63298794
|
C | T | 7 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(4): Show | 15 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.479-3551C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63298794 | ||||||
chr15:63298840
|
TAATATA | T | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG02258.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-3504_479-3499d others(8): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63298840 | ||||||
chr15:63298897
|
T | TA | 18 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(15): Show | 24 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.479-3433dupA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63298897 | |||||
chr15:63298897
|
TA | T | 130 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(127): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.479-3433delA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63298897 | |||||
chr15:63299120
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 37 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.479-3225T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299120 | ||||||
chr15:63299158
|
G | C | 1 | a0001c0001t0012g0193 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.479-3187G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299158 | ||||||
chr15:63299342
|
T | C | 17 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(14): Show | 23 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.479-3003T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299342 | ||||||
chr15:63299379
|
A | G | 190 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0022others(187): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.479-2966A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299379 | ||||||
chr15:63299444
|
AC | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(20): Show | 37 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.479-2898delC | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63299444 | |||||
chr15:63299471
|
C | G | 1 | a0001c0001t0002g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.479-2874C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299471 | ||||||
chr15:63299703
|
C | G | 130 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(127): Show | 194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.479-2642C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299703 | ||||||
chr15:63299741
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.479-2604A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299741 | ||||||
chr15:63299835
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066others(1): Show | 7 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-2510A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299835 | ||||||
chr15:63299838
|
G | A | 3 | a0001c0001t0005g0238a0001c0001t0005g0239a0001c0001t0005g0240 | 3 | HG02965.hp1 HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.479-2507G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63299838 | ||||||
chr15:63300002
|
T | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(31): Show | 50 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.479-2343T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300002 | ||||||
chr15:63300036
|
G | A | 1 | a0001c0001t0023g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.479-2309G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300036 | ||||||
chr15:63300151
|
T | G | 1 | a0001c0001t0018g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.479-2194T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300151 | ||||||
chr15:63300273
|
G | T | 4 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(1): Show | 12 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.479-2072G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300273 | ||||||
chr15:63300283
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0066 | 6 | HG02486.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-2062G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300283 | ||||||
chr15:63300320
|
T | G | 1 | a0001c0001t0003g0175 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.479-2025T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300320 | ||||||
chr15:63300372
|
C | T | 1 | a0001c0001t0010g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.479-1973C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300372 | ||||||
chr15:63300501
|
CA | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(60): Show | 97 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.479-1839delA | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63300501 | |||||
chr15:63300586
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.479-1759G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300586 | ||||||
chr15:63300599
|
G | A | 177 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0022others(174): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.479-1746G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300599 | ||||||
chr15:63300614
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.479-1731G>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300614 | ||||||
chr15:63300702
|
C | T | 1 | a0001c0001t0003g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.479-1643C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300702 | ||||||
chr15:63300825
|
G | A | 2 | a0001c0001t0003g0152a0001c0001t0022g0180 | 2 | NA18949.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.479-1520G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300825 | ||||||
chr15:63300826
|
A | C | 4 | a0001c0001t0005g0027a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 6 | HG02886.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.479-1519A>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63300826 | ||||||
chr15:63301414
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0079a0001c0001t0008g0078 | 4 | HG02976.hp2 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-931A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63301414 | ||||||
chr15:63301612
|
T | G | 4 | a0001c0001t0003g0046a0001c0001t0003g0178a0001c0001t0003g0181others(1): Show | 4 | NA18966.hp2 NA18972.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-733T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63301612 | ||||||
chr15:63301686
|
A | T | 6 | a0001c0001t0002g0034a0001c0001t0002g0091a0001c0001t0002g0106others(3): Show | 7 | HG00408.hp1 HG00597.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-659A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63301686 | ||||||
chr15:63301699
|
AGCCTCCC others(24): Show |
A | 1 | a0001c0001t0002g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.479-611_479-581del others(31): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 63301699 | |||||
chr15:63302032
|
C | T | 56 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0030others(53): Show | 109 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.479-313C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63302032 | ||||||
chr15:63302103
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.479-242G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63302103 | ||||||
chr15:63302256
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.479-89T>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63302256 | ||||||
chr15:63302265
|
C | T | 20 | a0001c0001t0001g0221a0001c0001t0001g0232a0002c0002t0002g0132others(17): Show | 49 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.479-80C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63302265 | ||||||
chr15:63302332
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.479-13G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 4/5 | chr15 | 63302332 | ||||||
chr15:63302557
|
C | G | 1 | a0001c0001t0005g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.606+85C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63302557 | ||||||
chr15:63302576
|
G | A | 8 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0064others(5): Show | 11 | HG02145.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.606+104G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63302576 | ||||||
chr15:63302675
|
T | G | 10 | a0001c0001t0001g0220a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 16 | HG01109.hp1 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.606+203T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63302675 | ||||||
chr15:63302829
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.606+357A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63302829 | ||||||
chr15:63302898
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0001g0222 | 3 | HG02976.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.606+426A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63302898 | ||||||
chr15:63303256
|
G | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0081a0001c0001t0001g0082others(1): Show | 6 | HG02257.hp1 HG02717.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+784G>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303256 | ||||||
chr15:63303345
|
TCA | T | 152 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0030others(149): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.606+878_606+879del others(2): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303345 | |||||
chr15:63303373
|
T | C | 42 | a0001c0001t0001g0009a0001c0001t0002g0002a0001c0001t0002g0003others(39): Show | 89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.606+901T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303373 | ||||||
chr15:63303452
|
A | G | 239 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0014others(236): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.606+980A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303452 | ||||||
chr15:63303499
|
T | C | 1 | a0001c0001t0023g0235 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.606+1027T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303499 | ||||||
chr15:63303627
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0066 | 4 | HG02615.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.606+1155C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303627 | ||||||
chr15:63303679
|
T | C | 4 | a0002c0002t0025g0137a0003c0003t0003g0024a0003c0003t0003g0213others(1): Show | 6 | HG00140.hp2 HG01099.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.606+1207T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303679 | ||||||
chr15:63303782
|
C | A | 160 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0030others(157): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.606+1310C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303782 | ||||||
chr15:63303865
|
C | A | 1 | a0001c0001t0019g0061 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.606+1393C>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303865 | ||||||
chr15:63303874
|
A | AAC | 55 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0028others(52): Show | 102 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.606+1435_606+1436d others(4): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
A | AACAC | 63 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0053others(60): Show | 99 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.606+1433_606+1436d others(6): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
A | AACACAC | 25 | a0001c0001t0001g0025a0001c0001t0001g0087a0001c0001t0001g0225others(22): Show | 44 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.606+1431_606+1436d others(8): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
A | AACACACA others(1): Show |
6 | a0001c0001t0001g0224a0001c0001t0003g0182a0001c0001t0003g0203others(3): Show | 6 | HG02809.hp2 HG03516.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.606+1429_606+1436d others(10): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
A | AACACACA others(3): Show |
1 | a0001c0001t0005g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.606+1427_606+1436d others(12): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
AAC | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0002g0037others(5): Show | 9 | HG00323.hp2 HG00438.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.606+1435_606+1436d others(4): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
AACAC | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 40 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.606+1433_606+1436d others(6): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
AACACACA others(3): Show |
A | 19 | a0001c0001t0003g0096a0001c0001t0003g0140a0001c0001t0005g0141others(16): Show | 36 | HG00099.hp2 HG00735.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.606+1427_606+1436d others(12): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
AACACACA others(5): Show |
A | 23 | a0002c0002t0003g0183a0002c0002t0004g0001a0002c0002t0004g0019others(20): Show | 53 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.606+1425_606+1436d others(14): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303874
|
AACACACA others(7): Show |
A | 2 | a0001c0001t0005g0237a0002c0002t0002g0132 | 2 | HG00558.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.606+1423_606+1436d others(16): Show |
APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 63303874 | |||||
chr15:63303965
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.606+1493C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63303965 | ||||||
chr15:63304241
|
G | A | 31 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0079others(28): Show | 49 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.607-1373G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63304241 | ||||||
chr15:63304396
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.607-1218G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63304396 | ||||||
chr15:63304559
|
C | T | 12 | a0001c0001t0001g0017a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 17 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.607-1055C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63304559 | ||||||
chr15:63304873
|
C | G | 6 | a0001c0001t0003g0096a0001c0001t0007g0007a0001c0001t0007g0018others(3): Show | 14 | HG00099.hp2 HG01074.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.607-741C>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63304873 | ||||||
chr15:63304916
|
C | T | 2 | a0002c0002t0004g0128a0002c0002t0004g0135 | 2 | HG02080.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.607-698C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63304916 | ||||||
chr15:63304923
|
T | G | 2 | a0001c0001t0010g0049a0001c0001t0010g0057 | 3 | HG02055.hp2 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.607-691T>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63304923 | ||||||
chr15:63305287
|
T | C | 3 | a0001c0001t0004g0013a0001c0001t0004g0190a0001c0001t0014g0202 | 6 | HG02109.hp1 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.607-327T>C | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63305287 | ||||||
chr15:63305352
|
G | A | 1 | a0001c0001t0008g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.607-262G>A | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63305352 | ||||||
chr15:63305440
|
C | T | 54 | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0032others(51): Show | 109 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.607-174C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63305440 | ||||||
chr15:63305451
|
A | T | 1 | a0001c0001t0005g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.607-163A>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63305451 | ||||||
chr15:63305474
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0066 | 4 | HG02615.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.607-140A>G | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63305474 | ||||||
chr15:63305530
|
C | T | 1 | a0003c0003t0002g0051 | 2 | HG00639.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.607-84C>T | APH1B | ENSG00000138613.14 | transcript | ENST00000261879.10 | protein_coding | 5/5 | chr15 | 63305530 |