geneid | 8943 |
---|---|
ensemblid | ENSG00000065000.20 |
hgncid | 568 |
symbol | AP3D1 |
name | adaptor related protein complex 3 subunit delta 1 |
refseq_nuc | NM_001261826.3 |
refseq_prot | NP_001248755.1 |
ensembl_nuc | ENST00000643116.3 |
ensembl_prot | ENSP00000495274.2 |
mane_status | MANE Select |
chr | chr19 |
start | 2100988 |
end | 2151566 |
strand | - |
ver | v1.2 |
region | chr19:2100988-2151566 |
region5000 | chr19:2095988-2156566 |
regionname0 | AP3D1_chr19_2100988_2151566 |
regionname5000 | AP3D1_chr19_2095988_2156566 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1215 | 387 | 91 | 68 | 174 | 16 | 36 | 128 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0002 | 0/0 | 1215 | 15 | 6 | 1 | 0 | 2 | 6 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0003 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0004 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0005 | 0/0 | 1215 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0006 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3648 | 182 | 49 | 30 | 77 | 4 | 21 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0002 | 0/1 | 3648 | 68 | 1 | 22 | 28 | 7 | 9 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0003 | 0/0 | 3648 | 53 | 25 | 0 | 23 | 2 | 3 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0004 | 0/0 | 3648 | 37 | 1 | 6 | 24 | 3 | 3 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0005 | 0/0 | 3648 | 14 | 0 | 6 | 8 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0006 | 0/0 | 3648 | 11 | 1 | 0 | 10 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0007 | 0/0 | 3648 | 10 | 1 | 1 | 0 | 2 | 6 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0008 | 0/0 | 3648 | 6 | 6 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0009 | 0/0 | 3648 | 5 | 5 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0010 | 0/0 | 3648 | 4 | 1 | 3 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0011 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0012 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0013 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0014 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0015 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0016 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0017 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0018 | 0/0 | 3648 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0019 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0020 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0021 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0022 | 0/0 | 3648 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0023 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
c0024 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1418 | 204 | 36 | 50 | 80 | 11 | 25 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0002 | 0/0 | 1428 | 131 | 46 | 13 | 63 | 5 | 4 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0003 | 0/0 | 1418 | 37 | 0 | 4 | 28 | 0 | 5 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0004 | 0/0 | 1428 | 10 | 1 | 1 | 0 | 2 | 6 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0005 | 0/0 | 1428 | 7 | 7 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0006 | 0/0 | 1418 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0007 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0008 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0009 | 0/0 | 1428 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0010 | 0/0 | 1418 | 2 | 1 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0011 | 0/0 | 1428 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0012 | 0/0 | 1418 | 2 | 0 | 2 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0013 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0014 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
t0015 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0392 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0393 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3648 | 182 | 49 | 30 | 77 | 4 | 21 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0002 | 0/1 | 3648 | 68 | 1 | 22 | 28 | 7 | 9 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0003 | 0/0 | 3648 | 53 | 25 | 0 | 23 | 2 | 3 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0004 | 0/0 | 3648 | 37 | 1 | 6 | 24 | 3 | 3 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0005 | 0/0 | 3648 | 14 | 0 | 6 | 8 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0006 | 0/0 | 3648 | 11 | 1 | 0 | 10 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0008 | 0/0 | 3648 | 6 | 6 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0010 | 0/0 | 3648 | 4 | 1 | 3 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0011 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0012 | 0/0 | 3648 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0014 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0015 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0016 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0017 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0020 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0021 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0022 | 0/0 | 3648 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0023 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0002c0007 | 0/0 | 3648 | 10 | 1 | 1 | 0 | 2 | 6 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0002c0009 | 0/0 | 3648 | 5 | 5 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0003c0024 | 0/0 | 3648 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0004c0013 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0005c0018 | 0/0 | 3648 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0006c0019 | 0/0 | 3648 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5065 | 128 | 32 | 25 | 51 | 4 | 15 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0001t0002 | 0/0 | 5075 | 15 | 14 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0001t0003 | 0/0 | 5065 | 35 | 0 | 4 | 26 | 0 | 5 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0001t0006 | 0/0 | 5065 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0001t0010 | 0/0 | 5065 | 2 | 1 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0002t0001 | 0/1 | 5065 | 66 | 1 | 20 | 28 | 7 | 9 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0002t0012 | 0/0 | 5065 | 2 | 0 | 2 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0003t0001 | 0/0 | 5065 | 2 | 1 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0003t0002 | 0/0 | 5075 | 45 | 20 | 0 | 21 | 2 | 2 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0003t0005 | 0/0 | 5075 | 4 | 4 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0003t0009 | 0/0 | 5075 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0004t0002 | 0/0 | 5075 | 36 | 1 | 6 | 24 | 3 | 2 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0004t0014 | 0/0 | 5075 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0005t0002 | 0/0 | 5075 | 14 | 0 | 6 | 8 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0006t0002 | 0/0 | 5075 | 8 | 1 | 0 | 7 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0006t0008 | 0/0 | 5075 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0006t0015 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0008t0002 | 0/0 | 5075 | 4 | 4 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0008t0011 | 0/0 | 5075 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0010t0001 | 0/0 | 5065 | 4 | 1 | 3 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0011t0005 | 0/0 | 5075 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0012t0007 | 0/0 | 5075 | 2 | 2 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0014t0013 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0015t0003 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0016t0002 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0017t0003 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0020t0002 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0021t0001 | 0/0 | 5065 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0022t0001 | 0/0 | 5065 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0001c0023t0005 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0002c0007t0004 | 0/0 | 5075 | 10 | 1 | 1 | 0 | 2 | 6 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0002c0009t0002 | 0/0 | 5075 | 5 | 5 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0003c0024t0001 | 0/0 | 5065 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0004c0013t0002 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0005c0018t0001 | 0/0 | 5065 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
a0006c0019t0002 | 0/0 | 5075 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | copy fasta | chr19 | 2095988 | 2156566 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0003g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0010g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0001t0010g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0002t0012g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0009g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0003t0009g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0004t0014g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0005t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0008g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0008g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0006t0015g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0008t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0008t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0008t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0008t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0008t0011g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0008t0011g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0010t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0010t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0010t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0010t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0011t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0011t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0012t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0012t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0014t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0015t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0016t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0017t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0020t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0021t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0022t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0001c0023t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0392 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0393 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0007t0004g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0009t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0009t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0009t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0009t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0002c0009t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0003c0024t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0004c0013t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0005c0018t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
a0006c0019t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0279 | EUR | GBR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0294 | EUR | GBR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0297 | EUR | GBR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | GBR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00280 | hp1 | a0001 | c0004 | t0002 | g0214 | EUR | FIN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00323 | hp1 | a0001 | c0004 | t0002 | g0233 | EUR | FIN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0250 | EUR | FIN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00408 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0377 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00438 | hp1 | a0001 | c0006 | t0015 | g0384 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00558 | hp2 | a0001 | c0004 | t0002 | g0241 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00597 | hp2 | a0001 | c0005 | t0002 | g0023 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0369 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0375 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00639 | hp1 | a0001 | c0010 | t0001 | g0286 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00639 | hp2 | a0001 | c0004 | t0002 | g0213 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00642 | hp1 | a0001 | c0005 | t0002 | g0019 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00673 | hp1 | a0001 | c0004 | t0002 | g0051 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00733 | hp1 | a0001 | c0010 | t0001 | g0299 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00735 | hp1 | a0002 | c0007 | t0004 | g0387 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0339 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01070 | hp2 | a0001 | c0005 | t0002 | g0029 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0340 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0287 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0288 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01167 | hp2 | a0001 | c0002 | t0012 | g0006 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01168 | hp2 | a0001 | c0010 | t0001 | g0293 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01169 | hp2 | a0001 | c0002 | t0012 | g0006 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0254 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0270 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0298 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0353 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0301 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01346 | hp2 | a0001 | c0022 | t0001 | g0082 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01433 | hp1 | a0001 | c0004 | t0002 | g0238 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0262 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01515 | hp2 | a0002 | c0007 | t0004 | g0393 | EUR | IBS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0295 | EUR | IBS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0190 | EUR | IBS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01517 | hp1 | a0002 | c0007 | t0004 | g0392 | EUR | IBS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0189 | EUR | IBS | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0186 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01891 | hp1 | a0001 | c0016 | t0002 | g0097 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01928 | hp2 | a0001 | c0005 | t0002 | g0047 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01952 | hp2 | a0001 | c0005 | t0002 | g0025 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0359 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01993 | hp1 | a0001 | c0005 | t0002 | g0040 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0357 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0373 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02040 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02055 | hp2 | a0001 | c0010 | t0001 | g0266 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0379 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02074 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02080 | hp1 | a0001 | c0006 | t0002 | g0317 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0382 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02083 | hp2 | a0001 | c0003 | t0002 | g0034 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0358 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0380 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02132 | hp1 | a0001 | c0021 | t0001 | g0165 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0351 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02145 | hp1 | a0001 | c0003 | t0002 | g0199 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02145 | hp2 | a0001 | c0008 | t0011 | g0399 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02148 | hp1 | a0001 | c0004 | t0002 | g0218 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | CDX | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02257 | hp2 | a0001 | c0006 | t0002 | g0009 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02258 | hp1 | a0002 | c0009 | t0002 | g0265 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02273 | hp1 | a0005 | c0018 | t0001 | g0100 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0362 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0196 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0326 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02293 | hp2 | a0001 | c0004 | t0002 | g0226 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02300 | hp1 | a0001 | c0005 | t0002 | g0033 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0370 | EAS | KHV | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02572 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02602 | hp1 | a0001 | c0004 | t0014 | g0237 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0289 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02622 | hp1 | a0001 | c0003 | t0002 | g0208 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02683 | hp1 | a0001 | c0003 | t0002 | g0026 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0267 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0303 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0219 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02717 | hp2 | a0003 | c0024 | t0001 | g0283 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02735 | hp1 | a0001 | c0003 | t0002 | g0027 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02735 | hp2 | a0002 | c0007 | t0004 | g0386 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0264 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0073 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0191 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02896 | hp1 | a0001 | c0008 | t0002 | g0184 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02897 | hp1 | a0001 | c0008 | t0002 | g0185 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02922 | hp1 | a0002 | c0009 | t0002 | g0277 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02922 | hp2 | a0001 | c0008 | t0002 | g0253 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02965 | hp1 | a0001 | c0011 | t0005 | g0210 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02970 | hp1 | a0001 | c0003 | t0002 | g0203 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02970 | hp2 | a0001 | c0012 | t0007 | g0182 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02976 | hp1 | a0001 | c0003 | t0002 | g0325 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0356 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0341 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03139 | hp1 | a0001 | c0003 | t0005 | g0207 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03139 | hp2 | a0001 | c0003 | t0005 | g0212 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03195 | hp1 | a0001 | c0003 | t0002 | g0192 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0198 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0201 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03225 | hp1 | a0001 | c0004 | t0002 | g0206 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0397 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03239 | hp1 | a0002 | c0007 | t0004 | g0389 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03453 | hp1 | a0001 | c0003 | t0002 | g0188 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03486 | hp1 | a0001 | c0003 | t0005 | g0211 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0355 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03491 | hp2 | a0002 | c0007 | t0004 | g0394 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0360 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03492 | hp2 | a0002 | c0007 | t0004 | g0390 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03516 | hp2 | a0001 | c0003 | t0002 | g0327 | AFR | ESN | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03579 | hp1 | a0001 | c0023 | t0005 | g0059 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03579 | hp2 | a0001 | c0003 | t0002 | g0195 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03654 | hp1 | a0002 | c0007 | t0004 | g0395 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0304 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0371 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0364 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03710 | hp2 | a0002 | c0007 | t0004 | g0391 | SAS | PJL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03942 | hp2 | a0001 | c0001 | t0010 | g0396 | SAS | BEB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | BEB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0259 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0342 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04204 | hp1 | a0001 | c0004 | t0002 | g0217 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0290 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | STU | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18522 | hp2 | a0001 | c0003 | t0002 | g0200 | AFR | YRI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0367 | EAS | CHB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0385 | EAS | CHB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18747 | hp2 | a0001 | c0003 | t0002 | g0048 | EAS | CHB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18940 | hp1 | a0001 | c0003 | t0002 | g0344 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18946 | hp2 | a0001 | c0015 | t0003 | g0363 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0315 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18947 | hp2 | a0001 | c0006 | t0002 | g0308 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18950 | hp1 | a0001 | c0004 | t0002 | g0225 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18950 | hp2 | a0001 | c0006 | t0002 | g0311 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18951 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18951 | hp2 | a0001 | c0006 | t0008 | g0319 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0376 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18957 | hp1 | a0001 | c0003 | t0002 | g0054 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18962 | hp1 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0372 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18965 | hp2 | a0001 | c0004 | t0002 | g0045 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0338 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18966 | hp2 | a0001 | c0004 | t0002 | g0240 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18967 | hp2 | a0001 | c0004 | t0002 | g0246 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18969 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18970 | hp2 | a0001 | c0020 | t0002 | g0232 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18971 | hp1 | a0001 | c0004 | t0002 | g0228 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18973 | hp1 | a0001 | c0004 | t0002 | g0230 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18975 | hp1 | a0001 | c0005 | t0002 | g0044 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18977 | hp1 | a0001 | c0005 | t0002 | g0021 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18977 | hp2 | a0001 | c0004 | t0002 | g0248 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18978 | hp1 | a0001 | c0006 | t0002 | g0312 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0378 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18980 | hp1 | a0001 | c0003 | t0002 | g0042 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18981 | hp1 | a0001 | c0004 | t0002 | g0247 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0383 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18984 | hp2 | a0001 | c0004 | t0002 | g0224 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0374 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18985 | hp2 | a0001 | c0005 | t0002 | g0022 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18989 | hp1 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18990 | hp1 | a0001 | c0006 | t0002 | g0314 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0381 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18992 | hp1 | a0001 | c0004 | t0002 | g0221 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18994 | hp1 | a0001 | c0005 | t0002 | g0039 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18994 | hp2 | a0004 | c0013 | t0002 | g0245 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18995 | hp1 | a0001 | c0004 | t0002 | g0244 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18995 | hp2 | a0001 | c0003 | t0002 | g0343 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18998 | hp2 | a0001 | c0004 | t0002 | g0239 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19002 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19003 | hp1 | a0001 | c0004 | t0002 | g0227 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19005 | hp2 | a0001 | c0003 | t0009 | g0349 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0030 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19010 | hp1 | a0001 | c0003 | t0002 | g0041 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19010 | hp2 | a0001 | c0004 | t0002 | g0231 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19011 | hp1 | a0001 | c0004 | t0002 | g0242 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19012 | hp1 | a0001 | c0006 | t0002 | g0330 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19030 | hp1 | a0001 | c0008 | t0011 | g0398 | AFR | LWK | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19043 | hp1 | a0002 | c0009 | t0002 | g0278 | AFR | LWK | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19055 | hp1 | a0001 | c0005 | t0002 | g0035 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19056 | hp2 | a0001 | c0006 | t0002 | g0260 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19057 | hp2 | a0001 | c0004 | t0002 | g0222 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19060 | hp1 | a0006 | c0019 | t0002 | g0038 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19062 | hp2 | a0001 | c0006 | t0008 | g0256 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19063 | hp1 | a0001 | c0004 | t0002 | g0236 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19063 | hp2 | a0001 | c0017 | t0003 | g0366 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19065 | hp1 | a0001 | c0003 | t0009 | g0348 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19068 | hp1 | a0001 | c0003 | t0002 | g0249 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19068 | hp2 | a0001 | c0005 | t0002 | g0018 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19074 | hp2 | a0001 | c0003 | t0002 | g0031 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19079 | hp1 | a0001 | c0004 | t0002 | g0147 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19079 | hp2 | a0001 | c0004 | t0002 | g0234 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19081 | hp1 | a0001 | c0004 | t0002 | g0220 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19085 | hp2 | a0001 | c0004 | t0002 | g0223 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19087 | hp1 | a0001 | c0004 | t0002 | g0229 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19088 | hp2 | a0001 | c0003 | t0002 | g0032 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19240 | hp1 | a0001 | c0012 | t0007 | g0183 | AFR | YRI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA19240 | hp2 | a0001 | c0003 | t0002 | g0194 | AFR | YRI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20129 | hp1 | a0001 | c0003 | t0002 | g0079 | AFR | ASW | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20129 | hp2 | a0001 | c0014 | t0013 | g0007 | AFR | ASW | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0296 | EUR | TSI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20805 | hp1 | a0001 | c0004 | t0002 | g0215 | EUR | TSI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | TSI | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0071 | SAS | GIH | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01123 | hp1 | a0001 | c0004 | t0002 | g0235 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG01123 | hp2 | a0001 | c0004 | t0002 | g0216 | AMR | CLM | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02486 | hp2 | a0002 | c0009 | t0002 | g0292 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02559 | hp1 | a0001 | c0003 | t0005 | g0114 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG02559 | hp2 | a0001 | c0008 | t0002 | g0181 | AFR | ACB | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03471 | hp1 | a0002 | c0009 | t0002 | g0276 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG06807 | hp1 | a0001 | c0011 | t0005 | g0209 | AFR | USA | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18955 | hp1 | a0001 | c0005 | t0002 | g0020 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20300 | hp1 | a0001 | c0003 | t0002 | g0329 | AFR | USA | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | USA | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0197 | AFR | LWK | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
NA21309 | hp2 | a0002 | c0007 | t0004 | g0388 | AFR | LWK | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0251 | REF | REF | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0129 | REF | REF | AP3D1_chr19_2095988_2156566 | AP3D1 | chr19 | 2095988 | 2156566 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2109158
|
T | C | 1 | a0002 | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
missense_variant | MODERATE | c.3400A>G | p.Ile1134Val | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 30/32 | 3632/5065 | 3400/3648 | 1134/1215 | chr19 | 2109158 | ||
chr19:2110773
|
T | C | 1 | a0005 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.3109A>G | p.Arg1037Gly | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/32 | 3341/5065 | 3109/3648 | 1037/1215 | chr19 | 2110773 | ||
chr19:2115322
|
T | C | 1 | a0006 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.2246A>G | p.Lys749Arg | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/32 | 2478/5065 | 2246/3648 | 749/1215 | chr19 | 2115322 | ||
chr19:2116623
|
G | C | 1 | a0006 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1983C>G | p.Asp661Glu | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/32 | 2215/5065 | 1983/3648 | 661/1215 | chr19 | 2116623 | ||
chr19:2118611
|
A | G | 1 | a0004 | 1 | NA18994.hp2 | missense_variant | MODERATE | c.1703T>C | p.Val568Ala | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/32 | 1935/5065 | 1703/3648 | 568/1215 | chr19 | 2118611 | ||
chr19:2118693
|
C | T | 1 | a0002 | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
missense_variant | MODERATE | c.1621G>A | p.Gly541Arg | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/32 | 1853/5065 | 1621/3648 | 541/1215 | chr19 | 2118693 | ||
chr19:2118738
|
C | T | 1 | a0003 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1576G>A | p.Val526Met | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/32 | 1808/5065 | 1576/3648 | 526/1215 | chr19 | 2118738 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2102206
|
T | C | 1 | a0001c0016 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.3615A>G | p.Leu1205Leu | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 3847/5065 | 3615/3648 | 1205/1215 | chr19 | 2102206 | ||
chr19:2102242
|
C | A | 1 | a0001c0017 | 1 | NA19063.hp2 | synonymous_variant | LOW | c.3579G>T | p.Gly1193Gly | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 3811/5065 | 3579/3648 | 1193/1215 | chr19 | 2102242 | ||
chr19:2108753
|
C | T | 1 | a0001c0014 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3486G>A | p.Val1162Val | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/32 | 3718/5065 | 3486/3648 | 1162/1215 | chr19 | 2108753 | ||
chr19:2110747
|
G | A | 13 | a0001c0003a0001c0004a0001c0005others(10): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
synonymous_variant | LOW | c.3135C>T | p.Ser1045Ser | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/32 | 3367/5065 | 3135/3648 | 1045/1215 | chr19 | 2110747 | ||
chr19:2110759
|
C | T | 1 | a0001c0015 | 1 | NA18946.hp2 | synonymous_variant | LOW | c.3123G>A | p.Pro1041Pro | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/32 | 3355/5065 | 3123/3648 | 1041/1215 | chr19 | 2110759 | ||
chr19:2113348
|
G | A | 1 | a0001c0010 | 4 | HG00639.hp1 HG00733.hp1 HG01168.hp2 others(1): Show |
synonymous_variant | LOW | c.2667C>T | p.Pro889Pro | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/32 | 2899/5065 | 2667/3648 | 889/1215 | chr19 | 2113348 | ||
chr19:2114176
|
T | C | 2 | a0002c0007a0002c0009 | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
synonymous_variant | LOW | c.2550A>G | p.Lys850Lys | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/32 | 2782/5065 | 2550/3648 | 850/1215 | chr19 | 2114176 | ||
chr19:2115384
|
C | T | 1 | a0001c0005 | 14 | HG00597.hp2 HG00642.hp1 HG01070.hp2 others(11): Show |
synonymous_variant | LOW | c.2184G>A | p.Glu728Glu | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/32 | 2416/5065 | 2184/3648 | 728/1215 | chr19 | 2115384 | ||
chr19:2115578
|
G | A | 1 | a0001c0011 | 2 | HG02965.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.2109C>T | p.Pro703Pro | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/32 | 2341/5065 | 2109/3648 | 703/1215 | chr19 | 2115578 | ||
chr19:2116617
|
T | C | 1 | a0001c0012 | 2 | HG02970.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.1989A>G | p.Glu663Glu | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/32 | 2221/5065 | 1989/3648 | 663/1215 | chr19 | 2116617 | ||
chr19:2116650
|
A | G | 7 | a0001c0004a0001c0006a0001c0014others(4): Show | 66 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(63): Show |
synonymous_variant | LOW | c.1956T>C | p.Arg652Arg | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/32 | 2188/5065 | 1956/3648 | 652/1215 | chr19 | 2116650 | ||
chr19:2117335
|
G | A | 1 | a0001c0020 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.1746C>T | p.Ile582Ile | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/32 | 1978/5065 | 1746/3648 | 582/1215 | chr19 | 2117335 | ||
chr19:2118625
|
G | A | 1 | a0001c0021 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.1689C>T | p.Ser563Ser | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/32 | 1921/5065 | 1689/3648 | 563/1215 | chr19 | 2118625 | ||
chr19:2118739
|
G | A | 1 | a0001c0022 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1575C>T | p.Asn525Asn | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/32 | 1807/5065 | 1575/3648 | 525/1215 | chr19 | 2118739 | ||
chr19:2129161
|
G | A | 1 | a0001c0023 | 1 | HG03579.hp1 | splice_region_variant&synonymous_variant | LOW | c.735C>T | p.Phe245Phe | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/32 | 967/5065 | 735/3648 | 245/1215 | chr19 | 2129161 | ||
chr19:2138655
|
T | G | 6 | a0001c0002a0001c0006a0001c0008others(3): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
synonymous_variant | LOW | c.156A>C | p.Ile52Ile | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/32 | 388/5065 | 156/3648 | 52/1215 | chr19 | 2138655 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2101171
|
C | G | 1 | a0001c0006t0008 | 2 | NA18951.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1002G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 1002 | chr19 | 2101171 | |||||
chr19:2101398
|
G | C | 3 | a0001c0003t0005a0001c0011t0005a0001c0023t0005 | 7 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*775C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 775 | chr19 | 2101398 | |||||
chr19:2101455
|
A | ACCACACA others(3): Show |
22 | a0001c0001t0002a0001c0003t0002a0001c0003t0005others(19): Show | 159 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*717_*718insGCGTGT others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 717 | chr19 | 2101455 | |||||
chr19:2101530
|
G | A | 1 | a0001c0004t0014 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*643C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 643 | chr19 | 2101530 | |||||
chr19:2101709
|
A | G | 1 | a0001c0012t0007 | 2 | HG02970.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*464T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 464 | chr19 | 2101709 | |||||
chr19:2101734
|
C | T | 1 | a0001c0001t0006 | 2 | HG02622.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*439G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 439 | chr19 | 2101734 | |||||
chr19:2102028
|
G | A | 1 | a0001c0014t0013 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 32/32 | 145 | chr19 | 2102028 | |||||
chr19:2151432
|
C | T | 1 | a0001c0014t0013 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-98G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | 98 | chr19 | 2151432 | |||||
chr19:2151465
|
G | A | 1 | a0001c0003t0009 | 2 | NA19005.hp2 NA19065.hp1 |
5_prime_UTR_variant | MODIFIER | c.-131C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | 131 | chr19 | 2151465 | |||||
chr19:2151511
|
G | C | 4 | a0001c0001t0003a0001c0006t0015a0001c0015t0003others(1): Show | 38 | HG00423.hp2 HG00438.hp1 HG00609.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-177C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | 177 | chr19 | 2151511 | |||||
chr19:2151516
|
G | A | 2 | a0001c0001t0010a0002c0007t0004 | 12 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-182C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | 182 | chr19 | 2151516 | |||||
chr19:2151528
|
C | A | 1 | a0001c0002t0012 | 2 | HG01167.hp2 HG01169.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-194G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | chr19 | 2151528 | ||||||
chr19:2151533
|
C | A | 1 | a0001c0008t0011 | 2 | HG02145.hp2 NA19030.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | chr19 | 2151533 | ||||||
chr19:2151535
|
G | A | 1 | a0001c0002t0012 | 2 | HG01167.hp2 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-201C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/32 | 201 | chr19 | 2151535 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:2102411
|
C | G | 5 | a0001c0008t0002g0184a0001c0008t0002g0185a0001c0008t0002g0253others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3553-143G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102411 | ||||||
chr19:2102450
|
C | G | 2 | a0001c0001t0003g0355a0001c0001t0003g0360 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3553-182G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102450 | ||||||
chr19:2102450
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3553-182G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102450 | ||||||
chr19:2102511
|
C | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-243G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102511 | ||||||
chr19:2102513
|
G | A | 1 | a0001c0003t0002g0046 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3553-245C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102513 | ||||||
chr19:2102544
|
G | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-276C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102544 | ||||||
chr19:2102553
|
C | T | 9 | a0001c0004t0002g0147a0001c0004t0002g0233a0001c0004t0002g0234others(6): Show | 9 | HG00323.hp1 HG00558.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.3553-285G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102553 | ||||||
chr19:2102558
|
C | G | 4 | a0001c0003t0001g0191a0001c0003t0002g0079a0001c0003t0002g0192others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-290G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102558 | ||||||
chr19:2102725
|
CAAAA | C | 3 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0023t0005g0059 | 3 | HG02630.hp1 HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3553-461_3553-458d others(6): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102725 | ||||||
chr19:2102728
|
AAAAT | A | 114 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0060others(111): Show | 115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.3553-464_3553-461d others(6): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102728 | ||||||
chr19:2102728
|
AAAATAAA others(1): Show |
A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(188): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.3553-468_3553-461d others(10): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102728 | ||||||
chr19:2102728
|
AAAATAAA others(5): Show |
A | 56 | a0001c0001t0001g0119a0001c0001t0001g0131a0001c0001t0001g0139others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.3553-472_3553-461d others(14): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102728 | ||||||
chr19:2102728
|
AAAATAAA others(9): Show |
A | 6 | a0001c0001t0001g0102a0001c0001t0001g0126a0001c0001t0001g0127others(3): Show | 6 | HG03017.hp1 HG03239.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.3553-476_3553-461d others(18): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102728 | ||||||
chr19:2102728
|
AAAATAAA others(13): Show |
A | 1 | a0001c0001t0001g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3553-480_3553-461d others(22): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102728 | ||||||
chr19:2102728
|
AAAATAAA others(17): Show |
A | 4 | a0001c0002t0001g0271a0001c0002t0001g0273a0001c0002t0001g0287others(1): Show | 4 | HG01074.hp1 HG01168.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-484_3553-461d others(26): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102728 | ||||||
chr19:2102767
|
A | G | 1 | a0001c0003t0002g0338 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3553-499T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102767 | ||||||
chr19:2102772
|
T | C | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3553-504A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102772 | ||||||
chr19:2102780
|
T | A | 2 | a0001c0002t0001g0320a0001c0014t0013g0007 | 2 | NA19057.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3553-512A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102780 | ||||||
chr19:2102825
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-557C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2102825 | ||||||
chr19:2103032
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3553-764C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103032 | ||||||
chr19:2103036
|
G | A | 1 | a0001c0001t0003g0350 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3553-768C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103036 | ||||||
chr19:2103115
|
T | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-847A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103115 | ||||||
chr19:2103187
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3553-919A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103187 | ||||||
chr19:2103220
|
TA | T | 131 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(128): Show | 131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.3553-953delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103220 | ||||||
chr19:2103301
|
T | G | 2 | a0001c0001t0003g0355a0001c0001t0003g0360 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3553-1033A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103301 | ||||||
chr19:2103315
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3553-1047C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103315 | ||||||
chr19:2103349
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0175 | 3 | NA18973.hp2 NA19002.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.3553-1081G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103349 | ||||||
chr19:2103350
|
G | A | 1 | a0001c0001t0003g0358 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3553-1082C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103350 | ||||||
chr19:2103350
|
G | C | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3553-1082C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103350 | ||||||
chr19:2103407
|
T | C | 2 | a0001c0001t0006g0123a0001c0001t0006g0137 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3553-1139A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103407 | ||||||
chr19:2103450
|
G | A | 1 | a0001c0001t0003g0370 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3553-1182C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103450 | ||||||
chr19:2103473
|
A | ACCAGAG | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-1211_3553-120 others(10): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103473 | ||||||
chr19:2103525
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3553-1257G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103525 | ||||||
chr19:2103556
|
G | A | 68 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(65): Show | 68 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.3553-1288C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103556 | ||||||
chr19:2103621
|
G | A | 3 | a0001c0001t0001g0081a0001c0002t0001g0289a0001c0002t0001g0290 | 3 | HG01243.hp1 HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.3553-1353C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103621 | ||||||
chr19:2103644
|
G | A | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3553-1376C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103644 | ||||||
chr19:2103817
|
CAGACCCC others(7): Show |
C | 1 | a0001c0001t0002g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3553-1563_3553-155 others(18): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103817 | ||||||
chr19:2103840
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 6 | HG01109.hp1 HG02615.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3553-1572C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103840 | ||||||
chr19:2103937
|
A | G | 1 | a0001c0003t0002g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3553-1669T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103937 | ||||||
chr19:2103942
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-1674C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103942 | ||||||
chr19:2103963
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-1695T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103963 | ||||||
chr19:2103990
|
C | T | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3553-1722G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2103990 | ||||||
chr19:2104030
|
G | A | 1 | a0001c0004t0002g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3553-1762C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104030 | ||||||
chr19:2104040
|
C | G | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3553-1772G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104040 | ||||||
chr19:2104098
|
G | A | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3553-1830C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104098 | ||||||
chr19:2104130
|
A | C | 68 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(65): Show | 68 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.3553-1862T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104130 | ||||||
chr19:2104156
|
TCAGACTC others(7): Show |
T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-1902_3553-188 others(18): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104156 | ||||||
chr19:2104173
|
G | A | 1 | a0001c0002t0001g0294 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3553-1905C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104173 | ||||||
chr19:2104225
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3553-1957G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104225 | ||||||
chr19:2104227
|
G | A | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3553-1959C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104227 | ||||||
chr19:2104273
|
C | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2005G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104273 | ||||||
chr19:2104299
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0202a0001c0001t0001g0347others(1): Show | 4 | HG02630.hp2 HG02647.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3553-2031C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104299 | ||||||
chr19:2104302
|
A | T | 16 | a0001c0006t0002g0009a0002c0007t0004g0386a0002c0007t0004g0387others(13): Show | 16 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.3553-2034T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104302 | ||||||
chr19:2104310
|
G | T | 65 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(62): Show | 65 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.3553-2042C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104310 | ||||||
chr19:2104311
|
C | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2043G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104311 | ||||||
chr19:2104316
|
C | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2048G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104316 | ||||||
chr19:2104322
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2054T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104322 | ||||||
chr19:2104324
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2056G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104324 | ||||||
chr19:2104325
|
C | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2057G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104325 | ||||||
chr19:2104331
|
C | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2063G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104331 | ||||||
chr19:2104335
|
T | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2067A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104335 | ||||||
chr19:2104336
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2068C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104336 | ||||||
chr19:2104344
|
C | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2076G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104344 | ||||||
chr19:2104345
|
G | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2077C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104345 | ||||||
chr19:2104353
|
G | GAGACGCC others(245): Show |
1 | a0001c0003t0002g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3553-2086_3553-208 others(256): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104353 | ||||||
chr19:2104353
|
G | GAGACGCC others(245): Show |
65 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(62): Show | 65 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.3553-2086_3553-208 others(256): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104353 | ||||||
chr19:2104353
|
G | GAGACGCC others(245): Show |
1 | a0001c0003t0002g0046 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3553-2086_3553-208 others(256): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104353 | ||||||
chr19:2104353
|
G | GAGACGCC others(245): Show |
1 | a0001c0003t0002g0338 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3553-2086_3553-208 others(256): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104353 | ||||||
chr19:2104358
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3553-2090C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104358 | ||||||
chr19:2104358
|
G | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2090C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104358 | ||||||
chr19:2104363
|
C | CACCGAGA others(7): Show |
15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2096_3553-209 others(18): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104363 | ||||||
chr19:2104378
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2110C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104378 | ||||||
chr19:2104381
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2113T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104381 | ||||||
chr19:2104381
|
AAGGCACC others(35): Show |
A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3553-2155_3553-211 others(46): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104381 | ||||||
chr19:2104503
|
T | C | 17 | a0001c0006t0002g0009a0001c0014t0013g0007a0002c0007t0004g0386others(14): Show | 17 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.3553-2235A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104503 | ||||||
chr19:2104516
|
A | C | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3553-2248T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104516 | ||||||
chr19:2104518
|
G | GCCAAGAC others(21): Show |
1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3553-2251_3553-225 others(32): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104518 | ||||||
chr19:2104546
|
G | A | 11 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(8): Show | 11 | HG02145.hp2 HG02559.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3553-2278C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104546 | ||||||
chr19:2104598
|
C | T | 4 | a0001c0001t0002g0096a0001c0001t0002g0098a0001c0001t0002g0103others(1): Show | 4 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3553-2330G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104598 | ||||||
chr19:2104628
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3553-2360C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104628 | ||||||
chr19:2104659
|
G | C | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3553-2391C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104659 | ||||||
chr19:2104666
|
G | GT | 58 | a0001c0001t0001g0011a0001c0001t0001g0074a0001c0001t0001g0081others(55): Show | 58 | HG00323.hp1 HG00423.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.3553-2399dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104666 | ||||||
chr19:2104666
|
GT | G | 23 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0099others(20): Show | 24 | HG01109.hp1 HG02622.hp2 HG02630.hp1 others(21): Show |
intron_variant | MODIFIER | c.3553-2399delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104666 | ||||||
chr19:2104673
|
T | TTG | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2406_3553-240 others(6): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104673 | ||||||
chr19:2104681
|
T | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3553-2413A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104681 | ||||||
chr19:2104707
|
C | T | 1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3553-2439G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104707 | ||||||
chr19:2104838
|
C | T | 47 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0213others(44): Show | 47 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.3553-2570G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104838 | ||||||
chr19:2104848
|
T | A | 2 | a0001c0002t0001g0307a0001c0004t0002g0226 | 2 | HG02293.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3553-2580A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104848 | ||||||
chr19:2104923
|
C | T | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3553-2655G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2104923 | ||||||
chr19:2105085
|
A | G | 3 | a0001c0001t0003g0367a0001c0001t0003g0368a0001c0001t0003g0377 | 3 | HG00423.hp2 NA18612.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.3553-2817T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105085 | ||||||
chr19:2105216
|
C | G | 1 | a0001c0001t0001g0130 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3553-2948G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105216 | ||||||
chr19:2105225
|
T | C | 1 | a0001c0001t0002g0096 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3553-2957A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105225 | ||||||
chr19:2105511
|
C | T | 23 | a0001c0001t0001g0081a0001c0001t0001g0089a0001c0001t0001g0090others(20): Show | 23 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.3552+3176G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105511 | ||||||
chr19:2105627
|
CTG | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+3058_3552+305 others(6): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105627 | ||||||
chr19:2105695
|
G | A | 2 | a0001c0002t0001g0303a0001c0002t0001g0304 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3552+2992C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105695 | ||||||
chr19:2105695
|
G | T | 1 | a0001c0004t0002g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3552+2992C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105695 | ||||||
chr19:2105705
|
T | A | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3552+2982A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105705 | ||||||
chr19:2105706
|
A | G | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3552+2981T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105706 | ||||||
chr19:2105770
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3552+2917T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105770 | ||||||
chr19:2105829
|
C | T | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3552+2858G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105829 | ||||||
chr19:2105856
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0328 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3552+2831C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105856 | ||||||
chr19:2105871
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3552+2816C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105871 | ||||||
chr19:2105888
|
C | T | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3552+2799G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105888 | ||||||
chr19:2105889
|
C | T | 8 | a0001c0001t0001g0172a0001c0002t0001g0004a0001c0002t0001g0257others(5): Show | 9 | HG01081.hp2 NA18945.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.3552+2798G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105889 | ||||||
chr19:2105914
|
T | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+2773A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2105914 | ||||||
chr19:2106072
|
G | A | 9 | a0001c0004t0002g0223a0001c0004t0002g0225a0001c0004t0002g0226others(6): Show | 9 | HG01123.hp1 HG02293.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.3552+2615C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106072 | ||||||
chr19:2106080
|
G | A | 1 | a0001c0008t0011g0399 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3552+2607C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106080 | ||||||
chr19:2106195
|
A | T | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3552+2492T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106195 | ||||||
chr19:2106228
|
A | T | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3552+2459T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106228 | ||||||
chr19:2106314
|
C | T | 1 | a0001c0005t0002g0018 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3552+2373G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106314 | ||||||
chr19:2106334
|
G | A | 145 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0063others(142): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3552+2353C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106334 | ||||||
chr19:2106560
|
T | TA | 48 | a0001c0001t0001g0180a0001c0004t0002g0051a0001c0004t0002g0147others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.3552+2126dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106560 | ||||||
chr19:2106570
|
C | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+2117G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106570 | ||||||
chr19:2106683
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3552+2004C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106683 | ||||||
chr19:2106697
|
T | C | 144 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3552+1990A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106697 | ||||||
chr19:2106751
|
G | A | 5 | a0001c0003t0002g0073a0001c0003t0002g0325a0001c0003t0002g0326others(2): Show | 5 | HG02280.hp2 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3552+1936C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106751 | ||||||
chr19:2106777
|
G | C | 1 | a0001c0001t0003g0358 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.3552+1910C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106777 | ||||||
chr19:2106893
|
C | G | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3552+1794G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106893 | ||||||
chr19:2106894
|
T | C | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3552+1793A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106894 | ||||||
chr19:2106895
|
G | T | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3552+1792C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106895 | ||||||
chr19:2106925
|
G | C | 1 | a0001c0008t0011g0399 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3552+1762C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2106925 | ||||||
chr19:2107018
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3552+1669G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107018 | ||||||
chr19:2107129
|
G | A | 1 | a0001c0008t0011g0398 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3552+1558C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107129 | ||||||
chr19:2107134
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3552+1553C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107134 | ||||||
chr19:2107135
|
C | T | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3552+1552G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107135 | ||||||
chr19:2107215
|
G | A | 1 | a0001c0003t0002g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3552+1472C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107215 | ||||||
chr19:2107259
|
C | CA | 20 | a0001c0001t0001g0179a0001c0002t0001g0310a0001c0003t0002g0050others(17): Show | 20 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.3552+1427dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107259 | ||||||
chr19:2107368
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3552+1319C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107368 | ||||||
chr19:2107370
|
G | A | 1 | a0001c0002t0001g0342 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3552+1317C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107370 | ||||||
chr19:2107386
|
C | T | 49 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(46): Show | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.3552+1301G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107386 | ||||||
chr19:2107407
|
T | C | 5 | a0001c0001t0003g0353a0001c0001t0003g0357a0001c0001t0003g0359others(2): Show | 5 | HG01256.hp1 HG01952.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3552+1280A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107407 | ||||||
chr19:2107462
|
C | T | 19 | a0001c0003t0001g0191a0001c0003t0002g0053a0001c0003t0002g0079others(16): Show | 19 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.3552+1225G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107462 | ||||||
chr19:2107663
|
C | T | 1 | a0001c0004t0002g0147 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3552+1024G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107663 | ||||||
chr19:2107664
|
A | G | 145 | a0001c0001t0001g0056a0001c0003t0001g0071a0001c0003t0001g0191others(142): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.3552+1023T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107664 | ||||||
chr19:2107693
|
C | T | 18 | a0001c0003t0001g0191a0001c0003t0002g0079a0001c0003t0002g0186others(15): Show | 18 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3552+994G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107693 | ||||||
chr19:2107694
|
T | C | 18 | a0001c0003t0001g0191a0001c0003t0002g0079a0001c0003t0002g0186others(15): Show | 18 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3552+993A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107694 | ||||||
chr19:2107696
|
C | T | 18 | a0001c0003t0001g0191a0001c0003t0002g0079a0001c0003t0002g0186others(15): Show | 18 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3552+991G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107696 | ||||||
chr19:2107697
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+990T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107697 | ||||||
chr19:2107739
|
C | CA | 56 | a0001c0001t0003g0358a0001c0001t0003g0372a0001c0001t0003g0374others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.3552+947dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107739 | ||||||
chr19:2107739
|
C | CAA | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3552+946_3552+947d others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107739 | ||||||
chr19:2107802
|
GAC | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3552+883_3552+884d others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107802 | ||||||
chr19:2107914
|
T | C | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3552+773A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107914 | ||||||
chr19:2107917
|
T | C | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.3552+770A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107917 | ||||||
chr19:2107950
|
C | T | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3552+737G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2107950 | ||||||
chr19:2108038
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3552+649T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108038 | ||||||
chr19:2108048
|
G | C | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3552+639C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108048 | ||||||
chr19:2108269
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3552+418G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108269 | ||||||
chr19:2108324
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3552+363C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108324 | ||||||
chr19:2108333
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0109 | 2 | HG02132.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.3552+354C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108333 | ||||||
chr19:2108341
|
A | G | 3 | a0001c0004t0002g0221a0001c0004t0002g0227a0001c0004t0002g0229 | 3 | NA18992.hp1 NA19003.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3552+346T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108341 | ||||||
chr19:2108469
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3552+218C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108469 | ||||||
chr19:2108479
|
G | A | 3 | a0001c0001t0003g0352a0001c0001t0003g0381a0001c0015t0003g0363 | 3 | NA18946.hp2 NA18990.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3552+208C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108479 | ||||||
chr19:2108540
|
C | A | 3 | a0001c0008t0002g0253a0001c0012t0007g0182a0001c0012t0007g0183 | 3 | HG02922.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3552+147G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 31/31 | chr19 | 2108540 | ||||||
chr19:2108930
|
C | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3472+156G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 30/31 | chr19 | 2108930 | ||||||
chr19:2109020
|
T | C | 144 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.3472+66A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 30/31 | chr19 | 2109020 | ||||||
chr19:2109039
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3472+47G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 30/31 | chr19 | 2109039 | ||||||
chr19:2109072
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3472+14G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 30/31 | chr19 | 2109072 | ||||||
chr19:2109293
|
C | T | 2 | a0001c0002t0001g0255a0001c0002t0001g0302 | 2 | HG00735.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.3351-86G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109293 | ||||||
chr19:2109380
|
G | A | 1 | a0001c0004t0014g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3351-173C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109380 | ||||||
chr19:2109434
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3351-227C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109434 | ||||||
chr19:2109481
|
G | A | 48 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.3351-274C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109481 | ||||||
chr19:2109541
|
G | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0108a0001c0001t0001g0109 | 3 | HG02132.hp2 HG04184.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.3350+332C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109541 | ||||||
chr19:2109542
|
G | C | 1 | a0001c0001t0010g0396 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3350+331C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109542 | ||||||
chr19:2109597
|
T | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3350+276A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109597 | ||||||
chr19:2109641
|
T | G | 3 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0043 | 3 | NA18980.hp1 NA18989.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.3350+232A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109641 | ||||||
chr19:2109668
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3350+205G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109668 | ||||||
chr19:2109708
|
G | A | 1 | a0001c0002t0001g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3350+165C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109708 | ||||||
chr19:2109798
|
G | A | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0111others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3350+75C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109798 | ||||||
chr19:2109813
|
G | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3350+60C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109813 | ||||||
chr19:2109835
|
G | A | 51 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.3350+38C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 29/31 | chr19 | 2109835 | ||||||
chr19:2109964
|
G | A | 1 | a0002c0009t0002g0277 | 1 | HG02922.hp1 | splice_region_variant&intron_variant | LOW | c.3265-6C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 28/31 | chr19 | 2109964 | ||||||
chr19:2109989
|
A | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3265-31T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 28/31 | chr19 | 2109989 | ||||||
chr19:2110020
|
T | C | 130 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.3265-62A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 28/31 | chr19 | 2110020 | ||||||
chr19:2110109
|
T | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.3264+27A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 28/31 | chr19 | 2110109 | ||||||
chr19:2110115
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3264+21C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 28/31 | chr19 | 2110115 | ||||||
chr19:2110259
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3176-35G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110259 | ||||||
chr19:2110334
|
G | A | 1 | a0001c0004t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3176-110C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110334 | ||||||
chr19:2110359
|
G | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0127 | 2 | HG01243.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.3176-135C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110359 | ||||||
chr19:2110366
|
G | A | 7 | a0001c0002t0001g0305a0001c0002t0001g0309a0001c0002t0001g0310others(4): Show | 7 | NA18943.hp2 NA18947.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.3176-142C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110366 | ||||||
chr19:2110388
|
G | A | 2 | a0001c0001t0006g0123a0001c0001t0006g0137 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3176-164C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110388 | ||||||
chr19:2110540
|
TCA | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0135 | 4 | HG01109.hp1 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3175+165_3175+166d others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110540 | ||||||
chr19:2110615
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3175+92C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110615 | ||||||
chr19:2110617
|
A | T | 1 | a0001c0001t0003g0365 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3175+90T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 27/31 | chr19 | 2110617 | ||||||
chr19:2110990
|
G | A | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2986-94C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2110990 | ||||||
chr19:2111013
|
C | T | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2986-117G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111013 | ||||||
chr19:2111036
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2986-140G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111036 | ||||||
chr19:2111039
|
G | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2986-143C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111039 | ||||||
chr19:2111064
|
T | C | 50 | a0001c0002t0001g0320a0001c0004t0002g0045a0001c0004t0002g0051others(47): Show | 50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.2986-168A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111064 | ||||||
chr19:2111132
|
C | T | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2985+153G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111132 | ||||||
chr19:2111204
|
G | A | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2985+81C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111204 | ||||||
chr19:2111213
|
C | T | 1 | a0001c0002t0001g0282 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2985+72G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 26/31 | chr19 | 2111213 | ||||||
chr19:2111340
|
T | C | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | splice_region_variant&intron_variant | LOW | c.2938-8A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111340 | ||||||
chr19:2111340
|
T | G | 1 | a0001c0001t0003g0350 | 1 | NA18974.hp1 | splice_region_variant&intron_variant | LOW | c.2938-8A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111340 | ||||||
chr19:2111383
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2938-51C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111383 | ||||||
chr19:2111398
|
T | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2938-66A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111398 | ||||||
chr19:2111427
|
A | C | 1 | a0001c0002t0001g0331 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2938-95T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111427 | ||||||
chr19:2111575
|
G | A | 2 | a0001c0001t0003g0372a0001c0001t0003g0374 | 2 | NA18962.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2937+104C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111575 | ||||||
chr19:2111596
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0302 | 2 | HG00735.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.2937+83C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111596 | ||||||
chr19:2111625
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2937+54C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111625 | ||||||
chr19:2111650
|
T | C | 144 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2937+29A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111650 | ||||||
chr19:2111656
|
G | A | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2937+23C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111656 | ||||||
chr19:2111662
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2937+17C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 25/31 | chr19 | 2111662 | ||||||
chr19:2111874
|
AC | A | 48 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2788-47delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2111874 | ||||||
chr19:2111916
|
C | G | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2788-88G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2111916 | ||||||
chr19:2112159
|
C | T | 1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2788-331G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2112159 | ||||||
chr19:2112171
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2788-343G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2112171 | ||||||
chr19:2112443
|
ATGAAATG others(12): Show |
A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2787+398_2787+416d others(21): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2112443 | ||||||
chr19:2112840
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0111others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787+20A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2112840 | ||||||
chr19:2112842
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2787+18C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2112842 | ||||||
chr19:2112845
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2787+15C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 24/31 | chr19 | 2112845 | ||||||
chr19:2113017
|
C | A | 1 | a0001c0003t0002g0024 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2680-50G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113017 | ||||||
chr19:2113098
|
G | A | 1 | a0001c0003t0002g0329 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2680-131C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113098 | ||||||
chr19:2113176
|
C | T | 1 | a0001c0001t0003g0369 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2679+160G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113176 | ||||||
chr19:2113274
|
G | A | 63 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(60): Show | 63 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.2679+62C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113274 | ||||||
chr19:2113278
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2679+58C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113278 | ||||||
chr19:2113285
|
A | G | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2679+51T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113285 | ||||||
chr19:2113302
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2679+34G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 23/31 | chr19 | 2113302 | ||||||
chr19:2113468
|
G | A | 7 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0002t0001g0267others(4): Show | 7 | HG00099.hp2 HG00408.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.2602-55C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113468 | ||||||
chr19:2113492
|
A | G | 1 | a0001c0001t0003g0365 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2602-79T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113492 | ||||||
chr19:2113519
|
G | A | 63 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(60): Show | 63 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.2602-106C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113519 | ||||||
chr19:2113551
|
G | C | 1 | a0001c0008t0011g0398 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2602-138C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113551 | ||||||
chr19:2113572
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2602-159C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113572 | ||||||
chr19:2113614
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2602-201C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113614 | ||||||
chr19:2113669
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2602-256C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113669 | ||||||
chr19:2113701
|
C | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2602-288G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113701 | ||||||
chr19:2113729
|
G | A | 1 | a0001c0003t0005g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2602-316C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113729 | ||||||
chr19:2113751
|
T | C | 18 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399others(15): Show | 18 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.2602-338A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113751 | ||||||
chr19:2113829
|
C | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2601+296G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113829 | ||||||
chr19:2113852
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2601+273C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113852 | ||||||
chr19:2113899
|
C | A | 5 | a0001c0003t0005g0114a0001c0003t0005g0211a0001c0003t0005g0212others(2): Show | 5 | HG02559.hp1 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2601+226G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113899 | ||||||
chr19:2113910
|
G | A | 49 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(46): Show | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2601+215C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113910 | ||||||
chr19:2113947
|
A | G | 1 | a0001c0002t0001g0307 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2601+178T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113947 | ||||||
chr19:2113977
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2601+148G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113977 | ||||||
chr19:2113985
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2601+140G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 22/31 | chr19 | 2113985 | ||||||
chr19:2114320
|
G | A | 3 | a0001c0010t0001g0266a0001c0010t0001g0293a0001c0010t0001g0299 | 3 | HG00733.hp1 HG01168.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2424-18C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114320 | ||||||
chr19:2114418
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2424-116G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114418 | ||||||
chr19:2114466
|
C | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2424-164G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114466 | ||||||
chr19:2114541
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2423+207C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114541 | ||||||
chr19:2114541
|
G | C | 2 | a0001c0008t0002g0181a0001c0008t0011g0399 | 2 | HG02145.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.2423+207C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114541 | ||||||
chr19:2114644
|
C | G | 2 | a0001c0002t0001g0284a0001c0002t0001g0285 | 2 | HG00408.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.2423+104G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114644 | ||||||
chr19:2114675
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2423+73C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114675 | ||||||
chr19:2114695
|
G | A | 50 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(47): Show | 50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.2423+53C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 21/31 | chr19 | 2114695 | ||||||
chr19:2114854
|
C | A | 2 | a0001c0004t0002g0216a0001c0004t0002g0218 | 2 | HG01123.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2350-33G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2114854 | ||||||
chr19:2114897
|
G | T | 1 | a0001c0003t0002g0027 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2350-76C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2114897 | ||||||
chr19:2115037
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(305): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2349+182A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2115037 | ||||||
chr19:2115063
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2349+156G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2115063 | ||||||
chr19:2115128
|
G | A | 52 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.2349+91C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2115128 | ||||||
chr19:2115132
|
A | G | 1 | a0001c0004t0002g0234 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2349+87T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2115132 | ||||||
chr19:2115198
|
G | A | 1 | a0001c0001t0003g0356 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2349+21C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 20/31 | chr19 | 2115198 | ||||||
chr19:2115423
|
G | A | 1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.2150-5C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/31 | chr19 | 2115423 | ||||||
chr19:2115440
|
C | G | 18 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399others(15): Show | 18 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.2150-22G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/31 | chr19 | 2115440 | ||||||
chr19:2115480
|
C | T | 48 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2149+58G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/31 | chr19 | 2115480 | ||||||
chr19:2115493
|
C | T | 2 | a0001c0004t0002g0234a0001c0006t0002g0009 | 2 | HG02257.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2149+45G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/31 | chr19 | 2115493 | ||||||
chr19:2115494
|
A | G | 144 | a0001c0001t0001g0337a0001c0003t0001g0071a0001c0003t0001g0191others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2149+44T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/31 | chr19 | 2115494 | ||||||
chr19:2115526
|
G | C | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2149+12C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 19/31 | chr19 | 2115526 | ||||||
chr19:2115669
|
G | A | 51 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.2074-56C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115669 | ||||||
chr19:2115675
|
C | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0175 | 3 | NA18973.hp2 NA19002.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2074-62G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115675 | ||||||
chr19:2115751
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | NA18979.hp2 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2074-138C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115751 | ||||||
chr19:2115791
|
T | C | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(309): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2074-178A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115791 | ||||||
chr19:2115799
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2074-186A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115799 | ||||||
chr19:2115919
|
C | T | 66 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(63): Show | 66 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.2073+288G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115919 | ||||||
chr19:2115955
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2073+252G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2115955 | ||||||
chr19:2116048
|
G | A | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2073+159C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116048 | ||||||
chr19:2116049
|
A | G | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2073+158T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116049 | ||||||
chr19:2116083
|
C | T | 1 | a0001c0023t0005g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2073+124G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116083 | ||||||
chr19:2116089
|
G | T | 8 | a0001c0002t0001g0003a0001c0002t0001g0255a0001c0002t0001g0302others(5): Show | 10 | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.2073+118C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116089 | ||||||
chr19:2116103
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2073+104G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116103 | ||||||
chr19:2116127
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2073+80C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116127 | ||||||
chr19:2116131
|
C | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0005c0018t0001g0100 | 3 | HG01081.hp1 HG02273.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2073+76G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116131 | ||||||
chr19:2116131
|
C | T | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2073+76G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116131 | ||||||
chr19:2116192
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2073+15C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 18/31 | chr19 | 2116192 | ||||||
chr19:2116282
|
T | C | 128 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(125): Show | 128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
splice_region_variant&intron_variant | LOW | c.2002-4A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/31 | chr19 | 2116282 | ||||||
chr19:2116314
|
C | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2002-36G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/31 | chr19 | 2116314 | ||||||
chr19:2116401
|
C | T | 143 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.2002-123G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/31 | chr19 | 2116401 | ||||||
chr19:2116450
|
G | C | 1 | a0001c0001t0003g0356 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2001+155C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/31 | chr19 | 2116450 | ||||||
chr19:2116460
|
C | T | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2001+145G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/31 | chr19 | 2116460 | ||||||
chr19:2116467
|
G | C | 143 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.2001+138C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 17/31 | chr19 | 2116467 | ||||||
chr19:2116758
|
A | G | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1860-12T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116758 | ||||||
chr19:2116761
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1860-15T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116761 | ||||||
chr19:2116765
|
C | T | 16 | a0001c0001t0001g0328a0002c0007t0004g0386a0002c0007t0004g0387others(13): Show | 16 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.1860-19G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116765 | ||||||
chr19:2116809
|
G | A | 2 | a0001c0006t0008g0256a0001c0006t0008g0319 | 2 | NA18951.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1860-63C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116809 | ||||||
chr19:2116834
|
T | C | 64 | a0001c0003t0001g0071a0001c0003t0001g0191a0001c0003t0002g0024others(61): Show | 64 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1860-88A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116834 | ||||||
chr19:2116835
|
G | T | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1860-89C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116835 | ||||||
chr19:2116885
|
G | A | 1 | a0001c0001t0003g0357 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1860-139C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116885 | ||||||
chr19:2116886
|
A | G | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1860-140T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116886 | ||||||
chr19:2116998
|
T | G | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1859+224A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2116998 | ||||||
chr19:2117075
|
C | T | 3 | a0001c0001t0002g0064a0001c0001t0003g0380a0001c0001t0003g0382 | 3 | HG02080.hp2 HG02129.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1859+147G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2117075 | ||||||
chr19:2117076
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.1859+146C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2117076 | ||||||
chr19:2117117
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1859+105G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2117117 | ||||||
chr19:2117133
|
C | T | 3 | a0001c0008t0002g0253a0001c0012t0007g0182a0001c0012t0007g0183 | 3 | HG02922.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1859+89G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 16/31 | chr19 | 2117133 | ||||||
chr19:2117466
|
T | C | 1 | a0001c0005t0002g0021 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1714-99A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117466 | ||||||
chr19:2117482
|
G | C | 1 | a0001c0008t0011g0398 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1714-115C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117482 | ||||||
chr19:2117515
|
C | T | 6 | a0001c0001t0002g0096a0001c0001t0002g0098a0001c0001t0002g0103others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1714-148G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117515 | ||||||
chr19:2117559
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1714-192G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117559 | ||||||
chr19:2117744
|
G | A | 3 | a0001c0001t0003g0352a0001c0001t0003g0381a0001c0015t0003g0363 | 3 | NA18946.hp2 NA18990.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1714-377C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117744 | ||||||
chr19:2117803
|
G | A | 50 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(47): Show | 50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1714-436C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117803 | ||||||
chr19:2117934
|
T | A | 1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1714-567A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117934 | ||||||
chr19:2117946
|
C | T | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1714-579G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2117946 | ||||||
chr19:2118014
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1713+587C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118014 | ||||||
chr19:2118016
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1713+585G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118016 | ||||||
chr19:2118017
|
G | A | 3 | a0001c0008t0002g0253a0001c0012t0007g0182a0001c0012t0007g0183 | 3 | HG02922.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1713+584C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118017 | ||||||
chr19:2118021
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1713+580C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118021 | ||||||
chr19:2118341
|
C | G | 2 | a0001c0002t0001g0280a0001c0002t0001g0294 | 2 | HG00099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1713+260G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118341 | ||||||
chr19:2118531
|
G | A | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1713+70C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118531 | ||||||
chr19:2118555
|
T | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1713+46A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118555 | ||||||
chr19:2118561
|
C | T | 1 | a0001c0003t0002g0024 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1713+40G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118561 | ||||||
chr19:2118563
|
C | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1713+38G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118563 | ||||||
chr19:2118564
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1713+37G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 15/31 | chr19 | 2118564 | ||||||
chr19:2118856
|
C | A | 2 | a0001c0001t0001g0328a0001c0003t0002g0079 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1482-24G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2118856 | ||||||
chr19:2118904
|
G | C | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1482-72C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2118904 | ||||||
chr19:2118917
|
C | T | 2 | a0001c0003t0002g0026a0001c0003t0002g0027 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1482-85G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2118917 | ||||||
chr19:2119014
|
G | A | 389 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(386): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1482-182C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119014 | ||||||
chr19:2119153
|
C | T | 1 | a0001c0003t0002g0054 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1482-321G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119153 | ||||||
chr19:2119220
|
T | C | 73 | a0001c0001t0001g0176a0001c0003t0001g0071a0001c0003t0001g0191others(70): Show | 73 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1482-388A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119220 | ||||||
chr19:2119319
|
G | T | 17 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0002t0001g0262others(14): Show | 17 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(14): Show |
intron_variant | MODIFIER | c.1482-487C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119319 | ||||||
chr19:2119421
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0111others(1): Show | 4 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482-589G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119421 | ||||||
chr19:2119457
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1482-625C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119457 | ||||||
chr19:2119597
|
G | A | 1 | a0001c0003t0002g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1482-765C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119597 | ||||||
chr19:2119699
|
C | CA | 20 | a0001c0001t0001g0008a0001c0001t0001g0090a0001c0001t0001g0115others(17): Show | 20 | HG01256.hp1 HG01934.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.1482-868dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119699 | ||||||
chr19:2119699
|
CA | C | 74 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0001g0075others(71): Show | 74 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1482-868delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119699 | ||||||
chr19:2119755
|
G | A | 48 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1482-923C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119755 | ||||||
chr19:2119832
|
C | T | 1 | a0001c0005t0002g0040 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1482-1000G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119832 | ||||||
chr19:2119883
|
A | C | 1 | a0004c0013t0002g0245 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1481+979T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119883 | ||||||
chr19:2119962
|
A | T | 1 | a0001c0023t0005g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1481+900T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2119962 | ||||||
chr19:2120137
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1481+725C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120137 | ||||||
chr19:2120155
|
A | G | 389 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(386): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1481+707T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120155 | ||||||
chr19:2120159
|
A | C | 2 | a0001c0005t0002g0019a0001c0005t0002g0029 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1481+703T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120159 | ||||||
chr19:2120179
|
G | C | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1481+683C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120179 | ||||||
chr19:2120199
|
C | T | 1 | a0001c0006t0002g0308 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1481+663G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120199 | ||||||
chr19:2120221
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1481+641G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120221 | ||||||
chr19:2120315
|
T | C | 140 | a0001c0001t0001g0049a0001c0001t0001g0176a0001c0003t0001g0071others(137): Show | 140 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1481+547A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120315 | ||||||
chr19:2120337
|
G | T | 2 | a0001c0001t0001g0328a0001c0003t0002g0079 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1481+525C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120337 | ||||||
chr19:2120460
|
G | A | 2 | a0001c0004t0002g0214a0001c0004t0002g0217 | 2 | HG00280.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1481+402C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120460 | ||||||
chr19:2120496
|
A | G | 1 | a0001c0001t0003g0379 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1481+366T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120496 | ||||||
chr19:2120512
|
C | T | 48 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(45): Show | 48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1481+350G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120512 | ||||||
chr19:2120643
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1481+219C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120643 | ||||||
chr19:2120674
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1481+188C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120674 | ||||||
chr19:2120763
|
G | A | 1 | a0001c0004t0002g0215 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1481+99C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120763 | ||||||
chr19:2120772
|
C | T | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1481+90G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120772 | ||||||
chr19:2120798
|
C | A | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1481+64G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120798 | ||||||
chr19:2120810
|
C | T | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1481+52G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 14/31 | chr19 | 2120810 | ||||||
chr19:2121317
|
C | T | 10 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(7): Show | 10 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1102-6G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121317 | ||||||
chr19:2121405
|
G | A | 1 | a0001c0003t0002g0036 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1102-94C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121405 | ||||||
chr19:2121416
|
G | A | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1102-105C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121416 | ||||||
chr19:2121462
|
G | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1102-151C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121462 | ||||||
chr19:2121549
|
C | T | 10 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(7): Show | 10 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.1101+185G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121549 | ||||||
chr19:2121550
|
C | T | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101+184G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121550 | ||||||
chr19:2121585
|
G | A | 1 | a0003c0024t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1101+149C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121585 | ||||||
chr19:2121656
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0110a0001c0001t0001g0115 | 3 | HG02040.hp1 HG03942.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1101+78G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121656 | ||||||
chr19:2121727
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
splice_region_variant&intron_variant | LOW | c.1101+7G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 12/31 | chr19 | 2121727 | ||||||
chr19:2121960
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.956-81C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2121960 | ||||||
chr19:2122088
|
C | T | 1 | a0001c0004t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.956-209G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122088 | ||||||
chr19:2122095
|
C | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.956-216G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122095 | ||||||
chr19:2122100
|
C | T | 49 | a0001c0004t0002g0051a0001c0004t0002g0147a0001c0004t0002g0206others(46): Show | 49 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.956-221G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122100 | ||||||
chr19:2122207
|
CCAG | C | 144 | a0001c0001t0001g0176a0001c0003t0001g0071a0001c0003t0001g0191others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.956-331_956-329del others(3): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122207 | ||||||
chr19:2122224
|
T | C | 141 | a0001c0001t0001g0176a0001c0003t0001g0071a0001c0003t0001g0191others(138): Show | 141 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.956-345A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122224 | ||||||
chr19:2122226
|
C | T | 3 | a0001c0002t0001g0275a0001c0002t0001g0281a0001c0002t0001g0282 | 3 | HG00597.hp1 HG02165.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.956-347G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122226 | ||||||
chr19:2122228
|
CT | C | 22 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0089others(19): Show | 22 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.956-350delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122228 | ||||||
chr19:2122230
|
T | C | 144 | a0001c0001t0001g0176a0001c0003t0001g0071a0001c0003t0001g0191others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.956-351A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122230 | ||||||
chr19:2122349
|
G | A | 2 | a0001c0001t0001g0328a0001c0003t0002g0079 | 2 | HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.956-470C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122349 | ||||||
chr19:2122384
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.956-505T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122384 | ||||||
chr19:2122459
|
C | T | 2 | a0001c0002t0001g0303a0001c0002t0001g0304 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.956-580G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122459 | ||||||
chr19:2122540
|
T | C | 1 | a0001c0008t0011g0398 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.956-661A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122540 | ||||||
chr19:2122548
|
G | A | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.956-669C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122548 | ||||||
chr19:2122564
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.956-685G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122564 | ||||||
chr19:2122663
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.955+695C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122663 | ||||||
chr19:2122900
|
T | C | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.955+458A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2122900 | ||||||
chr19:2123039
|
G | A | 3 | a0001c0008t0002g0253a0001c0012t0007g0182a0001c0012t0007g0183 | 3 | HG02922.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.955+319C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2123039 | ||||||
chr19:2123313
|
A | AGCTGGGG others(16): Show |
1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.955+22_955+44dupGC others(21): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2123313 | ||||||
chr19:2123329
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.955+29T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 11/31 | chr19 | 2123329 | ||||||
chr19:2123517
|
A | G | 80 | a0001c0001t0001g0049a0001c0001t0001g0176a0001c0003t0001g0071others(77): Show | 80 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.907-111T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 10/31 | chr19 | 2123517 | ||||||
chr19:2123609
|
C | G | 2 | a0001c0002t0001g0268a0001c0002t0001g0320 | 2 | NA19057.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.907-203G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 10/31 | chr19 | 2123609 | ||||||
chr19:2123621
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.906+209G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 10/31 | chr19 | 2123621 | ||||||
chr19:2123703
|
C | T | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.906+127G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 10/31 | chr19 | 2123703 | ||||||
chr19:2123713
|
G | C | 134 | a0001c0001t0001g0049a0001c0001t0001g0074a0001c0001t0001g0075others(131): Show | 134 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.906+117C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 10/31 | chr19 | 2123713 | ||||||
chr19:2123882
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | splice_region_variant&intron_variant | LOW | c.857-3C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2123882 | ||||||
chr19:2123929
|
C | T | 10 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(7): Show | 10 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.857-50G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2123929 | ||||||
chr19:2123994
|
C | A | 4 | a0002c0009t0002g0265a0002c0009t0002g0277a0002c0009t0002g0278others(1): Show | 4 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.857-115G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2123994 | ||||||
chr19:2124035
|
T | C | 6 | a0001c0003t0005g0114a0001c0003t0005g0207a0001c0003t0005g0211others(3): Show | 6 | HG02559.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.857-156A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124035 | ||||||
chr19:2124141
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.857-262C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124141 | ||||||
chr19:2124207
|
C | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0078others(49): Show | 53 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.857-328G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124207 | ||||||
chr19:2124223
|
A | G | 51 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0147others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.857-344T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124223 | ||||||
chr19:2124224
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-345C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124224 | ||||||
chr19:2124370
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-491G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124370 | ||||||
chr19:2124413
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0142 | 2 | HG02300.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.857-534C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124413 | ||||||
chr19:2124484
|
C | A | 5 | a0001c0001t0002g0096a0001c0001t0002g0098a0001c0001t0002g0103others(2): Show | 5 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.857-605G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124484 | ||||||
chr19:2124572
|
T | C | 1 | a0001c0001t0002g0103 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.857-693A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124572 | ||||||
chr19:2124575
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.857-696C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124575 | ||||||
chr19:2124678
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.857-799A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124678 | ||||||
chr19:2124808
|
A | G | 1 | a0001c0004t0002g0224 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.857-929T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124808 | ||||||
chr19:2124874
|
G | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-995C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124874 | ||||||
chr19:2124932
|
T | C | 1 | a0001c0001t0003g0379 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.857-1053A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124932 | ||||||
chr19:2124957
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.857-1078T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2124957 | ||||||
chr19:2125057
|
CACATAAA others(32): Show |
C | 1 | a0001c0002t0001g0323 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.857-1217_857-1179d others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125057 | ||||||
chr19:2125155
|
C | T | 2 | a0001c0001t0003g0355a0001c0001t0003g0360 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.857-1276G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125155 | ||||||
chr19:2125157
|
A | G | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.857-1278T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125157 | ||||||
chr19:2125278
|
C | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 6 | HG01109.hp1 HG02615.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.857-1399G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125278 | ||||||
chr19:2125325
|
C | T | 81 | a0001c0001t0001g0049a0001c0003t0001g0071a0001c0003t0001g0191others(78): Show | 81 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.857-1446G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125325 | ||||||
chr19:2125465
|
G | A | 1 | a0003c0024t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.857-1586C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125465 | ||||||
chr19:2125476
|
C | T | 2 | a0001c0004t0002g0216a0001c0004t0002g0218 | 2 | HG01123.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.857-1597G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125476 | ||||||
chr19:2125496
|
T | A | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.857-1617A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125496 | ||||||
chr19:2125599
|
G | A | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.856+1553C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125599 | ||||||
chr19:2125631
|
T | C | 1 | a0001c0006t0002g0314 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.856+1521A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125631 | ||||||
chr19:2125645
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.856+1507C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125645 | ||||||
chr19:2125724
|
C | T | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.856+1428G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125724 | ||||||
chr19:2125771
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.856+1381G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125771 | ||||||
chr19:2125806
|
T | C | 9 | a0001c0004t0002g0147a0001c0004t0002g0233a0001c0004t0002g0234others(6): Show | 9 | HG00323.hp1 HG00558.hp2 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.856+1346A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125806 | ||||||
chr19:2125835
|
G | GA | 145 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0001t0002g0205others(142): Show | 145 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.856+1316dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125835 | ||||||
chr19:2125857
|
G | A | 7 | a0001c0003t0005g0114a0001c0003t0005g0211a0001c0003t0005g0212others(4): Show | 7 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.856+1295C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125857 | ||||||
chr19:2125898
|
T | C | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.856+1254A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2125898 | ||||||
chr19:2126002
|
C | T | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.856+1150G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126002 | ||||||
chr19:2126039
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856+1113T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126039 | ||||||
chr19:2126107
|
G | A | 1 | a0002c0007t0004g0395 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.856+1045C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126107 | ||||||
chr19:2126150
|
C | CAAGTGAT others(86): Show |
5 | a0001c0008t0002g0184a0001c0008t0002g0185a0001c0008t0002g0253others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+909_856+1001du others(94): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126150 | ||||||
chr19:2126270
|
G | C | 4 | a0001c0003t0005g0211a0001c0003t0005g0212a0001c0011t0005g0209others(1): Show | 4 | HG02965.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+882C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126270 | ||||||
chr19:2126350
|
TCTGC | T | 7 | a0001c0001t0003g0351a0001c0001t0003g0365a0001c0001t0003g0370others(4): Show | 7 | HG00621.hp2 HG02071.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.856+798_856+801del others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126350 | ||||||
chr19:2126431
|
G | A | 65 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0003t0001g0071others(62): Show | 65 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.856+721C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126431 | ||||||
chr19:2126514
|
C | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.856+638G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126514 | ||||||
chr19:2126522
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.856+630G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126522 | ||||||
chr19:2126585
|
C | T | 1 | a0001c0010t0001g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.856+567G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126585 | ||||||
chr19:2126586
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.856+566C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126586 | ||||||
chr19:2126596
|
G | A | 1 | a0001c0003t0002g0046 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.856+556C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126596 | ||||||
chr19:2126609
|
C | T | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.856+543G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126609 | ||||||
chr19:2126640
|
G | A | 15 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(12): Show | 15 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.856+512C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126640 | ||||||
chr19:2126652
|
C | CA | 44 | a0001c0001t0001g0334a0001c0001t0003g0350a0001c0001t0003g0354others(41): Show | 44 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.856+499dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126652 | ||||||
chr19:2126652
|
C | CAA | 16 | a0001c0004t0002g0045a0001c0004t0002g0051a0001c0004t0002g0219others(13): Show | 16 | HG00438.hp1 HG00673.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.856+498_856+499dup others(2): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126652 | ||||||
chr19:2126652
|
CA | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0055others(18): Show | 21 | HG01074.hp2 HG01243.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.856+499delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126652 | ||||||
chr19:2126668
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.856+484T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126668 | ||||||
chr19:2126671
|
AG | A | 3 | a0001c0005t0002g0021a0001c0008t0002g0185a0002c0009t0002g0278 | 3 | HG02897.hp1 NA18977.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.856+480delC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126671 | ||||||
chr19:2126672
|
G | A | 132 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0003t0001g0071others(129): Show | 132 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.856+480C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126672 | ||||||
chr19:2126686
|
A | G | 2 | a0002c0007t0004g0392a0002c0007t0004g0393 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.856+466T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126686 | ||||||
chr19:2126753
|
T | C | 5 | a0001c0004t0002g0147a0001c0004t0002g0234a0001c0004t0002g0239others(2): Show | 5 | HG00558.hp2 NA18967.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.856+399A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126753 | ||||||
chr19:2126805
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.856+347C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2126805 | ||||||
chr19:2127022
|
G | A | 1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.856+130C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2127022 | ||||||
chr19:2127056
|
G | A | 3 | a0001c0001t0001g0072a0001c0004t0002g0220a0001c0004t0002g0228 | 3 | HG03453.hp2 NA18971.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.856+96C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2127056 | ||||||
chr19:2127141
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856+11G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2127141 | ||||||
chr19:2127142
|
C | T | 4 | a0001c0003t0005g0211a0001c0003t0005g0212a0001c0011t0005g0209others(1): Show | 4 | HG02965.hp1 HG03139.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.856+10G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 9/31 | chr19 | 2127142 | ||||||
chr19:2127257
|
G | A | 2 | a0001c0001t0001g0157a0001c0001t0001g0170 | 2 | NA18940.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.807-56C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127257 | ||||||
chr19:2127273
|
A | G | 154 | a0001c0001t0001g0049a0001c0001t0001g0180a0001c0001t0001g0328others(151): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.807-72T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127273 | ||||||
chr19:2127296
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.807-95G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127296 | ||||||
chr19:2127440
|
C | T | 1 | a0001c0002t0001g0288 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.807-239G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127440 | ||||||
chr19:2127441
|
G | A | 4 | a0001c0002t0001g0275a0001c0002t0001g0281a0001c0002t0001g0282others(1): Show | 4 | HG00597.hp1 HG02135.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.807-240C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127441 | ||||||
chr19:2127448
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.807-247G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127448 | ||||||
chr19:2127456
|
G | A | 1 | a0001c0008t0011g0399 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.807-255C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127456 | ||||||
chr19:2127465
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.807-264C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127465 | ||||||
chr19:2127466
|
C | T | 14 | a0001c0005t0002g0018a0001c0005t0002g0019a0001c0005t0002g0020others(11): Show | 14 | HG00597.hp2 HG00642.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.807-265G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127466 | ||||||
chr19:2127490
|
CT | C | 65 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0003t0001g0071others(62): Show | 65 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.807-290delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127490 | ||||||
chr19:2127494
|
C | G | 2 | a0001c0001t0003g0372a0001c0001t0003g0374 | 2 | NA18962.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.807-293G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127494 | ||||||
chr19:2127514
|
T | G | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.807-313A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127514 | ||||||
chr19:2127547
|
C | T | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.807-346G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127547 | ||||||
chr19:2127568
|
A | G | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.807-367T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127568 | ||||||
chr19:2127572
|
C | T | 3 | a0001c0003t0005g0211a0001c0011t0005g0209a0001c0011t0005g0210 | 3 | HG02965.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.807-371G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127572 | ||||||
chr19:2127573
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.807-372C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127573 | ||||||
chr19:2127610
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.807-409G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127610 | ||||||
chr19:2127628
|
G | T | 65 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0003t0001g0071others(62): Show | 65 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.807-427C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127628 | ||||||
chr19:2127698
|
T | C | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.807-497A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127698 | ||||||
chr19:2127791
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02647.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.807-590G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127791 | ||||||
chr19:2127824
|
G | C | 1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.807-623C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127824 | ||||||
chr19:2127832
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.807-631G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127832 | ||||||
chr19:2127909
|
C | G | 385 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(382): Show | 392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.807-708G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127909 | ||||||
chr19:2127937
|
C | T | 1 | a0001c0003t0005g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.807-736G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127937 | ||||||
chr19:2127939
|
C | T | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.807-738G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127939 | ||||||
chr19:2127960
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.807-759G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2127960 | ||||||
chr19:2128030
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.807-829G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128030 | ||||||
chr19:2128053
|
G | A | 15 | a0001c0001t0001g0263a0001c0002t0001g0259a0001c0002t0001g0261others(12): Show | 15 | HG03927.hp2 HG04199.hp1 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.807-852C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128053 | ||||||
chr19:2128055
|
C | T | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(314): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.807-854G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128055 | ||||||
chr19:2128065
|
C | G | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.807-864G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128065 | ||||||
chr19:2128102
|
C | T | 1 | a0001c0001t0003g0369 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.807-901G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128102 | ||||||
chr19:2128335
|
CG | C | 67 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0002t0001g0004others(64): Show | 68 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.806+754delC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128335 | ||||||
chr19:2128338
|
G | A | 67 | a0001c0001t0001g0049a0001c0001t0001g0328a0001c0002t0001g0004others(64): Show | 68 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.806+752C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128338 | ||||||
chr19:2128361
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.806+729G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128361 | ||||||
chr19:2128394
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.806+696C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128394 | ||||||
chr19:2128405
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.806+685C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128405 | ||||||
chr19:2128442
|
G | GCACTGCA others(32): Show |
1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.806+647_806+648ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(462): Show |
1 | a0001c0001t0001g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.806+647_806+648ins others(469): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(505): Show |
1 | a0001c0001t0001g0110 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(512): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(111): Show |
1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(32): Show |
8 | a0001c0001t0001g0111a0001c0003t0002g0196a0001c0004t0002g0051others(5): Show | 8 | HG00673.hp1 HG01123.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.806+647_806+648ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(71): Show |
1 | a0001c0004t0002g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.806+647_806+648ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(308): Show |
1 | a0001c0003t0005g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(315): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(72): Show |
7 | a0001c0003t0002g0329a0001c0004t0002g0213a0001c0004t0002g0214others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.806+647_806+648ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(112): Show |
1 | a0001c0003t0002g0326 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.806+647_806+648ins others(119): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(190): Show |
1 | a0001c0003t0002g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(197): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(191): Show |
1 | a0001c0003t0002g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(198): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(152): Show |
1 | a0001c0003t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(159): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(33): Show |
4 | a0001c0001t0001g0328a0001c0002t0001g0339a0001c0002t0001g0340others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+608_806+647dup others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(72): Show |
2 | a0001c0001t0001g0077a0001c0001t0003g0365 | 2 | HG01928.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.806+569_806+647dup others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(73): Show |
2 | a0001c0002t0001g0332a0001c0003t0002g0032 | 2 | NA18945.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.806+647_806+648ins others(80): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(113): Show |
2 | a0001c0001t0002g0013a0001c0002t0001g0261 | 2 | HG02258.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.806+647_806+648ins others(120): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(191): Show |
2 | a0001c0002t0001g0187a0001c0002t0001g0300 | 2 | NA18956.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.806+647_806+648ins others(198): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(193): Show |
1 | a0001c0001t0002g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.806+647_806+648ins others(200): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
G | GCACTGCA others(72): Show |
1 | a0001c0002t0001g0258 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.806+647_806+648ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(33): Show |
G | 13 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0120others(10): Show | 13 | HG00733.hp2 HG01243.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.806+608_806+647del others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(72): Show |
G | 15 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0085others(12): Show | 18 | HG00558.hp1 HG00621.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.806+569_806+647del others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(111): Show |
G | 2 | a0001c0001t0002g0103a0001c0004t0002g0239 | 2 | HG01884.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.806+530_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(151): Show |
G | 4 | a0001c0001t0001g0156a0001c0001t0003g0380a0001c0001t0003g0382others(1): Show | 4 | HG01934.hp2 HG02080.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+490_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(191): Show |
G | 2 | a0001c0001t0001g0157a0001c0001t0001g0177 | 2 | HG02074.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.806+450_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(230): Show |
G | 2 | a0001c0001t0001g0154a0005c0018t0001g0100 | 2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.806+411_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(270): Show |
G | 2 | a0001c0001t0001g0180a0001c0023t0005g0059 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.806+371_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(388): Show |
G | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.806+253_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(428): Show |
G | 4 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | NA18956.hp2 NA18979.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+213_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(468): Show |
G | 3 | a0001c0002t0001g0297a0001c0002t0001g0298a0001c0002t0001g0321 | 3 | HG00140.hp1 HG01255.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.806+173_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(508): Show |
G | 9 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0162others(6): Show | 9 | HG00423.hp1 HG00438.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+133_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128442
|
GCACTGCA others(548): Show |
G | 8 | a0001c0001t0001g0017a0001c0001t0001g0117a0001c0001t0001g0119others(5): Show | 8 | HG02523.hp1 NA18939.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.806+93_806+647del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128442 | ||||||
chr19:2128461
|
C | CGGCCCGC others(153): Show |
1 | a0001c0003t0002g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.806+628_806+629ins others(160): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128461 | ||||||
chr19:2128466
|
CG | C | 15 | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0089others(12): Show | 15 | HG01243.hp1 HG02132.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.806+623delC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128466 | ||||||
chr19:2128467
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0116 | 3 | HG01109.hp2 HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.806+623C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128467 | ||||||
chr19:2128467
|
G | GCCCCCGC others(472): Show |
1 | a0001c0002t0001g0324 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.806+622_806+623ins others(479): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128467 | ||||||
chr19:2128467
|
GC | G | 35 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(32): Show | 35 | HG01433.hp1 HG01516.hp1 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.806+622delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128467 | ||||||
chr19:2128467
|
GCCCCCGC others(112): Show |
G | 1 | a0001c0003t0005g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.806+504_806+622del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128467 | ||||||
chr19:2128468
|
C | A | 15 | a0001c0001t0001g0065a0001c0001t0001g0081a0001c0001t0001g0089others(12): Show | 15 | HG01243.hp1 HG02132.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.806+622G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128468 | ||||||
chr19:2128468
|
C | CCCCACAG others(31): Show |
3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0116 | 3 | HG01109.hp2 HG01358.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.806+621_806+622ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128468 | ||||||
chr19:2128468
|
C | CCCCACAG others(149): Show |
4 | a0001c0004t0002g0223a0001c0004t0002g0231a0001c0004t0002g0247others(1): Show | 4 | NA18981.hp1 NA18994.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+621_806+622ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128468 | ||||||
chr19:2128473
|
G | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 57 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(54): Show |
intron_variant | MODIFIER | c.806+617C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128473 | ||||||
chr19:2128475
|
C | A | 57 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0056others(54): Show | 57 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(54): Show |
intron_variant | MODIFIER | c.806+615G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(112): Show |
1 | a0001c0001t0002g0015 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.806+614_806+615ins others(119): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(228): Show |
2 | a0001c0003t0002g0026a0001c0003t0002g0027 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.806+614_806+615ins others(235): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(111): Show |
2 | a0001c0001t0001g0243a0001c0017t0003g0366 | 2 | HG02004.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.806+614_806+615ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(229): Show |
1 | a0001c0001t0003g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(236): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(111): Show |
1 | a0001c0003t0002g0050 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(72): Show |
3 | a0001c0002t0001g0342a0001c0004t0002g0045a0001c0006t0002g0308 | 3 | HG04199.hp2 NA18947.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.806+614_806+615ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(150): Show |
2 | a0001c0001t0001g0011a0001c0002t0001g0250 | 2 | HG00323.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.806+614_806+615ins others(157): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(346): Show |
1 | a0001c0006t0002g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.806+614_806+615ins others(353): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(229): Show |
1 | a0001c0001t0001g0095 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.806+614_806+615ins others(236): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(190): Show |
1 | a0001c0002t0001g0318 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.806+614_806+615ins others(197): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(229): Show |
1 | a0001c0010t0001g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(236): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(230): Show |
1 | a0001c0002t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(237): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(152): Show |
1 | a0001c0006t0002g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(159): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(191): Show |
1 | a0001c0002t0001g0275 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.806+614_806+615ins others(198): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(389): Show |
1 | a0001c0002t0001g0282 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(396): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
C | CGCTCCGA others(72): Show |
1 | a0001c0005t0002g0035 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.806+614_806+615ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
CGCTCCGA others(32): Show |
C | 11 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0124others(8): Show | 11 | HG00642.hp2 HG00738.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.806+576_806+614del others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
CGCTCCGA others(71): Show |
C | 22 | a0001c0001t0001g0263a0001c0001t0003g0356a0001c0002t0001g0003others(19): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.806+537_806+614del others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
CGCTCCGA others(190): Show |
C | 6 | a0001c0001t0003g0355a0001c0001t0003g0360a0001c0001t0003g0364others(3): Show | 6 | HG02300.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+418_806+614del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
CGCTCCGA others(269): Show |
C | 2 | a0001c0005t0002g0023a0002c0009t0002g0277 | 2 | HG00597.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.806+339_806+614del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128475
|
CGCTCCGA others(348): Show |
C | 1 | a0001c0001t0001g0336 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.806+260_806+614del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128475 | ||||||
chr19:2128481
|
GACACTGC others(428): Show |
G | 4 | a0001c0001t0001g0174a0001c0001t0001g0337a0001c0008t0011g0398others(1): Show | 4 | HG03471.hp1 HG04184.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+174_806+608del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128481 | ||||||
chr19:2128494
|
G | A | 2 | a0001c0002t0001g0303a0001c0002t0001g0304 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.806+596C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128494 | ||||||
chr19:2128501
|
C | CGGCCCGC others(268): Show |
1 | a0001c0002t0001g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.806+588_806+589ins others(275): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128501 | ||||||
chr19:2128501
|
C | CGGCCCGC others(586): Show |
1 | a0001c0002t0001g0281 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.806+588_806+589ins others(593): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128501 | ||||||
chr19:2128501
|
C | CGGCCCGC others(73): Show |
1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.806+588_806+589ins others(80): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128501 | ||||||
chr19:2128501
|
C | CGGCCCGC others(33): Show |
4 | a0001c0003t0002g0034a0001c0003t0009g0348a0001c0003t0009g0349others(1): Show | 4 | HG02083.hp2 NA18985.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+588_806+589ins others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128501 | ||||||
chr19:2128501
|
C | T | 3 | a0001c0001t0003g0359a0001c0005t0002g0021a0001c0005t0002g0044 | 3 | HG01981.hp1 NA18975.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.806+589G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128501 | ||||||
chr19:2128507
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0002g0063others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+583C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128507
|
G | GC | 77 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0093others(74): Show | 78 | HG00673.hp1 HG00733.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.806+582dupG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128507
|
G | GCCCCACA others(32): Show |
1 | a0001c0001t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.806+582_806+583ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128507
|
G | GCCCCCGC others(34): Show |
2 | a0001c0001t0001g0094a0001c0003t0002g0024 | 2 | HG00408.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.806+582_806+583ins others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128507
|
G | GCCCCCGC others(74): Show |
2 | a0001c0003t0002g0189a0001c0003t0002g0190 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.806+582_806+583ins others(81): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128507
|
G | GCCCCCGC others(73): Show |
1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.806+582_806+583ins others(80): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128507
|
G | T | 1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806+583C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128507 | ||||||
chr19:2128508
|
CCCCACAG others(150): Show |
C | 1 | a0001c0021t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.806+425_806+581del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128508 | ||||||
chr19:2128508
|
CCCCACAG others(308): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.806+267_806+581del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128508 | ||||||
chr19:2128512
|
A | G | 73 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0094others(70): Show | 74 | HG00408.hp1 HG00673.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.806+578T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128512 | ||||||
chr19:2128514
|
A | AGCTCCGA others(229): Show |
1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.806+575_806+576ins others(236): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(666): Show |
1 | a0001c0001t0001g0128 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.806+575_806+576ins others(673): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(33): Show |
4 | a0001c0001t0003g0351a0001c0001t0003g0368a0001c0001t0003g0375others(1): Show | 4 | HG00423.hp2 HG00621.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+575_806+576ins others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(190): Show |
1 | a0001c0001t0003g0370 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.806+575_806+576ins others(197): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(308): Show |
1 | a0001c0001t0003g0369 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.806+575_806+576ins others(315): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(73): Show |
1 | a0001c0001t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.806+575_806+576ins others(80): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(191): Show |
1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.806+575_806+576ins others(198): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(152): Show |
1 | a0001c0001t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.806+575_806+576ins others(159): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | AGCTCCGA others(33): Show |
1 | a0001c0001t0003g0378 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.806+575_806+576ins others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | C | 72 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0094others(69): Show | 73 | HG00408.hp1 HG00673.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.806+576T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
A | CGCTCCGA others(623): Show |
1 | a0001c0001t0002g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.806+576_806+577ins others(630): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
AGCTCCGA others(72): Show |
A | 2 | a0001c0001t0001g0142a0001c0002t0001g0004 | 3 | HG03669.hp2 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.806+497_806+575del others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
AGCTCCGA others(429): Show |
A | 1 | a0001c0002t0001g0295 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.806+140_806+575del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
AGCTCCGA others(469): Show |
A | 3 | a0001c0001t0001g0074a0001c0002t0001g0303a0001c0002t0001g0304 | 3 | HG02572.hp1 HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.806+100_806+575del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128514
|
AGCTCCGA others(509): Show |
A | 4 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0043others(1): Show | 4 | HG02258.hp1 NA18980.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+60_806+575del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128514 | ||||||
chr19:2128520
|
GACACTGC others(389): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.806+174_806+569del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128520 | ||||||
chr19:2128528
|
A | G | 3 | a0001c0001t0001g0011a0001c0001t0002g0015a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.806+562T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128528 | ||||||
chr19:2128540
|
C | CGGCCCGC others(73): Show |
1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.806+549_806+550ins others(80): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128540 | ||||||
chr19:2128540
|
C | T | 16 | a0001c0001t0001g0014a0001c0001t0001g0124a0001c0001t0001g0125others(13): Show | 16 | HG01928.hp2 HG01952.hp2 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.806+550G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128540 | ||||||
chr19:2128541
|
G | A | 1 | a0001c0003t0002g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.806+549C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128541 | ||||||
chr19:2128546
|
G | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0347a0001c0003t0002g0054others(3): Show | 6 | HG02630.hp2 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+544C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
G | C | 1 | a0001c0003t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806+544C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
G | GC | 38 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0066others(35): Show | 38 | HG01081.hp2 HG01175.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.806+543dupG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
G | GCCCCACA others(32): Show |
1 | a0001c0003t0002g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.806+543_806+544ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
G | GCCCCCGC others(74): Show |
1 | a0001c0003t0002g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.806+543_806+544ins others(81): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
G | GCCCCCGC others(193): Show |
1 | a0001c0003t0002g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.806+543_806+544ins others(200): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
G | T | 1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.806+544C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128546
|
GCCCCACA others(390): Show |
G | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.806+147_806+543del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128546 | ||||||
chr19:2128547
|
CCCCACAG others(150): Show |
C | 1 | a0001c0002t0001g0306 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.806+386_806+542del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128547 | ||||||
chr19:2128549
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0347 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.806+541G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128549 | ||||||
chr19:2128551
|
A | G | 52 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0066others(49): Show | 52 | HG00733.hp1 HG01081.hp2 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.806+539T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128551 | ||||||
chr19:2128553
|
A | AGCTCCGA others(71): Show |
1 | a0001c0004t0002g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.806+536_806+537ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128553 | ||||||
chr19:2128553
|
A | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0057a0001c0001t0001g0066others(49): Show | 52 | HG00733.hp1 HG01081.hp2 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.806+537T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128553 | ||||||
chr19:2128553
|
AGCTCCGA others(33): Show |
A | 6 | a0001c0001t0001g0085a0001c0001t0001g0112a0001c0001t0002g0063others(3): Show | 6 | HG01243.hp2 HG01978.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+497_806+536del others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128553 | ||||||
chr19:2128553
|
AGCTCCGA others(231): Show |
A | 1 | a0001c0001t0003g0357 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.806+299_806+536del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128553 | ||||||
chr19:2128553
|
AGCTCCGA others(430): Show |
A | 9 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0002g0096others(6): Show | 9 | HG01175.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+100_806+536del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128553 | ||||||
chr19:2128553
|
AGCTCCGA others(470): Show |
A | 3 | a0001c0001t0001g0070a0001c0008t0002g0184a0001c0008t0002g0185 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.806+60_806+536del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128553 | ||||||
chr19:2128567
|
A | G | 1 | a0001c0008t0011g0399 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.806+523T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128567 | ||||||
chr19:2128579
|
C | T | 7 | a0001c0001t0003g0352a0001c0001t0003g0353a0001c0001t0003g0362others(4): Show | 7 | HG01256.hp1 HG02027.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.806+511G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128579 | ||||||
chr19:2128580
|
G | A | 3 | a0001c0003t0002g0199a0001c0003t0002g0325a0001c0006t0002g0009 | 3 | HG02145.hp1 HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.806+510C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128580 | ||||||
chr19:2128584
|
CGCCCCCG others(34): Show |
C | 2 | a0001c0001t0001g0143a0001c0003t0002g0188 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.806+465_806+505del others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128584 | ||||||
chr19:2128585
|
GC | G | 93 | a0001c0001t0001g0049a0001c0001t0001g0078a0001c0001t0001g0088others(90): Show | 94 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.806+504delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128585 | ||||||
chr19:2128585
|
GCCCCCGC others(34): Show |
G | 13 | a0001c0001t0001g0069a0001c0001t0001g0149a0001c0001t0001g0170others(10): Show | 13 | HG01361.hp1 HG01993.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+464_806+504del others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128585 | ||||||
chr19:2128585
|
GCCCCCGC others(113): Show |
G | 1 | a0001c0012t0007g0183 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.806+385_806+504del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128585 | ||||||
chr19:2128585
|
GCCCCCGC others(192): Show |
G | 2 | a0001c0005t0002g0047a0001c0008t0002g0181 | 2 | HG01928.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.806+306_806+504del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128585 | ||||||
chr19:2128585
|
GCCCCCGC others(351): Show |
G | 3 | a0001c0001t0001g0068a0001c0001t0001g0072a0001c0008t0002g0253 | 3 | HG02300.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.806+147_806+504del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128585 | ||||||
chr19:2128585
|
GCCCCCGC others(391): Show |
G | 16 | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0001g0155others(13): Show | 16 | HG00099.hp2 HG00408.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.806+107_806+504del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128585 | ||||||
chr19:2128586
|
C | A | 1 | a0002c0009t0002g0278 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.806+504G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128586 | ||||||
chr19:2128586
|
C | CCCCACAG others(70): Show |
1 | a0001c0001t0001g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.806+503_806+504ins others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128586 | ||||||
chr19:2128586
|
C | CCCCACAG others(31): Show |
1 | a0001c0001t0001g0118 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.806+503_806+504ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128586 | ||||||
chr19:2128586
|
C | CCCCACAG others(188): Show |
1 | a0001c0001t0002g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806+503_806+504ins others(195): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128586 | ||||||
chr19:2128586
|
C | CCCCACAG others(71): Show |
1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806+503_806+504ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128586 | ||||||
chr19:2128586
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.806+504G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128586 | ||||||
chr19:2128589
|
C | T | 1 | a0001c0001t0003g0350 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.806+501G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128589 | ||||||
chr19:2128591
|
G | A | 100 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0078others(97): Show | 101 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.806+499C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128591 | ||||||
chr19:2128593
|
C | A | 100 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0078others(97): Show | 101 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.806+497G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128593 | ||||||
chr19:2128593
|
C | CGCTCCGA others(32): Show |
3 | a0001c0001t0001g0084a0001c0001t0002g0062a0001c0002t0001g0281 | 3 | HG01981.hp2 HG02055.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.806+496_806+497ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128593 | ||||||
chr19:2128593
|
C | CGCTCCGA others(228): Show |
1 | a0001c0003t0005g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.806+496_806+497ins others(235): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128593 | ||||||
chr19:2128593
|
C | CGCTCCGA others(191): Show |
1 | a0001c0003t0002g0194 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.806+496_806+497ins others(198): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128593 | ||||||
chr19:2128593
|
CGCTCCGA others(151): Show |
C | 1 | a0001c0003t0002g0192 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.806+339_806+496del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128593 | ||||||
chr19:2128599
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.806+491C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128599 | ||||||
chr19:2128604
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.806+486A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128604 | ||||||
chr19:2128608
|
C | T | 2 | a0001c0002t0001g0255a0001c0002t0001g0302 | 2 | HG00735.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.806+482G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128608 | ||||||
chr19:2128612
|
G | A | 2 | a0001c0004t0002g0045a0001c0006t0002g0308 | 2 | NA18947.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.806+478C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128612 | ||||||
chr19:2128619
|
C | T | 3 | a0001c0001t0003g0359a0001c0001t0003g0370a0001c0002t0001g0250 | 3 | HG00323.hp2 HG01981.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.806+471G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128619 | ||||||
chr19:2128620
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+470C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128620 | ||||||
chr19:2128625
|
GC | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(109): Show | 116 | HG00280.hp2 HG00558.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.806+464delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128625 | ||||||
chr19:2128625
|
GCCCCCGC others(271): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.806+187_806+464del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128625 | ||||||
chr19:2128625
|
GCCCCCGC others(311): Show |
G | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.806+147_806+464del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128625 | ||||||
chr19:2128625
|
GCCCCCGC others(391): Show |
G | 1 | a0001c0001t0003g0362 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.806+67_806+464del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128625 | ||||||
chr19:2128626
|
C | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0143a0001c0001t0003g0356others(1): Show | 4 | HG02818.hp1 HG02818.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+464G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128626 | ||||||
chr19:2128626
|
C | CCCCACAG others(344): Show |
1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.806+463_806+464ins others(351): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128626 | ||||||
chr19:2128626
|
C | CCCCACAG others(31): Show |
5 | a0001c0001t0001g0347a0001c0001t0003g0359a0001c0002t0001g0250others(2): Show | 5 | HG00323.hp2 HG01981.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.806+463_806+464ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128626 | ||||||
chr19:2128626
|
C | CCCCACAG others(70): Show |
2 | a0001c0004t0002g0045a0001c0006t0002g0308 | 2 | NA18947.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.806+463_806+464ins others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128626 | ||||||
chr19:2128626
|
C | CCCCACAG others(187): Show |
1 | a0001c0006t0002g0317 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.806+463_806+464ins others(194): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128626 | ||||||
chr19:2128629
|
C | T | 2 | a0001c0001t0001g0143a0001c0003t0002g0188 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.806+461G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128629 | ||||||
chr19:2128630
|
C | T | 1 | a0001c0003t0005g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.806+460G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128630 | ||||||
chr19:2128631
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(131): Show | 138 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.806+459C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128631 | ||||||
chr19:2128633
|
C | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(130): Show | 137 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.806+457G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128633
|
C | CGCTCCGA others(32): Show |
1 | a0001c0001t0001g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.806+418_806+456dup others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128633
|
C | CGCTCCGA others(383): Show |
1 | a0001c0001t0002g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.806+456_806+457ins others(390): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128633
|
C | CGCTCCGA others(72): Show |
2 | a0001c0001t0001g0060a0001c0004t0002g0224 | 2 | HG02896.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.806+456_806+457ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128633
|
C | CGCTCCGA others(467): Show |
1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+456_806+457ins others(474): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128633
|
C | CGCTCCGA others(779): Show |
1 | a0001c0003t0002g0326 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.806+456_806+457ins others(786): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128633
|
CGCTCCGA others(32): Show |
C | 1 | a0001c0001t0001g0138 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.806+418_806+456del others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128633 | ||||||
chr19:2128639
|
G | A | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.806+451C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128639 | ||||||
chr19:2128643
|
C | G | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.806+447G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128643 | ||||||
chr19:2128659
|
C | T | 12 | a0001c0002t0001g0004a0001c0003t0002g0028a0001c0003t0002g0034others(9): Show | 13 | HG01952.hp2 HG02040.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+431G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128659 | ||||||
chr19:2128665
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0347a0001c0003t0002g0196 | 3 | HG02280.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.806+425C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128665 | ||||||
chr19:2128665
|
G | GC | 22 | a0001c0001t0001g0093a0001c0001t0001g0130a0001c0001t0001g0202others(19): Show | 23 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.806+424dupG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128665 | ||||||
chr19:2128665
|
G | GCCCCCGC others(232): Show |
2 | a0001c0003t0009g0348a0001c0003t0009g0349 | 2 | NA19005.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.806+424_806+425ins others(239): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128665 | ||||||
chr19:2128665
|
G | GCCCCCGC others(153): Show |
1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.806+424_806+425ins others(160): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128665 | ||||||
chr19:2128668
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0347 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.806+422G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128668 | ||||||
chr19:2128670
|
A | G | 24 | a0001c0001t0001g0202a0001c0001t0003g0378a0001c0001t0006g0137others(21): Show | 25 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.806+420T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128670 | ||||||
chr19:2128672
|
A | AGCTCCGA others(33): Show |
1 | a0001c0003t0002g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.806+417_806+418ins others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
A | AGCTCCGA others(72): Show |
2 | a0001c0001t0001g0088a0001c0001t0001g0140 | 2 | HG01071.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.806+417_806+418ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
A | AGCTCCGA others(33): Show |
1 | a0001c0001t0002g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.806+378_806+417dup others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
A | C | 25 | a0001c0001t0001g0202a0001c0001t0003g0378a0001c0001t0006g0137others(22): Show | 26 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.806+418T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
AGCTCCGA others(33): Show |
A | 6 | a0001c0001t0001g0002a0001c0001t0001g0134a0001c0002t0001g0003others(3): Show | 8 | HG00140.hp2 HG01074.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.806+378_806+417del others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
AGCTCCGA others(112): Show |
A | 1 | a0001c0001t0003g0371 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.806+299_806+417del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
AGCTCCGA others(271): Show |
A | 1 | a0001c0002t0001g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.806+140_806+417del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
AGCTCCGA others(311): Show |
A | 2 | a0001c0001t0001g0122a0001c0002t0001g0289 | 2 | HG00280.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.806+100_806+417del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128672
|
AGCTCCGA others(351): Show |
A | 1 | a0002c0007t0004g0391 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.806+60_806+417del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128672 | ||||||
chr19:2128678
|
G | A | 1 | a0001c0021t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.806+412C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128678 | ||||||
chr19:2128679
|
A | G | 1 | a0001c0021t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.806+411T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128679 | ||||||
chr19:2128686
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+404T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128686 | ||||||
chr19:2128698
|
C | T | 7 | a0001c0001t0003g0005a0001c0001t0003g0353a0001c0001t0003g0358others(4): Show | 8 | HG01256.hp1 HG02080.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.806+392G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128698 | ||||||
chr19:2128703
|
C | T | 1 | a0001c0001t0003g0361 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.806+387G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128703 | ||||||
chr19:2128703
|
CG | C | 3 | a0001c0001t0002g0015a0001c0001t0002g0063a0001c0011t0005g0210 | 3 | HG01243.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.806+386delC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128703 | ||||||
chr19:2128704
|
GC | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(116): Show | 122 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.806+385delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128704 | ||||||
chr19:2128704
|
GCCCCCGC others(232): Show |
G | 1 | a0001c0001t0003g0350 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.806+147_806+385del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128704 | ||||||
chr19:2128704
|
GCCCCCGC others(272): Show |
G | 1 | a0001c0003t0005g0212 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.806+107_806+385del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128704 | ||||||
chr19:2128704
|
GCCCCCGC others(312): Show |
G | 4 | a0001c0004t0002g0240a0001c0004t0002g0248a0001c0020t0002g0232others(1): Show | 4 | NA18966.hp2 NA18970.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+67_806+385del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128704 | ||||||
chr19:2128705
|
C | A | 3 | a0001c0001t0002g0015a0001c0001t0002g0063a0001c0011t0005g0210 | 3 | HG01243.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.806+385G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(31): Show |
3 | a0001c0002t0001g0324a0001c0003t0002g0034a0001c0003t0002g0208 | 3 | HG02083.hp2 HG02135.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.806+384_806+385ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(70): Show |
1 | a0001c0006t0002g0330 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.806+384_806+385ins others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(109): Show |
1 | a0001c0002t0001g0307 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.806+384_806+385ins others(116): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(187): Show |
1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.806+384_806+385ins others(194): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(463): Show |
1 | a0001c0004t0002g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.806+384_806+385ins others(470): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(503): Show |
1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.806+384_806+385ins others(510): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(149): Show |
1 | a0001c0002t0001g0275 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.806+384_806+385ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(149): Show |
1 | a0001c0003t0002g0024 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.806+384_806+385ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(149): Show |
1 | a0001c0001t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.806+384_806+385ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(111): Show |
1 | a0001c0001t0002g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.806+384_806+385ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128705
|
C | CCCCACAG others(460): Show |
1 | a0001c0001t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+384_806+385ins others(467): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128705 | ||||||
chr19:2128710
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(133): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.806+380C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128710 | ||||||
chr19:2128712
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(132): Show | 139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.806+378G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
C | CGCTCCGA others(32): Show |
3 | a0001c0001t0001g0243a0001c0001t0003g0370a0001c0002t0001g0291 | 3 | HG01081.hp2 HG02004.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.806+339_806+377dup others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
C | CGCTCCGA others(269): Show |
1 | a0001c0001t0002g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.806+377_806+378ins others(276): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
C | CGCTCCGA others(72): Show |
1 | a0001c0010t0001g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.806+377_806+378ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
C | CGCTCCGA others(584): Show |
1 | a0003c0024t0001g0283 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.806+377_806+378ins others(591): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
C | CGCTCCGA others(112): Show |
1 | a0001c0003t0002g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.806+377_806+378ins others(119): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
C | CGCTCCGA others(189): Show |
1 | a0001c0001t0003g0361 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.806+377_806+378ins others(196): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128712
|
CGCTCCGA others(32): Show |
C | 7 | a0001c0001t0001g0133a0001c0001t0001g0142a0001c0001t0001g0179others(4): Show | 7 | HG02615.hp2 HG03225.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.806+339_806+377del others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128712 | ||||||
chr19:2128718
|
G | A | 3 | a0001c0001t0001g0011a0001c0011t0005g0209a0001c0021t0001g0165 | 3 | HG02132.hp1 HG02486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.806+372C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128718 | ||||||
chr19:2128718
|
GACACTGC others(191): Show |
G | 1 | a0001c0001t0001g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.806+174_806+371del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128718 | ||||||
chr19:2128719
|
A | G | 1 | a0001c0021t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.806+371T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128719 | ||||||
chr19:2128726
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+364T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128726 | ||||||
chr19:2128738
|
C | T | 11 | a0001c0002t0001g0187a0001c0002t0001g0282a0001c0003t0001g0191others(8): Show | 11 | HG00597.hp1 HG00642.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.806+352G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128738 | ||||||
chr19:2128739
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+351C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128739 | ||||||
chr19:2128744
|
G | A | 1 | a0001c0003t0002g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.806+346C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128744 | ||||||
chr19:2128744
|
G | GC | 31 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0065others(28): Show | 31 | HG00738.hp2 HG01071.hp1 HG01516.hp2 others(28): Show |
intron_variant | MODIFIER | c.806+345dupG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128744 | ||||||
chr19:2128745
|
CCCCACAG others(71): Show |
C | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.806+267_806+344del others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128745 | ||||||
chr19:2128749
|
A | G | 30 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0065others(27): Show | 30 | HG00738.hp2 HG01071.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.806+341T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128749 | ||||||
chr19:2128751
|
A | AGCTCCGA others(72): Show |
1 | a0001c0002t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.806+338_806+339ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
A | AGCTCCGA others(232): Show |
1 | a0001c0002t0001g0258 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.806+338_806+339ins others(239): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
A | AGCTCCGA others(33): Show |
1 | a0001c0001t0003g0359 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.806+299_806+338dup others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
A | AGCTCCGA others(111): Show |
2 | a0001c0003t0002g0026a0001c0003t0002g0027 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.806+338_806+339ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
A | C | 29 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0065others(26): Show | 29 | HG00738.hp2 HG01071.hp1 HG01516.hp2 others(26): Show |
intron_variant | MODIFIER | c.806+339T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
AGCTCCGA others(33): Show |
A | 9 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0132others(6): Show | 10 | HG01433.hp2 HG02129.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.806+299_806+338del others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
AGCTCCGA others(232): Show |
A | 13 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0099others(10): Show | 15 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.806+100_806+338del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128751
|
AGCTCCGA others(272): Show |
A | 2 | a0001c0001t0003g0385a0002c0007t0004g0386 | 2 | HG02735.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.806+60_806+338del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128751 | ||||||
chr19:2128757
|
GACACTGC others(152): Show |
G | 1 | a0001c0003t0002g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.806+174_806+332del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128757 | ||||||
chr19:2128765
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+325T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128765 | ||||||
chr19:2128777
|
C | T | 1 | a0001c0003t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806+313G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128777 | ||||||
chr19:2128783
|
GC | G | 103 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0069others(100): Show | 105 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.806+306delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128783 | ||||||
chr19:2128783
|
GCCCCCGC others(113): Show |
G | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0175others(1): Show | 4 | HG03017.hp1 NA18973.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+187_806+306del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128783 | ||||||
chr19:2128783
|
GCCCCCGC others(153): Show |
G | 2 | a0001c0001t0003g0353a0001c0001t0003g0379 | 2 | HG01256.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.806+147_806+306del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128783 | ||||||
chr19:2128783
|
GCCCCCGC others(193): Show |
G | 7 | a0001c0001t0001g0113a0001c0001t0001g0149a0001c0001t0001g0176others(4): Show | 7 | HG02293.hp1 NA18747.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.806+107_806+306del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128783 | ||||||
chr19:2128783
|
GCCCCCGC others(233): Show |
G | 2 | a0002c0007t0004g0390a0002c0007t0004g0394 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.806+67_806+306del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128783 | ||||||
chr19:2128784
|
C | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.806+306G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(265): Show |
1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.806+305_806+306ins others(272): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(31): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0101a0001c0001t0003g0376others(4): Show | 7 | HG00438.hp1 HG00673.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.806+305_806+306ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(187): Show |
1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.806+305_806+306ins others(194): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(265): Show |
1 | a0001c0001t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.806+305_806+306ins others(272): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(306): Show |
1 | a0001c0001t0002g0012 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.806+305_806+306ins others(313): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(895): Show |
1 | a0001c0004t0002g0220 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.806+305_806+306ins others(902): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(150): Show |
2 | a0001c0002t0001g0331a0001c0002t0001g0332 | 2 | NA18945.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.806+305_806+306ins others(157): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(307): Show |
1 | a0001c0003t0002g0050 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.806+305_806+306ins others(314): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCACAG others(461): Show |
1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.806+305_806+306ins others(468): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
C | CCCCCGCC others(150): Show |
1 | a0001c0001t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.806+305_806+306ins others(157): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128784
|
CCCCCGCC others(32): Show |
C | 1 | a0001c0003t0002g0327 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.806+267_806+305del others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128784 | ||||||
chr19:2128789
|
G | A | 123 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(120): Show | 125 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.806+301C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128789 | ||||||
chr19:2128791
|
C | A | 123 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0057others(120): Show | 125 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.806+299G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(32): Show |
1 | a0001c0001t0001g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.806+298_806+299ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(32): Show |
3 | a0001c0001t0001g0065a0001c0003t0002g0195a0001c0003t0005g0114 | 3 | HG02559.hp1 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.806+260_806+298dup others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(424): Show |
1 | a0001c0002t0001g0300 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.806+298_806+299ins others(431): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(580): Show |
1 | a0001c0006t0002g0311 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.806+298_806+299ins others(587): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(72): Show |
2 | a0001c0003t0002g0189a0001c0003t0002g0190 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.806+298_806+299ins others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(111): Show |
2 | a0001c0001t0001g0328a0001c0003t0002g0194 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.806+298_806+299ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
C | CGCTCCGA others(266): Show |
1 | a0001c0004t0002g0228 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.806+298_806+299ins others(273): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128791
|
CGCTCCGA others(32): Show |
C | 2 | a0001c0001t0001g0112a0001c0003t0002g0037 | 2 | HG01978.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.806+260_806+298del others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128791 | ||||||
chr19:2128797
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.806+293C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128797 | ||||||
chr19:2128805
|
A | G | 1 | a0001c0001t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+285T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128805 | ||||||
chr19:2128817
|
C | T | 24 | a0001c0002t0001g0252a0001c0002t0001g0268a0001c0002t0001g0269others(21): Show | 24 | HG00597.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.806+273G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128817 | ||||||
chr19:2128823
|
G | A | 3 | a0001c0001t0001g0204a0001c0003t0002g0053a0001c0011t0005g0210 | 3 | HG02965.hp1 NA18983.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.806+267C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128823 | ||||||
chr19:2128823
|
G | GC | 24 | a0001c0001t0001g0049a0001c0001t0001g0081a0001c0001t0001g0086others(21): Show | 24 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.806+266dupG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128823 | ||||||
chr19:2128823
|
G | GCCCCACA others(149): Show |
1 | a0001c0001t0001g0347 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.806+266_806+267ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128823 | ||||||
chr19:2128823
|
GCCCCACA others(33): Show |
G | 1 | a0001c0004t0002g0222 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.806+227_806+266del others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128823 | ||||||
chr19:2128826
|
C | CCACAGCT others(32): Show |
1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.806+263_806+264ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128826 | ||||||
chr19:2128826
|
C | T | 1 | a0001c0006t0002g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.806+264G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128826 | ||||||
chr19:2128828
|
A | G | 30 | a0001c0001t0001g0049a0001c0001t0001g0081a0001c0001t0001g0086others(27): Show | 30 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.806+262T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128828 | ||||||
chr19:2128830
|
A | AGCTCCGA others(584): Show |
1 | a0001c0001t0002g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806+259_806+260ins others(591): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128830 | ||||||
chr19:2128830
|
A | C | 31 | a0001c0001t0001g0049a0001c0001t0001g0081a0001c0001t0001g0086others(28): Show | 31 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.806+260T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128830 | ||||||
chr19:2128830
|
AGCTCCGA others(113): Show |
A | 3 | a0001c0003t0002g0188a0001c0005t0002g0019a0001c0005t0002g0029 | 3 | HG00642.hp1 HG01070.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.806+140_806+259del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128830 | ||||||
chr19:2128830
|
AGCTCCGA others(153): Show |
A | 8 | a0001c0001t0001g0010a0001c0001t0001g0136a0001c0001t0001g0180others(5): Show | 8 | HG00642.hp2 HG00733.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.806+100_806+259del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128830 | ||||||
chr19:2128830
|
AGCTCCGA others(193): Show |
A | 2 | a0001c0001t0006g0123a0001c0023t0005g0059 | 2 | HG02622.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.806+60_806+259del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128830 | ||||||
chr19:2128836
|
GACACTGC others(73): Show |
G | 1 | a0001c0001t0002g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.806+174_806+253del others(80): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128836 | ||||||
chr19:2128856
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0093a0001c0001t0001g0130others(1): Show | 4 | HG00738.hp2 HG02015.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+234G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128856 | ||||||
chr19:2128857
|
G | GGCCCGCC others(230): Show |
1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.806+232_806+233ins others(237): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128857 | ||||||
chr19:2128862
|
GC | G | 81 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0060others(78): Show | 81 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.806+227delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128862 | ||||||
chr19:2128862
|
GCCCCCGC others(34): Show |
G | 2 | a0001c0001t0001g0002a0001c0001t0002g0098 | 3 | HG01109.hp1 HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.806+187_806+227del others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128862 | ||||||
chr19:2128862
|
GCCCCCGC others(74): Show |
G | 12 | a0001c0001t0001g0093a0001c0001t0001g0121a0001c0001t0001g0130others(9): Show | 13 | HG00140.hp2 HG01168.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+147_806+227del others(81): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128862 | ||||||
chr19:2128862
|
GCCCCCGC others(114): Show |
G | 12 | a0001c0001t0001g0134a0001c0001t0001g0138a0001c0001t0001g0154others(9): Show | 13 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.806+107_806+227del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128862 | ||||||
chr19:2128862
|
GCCCCCGC others(154): Show |
G | 4 | a0001c0004t0002g0233a0001c0004t0002g0234a0001c0004t0002g0239others(1): Show | 4 | HG00323.hp1 HG00558.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+67_806+227del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128862 | ||||||
chr19:2128863
|
C | CCCCACAG others(31): Show |
3 | a0001c0001t0001g0011a0001c0004t0002g0247a0004c0013t0002g0245 | 3 | HG02486.hp1 NA18981.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.806+226_806+227ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128863 | ||||||
chr19:2128863
|
C | CCCCACAG others(70): Show |
1 | a0001c0003t0001g0191 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.806+226_806+227ins others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128863 | ||||||
chr19:2128863
|
C | CCCCACAG others(109): Show |
2 | a0001c0004t0002g0223a0001c0004t0002g0231 | 2 | NA19010.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.806+226_806+227ins others(116): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128863 | ||||||
chr19:2128863
|
C | CCCCACAG others(581): Show |
1 | a0001c0017t0003g0366 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.806+226_806+227ins others(588): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128863 | ||||||
chr19:2128863
|
C | CCCCACAG others(148): Show |
1 | a0001c0002t0001g0341 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.806+226_806+227ins others(155): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128863 | ||||||
chr19:2128868
|
G | A | 80 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0060others(77): Show | 80 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.806+222C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128868 | ||||||
chr19:2128868
|
GCCGCTCC others(193): Show |
G | 2 | a0001c0001t0001g0157a0001c0004t0002g0246 | 2 | NA18954.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.806+22_806+221del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128868 | ||||||
chr19:2128870
|
C | A | 79 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0060others(76): Show | 79 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.806+220G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCAA others(228): Show |
1 | a0001c0001t0001g0014 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.806+219_806+220ins others(235): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(32): Show |
1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.806+219_806+220ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(32): Show |
2 | a0001c0001t0001g0328a0001c0003t0002g0195 | 2 | HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.806+219_806+220ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(71): Show |
2 | a0001c0001t0001g0094a0001c0001t0001g0141 | 2 | NA18906.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.806+219_806+220ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(110): Show |
1 | a0001c0001t0002g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.806+219_806+220ins others(117): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(1366): Show |
1 | a0001c0004t0002g0229 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.806+219_806+220ins others(1373): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(1217): Show |
1 | a0001c0004t0002g0221 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.806+219_806+220ins others(1224): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(1639): Show |
1 | a0001c0004t0002g0227 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.806+219_806+220ins others(1646): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128870
|
C | CGCTCCGA others(270): Show |
1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806+219_806+220ins others(277): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128870 | ||||||
chr19:2128876
|
GACACTGC others(33): Show |
G | 1 | a0001c0016t0002g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.806+174_806+213del others(40): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128876 | ||||||
chr19:2128896
|
C | CGGCCCGC others(32): Show |
1 | a0001c0001t0003g0359 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.806+193_806+194ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128896 | ||||||
chr19:2128896
|
C | T | 14 | a0001c0001t0003g0358a0001c0001t0003g0380a0001c0001t0003g0382others(11): Show | 14 | HG00597.hp1 HG01074.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.806+194G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128896 | ||||||
chr19:2128897
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0346 | 2 | HG02630.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.806+193C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128897 | ||||||
chr19:2128901
|
CG | C | 3 | a0001c0003t0002g0054a0001c0003t0002g0249a0001c0003t0002g0343 | 3 | NA18957.hp1 NA18995.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.806+188delC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128901 | ||||||
chr19:2128902
|
G | A | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.806+188C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128902 | ||||||
chr19:2128902
|
GC | G | 90 | a0001c0001t0001g0011a0001c0001t0001g0055a0001c0001t0001g0060others(87): Show | 91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.806+187delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128902 | ||||||
chr19:2128902
|
GCCCCCGC others(34): Show |
G | 8 | a0001c0001t0001g0143a0001c0001t0001g0168a0001c0001t0001g0170others(5): Show | 8 | HG02074.hp2 HG02818.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.806+147_806+187del others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128902 | ||||||
chr19:2128903
|
C | A | 3 | a0001c0003t0002g0054a0001c0003t0002g0249a0001c0003t0002g0343 | 3 | NA18957.hp1 NA18995.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.806+187G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128903
|
C | CCCCACAG others(31): Show |
3 | a0001c0002t0001g0291a0001c0002t0001g0339a0001c0002t0001g0340 | 3 | HG01070.hp1 HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.806+186_806+187ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128903
|
C | CCCCACAG others(148): Show |
1 | a0001c0001t0003g0370 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.806+186_806+187ins others(155): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128903
|
C | CCCCACAG others(502): Show |
1 | a0001c0001t0001g0091 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.806+186_806+187ins others(509): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128903
|
C | CCCCACAG others(385): Show |
1 | a0001c0003t0002g0326 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.806+186_806+187ins others(392): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128903
|
C | CCCCACAG others(190): Show |
1 | a0001c0002t0001g0282 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.806+186_806+187ins others(197): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128903
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.806+187G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128903 | ||||||
chr19:2128908
|
G | A | 114 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0055others(111): Show | 117 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.806+182C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128908 | ||||||
chr19:2128908
|
GCCGCTCC others(153): Show |
G | 4 | a0001c0001t0001g0069a0001c0001t0001g0169a0001c0001t0001g0177others(1): Show | 4 | HG01993.hp2 HG02074.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+22_806+181del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128908 | ||||||
chr19:2128910
|
C | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0055others(110): Show | 116 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.806+180G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128910 | ||||||
chr19:2128910
|
C | CGCTCCGA others(32): Show |
1 | a0001c0003t0002g0052 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.806+179_806+180ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128910 | ||||||
chr19:2128910
|
C | CGCTCCGA others(71): Show |
2 | a0001c0001t0001g0116a0001c0003t0002g0193 | 2 | HG01109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.806+179_806+180ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128910 | ||||||
chr19:2128910
|
C | CGCTCCGA others(543): Show |
1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.806+179_806+180ins others(550): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128910 | ||||||
chr19:2128910
|
C | CGCTCCGA others(71): Show |
2 | a0001c0001t0001g0077a0001c0022t0001g0082 | 2 | HG01346.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.806+179_806+180ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128910 | ||||||
chr19:2128915
|
C | T | 1 | a0001c0005t0002g0022 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.806+175G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128915 | ||||||
chr19:2128916
|
A | G | 227 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0011others(224): Show | 230 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.806+174T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128916 | ||||||
chr19:2128916
|
AACACTGC others(73): Show |
A | 1 | a0001c0021t0001g0165 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.806+94_806+173delC others(79): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128916 | ||||||
chr19:2128917
|
A | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | NA18956.hp2 NA18979.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+173T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128917 | ||||||
chr19:2128924
|
A | G | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.806+166T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128924 | ||||||
chr19:2128936
|
C | T | 7 | a0001c0001t0001g0049a0001c0001t0001g0090a0001c0001t0001g0336others(4): Show | 7 | HG00738.hp2 HG01928.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.806+154G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128936 | ||||||
chr19:2128942
|
GC | G | 85 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0055others(82): Show | 87 | HG00323.hp2 HG00423.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.806+147delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128942 | ||||||
chr19:2128942
|
GCCCCCGC others(34): Show |
G | 2 | a0001c0001t0001g0085a0001c0011t0005g0209 | 2 | HG02040.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.806+107_806+147del others(41): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128942 | ||||||
chr19:2128943
|
C | A | 1 | a0001c0003t0002g0053 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.806+147G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(31): Show |
3 | a0001c0004t0002g0226a0001c0004t0002g0230a0001c0004t0002g0238 | 3 | HG01433.hp1 HG02293.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.806+146_806+147ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(70): Show |
1 | a0001c0001t0001g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(344): Show |
1 | a0001c0001t0003g0365 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(351): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(227): Show |
1 | a0001c0010t0001g0286 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(234): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(267): Show |
1 | a0001c0001t0001g0110 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(274): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(149): Show |
1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(227): Show |
1 | a0001c0003t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(234): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(110): Show |
1 | a0001c0001t0001g0111 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(117): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCACAG others(189): Show |
1 | a0001c0001t0001g0106 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.806+146_806+147ins others(196): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128943
|
C | CCCCCACA others(71): Show |
1 | a0001c0002t0001g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.806+146_806+147ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128943 | ||||||
chr19:2128946
|
C | CACAGCTC others(187): Show |
1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.806+143_806+144ins others(194): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128946 | ||||||
chr19:2128948
|
G | A | 120 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0049others(117): Show | 123 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.806+142C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128948 | ||||||
chr19:2128948
|
G | GCCGCTCC others(112): Show |
1 | a0001c0003t0002g0325 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.806+141_806+142ins others(119): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128948 | ||||||
chr19:2128950
|
C | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0049others(113): Show | 119 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.806+140G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128950
|
C | CGCTCCGA others(32): Show |
1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.806+139_806+140ins others(39): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128950
|
C | CGCTCCGA others(110): Show |
1 | a0001c0003t0002g0194 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.806+139_806+140ins others(117): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128950
|
C | CGCTCCGA others(230): Show |
1 | a0001c0003t0002g0200 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.806+139_806+140ins others(237): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128950
|
C | CGCTCCGA others(111): Show |
1 | a0001c0001t0001g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.806+139_806+140ins others(118): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128950
|
C | CGCTCCGA others(428): Show |
1 | a0001c0003t0002g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.806+139_806+140ins others(435): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128950
|
C | CGCTCCGA others(387): Show |
1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.806+139_806+140ins others(394): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128950 | ||||||
chr19:2128956
|
G | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG02572.hp2 HG02965.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+134C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128956 | ||||||
chr19:2128957
|
A | G | 4 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | NA18956.hp2 NA18979.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+133T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128957 | ||||||
chr19:2128976
|
C | T | 12 | a0001c0002t0001g0254a0001c0002t0001g0318a0001c0002t0001g0323others(9): Show | 12 | HG01175.hp2 HG02300.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.806+114G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128976 | ||||||
chr19:2128977
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.806+113C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128977 | ||||||
chr19:2128982
|
GC | G | 141 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0058others(138): Show | 144 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.806+107delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128982 | ||||||
chr19:2128983
|
C | CCCCACAG others(31): Show |
2 | a0001c0004t0002g0236a0001c0004t0002g0244 | 2 | NA18995.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.806+106_806+107ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(70): Show |
1 | a0001c0002t0001g0254 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.806+106_806+107ins others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(187): Show |
1 | a0001c0001t0003g0370 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.806+106_806+107ins others(194): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(188): Show |
2 | a0001c0001t0003g0372a0001c0001t0003g0374 | 2 | NA18962.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.806+106_806+107ins others(195): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(228): Show |
1 | a0001c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.806+106_806+107ins others(235): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(305): Show |
1 | a0001c0001t0003g0369 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.806+106_806+107ins others(312): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(188): Show |
1 | a0001c0003t0002g0024 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.806+106_806+107ins others(195): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(71): Show |
2 | a0001c0001t0001g0080a0001c0001t0001g0128 | 2 | HG02148.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.806+106_806+107ins others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(344): Show |
1 | a0001c0001t0001g0347 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.806+106_806+107ins others(351): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(149): Show |
1 | a0001c0001t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.806+106_806+107ins others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(345): Show |
1 | a0001c0001t0001g0118 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.806+106_806+107ins others(352): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128983
|
C | CCCCACAG others(31): Show |
1 | a0001c0003t0002g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.806+106_806+107ins others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128983 | ||||||
chr19:2128986
|
C | T | 1 | a0001c0001t0003g0350 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.806+104G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128986 | ||||||
chr19:2128987
|
C | T | 1 | a0001c0003t0002g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.806+103G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128987 | ||||||
chr19:2128988
|
G | A | 193 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0058others(190): Show | 197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.806+102C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128988 | ||||||
chr19:2128990
|
C | A | 192 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0058others(189): Show | 196 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.806+100G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(32): Show |
1 | a0001c0003t0002g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.806+99_806+100insT others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(71): Show |
1 | a0001c0001t0001g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(77): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(423): Show |
1 | a0001c0001t0003g0375 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(429): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(462): Show |
1 | a0001c0001t0003g0351 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(468): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(345): Show |
2 | a0001c0001t0003g0368a0001c0001t0003g0377 | 2 | HG00423.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.806+99_806+100insT others(351): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(151): Show |
1 | a0001c0003t0005g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.806+99_806+100insT others(157): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(898): Show |
1 | a0001c0001t0002g0092 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(904): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(269): Show |
1 | a0001c0002t0001g0258 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(275): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(72): Show |
1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.806+99_806+100insT others(78): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(230): Show |
1 | a0001c0003t0002g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(236): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(32): Show |
1 | a0006c0019t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.806+99_806+100insT others(38): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(150): Show |
1 | a0001c0003t0002g0050 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.806+99_806+100insT others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128990
|
C | CGCTCCGA others(189): Show |
1 | a0001c0003t0002g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.806+99_806+100insT others(195): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128990 | ||||||
chr19:2128996
|
G | A | 6 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG03453.hp1 NA18956.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+94C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128996 | ||||||
chr19:2128997
|
A | G | 6 | a0001c0001t0001g0144a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG02132.hp1 NA18956.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+93T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2128997 | ||||||
chr19:2129001
|
T | C | 1 | a0001c0004t0002g0222 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.806+89A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129001 | ||||||
chr19:2129016
|
C | T | 3 | a0001c0001t0003g0353a0001c0003t0002g0036a0001c0003t0002g0053 | 3 | HG01256.hp1 NA18951.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.806+74G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129016 | ||||||
chr19:2129017
|
G | A | 1 | a0001c0003t0002g0197 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.806+73C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129017 | ||||||
chr19:2129022
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.806+68C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129022 | ||||||
chr19:2129022
|
GC | G | 55 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(52): Show | 56 | HG00280.hp1 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.806+67delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129022 | ||||||
chr19:2129023
|
C | CCCCACAG others(31): Show |
2 | a0001c0001t0006g0137a0001c0004t0014g0237 | 2 | HG02602.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.806+66_806+67insCG others(36): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129023
|
C | CCCCACAG others(580): Show |
1 | a0001c0004t0002g0228 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.806+66_806+67insCG others(585): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129023
|
C | CCCCACAG others(110): Show |
1 | a0001c0003t0002g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.806+66_806+67insCG others(115): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129023
|
C | CCCCACAG others(228): Show |
1 | a0001c0001t0001g0078 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.806+66_806+67insCG others(233): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129023
|
C | CCCCCACA others(583): Show |
1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.806+66_806+67insCG others(588): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129023
|
C | CCCCCGCC others(110): Show |
2 | a0001c0005t0002g0022a0001c0005t0002g0035 | 2 | NA18985.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.806+66_806+67insCG others(115): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129023
|
C | CCTCACAG others(70): Show |
1 | a0001c0001t0001g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.806+66_806+67insCG others(75): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129023 | ||||||
chr19:2129028
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0055others(75): Show | 79 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.806+62C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129028 | ||||||
chr19:2129030
|
C | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0057others(71): Show | 75 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.806+60G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129030 | ||||||
chr19:2129030
|
C | CGCTCCGA others(71): Show |
6 | a0001c0004t0002g0051a0001c0004t0002g0216a0001c0004t0002g0218others(3): Show | 6 | HG00673.hp1 HG01123.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+59_806+60insTG others(76): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129030 | ||||||
chr19:2129030
|
C | CGCTCCGA others(151): Show |
1 | a0001c0004t0002g0225 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.806+59_806+60insTG others(156): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129030 | ||||||
chr19:2129030
|
C | CGCTCCGA others(71): Show |
2 | a0001c0003t0002g0026a0001c0003t0002g0027 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.806+59_806+60insTG others(76): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129030 | ||||||
chr19:2129036
|
G | A | 4 | a0001c0001t0001g0085a0001c0011t0005g0209a0001c0011t0005g0210others(1): Show | 4 | HG02040.hp1 HG02965.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.806+54C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129036 | ||||||
chr19:2129040
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.806+50G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129040 | ||||||
chr19:2129048
|
C | CGTGGAGC others(426): Show |
1 | a0001c0001t0001g0109 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.806+41_806+42insAG others(431): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129048 | ||||||
chr19:2129048
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0108 | 2 | HG04184.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.806+42G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129048 | ||||||
chr19:2129068
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0081a0001c0001t0001g0085others(39): Show | 44 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.806+22T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | 2129068 | ||||||
chr19:2129177
|
AGGGCCTC others(43): Show |
A | 3 | a0001c0008t0002g0184a0001c0008t0002g0185a0001c0008t0002g0253 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.733-64_733-15delCC others(48): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 7/31 | chr19 | 2129177 | ||||||
chr19:2129218
|
G | C | 1 | a0001c0001t0001g0347 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733-55C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 7/31 | chr19 | 2129218 | ||||||
chr19:2129222
|
CA | C | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.733-60delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 7/31 | chr19 | 2129222 | ||||||
chr19:2129244
|
CAGGGAAT others(15): Show |
C | 4 | a0001c0001t0001g0333a0001c0001t0001g0334a0001c0001t0001g0335others(1): Show | 4 | HG00438.hp2 HG02071.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+52_732+73delCA others(20): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 7/31 | chr19 | 2129244 | ||||||
chr19:2129474
|
T | C | 91 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0263others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.593-17A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129474 | ||||||
chr19:2129475
|
C | G | 91 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0263others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.593-18G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129475 | ||||||
chr19:2129533
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.593-76C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129533 | ||||||
chr19:2129543
|
T | G | 1 | a0001c0002t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.593-86A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129543 | ||||||
chr19:2129614
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0128 | 2 | HG03491.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.593-157G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129614 | ||||||
chr19:2129707
|
A | G | 39 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0147others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.593-250T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129707 | ||||||
chr19:2129851
|
C | T | 4 | a0001c0002t0001g0187a0001c0002t0001g0257a0001c0002t0001g0331others(1): Show | 4 | NA18945.hp2 NA18956.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-394G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129851 | ||||||
chr19:2129867
|
G | T | 114 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(111): Show | 114 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.593-410C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129867 | ||||||
chr19:2129881
|
G | T | 1 | a0001c0005t0002g0022 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.593-424C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2129881 | ||||||
chr19:2130014
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 8 | HG01109.hp1 HG02559.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+394C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130014 | ||||||
chr19:2130140
|
GA | G | 4 | a0001c0006t0002g0009a0001c0008t0002g0184a0001c0008t0002g0185others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+267delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130140 | ||||||
chr19:2130148
|
G | A | 3 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0043 | 3 | NA18980.hp1 NA18989.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.592+260C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130148 | ||||||
chr19:2130179
|
A | G | 2 | a0001c0011t0005g0209a0001c0011t0005g0210 | 2 | HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.592+229T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130179 | ||||||
chr19:2130209
|
G | C | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.592+199C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130209 | ||||||
chr19:2130310
|
A | G | 1 | a0001c0003t0002g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.592+98T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130310 | ||||||
chr19:2130397
|
A | G | 1 | a0001c0003t0002g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.592+11T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 6/31 | chr19 | 2130397 | ||||||
chr19:2130541
|
C | T | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | splice_region_variant&intron_variant | LOW | c.463-4G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2130541 | ||||||
chr19:2130563
|
C | T | 1 | a0001c0006t0002g0311 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.463-26G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2130563 | ||||||
chr19:2130577
|
G | A | 2 | a0001c0003t0002g0026a0001c0003t0002g0027 | 2 | HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.463-40C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2130577 | ||||||
chr19:2130669
|
G | A | 1 | a0001c0004t0002g0222 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.463-132C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2130669 | ||||||
chr19:2130924
|
A | G | 58 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0003t0001g0071others(55): Show | 58 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.463-387T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2130924 | ||||||
chr19:2131033
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0132a0001c0001t0001g0135 | 4 | HG01109.hp1 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.463-496C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131033 | ||||||
chr19:2131075
|
G | A | 1 | a0001c0005t0002g0039 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.463-538C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131075 | ||||||
chr19:2131082
|
C | A | 1 | a0001c0003t0002g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.463-545G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131082 | ||||||
chr19:2131102
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.463-565G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131102 | ||||||
chr19:2131146
|
G | A | 1 | a0001c0003t0002g0326 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.463-609C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131146 | ||||||
chr19:2131149
|
A | G | 211 | a0001c0001t0001g0049a0001c0001t0001g0180a0001c0001t0001g0202others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.463-612T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131149 | ||||||
chr19:2131256
|
T | C | 1 | a0001c0005t0002g0035 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.463-719A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131256 | ||||||
chr19:2131294
|
C | T | 35 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(32): Show | 35 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.463-757G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131294 | ||||||
chr19:2131341
|
G | A | 58 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0003t0001g0071others(55): Show | 58 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.463-804C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131341 | ||||||
chr19:2131349
|
A | G | 3 | a0001c0001t0001g0167a0001c0008t0002g0184a0001c0008t0002g0185 | 3 | HG00609.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.463-812T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131349 | ||||||
chr19:2131351
|
T | C | 2 | a0001c0001t0001g0144a0001c0003t0002g0344 | 2 | NA18940.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.463-814A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131351 | ||||||
chr19:2131364
|
C | T | 182 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.463-827G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131364 | ||||||
chr19:2131405
|
C | CGCCCATC others(47): Show |
58 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0003t0001g0071others(55): Show | 58 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.463-869_463-868ins others(54): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131405 | ||||||
chr19:2131430
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.463-893G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131430 | ||||||
chr19:2131448
|
C | T | 89 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.463-911G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131448 | ||||||
chr19:2131450
|
A | T | 89 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.463-913T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131450 | ||||||
chr19:2131459
|
G | T | 89 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.463-922C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131459 | ||||||
chr19:2131480
|
ACACCCGG others(47): Show |
A | 3 | a0001c0001t0002g0096a0001c0001t0002g0103a0001c0001t0002g0107 | 3 | HG01884.hp2 HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.462+937_463-944del others(54): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131480 | ||||||
chr19:2131484
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.463-947G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131484 | ||||||
chr19:2131485
|
C | G | 89 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.463-948G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131485 | ||||||
chr19:2131485
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.463-948G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131485 | ||||||
chr19:2131488
|
TGGACAGG others(386): Show |
T | 12 | a0001c0001t0001g0328a0001c0001t0002g0345a0001c0003t0002g0208others(9): Show | 12 | HG02280.hp2 HG02622.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.462+590_463-952del | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131488 | ||||||
chr19:2131503
|
G | A | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.463-966C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131503 | ||||||
chr19:2131513
|
GGCCCATC others(47): Show |
G | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.462+904_462+957del others(54): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131513 | ||||||
chr19:2131521
|
G | A | 6 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0215others(3): Show | 6 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.462+950C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131521 | ||||||
chr19:2131534
|
G | A | 191 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(188): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.462+937C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131534 | ||||||
chr19:2131539
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.462+932G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131539 | ||||||
chr19:2131539
|
C | CGGTGGAC others(47): Show |
10 | a0001c0004t0002g0222a0001c0004t0002g0233a0001c0004t0002g0234others(7): Show | 10 | HG00323.hp1 HG00558.hp2 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.462+878_462+931dup others(54): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131539 | ||||||
chr19:2131567
|
C | T | 86 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.462+904G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131567 | ||||||
chr19:2131581
|
G | A | 86 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.462+890C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131581 | ||||||
chr19:2131593
|
A | C | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.462+878T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131593 | ||||||
chr19:2131619
|
A | AGCGCCCA others(104): Show |
1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.462+851_462+852ins others(111): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131619 | ||||||
chr19:2131619
|
AGCGCCCA others(50): Show |
A | 1 | a0001c0004t0002g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.462+795_462+851del others(57): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131619 | ||||||
chr19:2131621
|
C | T | 7 | a0002c0007t0004g0392a0002c0007t0004g0393a0002c0009t0002g0265others(4): Show | 7 | HG01515.hp2 HG01517.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.462+850G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131621 | ||||||
chr19:2131634
|
C | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0111others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+837G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131634 | ||||||
chr19:2131635
|
G | A | 3 | a0001c0002t0001g0250a0001c0002t0001g0251a0001c0002t0001g0252 | 3 | HG00323.hp2 HG01361.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.462+836C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131635 | ||||||
chr19:2131644
|
ACCT | A | 27 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(24): Show | 27 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.462+824_462+826del others(3): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131644 | ||||||
chr19:2131650
|
AGGCGGAC others(50): Show |
A | 86 | a0001c0001t0001g0263a0001c0001t0001g0336a0001c0002t0001g0003others(83): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.462+764_462+820del others(57): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131650 | ||||||
chr19:2131653
|
C | T | 27 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(24): Show | 27 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.462+818G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131653 | ||||||
chr19:2131676
|
T | A | 27 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(24): Show | 27 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.462+795A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131676 | ||||||
chr19:2131676
|
T | C | 83 | a0001c0001t0001g0049a0001c0001t0001g0072a0001c0001t0001g0084others(80): Show | 83 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.462+795A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131676 | ||||||
chr19:2131676
|
TGCGCCCA others(50): Show |
T | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.462+738_462+794del others(57): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131676 | ||||||
chr19:2131707
|
G | A | 28 | a0001c0001t0001g0243a0001c0003t0002g0188a0001c0004t0002g0051others(25): Show | 28 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.462+764C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131707 | ||||||
chr19:2131725
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(257): Show | 264 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.462+746C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131725 | ||||||
chr19:2131734
|
G | A | 4 | a0001c0003t0002g0188a0001c0008t0002g0184a0001c0008t0002g0185others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.462+737C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131734 | ||||||
chr19:2131763
|
C | T | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.462+708G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131763 | ||||||
chr19:2131791
|
G | A | 348 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(345): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.462+680C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131791 | ||||||
chr19:2131791
|
G | GCGCCCAT others(50): Show |
27 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(24): Show | 27 | HG00280.hp1 HG00639.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.462+679_462+680ins others(57): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131791 | ||||||
chr19:2131793
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.462+678C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131793 | ||||||
chr19:2131810
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.462+661A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131810 | ||||||
chr19:2131821
|
G | A | 51 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0078others(48): Show | 52 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.462+650C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131821 | ||||||
chr19:2131826
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0127 | 2 | HG01243.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.462+645C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131826 | ||||||
chr19:2131839
|
G | A | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.462+632C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131839 | ||||||
chr19:2131847
|
A | C | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.462+624T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131847 | ||||||
chr19:2131847
|
A | G | 192 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.462+624T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131847 | ||||||
chr19:2131848
|
G | A | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.462+623C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131848 | ||||||
chr19:2131850
|
G | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.462+621C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131850 | ||||||
chr19:2131877
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.462+594G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2131877 | ||||||
chr19:2132165
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.462+306C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132165 | ||||||
chr19:2132167
|
C | A | 1 | a0001c0003t0002g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.462+304G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132167 | ||||||
chr19:2132232
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.462+239C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132232 | ||||||
chr19:2132297
|
A | C | 1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.462+174T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132297 | ||||||
chr19:2132311
|
C | T | 1 | a0001c0001t0003g0383 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.462+160G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132311 | ||||||
chr19:2132363
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0122a0001c0001t0001g0142 | 3 | HG00280.hp2 HG02300.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.462+108C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132363 | ||||||
chr19:2132371
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.462+100G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 5/31 | chr19 | 2132371 | ||||||
chr19:2132881
|
C | G | 1 | a0001c0017t0003g0366 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.355-303G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2132881 | ||||||
chr19:2133009
|
G | A | 1 | a0002c0007t0004g0391 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.355-431C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133009 | ||||||
chr19:2133275
|
C | G | 1 | a0001c0006t0002g0311 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.355-697G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133275 | ||||||
chr19:2133297
|
C | A | 1 | a0001c0016t0002g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.355-719G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133297 | ||||||
chr19:2133333
|
C | G | 85 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(82): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.355-755G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133333 | ||||||
chr19:2133348
|
C | G | 1 | a0001c0001t0001g0328 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.355-770G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133348 | ||||||
chr19:2133466
|
C | T | 91 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.355-888G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133466 | ||||||
chr19:2133508
|
C | A | 1 | a0001c0003t0002g0344 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.355-930G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133508 | ||||||
chr19:2133511
|
C | CT | 9 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(6): Show | 9 | HG01109.hp2 HG01358.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.355-934dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133511 | ||||||
chr19:2133777
|
C | T | 1 | a0001c0003t0002g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.355-1199G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133777 | ||||||
chr19:2133832
|
G | A | 87 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.355-1254C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133832 | ||||||
chr19:2133848
|
G | T | 1 | a0001c0003t0002g0338 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.355-1270C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133848 | ||||||
chr19:2133894
|
G | A | 2 | a0002c0007t0004g0392a0002c0007t0004g0393 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.355-1316C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2133894 | ||||||
chr19:2134180
|
G | A | 1 | a0001c0002t0001g0291 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.355-1602C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134180 | ||||||
chr19:2134319
|
G | A | 1 | a0001c0002t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.355-1741C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134319 | ||||||
chr19:2134353
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.355-1775G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134353 | ||||||
chr19:2134382
|
C | T | 1 | a0001c0002t0001g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.355-1804G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134382 | ||||||
chr19:2134420
|
C | CA | 100 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(97): Show | 100 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.355-1843dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134420 | ||||||
chr19:2134457
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.355-1879G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134457 | ||||||
chr19:2134462
|
C | T | 2 | a0001c0002t0001g0339a0001c0002t0001g0340 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.355-1884G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134462 | ||||||
chr19:2134555
|
T | C | 1 | a0001c0002t0001g0320 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.355-1977A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134555 | ||||||
chr19:2134560
|
T | C | 93 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.355-1982A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134560 | ||||||
chr19:2134583
|
TA | T | 93 | a0001c0001t0001g0263a0001c0001t0003g0355a0001c0002t0001g0003others(90): Show | 96 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(93): Show |
intron_variant | MODIFIER | c.355-2006delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134583 | ||||||
chr19:2134608
|
T | C | 4 | a0001c0006t0002g0009a0001c0008t0002g0184a0001c0008t0002g0185others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.355-2030A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134608 | ||||||
chr19:2134687
|
C | T | 1 | a0001c0002t0001g0280 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.355-2109G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134687 | ||||||
chr19:2134688
|
G | A | 1 | a0001c0003t0002g0052 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.355-2110C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134688 | ||||||
chr19:2134748
|
C | T | 4 | a0001c0001t0002g0096a0001c0001t0002g0103a0001c0001t0002g0107others(1): Show | 4 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-2170G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134748 | ||||||
chr19:2134774
|
T | C | 13 | a0001c0001t0001g0328a0001c0001t0002g0205a0001c0001t0002g0345others(10): Show | 13 | HG02280.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.355-2196A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134774 | ||||||
chr19:2134937
|
C | A | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.354+2074G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134937 | ||||||
chr19:2134950
|
G | C | 1 | a0001c0004t0002g0236 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.354+2061C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2134950 | ||||||
chr19:2135157
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.354+1854G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135157 | ||||||
chr19:2135180
|
G | A | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0111others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.354+1831C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135180 | ||||||
chr19:2135307
|
G | A | 2 | a0001c0002t0001g0255a0001c0002t0001g0302 | 2 | HG00735.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.354+1704C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135307 | ||||||
chr19:2135315
|
C | G | 1 | a0001c0002t0001g0251 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.354+1696G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135315 | ||||||
chr19:2135533
|
CTCAAAAC others(3): Show |
C | 1 | a0001c0003t0005g0114 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.354+1468_354+1477d others(12): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135533 | ||||||
chr19:2135587
|
G | C | 40 | a0001c0001t0001g0243a0001c0003t0002g0188a0001c0004t0002g0051others(37): Show | 40 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.354+1424C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135587 | ||||||
chr19:2135593
|
C | T | 10 | a0001c0001t0001g0328a0001c0003t0002g0208a0001c0003t0002g0325others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+1418G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135593 | ||||||
chr19:2135597
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.354+1414T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135597 | ||||||
chr19:2135715
|
T | G | 49 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0078others(46): Show | 50 | HG00280.hp2 HG00423.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.354+1296A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135715 | ||||||
chr19:2135738
|
G | A | 1 | a0001c0003t0002g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.354+1273C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135738 | ||||||
chr19:2135750
|
C | T | 1 | a0001c0003t0002g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.354+1261G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135750 | ||||||
chr19:2135778
|
C | T | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.354+1233G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135778 | ||||||
chr19:2135784
|
G | A | 58 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0003t0001g0071others(55): Show | 58 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.354+1227C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135784 | ||||||
chr19:2135821
|
C | T | 59 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0263others(56): Show | 59 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.354+1190G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135821 | ||||||
chr19:2135983
|
GAGACTCC others(38): Show |
G | 1 | a0001c0002t0001g0279 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.354+983_354+1027de others(46): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2135983 | ||||||
chr19:2136013
|
C | T | 1 | a0001c0003t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.354+998G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136013 | ||||||
chr19:2136014
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0102others(3): Show | 6 | HG03239.hp2 HG03490.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+997C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136014 | ||||||
chr19:2136017
|
C | A | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.354+994G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136017 | ||||||
chr19:2136102
|
A | T | 1 | a0002c0007t0004g0388 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.354+909T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136102 | ||||||
chr19:2136103
|
T | C | 208 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.354+908A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136103 | ||||||
chr19:2136109
|
T | C | 2 | a0001c0001t0002g0345a0001c0003t0005g0207 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.354+902A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136109 | ||||||
chr19:2136150
|
C | T | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.354+861G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136150 | ||||||
chr19:2136159
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.354+852G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136159 | ||||||
chr19:2136168
|
C | T | 5 | a0001c0005t0002g0018a0001c0005t0002g0020a0001c0005t0002g0021others(2): Show | 5 | NA18955.hp1 NA18975.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.354+843G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136168 | ||||||
chr19:2136264
|
C | T | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.354+747G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136264 | ||||||
chr19:2136274
|
T | C | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.354+737A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136274 | ||||||
chr19:2136380
|
G | A | 59 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0263others(56): Show | 59 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.354+631C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136380 | ||||||
chr19:2136440
|
G | A | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.354+571C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136440 | ||||||
chr19:2136516
|
T | C | 207 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.354+495A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136516 | ||||||
chr19:2136554
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.354+457A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136554 | ||||||
chr19:2136640
|
C | T | 37 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(34): Show | 37 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.354+371G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136640 | ||||||
chr19:2136681
|
G | C | 10 | a0002c0007t0004g0386a0002c0007t0004g0387a0002c0007t0004g0388others(7): Show | 10 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.354+330C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136681 | ||||||
chr19:2136704
|
C | T | 154 | a0001c0001t0001g0049a0001c0001t0001g0113a0001c0001t0001g0138others(151): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.354+307G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136704 | ||||||
chr19:2136746
|
G | T | 1 | a0001c0002t0001g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.354+265C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136746 | ||||||
chr19:2136765
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.354+246G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136765 | ||||||
chr19:2136842
|
G | A | 2 | a0001c0002t0001g0004a0001c0002t0001g0269 | 3 | NA18967.hp1 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.354+169C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136842 | ||||||
chr19:2136993
|
C | T | 38 | a0001c0001t0001g0085a0001c0001t0001g0243a0001c0004t0002g0051others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.354+18G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2136993 | ||||||
chr19:2137001
|
G | C | 60 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0263others(57): Show | 60 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.354+10C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 4/31 | chr19 | 2137001 | ||||||
chr19:2137176
|
G | C | 1 | a0001c0003t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.274-85C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137176 | ||||||
chr19:2137191
|
G | T | 5 | a0002c0009t0002g0265a0002c0009t0002g0276a0002c0009t0002g0277others(2): Show | 5 | HG02258.hp1 HG02486.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-100C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137191 | ||||||
chr19:2137286
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.274-195C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137286 | ||||||
chr19:2137314
|
G | GT | 17 | a0001c0001t0001g0084a0001c0001t0001g0328a0001c0001t0002g0062others(14): Show | 17 | HG01981.hp2 HG02055.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-224dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137314 | ||||||
chr19:2137319
|
T | G | 1 | a0001c0014t0013g0007 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.274-228A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137319 | ||||||
chr19:2137426
|
G | A | 9 | a0001c0002t0001g0004a0001c0002t0001g0187a0001c0002t0001g0257others(6): Show | 10 | HG01081.hp2 NA18945.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+301C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137426 | ||||||
chr19:2137461
|
G | A | 2 | a0001c0001t0001g0163a0001c0004t0014g0237 | 2 | HG02155.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.273+266C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137461 | ||||||
chr19:2137464
|
C | T | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273+263G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137464 | ||||||
chr19:2137496
|
A | G | 92 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.273+231T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137496 | ||||||
chr19:2137695
|
AC | A | 61 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(58): Show | 61 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.273+31delG | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 3/31 | chr19 | 2137695 | ||||||
chr19:2137820
|
G | A | 1 | a0001c0003t0002g0344 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.193-13C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2137820 | ||||||
chr19:2137871
|
C | T | 85 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(82): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.193-64G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2137871 | ||||||
chr19:2137886
|
C | T | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.193-79G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2137886 | ||||||
chr19:2137949
|
CT | C | 3 | a0001c0003t0002g0036a0001c0003t0002g0037a0001c0003t0002g0046 | 3 | HG02040.hp2 HG02074.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.193-143delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2137949 | ||||||
chr19:2138042
|
T | C | 92 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(89): Show | 95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.193-235A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138042 | ||||||
chr19:2138087
|
C | G | 5 | a0001c0001t0002g0096a0001c0001t0002g0098a0001c0001t0002g0103others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.193-280G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138087 | ||||||
chr19:2138192
|
C | T | 3 | a0001c0008t0002g0184a0001c0008t0002g0185a0001c0008t0002g0253 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.193-385G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138192 | ||||||
chr19:2138226
|
C | A | 3 | a0001c0001t0002g0096a0001c0001t0002g0103a0001c0001t0002g0107 | 3 | HG01884.hp2 HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.192+393G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138226 | ||||||
chr19:2138261
|
C | T | 1 | a0001c0004t0014g0237 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.192+358G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138261 | ||||||
chr19:2138371
|
G | A | 1 | a0001c0008t0002g0181 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.192+248C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138371 | ||||||
chr19:2138502
|
G | A | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.192+117C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138502 | ||||||
chr19:2138508
|
A | G | 207 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.192+111T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138508 | ||||||
chr19:2138548
|
G | A | 1 | a0001c0001t0003g0350 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.192+71C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138548 | ||||||
chr19:2138581
|
C | T | 1 | a0001c0002t0001g0258 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.192+38G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 2/31 | chr19 | 2138581 | ||||||
chr19:2138720
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp2 | splice_region_variant&intron_variant | LOW | c.97-6T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2138720 | ||||||
chr19:2138843
|
C | T | 61 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(58): Show | 61 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.97-129G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2138843 | ||||||
chr19:2138849
|
C | T | 87 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.97-135G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2138849 | ||||||
chr19:2138959
|
C | T | 4 | a0001c0002t0001g0271a0001c0002t0001g0272a0001c0002t0001g0273others(1): Show | 4 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-245G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2138959 | ||||||
chr19:2138974
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-260G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2138974 | ||||||
chr19:2139059
|
C | CA | 30 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(27): Show | 30 | HG00621.hp2 HG01891.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.97-346dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139059
|
CA | C | 62 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0128others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.97-346delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139059
|
CAA | C | 84 | a0001c0001t0002g0345a0001c0002t0001g0003a0001c0002t0001g0004others(81): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.97-347_97-346delTT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139059
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0001g0102a0001c0003t0002g0200a0001c0003t0002g0344others(2): Show | 5 | HG03239.hp2 NA18522.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-355_97-346delTT others(8): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139059
|
CAAAAAAA others(4): Show |
C | 56 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(53): Show | 56 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.97-356_97-346delTT others(9): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139059
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0002g0052 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.97-357_97-346delTT others(10): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139059
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.97-361_97-346delTT others(14): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139059 | ||||||
chr19:2139103
|
T | C | 1 | a0001c0004t0002g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.97-389A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139103 | ||||||
chr19:2139104
|
A | C | 1 | a0001c0004t0002g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.97-390T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139104 | ||||||
chr19:2139129
|
T | A | 1 | a0001c0004t0002g0248 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.97-415A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139129 | ||||||
chr19:2139141
|
G | C | 1 | a0001c0001t0003g0378 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.97-427C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139141 | ||||||
chr19:2139194
|
T | C | 61 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(58): Show | 61 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.97-480A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139194 | ||||||
chr19:2139277
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.97-563G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139277 | ||||||
chr19:2139294
|
C | T | 1 | a0001c0003t0002g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.97-580G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139294 | ||||||
chr19:2139317
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.97-603C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139317 | ||||||
chr19:2139358
|
A | G | 206 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.97-644T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139358 | ||||||
chr19:2139416
|
C | T | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.97-702G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139416 | ||||||
chr19:2139421
|
G | A | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-707C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139421 | ||||||
chr19:2139691
|
AG | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01358.hp2 HG01496.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.97-978delC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139691 | ||||||
chr19:2139810
|
A | T | 61 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(58): Show | 61 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.97-1096T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139810 | ||||||
chr19:2139893
|
C | T | 1 | a0001c0002t0001g0270 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.97-1179G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139893 | ||||||
chr19:2139916
|
C | T | 2 | a0001c0002t0001g0004a0001c0002t0001g0269 | 3 | NA18967.hp1 NA18971.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.97-1202G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139916 | ||||||
chr19:2139932
|
C | T | 1 | a0001c0002t0001g0320 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.97-1218G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139932 | ||||||
chr19:2139933
|
G | A | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG02647.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.97-1219C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2139933 | ||||||
chr19:2140010
|
C | T | 208 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.97-1296G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140010 | ||||||
chr19:2140035
|
G | T | 37 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(34): Show | 37 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.97-1321C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140035 | ||||||
chr19:2140152
|
G | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-1438C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140152 | ||||||
chr19:2140180
|
A | T | 13 | a0001c0001t0001g0328a0001c0001t0002g0205a0001c0001t0002g0345others(10): Show | 13 | HG02280.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-1466T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140180 | ||||||
chr19:2140233
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.97-1519T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140233 | ||||||
chr19:2140333
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.97-1619C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140333 | ||||||
chr19:2140365
|
C | T | 1 | a0001c0003t0005g0207 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97-1651G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140365 | ||||||
chr19:2140375
|
G | T | 208 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(205): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.97-1661C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140375 | ||||||
chr19:2140450
|
T | C | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-1736A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140450 | ||||||
chr19:2140480
|
C | CT | 206 | a0001c0001t0001g0049a0001c0001t0001g0069a0001c0001t0001g0078others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.97-1767dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140480 | ||||||
chr19:2140515
|
G | A | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-1801C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140515 | ||||||
chr19:2140624
|
G | A | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.97-1910C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140624 | ||||||
chr19:2140755
|
C | CT | 106 | a0001c0001t0001g0072a0001c0001t0001g0112a0001c0001t0001g0126others(103): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.97-2042dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140755 | ||||||
chr19:2140755
|
C | CTT | 8 | a0001c0002t0001g0252a0001c0002t0001g0254a0001c0002t0001g0305others(5): Show | 8 | HG01175.hp1 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.97-2043_97-2042dup others(2): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140755 | ||||||
chr19:2140755
|
CT | C | 10 | a0001c0001t0001g0060a0001c0001t0001g0099a0001c0001t0001g0110others(7): Show | 10 | HG02257.hp1 HG02723.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.97-2042delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140755 | ||||||
chr19:2140755
|
CTTTT | C | 56 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(53): Show | 56 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.97-2045_97-2042del others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140755 | ||||||
chr19:2140755
|
CTTTTTTT others(2): Show |
C | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-2050_97-2042del others(9): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140755 | ||||||
chr19:2140759
|
T | A | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.97-2045A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140759 | ||||||
chr19:2140945
|
G | C | 3 | a0001c0006t0002g0009a0001c0008t0002g0184a0001c0008t0002g0185 | 3 | HG02257.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.97-2231C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140945 | ||||||
chr19:2140979
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.97-2265C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2140979 | ||||||
chr19:2141018
|
C | A | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.97-2304G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141018 | ||||||
chr19:2141050
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-2336G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141050 | ||||||
chr19:2141104
|
T | C | 2 | a0002c0007t0004g0392a0002c0007t0004g0393 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.97-2390A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141104 | ||||||
chr19:2141111
|
A | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.97-2397T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141111 | ||||||
chr19:2141151
|
C | G | 206 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(203): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.97-2437G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141151 | ||||||
chr19:2141195
|
G | A | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.97-2481C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141195 | ||||||
chr19:2141210
|
C | T | 89 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.97-2496G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141210 | ||||||
chr19:2141350
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97-2636G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141350 | ||||||
chr19:2141351
|
G | A | 59 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0263others(56): Show | 59 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.97-2637C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141351 | ||||||
chr19:2141405
|
C | T | 1 | a0001c0003t0002g0343 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.97-2691G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141405 | ||||||
chr19:2141430
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.97-2716C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141430 | ||||||
chr19:2141436
|
C | CT | 6 | a0001c0001t0001g0110a0001c0001t0001g0180a0001c0003t0002g0027others(3): Show | 6 | HG02257.hp1 HG02735.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-2723dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141436 | ||||||
chr19:2141436
|
CT | C | 27 | a0001c0001t0001g0139a0001c0001t0001g0167a0001c0001t0001g0168others(24): Show | 27 | HG00099.hp2 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.97-2723delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141436 | ||||||
chr19:2141503
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-2789C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141503 | ||||||
chr19:2141520
|
G | A | 1 | a0001c0002t0001g0296 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.97-2806C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141520 | ||||||
chr19:2141528
|
GTTCAAGT others(2): Show |
G | 207 | a0001c0001t0001g0049a0001c0001t0001g0130a0001c0001t0001g0202others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-2823_97-2815del others(9): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141528 | ||||||
chr19:2141537
|
A | G | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.97-2823T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141537 | ||||||
chr19:2141661
|
C | T | 1 | a0001c0002t0001g0268 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.97-2947G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141661 | ||||||
chr19:2141709
|
G | A | 2 | a0001c0001t0002g0345a0001c0003t0005g0207 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.97-2995C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141709 | ||||||
chr19:2141735
|
C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0127a0001c0001t0001g0151 | 3 | HG01243.hp1 HG04228.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.97-3021G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141735 | ||||||
chr19:2141944
|
A | G | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-3230T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141944 | ||||||
chr19:2141955
|
C | T | 1 | a0001c0006t0002g0308 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.97-3241G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141955 | ||||||
chr19:2141957
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97-3243A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141957 | ||||||
chr19:2141962
|
T | G | 5 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.97-3248A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141962 | ||||||
chr19:2141972
|
A | G | 2 | a0001c0002t0001g0295a0001c0002t0001g0296 | 2 | HG01516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.97-3258T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141972 | ||||||
chr19:2141983
|
T | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.97-3269A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2141983 | ||||||
chr19:2142014
|
T | TTA | 61 | a0001c0001t0001g0049a0001c0001t0001g0150a0001c0001t0001g0202others(58): Show | 61 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.97-3302_97-3301dup others(2): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142014 | ||||||
chr19:2142025
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0140 | 2 | HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.97-3311A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142025 | ||||||
chr19:2142027
|
T | C | 89 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.97-3313A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142027 | ||||||
chr19:2142036
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.97-3322A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142036 | ||||||
chr19:2142056
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.97-3342G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142056 | ||||||
chr19:2142074
|
G | A | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-3360C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142074 | ||||||
chr19:2142103
|
C | T | 1 | a0001c0004t0002g0222 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.97-3389G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142103 | ||||||
chr19:2142216
|
T | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01346.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.97-3502A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142216 | ||||||
chr19:2142338
|
T | TG | 5 | a0001c0002t0001g0295a0001c0002t0001g0296a0001c0002t0001g0297others(2): Show | 5 | HG00140.hp1 HG01255.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-3625dupC | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142338 | ||||||
chr19:2142475
|
C | T | 1 | a0001c0002t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.97-3761G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142475 | ||||||
chr19:2142626
|
G | A | 1 | a0001c0001t0010g0397 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.97-3912C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142626 | ||||||
chr19:2142634
|
C | G | 207 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.97-3920G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142634 | ||||||
chr19:2142642
|
G | A | 10 | a0001c0001t0001g0328a0001c0003t0002g0208a0001c0003t0002g0325others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.97-3928C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142642 | ||||||
chr19:2142687
|
C | G | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.97-3973G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142687 | ||||||
chr19:2142688
|
T | C | 60 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0263others(57): Show | 60 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.97-3974A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142688 | ||||||
chr19:2142755
|
G | GT | 18 | a0001c0001t0001g0077a0001c0001t0001g0143a0001c0001t0001g0144others(15): Show | 18 | HG01928.hp1 HG02280.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.97-4042dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142755 | ||||||
chr19:2142755
|
GT | G | 90 | a0001c0001t0003g0350a0001c0002t0001g0003a0001c0002t0001g0004others(87): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.97-4042delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142755 | ||||||
chr19:2142829
|
C | T | 13 | a0001c0001t0001g0328a0001c0001t0002g0205a0001c0001t0002g0345others(10): Show | 13 | HG02280.hp2 HG02622.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-4115G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142829 | ||||||
chr19:2142867
|
T | C | 1 | a0001c0002t0001g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.97-4153A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142867 | ||||||
chr19:2142926
|
A | G | 89 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0187others(86): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.97-4212T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142926 | ||||||
chr19:2142965
|
T | C | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.97-4251A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2142965 | ||||||
chr19:2143012
|
C | A | 3 | a0001c0008t0002g0184a0001c0008t0002g0185a0001c0008t0002g0253 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.97-4298G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143012 | ||||||
chr19:2143081
|
T | C | 1 | a0001c0004t0002g0224 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.97-4367A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143081 | ||||||
chr19:2143230
|
A | AT | 75 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0055others(72): Show | 75 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.97-4517dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143230 | ||||||
chr19:2143230
|
A | ATT | 61 | a0001c0001t0001g0202a0001c0001t0001g0328a0001c0001t0002g0345others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.97-4518_97-4517dup others(2): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143230 | ||||||
chr19:2143230
|
AT | A | 13 | a0001c0001t0001g0060a0001c0001t0001g0067a0001c0001t0001g0104others(10): Show | 13 | HG01358.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.97-4517delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143230 | ||||||
chr19:2143230
|
ATT | A | 15 | a0001c0002t0001g0261a0001c0002t0001g0264a0001c0002t0001g0305others(12): Show | 15 | HG00438.hp1 HG01952.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-4518_97-4517del others(2): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143230 | ||||||
chr19:2143230
|
ATTT | A | 69 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0251others(66): Show | 72 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(69): Show |
intron_variant | MODIFIER | c.97-4519_97-4517del others(3): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143230 | ||||||
chr19:2143230
|
ATTTT | A | 6 | a0001c0002t0001g0187a0001c0002t0001g0300a0001c0002t0001g0301others(3): Show | 6 | HG00733.hp1 HG01256.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.97-4520_97-4517del others(4): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143230 | ||||||
chr19:2143290
|
G | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-4576C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143290 | ||||||
chr19:2143353
|
G | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-4639C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143353 | ||||||
chr19:2143434
|
A | T | 1 | a0001c0002t0001g0262 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.97-4720T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143434 | ||||||
chr19:2143439
|
G | A | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-4725C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143439 | ||||||
chr19:2143464
|
T | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | HG02132.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.97-4750A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143464 | ||||||
chr19:2143483
|
G | A | 1 | a0001c0002t0001g0302 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.97-4769C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143483 | ||||||
chr19:2143504
|
T | C | 1 | a0001c0001t0001g0110 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.97-4790A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143504 | ||||||
chr19:2143632
|
G | A | 2 | a0001c0002t0001g0303a0001c0002t0001g0304 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.97-4918C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143632 | ||||||
chr19:2143717
|
C | T | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97-5003G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143717 | ||||||
chr19:2143854
|
G | A | 1 | a0001c0002t0001g0259 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97-5140C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2143854 | ||||||
chr19:2144028
|
G | A | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-5314C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144028 | ||||||
chr19:2144047
|
T | C | 38 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0206others(35): Show | 38 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.97-5333A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144047 | ||||||
chr19:2144082
|
G | A | 3 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0043 | 3 | NA18980.hp1 NA18989.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.97-5368C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144082 | ||||||
chr19:2144086
|
C | CA | 126 | a0001c0001t0001g0243a0001c0001t0001g0263a0001c0001t0003g0378others(123): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.97-5373dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144086 | ||||||
chr19:2144117
|
A | G | 1 | a0001c0003t0002g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.97-5403T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144117 | ||||||
chr19:2144303
|
C | A | 1 | a0001c0001t0006g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97-5589G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144303 | ||||||
chr19:2144339
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-5625G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144339 | ||||||
chr19:2144367
|
C | T | 1 | a0001c0008t0002g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.97-5653G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144367 | ||||||
chr19:2144430
|
A | G | 91 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.97-5716T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144430 | ||||||
chr19:2144472
|
A | G | 91 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.97-5758T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144472 | ||||||
chr19:2144560
|
C | T | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-5846G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144560 | ||||||
chr19:2144682
|
C | G | 1 | a0001c0002t0001g0258 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.97-5968G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144682 | ||||||
chr19:2144759
|
T | C | 192 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.97-6045A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144759 | ||||||
chr19:2144762
|
G | T | 1 | a0001c0004t0002g0045 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.97-6048C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144762 | ||||||
chr19:2144805
|
A | C | 91 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.97-6091T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144805 | ||||||
chr19:2144990
|
T | C | 91 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.96+6249A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2144990 | ||||||
chr19:2145006
|
G | A | 22 | a0001c0002t0001g0261a0001c0002t0001g0305a0001c0002t0001g0306others(19): Show | 22 | HG00438.hp1 HG01952.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+6233C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145006 | ||||||
chr19:2145028
|
G | A | 1 | a0001c0001t0003g0380 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.96+6211C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145028 | ||||||
chr19:2145047
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.96+6192A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145047 | ||||||
chr19:2145105
|
C | G | 1 | a0001c0001t0002g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.96+6134G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145105 | ||||||
chr19:2145325
|
G | A | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+5914C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145325 | ||||||
chr19:2145331
|
A | G | 91 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.96+5908T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145331 | ||||||
chr19:2145447
|
T | C | 1 | a0001c0004t0002g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.96+5792A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145447 | ||||||
chr19:2145451
|
T | C | 87 | a0001c0001t0001g0263a0001c0002t0001g0003a0001c0002t0001g0004others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.96+5788A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145451 | ||||||
chr19:2145482
|
T | G | 192 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0243others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.96+5757A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145482 | ||||||
chr19:2145846
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+5393G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145846 | ||||||
chr19:2145974
|
G | A | 3 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399 | 3 | HG02145.hp2 HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+5265C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2145974 | ||||||
chr19:2146007
|
TGGGAGAA others(8): Show |
T | 4 | a0001c0006t0002g0009a0001c0008t0002g0184a0001c0008t0002g0185others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+5217_96+5231del others(15): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146007 | ||||||
chr19:2146016
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.96+5223G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146016 | ||||||
chr19:2146067
|
C | G | 2 | a0001c0003t0002g0188a0001c0014t0013g0007 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.96+5172G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146067 | ||||||
chr19:2146074
|
C | T | 1 | a0001c0002t0001g0261 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.96+5165G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146074 | ||||||
chr19:2146102
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+5137G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146102 | ||||||
chr19:2146113
|
T | C | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.96+5126A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146113 | ||||||
chr19:2146432
|
C | T | 5 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0111others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+4807G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146432 | ||||||
chr19:2146564
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.96+4675C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146564 | ||||||
chr19:2146607
|
C | CA | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(123): Show | 129 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.96+4631dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146607 | ||||||
chr19:2146607
|
C | CAA | 11 | a0001c0001t0001g0049a0001c0001t0001g0069a0001c0001t0001g0170others(8): Show | 11 | HG00438.hp2 HG00738.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+4630_96+4631dup others(2): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146607 | ||||||
chr19:2146607
|
CA | C | 7 | a0001c0001t0001g0072a0001c0001t0003g0350a0001c0002t0001g0187others(4): Show | 7 | HG03453.hp2 HG04199.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+4631delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146607 | ||||||
chr19:2146630
|
C | T | 201 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.96+4609G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146630 | ||||||
chr19:2146727
|
G | C | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+4512C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146727 | ||||||
chr19:2146793
|
C | T | 1 | a0001c0001t0003g0378 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.96+4446G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146793 | ||||||
chr19:2146794
|
T | C | 1 | a0001c0001t0003g0378 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.96+4445A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146794 | ||||||
chr19:2146853
|
T | C | 201 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(198): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.96+4386A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2146853 | ||||||
chr19:2147038
|
A | G | 1 | a0001c0002t0001g0257 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.96+4201T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147038 | ||||||
chr19:2147070
|
C | T | 1 | a0001c0004t0002g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.96+4169G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147070 | ||||||
chr19:2147173
|
C | T | 1 | a0001c0006t0008g0256 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.96+4066G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147173 | ||||||
chr19:2147179
|
T | A | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0175 | 3 | NA18973.hp2 NA19002.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.96+4060A>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147179 | ||||||
chr19:2147276
|
C | T | 3 | a0001c0003t0001g0191a0001c0003t0002g0192a0001c0003t0002g0193 | 3 | HG02572.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.96+3963G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147276 | ||||||
chr19:2147285
|
C | T | 1 | a0001c0002t0001g0003 | 2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.96+3954G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147285 | ||||||
chr19:2147302
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.96+3937C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147302 | ||||||
chr19:2147345
|
C | CA | 11 | a0001c0002t0001g0323a0001c0002t0001g0324a0001c0002t0001g0342others(8): Show | 11 | HG00642.hp1 HG01928.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+3893dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147345 | ||||||
chr19:2147345
|
CA | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(177): Show | 184 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.96+3893delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147345 | ||||||
chr19:2147360
|
A | G | 1 | a0001c0004t0002g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.96+3879T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147360 | ||||||
chr19:2147361
|
A | G | 3 | a0001c0006t0002g0009a0001c0012t0007g0182a0001c0012t0007g0183 | 3 | HG02257.hp2 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.96+3878T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147361 | ||||||
chr19:2147416
|
C | CT | 56 | a0001c0001t0001g0070a0001c0001t0001g0202a0001c0003t0001g0071others(53): Show | 56 | HG00408.hp1 HG00597.hp2 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.96+3822dupA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147416 | ||||||
chr19:2147416
|
CT | C | 114 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0131others(111): Show | 118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.96+3822delA | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147416 | ||||||
chr19:2147513
|
G | T | 1 | a0001c0005t0002g0019 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.96+3726C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147513 | ||||||
chr19:2147586
|
C | G | 2 | a0001c0003t0002g0189a0001c0003t0002g0190 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.96+3653G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147586 | ||||||
chr19:2147811
|
G | A | 1 | a0001c0002t0001g0252 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.96+3428C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147811 | ||||||
chr19:2147834
|
G | A | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.96+3405C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147834 | ||||||
chr19:2147862
|
C | A | 1 | a0001c0003t0002g0203 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.96+3377G>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147862 | ||||||
chr19:2147894
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.96+3345T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147894 | ||||||
chr19:2147895
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.96+3344C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147895 | ||||||
chr19:2147913
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0002g0205 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.96+3326G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147913 | ||||||
chr19:2147988
|
G | A | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.96+3251C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2147988 | ||||||
chr19:2148039
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0002g0205 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.96+3200G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148039 | ||||||
chr19:2148094
|
C | T | 1 | a0001c0002t0001g0254 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.96+3145G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148094 | ||||||
chr19:2148097
|
A | G | 1 | a0001c0004t0002g0220 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.96+3142T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148097 | ||||||
chr19:2148146
|
C | CA | 22 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0176others(19): Show | 22 | HG02074.hp1 HG02080.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.96+3092dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148146 | ||||||
chr19:2148146
|
CA | C | 131 | a0001c0001t0001g0010a0001c0001t0001g0068a0001c0001t0001g0069others(128): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.96+3092delT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148146 | ||||||
chr19:2148164
|
G | A | 2 | a0001c0012t0007g0182a0001c0012t0007g0183 | 2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.96+3075C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148164 | ||||||
chr19:2148211
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+3028A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148211 | ||||||
chr19:2148421
|
C | G | 4 | a0001c0006t0002g0009a0001c0008t0002g0184a0001c0008t0002g0185others(1): Show | 4 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2818G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148421 | ||||||
chr19:2148495
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.96+2744A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148495 | ||||||
chr19:2148543
|
A | G | 1 | a0001c0003t0002g0052 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.96+2696T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148543 | ||||||
chr19:2148645
|
C | T | 3 | a0001c0002t0001g0250a0001c0002t0001g0251a0001c0002t0001g0252 | 3 | HG00323.hp2 HG01361.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.96+2594G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148645 | ||||||
chr19:2148677
|
G | A | 1 | a0001c0006t0002g0330 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.96+2562C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148677 | ||||||
chr19:2148697
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.96+2542A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148697 | ||||||
chr19:2148758
|
A | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0055others(16): Show | 19 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.96+2481T>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148758 | ||||||
chr19:2148825
|
A | C | 1 | a0002c0007t0004g0386 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.96+2414T>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148825 | ||||||
chr19:2148896
|
C | T | 7 | a0001c0004t0002g0213a0001c0004t0002g0214a0001c0004t0002g0215others(4): Show | 7 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+2343G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2148896 | ||||||
chr19:2149001
|
G | A | 37 | a0001c0001t0001g0243a0001c0004t0002g0051a0001c0004t0002g0213others(34): Show | 37 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.96+2238C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149001 | ||||||
chr19:2149110
|
C | T | 2 | a0001c0008t0002g0184a0001c0008t0002g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.96+2129G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149110 | ||||||
chr19:2149216
|
G | A | 39 | a0001c0001t0001g0243a0001c0002t0001g0331a0001c0002t0001g0332others(36): Show | 39 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.96+2023C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149216 | ||||||
chr19:2149299
|
A | G | 5 | a0001c0008t0002g0181a0001c0008t0011g0398a0001c0008t0011g0399others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1940T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149299 | ||||||
chr19:2149497
|
C | T | 1 | a0001c0005t0002g0018 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.96+1742G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149497 | ||||||
chr19:2149504
|
C | T | 200 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(197): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.96+1735G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149504 | ||||||
chr19:2149543
|
C | CA | 138 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0142others(135): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.96+1695dupT | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149543 | ||||||
chr19:2149649
|
G | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | HG01346.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.96+1590C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149649 | ||||||
chr19:2149665
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.96+1574C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149665 | ||||||
chr19:2149695
|
T | C | 213 | a0001c0001t0001g0049a0001c0001t0001g0202a0001c0001t0001g0204others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.96+1544A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149695 | ||||||
chr19:2149745
|
C | T | 1 | a0001c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.96+1494G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149745 | ||||||
chr19:2149830
|
A | G | 42 | a0001c0001t0001g0049a0001c0003t0002g0024a0001c0003t0002g0026others(39): Show | 42 | HG00408.hp1 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.96+1409T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2149830 | ||||||
chr19:2150001
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.96+1238C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150001 | ||||||
chr19:2150004
|
G | A | 1 | a0001c0008t0011g0399 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.96+1235C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150004 | ||||||
chr19:2150032
|
G | C | 1 | a0001c0003t0002g0338 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.96+1207C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150032 | ||||||
chr19:2150197
|
C | G | 1 | a0001c0001t0001g0017 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.96+1042G>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150197 | ||||||
chr19:2150219
|
G | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0002g0012others(3): Show | 6 | HG02258.hp2 HG02486.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1020C>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150219 | ||||||
chr19:2150242
|
G | A | 4 | a0001c0002t0001g0339a0001c0002t0001g0340a0001c0002t0001g0341others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+997C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150242 | ||||||
chr19:2150396
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.96+843T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150396 | ||||||
chr19:2150474
|
A | G | 1 | a0001c0006t0002g0009 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.96+765T>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150474 | ||||||
chr19:2150596
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+643G>A | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150596 | ||||||
chr19:2150740
|
T | G | 1 | a0001c0003t0002g0343 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.96+499A>C | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150740 | ||||||
chr19:2150928
|
G | A | 1 | a0001c0003t0002g0344 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.96+311C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150928 | ||||||
chr19:2150973
|
G | C | 1 | a0001c0001t0002g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.96+266C>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2150973 | ||||||
chr19:2151015
|
T | C | 1 | a0001c0001t0001g0346 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.96+224A>G | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2151015 | ||||||
chr19:2151228
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.96+11C>T | AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 1/31 | chr19 | 2151228 |