geneid | 64430 |
---|---|
ensemblid | ENSG00000126773.13 |
hgncid | 20349 |
symbol | PCNX4 |
name | pecanex 4 |
refseq_nuc | NM_001330177.2 |
refseq_prot | NP_001317106.1 |
ensembl_nuc | ENST00000406854.6 |
ensembl_prot | ENSP00000384801.1 |
mane_status | MANE Select |
chr | chr14 |
start | 60091923 |
end | 60148221 |
strand | + |
ver | v1.2 |
region | chr14:60091923-60148221 |
region5000 | chr14:60086923-60153221 |
regionname0 | PCNX4_chr14_60091923_60148221 |
regionname5000 | PCNX4_chr14_60086923_60153221 |
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 | 0/1 | 1172 | 134 | 28 | 25 | 58 | 7 | 15 | 49 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002 | 0/0 | 1172 | 65 | 33 | 13 | 9 | 0 | 10 | 4 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003 | 0/0 | 1172 | 40 | 2 | 0 | 37 | 0 | 1 | 30 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004 | 0/0 | 1172 | 24 | 0 | 0 | 24 | 0 | 0 | 24 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0005 | 0/0 | 1172 | 8 | 0 | 1 | 7 | 0 | 0 | 5 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0006 | 0/0 | 1172 | 8 | 0 | 2 | 3 | 1 | 2 | 3 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0007 | 0/0 | 1173 | 7 | 4 | 1 | 0 | 0 | 2 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0008 | 0/0 | 1172 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0009 | 0/0 | 1172 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0010 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0011 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0012 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0013 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0014 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0015 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0016 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0017 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0018 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0019 | 1/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0020 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0021 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0022 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0023 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0024 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0025 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
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 | 0/1 | 3519 | 131 | 27 | 25 | 57 | 7 | 14 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0002 | 0/0 | 3519 | 50 | 20 | 11 | 9 | 0 | 10 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0003 | 0/0 | 3519 | 40 | 2 | 0 | 37 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0004 | 0/0 | 3519 | 24 | 0 | 0 | 24 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0005 | 0/0 | 3519 | 8 | 0 | 1 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0006 | 0/0 | 3519 | 8 | 0 | 2 | 3 | 1 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0007 | 0/0 | 3519 | 7 | 6 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0008 | 0/0 | 3522 | 7 | 4 | 1 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0009 | 0/0 | 3519 | 6 | 6 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0010 | 0/0 | 3519 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0011 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0012 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0013 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0014 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0015 | 1/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0016 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0017 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0018 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0019 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0020 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0021 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0022 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0023 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0024 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0025 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0026 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0027 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0028 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0029 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0030 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0031 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
c0032 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
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 | 14551 | 71 | 22 | 10 | 24 | 4 | 10 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0002 | 0/0 | 14550 | 37 | 2 | 0 | 34 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0003 | 0/0 | 14544 | 31 | 20 | 8 | 0 | 0 | 3 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0004 | 0/0 | 14557 | 18 | 0 | 0 | 18 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0005 | 0/0 | 14544 | 13 | 0 | 1 | 9 | 0 | 3 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0006 | 0/0 | 14549 | 11 | 0 | 1 | 9 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0007 | 0/0 | 14551 | 8 | 0 | 0 | 8 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0008 | 0/0 | 14551 | 8 | 1 | 7 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0009 | 0/0 | 14547 | 6 | 0 | 3 | 2 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0010 | 0/0 | 14551 | 5 | 0 | 0 | 5 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0011 | 0/0 | 14551 | 4 | 0 | 4 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0012 | 0/0 | 14551 | 4 | 1 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0013 | 0/0 | 14540 | 4 | 4 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0014 | 0/0 | 14544 | 3 | 0 | 3 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0015 | 0/0 | 14549 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0016 | 0/0 | 14544 | 3 | 3 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0017 | 0/0 | 14551 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0018 | 0/0 | 14551 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0019 | 0/0 | 14551 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0020 | 0/0 | 14551 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0021 | 0/0 | 14551 | 2 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0022 | 0/0 | 14551 | 2 | 0 | 0 | 0 | 2 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0023 | 0/0 | 14551 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0024 | 0/0 | 14551 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0025 | 0/0 | 14558 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0026 | 0/0 | 14540 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0027 | 0/0 | 14544 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0028 | 0/0 | 14544 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0029 | 0/0 | 14550 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0030 | 0/0 | 14551 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0031 | 0/0 | 14544 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0032 | 0/0 | 14549 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0033 | 0/0 | 14551 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0034 | 0/0 | 14551 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0035 | 0/0 | 14551 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0036 | 0/0 | 14551 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0037 | 0/0 | 14551 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0038 | 0/0 | 14640 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0039 | 0/0 | 14549 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0040 | 0/0 | 14550 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0041 | 0/0 | 14551 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0042 | 0/0 | 14552 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0043 | 0/0 | 14551 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0044 | 0/0 | 14549 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0045 | 0/0 | 14551 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0046 | 0/0 | 14551 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0047 | 0/0 | 14551 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0048 | 0/0 | 14551 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0049 | 0/0 | 14551 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0050 | 0/0 | 14551 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0051 | 0/0 | 14547 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0052 | 1/0 | 14551 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0053 | 0/0 | 14557 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0054 | 0/0 | 14558 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0055 | 0/0 | 14550 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0056 | 0/0 | 14544 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0057 | 0/0 | 14541 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0058 | 0/0 | 14544 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0059 | 0/0 | 14550 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0060 | 0/0 | 14550 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0061 | 0/0 | 14547 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0062 | 0/0 | 14550 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0063 | 0/0 | 14544 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0064 | 0/0 | 14540 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0065 | 0/0 | 14544 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0066 | 0/0 | 14542 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0067 | 0/0 | 14544 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0068 | 0/0 | 14544 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0069 | 0/0 | 14544 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0070 | 0/0 | 14544 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0071 | 0/0 | 14544 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0072 | 0/0 | 14543 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0073 | 0/0 | 14550 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0074 | 0/0 | 14551 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0075 | 0/0 | 14545 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0076 | 0/0 | 14547 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0077 | 0/0 | 14544 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0078 | 0/0 | 14554 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0079 | 0/0 | 14550 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0080 | 0/0 | 14544 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
t0081 | 0/0 | 14544 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
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 | 17 | 0 | 0 | 16 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0002 | 0/0 | 14 | 1 | 5 | 5 | 0 | 3 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0003 | 0/0 | 13 | 9 | 3 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0004 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0007 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0012 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0019 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0038 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
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 | 0/1 | 3519 | 131 | 27 | 25 | 57 | 7 | 14 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0021 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0023 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0030 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002 | 0/0 | 3519 | 50 | 20 | 11 | 9 | 0 | 10 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0007 | 0/0 | 3519 | 7 | 6 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0009 | 0/0 | 3519 | 6 | 6 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0013 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0025 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003c0003 | 0/0 | 3519 | 40 | 2 | 0 | 37 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004c0004 | 0/0 | 3519 | 24 | 0 | 0 | 24 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0005c0005 | 0/0 | 3519 | 8 | 0 | 1 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0006c0006 | 0/0 | 3519 | 8 | 0 | 2 | 3 | 1 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0007c0008 | 0/0 | 3522 | 7 | 4 | 1 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0008c0010 | 0/0 | 3519 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0009c0011 | 0/0 | 3519 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0010c0029 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0011c0020 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0012c0022 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0013c0014 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0014c0017 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0015c0028 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0016c0027 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0017c0016 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0018c0026 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0019c0015 | 1/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0020c0024 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0021c0018 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0022c0019 | 0/0 | 3519 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0023c0031 | 0/0 | 3519 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0024c0012 | 0/0 | 3519 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0025c0032 | 0/0 | 3519 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 18069 | 68 | 20 | 10 | 23 | 4 | 10 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0006 | 0/0 | 18067 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0007 | 0/0 | 18069 | 7 | 0 | 0 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0008 | 0/0 | 18069 | 8 | 1 | 7 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0010 | 0/0 | 18069 | 5 | 0 | 0 | 5 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0011 | 0/0 | 18069 | 4 | 0 | 4 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0012 | 0/0 | 18069 | 4 | 1 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0015 | 0/0 | 18067 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0017 | 0/0 | 18069 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0018 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0019 | 0/0 | 18069 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0020 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0021 | 0/0 | 18069 | 2 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0022 | 0/0 | 18069 | 2 | 0 | 0 | 0 | 2 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0023 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0030 | 0/0 | 18069 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0033 | 0/0 | 18069 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0034 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0036 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0038 | 0/0 | 18158 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0040 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0042 | 0/0 | 18070 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0043 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0044 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0046 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0047 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0048 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0001t0049 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0021t0032 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0023t0001 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0001c0030t0006 | 0/0 | 18067 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0003 | 0/0 | 18062 | 23 | 15 | 6 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0005 | 0/0 | 18062 | 9 | 0 | 1 | 6 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0014 | 0/0 | 18062 | 3 | 0 | 3 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0016 | 0/0 | 18062 | 3 | 3 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0028 | 0/0 | 18062 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0031 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0064 | 0/0 | 18058 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0066 | 0/0 | 18060 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0067 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0069 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0070 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0071 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0077 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0080 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0002t0081 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0007t0003 | 0/0 | 18062 | 5 | 4 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0007t0061 | 0/0 | 18065 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0007t0063 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0009t0027 | 0/0 | 18062 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0009t0029 | 0/0 | 18068 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0009t0056 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0009t0073 | 0/0 | 18068 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0013t0003 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0002c0025t0079 | 0/0 | 18068 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003c0003t0002 | 0/0 | 18068 | 36 | 2 | 0 | 33 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003c0003t0059 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003c0003t0060 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003c0003t0062 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0003c0003t0074 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004c0004t0004 | 0/0 | 18075 | 18 | 0 | 0 | 18 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004c0004t0024 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004c0004t0025 | 0/0 | 18076 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004c0004t0053 | 0/0 | 18075 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0004c0004t0054 | 0/0 | 18076 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0005c0005t0001 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0005c0005t0006 | 0/0 | 18067 | 6 | 0 | 1 | 5 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0005c0005t0039 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0006c0006t0009 | 0/0 | 18065 | 5 | 0 | 2 | 2 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0006c0006t0051 | 0/0 | 18065 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0006c0006t0075 | 0/0 | 18063 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0006c0006t0076 | 0/0 | 18065 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0007c0008t0013 | 0/0 | 18061 | 4 | 4 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0007c0008t0026 | 0/0 | 18061 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0007c0008t0057 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0008c0010t0005 | 0/0 | 18062 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0008c0010t0068 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0009c0011t0001 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0009c0011t0037 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0010c0029t0058 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0011c0020t0007 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0012c0022t0041 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0013c0014t0065 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0014c0017t0003 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0015c0028t0055 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0016c0027t0002 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0017c0016t0005 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0018c0026t0072 | 0/0 | 18061 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0019c0015t0052 | 1/0 | 18069 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0020c0024t0045 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0021c0018t0078 | 0/0 | 18072 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0022c0019t0050 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0023c0031t0035 | 0/0 | 18069 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0024c0012t0003 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
a0025c0032t0009 | 0/0 | 18065 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | copy fasta | chr14 | 60086923 | 60153221 |
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 | 7 | 0 | 0 | 6 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0003 | 0/0 | 10 | 8 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0011g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0015g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0015g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0017g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0017g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0018g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0019g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0020g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0021g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0021g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0022g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0023g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0023g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0030g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0033g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0036g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0038g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0040g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0042g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0043g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0044g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0046g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0047g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0048g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0049g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0021t0032g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0023t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0030t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0014g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0016g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0016g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0028g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0028g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0031g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0064g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0066g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0067g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0069g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0070g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0071g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0077g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0080g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0081g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0061g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0063g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0027g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0027g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0029g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0056g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0073g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0013t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0025t0079g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0059g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0060g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0062g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0074g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0024g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0024g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0025g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0025g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0053g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0054g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0006g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0005t0039g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0006t0009g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0006t0009g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0006t0051g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0006t0075g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0006t0076g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0013g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0026g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0026g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0057g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0008c0010t0005g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0008c0010t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0008c0010t0068g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0009c0011t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0009c0011t0037g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0010c0029t0058g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0011c0020t0007g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0012c0022t0041g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0013c0014t0065g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0014c0017t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0015c0028t0055g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0016c0027t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0017c0016t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0018c0026t0072g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0019c0015t0052g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0020c0024t0045g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0021c0018t0078g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0022c0019t0050g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0023c0031t0035g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0024c0012t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0025c0032t0009g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0022 | g0146 | EUR | GBR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00280 | hp2 | a0001 | c0001 | t0022 | g0165 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00323 | hp2 | a0006 | c0006 | t0076 | g0018 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00558 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00609 | hp1 | a0003 | c0003 | t0002 | g0069 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00639 | hp1 | a0002 | c0002 | t0003 | g0013 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00642 | hp1 | a0006 | c0006 | t0009 | g0017 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00642 | hp2 | a0001 | c0001 | t0046 | g0127 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00673 | hp1 | a0002 | c0002 | t0077 | g0007 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00673 | hp2 | a0001 | c0001 | t0049 | g0176 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00735 | hp1 | a0012 | c0022 | t0041 | g0157 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00735 | hp2 | a0006 | c0006 | t0009 | g0017 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01081 | hp2 | a0002 | c0007 | t0003 | g0080 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01109 | hp1 | a0002 | c0002 | t0003 | g0083 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01109 | hp2 | a0002 | c0002 | t0081 | g0007 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01175 | hp1 | a0001 | c0001 | t0021 | g0145 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0184 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01192 | hp1 | a0001 | c0001 | t0011 | g0010 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01192 | hp2 | a0002 | c0002 | t0014 | g0021 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01243 | hp1 | a0002 | c0013 | t0003 | g0057 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01243 | hp2 | a0010 | c0029 | t0058 | g0111 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01255 | hp1 | a0002 | c0002 | t0005 | g0007 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0039 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01258 | hp1 | a0002 | c0002 | t0003 | g0039 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01258 | hp2 | a0001 | c0001 | t0036 | g0003 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01346 | hp1 | a0002 | c0002 | t0003 | g0013 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01358 | hp2 | a0007 | c0008 | t0057 | g0112 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01361 | hp1 | a0025 | c0032 | t0009 | g0106 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0138 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01433 | hp2 | a0002 | c0002 | t0014 | g0021 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01496 | hp1 | a0020 | c0024 | t0045 | g0117 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01496 | hp2 | a0005 | c0005 | t0006 | g0152 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01884 | hp1 | a0002 | c0007 | t0063 | g0078 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0144 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01928 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01934 | hp2 | a0001 | c0001 | t0011 | g0140 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0134 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0037 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01978 | hp1 | a0001 | c0001 | t0008 | g0148 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01981 | hp1 | a0002 | c0002 | t0014 | g0013 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0010 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02004 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02004 | hp2 | a0001 | c0001 | t0047 | g0010 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02015 | hp1 | a0003 | c0003 | t0002 | g0026 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02040 | hp1 | a0016 | c0027 | t0002 | g0075 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02055 | hp2 | a0007 | c0008 | t0013 | g0028 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02071 | hp1 | a0003 | c0003 | t0002 | g0067 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02074 | hp1 | a0002 | c0002 | t0005 | g0092 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02074 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02080 | hp1 | a0002 | c0002 | t0005 | g0015 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0025 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02132 | hp1 | a0003 | c0003 | t0002 | g0025 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02132 | hp2 | a0002 | c0002 | t0067 | g0100 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02145 | hp1 | a0007 | c0008 | t0013 | g0114 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02145 | hp2 | a0002 | c0007 | t0003 | g0027 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02155 | hp1 | a0001 | c0001 | t0012 | g0131 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02155 | hp2 | a0001 | c0001 | t0044 | g0012 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02165 | hp1 | a0003 | c0003 | t0002 | g0072 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02165 | hp2 | a0005 | c0005 | t0006 | g0153 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02257 | hp2 | a0002 | c0025 | t0079 | g0055 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0059 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02280 | hp1 | a0007 | c0008 | t0013 | g0113 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02572 | hp1 | a0003 | c0003 | t0002 | g0115 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02572 | hp2 | a0001 | c0001 | t0017 | g0136 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02602 | hp1 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02615 | hp2 | a0002 | c0007 | t0061 | g0061 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02683 | hp1 | a0002 | c0002 | t0005 | g0095 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02683 | hp2 | a0001 | c0001 | t0021 | g0129 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02723 | hp1 | a0002 | c0002 | t0069 | g0024 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0186 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02735 | hp2 | a0007 | c0008 | t0026 | g0109 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02738 | hp1 | a0001 | c0030 | t0006 | g0177 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02738 | hp2 | a0002 | c0002 | t0080 | g0093 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02818 | hp2 | a0002 | c0002 | t0003 | g0086 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0088 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02896 | hp2 | a0001 | c0001 | t0038 | g0130 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02922 | hp1 | a0002 | c0009 | t0056 | g0056 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02970 | hp1 | a0002 | c0007 | t0003 | g0077 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02970 | hp2 | a0002 | c0002 | t0070 | g0181 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02976 | hp1 | a0001 | c0001 | t0019 | g0003 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03139 | hp1 | a0009 | c0011 | t0037 | g0034 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03139 | hp2 | a0002 | c0009 | t0027 | g0076 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03195 | hp2 | a0002 | c0002 | t0016 | g0084 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03209 | hp1 | a0001 | c0023 | t0001 | g0120 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0089 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03453 | hp1 | a0002 | c0009 | t0073 | g0104 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03486 | hp1 | a0002 | c0002 | t0003 | g0182 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03486 | hp2 | a0002 | c0002 | t0016 | g0085 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03490 | hp1 | a0001 | c0001 | t0030 | g0030 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03490 | hp2 | a0002 | c0002 | t0031 | g0183 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03491 | hp1 | a0001 | c0001 | t0030 | g0030 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03491 | hp2 | a0002 | c0002 | t0005 | g0097 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03516 | hp2 | a0002 | c0002 | t0016 | g0082 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03540 | hp2 | a0007 | c0008 | t0013 | g0028 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03579 | hp1 | a0001 | c0001 | t0019 | g0019 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03579 | hp2 | a0002 | c0002 | t0003 | g0062 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03654 | hp2 | a0002 | c0002 | t0064 | g0007 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03669 | hp1 | a0002 | c0002 | t0028 | g0101 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03688 | hp1 | a0013 | c0014 | t0065 | g0098 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03704 | hp1 | a0003 | c0003 | t0002 | g0014 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03704 | hp2 | a0023 | c0031 | t0035 | g0002 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03710 | hp2 | a0006 | c0006 | t0075 | g0108 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03831 | hp2 | a0002 | c0002 | t0028 | g0102 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0013 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03942 | hp1 | a0007 | c0008 | t0026 | g0110 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04115 | hp1 | a0002 | c0002 | t0071 | g0094 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04115 | hp2 | a0014 | c0017 | t0003 | g0185 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04204 | hp1 | a0006 | c0006 | t0009 | g0017 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04204 | hp2 | a0001 | c0001 | t0042 | g0141 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04228 | hp1 | a0017 | c0016 | t0005 | g0096 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18522 | hp2 | a0002 | c0002 | t0003 | g0060 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18612 | hp1 | a0005 | c0005 | t0039 | g0175 | EAS | CHB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18612 | hp2 | a0002 | c0002 | t0005 | g0015 | EAS | CHB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18906 | hp2 | a0018 | c0026 | t0072 | g0180 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18939 | hp2 | a0004 | c0004 | t0024 | g0023 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18940 | hp1 | a0004 | c0004 | t0025 | g0052 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18940 | hp2 | a0022 | c0019 | t0050 | g0160 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18941 | hp1 | a0004 | c0004 | t0004 | g0023 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18941 | hp2 | a0002 | c0002 | t0066 | g0007 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18942 | hp1 | a0011 | c0020 | t0007 | g0040 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18943 | hp1 | a0003 | c0003 | t0059 | g0008 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18944 | hp1 | a0008 | c0010 | t0068 | g0016 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18944 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18945 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18945 | hp2 | a0004 | c0004 | t0004 | g0045 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18946 | hp1 | a0006 | c0006 | t0009 | g0018 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18946 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18948 | hp2 | a0006 | c0006 | t0051 | g0107 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18950 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18960 | hp1 | a0001 | c0001 | t0040 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18960 | hp2 | a0004 | c0004 | t0024 | g0049 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18961 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18961 | hp2 | a0001 | c0001 | t0048 | g0035 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18962 | hp1 | a0015 | c0028 | t0055 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18962 | hp2 | a0006 | c0006 | t0009 | g0018 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18964 | hp1 | a0004 | c0004 | t0004 | g0051 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18964 | hp2 | a0003 | c0003 | t0002 | g0074 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18966 | hp1 | a0005 | c0005 | t0006 | g0174 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18968 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18968 | hp2 | a0001 | c0001 | t0010 | g0171 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18975 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18975 | hp2 | a0004 | c0004 | t0004 | g0042 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18977 | hp1 | a0005 | c0005 | t0006 | g0119 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18977 | hp2 | a0004 | c0004 | t0004 | g0048 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18978 | hp1 | a0002 | c0002 | t0005 | g0029 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18979 | hp1 | a0001 | c0021 | t0032 | g0168 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18979 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18980 | hp2 | a0001 | c0001 | t0015 | g0012 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18981 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18981 | hp2 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18982 | hp1 | a0001 | c0001 | t0015 | g0166 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18983 | hp2 | a0004 | c0004 | t0004 | g0022 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18984 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18986 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18986 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18988 | hp1 | a0004 | c0004 | t0053 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18988 | hp2 | a0003 | c0003 | t0002 | g0014 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18989 | hp1 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18989 | hp2 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18992 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18992 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0172 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18994 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18995 | hp2 | a0004 | c0004 | t0004 | g0046 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18998 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18999 | hp1 | a0001 | c0001 | t0023 | g0173 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18999 | hp2 | a0004 | c0004 | t0004 | g0044 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19002 | hp1 | a0002 | c0002 | t0005 | g0029 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19004 | hp1 | a0004 | c0004 | t0054 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19004 | hp2 | a0001 | c0001 | t0023 | g0035 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19006 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19006 | hp2 | a0005 | c0005 | t0001 | g0154 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19007 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19007 | hp2 | a0003 | c0003 | t0060 | g0066 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19009 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19009 | hp2 | a0001 | c0001 | t0020 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19011 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19012 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19043 | hp1 | a0002 | c0007 | t0003 | g0027 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19043 | hp2 | a0001 | c0001 | t0017 | g0125 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19057 | hp1 | a0003 | c0003 | t0062 | g0014 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19059 | hp1 | a0003 | c0003 | t0002 | g0105 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19059 | hp2 | a0001 | c0001 | t0043 | g0137 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19065 | hp1 | a0004 | c0004 | t0025 | g0047 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19065 | hp2 | a0008 | c0010 | t0005 | g0099 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19066 | hp2 | a0008 | c0010 | t0005 | g0016 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19068 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19068 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19070 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0041 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19075 | hp1 | a0008 | c0010 | t0005 | g0016 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19075 | hp2 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19078 | hp1 | a0003 | c0003 | t0074 | g0008 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19079 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19079 | hp2 | a0005 | c0005 | t0006 | g0036 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0065 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19080 | hp2 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19081 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19081 | hp2 | a0004 | c0004 | t0004 | g0050 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19082 | hp1 | a0002 | c0002 | t0005 | g0015 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19083 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19084 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19085 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19086 | hp1 | a0004 | c0004 | t0004 | g0043 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19087 | hp1 | a0005 | c0005 | t0006 | g0036 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19087 | hp2 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19088 | hp1 | a0004 | c0004 | t0004 | g0022 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19088 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19090 | hp1 | a0003 | c0003 | t0002 | g0026 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19090 | hp2 | a0001 | c0001 | t0010 | g0150 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19240 | hp2 | a0021 | c0018 | t0078 | g0116 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0058 | AFR | ASW | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20805 | hp1 | a0001 | c0001 | t0033 | g0038 | EUR | TSI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0087 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02486 | hp2 | a0002 | c0009 | t0029 | g0053 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02559 | hp1 | a0009 | c0011 | t0001 | g0034 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0073 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03471 | hp1 | a0002 | c0007 | t0003 | g0079 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03471 | hp2 | a0002 | c0009 | t0029 | g0054 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20300 | hp1 | a0002 | c0009 | t0027 | g0103 | AFR | USA | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | USA | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA21309 | hp2 | a0024 | c0012 | t0003 | g0081 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0121 | REF | REF | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
homoSapiens_grch38 | hp1 | a0019 | c0015 | t0052 | g0090 | REF | REF | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60107708
|
G | A | 1 | a0005 | 8 | HG01496.hp2 HG02165.hp2 NA18612.hp1 others(5): Show |
missense_variant | MODERATE | c.70G>A | p.Val24Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 620/18069 | 70/3519 | 24/1172 | chr14 | 60107708 | ||
chr14:60107730
|
A | G | 2 | a0006a0025 | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
missense_variant | MODERATE | c.92A>G | p.Lys31Arg | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 642/18069 | 92/3519 | 31/1172 | chr14 | 60107730 | ||
chr14:60107789
|
C | A | 1 | a0024 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.151C>A | p.Pro51Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 701/18069 | 151/3519 | 51/1172 | chr14 | 60107789 | ||
chr14:60108087
|
C | T | 1 | a0023 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.449C>T | p.Ala150Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 999/18069 | 449/3519 | 150/1172 | chr14 | 60108087 | ||
chr14:60108279
|
T | C | 1 | a0022 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.641T>C | p.Met214Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 1191/18069 | 641/3519 | 214/1172 | chr14 | 60108279 | ||
chr14:60115091
|
A | C | 1 | a0010 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.987A>C | p.Leu329Phe | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1537/18069 | 987/3519 | 329/1172 | chr14 | 60115091 | ||
chr14:60115188
|
A | G | 1 | a0004 | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
missense_variant | MODERATE | c.1084A>G | p.Ile362Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1634/18069 | 1084/3519 | 362/1172 | chr14 | 60115188 | ||
chr14:60115335
|
G | A | 7 | a0001a0005a0009others(4): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
missense_variant | MODERATE | c.1231G>A | p.Val411Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1781/18069 | 1231/3519 | 411/1172 | chr14 | 60115335 | ||
chr14:60115743
|
T | A | 1 | a0025 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1382T>A | p.Phe461Tyr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 5/11 | 1932/18069 | 1382/3519 | 461/1172 | chr14 | 60115743 | ||
chr14:60116008
|
G | A | 1 | a0013 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1526G>A | p.Ser509Asn | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/11 | 2076/18069 | 1526/3519 | 509/1172 | chr14 | 60116008 | ||
chr14:60118413
|
A | G | 15 | a0002a0003a0004others(12): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
missense_variant | MODERATE | c.1663A>G | p.Lys555Glu | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2213/18069 | 1663/3519 | 555/1172 | chr14 | 60118413 | ||
chr14:60118564
|
G | A | 1 | a0009 | 2 | HG02559.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.1814G>A | p.Arg605Gln | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2364/18069 | 1814/3519 | 605/1172 | chr14 | 60118564 | ||
chr14:60118621
|
C | T | 1 | a0014 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1871C>T | p.Thr624Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2421/18069 | 1871/3519 | 624/1172 | chr14 | 60118621 | ||
chr14:60121226
|
G | T | 1 | a0012 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.1973G>T | p.Gly658Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/11 | 2523/18069 | 1973/3519 | 658/1172 | chr14 | 60121226 | ||
chr14:60124345
|
T | A | 1 | a0011 | 1 | NA18942.hp1 | stop_gained | HIGH | c.2174T>A | p.Leu725* | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2724/18069 | 2174/3519 | 725/1172 | chr14 | 60124345 | ||
chr14:60124446
|
G | A | 1 | a0018 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.2275G>A | p.Asp759Asn | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2825/18069 | 2275/3519 | 759/1172 | chr14 | 60124446 | ||
chr14:60124481
|
A | T | 3 | a0003a0015a0016 | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
missense_variant | MODERATE | c.2310A>T | p.Gln770His | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2860/18069 | 2310/3519 | 770/1172 | chr14 | 60124481 | ||
chr14:60124509
|
G | A | 1 | a0016 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.2338G>A | p.Glu780Lys | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2888/18069 | 2338/3519 | 780/1172 | chr14 | 60124509 | ||
chr14:60124746
|
T | C | 1 | a0011 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2575T>C | p.Ser859Pro | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3125/18069 | 2575/3519 | 859/1172 | chr14 | 60124746 | ||
chr14:60124899
|
G | A | 1 | a0024 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2728G>A | p.Val910Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3278/18069 | 2728/3519 | 910/1172 | chr14 | 60124899 | ||
chr14:60124983
|
T | C | 1 | a0008 | 4 | NA18944.hp1 NA19065.hp2 NA19066.hp2 others(1): Show |
missense_variant | MODERATE | c.2812T>C | p.Tyr938His | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3362/18069 | 2812/3519 | 938/1172 | chr14 | 60124983 | ||
chr14:60125088
|
C | T | 1 | a0017 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2917C>T | p.His973Tyr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3467/18069 | 2917/3519 | 973/1172 | chr14 | 60125088 | ||
chr14:60125169
|
G | A | 17 | a0002a0003a0004others(14): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
missense_variant | MODERATE | c.2998G>A | p.Gly1000Ser | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3548/18069 | 2998/3519 | 1000/1172 | chr14 | 60125169 | ||
chr14:60125235
|
G | A | 1 | a0021 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.3064G>A | p.Ala1022Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3614/18069 | 3064/3519 | 1022/1172 | chr14 | 60125235 | ||
chr14:60125677
|
C | CTAT | 1 | a0007 | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
disruptive_inframe_insertion | MODERATE | c.3121_3122insTAT | p.Pro1041delinsLeuSe others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/11 | 3672/18069 | 3122/3519 | 1041/1172 | chr14 | 60125677 | ||
chr14:60134160
|
C | T | 1 | a0015 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.3458C>T | p.Ala1153Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4008/18069 | 3458/3519 | 1153/1172 | chr14 | 60134160 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60107821
|
A | G | 24 | a0001c0001a0001c0021a0001c0023others(21): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
synonymous_variant | LOW | c.183A>G | p.Leu61Leu | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 733/18069 | 183/3519 | 61/1172 | chr14 | 60107821 | ||
chr14:60108148
|
A | G | 1 | a0001c0030 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.510A>G | p.Thr170Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 1060/18069 | 510/3519 | 170/1172 | chr14 | 60108148 | ||
chr14:60108157
|
T | C | 1 | a0021c0018 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.519T>C | p.Thr173Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 1069/18069 | 519/3519 | 173/1172 | chr14 | 60108157 | ||
chr14:60115145
|
G | A | 15 | a0001c0001a0001c0021a0001c0023others(12): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
synonymous_variant | LOW | c.1041G>A | p.Pro347Pro | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1591/18069 | 1041/3519 | 347/1172 | chr14 | 60115145 | ||
chr14:60115217
|
C | T | 23 | a0001c0001a0001c0021a0001c0023others(20): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
synonymous_variant | LOW | c.1113C>T | p.Ser371Ser | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1663/18069 | 1113/3519 | 371/1172 | chr14 | 60115217 | ||
chr14:60115391
|
G | C | 1 | a0002c0013 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1287G>C | p.Val429Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1837/18069 | 1287/3519 | 429/1172 | chr14 | 60115391 | ||
chr14:60118385
|
G | T | 1 | a0025c0032 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.1635G>T | p.Val545Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2185/18069 | 1635/3519 | 545/1172 | chr14 | 60118385 | ||
chr14:60118508
|
C | T | 1 | a0001c0023 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1758C>T | p.Leu586Leu | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2308/18069 | 1758/3519 | 586/1172 | chr14 | 60118508 | ||
chr14:60118610
|
G | A | 1 | a0002c0025 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1860G>A | p.Val620Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2410/18069 | 1860/3519 | 620/1172 | chr14 | 60118610 | ||
chr14:60124538
|
G | A | 1 | a0001c0021 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.2367G>A | p.Gly789Gly | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2917/18069 | 2367/3519 | 789/1172 | chr14 | 60124538 | ||
chr14:60125111
|
T | C | 18 | a0002c0002a0002c0007a0002c0009others(15): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
synonymous_variant | LOW | c.2940T>C | p.Phe980Phe | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3490/18069 | 2940/3519 | 980/1172 | chr14 | 60125111 | ||
chr14:60134014
|
C | A | 1 | a0021c0018 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.3312C>A | p.Ile1104Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3862/18069 | 3312/3519 | 1104/1172 | chr14 | 60134014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60091946
|
A | T | 3 | a0001c0001t0030a0002c0002t0080a0002c0002t0081 | 4 | HG01109.hp2 HG02738.hp2 HG03490.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-527A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15693 | chr14 | 60091946 | |||||
chr14:60091961
|
C | A | 2 | a0002c0002t0014a0002c0002t0031 | 4 | HG01192.hp2 HG01433.hp2 HG01981.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-512C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15678 | chr14 | 60091961 | |||||
chr14:60091966
|
T | C | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(36): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-507T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15673 | chr14 | 60091966 | |||||
chr14:60092011
|
G | T | 5 | a0001c0001t0010a0001c0001t0023a0001c0001t0048others(2): Show | 10 | HG00673.hp2 NA18940.hp2 NA18944.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-462G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15628 | chr14 | 60092011 | |||||
chr14:60092048
|
C | T | 1 | a0001c0001t0047 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-425C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15591 | chr14 | 60092048 | |||||
chr14:60092081
|
C | T | 1 | a0001c0001t0046 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-392C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15558 | chr14 | 60092081 | |||||
chr14:60092120
|
C | G | 1 | a0002c0025t0079 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-353C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15519 | chr14 | 60092120 | |||||
chr14:60092314
|
T | A | 2 | a0001c0001t0007a0011c0020t0007 | 8 | HG02074.hp2 NA18942.hp1 NA18945.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-159T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15325 | chr14 | 60092314 | |||||
chr14:60092315
|
C | T | 2 | a0001c0001t0007a0011c0020t0007 | 8 | HG02074.hp2 NA18942.hp1 NA18945.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | chr14 | 60092315 | ||||||
chr14:60092342
|
G | T | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(36): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-131G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15297 | chr14 | 60092342 | |||||
chr14:60092354
|
A | G | 39 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(36): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
5_prime_UTR_variant | MODIFIER | c.-119A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15285 | chr14 | 60092354 | |||||
chr14:60092362
|
T | A | 1 | a0001c0021t0032 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15277 | chr14 | 60092362 | |||||
chr14:60134490
|
T | C | 1 | a0006c0006t0051 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 269 | chr14 | 60134490 | |||||
chr14:60134501
|
C | T | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 280 | chr14 | 60134501 | |||||
chr14:60134590
|
G | A | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*369G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 369 | chr14 | 60134590 | |||||
chr14:60134618
|
T | C | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*397T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 397 | chr14 | 60134618 | |||||
chr14:60134793
|
T | C | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*572T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 572 | chr14 | 60134793 | |||||
chr14:60134828
|
T | C | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*607T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 607 | chr14 | 60134828 | |||||
chr14:60134900
|
A | G | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 679 | chr14 | 60134900 | |||||
chr14:60134986
|
A | C | 1 | a0001c0001t0044 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*765A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 765 | chr14 | 60134986 | |||||
chr14:60134987
|
C | A | 1 | a0015c0028t0055 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 766 | chr14 | 60134987 | |||||
chr14:60135079
|
C | A | 1 | a0002c0009t0056 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*858C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 858 | chr14 | 60135079 | |||||
chr14:60135087
|
G | A | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*866G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 866 | chr14 | 60135087 | |||||
chr14:60135272
|
T | C | 1 | a0001c0001t0017 | 2 | HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1051T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1051 | chr14 | 60135272 | |||||
chr14:60135300
|
C | T | 1 | a0002c0002t0077 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1079C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1079 | chr14 | 60135300 | |||||
chr14:60135338
|
G | A | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1117 | chr14 | 60135338 | |||||
chr14:60135381
|
C | CT | 5 | a0006c0006t0009a0006c0006t0051a0006c0006t0075others(2): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1167dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1168 | INFO_REALIGN_3_PRIME | chr14 | 60135381 | ||||
chr14:60135418
|
G | A | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1197 | chr14 | 60135418 | |||||
chr14:60135556
|
C | CT | 5 | a0001c0001t0042a0001c0001t0043a0003c0003t0074others(2): Show | 6 | HG04204.hp2 NA18940.hp1 NA19004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1347dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1348 | INFO_REALIGN_3_PRIME | chr14 | 60135556 | ||||
chr14:60135698
|
G | A | 4 | a0007c0008t0013a0007c0008t0026a0007c0008t0057others(1): Show | 8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1477G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1477 | chr14 | 60135698 | |||||
chr14:60135705
|
A | G | 3 | a0002c0009t0029a0002c0009t0073a0002c0025t0079 | 4 | HG02257.hp2 HG02486.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1484 | chr14 | 60135705 | |||||
chr14:60135771
|
C | T | 1 | a0012c0022t0041 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1550C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1550 | chr14 | 60135771 | |||||
chr14:60135796
|
C | T | 2 | a0010c0029t0058a0020c0024t0045 | 2 | HG01243.hp2 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1575C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1575 | chr14 | 60135796 | |||||
chr14:60135886
|
TGATA | T | 27 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(24): Show | 69 | HG00639.hp1 HG00673.hp1 HG01081.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1670_*1673delGATA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1670 | INFO_REALIGN_3_PRIME | chr14 | 60135886 | ||||
chr14:60135921
|
A | G | 1 | a0001c0001t0022 | 2 | HG00099.hp1 HG00280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1700A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1700 | chr14 | 60135921 | |||||
chr14:60136058
|
C | T | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1837C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1837 | chr14 | 60136058 | |||||
chr14:60136069
|
A | G | 1 | a0001c0001t0021 | 2 | HG01175.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1848A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1848 | chr14 | 60136069 | |||||
chr14:60136107
|
TA | T | 53 | a0001c0001t0040a0001c0001t0043a0002c0002t0003others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1899delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1899 | INFO_REALIGN_3_PRIME | chr14 | 60136107 | ||||
chr14:60136650
|
C | T | 1 | a0001c0001t0015 | 3 | NA18946.hp2 NA18980.hp2 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2429C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2429 | chr14 | 60136650 | |||||
chr14:60136668
|
C | T | 1 | a0006c0006t0076 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2447C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2447 | chr14 | 60136668 | |||||
chr14:60136686
|
TGA | T | 7 | a0001c0001t0006a0001c0001t0015a0001c0001t0044others(4): Show | 17 | HG01496.hp2 HG02155.hp2 HG02165.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2469_*2470delAG | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2469 | INFO_REALIGN_3_PRIME | chr14 | 60136686 | ||||
chr14:60136694
|
G | C | 2 | a0001c0001t0011a0001c0001t0047 | 5 | HG01192.hp1 HG01928.hp2 HG01934.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2473 | chr14 | 60136694 | |||||
chr14:60136746
|
G | T | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2525G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2525 | chr14 | 60136746 | |||||
chr14:60136787
|
T | C | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2566T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2566 | chr14 | 60136787 | |||||
chr14:60136913
|
T | A | 1 | a0001c0001t0018 | 2 | NA18975.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2692T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2692 | chr14 | 60136913 | |||||
chr14:60136941
|
G | A | 1 | a0001c0001t0033 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2720 | chr14 | 60136941 | |||||
chr14:60137046
|
T | C | 1 | a0001c0001t0034 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2825T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2825 | chr14 | 60137046 | |||||
chr14:60137086
|
A | G | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2865A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2865 | chr14 | 60137086 | |||||
chr14:60137165
|
G | C | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2944G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2944 | chr14 | 60137165 | |||||
chr14:60137315
|
G | A | 2 | a0002c0009t0027a0002c0009t0056 | 3 | HG02922.hp1 HG03139.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3094G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3094 | chr14 | 60137315 | |||||
chr14:60137353
|
C | G | 1 | a0003c0003t0062 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3132C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3132 | chr14 | 60137353 | |||||
chr14:60137579
|
A | G | 93 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(90): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
3_prime_UTR_variant | MODIFIER | c.*3358A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3358 | chr14 | 60137579 | |||||
chr14:60137899
|
C | G | 1 | a0018c0026t0072 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3678C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3678 | chr14 | 60137899 | |||||
chr14:60137931
|
T | TA | 3 | a0007c0008t0013a0007c0008t0026a0007c0008t0057 | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3721dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3722 | INFO_REALIGN_3_PRIME | chr14 | 60137931 | ||||
chr14:60137952
|
G | A | 1 | a0007c0008t0026 | 2 | HG02735.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3731 | chr14 | 60137952 | |||||
chr14:60138050
|
C | T | 1 | a0002c0009t0056 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3829C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3829 | chr14 | 60138050 | |||||
chr14:60138069
|
C | T | 3 | a0007c0008t0013a0007c0008t0026a0007c0008t0057 | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3848C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3848 | chr14 | 60138069 | |||||
chr14:60138078
|
G | A | 5 | a0006c0006t0009a0006c0006t0051a0006c0006t0075others(2): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3857G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3857 | chr14 | 60138078 | |||||
chr14:60138126
|
G | A | 1 | a0002c0002t0016 | 3 | HG03195.hp2 HG03486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3905G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3905 | chr14 | 60138126 | |||||
chr14:60138245
|
A | G | 1 | a0002c0002t0028 | 2 | HG03669.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4024A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4024 | chr14 | 60138245 | |||||
chr14:60138446
|
A | T | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4225A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4225 | chr14 | 60138446 | |||||
chr14:60138453
|
G | A | 1 | a0002c0007t0063 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4232G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4232 | chr14 | 60138453 | |||||
chr14:60138998
|
TAAAAC | T | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*4780_*4784delAACA others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4780 | INFO_REALIGN_3_PRIME | chr14 | 60138998 | ||||
chr14:60139070
|
A | G | 25 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(22): Show | 66 | HG00639.hp1 HG00673.hp1 HG01081.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4849A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4849 | chr14 | 60139070 | |||||
chr14:60139123
|
T | C | 1 | a0002c0002t0080 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4902T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4902 | chr14 | 60139123 | |||||
chr14:60139184
|
AAAAG | A | 4 | a0002c0002t0064a0007c0008t0013a0007c0008t0026others(1): Show | 8 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4971_*4974delGAAA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4971 | INFO_REALIGN_3_PRIME | chr14 | 60139184 | ||||
chr14:60139208
|
C | G | 1 | a0018c0026t0072 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4987C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4987 | chr14 | 60139208 | |||||
chr14:60139225
|
T | C | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*5004T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5004 | chr14 | 60139225 | |||||
chr14:60139320
|
G | C | 7 | a0003c0003t0002a0003c0003t0059a0003c0003t0060others(4): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5099G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5099 | chr14 | 60139320 | |||||
chr14:60139370
|
C | T | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*5149C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5149 | chr14 | 60139370 | |||||
chr14:60139378
|
GAC | G | 5 | a0006c0006t0009a0006c0006t0051a0006c0006t0075others(2): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5159_*5160delCA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5159 | INFO_REALIGN_3_PRIME | chr14 | 60139378 | ||||
chr14:60139809
|
T | C | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*5588T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5588 | chr14 | 60139809 | |||||
chr14:60139914
|
C | T | 1 | a0002c0002t0031 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5693C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5693 | chr14 | 60139914 | |||||
chr14:60139952
|
T | TA | 50 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(47): Show | 155 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*5741dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5742 | INFO_REALIGN_3_PRIME | chr14 | 60139952 | ||||
chr14:60139999
|
A | G | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5778A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5778 | chr14 | 60139999 | |||||
chr14:60140098
|
G | A | 47 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(44): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*5877G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5877 | chr14 | 60140098 | |||||
chr14:60140119
|
A | G | 1 | a0002c0002t0071 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5898A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5898 | chr14 | 60140119 | |||||
chr14:60140248
|
A | C | 1 | a0010c0029t0058 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6027A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6027 | chr14 | 60140248 | |||||
chr14:60140308
|
G | C | 2 | a0007c0008t0013a0007c0008t0057 | 5 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6087G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6087 | chr14 | 60140308 | |||||
chr14:60140341
|
G | A | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*6120G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6120 | chr14 | 60140341 | |||||
chr14:60140350
|
A | C | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6129A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6129 | chr14 | 60140350 | |||||
chr14:60140521
|
T | C | 13 | a0002c0002t0005a0002c0002t0028a0002c0002t0064others(10): Show | 24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6300T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6300 | chr14 | 60140521 | |||||
chr14:60140601
|
T | TAC | 37 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(34): Show | 87 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6397_*6398dupAC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6399 | INFO_REALIGN_3_PRIME | chr14 | 60140601 | ||||
chr14:60140601
|
T | TACAC | 10 | a0002c0009t0029a0002c0009t0073a0002c0025t0079others(7): Show | 46 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*6395_*6398dupACAC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6399 | INFO_REALIGN_3_PRIME | chr14 | 60140601 | ||||
chr14:60140601
|
T | TACACAC | 4 | a0004c0004t0004a0004c0004t0025a0004c0004t0053others(1): Show | 22 | NA18940.hp1 NA18941.hp1 NA18945.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*6393_*6398dupACAC others(2): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6399 | INFO_REALIGN_3_PRIME | chr14 | 60140601 | ||||
chr14:60140696
|
C | G | 6 | a0002c0009t0029a0002c0009t0073a0007c0008t0013others(3): Show | 11 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6475C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6475 | chr14 | 60140696 | |||||
chr14:60140814
|
C | T | 1 | a0004c0004t0053 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6593C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6593 | chr14 | 60140814 | |||||
chr14:60140858
|
A | G | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6637A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6637 | chr14 | 60140858 | |||||
chr14:60140899
|
A | C | 5 | a0006c0006t0009a0006c0006t0051a0006c0006t0075others(2): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6678A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6678 | chr14 | 60140899 | |||||
chr14:60140947
|
GA | G | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6729delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6729 | INFO_REALIGN_3_PRIME | chr14 | 60140947 | ||||
chr14:60141047
|
A | G | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*6826A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6826 | chr14 | 60141047 | |||||
chr14:60141165
|
G | T | 1 | a0002c0025t0079 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6944G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6944 | chr14 | 60141165 | |||||
chr14:60141267
|
A | G | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*7046A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7046 | chr14 | 60141267 | |||||
chr14:60141356
|
A | G | 1 | a0022c0019t0050 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7135A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7135 | chr14 | 60141356 | |||||
chr14:60141359
|
ACAAT | A | 4 | a0007c0008t0013a0007c0008t0026a0007c0008t0057others(1): Show | 8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7142_*7145delTCAA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7142 | INFO_REALIGN_3_PRIME | chr14 | 60141359 | ||||
chr14:60141361
|
A | G | 1 | a0004c0004t0054 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7140A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7140 | chr14 | 60141361 | |||||
chr14:60141364
|
C | G | 1 | a0003c0003t0060 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7143C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7143 | chr14 | 60141364 | |||||
chr14:60141367
|
G | T | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7146G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7146 | chr14 | 60141367 | |||||
chr14:60141622
|
T | A | 2 | a0001c0001t0023a0001c0001t0048 | 3 | NA18961.hp2 NA18999.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7401T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7401 | chr14 | 60141622 | |||||
chr14:60141635
|
TAAAAG | T | 47 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(44): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*7418_*7422delAGAA others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7418 | INFO_REALIGN_3_PRIME | chr14 | 60141635 | ||||
chr14:60141739
|
G | T | 49 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(46): Show | 135 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*7518G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7518 | chr14 | 60141739 | |||||
chr14:60142006
|
A | C | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7785A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7785 | chr14 | 60142006 | |||||
chr14:60142089
|
G | A | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7868G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7868 | chr14 | 60142089 | |||||
chr14:60142369
|
G | C | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8148G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8148 | chr14 | 60142369 | |||||
chr14:60142478
|
T | TA | 52 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(49): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*8261dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8262 | INFO_REALIGN_3_PRIME | chr14 | 60142478 | ||||
chr14:60142528
|
A | T | 1 | a0001c0001t0043 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8307A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8307 | chr14 | 60142528 | |||||
chr14:60142590
|
G | A | 1 | a0023c0031t0035 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8369G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8369 | chr14 | 60142590 | |||||
chr14:60142681
|
T | C | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8460T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8460 | chr14 | 60142681 | |||||
chr14:60142969
|
G | A | 51 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(48): Show | 156 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*8748G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8748 | chr14 | 60142969 | |||||
chr14:60142985
|
G | A | 1 | a0001c0001t0019 | 2 | HG02976.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8764G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8764 | chr14 | 60142985 | |||||
chr14:60142989
|
A | G | 1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8768A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8768 | chr14 | 60142989 | |||||
chr14:60143000
|
C | G | 1 | a0006c0006t0051 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8779C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8779 | chr14 | 60143000 | |||||
chr14:60143046
|
T | C | 42 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(39): Show | 124 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*8825T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8825 | chr14 | 60143046 | |||||
chr14:60143276
|
G | C | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*9055G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9055 | chr14 | 60143276 | |||||
chr14:60143404
|
C | T | 1 | a0001c0001t0030 | 2 | HG03490.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9183C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9183 | chr14 | 60143404 | |||||
chr14:60143449
|
C | T | 2 | a0001c0001t0049a0022c0019t0050 | 2 | HG00673.hp2 NA18940.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9228C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9228 | chr14 | 60143449 | |||||
chr14:60143496
|
C | CTAATTAG others(82): Show |
1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9277_*9365dupAATT others(85): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9366 | INFO_REALIGN_3_PRIME | chr14 | 60143496 | ||||
chr14:60143598
|
C | T | 47 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(44): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*9377C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9377 | chr14 | 60143598 | |||||
chr14:60143679
|
G | A | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9458G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9458 | chr14 | 60143679 | |||||
chr14:60143760
|
T | C | 1 | a0002c0002t0069 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9539T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9539 | chr14 | 60143760 | |||||
chr14:60143825
|
A | G | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9604A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9604 | chr14 | 60143825 | |||||
chr14:60143839
|
C | T | 1 | a0002c0002t0070 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9618C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9618 | chr14 | 60143839 | |||||
chr14:60143881
|
T | C | 1 | a0010c0029t0058 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9660T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9660 | chr14 | 60143881 | |||||
chr14:60144087
|
A | G | 1 | a0009c0011t0037 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9866A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9866 | chr14 | 60144087 | |||||
chr14:60144383
|
C | T | 1 | a0002c0002t0067 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10162C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10162 | chr14 | 60144383 | |||||
chr14:60144399
|
G | C | 1 | a0002c0002t0067 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10178G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10178 | chr14 | 60144399 | |||||
chr14:60144476
|
C | T | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10255C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10255 | chr14 | 60144476 | |||||
chr14:60144675
|
G | A | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10454G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10454 | chr14 | 60144675 | |||||
chr14:60144810
|
T | C | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10589T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10589 | chr14 | 60144810 | |||||
chr14:60144867
|
T | C | 47 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(44): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*10646T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10646 | chr14 | 60144867 | |||||
chr14:60144930
|
C | T | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10709C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10709 | chr14 | 60144930 | |||||
chr14:60144957
|
G | A | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10736G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10736 | chr14 | 60144957 | |||||
chr14:60145029
|
A | C | 1 | a0010c0029t0058 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10808A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10808 | chr14 | 60145029 | |||||
chr14:60145075
|
T | C | 1 | a0001c0001t0048 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10854T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10854 | chr14 | 60145075 | |||||
chr14:60145120
|
T | C | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*10899T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10899 | chr14 | 60145120 | |||||
chr14:60145184
|
C | T | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10963C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10963 | chr14 | 60145184 | |||||
chr14:60145312
|
A | G | 1 | a0020c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11091A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11091 | chr14 | 60145312 | |||||
chr14:60145401
|
A | G | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11180A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11180 | chr14 | 60145401 | |||||
chr14:60145683
|
T | C | 1 | a0003c0003t0059 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11462T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11462 | chr14 | 60145683 | |||||
chr14:60145689
|
GA | G | 3 | a0007c0008t0013a0007c0008t0026a0007c0008t0057 | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11477delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11477 | INFO_REALIGN_3_PRIME | chr14 | 60145689 | ||||
chr14:60145697
|
A | C | 3 | a0007c0008t0013a0007c0008t0026a0007c0008t0057 | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11476A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11476 | chr14 | 60145697 | |||||
chr14:60145744
|
A | G | 1 | a0021c0018t0078 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11523A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11523 | chr14 | 60145744 | |||||
chr14:60145969
|
G | A | 6 | a0002c0009t0029a0002c0009t0073a0007c0008t0013others(3): Show | 11 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*11748G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11748 | chr14 | 60145969 | |||||
chr14:60145996
|
C | T | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11775C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11775 | chr14 | 60145996 | |||||
chr14:60146048
|
G | A | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11827G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11827 | chr14 | 60146048 | |||||
chr14:60146132
|
T | TATC | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11913_*11914insCA others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11914 | INFO_REALIGN_3_PRIME | chr14 | 60146132 | ||||
chr14:60146245
|
C | T | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*12024C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12024 | chr14 | 60146245 | |||||
chr14:60146605
|
T | C | 1 | a0001c0001t0036 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12384T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12384 | chr14 | 60146605 | |||||
chr14:60146683
|
G | GTC | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*12463_*12464insCT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12464 | INFO_REALIGN_3_PRIME | chr14 | 60146683 | ||||
chr14:60146687
|
G | A | 6 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(3): Show | 25 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*12466G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12466 | chr14 | 60146687 | |||||
chr14:60146687
|
G | GTA | 45 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(42): Show | 131 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*12467_*12468insAT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12468 | INFO_REALIGN_3_PRIME | chr14 | 60146687 | ||||
chr14:60146689
|
G | A | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*12468G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12468 | chr14 | 60146689 | |||||
chr14:60146846
|
C | A | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*12625C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12625 | chr14 | 60146846 | |||||
chr14:60147134
|
G | A | 5 | a0006c0006t0009a0006c0006t0051a0006c0006t0075others(2): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*12913G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12913 | chr14 | 60147134 | |||||
chr14:60147173
|
G | C | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*12952G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12952 | chr14 | 60147173 | |||||
chr14:60147222
|
G | A | 1 | a0002c0009t0073 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13001G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13001 | chr14 | 60147222 | |||||
chr14:60147279
|
T | G | 8 | a0002c0007t0061a0002c0009t0029a0002c0009t0073others(5): Show | 13 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*13058T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13058 | chr14 | 60147279 | |||||
chr14:60147293
|
T | C | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*13072T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13072 | chr14 | 60147293 | |||||
chr14:60147320
|
C | A | 54 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(51): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*13099C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13099 | chr14 | 60147320 | |||||
chr14:60147320
|
C | T | 2 | a0001c0001t0020a0001c0001t0034 | 3 | NA18986.hp2 NA19009.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13099C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13099 | chr14 | 60147320 | |||||
chr14:60147401
|
A | C | 13 | a0002c0002t0005a0002c0002t0028a0002c0002t0064others(10): Show | 24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*13180A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13180 | chr14 | 60147401 | |||||
chr14:60147458
|
G | C | 53 | a0002c0002t0003a0002c0002t0005a0002c0002t0014others(50): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*13237G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13237 | chr14 | 60147458 | |||||
chr14:60147596
|
A | G | 1 | a0013c0014t0065 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13375A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13375 | chr14 | 60147596 | |||||
chr14:60148028
|
T | A | 5 | a0004c0004t0004a0004c0004t0024a0004c0004t0025others(2): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*13807T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13807 | chr14 | 60148028 | |||||
chr14:60148169
|
T | C | 1 | a0005c0005t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13948T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13948 | chr14 | 60148169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60092494
|
T | G | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+75T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092494 | ||||||
chr14:60092511
|
A | G | 4 | a0001c0001t0007g0040a0001c0001t0007g0041a0001c0001t0007g0187others(1): Show | 5 | HG02074.hp2 NA18942.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+92A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092511 | ||||||
chr14:60092521
|
G | T | 11 | a0001c0001t0012g0186a0002c0002t0003g0013a0002c0002t0003g0021others(8): Show | 15 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-54+102G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092521 | ||||||
chr14:60092769
|
C | T | 1 | a0018c0026t0072g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+350C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092769 | ||||||
chr14:60092855
|
C | A | 3 | a0002c0009t0029g0053a0002c0009t0029g0054a0002c0025t0079g0055 | 3 | HG02257.hp2 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+436C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092855 | ||||||
chr14:60092943
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-54+524C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092943 | ||||||
chr14:60092966
|
G | A | 1 | a0002c0009t0056g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+547G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092966 | ||||||
chr14:60093114
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+695T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093114 | ||||||
chr14:60093238
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-54+819C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093238 | ||||||
chr14:60093272
|
C | A | 7 | a0002c0002t0003g0024a0002c0002t0003g0058a0002c0002t0003g0059others(4): Show | 7 | HG01243.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54+853C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093272 | ||||||
chr14:60093445
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-54+1026G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093445 | ||||||
chr14:60093465
|
C | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+1046C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093465 | ||||||
chr14:60093854
|
T | G | 2 | a0018c0026t0072g0180a0021c0018t0078g0116 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-54+1435T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093854 | ||||||
chr14:60093889
|
A | G | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.-54+1470A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093889 | ||||||
chr14:60094064
|
A | C | 1 | a0003c0003t0002g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-54+1645A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094064 | ||||||
chr14:60094151
|
T | A | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+1732T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094151 | ||||||
chr14:60094318
|
T | TC | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+1904dupC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094318 | |||||
chr14:60094428
|
C | A | 1 | a0002c0002t0003g0062 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-54+2009C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094428 | ||||||
chr14:60094447
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-54+2028T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094447 | ||||||
chr14:60094611
|
C | G | 1 | a0002c0002t0005g0029 | 2 | NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-54+2192C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094611 | ||||||
chr14:60094624
|
C | T | 4 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(1): Show | 5 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+2205C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094624 | ||||||
chr14:60094657
|
G | GCC | 7 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(4): Show | 8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54+2240_-54+2241d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094657 | |||||
chr14:60094761
|
G | GC | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(74): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-54+2351dupC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | |||||
chr14:60094761
|
G | GCC | 39 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0037others(36): Show | 50 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-54+2350_-54+2351d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | |||||
chr14:60094761
|
G | GCCC | 13 | a0001c0001t0001g0012a0001c0001t0001g0038a0001c0001t0001g0170others(10): Show | 14 | HG00673.hp2 HG02071.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.-54+2349_-54+2351d others(5): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | |||||
chr14:60094761
|
GC | G | 24 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(21): Show | 41 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.-54+2351delC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | |||||
chr14:60094770
|
C | A | 1 | a0005c0005t0006g0119 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-54+2351C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094770 | ||||||
chr14:60094771
|
A | C | 2 | a0001c0001t0001g0178a0014c0017t0003g0185 | 2 | HG01884.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-54+2352A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094771 | ||||||
chr14:60094805
|
A | T | 1 | a0003c0003t0002g0105 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-54+2386A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094805 | ||||||
chr14:60094912
|
T | C | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+2493T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094912 | ||||||
chr14:60094943
|
T | C | 25 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(22): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.-54+2524T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094943 | ||||||
chr14:60095162
|
G | A | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+2743G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095162 | ||||||
chr14:60095256
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+2837A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095256 | ||||||
chr14:60095342
|
A | G | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+2923A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095342 | ||||||
chr14:60095372
|
G | A | 1 | a0002c0009t0027g0076 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-54+2953G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095372 | ||||||
chr14:60095411
|
G | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-54+2992G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095411 | ||||||
chr14:60095455
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+3036T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095455 | ||||||
chr14:60095463
|
G | A | 8 | a0003c0003t0002g0004a0003c0003t0002g0008a0003c0003t0002g0063others(5): Show | 17 | HG00558.hp2 NA18942.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.-54+3044G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095463 | ||||||
chr14:60095509
|
G | T | 11 | a0002c0009t0029g0053a0002c0009t0029g0054a0002c0009t0073g0104others(8): Show | 12 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54+3090G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095509 | ||||||
chr14:60095600
|
C | T | 1 | a0004c0004t0004g0051 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-54+3181C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095600 | ||||||
chr14:60095655
|
C | T | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+3236C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095655 | ||||||
chr14:60095694
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-54+3275G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095694 | ||||||
chr14:60095882
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-54+3463C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095882 | ||||||
chr14:60095996
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0123 | 4 | HG00280.hp1 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+3577G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095996 | ||||||
chr14:60096076
|
T | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+3657T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096076 | ||||||
chr14:60096147
|
A | ATCTGGGT others(2): Show |
109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+3731_-54+3739d others(11): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60096147 | |||||
chr14:60096151
|
G | A | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+3732G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096151 | ||||||
chr14:60096236
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-54+3817G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096236 | ||||||
chr14:60096254
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+3835C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096254 | ||||||
chr14:60096317
|
G | C | 1 | a0002c0013t0003g0057 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-54+3898G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096317 | ||||||
chr14:60096361
|
G | A | 2 | a0004c0004t0004g0022a0004c0004t0004g0042 | 3 | NA18975.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-54+3942G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096361 | ||||||
chr14:60096423
|
A | G | 2 | a0002c0009t0027g0076a0002c0009t0027g0103 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-54+4004A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096423 | ||||||
chr14:60096521
|
C | T | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+4102C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096521 | ||||||
chr14:60096585
|
A | G | 1 | a0010c0029t0058g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-54+4166A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096585 | ||||||
chr14:60096766
|
T | A | 1 | a0002c0007t0003g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-54+4347T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096766 | ||||||
chr14:60096947
|
G | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54+4528G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096947 | ||||||
chr14:60097050
|
T | TTTAAA | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+4634_-54+4638d others(7): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60097050 | |||||
chr14:60097275
|
A | G | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+4856A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097275 | ||||||
chr14:60097284
|
A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0122a0001c0001t0001g0123 | 4 | HG00280.hp1 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+4865A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097284 | ||||||
chr14:60097350
|
G | A | 1 | a0001c0001t0008g0148 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-54+4931G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097350 | ||||||
chr14:60097392
|
A | G | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+4973A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097392 | ||||||
chr14:60097648
|
T | TA | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+5232dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60097648 | |||||
chr14:60097669
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-54+5250G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097669 | ||||||
chr14:60097768
|
A | G | 1 | a0001c0021t0032g0168 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-54+5349A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097768 | ||||||
chr14:60097837
|
A | T | 1 | a0004c0004t0004g0050 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-54+5418A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097837 | ||||||
chr14:60097843
|
A | G | 1 | a0003c0003t0002g0026 | 2 | HG02015.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-54+5424A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097843 | ||||||
chr14:60097855
|
C | G | 2 | a0002c0002t0028g0101a0002c0002t0028g0102 | 2 | HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-54+5436C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097855 | ||||||
chr14:60097933
|
C | A | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+5514C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097933 | ||||||
chr14:60097946
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+5527G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097946 | ||||||
chr14:60098006
|
C | T | 1 | a0004c0004t0024g0049 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-54+5587C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098006 | ||||||
chr14:60098010
|
G | A | 5 | a0002c0007t0003g0027a0002c0007t0003g0077a0002c0007t0003g0079others(2): Show | 6 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+5591G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098010 | ||||||
chr14:60098074
|
A | G | 20 | a0002c0002t0005g0007a0002c0002t0005g0015a0002c0002t0005g0029others(17): Show | 24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+5655A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098074 | ||||||
chr14:60098090
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+5671T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098090 | ||||||
chr14:60098109
|
A | C | 1 | a0002c0002t0031g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-54+5690A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098109 | ||||||
chr14:60098162
|
C | T | 1 | a0003c0003t0002g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-54+5743C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098162 | ||||||
chr14:60098312
|
C | A | 1 | a0001c0001t0001g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-54+5893C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098312 | ||||||
chr14:60098395
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-54+5976T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098395 | ||||||
chr14:60098525
|
C | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+6106C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098525 | ||||||
chr14:60098559
|
G | C | 3 | a0002c0009t0029g0053a0002c0009t0029g0054a0002c0009t0073g0104 | 3 | HG02486.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+6140G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098559 | ||||||
chr14:60098648
|
A | G | 1 | a0010c0029t0058g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-54+6229A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098648 | ||||||
chr14:60098768
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+6349T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098768 | ||||||
chr14:60098843
|
C | G | 2 | a0001c0001t0001g0167a0001c0001t0015g0166 | 2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-54+6424C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098843 | ||||||
chr14:60098856
|
T | C | 1 | a0001c0001t0017g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-54+6437T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098856 | ||||||
chr14:60099009
|
T | C | 3 | a0002c0009t0027g0076a0002c0009t0027g0103a0002c0009t0056g0056 | 3 | HG02922.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-54+6590T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099009 | ||||||
chr14:60099023
|
G | A | 3 | a0002c0007t0003g0027a0002c0007t0003g0079a0002c0007t0063g0078 | 4 | HG01884.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+6604G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099023 | ||||||
chr14:60099094
|
C | G | 3 | a0002c0009t0029g0053a0002c0009t0029g0054a0002c0009t0073g0104 | 3 | HG02486.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+6675C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099094 | ||||||
chr14:60099251
|
A | G | 3 | a0002c0009t0029g0053a0002c0009t0029g0054a0002c0009t0073g0104 | 3 | HG02486.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+6832A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099251 | ||||||
chr14:60099415
|
T | G | 3 | a0004c0004t0004g0043a0004c0004t0004g0050a0004c0004t0004g0051 | 3 | NA18964.hp1 NA19081.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-54+6996T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099415 | ||||||
chr14:60099795
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-54+7376G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099795 | ||||||
chr14:60099897
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-54+7478C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099897 | ||||||
chr14:60099947
|
C | T | 2 | a0001c0001t0022g0146a0001c0001t0022g0165 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.-54+7528C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099947 | ||||||
chr14:60099949
|
C | T | 1 | a0002c0002t0003g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-54+7530C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099949 | ||||||
chr14:60100143
|
A | G | 5 | a0002c0007t0061g0061a0002c0009t0029g0053a0002c0009t0029g0054others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-7443A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60100143 | ||||||
chr14:60100258
|
A | G | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53-7328A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60100258 | ||||||
chr14:60100371
|
T | A | 1 | a0024c0012t0003g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-53-7215T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60100371 | ||||||
chr14:60101083
|
T | C | 1 | a0004c0004t0004g0044 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-53-6503T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101083 | ||||||
chr14:60101140
|
T | A | 1 | a0001c0001t0015g0166 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-53-6446T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101140 | ||||||
chr14:60101168
|
T | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-6418T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101168 | ||||||
chr14:60101226
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-53-6360G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101226 | ||||||
chr14:60101412
|
CAGATT | C | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-6172_-53-6168d others(7): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60101412 | |||||
chr14:60101421
|
G | C | 1 | a0018c0026t0072g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53-6165G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101421 | ||||||
chr14:60101697
|
T | TA | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-53-5881dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60101697 | |||||
chr14:60101710
|
T | A | 1 | a0003c0003t0002g0105 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-53-5876T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101710 | ||||||
chr14:60101711
|
A | T | 1 | a0003c0003t0002g0105 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-53-5875A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101711 | ||||||
chr14:60101828
|
T | C | 26 | a0002c0025t0079g0055a0003c0003t0002g0004a0003c0003t0002g0006others(23): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(40): Show |
intron_variant | MODIFIER | c.-53-5758T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101828 | ||||||
chr14:60102329
|
T | TTAAAAA | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-53-5256_-53-5255i others(8): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60102329 | |||||
chr14:60102446
|
A | G | 1 | a0002c0007t0061g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-53-5140A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102446 | ||||||
chr14:60102557
|
C | A | 1 | a0018c0026t0072g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53-5029C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102557 | ||||||
chr14:60102661
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-53-4925T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102661 | ||||||
chr14:60102773
|
G | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-53-4813G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102773 | ||||||
chr14:60102796
|
T | A | 1 | a0003c0003t0002g0105 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-53-4790T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102796 | ||||||
chr14:60102842
|
T | C | 3 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0171 | 3 | NA18968.hp2 NA19080.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-53-4744T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102842 | ||||||
chr14:60102914
|
AT | A | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-4668delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60102914 | |||||
chr14:60102940
|
A | G | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-4646A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102940 | ||||||
chr14:60103088
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0006g0172 | 2 | NA18994.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-53-4498G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103088 | ||||||
chr14:60103276
|
A | G | 1 | a0003c0003t0002g0063 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-53-4310A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103276 | ||||||
chr14:60103330
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-53-4256C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103330 | ||||||
chr14:60103357
|
T | G | 30 | a0002c0007t0061g0061a0002c0009t0029g0053a0002c0009t0029g0054others(27): Show | 47 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.-53-4229T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103357 | ||||||
chr14:60103395
|
T | C | 1 | a0001c0001t0046g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-53-4191T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103395 | ||||||
chr14:60103446
|
G | A | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-4140G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103446 | ||||||
chr14:60103509
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-53-4077C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103509 | ||||||
chr14:60103816
|
G | A | 25 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(22): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.-53-3770G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103816 | ||||||
chr14:60103858
|
T | C | 1 | a0001c0001t0046g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-53-3728T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103858 | ||||||
chr14:60103925
|
G | A | 2 | a0002c0009t0027g0076a0002c0009t0027g0103 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-53-3661G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103925 | ||||||
chr14:60104012
|
C | A | 5 | a0002c0002t0003g0083a0002c0002t0003g0086a0002c0002t0016g0082others(2): Show | 5 | HG01109.hp1 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-3574C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104012 | ||||||
chr14:60104092
|
G | A | 1 | a0003c0003t0002g0065 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-53-3494G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104092 | ||||||
chr14:60104154
|
A | G | 1 | a0001c0030t0006g0177 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-53-3432A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104154 | ||||||
chr14:60104203
|
C | A | 1 | a0001c0001t0001g0032 | 2 | NA18984.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-53-3383C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104203 | ||||||
chr14:60104228
|
A | T | 1 | a0006c0006t0075g0108 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-53-3358A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104228 | ||||||
chr14:60104250
|
C | T | 1 | a0002c0002t0067g0100 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-53-3336C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104250 | ||||||
chr14:60104318
|
C | CA | 17 | a0002c0002t0003g0060a0002c0002t0003g0087a0002c0002t0005g0015others(14): Show | 22 | HG02071.hp1 HG02080.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.-53-3239dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | |||||
chr14:60104318
|
C | CAA | 7 | a0002c0002t0003g0024a0002c0002t0003g0058a0002c0002t0003g0059others(4): Show | 7 | HG01243.hp1 HG02074.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53-3240_-53-3239d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | |||||
chr14:60104318
|
CA | C | 34 | a0002c0002t0003g0021a0002c0002t0003g0039a0002c0002t0003g0083others(31): Show | 44 | HG01081.hp2 HG01109.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.-53-3239delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | |||||
chr14:60104318
|
CAAAAAAA others(4): Show |
C | 8 | a0002c0009t0027g0076a0002c0009t0027g0103a0006c0006t0009g0017others(5): Show | 11 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.-53-3249_-53-3239d others(13): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | |||||
chr14:60104318
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0023g0035a0001c0001t0023g0173a0001c0001t0048g0035 | 3 | NA18961.hp2 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-53-3253_-53-3239d others(17): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | |||||
chr14:60104318
|
CAAAAAAA others(9): Show |
C | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-53-3254_-53-3239d others(18): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | |||||
chr14:60104366
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-3220C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104366 | ||||||
chr14:60104511
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-53-3075T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104511 | ||||||
chr14:60104752
|
G | T | 1 | a0001c0001t0021g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-53-2834G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104752 | ||||||
chr14:60104772
|
A | C | 1 | a0002c0002t0071g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-53-2814A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104772 | ||||||
chr14:60104776
|
T | A | 4 | a0002c0002t0003g0083a0002c0002t0016g0082a0002c0002t0016g0084others(1): Show | 4 | HG01109.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-2810T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104776 | ||||||
chr14:60104939
|
T | A | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-2647T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104939 | ||||||
chr14:60105301
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-2285A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105301 | ||||||
chr14:60105320
|
G | C | 1 | a0002c0007t0063g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-53-2266G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105320 | ||||||
chr14:60105409
|
AT | A | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-2174delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60105409 | |||||
chr14:60105455
|
T | C | 7 | a0005c0005t0001g0154a0005c0005t0006g0036a0005c0005t0006g0119others(4): Show | 8 | HG01496.hp2 HG02165.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-2131T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105455 | ||||||
chr14:60105514
|
C | CTA | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-2063_-53-2062d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60105514 | |||||
chr14:60105539
|
T | C | 1 | a0004c0004t0004g0046 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-53-2047T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105539 | ||||||
chr14:60105642
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-53-1944T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105642 | ||||||
chr14:60105753
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-53-1833T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105753 | ||||||
chr14:60106019
|
A | T | 1 | a0005c0005t0039g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-53-1567A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106019 | ||||||
chr14:60106058
|
G | T | 1 | a0002c0009t0029g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-53-1528G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106058 | ||||||
chr14:60106065
|
A | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-53-1521A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106065 | ||||||
chr14:60106105
|
T | G | 6 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(3): Show | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-1481T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106105 | ||||||
chr14:60106168
|
A | G | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-1418A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106168 | ||||||
chr14:60106205
|
C | T | 1 | a0002c0007t0063g0078 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-53-1381C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106205 | ||||||
chr14:60106275
|
G | A | 25 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(22): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.-53-1311G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106275 | ||||||
chr14:60106282
|
C | G | 1 | a0001c0001t0008g0144 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-53-1304C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106282 | ||||||
chr14:60106403
|
T | A | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-1183T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106403 | ||||||
chr14:60106472
|
A | G | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-1114A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106472 | ||||||
chr14:60106494
|
G | A | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-1092G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106494 | ||||||
chr14:60106591
|
G | A | 1 | a0002c0002t0080g0093 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-53-995G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106591 | ||||||
chr14:60106767
|
TTTAA | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53-816_-53-813del others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60106767 | |||||
chr14:60106945
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-53-641A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106945 | ||||||
chr14:60107084
|
A | T | 1 | a0001c0001t0001g0143 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-53-502A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107084 | ||||||
chr14:60107249
|
C | T | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53-337C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107249 | ||||||
chr14:60107288
|
G | A | 1 | a0002c0025t0079g0055 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-53-298G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107288 | ||||||
chr14:60107520
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53-66G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107520 | ||||||
chr14:60108431
|
A | G | 1 | a0007c0008t0013g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.689+104A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108431 | ||||||
chr14:60108472
|
C | A | 2 | a0003c0003t0002g0069a0003c0003t0002g0074 | 2 | HG00609.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.689+145C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108472 | ||||||
chr14:60108522
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.689+195T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108522 | ||||||
chr14:60108768
|
A | AATATTGA others(301): Show |
1 | a0001c0001t0001g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.689+454_689+455ins others(308): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | |||||
chr14:60108768
|
A | AATATTGA others(307): Show |
5 | a0001c0001t0007g0040a0001c0001t0021g0129a0001c0001t0021g0145others(2): Show | 5 | HG01175.hp1 HG02683.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+454_689+455ins others(314): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | |||||
chr14:60108768
|
A | AATATTGA others(308): Show |
71 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(68): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.689+454_689+455ins others(315): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | |||||
chr14:60108768
|
A | AATATTGA others(309): Show |
30 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0037others(27): Show | 35 | HG00609.hp2 HG01361.hp2 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.689+454_689+455ins others(316): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | |||||
chr14:60108794
|
G | A | 34 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0031others(31): Show | 47 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.689+467G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108794 | ||||||
chr14:60109083
|
A | G | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+756A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109083 | ||||||
chr14:60109113
|
G | T | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+786G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109113 | ||||||
chr14:60109151
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.689+824A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109151 | ||||||
chr14:60109321
|
T | C | 1 | a0001c0001t0012g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.689+994T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109321 | ||||||
chr14:60109377
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.689+1050G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109377 | ||||||
chr14:60109523
|
G | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.689+1196G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109523 | ||||||
chr14:60109590
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.689+1263G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109590 | ||||||
chr14:60109632
|
G | T | 1 | a0002c0009t0056g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.689+1305G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109632 | ||||||
chr14:60109919
|
A | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.689+1592A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109919 | ||||||
chr14:60110032
|
T | G | 25 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(22): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.689+1705T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110032 | ||||||
chr14:60110068
|
A | G | 2 | a0001c0001t0022g0146a0001c0001t0022g0165 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.689+1741A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110068 | ||||||
chr14:60110071
|
A | G | 3 | a0008c0010t0005g0016a0008c0010t0005g0099a0008c0010t0068g0016 | 4 | NA18944.hp1 NA19065.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+1744A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110071 | ||||||
chr14:60110121
|
C | A | 1 | a0002c0002t0005g0095 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.689+1794C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110121 | ||||||
chr14:60110143
|
A | G | 4 | a0001c0001t0007g0040a0001c0001t0007g0041a0001c0001t0007g0187others(1): Show | 5 | HG02074.hp2 NA18942.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+1816A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110143 | ||||||
chr14:60110233
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.689+1906A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110233 | ||||||
chr14:60110300
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.689+1973C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110300 | ||||||
chr14:60110366
|
A | C | 1 | a0001c0001t0017g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.689+2039A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110366 | ||||||
chr14:60110500
|
T | G | 1 | a0002c0002t0003g0060 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.689+2173T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110500 | ||||||
chr14:60110930
|
G | T | 1 | a0003c0003t0002g0073 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.689+2603G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110930 | ||||||
chr14:60110994
|
A | G | 31 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(28): Show | 49 | HG00558.hp2 HG00609.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.689+2667A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110994 | ||||||
chr14:60111084
|
A | T | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.689+2757A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111084 | ||||||
chr14:60111155
|
C | G | 25 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(22): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.689+2828C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111155 | ||||||
chr14:60111243
|
T | G | 1 | a0024c0012t0003g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.689+2916T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111243 | ||||||
chr14:60111355
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.689+3028G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111355 | ||||||
chr14:60111437
|
A | G | 1 | a0002c0009t0073g0104 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.689+3110A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111437 | ||||||
chr14:60111634
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.690-3066G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111634 | ||||||
chr14:60111847
|
A | G | 12 | a0002c0007t0061g0061a0002c0009t0029g0053a0002c0009t0029g0054others(9): Show | 13 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.690-2853A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111847 | ||||||
chr14:60112004
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.690-2696T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112004 | ||||||
chr14:60112167
|
AAGAC | A | 6 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(3): Show | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-2527_690-2524d others(6): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60112167 | |||||
chr14:60112271
|
T | C | 1 | a0003c0003t0002g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.690-2429T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112271 | ||||||
chr14:60112323
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.690-2377T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112323 | ||||||
chr14:60112352
|
A | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0031a0001c0001t0001g0032others(26): Show | 41 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.690-2348A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112352 | ||||||
chr14:60112430
|
T | C | 2 | a0002c0002t0003g0058a0002c0002t0003g0060 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.690-2270T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112430 | ||||||
chr14:60112451
|
A | T | 2 | a0002c0002t0003g0058a0002c0002t0003g0060 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.690-2249A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112451 | ||||||
chr14:60112623
|
G | T | 2 | a0001c0001t0017g0125a0001c0001t0017g0136 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.690-2077G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112623 | ||||||
chr14:60112646
|
A | G | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.690-2054A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112646 | ||||||
chr14:60112910
|
G | A | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-1790G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112910 | ||||||
chr14:60112921
|
C | T | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.690-1779C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112921 | ||||||
chr14:60112955
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.690-1745A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112955 | ||||||
chr14:60113038
|
T | C | 1 | a0018c0026t0072g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.690-1662T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113038 | ||||||
chr14:60113270
|
G | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.690-1430G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113270 | ||||||
chr14:60113280
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.690-1420A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113280 | ||||||
chr14:60113568
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.690-1132C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113568 | ||||||
chr14:60113661
|
G | A | 1 | a0001c0001t0021g0129 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.690-1039G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113661 | ||||||
chr14:60113780
|
C | T | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.690-920C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113780 | ||||||
chr14:60113785
|
A | G | 7 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(4): Show | 8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-915A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113785 | ||||||
chr14:60113890
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.690-810T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113890 | ||||||
chr14:60113952
|
C | T | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.690-748C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113952 | ||||||
chr14:60113982
|
T | C | 1 | a0001c0001t0008g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.690-718T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113982 | ||||||
chr14:60114086
|
A | G | 2 | a0001c0001t0049g0176a0022c0019t0050g0160 | 2 | HG00673.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.690-614A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114086 | ||||||
chr14:60114228
|
G | C | 1 | a0001c0001t0010g0149 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.690-472G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114228 | ||||||
chr14:60114591
|
G | GT | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(107): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.690-100dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60114591 | |||||
chr14:60114652
|
C | T | 1 | a0002c0009t0029g0054 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.690-48C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114652 | ||||||
chr14:60114659
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.690-41A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114659 | ||||||
chr14:60114885
|
T | C | 1 | a0003c0003t0060g0066 | 1 | NA19007.hp2 | splice_region_variant&intron_variant | LOW | c.869+6T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 3/10 | chr14 | 60114885 | ||||||
chr14:60114955
|
CT | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.870-9delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr14 | 60114955 | |||||
chr14:60114965
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0038g0130 | 3 | HG02615.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.870-9T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 3/10 | chr14 | 60114965 | ||||||
chr14:60115558
|
A | G | 1 | a0002c0007t0003g0027 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1357+97A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/10 | chr14 | 60115558 | ||||||
chr14:60115598
|
T | C | 1 | a0001c0023t0001g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1358-121T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/10 | chr14 | 60115598 | ||||||
chr14:60115611
|
G | T | 1 | a0002c0007t0003g0077 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1358-108G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/10 | chr14 | 60115611 | ||||||
chr14:60115842
|
A | G | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1458+23A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 5/10 | chr14 | 60115842 | ||||||
chr14:60116344
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1578+284A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116344 | ||||||
chr14:60116456
|
C | T | 1 | a0003c0003t0002g0072 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1578+396C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116456 | ||||||
chr14:60116519
|
T | C | 1 | a0002c0002t0003g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1578+459T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116519 | ||||||
chr14:60116535
|
T | C | 3 | a0003c0003t0002g0067a0003c0003t0002g0070a0016c0027t0002g0075 | 3 | HG02040.hp1 HG02071.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1578+475T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116535 | ||||||
chr14:60116625
|
G | A | 118 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(115): Show | 158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.1578+565G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116625 | ||||||
chr14:60116641
|
A | C | 1 | a0006c0006t0051g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1578+581A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116641 | ||||||
chr14:60116650
|
T | G | 3 | a0002c0002t0003g0058a0002c0002t0003g0060a0002c0007t0061g0061 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1578+590T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116650 | ||||||
chr14:60117055
|
G | T | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1578+995G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117055 | ||||||
chr14:60117112
|
A | G | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1578+1052A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117112 | ||||||
chr14:60117363
|
G | A | 1 | a0002c0002t0003g0184 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1579-966G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117363 | ||||||
chr14:60117367
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579-962A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117367 | ||||||
chr14:60117456
|
C | T | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1579-873C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117456 | ||||||
chr14:60117497
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1579-832A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117497 | ||||||
chr14:60117508
|
C | T | 1 | a0004c0004t0004g0044 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1579-821C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117508 | ||||||
chr14:60117533
|
T | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1579-796T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117533 | ||||||
chr14:60117549
|
C | G | 119 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(116): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.1579-780C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117549 | ||||||
chr14:60117695
|
G | A | 1 | a0004c0004t0025g0047 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1579-634G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117695 | ||||||
chr14:60117744
|
G | T | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1579-585G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117744 | ||||||
chr14:60117808
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1579-521G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117808 | ||||||
chr14:60117851
|
A | G | 94 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(91): Show | 124 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1579-478A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117851 | ||||||
chr14:60117924
|
G | A | 1 | a0018c0026t0072g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1579-405G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117924 | ||||||
chr14:60118117
|
G | GT | 90 | a0001c0001t0001g0124a0002c0002t0003g0009a0002c0002t0003g0013others(87): Show | 123 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1579-200dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr14 | 60118117 | |||||
chr14:60118117
|
G | GTT | 9 | a0002c0002t0003g0024a0002c0002t0003g0059a0002c0002t0069g0024others(6): Show | 9 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579-201_1579-200d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr14 | 60118117 | |||||
chr14:60118244
|
T | A | 1 | a0017c0016t0005g0096 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1579-85T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60118244 | ||||||
chr14:60118317
|
A | T | 1 | a0010c0029t0058g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1579-12A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60118317 | ||||||
chr14:60118929
|
T | G | 37 | a0002c0007t0003g0027a0002c0007t0003g0077a0002c0007t0003g0079others(34): Show | 58 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1942+237T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60118929 | ||||||
chr14:60118963
|
C | A | 1 | a0025c0032t0009g0106 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1942+271C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60118963 | ||||||
chr14:60119328
|
A | G | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1942+636A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119328 | ||||||
chr14:60119360
|
T | G | 119 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(116): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.1942+668T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119360 | ||||||
chr14:60119615
|
T | TA | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.1942+924dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | 60119615 | |||||
chr14:60119677
|
C | T | 1 | a0010c0029t0058g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1942+985C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119677 | ||||||
chr14:60119919
|
T | C | 2 | a0002c0002t0003g0024a0002c0002t0069g0024 | 2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1942+1227T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119919 | ||||||
chr14:60119922
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1942+1230A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119922 | ||||||
chr14:60119943
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1942+1251A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119943 | ||||||
chr14:60119975
|
G | A | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1943-1221G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119975 | ||||||
chr14:60120032
|
A | G | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1943-1164A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120032 | ||||||
chr14:60120311
|
C | T | 7 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(4): Show | 8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1943-885C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120311 | ||||||
chr14:60120338
|
G | C | 119 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(116): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.1943-858G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120338 | ||||||
chr14:60120428
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1943-768A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120428 | ||||||
chr14:60120429
|
T | TCAGGTAG others(15): Show |
1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1943-762_1943-741d others(24): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | 60120429 | |||||
chr14:60120513
|
A | G | 1 | a0003c0003t0002g0068 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1943-683A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120513 | ||||||
chr14:60120781
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0043g0137 | 2 | NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1943-415G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120781 | ||||||
chr14:60120957
|
T | G | 1 | a0003c0003t0060g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1943-239T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120957 | ||||||
chr14:60121071
|
T | C | 1 | a0001c0001t0001g0159 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1943-125T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60121071 | ||||||
chr14:60121161
|
C | CT | 16 | a0003c0003t0002g0025a0005c0005t0001g0154a0006c0006t0009g0017others(13): Show | 21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1943-15dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | 60121161 | |||||
chr14:60121166
|
T | C | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1943-30T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60121166 | ||||||
chr14:60121181
|
T | C | 10 | a0002c0002t0003g0013a0002c0002t0003g0021a0002c0002t0003g0039others(7): Show | 14 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1943-15T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60121181 | ||||||
chr14:60121328
|
A | G | 26 | a0002c0025t0079g0055a0003c0003t0002g0004a0003c0003t0002g0006others(23): Show | 43 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(40): Show |
intron_variant | MODIFIER | c.2046+29A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121328 | ||||||
chr14:60121448
|
A | G | 117 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(114): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2046+149A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121448 | ||||||
chr14:60121519
|
C | CT | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.2046+224dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr14 | 60121519 | |||||
chr14:60121532
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0167 | 2 | NA18982.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2046+233C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121532 | ||||||
chr14:60121584
|
AT | A | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.2046+294delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr14 | 60121584 | |||||
chr14:60121632
|
A | G | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.2046+333A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121632 | ||||||
chr14:60121726
|
A | G | 2 | a0002c0009t0027g0076a0002c0009t0027g0103 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2046+427A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121726 | ||||||
chr14:60121851
|
T | C | 1 | a0002c0002t0005g0029 | 2 | NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2046+552T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121851 | ||||||
chr14:60121912
|
A | C | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.2046+613A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121912 | ||||||
chr14:60122013
|
C | T | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2046+714C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122013 | ||||||
chr14:60122061
|
C | T | 2 | a0020c0024t0045g0117a0021c0018t0078g0116 | 2 | HG01496.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+762C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122061 | ||||||
chr14:60122238
|
C | A | 1 | a0012c0022t0041g0157 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2046+939C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122238 | ||||||
chr14:60122436
|
G | A | 1 | a0002c0002t0003g0088 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2046+1137G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122436 | ||||||
chr14:60122447
|
T | G | 2 | a0002c0002t0028g0101a0002c0002t0028g0102 | 2 | HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2046+1148T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122447 | ||||||
chr14:60122454
|
G | T | 117 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(114): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2046+1155G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122454 | ||||||
chr14:60122619
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0167 | 2 | NA18982.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2046+1320A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122619 | ||||||
chr14:60122848
|
C | A | 1 | a0001c0001t0007g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2047-1370C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122848 | ||||||
chr14:60122848
|
C | T | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2047-1370C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122848 | ||||||
chr14:60123063
|
A | G | 3 | a0003c0003t0002g0067a0003c0003t0002g0070a0016c0027t0002g0075 | 3 | HG02040.hp1 HG02071.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2047-1155A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123063 | ||||||
chr14:60123102
|
A | C | 1 | a0003c0003t0002g0065 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2047-1116A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123102 | ||||||
chr14:60123240
|
T | G | 117 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(114): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2047-978T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123240 | ||||||
chr14:60123504
|
C | CAATATTT others(1): Show |
119 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(116): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.2047-709_2047-702d others(10): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr14 | 60123504 | |||||
chr14:60123928
|
C | G | 119 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(116): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.2047-290C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123928 | ||||||
chr14:60125312
|
A | G | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3080+61A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/10 | chr14 | 60125312 | ||||||
chr14:60125403
|
A | G | 20 | a0002c0002t0005g0007a0002c0002t0005g0015a0002c0002t0005g0029others(17): Show | 24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.3080+152A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/10 | chr14 | 60125403 | ||||||
chr14:60126146
|
G | A | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.3267+323G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126146 | ||||||
chr14:60126309
|
T | G | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3267+486T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126309 | ||||||
chr14:60126631
|
G | A | 1 | a0003c0003t0002g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3267+808G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126631 | ||||||
chr14:60126732
|
A | G | 1 | a0002c0002t0016g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3267+909A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126732 | ||||||
chr14:60126817
|
A | G | 1 | a0001c0001t0042g0141 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3267+994A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126817 | ||||||
chr14:60126971
|
A | G | 1 | a0002c0002t0003g0089 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3267+1148A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126971 | ||||||
chr14:60127607
|
A | G | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.3267+1784A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127607 | ||||||
chr14:60127622
|
A | C | 1 | a0013c0014t0065g0098 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3267+1799A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127622 | ||||||
chr14:60127759
|
A | G | 1 | a0005c0005t0006g0153 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3267+1936A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127759 | ||||||
chr14:60127971
|
G | A | 1 | a0008c0010t0005g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3267+2148G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127971 | ||||||
chr14:60127985
|
T | C | 7 | a0007c0008t0013g0028a0007c0008t0013g0113a0007c0008t0013g0114others(4): Show | 8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3267+2162T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127985 | ||||||
chr14:60128034
|
T | C | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3267+2211T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128034 | ||||||
chr14:60128061
|
A | G | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3267+2238A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128061 | ||||||
chr14:60128098
|
G | A | 1 | a0018c0026t0072g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3267+2275G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128098 | ||||||
chr14:60128164
|
GA | G | 116 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(113): Show | 156 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.3267+2349delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60128164 | |||||
chr14:60128236
|
G | A | 1 | a0021c0018t0078g0116 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3267+2413G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128236 | ||||||
chr14:60128464
|
C | T | 10 | a0002c0002t0003g0013a0002c0002t0003g0021a0002c0002t0003g0039others(7): Show | 14 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.3267+2641C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128464 | ||||||
chr14:60128465
|
A | G | 119 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(116): Show | 159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.3267+2642A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128465 | ||||||
chr14:60128564
|
T | C | 6 | a0006c0006t0009g0017a0006c0006t0009g0018a0006c0006t0051g0107others(3): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.3267+2741T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128564 | ||||||
chr14:60128615
|
T | C | 2 | a0020c0024t0045g0117a0021c0018t0078g0116 | 2 | HG01496.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3267+2792T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128615 | ||||||
chr14:60128784
|
G | C | 1 | a0006c0006t0051g0107 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3267+2961G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128784 | ||||||
chr14:60128784
|
G | T | 1 | a0001c0023t0001g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3267+2961G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128784 | ||||||
chr14:60128807
|
A | G | 20 | a0002c0002t0005g0007a0002c0002t0005g0015a0002c0002t0005g0029others(17): Show | 24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.3267+2984A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128807 | ||||||
chr14:60128841
|
A | G | 5 | a0002c0007t0061g0061a0002c0009t0029g0053a0002c0009t0029g0054others(2): Show | 5 | HG02257.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3267+3018A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128841 | ||||||
chr14:60128978
|
C | T | 1 | a0002c0002t0003g0182 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3267+3155C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128978 | ||||||
chr14:60128987
|
C | T | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3267+3164C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128987 | ||||||
chr14:60129240
|
C | CAA | 111 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(108): Show | 151 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.3267+3429_3267+343 others(6): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60129240 | |||||
chr14:60129363
|
G | A | 1 | a0024c0012t0003g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3267+3540G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60129363 | ||||||
chr14:60129958
|
CAAAG | C | 2 | a0006c0006t0009g0017a0006c0006t0075g0108 | 4 | HG00642.hp1 HG00735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3268-4008_3268-400 others(8): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60129958 | |||||
chr14:60130229
|
A | G | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3268-3741A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130229 | ||||||
chr14:60130342
|
AC | A | 48 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(45): Show | 59 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.3268-3626delC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60130342 | |||||
chr14:60130479
|
T | C | 6 | a0002c0002t0003g0013a0002c0002t0003g0021a0002c0002t0014g0013others(3): Show | 9 | HG00639.hp1 HG01192.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3268-3491T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130479 | ||||||
chr14:60130487
|
A | C | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-3483A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130487 | ||||||
chr14:60130689
|
T | C | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-3281T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130689 | ||||||
chr14:60130794
|
A | AT | 28 | a0002c0007t0061g0061a0002c0009t0029g0053a0002c0009t0029g0054others(25): Show | 36 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.3268-3164dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60130794 | |||||
chr14:60131016
|
C | A | 5 | a0002c0007t0003g0027a0002c0007t0003g0077a0002c0007t0003g0079others(2): Show | 6 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3268-2954C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131016 | ||||||
chr14:60131039
|
G | T | 1 | a0002c0002t0003g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3268-2931G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131039 | ||||||
chr14:60131041
|
T | TG | 117 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(114): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.3268-2929_3268-292 others(5): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131041 | ||||||
chr14:60131466
|
G | A | 25 | a0003c0003t0002g0004a0003c0003t0002g0006a0003c0003t0002g0008others(22): Show | 42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.3268-2504G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131466 | ||||||
chr14:60131559
|
C | A | 117 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(114): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.3268-2411C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131559 | ||||||
chr14:60131618
|
A | G | 8 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0042others(5): Show | 15 | NA18940.hp1 NA18975.hp2 NA18983.hp2 others(12): Show |
intron_variant | MODIFIER | c.3268-2352A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131618 | ||||||
chr14:60131771
|
G | A | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-2199G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131771 | ||||||
chr14:60132211
|
T | C | 3 | a0001c0001t0011g0010a0001c0001t0011g0140a0001c0001t0047g0010 | 5 | HG01192.hp1 HG01928.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3268-1759T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60132211 | ||||||
chr14:60132260
|
A | G | 1 | a0020c0024t0045g0117 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-1710A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60132260 | ||||||
chr14:60132805
|
T | C | 2 | a0009c0011t0001g0034a0009c0011t0037g0034 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3268-1165T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60132805 | ||||||
chr14:60133019
|
GAA | G | 4 | a0002c0002t0003g0083a0002c0002t0016g0082a0002c0002t0016g0084others(1): Show | 4 | HG01109.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3268-948_3268-947d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60133019 | |||||
chr14:60133117
|
A | G | 1 | a0003c0003t0002g0070 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3268-853A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133117 | ||||||
chr14:60133175
|
G | A | 117 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(114): Show | 157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.3268-795G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133175 | ||||||
chr14:60133503
|
T | G | 1 | a0002c0007t0061g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3268-467T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133503 | ||||||
chr14:60133637
|
A | G | 5 | a0002c0002t0003g0009a0002c0002t0003g0087a0002c0002t0003g0088others(2): Show | 8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3268-333A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133637 | ||||||
chr14:60133759
|
T | A | 100 | a0002c0002t0003g0009a0002c0002t0003g0013a0002c0002t0003g0021others(97): Show | 133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3268-211T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133759 | ||||||
chr14:60133890
|
C | CT | 17 | a0004c0004t0004g0005a0004c0004t0004g0022a0004c0004t0004g0023others(14): Show | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.3268-79dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60133890 |