geneid | 64411 |
---|---|
ensemblid | ENSG00000120318.16 |
hgncid | 24097 |
symbol | ARAP3 |
name | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 |
refseq_nuc | NM_022481.6 |
refseq_prot | NP_071926.4 |
ensembl_nuc | ENST00000239440.9 |
ensembl_prot | ENSP00000239440.4 |
mane_status | MANE Select |
chr | chr5 |
start | 141653402 |
end | 141682230 |
strand | - |
ver | v1.2 |
region | chr5:141653402-141682230 |
region5000 | chr5:141648402-141687230 |
regionname0 | ARAP3_chr5_141653402_141682230 |
regionname5000 | ARAP3_chr5_141648402_141687230 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1544 | 340 | 88 | 58 | 145 | 13 | 34 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002 | 0/0 | 1544 | 35 | 3 | 7 | 18 | 1 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0003 | 0/0 | 1544 | 7 | 0 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0004 | 0/0 | 1544 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0005 | 0/0 | 1544 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0006 | 0/0 | 1544 | 3 | 0 | 0 | 0 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0007 | 0/0 | 1544 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0008 | 0/0 | 1544 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0009 | 0/0 | 1540 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0010 | 0/0 | 1544 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0011 | 0/0 | 1544 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0012 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0013 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0014 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0015 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0016 | 0/0 | 1544 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0017 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0018 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0019 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0020 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0021 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0022 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 4635 | 82 | 2 | 14 | 54 | 4 | 7 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0002 | 0/1 | 4635 | 66 | 9 | 10 | 35 | 3 | 8 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0003 | 0/0 | 4635 | 55 | 5 | 13 | 31 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0004 | 0/0 | 4635 | 33 | 3 | 7 | 17 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0005 | 0/0 | 4635 | 30 | 12 | 8 | 7 | 1 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0006 | 0/0 | 4635 | 29 | 28 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0007 | 0/0 | 4635 | 16 | 0 | 6 | 7 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0008 | 0/0 | 4635 | 15 | 3 | 1 | 7 | 0 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0009 | 0/0 | 4635 | 8 | 5 | 0 | 0 | 2 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0010 | 0/0 | 4635 | 7 | 0 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0011 | 0/0 | 4635 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0012 | 0/0 | 4635 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0013 | 0/0 | 4635 | 4 | 0 | 1 | 0 | 3 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0014 | 0/0 | 4635 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0015 | 0/0 | 4635 | 3 | 0 | 0 | 0 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0016 | 0/0 | 4635 | 3 | 0 | 1 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0017 | 0/0 | 4635 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0018 | 0/0 | 4635 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0019 | 0/0 | 4635 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0020 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0021 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0022 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0023 | 0/0 | 4623 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0024 | 0/0 | 4635 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0025 | 0/0 | 4635 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0026 | 0/0 | 4635 | 2 | 1 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0027 | 0/0 | 4635 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0028 | 0/0 | 4635 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0029 | 0/0 | 4635 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0030 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0031 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0032 | 0/0 | 4622 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0033 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0034 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0035 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0036 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0037 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0038 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0039 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0040 | 0/0 | 4635 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0041 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0042 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0043 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0044 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0045 | 0/0 | 4635 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0046 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0047 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0048 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0049 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0050 | 0/0 | 4635 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
c0051 | 0/0 | 4635 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 624 | 404 | 89 | 75 | 176 | 16 | 46 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
t0002 | 0/0 | 624 | 5 | 5 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
t0003 | 0/0 | 624 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
t0004 | 0/0 | 624 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
t0005 | 0/0 | 624 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 32 | 0 | 3 | 24 | 1 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0002 | 0/0 | 8 | 1 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0003 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0006 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0041 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/0 | 82 | 2 | 14 | 54 | 4 | 7 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0002 | a0001 | c0002 | 0/1 | 66 | 9 | 10 | 35 | 3 | 8 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 55 | 5 | 13 | 31 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 30 | 12 | 8 | 7 | 1 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 29 | 28 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0007 | a0001 | c0007 | 0/0 | 16 | 0 | 6 | 7 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0008 | a0001 | c0008 | 0/0 | 15 | 3 | 1 | 7 | 0 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0009 | a0001 | c0009 | 0/0 | 8 | 5 | 0 | 0 | 2 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0011 | a0001 | c0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0013 | a0001 | c0013 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0016 | a0001 | c0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0018 | a0001 | c0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0020 | a0001 | c0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0021 | a0001 | c0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0022 | a0001 | c0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0025 | a0001 | c0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0026 | a0001 | c0026 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0027 | a0001 | c0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0028 | a0001 | c0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0029 | a0001 | c0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0033 | a0001 | c0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0034 | a0001 | c0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0038 | a0001 | c0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0042 | a0001 | c0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0043 | a0001 | c0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0044 | a0001 | c0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0051 | a0001 | c0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002c0004 | a0002 | c0004 | 0/0 | 33 | 3 | 7 | 17 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002c0030 | a0002 | c0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002c0031 | a0002 | c0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0003c0010 | a0003 | c0010 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0004c0012 | a0004 | c0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0005c0014 | a0005 | c0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0006c0015 | a0006 | c0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0007c0019 | a0007 | c0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0008c0017 | a0008 | c0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0009c0023 | a0009 | c0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0010c0047 | a0010 | c0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0010c0049 | a0010 | c0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0011c0024 | a0011 | c0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0012c0035 | a0012 | c0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0013c0036 | a0013 | c0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0014c0037 | a0014 | c0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0015c0048 | a0015 | c0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0016c0040 | a0016 | c0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0017c0050 | a0017 | c0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0018c0045 | a0018 | c0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0019c0046 | a0019 | c0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0020c0041 | a0020 | c0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0021c0032 | a0021 | c0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0022c0039 | a0022 | c0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 1/0 | 82 | 2 | 14 | 54 | 4 | 7 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0002t0001 | a0001 | c0002 | t0001 | 0/1 | 66 | 9 | 10 | 35 | 3 | 8 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 52 | 2 | 13 | 31 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0003t0004 | a0001 | c0003 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0003t0005 | a0001 | c0003 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 27 | 10 | 7 | 7 | 1 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0005t0003 | a0001 | c0005 | t0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 29 | 28 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0007t0001 | a0001 | c0007 | t0001 | 0/0 | 16 | 0 | 6 | 7 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 15 | 3 | 1 | 7 | 0 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 7 | 4 | 0 | 0 | 2 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0009t0002 | a0001 | c0009 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0011t0001 | a0001 | c0011 | t0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0011t0002 | a0001 | c0011 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0016t0001 | a0001 | c0016 | t0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0018t0002 | a0001 | c0018 | t0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0020t0001 | a0001 | c0020 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0021t0001 | a0001 | c0021 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0021t0004 | a0001 | c0021 | t0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0022t0001 | a0001 | c0022 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0025t0001 | a0001 | c0025 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0026t0001 | a0001 | c0026 | t0001 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0027t0001 | a0001 | c0027 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0028t0001 | a0001 | c0028 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0029t0001 | a0001 | c0029 | t0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0033t0001 | a0001 | c0033 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0034t0001 | a0001 | c0034 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0038t0001 | a0001 | c0038 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0042t0001 | a0001 | c0042 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0043t0001 | a0001 | c0043 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0044t0001 | a0001 | c0044 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0001c0051t0001 | a0001 | c0051 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 33 | 3 | 7 | 17 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002c0030t0001 | a0002 | c0030 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0002c0031t0001 | a0002 | c0031 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0003c0010t0001 | a0003 | c0010 | t0001 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0004c0012t0001 | a0004 | c0012 | t0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0005c0014t0001 | a0005 | c0014 | t0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0006c0015t0001 | a0006 | c0015 | t0001 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0007c0019t0001 | a0007 | c0019 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0008c0017t0001 | a0008 | c0017 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0009c0023t0001 | a0009 | c0023 | t0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0010c0047t0001 | a0010 | c0047 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0010c0049t0001 | a0010 | c0049 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0011c0024t0001 | a0011 | c0024 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0012c0035t0001 | a0012 | c0035 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0013c0036t0001 | a0013 | c0036 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0014c0037t0001 | a0014 | c0037 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0015c0048t0001 | a0015 | c0048 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0016c0040t0001 | a0016 | c0040 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0017c0050t0001 | a0017 | c0050 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0018c0045t0001 | a0018 | c0045 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0019c0046t0001 | a0019 | c0046 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0020c0041t0001 | a0020 | c0041 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0021c0032t0001 | a0021 | c0032 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
a0022c0039t0001 | a0022 | c0039 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 32 | 0 | 3 | 24 | 1 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 8 | 1 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0185 | a0001 | c0001 | t0001 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0004 | a0001 | c0002 | t0001 | g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0005 | a0001 | c0002 | t0001 | g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0007 | a0001 | c0002 | t0001 | g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0008 | a0001 | c0002 | t0001 | g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0023 | a0001 | c0002 | t0001 | g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0024 | a0001 | c0002 | t0001 | g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0053 | a0001 | c0002 | t0001 | g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0054 | a0001 | c0002 | t0001 | g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0065 | a0001 | c0002 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0068 | a0001 | c0002 | t0001 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0069 | a0001 | c0002 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0072 | a0001 | c0002 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0073 | a0001 | c0002 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0074 | a0001 | c0002 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0075 | a0001 | c0002 | t0001 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0076 | a0001 | c0002 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0077 | a0001 | c0002 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0078 | a0001 | c0002 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0079 | a0001 | c0002 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0081 | a0001 | c0002 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0082 | a0001 | c0002 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0083 | a0001 | c0002 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0084 | a0001 | c0002 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0085 | a0001 | c0002 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0086 | a0001 | c0002 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0090 | a0001 | c0002 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0091 | a0001 | c0002 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0092 | a0001 | c0002 | t0001 | g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0093 | a0001 | c0002 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0095 | a0001 | c0002 | t0001 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0096 | a0001 | c0002 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0098 | a0001 | c0002 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0099 | a0001 | c0002 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0215 | a0001 | c0002 | t0001 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0219 | a0001 | c0002 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0225 | a0001 | c0002 | t0001 | g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0226 | a0001 | c0002 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0227 | a0001 | c0002 | t0001 | g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0228 | a0001 | c0002 | t0001 | g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0229 | a0001 | c0002 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0230 | a0001 | c0002 | t0001 | g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0254 | a0001 | c0002 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0268 | a0001 | c0002 | t0001 | g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0002t0001g0271 | a0001 | c0002 | t0001 | g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0006 | a0001 | c0003 | t0001 | g0006 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0011 | a0001 | c0003 | t0001 | g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0012 | a0001 | c0003 | t0001 | g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0017 | a0001 | c0003 | t0001 | g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0048 | a0001 | c0003 | t0001 | g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0049 | a0001 | c0003 | t0001 | g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0050 | a0001 | c0003 | t0001 | g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0051 | a0001 | c0003 | t0001 | g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0052 | a0001 | c0003 | t0001 | g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0063 | a0001 | c0003 | t0001 | g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0209 | a0001 | c0003 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0211 | a0001 | c0003 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0216 | a0001 | c0003 | t0001 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0217 | a0001 | c0003 | t0001 | g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0231 | a0001 | c0003 | t0001 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0233 | a0001 | c0003 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0234 | a0001 | c0003 | t0001 | g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0236 | a0001 | c0003 | t0001 | g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0237 | a0001 | c0003 | t0001 | g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0238 | a0001 | c0003 | t0001 | g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0240 | a0001 | c0003 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0241 | a0001 | c0003 | t0001 | g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0242 | a0001 | c0003 | t0001 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0244 | a0001 | c0003 | t0001 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0245 | a0001 | c0003 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0246 | a0001 | c0003 | t0001 | g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0248 | a0001 | c0003 | t0001 | g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0249 | a0001 | c0003 | t0001 | g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0251 | a0001 | c0003 | t0001 | g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0255 | a0001 | c0003 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0256 | a0001 | c0003 | t0001 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0257 | a0001 | c0003 | t0001 | g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0259 | a0001 | c0003 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0260 | a0001 | c0003 | t0001 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0001g0261 | a0001 | c0003 | t0001 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0004g0202 | a0001 | c0003 | t0004 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0004g0203 | a0001 | c0003 | t0004 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0003t0005g0243 | a0001 | c0003 | t0005 | g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0010 | a0001 | c0005 | t0001 | g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0033 | a0001 | c0005 | t0001 | g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0035 | a0001 | c0005 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0037 | a0001 | c0005 | t0001 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0129 | a0001 | c0005 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0130 | a0001 | c0005 | t0001 | g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0131 | a0001 | c0005 | t0001 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0132 | a0001 | c0005 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0133 | a0001 | c0005 | t0001 | g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0144 | a0001 | c0005 | t0001 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0145 | a0001 | c0005 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0147 | a0001 | c0005 | t0001 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0149 | a0001 | c0005 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0152 | a0001 | c0005 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0153 | a0001 | c0005 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0154 | a0001 | c0005 | t0001 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0155 | a0001 | c0005 | t0001 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0162 | a0001 | c0005 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0164 | a0001 | c0005 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0165 | a0001 | c0005 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0001g0166 | a0001 | c0005 | t0001 | g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0005t0003g0016 | a0001 | c0005 | t0003 | g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0018 | a0001 | c0006 | t0001 | g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0032 | a0001 | c0006 | t0001 | g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0034 | a0001 | c0006 | t0001 | g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0136 | a0001 | c0006 | t0001 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0137 | a0001 | c0006 | t0001 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0138 | a0001 | c0006 | t0001 | g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0139 | a0001 | c0006 | t0001 | g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0140 | a0001 | c0006 | t0001 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0141 | a0001 | c0006 | t0001 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0142 | a0001 | c0006 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0143 | a0001 | c0006 | t0001 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0148 | a0001 | c0006 | t0001 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0158 | a0001 | c0006 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0272 | a0001 | c0006 | t0001 | g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0273 | a0001 | c0006 | t0001 | g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0274 | a0001 | c0006 | t0001 | g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0275 | a0001 | c0006 | t0001 | g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0276 | a0001 | c0006 | t0001 | g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0277 | a0001 | c0006 | t0001 | g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0278 | a0001 | c0006 | t0001 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0279 | a0001 | c0006 | t0001 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0280 | a0001 | c0006 | t0001 | g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0281 | a0001 | c0006 | t0001 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0282 | a0001 | c0006 | t0001 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0006t0001g0284 | a0001 | c0006 | t0001 | g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0014 | a0001 | c0007 | t0001 | g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0019 | a0001 | c0007 | t0001 | g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0020 | a0001 | c0007 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0025 | a0001 | c0007 | t0001 | g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0057 | a0001 | c0007 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0058 | a0001 | c0007 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0059 | a0001 | c0007 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0061 | a0001 | c0007 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0087 | a0001 | c0007 | t0001 | g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0088 | a0001 | c0007 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0007t0001g0204 | a0001 | c0007 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0021 | a0001 | c0008 | t0001 | g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0022 | a0001 | c0008 | t0001 | g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0044 | a0001 | c0008 | t0001 | g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0056 | a0001 | c0008 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0064 | a0001 | c0008 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0066 | a0001 | c0008 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0070 | a0001 | c0008 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0071 | a0001 | c0008 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0208 | a0001 | c0008 | t0001 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0212 | a0001 | c0008 | t0001 | g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0213 | a0001 | c0008 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0008t0001g0258 | a0001 | c0008 | t0001 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0009t0001g0013 | a0001 | c0009 | t0001 | g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0009t0001g0027 | a0001 | c0009 | t0001 | g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0009t0001g0089 | a0001 | c0009 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0009t0002g0270 | a0001 | c0009 | t0002 | g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0011t0001g0134 | a0001 | c0011 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0011t0001g0135 | a0001 | c0011 | t0001 | g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0011t0001g0150 | a0001 | c0011 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0011t0001g0156 | a0001 | c0011 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0011t0001g0163 | a0001 | c0011 | t0001 | g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0011t0002g0097 | a0001 | c0011 | t0002 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0013t0001g0045 | a0001 | c0013 | t0001 | g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0013t0001g0220 | a0001 | c0013 | t0001 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0013t0001g0250 | a0001 | c0013 | t0001 | g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0016t0001g0191 | a0001 | c0016 | t0001 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0016t0001g0194 | a0001 | c0016 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0016t0001g0195 | a0001 | c0016 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0018t0002g0262 | a0001 | c0018 | t0002 | g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0018t0002g0263 | a0001 | c0018 | t0002 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0018t0002g0264 | a0001 | c0018 | t0002 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0020t0001g0151 | a0001 | c0020 | t0001 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0020t0001g0161 | a0001 | c0020 | t0001 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0021t0001g0283 | a0001 | c0021 | t0001 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0021t0004g0160 | a0001 | c0021 | t0004 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0022t0001g0036 | a0001 | c0022 | t0001 | g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0025t0001g0189 | a0001 | c0025 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0025t0001g0193 | a0001 | c0025 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0026t0001g0235 | a0001 | c0026 | t0001 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0026t0001g0239 | a0001 | c0026 | t0001 | g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0027t0001g0252 | a0001 | c0027 | t0001 | g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0027t0001g0253 | a0001 | c0027 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0028t0001g0026 | a0001 | c0028 | t0001 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0029t0001g0266 | a0001 | c0029 | t0001 | g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0029t0001g0267 | a0001 | c0029 | t0001 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0033t0001g0157 | a0001 | c0033 | t0001 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0034t0001g0159 | a0001 | c0034 | t0001 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0038t0001g0200 | a0001 | c0038 | t0001 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0042t0001g0232 | a0001 | c0042 | t0001 | g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0043t0001g0247 | a0001 | c0043 | t0001 | g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0044t0001g0101 | a0001 | c0044 | t0001 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0001c0051t0001g0269 | a0001 | c0051 | t0001 | g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0009 | a0002 | c0004 | t0001 | g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0015 | a0002 | c0004 | t0001 | g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0029 | a0002 | c0004 | t0001 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0030 | a0002 | c0004 | t0001 | g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0105 | a0002 | c0004 | t0001 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0108 | a0002 | c0004 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0109 | a0002 | c0004 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0110 | a0002 | c0004 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0111 | a0002 | c0004 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0112 | a0002 | c0004 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0113 | a0002 | c0004 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0114 | a0002 | c0004 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0115 | a0002 | c0004 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0118 | a0002 | c0004 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0119 | a0002 | c0004 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0120 | a0002 | c0004 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0121 | a0002 | c0004 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0122 | a0002 | c0004 | t0001 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0123 | a0002 | c0004 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0126 | a0002 | c0004 | t0001 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0127 | a0002 | c0004 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0128 | a0002 | c0004 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0285 | a0002 | c0004 | t0001 | g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0286 | a0002 | c0004 | t0001 | g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0287 | a0002 | c0004 | t0001 | g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0004t0001g0288 | a0002 | c0004 | t0001 | g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0030t0001g0124 | a0002 | c0030 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0002c0031t0001g0106 | a0002 | c0031 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0003c0010t0001g0046 | a0003 | c0010 | t0001 | g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0003c0010t0001g0047 | a0003 | c0010 | t0001 | g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0003c0010t0001g0062 | a0003 | c0010 | t0001 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0003c0010t0001g0210 | a0003 | c0010 | t0001 | g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0003c0010t0001g0221 | a0003 | c0010 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0004c0012t0001g0028 | a0004 | c0012 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0004c0012t0001g0107 | a0004 | c0012 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0004c0012t0001g0116 | a0004 | c0012 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0004c0012t0001g0117 | a0004 | c0012 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0005c0014t0001g0102 | a0005 | c0014 | t0001 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0005c0014t0001g0103 | a0005 | c0014 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0005c0014t0001g0104 | a0005 | c0014 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0006c0015t0001g0039 | a0006 | c0015 | t0001 | g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0006c0015t0001g0176 | a0006 | c0015 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0007c0019t0001g0222 | a0007 | c0019 | t0001 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0007c0019t0001g0223 | a0007 | c0019 | t0001 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0007c0019t0001g0224 | a0007 | c0019 | t0001 | g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0008c0017t0001g0205 | a0008 | c0017 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0008c0017t0001g0206 | a0008 | c0017 | t0001 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0008c0017t0001g0207 | a0008 | c0017 | t0001 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0009c0023t0001g0031 | a0009 | c0023 | t0001 | g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0010c0047t0001g0100 | a0010 | c0047 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0010c0049t0001g0094 | a0010 | c0049 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0011c0024t0001g0042 | a0011 | c0024 | t0001 | g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0012c0035t0001g0146 | a0012 | c0035 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0013c0036t0001g0168 | a0013 | c0036 | t0001 | g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0014c0037t0001g0167 | a0014 | c0037 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0015c0048t0001g0080 | a0015 | c0048 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0016c0040t0001g0060 | a0016 | c0040 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0017c0050t0001g0214 | a0017 | c0050 | t0001 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0018c0045t0001g0218 | a0018 | c0045 | t0001 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0019c0046t0001g0067 | a0019 | c0046 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0020c0041t0001g0265 | a0020 | c0041 | t0001 | g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0021c0032t0001g0125 | a0021 | c0032 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
a0022c0039t0001g0201 | a0022 | c0039 | t0001 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0091 | EUR | GBR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00140 | hp2 | a0003 | c0010 | t0001 | g0221 | EUR | GBR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00280 | hp1 | a0003 | c0010 | t0001 | g0046 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0065 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00323 | hp1 | a0002 | c0030 | t0001 | g0124 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00408 | hp1 | a0019 | c0046 | t0001 | g0067 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00438 | hp1 | a0002 | c0004 | t0001 | g0114 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00544 | hp1 | a0001 | c0007 | t0001 | g0014 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00558 | hp1 | a0001 | c0005 | t0001 | g0162 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00609 | hp2 | a0002 | c0004 | t0001 | g0009 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0256 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00639 | hp2 | a0003 | c0010 | t0001 | g0047 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00673 | hp1 | a0001 | c0008 | t0001 | g0022 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00673 | hp2 | a0007 | c0019 | t0001 | g0222 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0048 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00735 | hp2 | a0003 | c0010 | t0001 | g0047 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00738 | hp1 | a0002 | c0004 | t0001 | g0030 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0246 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG00741 | hp2 | a0001 | c0008 | t0001 | g0056 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01070 | hp1 | a0009 | c0023 | t0001 | g0031 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01071 | hp2 | a0009 | c0023 | t0001 | g0031 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01074 | hp2 | a0001 | c0007 | t0001 | g0025 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01081 | hp2 | a0001 | c0005 | t0001 | g0010 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01099 | hp1 | a0001 | c0005 | t0001 | g0165 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0049 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01168 | hp2 | a0001 | c0007 | t0001 | g0019 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01169 | hp1 | a0001 | c0005 | t0001 | g0133 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01169 | hp2 | a0001 | c0007 | t0001 | g0019 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01175 | hp1 | a0001 | c0044 | t0001 | g0101 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01175 | hp2 | a0001 | c0006 | t0001 | g0273 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01192 | hp2 | a0003 | c0010 | t0001 | g0046 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0033 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01243 | hp2 | a0012 | c0035 | t0001 | g0146 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01256 | hp1 | a0001 | c0007 | t0001 | g0058 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0288 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01257 | hp2 | a0001 | c0013 | t0001 | g0250 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01258 | hp2 | a0002 | c0004 | t0001 | g0287 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01346 | hp1 | a0005 | c0014 | t0001 | g0102 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01346 | hp2 | a0003 | c0010 | t0001 | g0062 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01358 | hp1 | a0001 | c0007 | t0001 | g0087 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0241 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01361 | hp1 | a0001 | c0007 | t0001 | g0025 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0217 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01433 | hp2 | a0020 | c0041 | t0001 | g0265 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01496 | hp1 | a0001 | c0029 | t0001 | g0266 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01496 | hp2 | a0001 | c0005 | t0001 | g0130 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01515 | hp2 | a0001 | c0013 | t0001 | g0045 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0010 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01516 | hp2 | a0001 | c0009 | t0001 | g0027 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01517 | hp1 | a0001 | c0013 | t0001 | g0045 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01517 | hp2 | a0001 | c0009 | t0001 | g0027 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01884 | hp1 | a0001 | c0006 | t0001 | g0148 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01891 | hp1 | a0001 | c0020 | t0001 | g0151 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01891 | hp2 | a0013 | c0036 | t0001 | g0168 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01928 | hp1 | a0001 | c0016 | t0001 | g0191 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01928 | hp2 | a0001 | c0042 | t0001 | g0232 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01934 | hp1 | a0002 | c0004 | t0001 | g0286 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01934 | hp2 | a0001 | c0005 | t0003 | g0016 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0248 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01978 | hp1 | a0002 | c0004 | t0001 | g0015 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01981 | hp2 | a0002 | c0004 | t0001 | g0015 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01993 | hp1 | a0001 | c0005 | t0001 | g0131 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0249 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02027 | hp1 | a0002 | c0004 | t0001 | g0118 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02040 | hp1 | a0002 | c0004 | t0001 | g0127 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02055 | hp1 | a0001 | c0006 | t0001 | g0018 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02055 | hp2 | a0001 | c0006 | t0001 | g0284 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02071 | hp2 | a0001 | c0008 | t0001 | g0066 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0011 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02074 | hp2 | a0001 | c0007 | t0001 | g0014 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02135 | hp1 | a0001 | c0007 | t0001 | g0204 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02135 | hp2 | a0002 | c0004 | t0001 | g0111 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02145 | hp1 | a0001 | c0011 | t0001 | g0150 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02145 | hp2 | a0001 | c0018 | t0002 | g0264 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CDX | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | CDX | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02257 | hp1 | a0002 | c0004 | t0001 | g0126 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0282 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02258 | hp1 | a0001 | c0006 | t0001 | g0143 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02273 | hp1 | a0002 | c0004 | t0001 | g0015 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0228 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02280 | hp2 | a0001 | c0006 | t0001 | g0139 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02300 | hp1 | a0001 | c0005 | t0001 | g0010 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02300 | hp2 | a0018 | c0045 | t0001 | g0218 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02451 | hp1 | a0001 | c0006 | t0001 | g0281 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02451 | hp2 | a0001 | c0005 | t0003 | g0016 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02572 | hp1 | a0001 | c0011 | t0002 | g0097 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02602 | hp1 | a0001 | c0008 | t0001 | g0070 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02602 | hp2 | a0001 | c0008 | t0001 | g0213 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02615 | hp1 | a0001 | c0011 | t0001 | g0134 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02615 | hp2 | a0001 | c0028 | t0001 | g0026 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02622 | hp1 | a0001 | c0006 | t0001 | g0032 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0141 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0203 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02630 | hp2 | a0001 | c0026 | t0001 | g0235 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02647 | hp1 | a0001 | c0009 | t0001 | g0013 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02647 | hp2 | a0001 | c0018 | t0002 | g0262 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0238 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02683 | hp2 | a0001 | c0027 | t0001 | g0253 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02717 | hp2 | a0001 | c0006 | t0001 | g0277 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02723 | hp1 | a0001 | c0028 | t0001 | g0026 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02723 | hp2 | a0001 | c0021 | t0004 | g0160 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02735 | hp2 | a0006 | c0015 | t0001 | g0039 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02738 | hp1 | a0001 | c0007 | t0001 | g0057 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0082 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02809 | hp1 | a0001 | c0006 | t0001 | g0275 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02809 | hp2 | a0001 | c0006 | t0001 | g0018 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02818 | hp1 | a0005 | c0014 | t0001 | g0103 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02818 | hp2 | a0001 | c0018 | t0002 | g0263 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02886 | hp1 | a0001 | c0006 | t0001 | g0276 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02886 | hp2 | a0001 | c0009 | t0001 | g0013 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02895 | hp1 | a0001 | c0005 | t0001 | g0132 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0136 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02896 | hp1 | a0001 | c0011 | t0001 | g0163 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0279 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02897 | hp1 | a0001 | c0011 | t0001 | g0156 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02897 | hp2 | a0001 | c0006 | t0001 | g0142 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02922 | hp1 | a0001 | c0011 | t0001 | g0135 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02922 | hp2 | a0001 | c0051 | t0001 | g0269 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0164 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02965 | hp2 | a0001 | c0029 | t0001 | g0267 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02970 | hp1 | a0001 | c0033 | t0001 | g0157 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0018 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02976 | hp1 | a0010 | c0049 | t0001 | g0094 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0271 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03041 | hp1 | a0001 | c0003 | t0004 | g0202 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03041 | hp2 | a0001 | c0006 | t0001 | g0280 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0129 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03098 | hp2 | a0008 | c0017 | t0001 | g0207 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0137 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03130 | hp2 | a0001 | c0006 | t0001 | g0034 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0033 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03139 | hp2 | a0001 | c0008 | t0001 | g0064 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03195 | hp1 | a0001 | c0008 | t0001 | g0021 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0063 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0032 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03225 | hp1 | a0008 | c0017 | t0001 | g0205 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03453 | hp1 | a0001 | c0006 | t0001 | g0138 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03453 | hp2 | a0005 | c0014 | t0001 | g0104 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03486 | hp1 | a0001 | c0003 | t0005 | g0243 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03486 | hp2 | a0001 | c0006 | t0001 | g0278 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03490 | hp1 | a0011 | c0024 | t0001 | g0042 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03490 | hp2 | a0001 | c0008 | t0001 | g0071 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03491 | hp1 | a0001 | c0005 | t0001 | g0166 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03492 | hp1 | a0011 | c0024 | t0001 | g0042 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03516 | hp1 | a0001 | c0022 | t0001 | g0036 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03516 | hp2 | a0001 | c0006 | t0001 | g0272 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03540 | hp1 | a0022 | c0039 | t0001 | g0201 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03579 | hp2 | a0001 | c0006 | t0001 | g0274 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03654 | hp1 | a0006 | c0015 | t0001 | g0039 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03654 | hp2 | a0002 | c0004 | t0001 | g0123 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03669 | hp1 | a0006 | c0015 | t0001 | g0176 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03688 | hp2 | a0001 | c0007 | t0001 | g0061 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03704 | hp1 | a0002 | c0004 | t0001 | g0122 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0234 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03710 | hp1 | a0002 | c0004 | t0001 | g0009 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03710 | hp2 | a0001 | c0005 | t0001 | g0010 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0233 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0245 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03942 | hp1 | a0001 | c0027 | t0001 | g0252 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03942 | hp2 | a0001 | c0007 | t0001 | g0088 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04115 | hp2 | a0001 | c0008 | t0001 | g0212 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04184 | hp1 | a0016 | c0040 | t0001 | g0060 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04199 | hp1 | a0002 | c0004 | t0001 | g0109 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04199 | hp2 | a0002 | c0004 | t0001 | g0030 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0081 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04204 | hp2 | a0001 | c0026 | t0001 | g0239 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0049 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG04228 | hp2 | a0002 | c0004 | t0001 | g0128 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18522 | hp1 | a0001 | c0022 | t0001 | g0036 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18522 | hp2 | a0001 | c0021 | t0001 | g0283 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18612 | hp1 | a0001 | c0016 | t0001 | g0194 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18747 | hp2 | a0001 | c0007 | t0001 | g0059 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18906 | hp1 | a0001 | c0034 | t0001 | g0159 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18906 | hp2 | a0001 | c0008 | t0001 | g0021 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18939 | hp1 | a0014 | c0037 | t0001 | g0167 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18941 | hp1 | a0002 | c0031 | t0001 | g0106 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0236 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18951 | hp2 | a0001 | c0025 | t0001 | g0189 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18952 | hp1 | a0001 | c0008 | t0001 | g0044 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18954 | hp2 | a0002 | c0004 | t0001 | g0029 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18961 | hp2 | a0001 | c0005 | t0001 | g0154 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18965 | hp2 | a0021 | c0032 | t0001 | g0125 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18966 | hp1 | a0007 | c0019 | t0001 | g0223 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18966 | hp2 | a0001 | c0003 | t0001 | g0216 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18968 | hp1 | a0001 | c0007 | t0001 | g0014 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18969 | hp1 | a0001 | c0008 | t0001 | g0208 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18969 | hp2 | a0001 | c0005 | t0001 | g0035 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18972 | hp2 | a0002 | c0004 | t0001 | g0113 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18979 | hp2 | a0002 | c0004 | t0001 | g0112 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18980 | hp2 | a0004 | c0012 | t0001 | g0117 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18981 | hp2 | a0001 | c0005 | t0001 | g0149 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18983 | hp1 | a0001 | c0007 | t0001 | g0020 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18984 | hp2 | a0001 | c0016 | t0001 | g0195 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18986 | hp1 | a0017 | c0050 | t0001 | g0214 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18989 | hp2 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18990 | hp2 | a0004 | c0012 | t0001 | g0028 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18994 | hp2 | a0004 | c0012 | t0001 | g0116 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18998 | hp1 | a0001 | c0008 | t0001 | g0258 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18998 | hp2 | a0001 | c0005 | t0001 | g0153 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18999 | hp1 | a0002 | c0004 | t0001 | g0029 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19003 | hp2 | a0002 | c0004 | t0001 | g0108 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19005 | hp2 | a0004 | c0012 | t0001 | g0028 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19007 | hp1 | a0002 | c0004 | t0001 | g0110 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19007 | hp2 | a0001 | c0005 | t0001 | g0152 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19010 | hp1 | a0001 | c0008 | t0001 | g0022 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19012 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19030 | hp1 | a0001 | c0005 | t0001 | g0145 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19030 | hp2 | a0002 | c0004 | t0001 | g0105 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0144 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19054 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19057 | hp1 | a0002 | c0004 | t0001 | g0115 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19057 | hp2 | a0002 | c0004 | t0001 | g0121 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19060 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0242 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19066 | hp1 | a0002 | c0004 | t0001 | g0119 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19066 | hp2 | a0015 | c0048 | t0001 | g0080 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19079 | hp2 | a0001 | c0025 | t0001 | g0193 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19082 | hp2 | a0002 | c0004 | t0001 | g0120 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19083 | hp2 | a0004 | c0012 | t0001 | g0107 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19085 | hp2 | a0001 | c0008 | t0001 | g0044 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19090 | hp2 | a0001 | c0005 | t0001 | g0035 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19091 | hp1 | a0007 | c0019 | t0001 | g0224 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0158 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA19240 | hp2 | a0001 | c0009 | t0001 | g0013 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20129 | hp1 | a0008 | c0017 | t0001 | g0206 | AFR | ASW | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20129 | hp2 | a0001 | c0005 | t0001 | g0037 | AFR | ASW | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20752 | hp1 | a0001 | c0013 | t0001 | g0220 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | GIH | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20905 | hp2 | a0001 | c0009 | t0001 | g0089 | SAS | GIH | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01123 | hp1 | a0003 | c0010 | t0001 | g0210 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02109 | hp2 | a0001 | c0006 | t0001 | g0034 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02486 | hp1 | a0001 | c0005 | t0003 | g0016 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02486 | hp2 | a0001 | c0006 | t0001 | g0140 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02559 | hp1 | a0001 | c0009 | t0002 | g0270 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG02559 | hp2 | a0001 | c0038 | t0001 | g0200 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03471 | hp1 | a0010 | c0047 | t0001 | g0100 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG03471 | hp2 | a0001 | c0043 | t0001 | g0247 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0285 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 |
HG06807 | hp2 | a0001 | c0009 | t0001 | g0013 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA18955 | hp2 | a0001 | c0007 | t0001 | g0020 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20300 | hp1 | a0001 | c0020 | t0001 | g0161 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA20300 | hp2 | a0001 | c0005 | t0001 | g0155 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0257 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0147 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0092 | REF | REF | ARAP3_chr5_141648402_141687230 | ARAP3 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0041 | REF | REF | ARAP3_chr5_141648402_141687230 | ARAP3 |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141654147
|
ACCCCCGT others(5): Show |
A | 1 | a0009 | 2 | HG01070.hp1 HG01071.hp2 |
conservative_inframe_deletion | MODERATE | c.4426_4437delCAGGCA others(6): Show |
p.Gln1476_Gly1479del | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4512/5258 | 4426/4635 | 1476/1544 | chr5 | 141654147 | ||
chr5:141654256
|
C | A | 1 | a0010 | 2 | HG02976.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.4329G>T | p.Lys1443Asn | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4404/5258 | 4329/4635 | 1443/1544 | chr5 | 141654256 | ||
chr5:141654303
|
T | G | 1 | a0003 | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
missense_variant | MODERATE | c.4282A>C | p.Thr1428Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4357/5258 | 4282/4635 | 1428/1544 | chr5 | 141654303 | ||
chr5:141655631
|
T | C | 1 | a0017 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.4100A>G | p.Asn1367Ser | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/33 | 4175/5258 | 4100/4635 | 1367/1544 | chr5 | 141655631 | ||
chr5:141656198
|
T | C | 1 | a0016 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.3868A>G | p.Thr1290Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 28/33 | 3943/5258 | 3868/4635 | 1290/1544 | chr5 | 141656198 | ||
chr5:141656532
|
C | T | 3 | a0004a0007a0021 | 9 | HG00673.hp2 NA18965.hp2 NA18966.hp1 others(6): Show |
missense_variant | MODERATE | c.3761G>A | p.Arg1254His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/33 | 3836/5258 | 3761/4635 | 1254/1544 | chr5 | 141656532 | ||
chr5:141656629
|
G | A | 1 | a0015 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.3664C>T | p.Arg1222Cys | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/33 | 3739/5258 | 3664/4635 | 1222/1544 | chr5 | 141656629 | ||
chr5:141658384
|
A | C | 1 | a0008 | 3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.3507T>G | p.Ile1169Met | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/33 | 3582/5258 | 3507/4635 | 1169/1544 | chr5 | 141658384 | ||
chr5:141658466
|
AGGGTTGG others(9): Show |
A | 1 | a0021 | 1 | NA18965.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.3412-3_3424delCAGG others(12): Show |
p.Val1138fs | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/33 | 3499/5258 | 3412/4635 | 1138/1544 | chr5 | 141658466 | ||
chr5:141659840
|
C | A | 1 | a0014 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.3206G>T | p.Arg1069Leu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/33 | 3281/5258 | 3206/4635 | 1069/1544 | chr5 | 141659840 | ||
chr5:141661751
|
C | A | 1 | a0018 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.3052G>T | p.Asp1018Tyr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/33 | 3127/5258 | 3052/4635 | 1018/1544 | chr5 | 141661751 | ||
chr5:141662178
|
C | T | 1 | a0011 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.2878G>A | p.Asp960Asn | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/33 | 2953/5258 | 2878/4635 | 960/1544 | chr5 | 141662178 | ||
chr5:141669750
|
C | T | 1 | a0019 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.2311G>A | p.Gly771Arg | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/33 | 2386/5258 | 2311/4635 | 771/1544 | chr5 | 141669750 | ||
chr5:141669947
|
G | A | 1 | a0020 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2224C>T | p.Pro742Ser | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 15/33 | 2299/5258 | 2224/4635 | 742/1544 | chr5 | 141669947 | ||
chr5:141672841
|
G | T | 1 | a0006 | 3 | HG02735.hp2 HG03654.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.1178C>A | p.Pro393His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 8/33 | 1253/5258 | 1178/4635 | 393/1544 | chr5 | 141672841 | ||
chr5:141673419
|
C | T | 1 | a0013 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.954G>A | p.Met318Ile | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/33 | 1029/5258 | 954/4635 | 318/1544 | chr5 | 141673419 | ||
chr5:141673693
|
G | A | 1 | a0012 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.814C>T | p.Leu272Phe | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 5/33 | 889/5258 | 814/4635 | 272/1544 | chr5 | 141673693 | ||
chr5:141679591
|
C | G | 3 | a0002a0004a0021 | 41 | HG00323.hp1 HG00438.hp1 HG00609.hp2 others(38): Show |
missense_variant | MODERATE | c.652G>C | p.Asp218His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/33 | 727/5258 | 652/4635 | 218/1544 | chr5 | 141679591 | ||
chr5:141679793
|
G | T | 1 | a0005 | 3 | HG01346.hp1 HG02818.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.554C>A | p.Pro185His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 3/33 | 629/5258 | 554/4635 | 185/1544 | chr5 | 141679793 | ||
chr5:141680003
|
C | T | 1 | a0022 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.484G>A | p.Gly162Ser | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 559/5258 | 484/4635 | 162/1544 | chr5 | 141680003 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141654160
|
G | T | 1 | a0001c0029 | 2 | HG01496.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.4425C>A | p.Pro1475Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4500/5258 | 4425/4635 | 1475/1544 | chr5 | 141654160 | ||
chr5:141655681
|
A | G | 6 | a0001c0007a0001c0011a0001c0018others(3): Show | 29 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(26): Show |
synonymous_variant | LOW | c.4050T>C | p.Pro1350Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/33 | 4125/5258 | 4050/4635 | 1350/1544 | chr5 | 141655681 | ||
chr5:141655747
|
C | T | 1 | a0001c0028 | 2 | HG02615.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.3984G>A | p.Gln1328Gln | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/33 | 4059/5258 | 3984/4635 | 1328/1544 | chr5 | 141655747 | ||
chr5:141656770
|
A | G | 32 | a0001c0002a0001c0003a0001c0006others(29): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
synonymous_variant | LOW | c.3603T>C | p.Ala1201Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 26/33 | 3678/5258 | 3603/4635 | 1201/1544 | chr5 | 141656770 | ||
chr5:141656824
|
T | C | 1 | a0001c0034 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3549A>G | p.Glu1183Glu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 26/33 | 3624/5258 | 3549/4635 | 1183/1544 | chr5 | 141656824 | ||
chr5:141659474
|
G | A | 1 | a0001c0043 | 1 | HG03471.hp2 | splice_region_variant&synonymous_variant | LOW | c.3270C>T | p.Ile1090Ile | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/33 | 3345/5258 | 3270/4635 | 1090/1544 | chr5 | 141659474 | ||
chr5:141659848
|
C | T | 1 | a0001c0033 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.3198G>A | p.Thr1066Thr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/33 | 3273/5258 | 3198/4635 | 1066/1544 | chr5 | 141659848 | ||
chr5:141659911
|
C | T | 1 | a0001c0042 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.3135G>A | p.Ala1045Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/33 | 3210/5258 | 3135/4635 | 1045/1544 | chr5 | 141659911 | ||
chr5:141661731
|
C | A | 1 | a0001c0044 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.3072G>T | p.Pro1024Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/33 | 3147/5258 | 3072/4635 | 1024/1544 | chr5 | 141661731 | ||
chr5:141661755
|
A | G | 2 | a0001c0022a0001c0033 | 3 | HG02970.hp1 HG03516.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.3048T>C | p.Tyr1016Tyr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/33 | 3123/5258 | 3048/4635 | 1016/1544 | chr5 | 141661755 | ||
chr5:141662095
|
G | A | 1 | a0001c0020 | 2 | HG01891.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2961C>T | p.Leu987Leu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/33 | 3036/5258 | 2961/4635 | 987/1544 | chr5 | 141662095 | ||
chr5:141665019
|
C | T | 1 | a0001c0020 | 2 | HG01891.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2703G>A | p.Ala901Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/33 | 2778/5258 | 2703/4635 | 901/1544 | chr5 | 141665019 | ||
chr5:141671669
|
C | T | 13 | a0001c0003a0001c0013a0001c0016others(10): Show | 76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
synonymous_variant | LOW | c.1755G>A | p.Ala585Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 12/33 | 1830/5258 | 1755/4635 | 585/1544 | chr5 | 141671669 | ||
chr5:141672849
|
G | T | 6 | a0001c0007a0001c0009a0001c0013others(3): Show | 33 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(30): Show |
synonymous_variant | LOW | c.1170C>A | p.Pro390Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 8/33 | 1245/5258 | 1170/4635 | 390/1544 | chr5 | 141672849 | ||
chr5:141680082
|
A | G | 44 | a0001c0002a0001c0003a0001c0005others(41): Show | 322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
synonymous_variant | LOW | c.405T>C | p.Pro135Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 480/5258 | 405/4635 | 135/1544 | chr5 | 141680082 | ||
chr5:141680187
|
G | A | 1 | a0001c0038 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.300C>T | p.Thr100Thr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 375/5258 | 300/4635 | 100/1544 | chr5 | 141680187 | ||
chr5:141680301
|
T | C | 27 | a0001c0002a0001c0003a0001c0007others(24): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
synonymous_variant | LOW | c.186A>G | p.Leu62Leu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 261/5258 | 186/4635 | 62/1544 | chr5 | 141680301 | ||
chr5:141680364
|
G | A | 1 | a0001c0051 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.123C>T | p.His41His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 198/5258 | 123/4635 | 41/1544 | chr5 | 141680364 |
chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141653547
|
G | A | 1 | a0001c0003t0005 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 403 | chr5 | 141653547 | |||||
chr5:141653631
|
G | A | 3 | a0001c0009t0002a0001c0011t0002a0001c0018t0002 | 5 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 319 | chr5 | 141653631 | |||||
chr5:141653740
|
C | A | 2 | a0001c0003t0004a0001c0021t0004 | 3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*210G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 210 | chr5 | 141653740 | |||||
chr5:141653757
|
G | C | 2 | a0001c0003t0004a0001c0021t0004 | 3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 193 | chr5 | 141653757 | |||||
chr5:141653931
|
C | G | 1 | a0001c0005t0003 | 3 | HG01934.hp2 HG02451.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 19 | chr5 | 141653931 |
chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141654473
|
TAA | T | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.4150-40_4150-39del others(2): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654473 | ||||||
chr5:141654556
|
T | A | 176 | a0001c0001t0001g0178a0001c0001t0001g0192a0001c0002t0001g0005others(173): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.4150-121A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654556 | ||||||
chr5:141654616
|
A | G | 47 | a0001c0001t0001g0178a0001c0002t0001g0226a0001c0003t0001g0006others(44): Show | 63 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.4150-181T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654616 | ||||||
chr5:141654678
|
A | C | 18 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(15): Show | 23 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.4150-243T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654678 | ||||||
chr5:141654741
|
C | CT | 28 | a0001c0001t0001g0182a0001c0003t0001g0063a0001c0003t0004g0202others(25): Show | 33 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.4150-307dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654741 | ||||||
chr5:141654741
|
CT | C | 6 | a0001c0001t0001g0192a0001c0003t0001g0209a0001c0006t0001g0136others(3): Show | 6 | HG02132.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4150-307delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654741 | ||||||
chr5:141654752
|
T | G | 2 | a0010c0047t0001g0100a0010c0049t0001g0094 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4150-317A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654752 | ||||||
chr5:141654803
|
G | A | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4150-368C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654803 | ||||||
chr5:141654825
|
C | T | 94 | a0001c0002t0001g0005a0001c0002t0001g0053a0001c0002t0001g0054others(91): Show | 123 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.4150-390G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654825 | ||||||
chr5:141654913
|
A | G | 1 | a0001c0006t0001g0282 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4149+449T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654913 | ||||||
chr5:141654965
|
C | G | 3 | a0001c0005t0003g0016a0001c0029t0001g0266a0001c0029t0001g0267 | 5 | HG01496.hp1 HG01934.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4149+397G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654965 | ||||||
chr5:141655156
|
T | TCA | 23 | a0001c0006t0001g0018a0001c0006t0001g0158a0001c0006t0001g0272others(20): Show | 30 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.4149+204_4149+205d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655156 | ||||||
chr5:141655182
|
T | TAC | 14 | a0001c0001t0001g0192a0001c0002t0001g0074a0001c0003t0001g0234others(11): Show | 14 | HG00323.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.4149+178_4149+179d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACAC | 41 | a0001c0002t0001g0053a0001c0002t0001g0226a0001c0003t0001g0006others(38): Show | 58 | HG00621.hp2 HG00735.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.4149+176_4149+179d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACAC | 35 | a0001c0003t0001g0217a0001c0003t0001g0249a0001c0003t0001g0257others(32): Show | 49 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.4149+174_4149+179d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACACA others(1): Show |
14 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0099others(11): Show | 15 | HG00140.hp1 HG00639.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.4149+172_4149+179d others(10): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACACA others(3): Show |
10 | a0001c0002t0001g0005a0001c0002t0001g0054a0001c0002t0001g0065others(7): Show | 17 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.4149+170_4149+179d others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACACA others(5): Show |
4 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0093others(1): Show | 4 | HG02965.hp1 HG03239.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.4149+168_4149+179d others(14): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACACA others(7): Show |
11 | a0001c0002t0001g0068a0001c0002t0001g0075a0001c0002t0001g0077others(8): Show | 11 | HG00642.hp2 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.4149+166_4149+179d others(16): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACACA others(9): Show |
7 | a0001c0002t0001g0079a0001c0006t0001g0274a0001c0006t0001g0277others(4): Show | 8 | HG02717.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.4149+164_4149+179d others(18): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
T | TACACACA others(11): Show |
3 | a0001c0006t0001g0136a0001c0006t0001g0142a0001c0006t0001g0275 | 3 | HG02809.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4149+162_4149+179d others(20): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
TAC | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 157 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.4149+178_4149+179d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
TACAC | T | 7 | a0001c0001t0001g0188a0001c0002t0001g0227a0001c0005t0001g0130others(4): Show | 10 | HG00408.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.4149+176_4149+179d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655182
|
TACACAC | T | 4 | a0001c0006t0001g0137a0001c0007t0001g0059a0001c0029t0001g0266others(1): Show | 4 | HG01496.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4149+174_4149+179d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | ||||||
chr5:141655206
|
C | CCCTGATG others(4): Show |
1 | a0001c0018t0002g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+155_4149+156i others(13): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655206 | ||||||
chr5:141655214
|
C | CACACACA others(8): Show |
1 | a0001c0002t0001g0082 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4149+147_4149+148i others(17): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655214 | ||||||
chr5:141655215
|
C | A | 1 | a0001c0018t0002g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+147G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655215 | ||||||
chr5:141655217
|
T | A | 1 | a0001c0018t0002g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+145A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655217 | ||||||
chr5:141655218
|
G | C | 1 | a0001c0018t0002g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+144C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655218 | ||||||
chr5:141655224
|
C | A | 1 | a0001c0018t0002g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+138G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655224 | ||||||
chr5:141655225
|
T | C | 1 | a0001c0018t0002g0262 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+137A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TAC | 10 | a0001c0003t0001g0017a0001c0003t0004g0203a0001c0005t0001g0033others(7): Show | 14 | HG00673.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.4149+135_4149+136d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACAC | 47 | a0001c0002t0001g0075a0001c0002t0001g0081a0001c0002t0001g0082others(44): Show | 59 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4149+133_4149+136d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACAC | 41 | a0001c0002t0001g0005a0001c0002t0001g0053a0001c0002t0001g0054others(38): Show | 56 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.4149+131_4149+136d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACACA others(1): Show |
10 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0002t0001g0268others(7): Show | 12 | HG00544.hp1 HG01891.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.4149+129_4149+136d others(10): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACACA others(3): Show |
9 | a0001c0002t0001g0099a0001c0006t0001g0140a0001c0007t0001g0019others(6): Show | 11 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4149+127_4149+136d others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACACA others(5): Show |
2 | a0001c0007t0001g0020a0001c0007t0001g0058 | 3 | HG01256.hp1 NA18955.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.4149+125_4149+136d others(14): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACACA others(7): Show |
2 | a0001c0018t0002g0263a0020c0041t0001g0265 | 2 | HG01433.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4149+123_4149+136d others(16): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACACA others(9): Show |
2 | a0001c0007t0001g0204a0001c0018t0002g0264 | 2 | HG02135.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.4149+121_4149+136d others(18): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
T | TACACACA others(13): Show |
1 | a0001c0011t0002g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4149+117_4149+136d others(22): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
TAC | T | 41 | a0001c0001t0001g0181a0001c0003t0001g0251a0001c0005t0001g0010others(38): Show | 54 | HG00609.hp2 HG00673.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.4149+135_4149+136d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
TACAC | T | 8 | a0001c0001t0001g0170a0001c0001t0001g0180a0001c0001t0001g0192others(5): Show | 8 | HG01106.hp1 HG02132.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.4149+133_4149+136d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655225
|
TACACAC | T | 6 | a0001c0008t0001g0056a0003c0010t0001g0046a0003c0010t0001g0047others(3): Show | 8 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.4149+131_4149+136d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | ||||||
chr5:141655248
|
A | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0179 | 3 | NA18947.hp2 NA18964.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.4149+114T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655248 | ||||||
chr5:141655258
|
ACC | A | 3 | a0001c0005t0003g0016a0002c0004t0001g0114a0002c0004t0001g0115 | 5 | HG00438.hp1 HG01934.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4149+102_4149+103d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655258 | ||||||
chr5:141655259
|
C | CACACACA others(4): Show |
2 | a0001c0007t0001g0087a0001c0026t0001g0239 | 2 | HG01358.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.4149+102_4149+103i others(13): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655259 | ||||||
chr5:141655260
|
C | A | 10 | a0001c0002t0001g0227a0001c0002t0001g0228a0001c0003t0001g0012others(7): Show | 13 | HG00621.hp2 HG01496.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.4149+102G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655260 | ||||||
chr5:141655274
|
C | T | 1 | a0001c0027t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4149+88G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655274 | ||||||
chr5:141655423
|
C | A | 1 | a0001c0043t0001g0247 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4111-23G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/32 | chr5 | 141655423 | ||||||
chr5:141655583
|
C | T | 2 | a0010c0047t0001g0100a0010c0049t0001g0094 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4110+38G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/32 | chr5 | 141655583 | ||||||
chr5:141655607
|
G | C | 26 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(23): Show | 31 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.4110+14C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/32 | chr5 | 141655607 | ||||||
chr5:141655799
|
G | A | 2 | a0001c0002t0001g0081a0001c0002t0001g0082 | 2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3973-41C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 30/32 | chr5 | 141655799 | ||||||
chr5:141655807
|
G | A | 40 | a0001c0001t0001g0183a0001c0002t0001g0005a0001c0002t0001g0053others(37): Show | 49 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.3973-49C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 30/32 | chr5 | 141655807 | ||||||
chr5:141655864
|
C | T | 2 | a0001c0006t0001g0279a0001c0006t0001g0281 | 2 | HG02451.hp1 HG02896.hp2 |
splice_region_variant&intron_variant | LOW | c.3972+5G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 30/32 | chr5 | 141655864 | ||||||
chr5:141656313
|
G | A | 12 | a0001c0005t0001g0130a0001c0005t0001g0131a0001c0005t0001g0132others(9): Show | 19 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.3790-37C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656313 | ||||||
chr5:141656384
|
C | T | 1 | a0001c0051t0001g0269 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3790-108G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656384 | ||||||
chr5:141656387
|
G | A | 1 | a0005c0014t0001g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3790-111C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656387 | ||||||
chr5:141656388
|
G | A | 68 | a0001c0001t0001g0184a0001c0001t0001g0192a0001c0003t0001g0245others(65): Show | 91 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.3790-112C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656388 | ||||||
chr5:141657000
|
C | T | 1 | a0001c0026t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3527-154G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657000 | ||||||
chr5:141657033
|
A | C | 1 | a0001c0006t0001g0273 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3527-187T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657033 | ||||||
chr5:141657109
|
A | G | 160 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(157): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3527-263T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657109 | ||||||
chr5:141657384
|
T | C | 160 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(157): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3527-538A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657384 | ||||||
chr5:141657710
|
T | G | 160 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(157): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3526+655A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657710 | ||||||
chr5:141657768
|
T | C | 3 | a0001c0003t0004g0202a0001c0003t0004g0203a0001c0021t0004g0160 | 3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3526+597A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657768 | ||||||
chr5:141657810
|
T | C | 160 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(157): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.3526+555A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657810 | ||||||
chr5:141658079
|
G | A | 155 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(152): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.3526+286C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658079 | ||||||
chr5:141658116
|
G | A | 55 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0012others(52): Show | 73 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.3526+249C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658116 | ||||||
chr5:141658136
|
G | A | 2 | a0001c0051t0001g0269a0005c0014t0001g0104 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3526+229C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658136 | ||||||
chr5:141658232
|
G | A | 3 | a0001c0003t0004g0202a0001c0003t0004g0203a0001c0021t0004g0160 | 3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3526+133C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658232 | ||||||
chr5:141658310
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3526+55G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658310 | ||||||
chr5:141658726
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3337-73C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141658726 | ||||||
chr5:141658787
|
C | A | 2 | a0001c0020t0001g0151a0001c0020t0001g0161 | 2 | HG01891.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3337-134G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141658787 | ||||||
chr5:141659049
|
G | T | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3336+359C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659049 | ||||||
chr5:141659091
|
T | C | 1 | a0001c0003t0001g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3336+317A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659091 | ||||||
chr5:141659122
|
T | C | 5 | a0001c0009t0001g0013a0001c0009t0002g0270a0008c0017t0001g0205others(2): Show | 8 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3336+286A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659122 | ||||||
chr5:141659206
|
T | C | 2 | a0008c0017t0001g0206a0008c0017t0001g0207 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3336+202A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659206 | ||||||
chr5:141659289
|
G | T | 1 | a0001c0006t0001g0282 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3336+119C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659289 | ||||||
chr5:141659353
|
C | T | 1 | a0001c0002t0001g0024 | 2 | NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3336+55G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659353 | ||||||
chr5:141659354
|
T | C | 2 | a0003c0010t0001g0047a0003c0010t0001g0210 | 3 | HG00639.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.3336+54A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659354 | ||||||
chr5:141659521
|
C | T | 1 | a0001c0038t0001g0200 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3268-45G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659521 | ||||||
chr5:141659593
|
G | T | 56 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0012others(53): Show | 74 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.3268-117C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659593 | ||||||
chr5:141659633
|
G | C | 36 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0271others(33): Show | 41 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.3267+146C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659633 | ||||||
chr5:141659707
|
A | G | 1 | a0003c0010t0001g0221 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3267+72T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659707 | ||||||
chr5:141659980
|
T | G | 1 | a0001c0005t0001g0145 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3120-54A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141659980 | ||||||
chr5:141660214
|
C | T | 1 | a0001c0002t0001g0226 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3120-288G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660214 | ||||||
chr5:141660215
|
G | A | 8 | a0001c0002t0001g0081a0001c0003t0001g0017a0001c0003t0001g0052others(5): Show | 11 | HG00558.hp2 HG02027.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3120-289C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660215 | ||||||
chr5:141660366
|
T | C | 162 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(159): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.3120-440A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660366 | ||||||
chr5:141660481
|
A | G | 225 | a0001c0001t0001g0192a0001c0002t0001g0004a0001c0002t0001g0005others(222): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.3120-555T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660481 | ||||||
chr5:141660650
|
T | G | 35 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0271others(32): Show | 40 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.3120-724A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660650 | ||||||
chr5:141660732
|
C | T | 109 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(106): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.3120-806G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660732 | ||||||
chr5:141660779
|
G | C | 1 | a0014c0037t0001g0167 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3120-853C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660779 | ||||||
chr5:141660912
|
C | G | 1 | a0021c0032t0001g0125 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3119+772G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660912 | ||||||
chr5:141660990
|
G | A | 1 | a0021c0032t0001g0125 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3119+694C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660990 | ||||||
chr5:141661059
|
T | C | 5 | a0001c0009t0001g0013a0001c0009t0002g0270a0008c0017t0001g0205others(2): Show | 8 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3119+625A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661059 | ||||||
chr5:141661067
|
C | CTT | 5 | a0001c0005t0001g0010a0001c0005t0001g0165a0001c0005t0001g0166others(2): Show | 8 | HG01081.hp2 HG01099.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3119+615_3119+616d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661067 | ||||||
chr5:141661226
|
G | C | 3 | a0008c0017t0001g0205a0008c0017t0001g0206a0008c0017t0001g0207 | 3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3119+458C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661226 | ||||||
chr5:141661357
|
G | A | 1 | a0010c0047t0001g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3119+327C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661357 | ||||||
chr5:141661461
|
C | G | 1 | a0001c0006t0001g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3119+223G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661461 | ||||||
chr5:141661482
|
C | T | 1 | a0001c0003t0001g0216 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3119+202G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661482 | ||||||
chr5:141661581
|
G | A | 52 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(49): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.3119+103C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661581 | ||||||
chr5:141661616
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3119+68T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661616 | ||||||
chr5:141661868
|
G | A | 221 | a0001c0001t0001g0192a0001c0002t0001g0004a0001c0002t0001g0005others(218): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.3014-79C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/32 | chr5 | 141661868 | ||||||
chr5:141661887
|
G | A | 1 | a0010c0047t0001g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-98C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/32 | chr5 | 141661887 | ||||||
chr5:141662333
|
T | A | 1 | a0001c0005t0001g0131 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2801-78A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662333 | ||||||
chr5:141662448
|
A | G | 4 | a0001c0005t0001g0035a0001c0005t0001g0152a0001c0005t0001g0153others(1): Show | 5 | HG00558.hp1 NA18969.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2801-193T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662448 | ||||||
chr5:141662455
|
T | G | 1 | a0010c0047t0001g0100 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2801-200A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662455 | ||||||
chr5:141662541
|
C | T | 1 | a0001c0005t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2801-286G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662541 | ||||||
chr5:141663222
|
G | A | 1 | a0001c0002t0001g0229 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2801-967C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663222 | ||||||
chr5:141663331
|
T | C | 2 | a0001c0002t0001g0099a0010c0047t0001g0100 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2801-1076A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663331 | ||||||
chr5:141663648
|
C | T | 5 | a0002c0004t0001g0111a0002c0004t0001g0112a0002c0004t0001g0113others(2): Show | 5 | HG00438.hp1 HG02135.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.2800+1274G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663648 | ||||||
chr5:141663701
|
C | T | 57 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0012others(54): Show | 75 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.2800+1221G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663701 | ||||||
chr5:141663732
|
T | C | 6 | a0001c0013t0001g0220a0003c0010t0001g0046a0003c0010t0001g0047others(3): Show | 8 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.2800+1190A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663732 | ||||||
chr5:141663756
|
A | G | 34 | a0001c0002t0001g0098a0001c0002t0001g0271a0001c0006t0001g0018others(31): Show | 39 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.2800+1166T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663756 | ||||||
chr5:141663773
|
T | C | 2 | a0001c0002t0001g0099a0010c0047t0001g0100 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2800+1149A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663773 | ||||||
chr5:141663785
|
T | G | 3 | a0008c0017t0001g0205a0008c0017t0001g0206a0008c0017t0001g0207 | 3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2800+1137A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663785 | ||||||
chr5:141663795
|
G | GT | 8 | a0001c0002t0001g0098a0001c0006t0001g0274a0001c0006t0001g0277others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2800+1126dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663795 | ||||||
chr5:141663820
|
T | G | 1 | a0001c0006t0001g0281 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2800+1102A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663820 | ||||||
chr5:141663991
|
C | G | 1 | a0001c0002t0001g0225 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2800+931G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663991 | ||||||
chr5:141664111
|
G | A | 1 | a0001c0003t0001g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2800+811C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664111 | ||||||
chr5:141664416
|
C | T | 1 | a0001c0002t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2800+506G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664416 | ||||||
chr5:141664432
|
G | A | 1 | a0001c0011t0002g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2800+490C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664432 | ||||||
chr5:141664535
|
C | T | 1 | a0001c0003t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2800+387G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664535 | ||||||
chr5:141664577
|
C | T | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800+345G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664577 | ||||||
chr5:141664612
|
C | T | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800+310G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664612 | ||||||
chr5:141664713
|
C | T | 2 | a0001c0006t0001g0137a0001c0006t0001g0138 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2800+209G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664713 | ||||||
chr5:141664885
|
A | C | 1 | a0004c0012t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2800+37T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664885 | ||||||
chr5:141664905
|
A | G | 52 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(49): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2800+17T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664905 | ||||||
chr5:141665197
|
T | A | 1 | a0001c0005t0001g0162 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2637-112A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 18/32 | chr5 | 141665197 | ||||||
chr5:141665437
|
T | C | 1 | a0001c0003t0001g0236 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2573-63A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665437 | ||||||
chr5:141665509
|
T | A | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2573-135A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665509 | ||||||
chr5:141665695
|
C | G | 54 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(51): Show | 79 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2573-321G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665695 | ||||||
chr5:141665714
|
C | G | 52 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(49): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2573-340G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665714 | ||||||
chr5:141665731
|
A | G | 10 | a0001c0005t0001g0010a0001c0005t0001g0165a0001c0005t0001g0166others(7): Show | 16 | HG01081.hp2 HG01099.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2573-357T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665731 | ||||||
chr5:141665745
|
T | C | 2 | a0001c0008t0001g0070a0001c0008t0001g0071 | 2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2573-371A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665745 | ||||||
chr5:141665808
|
A | C | 1 | a0001c0002t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2573-434T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665808 | ||||||
chr5:141665847
|
A | C | 1 | a0001c0006t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2573-473T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665847 | ||||||
chr5:141665875
|
A | C | 2 | a0006c0015t0001g0039a0006c0015t0001g0176 | 3 | HG02735.hp2 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2573-501T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665875 | ||||||
chr5:141665899
|
C | T | 3 | a0001c0003t0004g0202a0001c0003t0004g0203a0001c0021t0004g0160 | 3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2572+525G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665899 | ||||||
chr5:141666026
|
G | A | 3 | a0001c0005t0001g0010a0001c0005t0001g0165a0001c0005t0001g0166 | 6 | HG01081.hp2 HG01099.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572+398C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666026 | ||||||
chr5:141666039
|
C | CA | 29 | a0001c0001t0001g0185a0001c0003t0001g0011a0001c0003t0001g0017others(26): Show | 37 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2572+384dupT | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666039 | ||||||
chr5:141666039
|
CA | C | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2572+384delT | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666039 | ||||||
chr5:141666049
|
A | T | 2 | a0001c0006t0001g0136a0001c0006t0001g0142 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2572+375T>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666049 | ||||||
chr5:141666052
|
A | AT | 3 | a0001c0003t0001g0233a0001c0020t0001g0151a0001c0042t0001g0232 | 3 | HG01891.hp1 HG01928.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2572+371_2572+372i others(3): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666052 | ||||||
chr5:141666052
|
A | T | 32 | a0001c0001t0001g0043a0001c0002t0001g0098a0001c0002t0001g0271others(29): Show | 38 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.2572+372T>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666052 | ||||||
chr5:141666054
|
AT | A | 35 | a0001c0001t0001g0192a0001c0005t0001g0147a0001c0005t0001g0154others(32): Show | 44 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.2572+369delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666054 | ||||||
chr5:141666055
|
T | A | 101 | a0001c0001t0001g0186a0001c0002t0001g0004a0001c0002t0001g0005others(98): Show | 140 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2572+369A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666055 | ||||||
chr5:141666056
|
A | T | 48 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(45): Show | 73 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.2572+368T>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666056 | ||||||
chr5:141666058
|
T | A | 85 | a0001c0001t0001g0192a0001c0002t0001g0004a0001c0002t0001g0005others(82): Show | 118 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.2572+366A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666058 | ||||||
chr5:141666061
|
T | A | 1 | a0001c0009t0002g0270 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2572+363A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666061 | ||||||
chr5:141666076
|
C | T | 190 | a0001c0001t0001g0192a0001c0001t0001g0196a0001c0002t0001g0004others(187): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.2572+348G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666076 | ||||||
chr5:141666409
|
A | G | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2572+15T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666409 | ||||||
chr5:141666789
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2353-146C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141666789 | ||||||
chr5:141666911
|
C | T | 52 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(49): Show | 77 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2353-268G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141666911 | ||||||
chr5:141666994
|
G | A | 1 | a0002c0004t0001g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2353-351C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141666994 | ||||||
chr5:141667061
|
C | T | 6 | a0001c0003t0001g0017a0001c0003t0001g0052a0001c0003t0001g0259others(3): Show | 9 | HG02027.hp2 HG02071.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.2353-418G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667061 | ||||||
chr5:141667105
|
G | A | 2 | a0001c0011t0001g0156a0001c0011t0001g0163 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2353-462C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667105 | ||||||
chr5:141667133
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2353-490G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667133 | ||||||
chr5:141667160
|
C | G | 139 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(136): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2353-517G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667160 | ||||||
chr5:141667294
|
A | G | 1 | a0001c0003t0001g0231 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2353-651T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667294 | ||||||
chr5:141667343
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2353-700A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667343 | ||||||
chr5:141667369
|
C | T | 58 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0012others(55): Show | 76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2353-726G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667369 | ||||||
chr5:141667435
|
C | CT | 56 | a0001c0002t0001g0090a0001c0003t0001g0006a0001c0003t0001g0011others(53): Show | 74 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.2353-793dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667435 | ||||||
chr5:141667435
|
CT | C | 7 | a0001c0001t0001g0171a0001c0002t0001g0069a0001c0002t0001g0084others(4): Show | 8 | HG01069.hp1 HG02572.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2353-793delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667435 | ||||||
chr5:141667546
|
G | C | 1 | a0001c0002t0001g0215 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2353-903C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667546 | ||||||
chr5:141667680
|
G | A | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353-1037C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667680 | ||||||
chr5:141667691
|
G | A | 1 | a0002c0004t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2353-1048C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667691 | ||||||
chr5:141667724
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2353-1081C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667724 | ||||||
chr5:141667899
|
G | A | 58 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0012others(55): Show | 76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2353-1256C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667899 | ||||||
chr5:141667915
|
G | A | 1 | a0001c0005t0001g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2353-1272C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667915 | ||||||
chr5:141668022
|
A | G | 1 | a0001c0006t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2353-1379T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668022 | ||||||
chr5:141668039
|
T | A | 2 | a0001c0021t0001g0283a0001c0043t0001g0247 | 2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2353-1396A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668039 | ||||||
chr5:141668040
|
C | G | 2 | a0001c0002t0001g0099a0010c0047t0001g0100 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2353-1397G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668040 | ||||||
chr5:141668266
|
C | T | 1 | a0001c0002t0001g0007 | 5 | NA18963.hp2 NA18971.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352+1443G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668266 | ||||||
chr5:141668522
|
C | T | 3 | a0001c0018t0002g0262a0001c0018t0002g0263a0001c0018t0002g0264 | 3 | HG02145.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2352+1187G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668522 | ||||||
chr5:141668663
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2352+1046A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668663 | ||||||
chr5:141669473
|
G | A | 5 | a0001c0006t0001g0274a0001c0006t0001g0278a0001c0006t0001g0279others(2): Show | 5 | HG02451.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2352+236C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141669473 | ||||||
chr5:141669568
|
C | T | 2 | a0001c0051t0001g0269a0005c0014t0001g0104 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2352+141G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141669568 | ||||||
chr5:141669840
|
G | A | 132 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(129): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.2250-29C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 15/32 | chr5 | 141669840 | ||||||
chr5:141670089
|
A | G | 18 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(15): Show | 26 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.2108-26T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 14/32 | chr5 | 141670089 | ||||||
chr5:141670175
|
T | G | 1 | a0001c0001t0001g0043 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2108-112A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 14/32 | chr5 | 141670175 | ||||||
chr5:141670340
|
C | T | 18 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(15): Show | 26 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.2107+172G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 14/32 | chr5 | 141670340 | ||||||
chr5:141670759
|
A | G | 4 | a0001c0005t0001g0035a0001c0005t0001g0152a0001c0005t0001g0153others(1): Show | 5 | HG00558.hp1 NA18969.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1991-131T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141670759 | ||||||
chr5:141670760
|
A | G | 1 | a0002c0004t0001g0029 | 2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1991-132T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141670760 | ||||||
chr5:141670806
|
G | C | 1 | a0002c0004t0001g0030 | 2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1991-178C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141670806 | ||||||
chr5:141671008
|
A | C | 5 | a0003c0010t0001g0046a0003c0010t0001g0047a0003c0010t0001g0062others(2): Show | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.1990+257T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671008 | ||||||
chr5:141671065
|
ACACCCAG others(3): Show |
A | 2 | a0001c0029t0001g0266a0001c0029t0001g0267 | 2 | HG01496.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1990+190_1990+199d others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671065 | ||||||
chr5:141671187
|
G | C | 1 | a0017c0050t0001g0214 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1990+78C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671187 | ||||||
chr5:141671202
|
C | A | 1 | a0001c0006t0001g0282 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1990+63G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671202 | ||||||
chr5:141671862
|
C | T | 34 | a0001c0002t0001g0098a0001c0002t0001g0271a0001c0006t0001g0018others(31): Show | 39 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.1671+33G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 11/32 | chr5 | 141671862 | ||||||
chr5:141671879
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1671+16G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 11/32 | chr5 | 141671879 | ||||||
chr5:141671988
|
GGTGTGAG others(3): Show |
G | 1 | a0001c0002t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1586-18_1586-9delA others(9): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 10/32 | chr5 | 141671988 | ||||||
chr5:141672029
|
T | C | 2 | a0001c0029t0001g0266a0001c0029t0001g0267 | 2 | HG01496.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1586-49A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 10/32 | chr5 | 141672029 | ||||||
chr5:141672358
|
CT | C | 58 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0012others(55): Show | 76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386-58delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 9/32 | chr5 | 141672358 | ||||||
chr5:141672491
|
T | C | 2 | a0006c0015t0001g0039a0006c0015t0001g0176 | 3 | HG02735.hp2 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1385+61A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 9/32 | chr5 | 141672491 | ||||||
chr5:141672975
|
C | CT | 12 | a0001c0005t0001g0035a0001c0005t0001g0152a0001c0005t0001g0153others(9): Show | 13 | HG00558.hp1 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093+37dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 7/32 | chr5 | 141672975 | ||||||
chr5:141672984
|
G | T | 1 | a0011c0024t0001g0042 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1093+29C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 7/32 | chr5 | 141672984 | ||||||
chr5:141673151
|
A | G | 2 | a0001c0002t0001g0098a0005c0014t0001g0102 | 2 | HG01346.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.973-18T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673151 | ||||||
chr5:141673303
|
G | C | 223 | a0001c0001t0001g0192a0001c0002t0001g0004a0001c0002t0001g0005others(220): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.972+98C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673303 | ||||||
chr5:141673335
|
A | G | 1 | a0001c0006t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.972+66T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673335 | ||||||
chr5:141673373
|
C | T | 1 | a0001c0003t0001g0259 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.972+28G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673373 | ||||||
chr5:141673554
|
A | G | 9 | a0001c0001t0001g0175a0001c0003t0001g0011a0001c0003t0001g0051others(6): Show | 13 | HG00735.hp1 HG01433.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.902+51T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 5/32 | chr5 | 141673554 | ||||||
chr5:141673959
|
C | CT | 9 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0008t0001g0208others(6): Show | 9 | HG02572.hp1 HG02922.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.699-152dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | ||||||
chr5:141673959
|
C | CTT | 9 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(6): Show | 14 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.699-153_699-152dup others(2): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | ||||||
chr5:141673959
|
CT | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0172a0001c0001t0001g0196others(179): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.699-152delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | ||||||
chr5:141673959
|
CTT | C | 15 | a0001c0001t0001g0199a0001c0002t0001g0095a0001c0003t0001g0051others(12): Show | 17 | HG00558.hp1 HG01099.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.699-153_699-152del others(2): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | ||||||
chr5:141673961
|
T | C | 1 | a0001c0008t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.699-153A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673961 | ||||||
chr5:141674109
|
A | G | 1 | a0001c0006t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699-301T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674109 | ||||||
chr5:141674162
|
C | T | 1 | a0001c0005t0001g0149 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.699-354G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674162 | ||||||
chr5:141674243
|
G | A | 1 | a0001c0005t0003g0016 | 3 | HG01934.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.699-435C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674243 | ||||||
chr5:141674261
|
C | A | 18 | a0001c0002t0001g0099a0001c0007t0001g0014a0001c0007t0001g0019others(15): Show | 23 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.699-453G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674261 | ||||||
chr5:141674398
|
T | C | 1 | a0016c0040t0001g0060 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.699-590A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674398 | ||||||
chr5:141674509
|
C | T | 1 | a0001c0007t0001g0058 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.699-701G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674509 | ||||||
chr5:141674510
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.699-702C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674510 | ||||||
chr5:141674518
|
G | A | 66 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0215others(63): Show | 97 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.699-710C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674518 | ||||||
chr5:141674580
|
G | C | 30 | a0001c0002t0001g0271a0001c0006t0001g0018a0001c0006t0001g0032others(27): Show | 34 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.699-772C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674580 | ||||||
chr5:141674613
|
T | A | 1 | a0001c0006t0001g0143 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.699-805A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674613 | ||||||
chr5:141674673
|
T | C | 66 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0215others(63): Show | 97 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.699-865A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674673 | ||||||
chr5:141674766
|
C | T | 1 | a0003c0010t0001g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.699-958G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674766 | ||||||
chr5:141675021
|
C | T | 125 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0215others(122): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.699-1213G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675021 | ||||||
chr5:141675038
|
G | A | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1230C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675038 | ||||||
chr5:141675050
|
C | T | 43 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(40): Show | 57 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.699-1242G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675050 | ||||||
chr5:141675161
|
C | A | 2 | a0001c0002t0001g0007a0001c0002t0001g0254 | 6 | NA18960.hp2 NA18963.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.699-1353G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675161 | ||||||
chr5:141675285
|
C | T | 1 | a0001c0003t0001g0211 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.699-1477G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675285 | ||||||
chr5:141675326
|
C | T | 1 | a0002c0004t0001g0108 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.699-1518G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675326 | ||||||
chr5:141675440
|
G | T | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1632C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675440 | ||||||
chr5:141675447
|
G | A | 1 | a0001c0002t0001g0086 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.699-1639C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675447 | ||||||
chr5:141675547
|
C | T | 2 | a0001c0008t0001g0022a0001c0008t0001g0066 | 3 | HG00673.hp1 HG02071.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.699-1739G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675547 | ||||||
chr5:141675592
|
G | A | 2 | a0001c0003t0001g0063a0001c0008t0001g0064 | 2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.699-1784C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675592 | ||||||
chr5:141675677
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 13 | HG00323.hp2 HG00642.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.699-1869G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675677 | ||||||
chr5:141675736
|
T | A | 2 | a0001c0003t0001g0051a0001c0003t0001g0255 | 3 | NA18940.hp1 NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.699-1928A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675736 | ||||||
chr5:141675913
|
T | C | 3 | a0001c0005t0001g0010a0001c0005t0001g0165a0001c0005t0001g0166 | 6 | HG01081.hp2 HG01099.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.699-2105A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675913 | ||||||
chr5:141675954
|
C | T | 12 | a0001c0006t0001g0032a0001c0006t0001g0136a0001c0006t0001g0137others(9): Show | 13 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.699-2146G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675954 | ||||||
chr5:141676044
|
T | C | 1 | a0001c0005t0003g0016 | 3 | HG01934.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.699-2236A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676044 | ||||||
chr5:141676176
|
C | T | 1 | a0001c0006t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699-2368G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676176 | ||||||
chr5:141676460
|
T | C | 1 | a0001c0003t0001g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.699-2652A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676460 | ||||||
chr5:141676567
|
T | TCAGCAGC others(7): Show |
1 | a0001c0003t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699-2760_699-2759i others(16): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676567 | ||||||
chr5:141676569
|
T | G | 1 | a0001c0003t0001g0257 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699-2761A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676569 | ||||||
chr5:141676614
|
C | T | 2 | a0004c0012t0001g0028a0004c0012t0001g0107 | 3 | NA18990.hp2 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.699-2806G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676614 | ||||||
chr5:141676669
|
C | T | 58 | a0001c0005t0001g0010a0001c0005t0001g0035a0001c0005t0001g0037others(55): Show | 72 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.699-2861G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676669 | ||||||
chr5:141676695
|
T | C | 1 | a0001c0005t0001g0147 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.698+2850A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676695 | ||||||
chr5:141676702
|
G | A | 43 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(40): Show | 57 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.698+2843C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676702 | ||||||
chr5:141676803
|
T | C | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.698+2742A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676803 | ||||||
chr5:141676897
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG00621.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.698+2648T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676897 | ||||||
chr5:141676975
|
G | A | 2 | a0001c0003t0004g0202a0001c0003t0004g0203 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.698+2570C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676975 | ||||||
chr5:141677002
|
C | T | 26 | a0001c0002t0001g0008a0001c0002t0001g0023a0001c0002t0001g0024others(23): Show | 32 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.698+2543G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677002 | ||||||
chr5:141677015
|
C | A | 1 | a0001c0007t0001g0020 | 2 | NA18955.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.698+2530G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677015 | ||||||
chr5:141677034
|
C | T | 1 | a0001c0008t0001g0021 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.698+2511G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677034 | ||||||
chr5:141677377
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.698+2168G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677377 | ||||||
chr5:141677473
|
C | CT | 118 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(115): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.698+2071dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677473 | ||||||
chr5:141677582
|
T | C | 1 | a0001c0006t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.698+1963A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677582 | ||||||
chr5:141677612
|
T | C | 2 | a0002c0004t0001g0015a0002c0004t0001g0126 | 4 | HG01978.hp1 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.698+1933A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677612 | ||||||
chr5:141677654
|
G | T | 194 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(191): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.698+1891C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677654 | ||||||
chr5:141677745
|
GT | G | 43 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(40): Show | 57 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.698+1799delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677745 | ||||||
chr5:141677750
|
T | C | 1 | a0002c0004t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.698+1795A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677750 | ||||||
chr5:141677753
|
G | A | 1 | a0001c0007t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.698+1792C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677753 | ||||||
chr5:141677764
|
GTTTTTTG others(8): Show |
G | 1 | a0003c0010t0001g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.698+1766_698+1780d others(17): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677764 | ||||||
chr5:141677780
|
T | TTTTTTG | 15 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(12): Show | 20 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.698+1759_698+1764d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677780 | ||||||
chr5:141677846
|
A | C | 1 | a0003c0010t0001g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.698+1699T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677846 | ||||||
chr5:141677934
|
G | A | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1611C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677934 | ||||||
chr5:141677950
|
A | AT | 121 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0007others(118): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.698+1594dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677950 | ||||||
chr5:141677970
|
C | T | 5 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0268others(2): Show | 7 | HG01496.hp1 HG02280.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.698+1575G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677970 | ||||||
chr5:141678303
|
C | T | 15 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(12): Show | 20 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.698+1242G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678303 | ||||||
chr5:141678328
|
T | A | 5 | a0001c0003t0001g0017a0001c0003t0001g0052a0001c0003t0001g0259others(2): Show | 8 | HG00558.hp2 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.698+1217A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678328 | ||||||
chr5:141678487
|
C | T | 6 | a0001c0003t0001g0063a0001c0008t0001g0064a0001c0009t0001g0013others(3): Show | 9 | HG02145.hp2 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.698+1058G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678487 | ||||||
chr5:141678581
|
C | G | 7 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0268others(4): Show | 9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+964G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678581 | ||||||
chr5:141678590
|
C | T | 6 | a0001c0005t0001g0129a0001c0005t0001g0130a0001c0005t0001g0131others(3): Show | 7 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.698+955G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678590 | ||||||
chr5:141678615
|
C | G | 78 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(75): Show | 102 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.698+930G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678615 | ||||||
chr5:141678711
|
C | T | 49 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(46): Show | 66 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.698+834G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678711 | ||||||
chr5:141678720
|
T | C | 17 | a0001c0002t0001g0099a0001c0007t0001g0014a0001c0007t0001g0019others(14): Show | 22 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.698+825A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678720 | ||||||
chr5:141678858
|
T | G | 7 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0268others(4): Show | 9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+687A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678858 | ||||||
chr5:141678920
|
G | A | 42 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(39): Show | 56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.698+625C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678920 | ||||||
chr5:141678947
|
G | A | 1 | a0001c0006t0001g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.698+598C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678947 | ||||||
chr5:141679096
|
C | T | 7 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0268others(4): Show | 9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+449G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679096 | ||||||
chr5:141679110
|
G | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG01175.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.698+435C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679110 | ||||||
chr5:141679146
|
G | A | 1 | a0002c0004t0001g0128 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.698+399C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679146 | ||||||
chr5:141679152
|
G | A | 125 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0215others(122): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.698+393C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679152 | ||||||
chr5:141679227
|
T | A | 67 | a0001c0002t0001g0005a0001c0002t0001g0008a0001c0002t0001g0023others(64): Show | 89 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.698+318A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679227 | ||||||
chr5:141679242
|
T | C | 7 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0268others(4): Show | 9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+303A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679242 | ||||||
chr5:141679487
|
A | G | 16 | a0001c0007t0001g0014a0001c0007t0001g0019a0001c0007t0001g0020others(13): Show | 21 | HG00544.hp1 HG00741.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.698+58T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679487 | ||||||
chr5:141679498
|
C | T | 2 | a0001c0003t0004g0202a0001c0003t0004g0203 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.698+47G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679498 | ||||||
chr5:141679669
|
G | A | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-13C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 3/32 | chr5 | 141679669 | ||||||
chr5:141679898
|
G | A | 1 | a0001c0001t0001g0043 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.524+65C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/32 | chr5 | 141679898 | ||||||
chr5:141680507
|
G | T | 1 | a0001c0044t0001g0101 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.-17-4C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680507 | ||||||
chr5:141680677
|
C | T | 2 | a0001c0002t0001g0099a0010c0047t0001g0100 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-17-174G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680677 | ||||||
chr5:141680890
|
G | C | 2 | a0001c0002t0001g0271a0001c0009t0002g0270 | 2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-17-387C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680890 | ||||||
chr5:141680981
|
A | G | 1 | a0001c0002t0001g0098 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-17-478T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680981 | ||||||
chr5:141681009
|
G | A | 2 | a0002c0004t0001g0287a0002c0004t0001g0288 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-17-506C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681009 | ||||||
chr5:141681111
|
G | A | 1 | a0001c0009t0001g0013 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-608C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681111 | ||||||
chr5:141681463
|
G | GCCTGACC others(5): Show |
4 | a0001c0006t0001g0018a0001c0006t0001g0272a0001c0006t0001g0273others(1): Show | 6 | HG01175.hp2 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+698_-18+709dup others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681463 | ||||||
chr5:141681465
|
C | T | 1 | a0001c0011t0002g0097 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18+708G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681465 | ||||||
chr5:141681600
|
G | T | 54 | a0001c0001t0001g0055a0001c0002t0001g0005a0001c0002t0001g0008others(51): Show | 72 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.-18+573C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681600 | ||||||
chr5:141681900
|
G | C | 2 | a0001c0006t0001g0275a0001c0006t0001g0276 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-18+273C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681900 | ||||||
chr5:141682067
|
G | C | 8 | a0001c0006t0001g0277a0001c0006t0001g0278a0001c0006t0001g0279others(5): Show | 8 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+106C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141682067 | ||||||
chr5:141682136
|
T | C | 4 | a0002c0004t0001g0285a0002c0004t0001g0286a0002c0004t0001g0287others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+37A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141682136 |