geneid | 5678 |
---|---|
ensemblid | ENSG00000183668.18 |
hgncid | 9526 |
symbol | PSG9 |
name | pregnancy specific beta-1-glycoprotein 9 |
refseq_nuc | NM_002784.5 |
refseq_prot | NP_002775.3 |
ensembl_nuc | ENST00000270077.8 |
ensembl_prot | ENSP00000270077.3 |
mane_status | MANE Select |
chr | chr19 |
start | 43253282 |
end | 43269530 |
strand | - |
ver | v1.2 |
region | chr19:43253282-43269530 |
region5000 | chr19:43248282-43274530 |
regionname0 | PSG9_chr19_43253282_43269530 |
regionname5000 | PSG9_chr19_43248282_43274530 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 426 | 140 | 28 | 39 | 44 | 4 | 23 | 29 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002 | 0/0 | 426 | 21 | 10 | 0 | 10 | 0 | 1 | 6 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0003 | 0/0 | 426 | 8 | 0 | 4 | 0 | 3 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0004 | 0/0 | 426 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0005 | 0/0 | 426 | 5 | 0 | 0 | 2 | 0 | 3 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0006 | 0/0 | 426 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0007 | 0/0 | 426 | 4 | 0 | 1 | 0 | 1 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0008 | 0/0 | 426 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0009 | 0/0 | 426 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0010 | 0/0 | 426 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0011 | 0/0 | 426 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0012 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0013 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0014 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0015 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0016 | 0/0 | 126 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0017 | 0/0 | 426 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0018 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0019 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0020 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0021 | 0/0 | 426 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0022 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0023 | 0/0 | 426 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0024 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0025 | 0/0 | 426 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1281 | 134 | 25 | 37 | 44 | 4 | 22 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0002 | 0/0 | 1281 | 20 | 9 | 0 | 10 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0003 | 0/0 | 1281 | 8 | 0 | 4 | 0 | 3 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0004 | 0/0 | 1281 | 5 | 0 | 0 | 2 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0005 | 0/0 | 1281 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0006 | 0/0 | 1281 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0007 | 0/0 | 1281 | 4 | 1 | 0 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0008 | 0/0 | 1281 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0009 | 0/0 | 1281 | 3 | 0 | 1 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0010 | 0/0 | 1281 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0011 | 0/0 | 1281 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0012 | 0/0 | 1281 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0013 | 0/0 | 1281 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0014 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0015 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0016 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0017 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0018 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0019 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0020 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0021 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0022 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0023 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0024 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0025 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0026 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0027 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0028 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0029 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
c0030 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 427 | 136 | 23 | 21 | 59 | 2 | 30 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0002 | 1/0 | 427 | 62 | 13 | 30 | 3 | 7 | 8 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0003 | 0/0 | 427 | 4 | 4 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0004 | 0/0 | 427 | 3 | 0 | 0 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0005 | 0/0 | 427 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0006 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0007 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0008 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0009 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0010 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
t0011 | 0/0 | 427 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 18 | 0 | 4 | 10 | 1 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0002 | 0/0 | 11 | 1 | 1 | 7 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0003 | 0/0 | 9 | 1 | 5 | 1 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0004 | 1/0 | 8 | 0 | 4 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0007 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0009 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1281 | 134 | 25 | 37 | 44 | 4 | 22 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0012 | 0/0 | 1281 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0013 | 0/0 | 1281 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0014 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0021 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002c0002 | 0/0 | 1281 | 20 | 9 | 0 | 10 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002c0029 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0003c0003 | 0/0 | 1281 | 8 | 0 | 4 | 0 | 3 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0004c0005 | 0/0 | 1281 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0005c0004 | 0/0 | 1281 | 5 | 0 | 0 | 2 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0006c0007 | 0/0 | 1281 | 4 | 1 | 0 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0007c0006 | 0/0 | 1281 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0008c0009 | 0/0 | 1281 | 3 | 0 | 1 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0009c0008 | 0/0 | 1281 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0010c0010 | 0/0 | 1281 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0011c0011 | 0/0 | 1281 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0012c0027 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0013c0030 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0014c0028 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0015c0026 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0016c0024 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0017c0023 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0018c0022 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0019c0016 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0020c0017 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0021c0018 | 0/0 | 1281 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0022c0020 | 0/0 | 1281 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0023c0019 | 0/0 | 1281 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0024c0015 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0025c0025 | 0/0 | 1281 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1707 | 80 | 8 | 14 | 42 | 1 | 14 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0001t0002 | 1/0 | 1707 | 45 | 12 | 22 | 2 | 2 | 6 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0001t0003 | 0/0 | 1707 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0001t0004 | 0/0 | 1707 | 3 | 0 | 0 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0001t0005 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0001t0008 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0001t0010 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0012t0001 | 0/0 | 1707 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0013t0001 | 0/0 | 1707 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0014t0006 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0001c0021t0003 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002c0002t0001 | 0/0 | 1707 | 18 | 7 | 0 | 10 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002c0002t0009 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002c0002t0011 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0002c0029t0001 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0003c0003t0001 | 0/0 | 1707 | 4 | 0 | 3 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0003c0003t0002 | 0/0 | 1707 | 4 | 0 | 1 | 0 | 3 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0004c0005t0001 | 0/0 | 1707 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0005c0004t0001 | 0/0 | 1707 | 4 | 0 | 0 | 1 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0005c0004t0002 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0006c0007t0001 | 0/0 | 1707 | 4 | 1 | 0 | 0 | 0 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0007c0006t0002 | 0/0 | 1707 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0008c0009t0001 | 0/0 | 1707 | 3 | 0 | 1 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0009c0008t0001 | 0/0 | 1707 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0010c0010t0002 | 0/0 | 1707 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0011c0011t0002 | 0/0 | 1707 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0012c0027t0001 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0013c0030t0001 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0014c0028t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0015c0026t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0016c0024t0007 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0017c0023t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0018c0022t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0019c0016t0002 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0020c0017t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0021c0018t0001 | 0/0 | 1707 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0022c0020t0002 | 0/0 | 1707 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0023c0019t0001 | 0/0 | 1707 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0024c0015t0002 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
a0025c0025t0001 | 0/0 | 1707 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | copy fasta | chr19 | 43248282 | 43274530 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 0 | 4 | 10 | 1 | 3 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0002 | 0/0 | 11 | 1 | 1 | 7 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0003 | 0/0 | 9 | 1 | 5 | 1 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0004 | 1/0 | 8 | 0 | 4 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0007 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0003g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0012t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0013t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0014t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0001c0021t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0002t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0002c0029t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0002g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0003c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0004c0005t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0005c0004t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0005c0004t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0005c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0006c0007t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0006c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0006c0007t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0007c0006t0002g0009 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0008c0009t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0008c0009t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0009c0008t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0009c0008t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0010c0010t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0011c0011t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0011c0011t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0012c0027t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0013c0030t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0014c0028t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0015c0026t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0016c0024t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0017c0023t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0018c0022t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0019c0016t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0020c0017t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0021c0018t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0022c0020t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0023c0019t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0024c0015t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
a0025c0025t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0003 | t0002 | g0034 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00099 | hp2 | a0003 | c0003 | t0002 | g0012 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00140 | hp1 | a0007 | c0006 | t0002 | g0009 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0057 | EUR | GBR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00280 | hp1 | a0017 | c0023 | t0001 | g0085 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00280 | hp2 | a0011 | c0011 | t0002 | g0044 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00609 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00621 | hp2 | a0004 | c0005 | t0001 | g0008 | EAS | CHS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00735 | hp2 | a0025 | c0025 | t0001 | g0090 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00738 | hp1 | a0001 | c0012 | t0001 | g0030 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG00741 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01070 | hp2 | a0007 | c0006 | t0002 | g0009 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01168 | hp1 | a0019 | c0016 | t0002 | g0036 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01168 | hp2 | a0010 | c0010 | t0002 | g0014 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01175 | hp2 | a0011 | c0011 | t0002 | g0043 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01192 | hp1 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01192 | hp2 | a0024 | c0015 | t0002 | g0035 | AMR | PUR | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01496 | hp1 | a0001 | c0013 | t0001 | g0026 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01515 | hp2 | a0003 | c0003 | t0002 | g0012 | EUR | IBS | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01934 | hp1 | a0010 | c0010 | t0002 | g0014 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ACB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02129 | hp1 | a0005 | c0004 | t0002 | g0041 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02300 | hp1 | a0008 | c0009 | t0001 | g0078 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02572 | hp2 | a0013 | c0030 | t0001 | g0097 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02622 | hp2 | a0016 | c0024 | t0007 | g0040 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02630 | hp1 | a0006 | c0007 | t0001 | g0099 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02683 | hp1 | a0014 | c0028 | t0001 | g0106 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02698 | hp1 | a0001 | c0013 | t0001 | g0026 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02717 | hp1 | a0022 | c0020 | t0002 | g0048 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02723 | hp2 | a0009 | c0008 | t0001 | g0055 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02735 | hp2 | a0020 | c0017 | t0001 | g0071 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02809 | hp2 | a0009 | c0008 | t0001 | g0021 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02818 | hp1 | a0001 | c0012 | t0001 | g0030 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0060 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0079 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03041 | hp1 | a0002 | c0002 | t0011 | g0101 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03195 | hp1 | a0001 | c0021 | t0003 | g0058 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03225 | hp1 | a0009 | c0008 | t0001 | g0021 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03490 | hp2 | a0008 | c0009 | t0001 | g0024 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03491 | hp2 | a0007 | c0006 | t0002 | g0009 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03492 | hp1 | a0008 | c0009 | t0001 | g0024 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03492 | hp2 | a0007 | c0006 | t0002 | g0009 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03710 | hp2 | a0021 | c0018 | t0001 | g0080 | SAS | PJL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03831 | hp2 | a0005 | c0004 | t0001 | g0025 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03834 | hp1 | a0015 | c0026 | t0001 | g0091 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03927 | hp1 | a0006 | c0007 | t0001 | g0031 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03927 | hp2 | a0006 | c0007 | t0001 | g0100 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03942 | hp1 | a0018 | c0022 | t0001 | g0076 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03942 | hp2 | a0005 | c0004 | t0001 | g0023 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04115 | hp2 | a0006 | c0007 | t0001 | g0031 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04204 | hp2 | a0005 | c0004 | t0001 | g0025 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18612 | hp1 | a0023 | c0019 | t0001 | g0072 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18747 | hp1 | a0005 | c0004 | t0001 | g0023 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHB | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18993 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19043 | hp2 | a0002 | c0002 | t0009 | g0112 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19056 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19090 | hp1 | a0004 | c0005 | t0001 | g0008 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | YRI | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | YRI | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA20129 | hp1 | a0001 | c0014 | t0006 | g0046 | AFR | ASW | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ASW | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01123 | hp1 | a0010 | c0010 | t0002 | g0014 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG03471 | hp2 | a0012 | c0027 | t0001 | g0098 | AFR | MSL | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | USA | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | USA | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
NA21309 | hp2 | a0002 | c0029 | t0001 | g0103 | AFR | LWK | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0004 | REF | REF | PSG9_chr19_43248282_43274530 | PSG9 | chr19 | 43248282 | 43274530 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43258277
|
C | T | 1 | a0010 | 3 | HG01123.hp1 HG01168.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.1168G>A | p.Gly390Arg | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1267/1707 | 1168/1281 | 390/426 | chr19 | 43258277 | ||
chr19:43258288
|
C | G | 1 | a0022 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1157G>C | p.Arg386Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1256/1707 | 1157/1281 | 386/426 | chr19 | 43258288 | ||
chr19:43258399
|
T | A | 1 | a0009 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
missense_variant | MODERATE | c.1046A>T | p.Asn349Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1145/1707 | 1046/1281 | 349/426 | chr19 | 43258399 | ||
chr19:43258871
|
A | G | 6 | a0005a0007a0013others(3): Show | 13 | HG00140.hp1 HG01070.hp2 HG01168.hp1 others(10): Show |
missense_variant | MODERATE | c.974T>C | p.Ile325Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1073/1707 | 974/1281 | 325/426 | chr19 | 43258871 | ||
chr19:43258881
|
T | A | 3 | a0007a0008a0021 | 8 | HG00140.hp1 HG01070.hp2 HG02300.hp1 others(5): Show |
missense_variant | MODERATE | c.964A>T | p.Asn322Tyr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1063/1707 | 964/1281 | 322/426 | chr19 | 43258881 | ||
chr19:43258881
|
T | C | 2 | a0014a0020 | 2 | HG02683.hp1 HG02735.hp2 |
missense_variant | MODERATE | c.964A>G | p.Asn322Asp | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1063/1707 | 964/1281 | 322/426 | chr19 | 43258881 | ||
chr19:43258883
|
C | G | 1 | a0023 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.962G>C | p.Ser321Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1061/1707 | 962/1281 | 321/426 | chr19 | 43258883 | ||
chr19:43258886
|
C | T | 1 | a0020 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.959G>A | p.Arg320His | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1058/1707 | 959/1281 | 320/426 | chr19 | 43258886 | ||
chr19:43258890
|
G | T | 7 | a0007a0008a0014others(4): Show | 12 | HG00140.hp1 HG01070.hp2 HG01168.hp1 others(9): Show |
missense_variant | MODERATE | c.955C>A | p.Leu319Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1054/1707 | 955/1281 | 319/426 | chr19 | 43258890 | ||
chr19:43258907
|
C | T | 4 | a0003a0008a0019others(1): Show | 13 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(10): Show |
missense_variant | MODERATE | c.938G>A | p.Arg313Gln | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1037/1707 | 938/1281 | 313/426 | chr19 | 43258907 | ||
chr19:43258920
|
G | C | 1 | a0018 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.925C>G | p.Gln309Glu | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1024/1707 | 925/1281 | 309/426 | chr19 | 43258920 | ||
chr19:43258992
|
C | T | 1 | a0011 | 2 | HG00280.hp2 HG01175.hp2 |
missense_variant | MODERATE | c.853G>A | p.Gly285Arg | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 952/1707 | 853/1281 | 285/426 | chr19 | 43258992 | ||
chr19:43261892
|
C | A | 3 | a0006a0012a0013 | 6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
missense_variant | MODERATE | c.677G>T | p.Ser226Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 776/1707 | 677/1281 | 226/426 | chr19 | 43261892 | ||
chr19:43261936
|
A | C | 1 | a0024 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.633T>G | p.Ile211Met | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 732/1707 | 633/1281 | 211/426 | chr19 | 43261936 | ||
chr19:43261961
|
T | C | 1 | a0004 | 5 | HG00609.hp1 HG00621.hp2 NA18993.hp1 others(2): Show |
missense_variant | MODERATE | c.608A>G | p.Tyr203Cys | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 707/1707 | 608/1281 | 203/426 | chr19 | 43261961 | ||
chr19:43262072
|
C | T | 1 | a0012 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.497G>A | p.Arg166His | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 596/1707 | 497/1281 | 166/426 | chr19 | 43262072 | ||
chr19:43262120
|
T | G | 1 | a0017 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.449A>C | p.Tyr150Ser | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 548/1707 | 449/1281 | 150/426 | chr19 | 43262120 | ||
chr19:43267835
|
G | A | 1 | a0016 | 1 | HG02622.hp2 | stop_gained | HIGH | c.379C>T | p.Arg127* | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 478/1707 | 379/1281 | 127/426 | chr19 | 43267835 | ||
chr19:43267874
|
G | A | 1 | a0025 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.340C>T | p.Arg114Trp | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 439/1707 | 340/1281 | 114/426 | chr19 | 43267874 | ||
chr19:43268125
|
G | A | 1 | a0015 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.89C>T | p.Pro30Leu | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 188/1707 | 89/1281 | 30/426 | chr19 | 43268125 | ||
chr19:43269422
|
G | A | 5 | a0002a0006a0012others(2): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
missense_variant | MODERATE | c.10C>T | p.Leu4Phe | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/6 | 109/1707 | 10/1281 | 4/426 | chr19 | 43269422 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43258431
|
G | A | 1 | a0001c0021 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1014C>T | p.Tyr338Tyr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/6 | 1113/1707 | 1014/1281 | 338/426 | chr19 | 43258431 | ||
chr19:43258867
|
T | C | 6 | a0005c0004a0007c0006a0013c0030others(3): Show | 13 | HG00140.hp1 HG01070.hp2 HG01168.hp1 others(10): Show |
synonymous_variant | LOW | c.978A>G | p.Leu326Leu | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1077/1707 | 978/1281 | 326/426 | chr19 | 43258867 | ||
chr19:43258918
|
T | C | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.927A>G | p.Gln309Gln | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 1026/1707 | 927/1281 | 309/426 | chr19 | 43258918 | ||
chr19:43258963
|
T | G | 3 | a0001c0012a0002c0029a0018c0022 | 4 | HG00738.hp1 HG02818.hp1 HG03942.hp1 others(1): Show |
synonymous_variant | LOW | c.882A>C | p.Ile294Ile | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 981/1707 | 882/1281 | 294/426 | chr19 | 43258963 | ||
chr19:43259038
|
G | A | 1 | a0001c0013 | 2 | HG01496.hp1 HG02698.hp1 |
synonymous_variant | LOW | c.807C>T | p.Tyr269Tyr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/6 | 906/1707 | 807/1281 | 269/426 | chr19 | 43259038 | ||
chr19:43261930
|
T | C | 1 | a0009c0008 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.639A>G | p.Gly213Gly | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/6 | 738/1707 | 639/1281 | 213/426 | chr19 | 43261930 | ||
chr19:43268118
|
G | T | 1 | a0009c0008 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.96C>A | p.Thr32Thr | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 195/1707 | 96/1281 | 32/426 | chr19 | 43268118 | ||
chr19:43268124
|
C | T | 1 | a0001c0014 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.90G>A | p.Pro30Pro | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/6 | 189/1707 | 90/1281 | 30/426 | chr19 | 43268124 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43253285
|
C | T | 1 | a0001c0001t0008 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*324G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 324 | chr19 | 43253285 | |||||
chr19:43253313
|
A | G | 2 | a0002c0002t0009a0016c0024t0007 | 2 | HG02622.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 296 | chr19 | 43253313 | |||||
chr19:43253321
|
A | G | 1 | a0001c0001t0004 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*288T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 288 | chr19 | 43253321 | |||||
chr19:43253461
|
A | C | 1 | a0001c0014t0006 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 148 | chr19 | 43253461 | |||||
chr19:43253508
|
T | G | 1 | a0001c0001t0010 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 101 | chr19 | 43253508 | |||||
chr19:43253516
|
T | C | 2 | a0001c0001t0003a0001c0021t0003 | 4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*93A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 93 | chr19 | 43253516 | |||||
chr19:43253602
|
G | T | 1 | a0001c0001t0005 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 7 | chr19 | 43253602 | |||||
chr19:43253606
|
C | A | 1 | a0002c0002t0011 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 6/6 | 3 | chr19 | 43253606 | |||||
chr19:43269447
|
T | C | 27 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(24): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/6 | 16 | chr19 | 43269447 | |||||
chr19:43269474
|
G | A | 27 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(24): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/6 | 43 | chr19 | 43269474 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:43253877
|
G | T | 1 | a0001c0001t0001g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1244-231C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253877 | ||||||
chr19:43253943
|
T | A | 3 | a0002c0002t0001g0096a0002c0002t0001g0108a0002c0029t0001g0103 | 3 | HG02055.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1244-297A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253943 | ||||||
chr19:43253962
|
C | T | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1244-316G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253962 | ||||||
chr19:43253963
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1244-317G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253963 | ||||||
chr19:43253965
|
T | C | 11 | a0002c0002t0001g0017a0002c0002t0001g0096a0002c0002t0001g0102others(8): Show | 14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244-319A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253965 | ||||||
chr19:43253968
|
A | C | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1244-322T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43253968 | ||||||
chr19:43254118
|
A | G | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1244-472T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254118 | ||||||
chr19:43254213
|
C | G | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-567G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254213 | ||||||
chr19:43254215
|
C | G | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-569G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254215 | ||||||
chr19:43254216
|
A | G | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-570T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254216 | ||||||
chr19:43254224
|
T | C | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-578A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254224 | ||||||
chr19:43254259
|
G | T | 2 | a0011c0011t0002g0043a0011c0011t0002g0044 | 2 | HG00280.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1244-613C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254259 | ||||||
chr19:43254431
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 143 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1244-785T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254431 | ||||||
chr19:43254700
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 143 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1244-1054T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254700 | ||||||
chr19:43254799
|
G | C | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1244-1153C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254799 | ||||||
chr19:43254807
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1244-1161T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254807 | ||||||
chr19:43254809
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 143 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1244-1163A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254809 | ||||||
chr19:43254932
|
TA | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(63): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1244-1287delT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254932 | ||||||
chr19:43254969
|
TAGTCCTA others(9): Show |
T | 1 | a0017c0023t0001g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1244-1339_1244-132 others(20): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43254969 | ||||||
chr19:43255040
|
G | A | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1244-1394C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255040 | ||||||
chr19:43255117
|
A | G | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0062 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1244-1471T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255117 | ||||||
chr19:43255117
|
AAAAG | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(52): Show | 114 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1244-1475_1244-147 others(8): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255117 | ||||||
chr19:43255230
|
G | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(90): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1244-1584C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255230 | ||||||
chr19:43255412
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1244-1766C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255412 | ||||||
chr19:43255476
|
T | A | 3 | a0002c0002t0001g0096a0002c0002t0001g0108a0002c0029t0001g0103 | 3 | HG02055.hp1 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1244-1830A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255476 | ||||||
chr19:43255481
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(52): Show | 114 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1244-1835A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255481 | ||||||
chr19:43255487
|
G | T | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1244-1841C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255487 | ||||||
chr19:43255688
|
T | A | 1 | a0001c0001t0002g0038 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1244-2042A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255688 | ||||||
chr19:43255848
|
T | G | 11 | a0002c0002t0001g0017a0002c0002t0001g0096a0002c0002t0001g0102others(8): Show | 14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244-2202A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255848 | ||||||
chr19:43255884
|
T | G | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(88): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1244-2238A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255884 | ||||||
chr19:43255903
|
C | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(63): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1244-2257G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255903 | ||||||
chr19:43255939
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1243+2263A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43255939 | ||||||
chr19:43256145
|
G | T | 1 | a0001c0001t0001g0006 | 8 | NA18949.hp2 NA18983.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243+2057C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256145 | ||||||
chr19:43256284
|
C | A | 1 | a0002c0002t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1243+1918G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256284 | ||||||
chr19:43256367
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1243+1835T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256367 | ||||||
chr19:43256482
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0004g0056a0001c0001t0004g0057others(2): Show | 6 | HG00140.hp2 HG00738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1243+1720C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256482 | ||||||
chr19:43256492
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0002g0045a0001c0001t0002g0047 | 3 | HG02055.hp2 HG04115.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1243+1710T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256492 | ||||||
chr19:43256579
|
C | T | 2 | a0001c0001t0003g0015a0001c0021t0003g0058 | 4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1243+1623G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256579 | ||||||
chr19:43256608
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 143 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1243+1594G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256608 | ||||||
chr19:43256712
|
G | T | 5 | a0006c0007t0001g0031a0006c0007t0001g0099a0006c0007t0001g0100others(2): Show | 6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+1490C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256712 | ||||||
chr19:43256811
|
A | C | 11 | a0002c0002t0001g0017a0002c0002t0001g0096a0002c0002t0001g0102others(8): Show | 14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243+1391T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256811 | ||||||
chr19:43256885
|
C | G | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0062 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1243+1317G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43256885 | ||||||
chr19:43257016
|
C | A | 11 | a0002c0002t0001g0017a0002c0002t0001g0096a0002c0002t0001g0102others(8): Show | 14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243+1186G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257016 | ||||||
chr19:43257047
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0086 | 2 | HG02273.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1243+1155A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257047 | ||||||
chr19:43257244
|
G | A | 2 | a0001c0001t0001g0095a0001c0012t0001g0030 | 3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1243+958C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257244 | ||||||
chr19:43257353
|
T | G | 5 | a0006c0007t0001g0031a0006c0007t0001g0099a0006c0007t0001g0100others(2): Show | 6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1243+849A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257353 | ||||||
chr19:43257440
|
C | T | 1 | a0009c0008t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1243+762G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257440 | ||||||
chr19:43257473
|
C | T | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0062 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1243+729G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257473 | ||||||
chr19:43257545
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 143 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1243+657A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257545 | ||||||
chr19:43257546
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0018c0022t0001g0076 | 3 | HG03490.hp1 HG03942.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1243+656C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257546 | ||||||
chr19:43257697
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(54): Show | 116 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1243+505C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257697 | ||||||
chr19:43257782
|
TG | T | 11 | a0002c0002t0001g0017a0002c0002t0001g0096a0002c0002t0001g0102others(8): Show | 14 | HG02055.hp1 HG02572.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.1243+419delC | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257782 | ||||||
chr19:43257790
|
A | C | 2 | a0001c0001t0001g0095a0001c0012t0001g0030 | 3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1243+412T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257790 | ||||||
chr19:43257821
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 143 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1243+381G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257821 | ||||||
chr19:43257830
|
C | G | 1 | a0001c0001t0002g0051 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1243+372G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43257830 | ||||||
chr19:43258164
|
A | C | 4 | a0001c0001t0002g0007a0001c0001t0002g0049a0007c0006t0002g0009others(1): Show | 13 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1243+38T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43258164 | ||||||
chr19:43258189
|
G | T | 1 | a0001c0001t0008g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1243+13C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 5/5 | chr19 | 43258189 | ||||||
chr19:43258534
|
T | TGACCCTC others(16): Show |
5 | a0006c0007t0001g0031a0006c0007t0001g0099a0006c0007t0001g0100others(2): Show | 6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.989-101_989-79dupG others(22): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258534 | ||||||
chr19:43258665
|
A | G | 1 | a0001c0001t0001g0006 | 8 | NA18949.hp2 NA18983.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.988+192T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258665 | ||||||
chr19:43258730
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.988+127A>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258730 | ||||||
chr19:43258743
|
T | G | 1 | a0023c0019t0001g0072 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.988+114A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258743 | ||||||
chr19:43258757
|
G | A | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.988+100C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258757 | ||||||
chr19:43258840
|
G | T | 19 | a0002c0002t0001g0011a0002c0002t0001g0017a0002c0002t0001g0032others(16): Show | 26 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(23): Show |
intron_variant | MODIFIER | c.988+17C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258840 | ||||||
chr19:43258847
|
A | G | 1 | a0019c0016t0002g0036 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.988+10T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258847 | ||||||
chr19:43258855
|
A | T | 1 | a0008c0009t0001g0078 | 1 | HG02300.hp1 | splice_donor_variant&intron_variant | HIGH | c.988+2T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 4/5 | chr19 | 43258855 | ||||||
chr19:43259171
|
G | A | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.710-36C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259171 | ||||||
chr19:43259192
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.710-57C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259192 | ||||||
chr19:43259317
|
G | T | 1 | a0001c0001t0002g0049 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.710-182C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259317 | ||||||
chr19:43259394
|
C | T | 5 | a0006c0007t0001g0031a0006c0007t0001g0099a0006c0007t0001g0100others(2): Show | 6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.710-259G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259394 | ||||||
chr19:43259400
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0008g0039 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.710-265C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259400 | ||||||
chr19:43259411
|
C | T | 1 | a0001c0001t0001g0022 | 2 | NA18991.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.710-276G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259411 | ||||||
chr19:43259419
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.710-284G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259419 | ||||||
chr19:43259489
|
G | A | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-354C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259489 | ||||||
chr19:43259526
|
C | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.710-391G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259526 | ||||||
chr19:43259529
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.710-394A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259529 | ||||||
chr19:43259581
|
T | G | 21 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0027others(18): Show | 51 | HG00280.hp1 HG00323.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.710-446A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259581 | ||||||
chr19:43259637
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.710-502T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259637 | ||||||
chr19:43259692
|
AGTTC | A | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-561_710-558del others(4): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259692 | ||||||
chr19:43259737
|
G | A | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0062 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.710-602C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259737 | ||||||
chr19:43259823
|
A | T | 1 | a0001c0001t0004g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.710-688T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259823 | ||||||
chr19:43259837
|
G | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.710-702C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259837 | ||||||
chr19:43259854
|
C | G | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.710-719G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259854 | ||||||
chr19:43259939
|
T | C | 5 | a0006c0007t0001g0031a0006c0007t0001g0099a0006c0007t0001g0100others(2): Show | 6 | HG02572.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.710-804A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259939 | ||||||
chr19:43259960
|
A | C | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.710-825T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43259960 | ||||||
chr19:43260043
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.710-908G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260043 | ||||||
chr19:43260089
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.710-954A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260089 | ||||||
chr19:43260114
|
T | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 104 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.710-979A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260114 | ||||||
chr19:43260142
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.710-1007C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260142 | ||||||
chr19:43260167
|
G | T | 14 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0033others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.710-1032C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260167 | ||||||
chr19:43260349
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(45): Show | 103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.710-1214A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260349 | ||||||
chr19:43260351
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.710-1216A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260351 | ||||||
chr19:43260369
|
A | G | 1 | a0002c0002t0001g0104 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.710-1234T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260369 | ||||||
chr19:43260411
|
C | G | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.710-1276G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260411 | ||||||
chr19:43260421
|
T | C | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.710-1286A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260421 | ||||||
chr19:43260439
|
C | T | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.710-1304G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260439 | ||||||
chr19:43260514
|
T | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.709+1346A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260514 | ||||||
chr19:43260593
|
G | A | 1 | a0002c0002t0001g0107 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.709+1267C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260593 | ||||||
chr19:43260619
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.709+1241A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260619 | ||||||
chr19:43260725
|
C | A | 2 | a0002c0002t0001g0108a0002c0029t0001g0103 | 2 | HG02055.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.709+1135G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260725 | ||||||
chr19:43260742
|
G | A | 2 | a0001c0001t0003g0015a0001c0021t0003g0058 | 4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+1118C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260742 | ||||||
chr19:43260763
|
G | T | 1 | a0001c0001t0002g0019 | 2 | HG01175.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.709+1097C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260763 | ||||||
chr19:43260786
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0004g0056a0001c0001t0004g0057others(2): Show | 6 | HG00140.hp2 HG00738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1074A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260786 | ||||||
chr19:43260863
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.709+997T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43260863 | ||||||
chr19:43261094
|
A | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.709+766T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261094 | ||||||
chr19:43261096
|
C | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.709+764G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261096 | ||||||
chr19:43261098
|
A | T | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.709+762T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261098 | ||||||
chr19:43261099
|
G | T | 1 | a0002c0002t0001g0111 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.709+761C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261099 | ||||||
chr19:43261107
|
T | G | 1 | a0001c0001t0001g0084 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.709+753A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261107 | ||||||
chr19:43261123
|
T | G | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.709+737A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261123 | ||||||
chr19:43261220
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.709+640G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261220 | ||||||
chr19:43261278
|
A | AC | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(90): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.709+581dupG | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261278 | ||||||
chr19:43261306
|
G | T | 1 | a0006c0007t0001g0031 | 2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.709+554C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261306 | ||||||
chr19:43261327
|
G | T | 2 | a0002c0002t0001g0105a0006c0007t0001g0031 | 3 | HG03927.hp1 HG04115.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.709+533C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261327 | ||||||
chr19:43261461
|
G | C | 1 | a0009c0008t0001g0021 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.709+399C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261461 | ||||||
chr19:43261613
|
A | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.709+247T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261613 | ||||||
chr19:43261648
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.709+212T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261648 | ||||||
chr19:43261678
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 104 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.709+182G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261678 | ||||||
chr19:43261786
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.709+74T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261786 | ||||||
chr19:43261850
|
A | G | 1 | a0003c0003t0001g0016 | 3 | HG00741.hp2 HG01081.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.709+10T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261850 | ||||||
chr19:43261851
|
G | T | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0051 | 5 | HG00323.hp1 HG01074.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+9C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 3/5 | chr19 | 43261851 | ||||||
chr19:43262231
|
A | G | 14 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0033others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.431-93T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262231 | ||||||
chr19:43262240
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.431-102G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262240 | ||||||
chr19:43262290
|
G | A | 2 | a0002c0002t0009g0112a0016c0024t0007g0040 | 2 | HG02622.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.431-152C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262290 | ||||||
chr19:43262373
|
G | A | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.431-235C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262373 | ||||||
chr19:43262422
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.431-284G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262422 | ||||||
chr19:43262426
|
T | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.431-288A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262426 | ||||||
chr19:43262453
|
A | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.431-315T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262453 | ||||||
chr19:43262462
|
A | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.431-324T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262462 | ||||||
chr19:43262492
|
C | T | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.431-354G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262492 | ||||||
chr19:43262507
|
T | G | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.431-369A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262507 | ||||||
chr19:43262527
|
C | A | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-389G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262527 | ||||||
chr19:43262652
|
G | T | 1 | a0003c0003t0002g0034 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.431-514C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262652 | ||||||
chr19:43262683
|
G | A | 1 | a0001c0014t0006g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.431-545C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262683 | ||||||
chr19:43262733
|
G | A | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.431-595C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262733 | ||||||
chr19:43262828
|
C | T | 1 | a0011c0011t0002g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.431-690G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262828 | ||||||
chr19:43262898
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.431-760G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262898 | ||||||
chr19:43262901
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.431-763A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262901 | ||||||
chr19:43262919
|
C | G | 1 | a0002c0002t0001g0032 | 2 | HG02074.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.431-781G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43262919 | ||||||
chr19:43263017
|
A | T | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.431-879T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263017 | ||||||
chr19:43263066
|
T | C | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.431-928A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263066 | ||||||
chr19:43263316
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-1178C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263316 | ||||||
chr19:43263429
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0027 | 10 | NA18949.hp2 NA18956.hp2 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.431-1291C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263429 | ||||||
chr19:43263575
|
G | A | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.431-1437C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263575 | ||||||
chr19:43263591
|
C | CA | 9 | a0001c0001t0002g0013a0001c0001t0002g0033a0001c0001t0008g0039others(6): Show | 12 | HG00280.hp2 HG01123.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-1454dupT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263591 | ||||||
chr19:43263591
|
CA | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0059others(10): Show | 21 | HG00642.hp2 HG00735.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.431-1454delT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263591 | ||||||
chr19:43263778
|
G | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.431-1640C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263778 | ||||||
chr19:43263823
|
C | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 104 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.431-1685G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263823 | ||||||
chr19:43263960
|
T | C | 2 | a0001c0001t0001g0028a0025c0025t0001g0090 | 3 | HG00735.hp2 HG03239.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.431-1822A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263960 | ||||||
chr19:43263973
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-1835C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43263973 | ||||||
chr19:43264030
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.431-1892G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264030 | ||||||
chr19:43264166
|
T | G | 8 | a0002c0002t0001g0011a0002c0002t0001g0032a0002c0002t0001g0104others(5): Show | 12 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-2028A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264166 | ||||||
chr19:43264178
|
C | T | 8 | a0002c0002t0001g0011a0002c0002t0001g0032a0002c0002t0001g0104others(5): Show | 12 | HG00544.hp1 HG02074.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.431-2040G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264178 | ||||||
chr19:43264220
|
T | C | 1 | a0022c0020t0002g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-2082A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264220 | ||||||
chr19:43264473
|
T | TC | 2 | a0001c0001t0001g0095a0001c0012t0001g0030 | 3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.431-2336dupG | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264473 | ||||||
chr19:43264602
|
C | T | 2 | a0006c0007t0001g0099a0012c0027t0001g0098 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.431-2464G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264602 | ||||||
chr19:43264619
|
G | A | 1 | a0002c0002t0011g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.431-2481C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264619 | ||||||
chr19:43264704
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-2566C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264704 | ||||||
chr19:43264833
|
C | A | 1 | a0022c0020t0002g0048 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-2695G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43264833 | ||||||
chr19:43265004
|
G | C | 22 | a0001c0001t0001g0054a0001c0001t0001g0087a0002c0002t0001g0011others(19): Show | 29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.430+2780C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265004 | ||||||
chr19:43265094
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.430+2690A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265094 | ||||||
chr19:43265192
|
A | G | 2 | a0001c0001t0004g0057a0001c0001t0004g0062 | 2 | HG00140.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.430+2592T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265192 | ||||||
chr19:43265285
|
T | C | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0062 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.430+2499A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265285 | ||||||
chr19:43265291
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 104 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.430+2493G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265291 | ||||||
chr19:43265529
|
CA | C | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+2254delT | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265529 | ||||||
chr19:43265634
|
A | C | 4 | a0001c0001t0001g0065a0001c0001t0004g0056a0001c0001t0004g0057others(1): Show | 4 | HG00140.hp2 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2150T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265634 | ||||||
chr19:43265637
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.430+2147G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265637 | ||||||
chr19:43265661
|
A | C | 1 | a0001c0001t0004g0062 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.430+2123T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265661 | ||||||
chr19:43265711
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+2073A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265711 | ||||||
chr19:43265711
|
T | G | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(45): Show | 103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.430+2073A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265711 | ||||||
chr19:43265721
|
G | A | 1 | a0001c0021t0003g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.430+2063C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265721 | ||||||
chr19:43265749
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.430+2035G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265749 | ||||||
chr19:43265791
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+1993A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265791 | ||||||
chr19:43265829
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 104 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.430+1955T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265829 | ||||||
chr19:43265862
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.430+1922A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265862 | ||||||
chr19:43265970
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.430+1814C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265970 | ||||||
chr19:43265997
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.430+1787A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43265997 | ||||||
chr19:43266005
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.430+1779T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266005 | ||||||
chr19:43266109
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 142 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.430+1675C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266109 | ||||||
chr19:43266131
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.430+1653C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266131 | ||||||
chr19:43266141
|
A | T | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+1643T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266141 | ||||||
chr19:43266142
|
G | T | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+1642C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266142 | ||||||
chr19:43266167
|
C | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(53): Show | 114 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.430+1617G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266167 | ||||||
chr19:43266232
|
G | A | 21 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(18): Show | 28 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.430+1552C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266232 | ||||||
chr19:43266243
|
A | G | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.430+1541T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266243 | ||||||
chr19:43266267
|
G | T | 1 | a0002c0002t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.430+1517C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266267 | ||||||
chr19:43266292
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.430+1492C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266292 | ||||||
chr19:43266343
|
G | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1441C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266343 | ||||||
chr19:43266344
|
G | A | 2 | a0001c0001t0002g0033a0001c0001t0008g0039 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.430+1440C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266344 | ||||||
chr19:43266354
|
G | C | 5 | a0001c0001t0001g0029a0001c0001t0002g0007a0001c0001t0002g0049others(2): Show | 15 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+1430C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266354 | ||||||
chr19:43266357
|
A | AC | 5 | a0001c0001t0001g0029a0001c0001t0002g0007a0001c0001t0002g0049others(2): Show | 15 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+1426_430+1427i others(3): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266357 | ||||||
chr19:43266360
|
T | C | 5 | a0001c0001t0001g0029a0001c0001t0002g0007a0001c0001t0002g0049others(2): Show | 15 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.430+1424A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266360 | ||||||
chr19:43266385
|
A | T | 1 | a0001c0001t0001g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.430+1399T>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266385 | ||||||
chr19:43266401
|
A | C | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1383T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266401 | ||||||
chr19:43266403
|
G | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1381C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266403 | ||||||
chr19:43266405
|
T | C | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1379A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266405 | ||||||
chr19:43266413
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.430+1371G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266413 | ||||||
chr19:43266414
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.430+1370T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266414 | ||||||
chr19:43266439
|
G | C | 1 | a0001c0001t0002g0013 | 3 | HG01123.hp2 HG03041.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.430+1345C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266439 | ||||||
chr19:43266446
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+1338C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266446 | ||||||
chr19:43266464
|
T | C | 2 | a0001c0001t0001g0029a0002c0002t0001g0109 | 3 | HG02717.hp2 HG02965.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.430+1320A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266464 | ||||||
chr19:43266618
|
G | C | 1 | a0009c0008t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.430+1166C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266618 | ||||||
chr19:43266690
|
G | A | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+1094C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266690 | ||||||
chr19:43266716
|
C | T | 7 | a0001c0001t0001g0095a0001c0001t0003g0015a0001c0001t0004g0056others(4): Show | 10 | HG00140.hp2 HG00738.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+1068G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266716 | ||||||
chr19:43266962
|
G | C | 1 | a0002c0002t0001g0110 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.430+822C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43266962 | ||||||
chr19:43267122
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.430+662T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267122 | ||||||
chr19:43267130
|
A | C | 1 | a0013c0030t0001g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.430+654T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267130 | ||||||
chr19:43267197
|
C | T | 1 | a0001c0001t0002g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.430+587G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267197 | ||||||
chr19:43267230
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(77): Show | 146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.430+554T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267230 | ||||||
chr19:43267258
|
A | G | 2 | a0001c0001t0003g0015a0001c0021t0003g0058 | 4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+526T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267258 | ||||||
chr19:43267260
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(46): Show | 104 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.430+524T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267260 | ||||||
chr19:43267274
|
C | T | 1 | a0001c0001t0002g0010 | 4 | HG02723.hp1 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+510G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267274 | ||||||
chr19:43267386
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.430+398C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267386 | ||||||
chr19:43267418
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(44): Show | 102 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.430+366A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267418 | ||||||
chr19:43267422
|
TGA | T | 2 | a0001c0001t0003g0015a0001c0021t0003g0058 | 4 | HG03139.hp2 HG03195.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+360_430+361del others(2): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267422 | ||||||
chr19:43267509
|
T | G | 1 | a0002c0002t0001g0111 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.430+275A>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267509 | ||||||
chr19:43267517
|
G | T | 2 | a0001c0001t0001g0095a0001c0012t0001g0030 | 3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.430+267C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267517 | ||||||
chr19:43267549
|
C | T | 1 | a0002c0029t0001g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.430+235G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267549 | ||||||
chr19:43267634
|
TGTGTGTG others(26): Show |
T | 1 | a0001c0001t0001g0063 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.430+117_430+149del others(33): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 2/5 | chr19 | 43267634 | ||||||
chr19:43268157
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0010g0060 | 2 | HG02886.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.65-8C>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268157 | ||||||
chr19:43268211
|
G | A | 1 | a0002c0002t0009g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.65-62C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268211 | ||||||
chr19:43268237
|
C | A | 1 | a0001c0001t0001g0092 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.65-88G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268237 | ||||||
chr19:43268237
|
C | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(76): Show | 145 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.65-88G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268237 | ||||||
chr19:43268246
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.65-97G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268246 | ||||||
chr19:43268263
|
C | T | 13 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0033others(10): Show | 18 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.65-114G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268263 | ||||||
chr19:43268267
|
C | CACAT | 12 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0033others(9): Show | 17 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-122_65-119dupAT others(2): Show |
PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268267 | ||||||
chr19:43268321
|
G | A | 1 | a0001c0001t0001g0029 | 2 | HG02717.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.65-172C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268321 | ||||||
chr19:43268332
|
C | G | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0062 | 3 | HG00140.hp2 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.65-183G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268332 | ||||||
chr19:43268484
|
A | C | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.65-335T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268484 | ||||||
chr19:43268519
|
G | A | 22 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(19): Show | 29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-370C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268519 | ||||||
chr19:43268591
|
C | G | 2 | a0001c0001t0002g0042a0005c0004t0002g0041 | 2 | HG02129.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.65-442G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268591 | ||||||
chr19:43268599
|
C | T | 2 | a0001c0001t0002g0042a0005c0004t0002g0041 | 2 | HG02129.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.65-450G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268599 | ||||||
chr19:43268600
|
G | A | 16 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(13): Show | 22 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-451C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268600 | ||||||
chr19:43268636
|
C | G | 22 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(19): Show | 29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-487G>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268636 | ||||||
chr19:43268724
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.65-575G>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268724 | ||||||
chr19:43268780
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+588A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268780 | ||||||
chr19:43268783
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+585A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268783 | ||||||
chr19:43268784
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64+584C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268784 | ||||||
chr19:43268865
|
G | T | 2 | a0009c0008t0001g0021a0009c0008t0001g0055 | 3 | HG02723.hp2 HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.64+503C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268865 | ||||||
chr19:43268940
|
C | A | 2 | a0001c0001t0002g0010a0001c0001t0003g0015 | 7 | HG02723.hp1 HG03098.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+428G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43268940 | ||||||
chr19:43269026
|
A | G | 1 | a0002c0002t0001g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.64+342T>C | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269026 | ||||||
chr19:43269056
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.64+312C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269056 | ||||||
chr19:43269064
|
G | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0033others(8): Show | 16 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+304C>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269064 | ||||||
chr19:43269067
|
G | T | 11 | a0001c0001t0002g0013a0001c0001t0002g0018a0001c0001t0002g0033others(8): Show | 16 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.64+301C>A | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269067 | ||||||
chr19:43269078
|
A | C | 22 | a0001c0001t0001g0054a0002c0002t0001g0011a0002c0002t0001g0017others(19): Show | 29 | HG00544.hp1 HG02055.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.64+290T>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269078 | ||||||
chr19:43269151
|
T | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(45): Show | 103 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.64+217A>G | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269151 | ||||||
chr19:43269292
|
C | A | 2 | a0001c0001t0001g0095a0001c0012t0001g0030 | 3 | HG00738.hp1 HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.64+76G>T | PSG9 | ENSG00000183668.18 | transcript | ENST00000270077.8 | protein_coding | 1/5 | chr19 | 43269292 |