geneid | 9907 |
---|---|
ensemblid | ENSG00000242802.9 |
hgncid | 22197 |
symbol | AP5Z1 |
name | adaptor related protein complex 5 subunit zeta 1 |
refseq_nuc | NM_014855.3 |
refseq_prot | NP_055670.1 |
ensembl_nuc | ENST00000649063.2 |
ensembl_prot | ENSP00000497815.1 |
mane_status | MANE Select |
chr | chr7 |
start | 4775623 |
end | 4794397 |
strand | + |
ver | v1.2 |
region | chr7:4775623-4794397 |
region5000 | chr7:4770623-4799397 |
regionname0 | AP5Z1_chr7_4775623_4794397 |
regionname5000 | AP5Z1_chr7_4770623_4799397 |
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 | 1/1 | 807 | 258 | 62 | 52 | 99 | 12 | 31 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002 | 0/0 | 807 | 31 | 2 | 2 | 14 | 0 | 13 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0003 | 0/0 | 803 | 19 | 17 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0004 | 0/0 | 807 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0005 | 0/0 | 807 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0006 | 0/0 | 807 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0007 | 0/0 | 803 | 3 | 2 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0008 | 0/0 | 807 | 2 | 0 | 1 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0009 | 0/0 | 807 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0010 | 0/0 | 807 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0011 | 0/0 | 803 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0012 | 0/0 | 807 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0013 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0014 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0015 | 0/0 | 803 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0016 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0017 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0018 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0019 | 0/0 | 807 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0020 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0021 | 0/0 | 807 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0022 | 0/0 | 807 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | 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 | 1/1 | 2424 | 203 | 18 | 48 | 96 | 10 | 29 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0002 | 0/0 | 2424 | 36 | 31 | 2 | 0 | 2 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0003 | 0/0 | 2424 | 29 | 2 | 2 | 13 | 0 | 12 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0004 | 0/0 | 2412 | 19 | 17 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0005 | 0/0 | 2424 | 6 | 4 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0006 | 0/0 | 2424 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0007 | 0/0 | 2424 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0008 | 0/0 | 2424 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0009 | 0/0 | 2424 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0010 | 0/0 | 2424 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0011 | 0/0 | 2412 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0012 | 0/0 | 2424 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0013 | 0/0 | 2412 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0014 | 0/0 | 2424 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0015 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0016 | 0/0 | 2424 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0017 | 0/0 | 2424 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0018 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0019 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0020 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0021 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0022 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0023 | 0/0 | 2424 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0024 | 0/0 | 2424 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0025 | 0/0 | 2424 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0026 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0027 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0028 | 0/0 | 2424 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0029 | 0/0 | 2412 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0030 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0031 | 0/0 | 2424 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0032 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0033 | 0/0 | 2424 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0034 | 0/0 | 2424 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
c0035 | 0/0 | 2424 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | 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 | 1/1 | 3106 | 175 | 3 | 41 | 97 | 8 | 24 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0002 | 0/0 | 3122 | 35 | 10 | 3 | 10 | 0 | 12 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0003 | 0/0 | 3106 | 21 | 19 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0004 | 0/0 | 3106 | 14 | 14 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0005 | 0/0 | 3106 | 12 | 0 | 6 | 1 | 1 | 4 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0006 | 0/0 | 3106 | 9 | 9 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0007 | 0/0 | 3106 | 8 | 5 | 3 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0008 | 0/0 | 3106 | 5 | 0 | 0 | 3 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0009 | 0/0 | 3105 | 5 | 3 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0010 | 0/0 | 3106 | 4 | 1 | 1 | 1 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0011 | 0/0 | 3122 | 4 | 0 | 0 | 4 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0012 | 0/0 | 3105 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0013 | 0/0 | 3100 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0014 | 0/0 | 3106 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0015 | 0/0 | 3106 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0016 | 0/0 | 3106 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0017 | 0/0 | 3105 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0018 | 0/0 | 3106 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0019 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0020 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0021 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0022 | 0/0 | 3106 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0023 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0024 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0025 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0026 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0027 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0028 | 0/0 | 3122 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0029 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0030 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0031 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0032 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0033 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0034 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0035 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0036 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0037 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0038 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0039 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0040 | 0/0 | 3106 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0041 | 0/0 | 3122 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0042 | 0/0 | 3106 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0043 | 0/0 | 3122 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0044 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0045 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0046 | 0/0 | 3106 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0047 | 0/0 | 3105 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0048 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
t0049 | 0/0 | 3105 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | 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 | 1/0 | 61 | 4 | 17 | 26 | 3 | 10 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0002 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0003 | 0/0 | 9 | 0 | 0 | 6 | 0 | 3 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0005 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0018 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0048 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
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 | 1/1 | 203 | 18 | 48 | 96 | 10 | 29 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 36 | 31 | 2 | 0 | 2 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0014 | a0001 | c0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0020 | a0001 | c0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0021 | a0001 | c0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0024 | a0001 | c0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0025 | a0001 | c0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0027 | a0001 | c0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0003 | a0002 | c0003 | 0/0 | 29 | 2 | 2 | 13 | 0 | 12 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0030 | a0002 | c0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0033 | a0002 | c0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0003c0004 | a0003 | c0004 | 0/0 | 19 | 17 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0004c0007 | a0004 | c0007 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0005c0008 | a0005 | c0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0006c0009 | a0006 | c0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0007c0011 | a0007 | c0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0007c0018 | a0007 | c0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0008c0034 | a0008 | c0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0008c0035 | a0008 | c0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0009c0010 | a0009 | c0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0010c0012 | a0010 | c0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0011c0013 | a0011 | c0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0012c0016 | a0012 | c0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0013c0032 | a0013 | c0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0014c0028 | a0014 | c0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0015c0029 | a0015 | c0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0016c0026 | a0016 | c0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0017c0023 | a0017 | c0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0018c0022 | a0018 | c0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0019c0017 | a0019 | c0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0020c0019 | a0020 | c0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0021c0031 | a0021 | c0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0022c0015 | a0022 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | 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 | 1/1 | 159 | 3 | 38 | 87 | 8 | 21 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 12 | 0 | 6 | 1 | 1 | 4 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 4 | 1 | 1 | 1 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0037 | a0001 | c0001 | t0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0039 | a0001 | c0001 | t0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0040 | a0001 | c0001 | t0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0041 | a0001 | c0001 | t0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0001t0049 | a0001 | c0001 | t0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 15 | 13 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0006 | a0001 | c0002 | t0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0015 | a0001 | c0002 | t0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0017 | a0001 | c0002 | t0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0018 | a0001 | c0002 | t0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0027 | a0001 | c0002 | t0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0031 | a0001 | c0002 | t0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0032 | a0001 | c0002 | t0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0033 | a0001 | c0002 | t0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0036 | a0001 | c0002 | t0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0038 | a0001 | c0002 | t0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0002t0044 | a0001 | c0002 | t0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0005t0009 | a0001 | c0005 | t0009 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0005t0048 | a0001 | c0005 | t0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0006t0003 | a0001 | c0006 | t0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0014t0006 | a0001 | c0014 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0014t0029 | a0001 | c0014 | t0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0020t0001 | a0001 | c0020 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0021t0001 | a0001 | c0021 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0024t0001 | a0001 | c0024 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0025t0006 | a0001 | c0025 | t0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0001c0027t0001 | a0001 | c0027 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0003t0002 | a0002 | c0003 | t0002 | 0/0 | 24 | 2 | 2 | 9 | 0 | 11 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0003t0011 | a0002 | c0003 | t0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0003t0043 | a0002 | c0003 | t0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0030t0002 | a0002 | c0030 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0002c0033t0002 | a0002 | c0033 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0003c0004t0004 | a0003 | c0004 | t0004 | 0/0 | 14 | 14 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0003c0004t0007 | a0003 | c0004 | t0007 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0004c0007t0012 | a0004 | c0007 | t0012 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0005c0008t0013 | a0005 | c0008 | t0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0006c0009t0001 | a0006 | c0009 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0007c0011t0007 | a0007 | c0011 | t0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0007c0018t0019 | a0007 | c0018 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0008c0034t0001 | a0008 | c0034 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0008c0035t0042 | a0008 | c0035 | t0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0009c0010t0023 | a0009 | c0010 | t0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0009c0010t0025 | a0009 | c0010 | t0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0010c0012t0007 | a0010 | c0012 | t0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0010c0012t0046 | a0010 | c0012 | t0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0011c0013t0021 | a0011 | c0013 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0011c0013t0045 | a0011 | c0013 | t0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0012c0016t0001 | a0012 | c0016 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0013c0032t0001 | a0013 | c0032 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0014c0028t0047 | a0014 | c0028 | t0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0015c0029t0020 | a0015 | c0029 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0016c0026t0001 | a0016 | c0026 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0017c0023t0001 | a0017 | c0023 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0018c0022t0001 | a0018 | c0022 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0019c0017t0024 | a0019 | c0017 | t0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0020c0019t0001 | a0020 | c0019 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0021c0031t0001 | a0021 | c0031 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | copy fasta |
a0022c0015t0008 | a0022 | c0015 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 1/0 | 47 | 2 | 16 | 17 | 3 | 8 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0009 | a0001 | c0001 | t0002 | g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0105 | a0001 | c0001 | t0002 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0005g0005 | a0001 | c0001 | t0005 | g0005 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0005g0012 | a0001 | c0001 | t0005 | g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0005g0112 | a0001 | c0001 | t0005 | g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0005g0116 | a0001 | c0001 | t0005 | g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0005g0117 | a0001 | c0001 | t0005 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0005g0118 | a0001 | c0001 | t0005 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0006g0009 | a0001 | c0001 | t0006 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0008g0001 | a0001 | c0001 | t0008 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0008g0041 | a0001 | c0001 | t0008 | g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0010g0020 | a0001 | c0001 | t0010 | g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0010g0129 | a0001 | c0001 | t0010 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0014g0012 | a0001 | c0001 | t0014 | g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0014g0170 | a0001 | c0001 | t0014 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0016g0051 | a0001 | c0001 | t0016 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0016g0052 | a0001 | c0001 | t0016 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0022g0001 | a0001 | c0001 | t0022 | g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0026g0149 | a0001 | c0001 | t0026 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0028g0001 | a0001 | c0001 | t0028 | g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0030g0128 | a0001 | c0001 | t0030 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0034g0173 | a0001 | c0001 | t0034 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0035g0167 | a0001 | c0001 | t0035 | g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0037g0001 | a0001 | c0001 | t0037 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0039g0002 | a0001 | c0001 | t0039 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0040g0012 | a0001 | c0001 | t0040 | g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0041g0122 | a0001 | c0001 | t0041 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0001t0049g0087 | a0001 | c0001 | t0049 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0001g0036 | a0001 | c0002 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0002g0007 | a0001 | c0002 | t0002 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0007 | a0001 | c0002 | t0003 | g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0008 | a0001 | c0002 | t0003 | g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0029 | a0001 | c0002 | t0003 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0073 | a0001 | c0002 | t0003 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0075 | a0001 | c0002 | t0003 | g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0076 | a0001 | c0002 | t0003 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0078 | a0001 | c0002 | t0003 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0080 | a0001 | c0002 | t0003 | g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0003g0086 | a0001 | c0002 | t0003 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0006g0011 | a0001 | c0002 | t0006 | g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0006g0094 | a0001 | c0002 | t0006 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0006g0095 | a0001 | c0002 | t0006 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0006g0175 | a0001 | c0002 | t0006 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0015g0049 | a0001 | c0002 | t0015 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0015g0084 | a0001 | c0002 | t0015 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0017g0024 | a0001 | c0002 | t0017 | g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0018g0071 | a0001 | c0002 | t0018 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0018g0072 | a0001 | c0002 | t0018 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0027g0088 | a0001 | c0002 | t0027 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0031g0060 | a0001 | c0002 | t0031 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0032g0083 | a0001 | c0002 | t0032 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0033g0074 | a0001 | c0002 | t0033 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0036g0053 | a0001 | c0002 | t0036 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0038g0011 | a0001 | c0002 | t0038 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0002t0044g0085 | a0001 | c0002 | t0044 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0005t0009g0031 | a0001 | c0005 | t0009 | g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0005t0009g0032 | a0001 | c0005 | t0009 | g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0005t0009g0089 | a0001 | c0005 | t0009 | g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0005t0009g0090 | a0001 | c0005 | t0009 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0005t0048g0031 | a0001 | c0005 | t0048 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0006t0003g0010 | a0001 | c0006 | t0003 | g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0006t0003g0079 | a0001 | c0006 | t0003 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0006t0003g0081 | a0001 | c0006 | t0003 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0014t0006g0096 | a0001 | c0014 | t0006 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0014t0029g0093 | a0001 | c0014 | t0029 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0020t0001g0001 | a0001 | c0020 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0021t0001g0142 | a0001 | c0021 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0024t0001g0001 | a0001 | c0024 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0025t0006g0009 | a0001 | c0025 | t0006 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0001c0027t0001g0043 | a0001 | c0027 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0003 | a0002 | c0003 | t0002 | g0003 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0014 | a0002 | c0003 | t0002 | g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0026 | a0002 | c0003 | t0002 | g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0027 | a0002 | c0003 | t0002 | g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0047 | a0002 | c0003 | t0002 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0058 | a0002 | c0003 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0059 | a0002 | c0003 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0061 | a0002 | c0003 | t0002 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0062 | a0002 | c0003 | t0002 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0063 | a0002 | c0003 | t0002 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0064 | a0002 | c0003 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0065 | a0002 | c0003 | t0002 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0066 | a0002 | c0003 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0104 | a0002 | c0003 | t0002 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0002g0174 | a0002 | c0003 | t0002 | g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0011g0003 | a0002 | c0003 | t0011 | g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0011g0025 | a0002 | c0003 | t0011 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0011g0057 | a0002 | c0003 | t0011 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0003t0043g0025 | a0002 | c0003 | t0043 | g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0030t0002g0014 | a0002 | c0030 | t0002 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0002c0033t0002g0047 | a0002 | c0033 | t0002 | g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0004g0004 | a0003 | c0004 | t0004 | g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0004g0016 | a0003 | c0004 | t0004 | g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0004g0056 | a0003 | c0004 | t0004 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0004g0068 | a0003 | c0004 | t0004 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0004g0069 | a0003 | c0004 | t0004 | g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0004g0070 | a0003 | c0004 | t0004 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0007g0017 | a0003 | c0004 | t0007 | g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0007g0077 | a0003 | c0004 | t0007 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0003c0004t0007g0101 | a0003 | c0004 | t0007 | g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0004c0007t0012g0015 | a0004 | c0007 | t0012 | g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0004c0007t0012g0067 | a0004 | c0007 | t0012 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0005c0008t0013g0033 | a0005 | c0008 | t0013 | g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0005c0008t0013g0092 | a0005 | c0008 | t0013 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0006c0009t0001g0001 | a0006 | c0009 | t0001 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0006c0009t0001g0134 | a0006 | c0009 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0007c0011t0007g0028 | a0007 | c0011 | t0007 | g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0007c0018t0019g0054 | a0007 | c0018 | t0019 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0008c0034t0001g0158 | a0008 | c0034 | t0001 | g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0008c0035t0042g0001 | a0008 | c0035 | t0042 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0009c0010t0023g0034 | a0009 | c0010 | t0023 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0009c0010t0025g0034 | a0009 | c0010 | t0025 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0010c0012t0007g0004 | a0010 | c0012 | t0007 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0010c0012t0046g0178 | a0010 | c0012 | t0046 | g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0011c0013t0021g0030 | a0011 | c0013 | t0021 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0011c0013t0045g0030 | a0011 | c0013 | t0045 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0012c0016t0001g0136 | a0012 | c0016 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0013c0032t0001g0022 | a0013 | c0032 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0014c0028t0047g0091 | a0014 | c0028 | t0047 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0015c0029t0020g0082 | a0015 | c0029 | t0020 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0016c0026t0001g0001 | a0016 | c0026 | t0001 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0017c0023t0001g0021 | a0017 | c0023 | t0001 | g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0018c0022t0001g0002 | a0018 | c0022 | t0001 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0019c0017t0024g0097 | a0019 | c0017 | t0024 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0020c0019t0001g0109 | a0020 | c0019 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0021c0031t0001g0001 | a0021 | c0031 | t0001 | g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
a0022c0015t0008g0001 | a0022 | c0015 | t0008 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0118 | EUR | GBR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00280 | hp1 | a0001 | c0001 | t0010 | g0020 | EUR | FIN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00597 | hp1 | a0002 | c0003 | t0011 | g0025 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00609 | hp2 | a0020 | c0019 | t0001 | g0109 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0116 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01070 | hp2 | a0003 | c0004 | t0007 | g0077 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01071 | hp1 | a0003 | c0004 | t0007 | g0017 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01074 | hp1 | a0002 | c0003 | t0002 | g0174 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01074 | hp2 | a0004 | c0007 | t0012 | g0015 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01081 | hp1 | a0001 | c0005 | t0009 | g0031 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01081 | hp2 | a0004 | c0007 | t0012 | g0015 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0012 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0020 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01169 | hp1 | a0001 | c0001 | t0014 | g0170 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01175 | hp1 | a0001 | c0002 | t0017 | g0024 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0073 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01243 | hp2 | a0007 | c0011 | t0007 | g0028 | AMR | PUR | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01261 | hp2 | a0002 | c0003 | t0002 | g0047 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0112 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01358 | hp1 | a0008 | c0034 | t0001 | g0158 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01361 | hp2 | a0004 | c0007 | t0012 | g0015 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01433 | hp1 | a0017 | c0023 | t0001 | g0021 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01496 | hp1 | a0001 | c0005 | t0009 | g0032 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01496 | hp2 | a0014 | c0028 | t0047 | g0091 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01515 | hp1 | a0001 | c0002 | t0017 | g0024 | EUR | IBS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01884 | hp2 | a0001 | c0005 | t0048 | g0031 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01891 | hp2 | a0005 | c0008 | t0013 | g0033 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01952 | hp1 | a0021 | c0031 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02055 | hp1 | a0001 | c0002 | t0006 | g0094 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02055 | hp2 | a0001 | c0025 | t0006 | g0009 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02074 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02083 | hp1 | a0022 | c0015 | t0008 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02132 | hp1 | a0008 | c0035 | t0042 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02145 | hp1 | a0003 | c0004 | t0004 | g0004 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02155 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02155 | hp2 | a0016 | c0026 | t0001 | g0001 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02257 | hp1 | a0003 | c0004 | t0004 | g0016 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02257 | hp2 | a0001 | c0002 | t0015 | g0084 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02258 | hp1 | a0003 | c0004 | t0004 | g0004 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02280 | hp1 | a0003 | c0004 | t0004 | g0004 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02280 | hp2 | a0001 | c0002 | t0006 | g0011 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02451 | hp1 | a0007 | c0018 | t0019 | g0054 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02451 | hp2 | a0003 | c0004 | t0004 | g0068 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02523 | hp2 | a0001 | c0020 | t0001 | g0001 | EAS | KHV | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02572 | hp1 | a0003 | c0004 | t0004 | g0056 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02572 | hp2 | a0001 | c0002 | t0038 | g0011 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02615 | hp1 | a0001 | c0002 | t0006 | g0011 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02622 | hp1 | a0001 | c0001 | t0028 | g0001 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02622 | hp2 | a0003 | c0004 | t0004 | g0070 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02630 | hp1 | a0003 | c0004 | t0004 | g0016 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02630 | hp2 | a0001 | c0005 | t0009 | g0032 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02647 | hp1 | a0001 | c0002 | t0015 | g0049 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0078 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02698 | hp1 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02717 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02717 | hp2 | a0001 | c0006 | t0003 | g0010 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02735 | hp1 | a0002 | c0003 | t0002 | g0059 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0117 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02738 | hp2 | a0001 | c0001 | t0022 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02809 | hp1 | a0001 | c0006 | t0003 | g0079 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02809 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02886 | hp2 | a0005 | c0008 | t0013 | g0092 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02896 | hp1 | a0001 | c0002 | t0006 | g0095 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02896 | hp2 | a0001 | c0002 | t0018 | g0071 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02897 | hp1 | a0001 | c0002 | t0018 | g0072 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02897 | hp2 | a0010 | c0012 | t0007 | g0004 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02922 | hp1 | a0011 | c0013 | t0021 | g0030 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02922 | hp2 | a0001 | c0014 | t0006 | g0096 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02965 | hp1 | a0001 | c0002 | t0006 | g0175 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02970 | hp1 | a0010 | c0012 | t0046 | g0178 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0086 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02976 | hp2 | a0001 | c0006 | t0003 | g0010 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03041 | hp1 | a0005 | c0008 | t0013 | g0033 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03041 | hp2 | a0001 | c0002 | t0027 | g0088 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03139 | hp1 | a0001 | c0002 | t0033 | g0074 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03139 | hp2 | a0019 | c0017 | t0024 | g0097 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03195 | hp1 | a0001 | c0005 | t0009 | g0089 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03195 | hp2 | a0003 | c0004 | t0004 | g0016 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03209 | hp1 | a0001 | c0001 | t0049 | g0087 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03209 | hp2 | a0001 | c0005 | t0009 | g0090 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03225 | hp1 | a0002 | c0003 | t0002 | g0061 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03225 | hp2 | a0011 | c0013 | t0045 | g0030 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03239 | hp1 | a0002 | c0003 | t0002 | g0026 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03453 | hp1 | a0001 | c0014 | t0029 | g0093 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03486 | hp1 | a0003 | c0004 | t0004 | g0004 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0076 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0041 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03491 | hp1 | a0004 | c0007 | t0012 | g0067 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03491 | hp2 | a0002 | c0003 | t0002 | g0027 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03492 | hp1 | a0002 | c0003 | t0002 | g0027 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0041 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03516 | hp1 | a0003 | c0004 | t0004 | g0004 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03516 | hp2 | a0001 | c0006 | t0003 | g0010 | AFR | ESN | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03540 | hp2 | a0001 | c0002 | t0032 | g0083 | AFR | GWD | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03579 | hp1 | a0001 | c0002 | t0006 | g0011 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03579 | hp2 | a0001 | c0002 | t0031 | g0060 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0063 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03669 | hp2 | a0002 | c0003 | t0002 | g0003 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03688 | hp1 | a0002 | c0003 | t0002 | g0062 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03704 | hp2 | a0012 | c0016 | t0001 | g0136 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03710 | hp1 | a0001 | c0024 | t0001 | g0001 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0064 | SAS | PJL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0003 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03927 | hp2 | a0002 | c0033 | t0002 | g0047 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03942 | hp2 | a0001 | c0001 | t0040 | g0012 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04115 | hp2 | a0002 | c0003 | t0002 | g0065 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04184 | hp1 | a0002 | c0003 | t0043 | g0025 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18522 | hp2 | a0009 | c0010 | t0023 | g0034 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18747 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | CHB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18906 | hp1 | a0003 | c0004 | t0007 | g0101 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18906 | hp2 | a0007 | c0011 | t0007 | g0028 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18940 | hp1 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18942 | hp2 | a0002 | c0003 | t0011 | g0003 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18947 | hp2 | a0018 | c0022 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18951 | hp1 | a0006 | c0009 | t0001 | g0134 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18951 | hp2 | a0002 | c0003 | t0002 | g0003 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18954 | hp2 | a0001 | c0001 | t0030 | g0128 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18960 | hp1 | a0001 | c0001 | t0034 | g0173 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18960 | hp2 | a0013 | c0032 | t0001 | g0022 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0026 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18966 | hp1 | a0001 | c0021 | t0001 | g0142 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18967 | hp2 | a0001 | c0001 | t0026 | g0149 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0129 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18975 | hp1 | a0006 | c0009 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19009 | hp2 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19030 | hp1 | a0001 | c0001 | t0041 | g0122 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0052 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19043 | hp1 | a0001 | c0001 | t0035 | g0167 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19043 | hp2 | a0003 | c0004 | t0004 | g0004 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19057 | hp2 | a0002 | c0003 | t0002 | g0058 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19064 | hp1 | a0006 | c0009 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19066 | hp1 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19070 | hp2 | a0002 | c0030 | t0002 | g0014 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19083 | hp2 | a0001 | c0001 | t0039 | g0002 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19085 | hp1 | a0002 | c0003 | t0011 | g0003 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19086 | hp2 | a0002 | c0003 | t0011 | g0057 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19089 | hp1 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19091 | hp1 | a0001 | c0027 | t0001 | g0043 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19091 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19240 | hp1 | a0003 | c0004 | t0004 | g0069 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA19240 | hp2 | a0001 | c0006 | t0003 | g0010 | AFR | YRI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0007 | AFR | ASW | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20129 | hp2 | a0003 | c0004 | t0007 | g0017 | AFR | ASW | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0080 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | GIH | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02109 | hp1 | a0001 | c0002 | t0044 | g0085 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02109 | hp2 | a0001 | c0002 | t0036 | g0053 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02486 | hp2 | a0002 | c0003 | t0002 | g0104 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG02559 | hp2 | a0003 | c0004 | t0004 | g0004 | AFR | ACB | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03471 | hp1 | a0015 | c0029 | t0020 | g0082 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG03471 | hp2 | a0003 | c0004 | t0007 | g0017 | AFR | MSL | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG06807 | hp1 | a0001 | c0001 | t0016 | g0051 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20300 | hp1 | a0009 | c0010 | t0025 | g0034 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | USA | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
NA21309 | hp2 | a0001 | c0006 | t0003 | g0081 | AFR | LWK | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0048 | REF | REF | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | AP5Z1_chr7_4770623_4799397 | AP5Z1 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4781188
|
G | A | 1 | a0022 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.55G>A | p.Glu19Lys | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/17 | 148/5529 | 55/2424 | 19/807 | chr7 | 4781188 | ||
chr7:4781297
|
C | T | 1 | a0008 | 2 | HG01358.hp1 HG02132.hp1 |
missense_variant | MODERATE | c.164C>T | p.Thr55Met | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/17 | 257/5529 | 164/2424 | 55/807 | chr7 | 4781297 | ||
chr7:4781669
|
C | G | 1 | a0004 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
missense_variant | MODERATE | c.281C>G | p.Ser94Cys | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/17 | 374/5529 | 281/2424 | 94/807 | chr7 | 4781669 | ||
chr7:4781717
|
G | A | 1 | a0012 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.329G>A | p.Arg110Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/17 | 422/5529 | 329/2424 | 110/807 | chr7 | 4781717 | ||
chr7:4781721
|
G | C | 1 | a0004 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
missense_variant | MODERATE | c.333G>C | p.Gln111His | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/17 | 426/5529 | 333/2424 | 111/807 | chr7 | 4781721 | ||
chr7:4783328
|
G | A | 1 | a0007 | 3 | HG01243.hp2 HG02451.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.379G>A | p.Glu127Lys | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 472/5529 | 379/2424 | 127/807 | chr7 | 4783328 | ||
chr7:4783439
|
A | G | 1 | a0013 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.490A>G | p.Ser164Gly | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 583/5529 | 490/2424 | 164/807 | chr7 | 4783439 | ||
chr7:4783761
|
A | G | 1 | a0006 | 3 | NA18951.hp1 NA18975.hp1 NA19064.hp1 |
missense_variant | MODERATE | c.584A>G | p.His195Arg | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/17 | 677/5529 | 584/2424 | 195/807 | chr7 | 4783761 | ||
chr7:4783784
|
C | T | 1 | a0021 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.607C>T | p.Pro203Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/17 | 700/5529 | 607/2424 | 203/807 | chr7 | 4783784 | ||
chr7:4784264
|
G | C | 1 | a0020 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.683G>C | p.Ser228Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 776/5529 | 683/2424 | 228/807 | chr7 | 4784264 | ||
chr7:4784354
|
C | T | 1 | a0014 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.773C>T | p.Pro258Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 866/5529 | 773/2424 | 258/807 | chr7 | 4784354 | ||
chr7:4785676
|
T | A | 1 | a0002 | 31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
missense_variant | MODERATE | c.1124T>A | p.Leu375Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/17 | 1217/5529 | 1124/2424 | 375/807 | chr7 | 4785676 | ||
chr7:4787707
|
C | G | 1 | a0015 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1385C>G | p.Thr462Arg | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1478/5529 | 1385/2424 | 462/807 | chr7 | 4787707 | ||
chr7:4788162
|
C | T | 1 | a0016 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.1463C>T | p.Pro488Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1556/5529 | 1463/2424 | 488/807 | chr7 | 4788162 | ||
chr7:4788222
|
C | G | 1 | a0011 | 2 | HG02922.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1523C>G | p.Ala508Gly | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1616/5529 | 1523/2424 | 508/807 | chr7 | 4788222 | ||
chr7:4788228
|
G | A | 1 | a0004 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
missense_variant | MODERATE | c.1529G>A | p.Arg510Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1622/5529 | 1529/2424 | 510/807 | chr7 | 4788228 | ||
chr7:4790763
|
C | G | 1 | a0019 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.2029C>G | p.Leu677Val | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2122/5529 | 2029/2424 | 677/807 | chr7 | 4790763 | ||
chr7:4790817
|
C | A | 1 | a0018 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.2083C>A | p.Pro695Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2176/5529 | 2083/2424 | 695/807 | chr7 | 4790817 | ||
chr7:4790832
|
G | A | 1 | a0017 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.2098G>A | p.Val700Met | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2191/5529 | 2098/2424 | 700/807 | chr7 | 4790832 | ||
chr7:4791165
|
CCAGCTCC others(5): Show |
C | 4 | a0003a0007a0011others(1): Show | 25 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(22): Show |
conservative_inframe_deletion | MODERATE | c.2209_2220delTCCACG others(6): Show |
p.Ser737_Ser740del | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2302/5529 | 2209/2424 | 737/807 | INFO_REALIGN_3_PRIME | chr7 | 4791165 | |
chr7:4791191
|
G | A | 3 | a0010a0011a0015 | 5 | HG02897.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
missense_variant | MODERATE | c.2230G>A | p.Ala744Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2323/5529 | 2230/2424 | 744/807 | chr7 | 4791191 | ||
chr7:4791266
|
A | G | 1 | a0005 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.2305A>G | p.Thr769Ala | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2398/5529 | 2305/2424 | 769/807 | chr7 | 4791266 | ||
chr7:4791289
|
C | A | 2 | a0009a0019 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.2328C>A | p.Ser776Arg | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2421/5529 | 2328/2424 | 776/807 | chr7 | 4791289 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4783318
|
T | C | 2 | a0009c0010a0019c0017 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
splice_region_variant&synonymous_variant | LOW | c.369T>C | p.Gly123Gly | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 462/5529 | 369/2424 | 123/807 | chr7 | 4783318 | ||
chr7:4783393
|
C | G | 1 | a0002c0033 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.444C>G | p.Pro148Pro | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/17 | 537/5529 | 444/2424 | 148/807 | chr7 | 4783393 | ||
chr7:4783765
|
C | T | 2 | a0008c0035a0013c0032 | 2 | HG02132.hp1 NA18960.hp2 |
synonymous_variant | LOW | c.588C>T | p.Ser196Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/17 | 681/5529 | 588/2424 | 196/807 | chr7 | 4783765 | ||
chr7:4784256
|
G | C | 1 | a0019c0017 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.675G>C | p.Val225Val | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 768/5529 | 675/2424 | 225/807 | chr7 | 4784256 | ||
chr7:4784340
|
C | T | 13 | a0001c0002a0001c0006a0001c0014others(10): Show | 103 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(100): Show |
synonymous_variant | LOW | c.759C>T | p.Ser253Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 852/5529 | 759/2424 | 253/807 | chr7 | 4784340 | ||
chr7:4784367
|
C | T | 1 | a0001c0027 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.786C>T | p.Asp262Asp | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/17 | 879/5529 | 786/2424 | 262/807 | chr7 | 4784367 | ||
chr7:4784951
|
C | T | 1 | a0002c0030 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.834C>T | p.Ser278Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/17 | 927/5529 | 834/2424 | 278/807 | chr7 | 4784951 | ||
chr7:4785683
|
C | T | 3 | a0002c0003a0002c0030a0002c0033 | 31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
splice_region_variant&synonymous_variant | LOW | c.1131C>T | p.His377His | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/17 | 1224/5529 | 1131/2424 | 377/807 | chr7 | 4785683 | ||
chr7:4786314
|
G | A | 1 | a0004c0007 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
synonymous_variant | LOW | c.1197G>A | p.Glu399Glu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/17 | 1290/5529 | 1197/2424 | 399/807 | chr7 | 4786314 | ||
chr7:4786353
|
G | A | 1 | a0001c0020 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.1236G>A | p.Gln412Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/17 | 1329/5529 | 1236/2424 | 412/807 | chr7 | 4786353 | ||
chr7:4787637
|
C | T | 1 | a0005c0008 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.1315C>T | p.Leu439Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1408/5529 | 1315/2424 | 439/807 | chr7 | 4787637 | ||
chr7:4787691
|
C | T | 1 | a0001c0006 | 6 | HG02717.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
synonymous_variant | LOW | c.1369C>T | p.Leu457Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1462/5529 | 1369/2424 | 457/807 | chr7 | 4787691 | ||
chr7:4787699
|
C | T | 4 | a0001c0014a0002c0003a0002c0030others(1): Show | 33 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(30): Show |
synonymous_variant | LOW | c.1377C>T | p.Asp459Asp | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/17 | 1470/5529 | 1377/2424 | 459/807 | chr7 | 4787699 | ||
chr7:4788253
|
C | T | 2 | a0001c0005a0014c0028 | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
synonymous_variant | LOW | c.1554C>T | p.Phe518Phe | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1647/5529 | 1554/2424 | 518/807 | chr7 | 4788253 | ||
chr7:4788256
|
A | G | 2 | a0011c0013a0015c0029 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.1557A>G | p.Gln519Gln | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1650/5529 | 1557/2424 | 519/807 | chr7 | 4788256 | ||
chr7:4788262
|
G | A | 1 | a0011c0013 | 2 | HG02922.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.1563G>A | p.Leu521Leu | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/17 | 1656/5529 | 1563/2424 | 521/807 | chr7 | 4788262 | ||
chr7:4790795
|
T | C | 1 | a0001c0021 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.2061T>C | p.Ser687Ser | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2154/5529 | 2061/2424 | 687/807 | chr7 | 4790795 | ||
chr7:4790825
|
G | T | 1 | a0001c0025 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2091G>T | p.Val697Val | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/17 | 2184/5529 | 2091/2424 | 697/807 | chr7 | 4790825 | ||
chr7:4791193
|
G | A | 1 | a0001c0024 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.2232G>A | p.Ala744Ala | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2325/5529 | 2232/2424 | 744/807 | chr7 | 4791193 | ||
chr7:4791340
|
G | T | 1 | a0004c0007 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
synonymous_variant | LOW | c.2379G>T | p.Thr793Thr | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2472/5529 | 2379/2424 | 793/807 | chr7 | 4791340 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4775713
|
G | A | 1 | a0007c0018t0019 | 1 | HG02451.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-3G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/17 | chr7 | 4775713 | ||||||
chr7:4775715
|
G | C | 3 | a0005c0008t0013a0011c0013t0021a0015c0029t0020 | 5 | HG01891.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/17 | 1 | chr7 | 4775715 | |||||
chr7:4791430
|
A | G | 9 | a0001c0001t0049a0001c0002t0017a0001c0002t0018others(6): Show | 20 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*45A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 45 | chr7 | 4791430 | |||||
chr7:4791453
|
G | A | 1 | a0003c0004t0004 | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 68 | chr7 | 4791453 | |||||
chr7:4791526
|
C | G | 2 | a0011c0013t0021a0011c0013t0045 | 2 | HG02922.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 141 | chr7 | 4791526 | |||||
chr7:4791533
|
G | A | 1 | a0001c0001t0022 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 148 | chr7 | 4791533 | |||||
chr7:4791535
|
G | A | 3 | a0009c0010t0023a0009c0010t0025a0019c0017t0024 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*150G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 150 | chr7 | 4791535 | |||||
chr7:4791540
|
TG | T | 3 | a0010c0012t0046a0011c0013t0021a0011c0013t0045 | 3 | HG02922.hp1 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*157delG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 157 | INFO_REALIGN_3_PRIME | chr7 | 4791540 | ||||
chr7:4791543
|
C | A | 3 | a0010c0012t0046a0011c0013t0021a0011c0013t0045 | 3 | HG02922.hp1 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*158C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 158 | chr7 | 4791543 | |||||
chr7:4791546
|
C | T | 1 | a0009c0010t0025 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*161C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 161 | chr7 | 4791546 | |||||
chr7:4791574
|
G | A | 1 | a0001c0001t0026 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 189 | chr7 | 4791574 | |||||
chr7:4791590
|
G | A | 14 | a0001c0001t0028a0001c0002t0027a0003c0004t0004others(11): Show | 32 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*205G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 205 | chr7 | 4791590 | |||||
chr7:4791596
|
ACTGAG | A | 1 | a0005c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*222_*226delCTGAG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 222 | INFO_REALIGN_3_PRIME | chr7 | 4791596 | ||||
chr7:4791635
|
T | G | 5 | a0001c0001t0049a0001c0002t0017a0001c0005t0009others(2): Show | 10 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*250T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 250 | chr7 | 4791635 | |||||
chr7:4791661
|
T | C | 7 | a0001c0001t0049a0001c0002t0017a0001c0005t0009others(4): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*276T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 276 | chr7 | 4791661 | |||||
chr7:4791763
|
T | C | 7 | a0001c0001t0049a0001c0002t0017a0001c0005t0009others(4): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 378 | chr7 | 4791763 | |||||
chr7:4791817
|
C | G | 1 | a0005c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*432C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 432 | chr7 | 4791817 | |||||
chr7:4791825
|
G | A | 1 | a0001c0014t0029 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*440G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 440 | chr7 | 4791825 | |||||
chr7:4791869
|
G | A | 1 | a0001c0001t0014 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*484G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 484 | chr7 | 4791869 | |||||
chr7:4791916
|
G | A | 2 | a0009c0010t0023a0009c0010t0025 | 2 | NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*531G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 531 | chr7 | 4791916 | |||||
chr7:4791922
|
G | A | 1 | a0005c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*537G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 537 | chr7 | 4791922 | |||||
chr7:4792044
|
G | A | 2 | a0001c0001t0010a0001c0001t0030 | 5 | HG00280.hp1 HG01168.hp1 HG02145.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 659 | chr7 | 4792044 | |||||
chr7:4792050
|
T | C | 5 | a0003c0004t0004a0003c0004t0007a0007c0011t0007others(2): Show | 23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*665T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 665 | chr7 | 4792050 | |||||
chr7:4792075
|
A | G | 1 | a0001c0001t0016 | 2 | HG06807.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 690 | chr7 | 4792075 | |||||
chr7:4792119
|
G | C | 1 | a0005c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*734G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 734 | chr7 | 4792119 | |||||
chr7:4792146
|
G | A | 11 | a0001c0001t0049a0001c0002t0015a0001c0002t0027others(8): Show | 21 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*761G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 761 | chr7 | 4792146 | |||||
chr7:4792150
|
C | G | 9 | a0003c0004t0004a0003c0004t0007a0007c0011t0007others(6): Show | 27 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*765C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 765 | chr7 | 4792150 | |||||
chr7:4792158
|
G | A | 1 | a0001c0001t0034 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 773 | chr7 | 4792158 | |||||
chr7:4792241
|
G | A | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 856 | chr7 | 4792241 | |||||
chr7:4792278
|
T | C | 1 | a0001c0001t0035 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*893T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 893 | chr7 | 4792278 | |||||
chr7:4792282
|
G | A | 1 | a0014c0028t0047 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*897G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 897 | chr7 | 4792282 | |||||
chr7:4792286
|
C | T | 3 | a0001c0002t0015a0001c0002t0027a0001c0002t0044 | 4 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*901C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 901 | chr7 | 4792286 | |||||
chr7:4792304
|
CT | C | 7 | a0001c0001t0049a0001c0002t0017a0001c0005t0009others(4): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*921delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 921 | INFO_REALIGN_3_PRIME | chr7 | 4792304 | ||||
chr7:4792307
|
C | T | 6 | a0002c0003t0043a0003c0004t0004a0003c0004t0007others(3): Show | 24 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*922C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 922 | chr7 | 4792307 | |||||
chr7:4792336
|
T | C | 1 | a0001c0002t0031 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*951T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 951 | chr7 | 4792336 | |||||
chr7:4792338
|
T | C | 20 | a0001c0001t0049a0001c0002t0017a0001c0002t0036others(17): Show | 48 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*953T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 953 | chr7 | 4792338 | |||||
chr7:4792424
|
G | C | 4 | a0001c0001t0049a0001c0005t0009a0001c0005t0048others(1): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1039G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1039 | chr7 | 4792424 | |||||
chr7:4792424
|
G | T | 2 | a0004c0007t0012a0005c0008t0013 | 7 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1039G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1039 | chr7 | 4792424 | |||||
chr7:4792479
|
G | A | 1 | a0005c0008t0013 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1094G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1094 | chr7 | 4792479 | |||||
chr7:4792517
|
G | A | 1 | a0001c0001t0037 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1132G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1132 | chr7 | 4792517 | |||||
chr7:4792518
|
CG | C | 4 | a0010c0012t0046a0011c0013t0021a0011c0013t0045others(1): Show | 4 | HG02922.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1136delG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1136 | INFO_REALIGN_3_PRIME | chr7 | 4792518 | ||||
chr7:4792567
|
C | T | 5 | a0003c0004t0004a0003c0004t0007a0007c0011t0007others(2): Show | 23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1182C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1182 | chr7 | 4792567 | |||||
chr7:4792572
|
G | A | 3 | a0009c0010t0023a0009c0010t0025a0019c0017t0024 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1187G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1187 | chr7 | 4792572 | |||||
chr7:4792643
|
C | T | 1 | a0008c0035t0042 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1258C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1258 | chr7 | 4792643 | |||||
chr7:4792650
|
C | A | 1 | a0001c0002t0038 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1265C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1265 | chr7 | 4792650 | |||||
chr7:4792740
|
G | A | 5 | a0001c0002t0003a0001c0002t0018a0001c0002t0031others(2): Show | 25 | HG01243.hp1 HG02109.hp2 HG02559.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1355G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1355 | chr7 | 4792740 | |||||
chr7:4792826
|
C | T | 4 | a0001c0001t0049a0001c0005t0009a0001c0005t0048others(1): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1441C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1441 | chr7 | 4792826 | |||||
chr7:4792888
|
C | A | 2 | a0009c0010t0023a0009c0010t0025 | 2 | NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1503C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1503 | chr7 | 4792888 | |||||
chr7:4792890
|
C | T | 17 | a0001c0001t0049a0001c0005t0009a0001c0005t0048others(14): Show | 44 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1505C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1505 | chr7 | 4792890 | |||||
chr7:4792940
|
C | G | 5 | a0003c0004t0004a0003c0004t0007a0007c0011t0007others(2): Show | 23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1555C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1555 | chr7 | 4792940 | |||||
chr7:4792979
|
C | A | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1594C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1594 | chr7 | 4792979 | |||||
chr7:4793026
|
A | C | 3 | a0009c0010t0023a0009c0010t0025a0019c0017t0024 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1641A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1641 | chr7 | 4793026 | |||||
chr7:4793072
|
T | C | 18 | a0001c0001t0049a0001c0005t0009a0001c0005t0048others(15): Show | 45 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1687T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1687 | chr7 | 4793072 | |||||
chr7:4793086
|
C | G | 17 | a0001c0001t0049a0001c0005t0009a0001c0005t0048others(14): Show | 44 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1701C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1701 | chr7 | 4793086 | |||||
chr7:4793179
|
C | T | 3 | a0009c0010t0023a0009c0010t0025a0019c0017t0024 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1794C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1794 | chr7 | 4793179 | |||||
chr7:4793362
|
C | T | 1 | a0001c0001t0030 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1977C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 1977 | chr7 | 4793362 | |||||
chr7:4793389
|
C | T | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2004 | chr7 | 4793389 | |||||
chr7:4793398
|
C | T | 3 | a0011c0013t0021a0011c0013t0045a0015c0029t0020 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2013C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2013 | chr7 | 4793398 | |||||
chr7:4793468
|
A | AGC | 3 | a0001c0002t0032a0001c0002t0033a0010c0012t0046 | 3 | HG02970.hp1 HG03139.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084_*2085dupGC | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2086 | INFO_REALIGN_3_PRIME | chr7 | 4793468 | ||||
chr7:4793478
|
A | G | 8 | a0001c0001t0049a0001c0002t0015a0001c0002t0044others(5): Show | 18 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2093A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2093 | chr7 | 4793478 | |||||
chr7:4793552
|
G | A | 2 | a0001c0001t0008a0022c0015t0008 | 5 | HG02083.hp1 HG02155.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2167G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2167 | chr7 | 4793552 | |||||
chr7:4793557
|
C | T | 1 | a0001c0001t0049 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2172C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2172 | chr7 | 4793557 | |||||
chr7:4793582
|
A | G | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2197A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2197 | chr7 | 4793582 | |||||
chr7:4793583
|
G | C | 3 | a0009c0010t0023a0009c0010t0025a0019c0017t0024 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2198G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2198 | chr7 | 4793583 | |||||
chr7:4793594
|
G | GCGTGGGC others(9): Show |
9 | a0001c0001t0002a0001c0001t0028a0001c0001t0041others(6): Show | 42 | HG00597.hp1 HG01074.hp1 HG01109.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2211_*2226dupGTGG others(12): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2227 | INFO_REALIGN_3_PRIME | chr7 | 4793594 | ||||
chr7:4793607
|
G | A | 2 | a0009c0010t0023a0009c0010t0025 | 2 | NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2222G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2222 | chr7 | 4793607 | |||||
chr7:4793613
|
C | T | 9 | a0001c0001t0002a0001c0001t0028a0001c0001t0041others(6): Show | 42 | HG00597.hp1 HG01074.hp1 HG01109.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2228C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2228 | chr7 | 4793613 | |||||
chr7:4793629
|
G | A | 1 | a0004c0007t0012 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2244G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2244 | chr7 | 4793629 | |||||
chr7:4793671
|
G | A | 5 | a0003c0004t0004a0003c0004t0007a0007c0011t0007others(2): Show | 23 | HG01070.hp2 HG01071.hp1 HG01243.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2286G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2286 | chr7 | 4793671 | |||||
chr7:4793687
|
G | A | 1 | a0019c0017t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2302G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2302 | chr7 | 4793687 | |||||
chr7:4793691
|
G | A | 2 | a0011c0013t0021a0011c0013t0045 | 2 | HG02922.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2306G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2306 | chr7 | 4793691 | |||||
chr7:4793719
|
C | T | 3 | a0001c0001t0041a0009c0010t0023a0009c0010t0025 | 3 | NA18522.hp2 NA19030.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2334C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2334 | chr7 | 4793719 | |||||
chr7:4793722
|
C | T | 1 | a0001c0001t0040 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2337C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2337 | chr7 | 4793722 | |||||
chr7:4793757
|
T | G | 1 | a0001c0001t0039 | 1 | NA19083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2372 | chr7 | 4793757 | |||||
chr7:4793789
|
C | T | 1 | a0019c0017t0024 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2404C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2404 | chr7 | 4793789 | |||||
chr7:4793885
|
C | T | 2 | a0001c0002t0015a0001c0002t0033 | 3 | HG02257.hp2 HG02647.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2500C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2500 | chr7 | 4793885 | |||||
chr7:4793886
|
G | A | 2 | a0001c0001t0049a0001c0005t0009 | 6 | HG01081.hp1 HG01496.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2501G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2501 | chr7 | 4793886 | |||||
chr7:4793984
|
T | C | 4 | a0001c0001t0049a0001c0005t0009a0001c0005t0048others(1): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2599T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2599 | chr7 | 4793984 | |||||
chr7:4794008
|
A | C | 46 | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(43): Show | 134 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2623A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2623 | chr7 | 4794008 | |||||
chr7:4794021
|
T | TCTGTATC others(34): Show |
3 | a0011c0013t0021a0011c0013t0045a0015c0029t0020 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2637_*2677dupCTGT others(37): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2678 | INFO_REALIGN_3_PRIME | chr7 | 4794021 | ||||
chr7:4794104
|
C | A | 3 | a0011c0013t0021a0011c0013t0045a0015c0029t0020 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2719C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2719 | chr7 | 4794104 | |||||
chr7:4794197
|
C | T | 1 | a0002c0003t0011 | 4 | HG00597.hp1 NA18942.hp2 NA19085.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2812C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2812 | chr7 | 4794197 | |||||
chr7:4794226
|
A | G | 3 | a0001c0001t0005a0001c0001t0014a0001c0001t0040 | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2841A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2841 | chr7 | 4794226 | |||||
chr7:4794234
|
G | T | 3 | a0001c0005t0009a0001c0005t0048a0014c0028t0047 | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2849G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2849 | chr7 | 4794234 | |||||
chr7:4794243
|
G | C | 3 | a0011c0013t0021a0011c0013t0045a0015c0029t0020 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2858G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2858 | chr7 | 4794243 | |||||
chr7:4794267
|
A | G | 7 | a0001c0002t0015a0001c0002t0017a0001c0002t0027others(4): Show | 9 | HG01175.hp1 HG01515.hp1 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2882A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2882 | chr7 | 4794267 | |||||
chr7:4794367
|
G | A | 1 | a0001c0001t0035 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2982G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 17/17 | 2982 | chr7 | 4794367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:4775757
|
G | C | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | splice_donor_variant&intron_variant | HIGH | c.41+1G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775757 | ||||||
chr7:4775843
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0050 | 3 | HG01433.hp2 HG01952.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.41+87G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775843 | ||||||
chr7:4775873
|
C | T | 1 | a0010c0012t0046g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.41+117C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775873 | ||||||
chr7:4775879
|
C | A | 2 | a0001c0001t0016g0051a0001c0001t0016g0052 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.41+123C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775879 | ||||||
chr7:4775897
|
T | G | 80 | a0001c0001t0002g0009a0001c0001t0002g0055a0001c0001t0006g0009others(77): Show | 118 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(115): Show |
intron_variant | MODIFIER | c.41+141T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775897 | ||||||
chr7:4775910
|
C | A | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.41+154C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775910 | ||||||
chr7:4775972
|
T | C | 80 | a0001c0001t0002g0009a0001c0001t0002g0055a0001c0001t0006g0009others(77): Show | 118 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(115): Show |
intron_variant | MODIFIER | c.41+216T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4775972 | ||||||
chr7:4776041
|
C | G | 9 | a0001c0002t0006g0011a0001c0002t0006g0094a0001c0002t0006g0095others(6): Show | 11 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.41+285C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776041 | ||||||
chr7:4776197
|
C | CGTGGGAG others(36): Show |
2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.41+444_41+486dupGG others(41): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776197 | |||||
chr7:4776355
|
T | C | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41+599T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776355 | ||||||
chr7:4776441
|
G | T | 6 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(3): Show | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+685G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776441 | ||||||
chr7:4776507
|
A | C | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.41+751A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776507 | ||||||
chr7:4776551
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.41+795T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776551 | ||||||
chr7:4776562
|
C | CA | 12 | a0001c0001t0001g0018a0001c0001t0001g0098a0001c0001t0001g0099others(9): Show | 13 | HG01981.hp1 HG02027.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+829dupA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | |||||
chr7:4776562
|
CA | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0171a0001c0001t0001g0172others(15): Show | 21 | HG00597.hp1 HG01074.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.41+829delA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | |||||
chr7:4776562
|
CAA | C | 22 | a0001c0002t0006g0011a0001c0002t0006g0094a0001c0002t0006g0095others(19): Show | 36 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.41+828_41+829delAA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | |||||
chr7:4776562
|
CAAAAAA | C | 20 | a0001c0001t0002g0009a0001c0001t0006g0009a0001c0002t0002g0007others(17): Show | 37 | HG01071.hp1 HG01109.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.41+824_41+829delAA others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | |||||
chr7:4776562
|
CAAAAAAA | C | 20 | a0001c0001t0001g0048a0001c0001t0049g0087a0001c0002t0003g0029others(17): Show | 25 | HG00280.hp2 HG01070.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.41+823_41+829delAA others(5): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | |||||
chr7:4776562
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41+817_41+829delAA others(11): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4776562 | |||||
chr7:4776689
|
G | A | 1 | a0007c0018t0019g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41+933G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776689 | ||||||
chr7:4776697
|
T | C | 47 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0002g0055others(44): Show | 73 | HG00544.hp2 HG00597.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.41+941T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776697 | ||||||
chr7:4776807
|
G | A | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41+1051G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776807 | ||||||
chr7:4776856
|
G | A | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41+1100G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776856 | ||||||
chr7:4776870
|
A | C | 1 | a0001c0001t0001g0169 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.41+1114A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776870 | ||||||
chr7:4776943
|
C | T | 18 | a0001c0002t0006g0011a0001c0002t0006g0095a0001c0002t0006g0175others(15): Show | 24 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.41+1187C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776943 | ||||||
chr7:4776989
|
G | T | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.41+1233G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776989 | ||||||
chr7:4776990
|
C | T | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.41+1234C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4776990 | ||||||
chr7:4777019
|
G | T | 1 | a0001c0001t0002g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.41+1263G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777019 | ||||||
chr7:4777037
|
C | A | 12 | a0001c0001t0001g0108a0001c0002t0017g0024a0001c0005t0009g0031others(9): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+1281C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777037 | ||||||
chr7:4777125
|
C | G | 23 | a0001c0001t0002g0055a0001c0014t0006g0096a0002c0003t0002g0003others(20): Show | 33 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.41+1369C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777125 | ||||||
chr7:4777145
|
C | A | 1 | a0020c0019t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.41+1389C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777145 | ||||||
chr7:4777156
|
A | T | 1 | a0001c0002t0003g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.41+1400A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777156 | ||||||
chr7:4777166
|
GAT | G | 20 | a0001c0001t0002g0055a0002c0003t0002g0003a0002c0003t0002g0014others(17): Show | 30 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.41+1413_41+1414del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777166 | |||||
chr7:4777170
|
T | C | 22 | a0001c0001t0002g0009a0001c0001t0006g0009a0001c0002t0002g0007others(19): Show | 39 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.41+1414T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777170 | ||||||
chr7:4777197
|
A | G | 8 | a0001c0002t0006g0011a0001c0002t0006g0094a0001c0002t0006g0095others(5): Show | 10 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+1441A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777197 | ||||||
chr7:4777353
|
C | CTTTA | 55 | a0001c0001t0001g0036a0001c0001t0001g0113a0001c0001t0001g0114others(52): Show | 72 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.41+1629_41+1632dup others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777353 | |||||
chr7:4777353
|
C | CTTTATTT others(1): Show |
19 | a0001c0001t0001g0035a0001c0001t0001g0110a0001c0001t0001g0111others(16): Show | 30 | HG01891.hp2 HG02055.hp1 HG02074.hp1 others(27): Show |
intron_variant | MODIFIER | c.41+1625_41+1632dup others(8): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777353 | |||||
chr7:4777353
|
C | CTTTATTT others(5): Show |
2 | a0001c0002t0003g0078a0001c0006t0003g0079 | 2 | HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.41+1621_41+1632dup others(12): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4777353 | |||||
chr7:4777426
|
C | T | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.41+1670C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777426 | ||||||
chr7:4777444
|
A | G | 1 | a0007c0018t0019g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41+1688A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777444 | ||||||
chr7:4777476
|
C | T | 2 | a0003c0004t0007g0017a0003c0004t0007g0077 | 4 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+1720C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777476 | ||||||
chr7:4777587
|
C | G | 1 | a0015c0029t0020g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.41+1831C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777587 | ||||||
chr7:4777623
|
A | G | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41+1867A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777623 | ||||||
chr7:4777648
|
C | T | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.41+1892C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777648 | ||||||
chr7:4777656
|
C | T | 2 | a0001c0001t0001g0168a0001c0001t0001g0169 | 2 | NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.41+1900C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777656 | ||||||
chr7:4777744
|
C | T | 1 | a0001c0001t0035g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+1988C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777744 | ||||||
chr7:4777756
|
T | C | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2000T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777756 | ||||||
chr7:4777822
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.41+2066A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777822 | ||||||
chr7:4777829
|
T | C | 11 | a0001c0002t0017g0024a0001c0005t0009g0031a0001c0005t0009g0032others(8): Show | 16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+2073T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777829 | ||||||
chr7:4777836
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.41+2080A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777836 | ||||||
chr7:4777932
|
C | T | 1 | a0019c0017t0024g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+2176C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777932 | ||||||
chr7:4777957
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.41+2201G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777957 | ||||||
chr7:4777985
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.41+2229G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4777985 | ||||||
chr7:4778039
|
C | T | 1 | a0002c0003t0002g0027 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.41+2283C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778039 | ||||||
chr7:4778047
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41+2291G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778047 | ||||||
chr7:4778082
|
A | G | 1 | a0019c0017t0024g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+2326A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778082 | ||||||
chr7:4778193
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.41+2437C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778193 | ||||||
chr7:4778321
|
G | T | 11 | a0001c0002t0017g0024a0001c0005t0009g0031a0001c0005t0009g0032others(8): Show | 16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+2565G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778321 | ||||||
chr7:4778377
|
G | A | 1 | a0020c0019t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.41+2621G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778377 | ||||||
chr7:4778390
|
G | A | 1 | a0001c0001t0041g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+2634G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778390 | ||||||
chr7:4778455
|
A | T | 65 | a0001c0001t0002g0009a0001c0001t0002g0055a0001c0001t0006g0009others(62): Show | 97 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(94): Show |
intron_variant | MODIFIER | c.41+2699A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778455 | ||||||
chr7:4778509
|
T | C | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42-2666T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778509 | ||||||
chr7:4778544
|
C | T | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-2631C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778544 | ||||||
chr7:4778660
|
T | A | 26 | a0001c0002t0017g0024a0001c0005t0009g0031a0001c0005t0009g0032others(23): Show | 40 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.42-2515T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778660 | ||||||
chr7:4778665
|
G | A | 5 | a0001c0002t0015g0049a0001c0002t0015g0084a0001c0002t0032g0083others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2510G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778665 | ||||||
chr7:4778713
|
A | G | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-2462A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778713 | ||||||
chr7:4778759
|
TTA | T | 6 | a0001c0001t0002g0009a0001c0001t0006g0009a0001c0002t0003g0008others(3): Show | 10 | HG01109.hp1 HG02055.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-2410_42-2409del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4778759 | |||||
chr7:4778766
|
T | G | 1 | a0001c0001t0002g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.42-2409T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778766 | ||||||
chr7:4778785
|
TATATA | T | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.42-2382_42-2378del others(5): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4778785 | |||||
chr7:4778817
|
GTTATA | G | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-2351_42-2347del others(5): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4778817 | |||||
chr7:4778829
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.42-2346A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778829 | ||||||
chr7:4778957
|
A | G | 1 | a0001c0002t0015g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.42-2218A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4778957 | ||||||
chr7:4779043
|
T | G | 2 | a0001c0001t0001g0037a0001c0002t0036g0053 | 3 | HG00438.hp2 HG02109.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.42-2132T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779043 | ||||||
chr7:4779043
|
TATAG | T | 9 | a0001c0001t0001g0119a0001c0001t0005g0005a0001c0001t0005g0012others(6): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.42-2116_42-2113del others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779043 | |||||
chr7:4779046
|
A | T | 1 | a0001c0014t0006g0096 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-2129A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779046 | ||||||
chr7:4779047
|
G | T | 22 | a0001c0001t0002g0055a0002c0003t0002g0003a0002c0003t0002g0014others(19): Show | 32 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.42-2128G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779047 | ||||||
chr7:4779057
|
T | C | 1 | a0002c0003t0002g0063 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.42-2118T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779057 | ||||||
chr7:4779161
|
A | G | 31 | a0001c0001t0002g0055a0001c0002t0006g0011a0001c0002t0006g0094others(28): Show | 43 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.42-2014A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779161 | ||||||
chr7:4779180
|
A | G | 1 | a0001c0006t0003g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.42-1995A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779180 | ||||||
chr7:4779208
|
A | T | 1 | a0001c0014t0006g0096 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-1967A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779208 | ||||||
chr7:4779221
|
CAT | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0046a0011c0013t0021g0030others(2): Show | 7 | HG00738.hp2 HG01071.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-1949_42-1948del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779221 | |||||
chr7:4779238
|
A | G | 26 | a0001c0002t0017g0024a0001c0002t0027g0088a0001c0002t0036g0053others(23): Show | 40 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.42-1937A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779238 | ||||||
chr7:4779316
|
CAT | C | 13 | a0001c0001t0005g0005a0001c0001t0005g0012a0001c0001t0005g0112others(10): Show | 20 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1857_42-1856del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779316 | |||||
chr7:4779319
|
A | G | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.42-1856A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779319 | ||||||
chr7:4779342
|
CAT | C | 4 | a0001c0001t0002g0123a0001c0002t0006g0095a0001c0002t0027g0088others(1): Show | 4 | HG01496.hp2 HG02896.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-1829_42-1828del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779342 | |||||
chr7:4779344
|
T | TAACACGT others(17): Show |
5 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(2): Show | 6 | HG01081.hp1 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-1830_42-1829ins others(24): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779344 | |||||
chr7:4779374
|
A | G | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1801A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779374 | ||||||
chr7:4779376
|
G | C | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1799G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779376 | ||||||
chr7:4779377
|
T | A | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1798T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779377 | ||||||
chr7:4779378
|
C | CAT | 16 | a0001c0002t0027g0088a0001c0002t0036g0053a0001c0005t0009g0031others(13): Show | 20 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1793_42-1792dup others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779378 | |||||
chr7:4779378
|
C | CATATAAC others(18): Show |
3 | a0001c0001t0002g0009a0001c0001t0006g0009a0001c0025t0006g0009 | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-1784_42-1760dup others(25): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779378 | |||||
chr7:4779378
|
C | T | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.42-1797C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779378 | ||||||
chr7:4779410
|
CATG | C | 7 | a0001c0002t0027g0088a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-1762_42-1760del others(3): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779410 | |||||
chr7:4779430
|
A | G | 1 | a0001c0001t0005g0118 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.42-1745A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779430 | ||||||
chr7:4779436
|
CAT | C | 13 | a0001c0002t0017g0024a0001c0002t0027g0088a0001c0005t0009g0031others(10): Show | 18 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.42-1733_42-1732del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779436 | |||||
chr7:4779439
|
A | G | 1 | a0001c0001t0002g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42-1736A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779439 | ||||||
chr7:4779457
|
CAT | C | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.42-1711_42-1710del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779457 | |||||
chr7:4779479
|
T | C | 12 | a0001c0002t0017g0024a0001c0002t0027g0088a0001c0005t0009g0031others(9): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-1696T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779479 | ||||||
chr7:4779481
|
TA | T | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-1693delA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779481 | ||||||
chr7:4779482
|
A | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0001t0001g0159others(4): Show | 7 | HG00099.hp2 HG00741.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-1693A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779482 | ||||||
chr7:4779482
|
AT | A | 14 | a0001c0002t0017g0024a0001c0002t0027g0088a0001c0005t0009g0031others(11): Show | 19 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-1684delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779482 | |||||
chr7:4779484
|
T | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0099a0001c0001t0001g0108others(69): Show | 110 | HG00099.hp1 HG00597.hp1 HG01070.hp2 others(107): Show |
intron_variant | MODIFIER | c.42-1691T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779484 | ||||||
chr7:4779485
|
T | A | 2 | a0002c0003t0011g0057a0019c0017t0024g0097 | 2 | HG03139.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.42-1690T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779485 | ||||||
chr7:4779641
|
T | A | 1 | a0001c0002t0003g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.42-1534T>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779641 | ||||||
chr7:4779685
|
A | C | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-1490A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779685 | ||||||
chr7:4779713
|
T | C | 12 | a0001c0002t0017g0024a0001c0002t0027g0088a0001c0005t0009g0031others(9): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.42-1462T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779713 | ||||||
chr7:4779757
|
C | T | 9 | a0001c0002t0017g0024a0001c0005t0009g0031a0001c0005t0009g0032others(6): Show | 13 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-1418C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779757 | ||||||
chr7:4779806
|
AT | A | 15 | a0001c0002t0017g0024a0001c0005t0009g0031a0001c0005t0009g0032others(12): Show | 20 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1360delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4779806 | |||||
chr7:4779884
|
C | G | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.42-1291C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779884 | ||||||
chr7:4779894
|
C | T | 6 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(3): Show | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-1281C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4779894 | ||||||
chr7:4780005
|
A | G | 5 | a0001c0002t0015g0049a0001c0002t0015g0084a0001c0002t0032g0083others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-1170A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780005 | ||||||
chr7:4780010
|
C | T | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.42-1165C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780010 | ||||||
chr7:4780083
|
G | A | 1 | a0001c0002t0006g0094 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-1092G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780083 | ||||||
chr7:4780093
|
C | T | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.42-1082C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780093 | ||||||
chr7:4780107
|
C | T | 6 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(3): Show | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-1068C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780107 | ||||||
chr7:4780110
|
A | T | 2 | a0011c0013t0021g0030a0011c0013t0045g0030 | 2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.42-1065A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780110 | ||||||
chr7:4780129
|
A | G | 11 | a0001c0002t0017g0024a0001c0005t0009g0031a0001c0005t0009g0032others(8): Show | 16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.42-1046A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780129 | ||||||
chr7:4780236
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.42-939T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780236 | ||||||
chr7:4780285
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.42-890A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780285 | ||||||
chr7:4780358
|
G | A | 1 | a0015c0029t0020g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.42-817G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780358 | ||||||
chr7:4780411
|
A | C | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.42-764A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780411 | ||||||
chr7:4780412
|
GT | G | 57 | a0001c0001t0001g0125a0001c0001t0001g0171a0001c0001t0002g0009others(54): Show | 80 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.42-759delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4780412 | |||||
chr7:4780485
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.42-690C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780485 | ||||||
chr7:4780487
|
A | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 10 | HG00621.hp2 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-688A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780487 | ||||||
chr7:4780517
|
C | T | 1 | a0001c0001t0001g0153 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.42-658C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780517 | ||||||
chr7:4780530
|
C | G | 1 | a0019c0017t0024g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42-645C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780530 | ||||||
chr7:4780531
|
G | C | 5 | a0001c0002t0006g0011a0001c0002t0006g0094a0001c0002t0006g0095others(2): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-644G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780531 | ||||||
chr7:4780637
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.42-538G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780637 | ||||||
chr7:4780639
|
G | T | 1 | a0001c0001t0001g0153 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.42-536G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780639 | ||||||
chr7:4780652
|
T | G | 72 | a0001c0001t0001g0127a0001c0001t0002g0009a0001c0001t0006g0009others(69): Show | 106 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(103): Show |
intron_variant | MODIFIER | c.42-523T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780652 | ||||||
chr7:4780715
|
G | A | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-460G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780715 | ||||||
chr7:4780765
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG02074.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.42-410C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780765 | ||||||
chr7:4780792
|
T | C | 18 | a0001c0002t0017g0024a0001c0002t0036g0053a0001c0005t0009g0031others(15): Show | 23 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.42-383T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780792 | ||||||
chr7:4780950
|
T | C | 24 | a0001c0001t0010g0129a0001c0001t0030g0128a0002c0003t0002g0003others(21): Show | 34 | HG00597.hp1 HG00609.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.42-225T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4780950 | ||||||
chr7:4781002
|
CAGCTCAG others(21): Show |
C | 1 | a0001c0001t0001g0130 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.42-170_42-143delCT others(26): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr7 | 4781002 | |||||
chr7:4781018
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.42-157C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781018 | ||||||
chr7:4781029
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0150 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42-146C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781029 | ||||||
chr7:4781031
|
A | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0150 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.42-144A>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781031 | ||||||
chr7:4781098
|
C | T | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-77C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 1/16 | chr7 | 4781098 | ||||||
chr7:4781425
|
T | G | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+113T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781425 | ||||||
chr7:4781491
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.180-77C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781491 | ||||||
chr7:4781523
|
C | T | 1 | a0001c0001t0001g0045 | 2 | NA19002.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.180-45C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781523 | ||||||
chr7:4781540
|
C | T | 5 | a0001c0002t0006g0011a0001c0002t0006g0094a0001c0002t0006g0095others(2): Show | 7 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.180-28C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 2/16 | chr7 | 4781540 | ||||||
chr7:4781924
|
G | A | 23 | a0001c0014t0006g0096a0001c0014t0029g0093a0002c0003t0002g0003others(20): Show | 33 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.366+170G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4781924 | ||||||
chr7:4781966
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.366+212A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4781966 | ||||||
chr7:4781996
|
C | G | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+242C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4781996 | ||||||
chr7:4782013
|
G | A | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.366+259G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782013 | ||||||
chr7:4782209
|
C | T | 1 | a0001c0001t0026g0149 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.366+455C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782209 | ||||||
chr7:4782340
|
C | T | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.366+586C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782340 | ||||||
chr7:4782426
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.366+672C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782426 | ||||||
chr7:4782473
|
G | A | 1 | a0014c0028t0047g0091 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.366+719G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782473 | ||||||
chr7:4782604
|
T | G | 1 | a0001c0001t0001g0038 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.367-712T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782604 | ||||||
chr7:4782677
|
C | T | 1 | a0001c0001t0001g0044 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.367-639C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782677 | ||||||
chr7:4782706
|
G | C | 1 | a0001c0001t0001g0038 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.367-610G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782706 | ||||||
chr7:4782769
|
TCTC | T | 24 | a0001c0002t0003g0075a0001c0014t0006g0096a0001c0014t0029g0093others(21): Show | 34 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.367-543_367-541del others(3): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 4782769 | |||||
chr7:4782785
|
A | G | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367-531A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782785 | ||||||
chr7:4782827
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.367-489C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782827 | ||||||
chr7:4782829
|
C | T | 8 | a0001c0001t0049g0087a0001c0002t0044g0085a0001c0005t0009g0031others(5): Show | 9 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-487C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782829 | ||||||
chr7:4782834
|
G | A | 1 | a0015c0029t0020g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.367-482G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782834 | ||||||
chr7:4782897
|
G | A | 5 | a0001c0001t0001g0039a0001c0001t0001g0126a0001c0001t0001g0131others(2): Show | 6 | HG00735.hp1 HG01099.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-419G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782897 | ||||||
chr7:4782945
|
C | T | 12 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(9): Show | 16 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.367-371C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782945 | ||||||
chr7:4782955
|
T | C | 5 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(2): Show | 6 | HG01081.hp1 HG01496.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.367-361T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4782955 | ||||||
chr7:4783006
|
C | G | 5 | a0001c0002t0002g0007a0001c0002t0003g0007a0001c0002t0003g0073others(2): Show | 7 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.367-310C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783006 | ||||||
chr7:4783011
|
C | T | 3 | a0003c0004t0007g0101a0007c0011t0007g0028a0007c0018t0019g0054 | 4 | HG01243.hp2 HG02451.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-305C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783011 | ||||||
chr7:4783022
|
G | T | 1 | a0001c0002t0044g0085 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367-294G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783022 | ||||||
chr7:4783035
|
G | A | 1 | a0020c0019t0001g0109 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.367-281G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783035 | ||||||
chr7:4783077
|
C | T | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.367-239C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783077 | ||||||
chr7:4783096
|
C | G | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.367-220C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783096 | ||||||
chr7:4783147
|
G | C | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.367-169G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783147 | ||||||
chr7:4783256
|
T | C | 12 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(9): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.367-60T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | chr7 | 4783256 | ||||||
chr7:4783258
|
GGGGAGCT others(13): Show |
G | 2 | a0001c0002t0032g0083a0001c0002t0033g0074 | 2 | HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.367-55_367-36delGA others(18): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr7 | 4783258 | |||||
chr7:4783526
|
A | G | 2 | a0001c0014t0006g0096a0001c0014t0029g0093 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.511+66A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783526 | ||||||
chr7:4783547
|
G | T | 21 | a0002c0003t0002g0003a0002c0003t0002g0014a0002c0003t0002g0026others(18): Show | 31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.511+87G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783547 | ||||||
chr7:4783555
|
G | T | 21 | a0002c0003t0002g0003a0002c0003t0002g0014a0002c0003t0002g0026others(18): Show | 31 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.511+95G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783555 | ||||||
chr7:4783564
|
G | A | 4 | a0005c0008t0013g0092a0011c0013t0021g0030a0011c0013t0045g0030others(1): Show | 4 | HG02886.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.511+104G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783564 | ||||||
chr7:4783573
|
C | T | 1 | a0001c0001t0026g0149 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.511+113C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783573 | ||||||
chr7:4783574
|
G | A | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.511+114G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783574 | ||||||
chr7:4783578
|
G | T | 5 | a0001c0002t0015g0049a0001c0002t0015g0084a0001c0002t0032g0083others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.512-111G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783578 | ||||||
chr7:4783643
|
C | A | 1 | a0001c0014t0006g0096 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.512-46C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783643 | ||||||
chr7:4783662
|
C | G | 1 | a0001c0002t0003g0008 | 4 | HG02559.hp1 HG02717.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.512-27C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783662 | ||||||
chr7:4783682
|
A | G | 27 | a0001c0001t0035g0167a0001c0002t0002g0007a0001c0002t0003g0007others(24): Show | 44 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(41): Show |
splice_region_variant&intron_variant | LOW | c.512-7A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 4/16 | chr7 | 4783682 | ||||||
chr7:4783874
|
A | G | 1 | a0001c0001t0026g0149 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.621+76A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4783874 | ||||||
chr7:4783929
|
G | T | 1 | a0001c0002t0003g0073 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.621+131G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4783929 | ||||||
chr7:4783966
|
G | A | 9 | a0001c0001t0005g0005a0001c0001t0005g0012a0001c0001t0005g0112others(6): Show | 15 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.621+168G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4783966 | ||||||
chr7:4784034
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.622-169C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784034 | ||||||
chr7:4784092
|
G | A | 6 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(3): Show | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.622-111G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784092 | ||||||
chr7:4784099
|
T | C | 1 | a0001c0002t0036g0053 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.622-104T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784099 | ||||||
chr7:4784113
|
C | T | 1 | a0001c0001t0049g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.622-90C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784113 | ||||||
chr7:4784151
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.622-52G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 5/16 | chr7 | 4784151 | ||||||
chr7:4784394
|
G | A | 1 | a0001c0001t0005g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.790+23G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784394 | ||||||
chr7:4784400
|
CAG | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0147a0001c0002t0036g0053 | 3 | HG02109.hp2 NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.790+30_790+31delAG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784400 | ||||||
chr7:4784453
|
G | A | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.790+82G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784453 | ||||||
chr7:4784500
|
A | G | 9 | a0001c0001t0049g0087a0001c0005t0009g0032a0001c0005t0009g0089others(6): Show | 13 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.790+129A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784500 | ||||||
chr7:4784680
|
C | T | 8 | a0001c0002t0002g0007a0001c0002t0003g0007a0001c0002t0003g0073others(5): Show | 12 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-228C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784680 | ||||||
chr7:4784686
|
G | A | 5 | a0001c0002t0015g0049a0001c0002t0015g0084a0001c0002t0032g0083others(2): Show | 5 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.791-222G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784686 | ||||||
chr7:4784798
|
C | T | 13 | a0003c0004t0004g0004a0003c0004t0004g0016a0003c0004t0004g0056others(10): Show | 22 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.791-110C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784798 | ||||||
chr7:4784903
|
C | T | 2 | a0001c0002t0003g0075a0001c0002t0031g0060 | 2 | HG03579.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.791-5C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 6/16 | chr7 | 4784903 | ||||||
chr7:4785256
|
A | G | 82 | a0001c0001t0049g0087a0001c0002t0002g0007a0001c0002t0003g0007others(79): Show | 119 | HG00597.hp1 HG01070.hp2 HG01071.hp1 others(116): Show |
intron_variant | MODIFIER | c.932-159A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/16 | chr7 | 4785256 | ||||||
chr7:4785312
|
C | A | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.932-103C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/16 | chr7 | 4785312 | ||||||
chr7:4785372
|
T | C | 9 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(6): Show | 12 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-43T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 7/16 | chr7 | 4785372 | ||||||
chr7:4785486
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0002g0150 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.969+34C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785486 | ||||||
chr7:4785491
|
C | T | 1 | a0001c0001t0049g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.970-31C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785491 | ||||||
chr7:4785492
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.970-30G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785492 | ||||||
chr7:4785509
|
C | T | 18 | a0001c0002t0002g0007a0001c0002t0003g0007a0001c0002t0003g0008others(15): Show | 29 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.970-13C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 8/16 | chr7 | 4785509 | ||||||
chr7:4785698
|
G | T | 2 | a0001c0014t0006g0096a0001c0014t0029g0093 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1132+14G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785698 | ||||||
chr7:4785713
|
C | CG | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132+33dupG | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785713 | |||||
chr7:4785743
|
A | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG00621.hp2 HG00642.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1132+59A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785743 | ||||||
chr7:4785760
|
C | CT | 26 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0146others(23): Show | 42 | HG00544.hp1 HG01175.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1132+96dupT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | |||||
chr7:4785760
|
C | CTT | 9 | a0001c0002t0003g0075a0001c0002t0006g0011a0001c0002t0006g0094others(6): Show | 13 | HG02055.hp1 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1132+95_1132+96dup others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | |||||
chr7:4785760
|
CT | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0110others(13): Show | 20 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1132+96delT | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | |||||
chr7:4785760
|
CTT | C | 5 | a0005c0008t0013g0033a0005c0008t0013g0092a0006c0009t0001g0134others(2): Show | 6 | HG01891.hp2 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132+95_1132+96del others(2): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | |||||
chr7:4785760
|
CTTT | C | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132+94_1132+96del others(3): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr7 | 4785760 | |||||
chr7:4785762
|
T | G | 1 | a0019c0017t0024g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1132+78T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785762 | ||||||
chr7:4785788
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1132+104T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785788 | ||||||
chr7:4785883
|
G | T | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1132+199G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785883 | ||||||
chr7:4785943
|
G | A | 6 | a0001c0002t0015g0049a0001c0002t0015g0084a0001c0002t0027g0088others(3): Show | 6 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132+259G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785943 | ||||||
chr7:4785966
|
G | C | 2 | a0009c0010t0023g0034a0009c0010t0025g0034 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1132+282G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785966 | ||||||
chr7:4785984
|
T | C | 1 | a0001c0001t0002g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1133-266T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785984 | ||||||
chr7:4785995
|
C | T | 8 | a0001c0002t0002g0007a0001c0002t0003g0007a0001c0002t0003g0073others(5): Show | 12 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1133-255C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4785995 | ||||||
chr7:4786011
|
C | T | 3 | a0001c0006t0003g0010a0001c0006t0003g0079a0001c0006t0003g0081 | 6 | HG02717.hp2 HG02809.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1133-239C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786011 | ||||||
chr7:4786055
|
G | T | 51 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(48): Show | 75 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(72): Show |
intron_variant | MODIFIER | c.1133-195G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786055 | ||||||
chr7:4786125
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1133-125G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786125 | ||||||
chr7:4786220
|
C | T | 13 | a0002c0003t0002g0003a0002c0003t0002g0014a0002c0003t0002g0026others(10): Show | 22 | HG00597.hp1 HG02074.hp2 HG02698.hp1 others(19): Show |
intron_variant | MODIFIER | c.1133-30C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 9/16 | chr7 | 4786220 | ||||||
chr7:4786469
|
T | TA | 24 | a0001c0002t0002g0007a0001c0002t0003g0007a0001c0002t0003g0008others(21): Show | 37 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1311+43dupA | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr7 | 4786469 | |||||
chr7:4786500
|
C | T | 1 | a0003c0004t0004g0070 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1311+72C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786500 | ||||||
chr7:4786518
|
C | G | 1 | a0002c0003t0002g0066 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1311+90C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786518 | ||||||
chr7:4786547
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0130 | 3 | HG00544.hp1 NA18944.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1311+119G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786547 | ||||||
chr7:4786557
|
T | C | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+129T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786557 | ||||||
chr7:4786560
|
G | A | 9 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(6): Show | 12 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1311+132G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786560 | ||||||
chr7:4786575
|
G | A | 2 | a0002c0003t0002g0014a0002c0030t0002g0014 | 3 | NA18969.hp2 NA19066.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1311+147G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786575 | ||||||
chr7:4786592
|
C | G | 1 | a0015c0029t0020g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1311+164C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786592 | ||||||
chr7:4786615
|
G | A | 2 | a0001c0001t0016g0051a0001c0001t0016g0052 | 2 | HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1311+187G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786615 | ||||||
chr7:4786667
|
A | G | 1 | a0001c0001t0010g0020 | 3 | HG00280.hp1 HG01168.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1311+239A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786667 | ||||||
chr7:4786672
|
G | C | 2 | a0001c0014t0006g0096a0001c0014t0029g0093 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1311+244G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786672 | ||||||
chr7:4786708
|
T | C | 49 | a0001c0001t0049g0087a0001c0002t0036g0053a0001c0005t0009g0031others(46): Show | 72 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.1311+280T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786708 | ||||||
chr7:4786885
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1311+457G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786885 | ||||||
chr7:4786951
|
T | C | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1311+523T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786951 | ||||||
chr7:4786969
|
G | A | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+541G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4786969 | ||||||
chr7:4787000
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1311+572G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787000 | ||||||
chr7:4787010
|
G | T | 1 | a0001c0001t0049g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1311+582G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787010 | ||||||
chr7:4787018
|
T | C | 26 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(23): Show | 39 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.1311+590T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787018 | ||||||
chr7:4787062
|
G | T | 1 | a0010c0012t0046g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1312-572G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787062 | ||||||
chr7:4787063
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1312-571C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787063 | ||||||
chr7:4787108
|
C | T | 3 | a0001c0001t0002g0009a0001c0001t0006g0009a0001c0025t0006g0009 | 4 | HG01109.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312-526C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787108 | ||||||
chr7:4787113
|
C | T | 1 | a0001c0002t0003g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1312-521C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787113 | ||||||
chr7:4787114
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0135a0001c0001t0001g0151 | 6 | HG02132.hp2 NA18952.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-520G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787114 | ||||||
chr7:4787198
|
G | A | 2 | a0007c0011t0007g0028a0010c0012t0046g0178 | 3 | HG01243.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1312-436G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787198 | ||||||
chr7:4787228
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1312-406C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787228 | ||||||
chr7:4787248
|
C | T | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1312-386C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787248 | ||||||
chr7:4787253
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1312-381G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787253 | ||||||
chr7:4787315
|
A | C | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312-319A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787315 | ||||||
chr7:4787336
|
A | C | 18 | a0001c0002t0015g0049a0001c0002t0015g0084a0001c0002t0032g0083others(15): Show | 27 | HG01243.hp2 HG02109.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1312-298A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787336 | ||||||
chr7:4787347
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0034g0173 | 2 | NA18960.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1312-287A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787347 | ||||||
chr7:4787429
|
T | G | 19 | a0001c0002t0017g0024a0003c0004t0004g0004a0003c0004t0004g0016others(16): Show | 30 | HG01175.hp1 HG01243.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.1312-205T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787429 | ||||||
chr7:4787450
|
C | T | 1 | a0001c0001t0008g0041 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1312-184C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787450 | ||||||
chr7:4787457
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1312-177G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787457 | ||||||
chr7:4787465
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0005g0012a0001c0001t0005g0116others(6): Show | 11 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1312-169G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787465 | ||||||
chr7:4787529
|
G | C | 17 | a0001c0002t0017g0024a0003c0004t0004g0004a0003c0004t0004g0016others(14): Show | 27 | HG01175.hp1 HG01243.hp2 HG01515.hp1 others(24): Show |
intron_variant | MODIFIER | c.1312-105G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787529 | ||||||
chr7:4787542
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1312-92C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787542 | ||||||
chr7:4787574
|
C | T | 3 | a0001c0002t0003g0076a0003c0004t0007g0017a0003c0004t0007g0077 | 5 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-60C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787574 | ||||||
chr7:4787614
|
C | T | 4 | a0001c0014t0006g0096a0001c0014t0029g0093a0005c0008t0013g0033others(1): Show | 5 | HG01891.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-20C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 10/16 | chr7 | 4787614 | ||||||
chr7:4787849
|
T | C | 32 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(29): Show | 46 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.1454+73T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4787849 | ||||||
chr7:4787867
|
C | T | 2 | a0001c0014t0006g0096a0001c0014t0029g0093 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1454+91C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4787867 | ||||||
chr7:4788006
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0176others(1): Show | 4 | HG00741.hp1 HG01070.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-148G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788006 | ||||||
chr7:4788015
|
T | G | 3 | a0001c0002t0003g0076a0003c0004t0007g0017a0003c0004t0007g0077 | 5 | HG01070.hp2 HG01071.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455-139T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788015 | ||||||
chr7:4788065
|
A | C | 12 | a0001c0002t0003g0029a0001c0002t0003g0078a0001c0002t0003g0080others(9): Show | 18 | HG02055.hp1 HG02280.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.1455-89A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788065 | ||||||
chr7:4788077
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1455-77C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788077 | ||||||
chr7:4788117
|
C | T | 4 | a0001c0021t0001g0142a0011c0013t0021g0030a0011c0013t0045g0030others(1): Show | 4 | HG02922.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455-37C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788117 | ||||||
chr7:4788118
|
G | A | 1 | a0004c0007t0012g0015 | 3 | HG01074.hp2 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1455-36G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 11/16 | chr7 | 4788118 | ||||||
chr7:4788323
|
C | A | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+29C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788323 | ||||||
chr7:4788341
|
G | A | 20 | a0002c0003t0002g0003a0002c0003t0002g0014a0002c0003t0002g0026others(17): Show | 30 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1595+47G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788341 | ||||||
chr7:4788365
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1595+71C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788365 | ||||||
chr7:4788397
|
T | G | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1595+103T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788397 | ||||||
chr7:4788446
|
C | T | 35 | a0001c0002t0017g0024a0002c0003t0002g0003a0002c0003t0002g0014others(32): Show | 55 | HG00597.hp1 HG01074.hp1 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.1595+152C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788446 | ||||||
chr7:4788470
|
G | A | 2 | a0009c0010t0023g0034a0009c0010t0025g0034 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1595+176G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788470 | ||||||
chr7:4788505
|
C | T | 1 | a0001c0001t0001g0039 | 2 | HG00735.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1595+211C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788505 | ||||||
chr7:4788528
|
A | G | 28 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(25): Show | 42 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1595+234A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788528 | ||||||
chr7:4788532
|
T | C | 46 | a0001c0001t0002g0123a0001c0001t0049g0087a0001c0002t0002g0007others(43): Show | 73 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.1595+238T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788532 | ||||||
chr7:4788535
|
C | T | 19 | a0001c0001t0002g0123a0001c0002t0002g0007a0001c0002t0003g0007others(16): Show | 30 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1595+241C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788535 | ||||||
chr7:4788598
|
G | A | 1 | a0010c0012t0046g0178 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1596-242G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788598 | ||||||
chr7:4788641
|
T | C | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1596-199T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788641 | ||||||
chr7:4788763
|
G | A | 1 | a0001c0014t0029g0093 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1596-77G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788763 | ||||||
chr7:4788765
|
A | G | 1 | a0003c0004t0004g0069 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1596-75A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788765 | ||||||
chr7:4788774
|
G | A | 28 | a0001c0002t0006g0011a0001c0002t0006g0094a0001c0002t0006g0095others(25): Show | 40 | HG00597.hp1 HG01074.hp1 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.1596-66G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788774 | ||||||
chr7:4788780
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1596-60C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788780 | ||||||
chr7:4788781
|
C | T | 2 | a0001c0014t0006g0096a0001c0014t0029g0093 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1596-59C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788781 | ||||||
chr7:4788808
|
G | A | 2 | a0009c0010t0023g0034a0009c0010t0025g0034 | 2 | NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1596-32G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 12/16 | chr7 | 4788808 | ||||||
chr7:4788959
|
C | T | 1 | a0008c0034t0001g0158 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.1707+8C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4788959 | ||||||
chr7:4788962
|
T | C | 53 | a0001c0001t0002g0009a0001c0001t0006g0009a0001c0002t0006g0011others(50): Show | 79 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(76): Show |
intron_variant | MODIFIER | c.1707+11T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4788962 | ||||||
chr7:4788997
|
T | C | 58 | a0001c0001t0049g0087a0001c0002t0006g0011a0001c0002t0006g0094others(55): Show | 84 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(81): Show |
intron_variant | MODIFIER | c.1707+46T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4788997 | ||||||
chr7:4789076
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1707+125G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789076 | ||||||
chr7:4789097
|
G | C | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1707+146G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789097 | ||||||
chr7:4789125
|
G | A | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1707+174G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789125 | ||||||
chr7:4789161
|
G | A | 9 | a0003c0004t0004g0004a0003c0004t0004g0016a0003c0004t0004g0056others(6): Show | 18 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1707+210G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789161 | ||||||
chr7:4789169
|
GTCCCCGT others(36): Show |
G | 1 | a0004c0007t0012g0015 | 3 | HG01074.hp2 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1707+249_1707+291d others(45): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 4789169 | |||||
chr7:4789183
|
C | T | 2 | a0001c0002t0015g0049a0001c0002t0044g0085 | 2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1707+232C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789183 | ||||||
chr7:4789188
|
C | T | 1 | a0004c0007t0012g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+237C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789188 | ||||||
chr7:4789189
|
A | G | 4 | a0001c0002t0015g0049a0001c0002t0032g0083a0001c0002t0033g0074others(1): Show | 4 | HG02109.hp1 HG02647.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1707+238A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789189 | ||||||
chr7:4789191
|
C | T | 1 | a0004c0007t0012g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+240C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789191 | ||||||
chr7:4789194
|
G | A | 1 | a0004c0007t0012g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+243G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789194 | ||||||
chr7:4789202
|
A | C | 1 | a0004c0007t0012g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+251A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789202 | ||||||
chr7:4789206
|
C | T | 1 | a0004c0007t0012g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+255C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789206 | ||||||
chr7:4789212
|
A | G | 1 | a0004c0007t0012g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1707+261A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789212 | ||||||
chr7:4789265
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1707+314C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789265 | ||||||
chr7:4789297
|
C | G | 16 | a0003c0004t0004g0004a0003c0004t0004g0016a0003c0004t0004g0056others(13): Show | 25 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1707+346C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789297 | ||||||
chr7:4789320
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1707+369A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789320 | ||||||
chr7:4789350
|
G | T | 10 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(7): Show | 13 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1707+399G>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789350 | ||||||
chr7:4789369
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1707+418C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789369 | ||||||
chr7:4789396
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1708-436C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789396 | ||||||
chr7:4789432
|
G | GCCCCCCA others(18): Show |
1 | a0001c0001t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1708-396_1708-372d others(27): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr7 | 4789432 | |||||
chr7:4789488
|
A | G | 10 | a0003c0004t0004g0004a0003c0004t0004g0016a0003c0004t0004g0056others(7): Show | 19 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1708-344A>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789488 | ||||||
chr7:4789541
|
C | T | 1 | a0001c0002t0017g0024 | 2 | HG01175.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1708-291C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789541 | ||||||
chr7:4789545
|
C | G | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1708-287C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789545 | ||||||
chr7:4789582
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1708-250G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789582 | ||||||
chr7:4789585
|
A | C | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1708-247A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789585 | ||||||
chr7:4789661
|
G | A | 10 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(7): Show | 13 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1708-171G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789661 | ||||||
chr7:4789730
|
C | T | 15 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0037others(12): Show | 28 | HG00438.hp2 HG02129.hp2 NA18747.hp1 others(25): Show |
intron_variant | MODIFIER | c.1708-102C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789730 | ||||||
chr7:4789733
|
C | T | 3 | a0009c0010t0023g0034a0009c0010t0025g0034a0019c0017t0024g0097 | 3 | HG03139.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1708-99C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789733 | ||||||
chr7:4789740
|
C | G | 28 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(25): Show | 42 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1708-92C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789740 | ||||||
chr7:4789818
|
C | T | 3 | a0002c0003t0002g0027a0002c0003t0002g0064a0002c0003t0002g0065 | 4 | HG03491.hp2 HG03492.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1708-14C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789818 | ||||||
chr7:4789827
|
C | T | 1 | a0002c0003t0002g0065 | 1 | HG04115.hp2 | splice_region_variant&intron_variant | LOW | c.1708-5C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 13/16 | chr7 | 4789827 | ||||||
chr7:4789969
|
T | G | 1 | a0019c0017t0024g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1805+40T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4789969 | ||||||
chr7:4789981
|
TCCTCCCC others(6): Show |
T | 1 | a0001c0001t0002g0105 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1805+61_1805+73del others(13): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789981 | |||||
chr7:4789984
|
TCCCCCTC others(7): Show |
T | 1 | a0007c0018t0019g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1805+63_1805+76del others(14): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789984 | |||||
chr7:4789985
|
CCCCCTCT | C | 4 | a0003c0004t0007g0101a0011c0013t0021g0030a0011c0013t0045g0030others(1): Show | 4 | HG02922.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1805+63_1805+69del others(7): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789985 | |||||
chr7:4789990
|
TCTCCCCT others(5): Show |
T | 10 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(7): Show | 13 | HG01081.hp1 HG01175.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1805+69_1805+80del others(12): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4789990 | |||||
chr7:4789992
|
T | C | 11 | a0003c0004t0004g0004a0003c0004t0004g0016a0003c0004t0004g0056others(8): Show | 20 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1805+63T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4789992 | ||||||
chr7:4790002
|
C | G | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1805+73C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790002 | ||||||
chr7:4790044
|
C | A | 3 | a0011c0013t0021g0030a0011c0013t0045g0030a0015c0029t0020g0082 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1805+115C>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790044 | ||||||
chr7:4790054
|
A | C | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1805+125A>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790054 | ||||||
chr7:4790070
|
ACCCACAG others(1): Show |
A | 20 | a0001c0001t0002g0123a0001c0002t0002g0007a0001c0002t0003g0007others(17): Show | 31 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1805+148_1805+155d others(10): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790070 | |||||
chr7:4790077
|
G | C | 1 | a0001c0001t0002g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1805+148G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790077 | ||||||
chr7:4790100
|
TTCTC | T | 13 | a0003c0004t0004g0004a0003c0004t0004g0016a0003c0004t0004g0056others(10): Show | 22 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1805+175_1805+178d others(6): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790100 | |||||
chr7:4790110
|
T | C | 56 | a0001c0001t0049g0087a0001c0002t0006g0011a0001c0002t0006g0094others(53): Show | 82 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(79): Show |
intron_variant | MODIFIER | c.1805+181T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790110 | ||||||
chr7:4790126
|
C | CCT | 63 | a0001c0001t0049g0087a0001c0002t0006g0011a0001c0002t0006g0094others(60): Show | 89 | HG00597.hp1 HG01074.hp1 HG01074.hp2 others(86): Show |
intron_variant | MODIFIER | c.1805+197_1805+198i others(4): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790126 | ||||||
chr7:4790132
|
T | C | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1805+203T>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790132 | ||||||
chr7:4790141
|
C | T | 3 | a0001c0002t0018g0071a0001c0002t0018g0072a0001c0002t0031g0060 | 3 | HG02896.hp2 HG02897.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1805+212C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790141 | ||||||
chr7:4790150
|
C | CCTCTTCA others(7): Show |
1 | a0001c0014t0006g0096 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1805+225_1805+238d others(16): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790150 | |||||
chr7:4790185
|
C | T | 1 | a0019c0017t0024g0097 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1805+256C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790185 | ||||||
chr7:4790198
|
G | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0050a0001c0001t0001g0164 | 4 | HG01433.hp2 HG01952.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1806-261G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790198 | ||||||
chr7:4790252
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1806-207C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790252 | ||||||
chr7:4790292
|
G | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0137a0012c0016t0001g0136 | 3 | HG02602.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1806-167G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790292 | ||||||
chr7:4790307
|
C | G | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1806-152C>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790307 | ||||||
chr7:4790324
|
C | T | 12 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(9): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1806-135C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790324 | ||||||
chr7:4790338
|
C | T | 6 | a0001c0005t0009g0031a0001c0005t0009g0032a0001c0005t0009g0089others(3): Show | 7 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1806-121C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790338 | ||||||
chr7:4790354
|
C | CACCTACC others(3): Show |
2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806-104_1806-95du others(11): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr7 | 4790354 | |||||
chr7:4790417
|
T | G | 12 | a0001c0001t0049g0087a0001c0002t0017g0024a0001c0005t0009g0031others(9): Show | 17 | HG01074.hp2 HG01081.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1806-42T>G | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790417 | ||||||
chr7:4790424
|
G | A | 1 | a0001c0002t0006g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1806-35G>A | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790424 | ||||||
chr7:4790447
|
C | T | 7 | a0001c0001t0049g0087a0001c0005t0009g0031a0001c0005t0009g0032others(4): Show | 8 | HG01081.hp1 HG01496.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1806-12C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 14/16 | chr7 | 4790447 | ||||||
chr7:4790602
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1938+11C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 15/16 | chr7 | 4790602 | ||||||
chr7:4790664
|
C | T | 12 | a0001c0002t0003g0008a0001c0002t0003g0029a0001c0002t0003g0075others(9): Show | 20 | HG01891.hp2 HG02559.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.1939-9C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 15/16 | chr7 | 4790664 | ||||||
chr7:4790932
|
G | C | 1 | a0001c0005t0009g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2153+45G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4790932 | ||||||
chr7:4791032
|
C | T | 2 | a0001c0002t0018g0071a0001c0002t0018g0072 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2154-83C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791032 | ||||||
chr7:4791045
|
G | C | 2 | a0005c0008t0013g0033a0005c0008t0013g0092 | 3 | HG01891.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2154-70G>C | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791045 | ||||||
chr7:4791047
|
C | T | 1 | a0001c0001t0002g0123 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2154-68C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791047 | ||||||
chr7:4791063
|
C | T | 2 | a0004c0007t0012g0015a0004c0007t0012g0067 | 4 | HG01074.hp2 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2154-52C>T | AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | chr7 | 4791063 | ||||||
chr7:4791074
|
G | GGGGAGCA others(15): Show |
1 | a0001c0005t0009g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2154-36_2154-15dup others(22): Show |
AP5Z1 | ENSG00000242802.9 | transcript | ENST00000649063.2 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr7 | 4791074 |