geneid | 129285 |
---|---|
ensemblid | ENSG00000162869.16 |
hgncid | 30595 |
symbol | PPP1R21 |
name | protein phosphatase 1 regulatory subunit 21 |
refseq_nuc | NM_001135629.3 |
refseq_prot | NP_001129101.1 |
ensembl_nuc | ENST00000294952.13 |
ensembl_prot | ENSP00000294952.8 |
mane_status | MANE Select |
chr | chr2 |
start | 48440766 |
end | 48515386 |
strand | + |
ver | v1.2 |
region | chr2:48440766-48515386 |
region5000 | chr2:48435766-48520386 |
regionname0 | PPP1R21_chr2_48440766_48515386 |
regionname5000 | PPP1R21_chr2_48435766_48520386 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 780 | 363 | 77 | 66 | 161 | 17 | 40 | 121 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0002 | 0/0 | 780 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0003 | 0/0 | 780 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0004 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0005 | 0/0 | 780 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0006 | 0/0 | 780 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0007 | 0/0 | 780 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2343 | 317 | 62 | 53 | 159 | 12 | 29 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0002 | 0/0 | 2343 | 20 | 1 | 7 | 1 | 2 | 9 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0003 | 0/0 | 2343 | 9 | 7 | 1 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0004 | 0/0 | 2343 | 7 | 0 | 3 | 0 | 3 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0005 | 0/0 | 2343 | 6 | 4 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0006 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0007 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0008 | 0/0 | 2343 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0009 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0010 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0011 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0012 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0013 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
c0014 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
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 | 0/0 | 841 | 80 | 1 | 13 | 51 | 5 | 10 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0002 | 0/0 | 839 | 47 | 18 | 10 | 5 | 2 | 12 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0003 | 1/0 | 831 | 33 | 4 | 3 | 22 | 0 | 3 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0004 | 0/0 | 848 | 26 | 0 | 9 | 16 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0005 | 0/0 | 834 | 25 | 0 | 0 | 25 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0006 | 0/0 | 843 | 25 | 13 | 2 | 8 | 1 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0007 | 0/0 | 845 | 21 | 10 | 1 | 6 | 2 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0008 | 0/0 | 849 | 10 | 5 | 3 | 0 | 2 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0009 | 0/0 | 826 | 7 | 0 | 3 | 0 | 3 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0010 | 0/0 | 847 | 7 | 4 | 1 | 1 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0011 | 0/0 | 851 | 5 | 0 | 2 | 3 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0012 | 0/0 | 837 | 5 | 0 | 2 | 2 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0013 | 0/1 | 844 | 4 | 0 | 2 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0014 | 0/0 | 839 | 4 | 3 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0015 | 0/0 | 846 | 4 | 1 | 2 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0016 | 0/0 | 844 | 4 | 0 | 0 | 3 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0017 | 0/0 | 847 | 3 | 2 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0018 | 0/0 | 839 | 3 | 1 | 0 | 0 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0019 | 0/0 | 831 | 3 | 1 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0020 | 0/0 | 851 | 3 | 0 | 1 | 0 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0021 | 0/0 | 852 | 3 | 2 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0022 | 0/0 | 850 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0023 | 0/0 | 842 | 3 | 0 | 3 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0024 | 0/0 | 852 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0025 | 0/0 | 846 | 3 | 1 | 0 | 2 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0026 | 0/0 | 833 | 3 | 0 | 0 | 1 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0027 | 0/0 | 840 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0028 | 0/0 | 835 | 2 | 1 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0029 | 0/0 | 843 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0030 | 0/0 | 833 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0031 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0032 | 0/0 | 852 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0033 | 0/0 | 837 | 2 | 0 | 0 | 1 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0034 | 0/0 | 838 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0035 | 0/0 | 835 | 2 | 1 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0036 | 0/0 | 829 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0037 | 0/0 | 856 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0038 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0039 | 0/0 | 853 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0040 | 0/0 | 845 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0041 | 0/0 | 838 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0042 | 0/0 | 841 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0043 | 0/0 | 841 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0044 | 0/0 | 845 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0045 | 0/0 | 833 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0046 | 0/0 | 848 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0047 | 0/0 | 842 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0048 | 0/0 | 863 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0049 | 0/0 | 859 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0050 | 0/0 | 857 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0051 | 0/0 | 829 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
t0052 | 0/0 | 845 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
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 | 2 | 0 | 1 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2343 | 317 | 62 | 53 | 159 | 12 | 29 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002 | 0/0 | 2343 | 20 | 1 | 7 | 1 | 2 | 9 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003 | 0/0 | 2343 | 9 | 7 | 1 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0004 | 0/0 | 2343 | 7 | 0 | 3 | 0 | 3 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0005 | 0/0 | 2343 | 6 | 4 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0007 | 0/0 | 2343 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0013 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0014 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0002c0006 | 0/0 | 2343 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0003c0008 | 0/0 | 2343 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0004c0010 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0005c0009 | 0/0 | 2343 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0006c0011 | 0/0 | 2343 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0007c0012 | 0/0 | 2343 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3183 | 73 | 1 | 12 | 50 | 3 | 7 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0002 | 0/0 | 3181 | 37 | 17 | 6 | 5 | 1 | 8 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0003 | 1/0 | 3173 | 29 | 1 | 3 | 22 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0004 | 0/0 | 3190 | 26 | 0 | 9 | 16 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0005 | 0/0 | 3176 | 25 | 0 | 0 | 25 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0006 | 0/0 | 3185 | 24 | 13 | 2 | 8 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0007 | 0/0 | 3187 | 19 | 8 | 1 | 6 | 2 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0008 | 0/0 | 3191 | 10 | 5 | 3 | 0 | 2 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0010 | 0/0 | 3189 | 7 | 4 | 1 | 1 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0011 | 0/0 | 3193 | 5 | 0 | 2 | 3 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0012 | 0/0 | 3179 | 5 | 0 | 2 | 2 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0013 | 0/1 | 3186 | 4 | 0 | 2 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0014 | 0/0 | 3181 | 4 | 3 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0015 | 0/0 | 3188 | 4 | 1 | 2 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0016 | 0/0 | 3186 | 4 | 0 | 0 | 3 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0017 | 0/0 | 3189 | 3 | 2 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0020 | 0/0 | 3193 | 3 | 0 | 1 | 0 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0021 | 0/0 | 3194 | 3 | 2 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0022 | 0/0 | 3192 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0023 | 0/0 | 3184 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0024 | 0/0 | 3194 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0025 | 0/0 | 3188 | 3 | 1 | 0 | 2 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0026 | 0/0 | 3175 | 3 | 0 | 0 | 1 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0027 | 0/0 | 3182 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0029 | 0/0 | 3185 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0032 | 0/0 | 3194 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0033 | 0/0 | 3179 | 2 | 0 | 0 | 1 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0037 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0038 | 0/0 | 3196 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0039 | 0/0 | 3195 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0040 | 0/0 | 3187 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0042 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0043 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0046 | 0/0 | 3190 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0047 | 0/0 | 3184 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0049 | 0/0 | 3201 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0050 | 0/0 | 3199 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0051 | 0/0 | 3171 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0001t0052 | 0/0 | 3187 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0001 | 0/0 | 3183 | 5 | 0 | 1 | 0 | 1 | 3 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0002 | 0/0 | 3181 | 9 | 0 | 4 | 0 | 1 | 4 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0003 | 0/0 | 3173 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0006 | 0/0 | 3185 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0007 | 0/0 | 3187 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0023 | 0/0 | 3184 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0002t0048 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003t0028 | 0/0 | 3177 | 2 | 1 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003t0034 | 0/0 | 3180 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003t0035 | 0/0 | 3177 | 2 | 1 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003t0041 | 0/0 | 3180 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003t0044 | 0/0 | 3187 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0003t0045 | 0/0 | 3175 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0004t0009 | 0/0 | 3168 | 7 | 0 | 3 | 0 | 3 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0005t0019 | 0/0 | 3173 | 3 | 1 | 2 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0005t0030 | 0/0 | 3175 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0005t0036 | 0/0 | 3171 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0007t0031 | 0/0 | 3170 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0013t0002 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0001c0014t0022 | 0/0 | 3192 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0002c0006t0003 | 0/0 | 3173 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0003c0008t0018 | 0/0 | 3181 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0004c0010t0018 | 0/0 | 3181 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0005c0009t0001 | 0/0 | 3183 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0006c0011t0001 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
a0007c0012t0007 | 0/0 | 3187 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | copy fasta | chr2 | 48435766 | 48520386 |
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 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0065 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0004g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0007g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0008g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0011g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0011g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0011g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0012g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0012g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0012g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0012g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0013g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0013g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0013g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0013g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0014g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0014g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0015g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0015g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0015g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0015g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0016g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0016g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0016g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0016g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0017g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0017g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0017g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0020g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0020g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0020g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0021g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0021g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0021g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0022g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0022g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0023g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0024g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0024g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0024g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0025g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0025g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0025g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0026g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0026g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0026g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0027g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0027g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0029g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0029g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0032g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0032g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0033g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0033g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0037g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0038g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0039g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0040g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0042g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0043g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0046g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0047g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0049g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0050g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0051g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0001t0052g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0006g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0023g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0023g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0002t0048g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0028g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0028g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0034g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0034g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0035g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0035g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0041g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0044g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0003t0045g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0004t0009g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0005t0019g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0005t0019g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0005t0019g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0005t0030g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0005t0030g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0005t0036g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0007t0031g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0007t0031g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0013t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0001c0014t0022g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0002c0006t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0002c0006t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0002c0006t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0003c0008t0018g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0003c0008t0018g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0004c0010t0018g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0005c0009t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0006c0011t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
a0007c0012t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0269 | EUR | GBR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0270 | EUR | GBR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0295 | EUR | GBR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | GBR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00280 | hp1 | a0001 | c0004 | t0009 | g0315 | EUR | FIN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00280 | hp2 | a0001 | c0001 | t0016 | g0214 | EUR | FIN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | FIN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00323 | hp2 | a0001 | c0001 | t0013 | g0284 | EUR | FIN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00408 | hp1 | a0001 | c0001 | t0022 | g0359 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0356 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00438 | hp2 | a0001 | c0001 | t0007 | g0082 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0354 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00597 | hp1 | a0001 | c0002 | t0048 | g0145 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0347 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0263 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00642 | hp1 | a0001 | c0001 | t0013 | g0288 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00642 | hp2 | a0001 | c0001 | t0008 | g0264 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00735 | hp2 | a0001 | c0001 | t0027 | g0286 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00738 | hp1 | a0001 | c0005 | t0019 | g0014 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01069 | hp1 | a0001 | c0001 | t0017 | g0326 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01070 | hp1 | a0001 | c0001 | t0012 | g0261 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01070 | hp2 | a0001 | c0004 | t0009 | g0314 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01081 | hp1 | a0001 | c0004 | t0009 | g0316 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0078 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01099 | hp2 | a0001 | c0001 | t0015 | g0362 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0300 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01106 | hp2 | a0001 | c0001 | t0012 | g0245 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0243 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01109 | hp2 | a0001 | c0005 | t0019 | g0013 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0296 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01168 | hp2 | a0001 | c0002 | t0023 | g0297 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0151 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0282 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01243 | hp1 | a0001 | c0003 | t0035 | g0332 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01243 | hp2 | a0001 | c0001 | t0010 | g0115 | AMR | PUR | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01255 | hp1 | a0001 | c0002 | t0023 | g0298 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01255 | hp2 | a0001 | c0004 | t0009 | g0317 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01257 | hp1 | a0001 | c0001 | t0023 | g0149 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01261 | hp1 | a0001 | c0001 | t0052 | g0260 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0267 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0181 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01346 | hp2 | a0001 | c0001 | t0008 | g0024 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01358 | hp2 | a0001 | c0001 | t0049 | g0275 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01433 | hp2 | a0001 | c0001 | t0014 | g0099 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0294 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0001 | EUR | IBS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01515 | hp2 | a0001 | c0001 | t0008 | g0265 | EUR | IBS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01516 | hp2 | a0001 | c0004 | t0009 | g0312 | EUR | IBS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01517 | hp1 | a0001 | c0004 | t0009 | g0313 | EUR | IBS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0266 | EUR | IBS | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01884 | hp2 | a0001 | c0003 | t0028 | g0334 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01891 | hp1 | a0001 | c0001 | t0015 | g0091 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0330 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0370 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0366 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0301 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01981 | hp1 | a0001 | c0001 | t0013 | g0289 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0342 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0367 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0368 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02004 | hp2 | a0001 | c0001 | t0027 | g0287 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0337 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02055 | hp2 | a0001 | c0001 | t0029 | g0328 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0352 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02083 | hp1 | a0001 | c0001 | t0037 | g0268 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0205 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02132 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02132 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0172 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0173 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0369 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | CDX | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0188 | EAS | CDX | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0220 | EAS | CDX | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02165 | hp2 | a0001 | c0001 | t0026 | g0200 | EAS | CDX | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0371 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0271 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02451 | hp1 | a0001 | c0001 | t0029 | g0329 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02572 | hp1 | a0001 | c0002 | t0007 | g0293 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02572 | hp2 | a0001 | c0001 | t0025 | g0093 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0299 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02615 | hp2 | a0002 | c0006 | t0003 | g0320 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0092 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02683 | hp1 | a0001 | c0001 | t0007 | g0278 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02683 | hp2 | a0001 | c0001 | t0040 | g0274 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02698 | hp2 | a0001 | c0001 | t0026 | g0063 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02717 | hp1 | a0001 | c0007 | t0031 | g0015 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02723 | hp1 | a0001 | c0003 | t0035 | g0333 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0109 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02735 | hp1 | a0001 | c0004 | t0009 | g0318 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02735 | hp2 | a0001 | c0001 | t0020 | g0341 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0304 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02818 | hp2 | a0001 | c0001 | t0014 | g0101 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02886 | hp1 | a0001 | c0001 | t0021 | g0114 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02895 | hp2 | a0001 | c0001 | t0021 | g0281 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0072 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02970 | hp1 | a0001 | c0001 | t0046 | g0017 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0127 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0085 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02976 | hp2 | a0001 | c0005 | t0030 | g0011 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03041 | hp1 | a0001 | c0001 | t0017 | g0331 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03098 | hp1 | a0001 | c0005 | t0030 | g0008 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03130 | hp1 | a0001 | c0001 | t0014 | g0100 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03130 | hp2 | a0001 | c0013 | t0002 | g0140 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03139 | hp2 | a0001 | c0001 | t0050 | g0144 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03195 | hp1 | a0001 | c0005 | t0019 | g0010 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0120 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03225 | hp2 | a0001 | c0003 | t0034 | g0153 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03239 | hp1 | a0001 | c0001 | t0039 | g0339 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03239 | hp2 | a0003 | c0008 | t0018 | g0324 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03453 | hp1 | a0001 | c0003 | t0045 | g0159 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03453 | hp2 | a0001 | c0003 | t0034 | g0152 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03490 | hp1 | a0001 | c0001 | t0020 | g0340 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0018 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03516 | hp2 | a0004 | c0010 | t0018 | g0327 | AFR | ESN | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0272 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03579 | hp2 | a0001 | c0007 | t0031 | g0009 | AFR | MSL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0306 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03688 | hp1 | a0001 | c0003 | t0028 | g0335 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0303 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0146 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03704 | hp2 | a0001 | c0001 | t0015 | g0344 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03831 | hp1 | a0001 | c0001 | t0033 | g0343 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03927 | hp1 | a0003 | c0008 | t0018 | g0325 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03927 | hp2 | a0001 | c0002 | t0003 | g0292 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG03942 | hp2 | a0001 | c0001 | t0007 | g0276 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04184 | hp1 | a0001 | c0002 | t0006 | g0111 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0238 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0351 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18522 | hp1 | a0001 | c0003 | t0044 | g0308 | AFR | YRI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0126 | AFR | YRI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18747 | hp1 | a0001 | c0001 | t0016 | g0361 | EAS | CHB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18747 | hp2 | a0001 | c0001 | t0012 | g0199 | EAS | CHB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18906 | hp1 | a0002 | c0006 | t0003 | g0322 | AFR | YRI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | YRI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0349 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18939 | hp2 | a0001 | c0001 | t0033 | g0043 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0365 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0045 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18942 | hp1 | a0001 | c0001 | t0024 | g0345 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18943 | hp2 | a0001 | c0001 | t0011 | g0226 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18944 | hp2 | a0001 | c0014 | t0022 | g0350 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18945 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18949 | hp1 | a0001 | c0001 | t0010 | g0168 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0240 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18962 | hp1 | a0001 | c0001 | t0032 | g0255 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0364 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18963 | hp2 | a0001 | c0001 | t0042 | g0179 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0353 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18968 | hp1 | a0001 | c0001 | t0025 | g0184 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18968 | hp2 | a0001 | c0001 | t0012 | g0229 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18972 | hp1 | a0001 | c0001 | t0016 | g0363 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18974 | hp1 | a0001 | c0001 | t0024 | g0346 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18975 | hp1 | a0001 | c0001 | t0047 | g0164 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18977 | hp1 | a0001 | c0001 | t0051 | g0038 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18977 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18978 | hp1 | a0001 | c0001 | t0011 | g0225 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18982 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18985 | hp2 | a0001 | c0001 | t0016 | g0355 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18989 | hp1 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18989 | hp2 | a0001 | c0001 | t0038 | g0262 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18990 | hp1 | a0001 | c0001 | t0043 | g0119 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18992 | hp2 | a0005 | c0009 | t0001 | g0211 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0046 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19006 | hp2 | a0001 | c0001 | t0022 | g0360 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19007 | hp1 | a0001 | c0001 | t0024 | g0357 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19030 | hp1 | a0002 | c0006 | t0003 | g0321 | AFR | LWK | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19030 | hp2 | a0007 | c0012 | t0007 | g0089 | AFR | LWK | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19072 | hp1 | a0001 | c0001 | t0005 | g0052 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19074 | hp1 | a0001 | c0001 | t0032 | g0256 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19077 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19078 | hp1 | a0001 | c0001 | t0025 | g0161 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0358 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19081 | hp2 | a0001 | c0001 | t0021 | g0348 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19087 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0227 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19090 | hp2 | a0001 | c0001 | t0011 | g0167 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0336 | AFR | YRI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA19240 | hp2 | a0001 | c0001 | t0014 | g0102 | AFR | YRI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0134 | AFR | ASW | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0139 | AFR | ASW | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0197 | EUR | TSI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0291 | EUR | TSI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0096 | EUR | TSI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20805 | hp2 | a0006 | c0011 | t0001 | g0103 | EUR | TSI | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20905 | hp1 | a0001 | c0001 | t0026 | g0064 | SAS | GIH | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | GIH | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | CLM | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0123 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG02559 | hp2 | a0001 | c0005 | t0036 | g0012 | AFR | ACB | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG06807 | hp1 | a0001 | c0001 | t0010 | g0108 | AFR | USA | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | USA | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20300 | hp1 | a0001 | c0003 | t0041 | g0081 | AFR | USA | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | USA | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA21309 | hp1 | a0001 | c0001 | t0007 | g0125 | AFR | LWK | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | LWK | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0285 | REF | REF | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0065 | REF | REF | PPP1R21_chr2_48435766_48520386 | PPP1R21 | chr2 | 48435766 | 48520386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48474798
|
A | G | 1 | a0007 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1204A>G | p.Ile402Val | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/22 | 1392/3173 | 1204/2343 | 402/780 | chr2 | 48474798 | ||
chr2:48480014
|
A | G | 1 | a0002 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
missense_variant&splice_region_variant | MODERATE | c.1316A>G | p.Lys439Arg | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/22 | 1504/3173 | 1316/2343 | 439/780 | chr2 | 48480014 | ||
chr2:48486669
|
C | T | 1 | a0006 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1357C>T | p.His453Tyr | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/22 | 1545/3173 | 1357/2343 | 453/780 | chr2 | 48486669 | ||
chr2:48491070
|
A | G | 1 | a0004 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1499A>G | p.Tyr500Cys | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/22 | 1687/3173 | 1499/2343 | 500/780 | chr2 | 48491070 | ||
chr2:48495758
|
G | T | 2 | a0003a0004 | 3 | HG03239.hp2 HG03516.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.1679G>T | p.Gly560Val | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/22 | 1867/3173 | 1679/2343 | 560/780 | chr2 | 48495758 | ||
chr2:48507315
|
T | G | 1 | a0005 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.2015T>G | p.Met672Arg | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/22 | 2203/3173 | 2015/2343 | 672/780 | chr2 | 48507315 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48454711
|
T | C | 2 | a0001c0005a0001c0007 | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.243T>C | p.Ala81Ala | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/22 | 431/3173 | 243/2343 | 81/780 | chr2 | 48454711 | ||
chr2:48454729
|
C | G | 1 | a0001c0004 | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
synonymous_variant | LOW | c.261C>G | p.Gly87Gly | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/22 | 449/3173 | 261/2343 | 87/780 | chr2 | 48454729 | ||
chr2:48464953
|
C | T | 1 | a0001c0014 | 1 | NA18944.hp2 | synonymous_variant | LOW | c.711C>T | p.Asn237Asn | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 8/22 | 899/3173 | 711/2343 | 237/780 | chr2 | 48464953 | ||
chr2:48471284
|
A | G | 1 | a0001c0013 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1005A>G | p.Thr335Thr | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/22 | 1193/3173 | 1005/2343 | 335/780 | chr2 | 48471284 | ||
chr2:48486638
|
C | T | 1 | a0001c0002 | 20 | HG00140.hp1 HG00597.hp1 HG00738.hp2 others(17): Show |
synonymous_variant | LOW | c.1326C>T | p.Ser442Ser | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/22 | 1514/3173 | 1326/2343 | 442/780 | chr2 | 48486638 | ||
chr2:48498618
|
T | C | 1 | a0001c0007 | 2 | HG02717.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1818T>C | p.Asn606Asn | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/22 | 2006/3173 | 1818/2343 | 606/780 | chr2 | 48498618 | ||
chr2:48510026
|
G | C | 2 | a0001c0003a0001c0007 | 11 | HG01243.hp1 HG01884.hp2 HG02717.hp1 others(8): Show |
synonymous_variant | LOW | c.2097G>C | p.Leu699Leu | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/22 | 2285/3173 | 2097/2343 | 699/780 | chr2 | 48510026 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48440766
|
A | T | 1 | a0001c0003t0035 | 2 | HG01243.hp1 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-188A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/22 | 188 | chr2 | 48440766 | |||||
chr2:48440788
|
G | C | 13 | a0001c0001t0013a0001c0001t0017a0001c0001t0027others(10): Show | 33 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-166G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/22 | 166 | chr2 | 48440788 | |||||
chr2:48440812
|
C | CGCG | 14 | a0001c0001t0004a0001c0001t0005a0001c0001t0013others(11): Show | 80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-121_-119dupGGC | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/22 | 118 | INFO_REALIGN_3_PRIME | chr2 | 48440812 | ||||
chr2:48440812
|
C | CGCGGCG | 5 | a0001c0001t0014a0001c0001t0020a0001c0001t0033others(2): Show | 11 | HG01433.hp2 HG01981.hp2 HG02683.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-124_-119dupGGCGGC | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/22 | 118 | INFO_REALIGN_3_PRIME | chr2 | 48440812 | ||||
chr2:48440812
|
C | CGCGGCGG others(2): Show |
3 | a0001c0001t0032a0001c0001t0037a0001c0001t0038 | 4 | HG02083.hp1 NA18962.hp1 NA18989.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-127_-119dupGGCGGC others(3): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/22 | 118 | INFO_REALIGN_3_PRIME | chr2 | 48440812 | ||||
chr2:48440812
|
CGCG | C | 5 | a0001c0004t0009a0001c0005t0019a0001c0005t0030others(2): Show | 15 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-121_-119delGGC | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/22 | 119 | INFO_REALIGN_3_PRIME | chr2 | 48440812 | ||||
chr2:48514769
|
G | A | 1 | a0001c0001t0042 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 25 | chr2 | 48514769 | |||||
chr2:48514835
|
T | C | 1 | a0001c0001t0043 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 91 | chr2 | 48514835 | |||||
chr2:48514985
|
T | C | 1 | a0001c0003t0041 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 241 | chr2 | 48514985 | |||||
chr2:48515084
|
A | G | 1 | a0001c0001t0024 | 3 | NA18942.hp1 NA18974.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*340A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 340 | chr2 | 48515084 | |||||
chr2:48515159
|
ACTT | A | 3 | a0001c0005t0019a0001c0005t0030a0001c0005t0036 | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*421delCTT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 419 | INFO_REALIGN_3_PRIME | chr2 | 48515159 | ||||
chr2:48515167
|
T | C | 8 | a0001c0003t0028a0001c0003t0034a0001c0003t0035others(5): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*423T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 423 | chr2 | 48515167 | |||||
chr2:48515216
|
T | TCTCTCTC others(4): Show |
1 | a0001c0001t0047 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472_*473insCTCTCT others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 473 | chr2 | 48515216 | |||||
chr2:48515216
|
T | TCTCTCTC others(8): Show |
1 | a0001c0001t0025 | 3 | HG02572.hp2 NA18968.hp1 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*472_*473insCTCTCT others(9): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 473 | chr2 | 48515216 | |||||
chr2:48515216
|
T | TCTCTCTC others(10): Show |
1 | a0001c0001t0046 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472_*473insCTCTCT others(11): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 473 | chr2 | 48515216 | |||||
chr2:48515216
|
T | TTC | 3 | a0001c0001t0014a0001c0001t0026a0001c0003t0045 | 8 | HG01433.hp2 HG02165.hp2 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*503dupCT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTC | 5 | a0001c0003t0028a0001c0003t0034a0001c0003t0035others(2): Show | 8 | HG01243.hp1 HG01884.hp2 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*500_*503dupCTCT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTC | 3 | a0001c0001t0012a0001c0001t0027a0001c0005t0019 | 10 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*498_*503dupCTCTCT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(1): Show |
9 | a0001c0001t0002a0001c0001t0023a0001c0001t0040others(6): Show | 56 | HG00140.hp1 HG00323.hp1 HG00609.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*496_*503dupCTCTCT others(2): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(3): Show |
8 | a0001c0001t0001a0001c0001t0013a0001c0001t0016others(5): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*494_*503dupCTCTCT others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(5): Show |
5 | a0001c0001t0006a0001c0001t0015a0001c0001t0029others(2): Show | 33 | HG01099.hp2 HG01175.hp2 HG01192.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*492_*503dupCTCTCT others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(7): Show |
7 | a0001c0001t0004a0001c0001t0007a0001c0001t0020others(4): Show | 52 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*490_*503dupCTCTCT others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(9): Show |
6 | a0001c0001t0010a0001c0001t0017a0001c0001t0022others(3): Show | 15 | HG00408.hp1 HG01069.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*488_*503dupCTCTCT others(10): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(11): Show |
3 | a0001c0001t0008a0001c0001t0021a0001c0001t0024 | 16 | HG00642.hp2 HG01081.hp2 HG01346.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*486_*503dupCTCTCT others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(13): Show |
1 | a0001c0001t0011 | 5 | HG00639.hp1 HG01261.hp2 NA18943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*484_*503dupCTCTCT others(14): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(19): Show |
1 | a0001c0001t0050 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*478_*503dupCTCTCT others(20): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(21): Show |
1 | a0001c0001t0049 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*476_*503dupCTCTCT others(22): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
T | TTCTCTCT others(25): Show |
1 | a0001c0002t0048 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*503_*504insCTCTCT others(26): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 504 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515216
|
TTC | T | 2 | a0001c0001t0051a0001c0004t0009 | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*503delCT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 502 | INFO_REALIGN_3_PRIME | chr2 | 48515216 | ||||
chr2:48515228
|
C | CTCTCTCT others(7): Show |
1 | a0001c0001t0052 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*497_*498insGTCTCT others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 22/22 | 498 | INFO_REALIGN_3_PRIME | chr2 | 48515228 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48441151
|
C | T | 34 | a0001c0001t0004g0338a0001c0001t0004g0347a0001c0001t0004g0349others(31): Show | 34 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.57+141C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441151 | ||||||
chr2:48441224
|
A | G | 1 | a0001c0001t0002g0337 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.57+214A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441224 | ||||||
chr2:48441346
|
A | C | 1 | a0001c0001t0008g0336 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+336A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441346 | ||||||
chr2:48441417
|
C | A | 1 | a0001c0001t0006g0002 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.57+407C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441417 | ||||||
chr2:48441428
|
T | C | 3 | a0001c0001t0007g0003a0001c0001t0007g0004a0001c0001t0007g0005 | 3 | HG02647.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.57+418T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441428 | ||||||
chr2:48441486
|
C | T | 12 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(9): Show | 12 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+476C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441486 | ||||||
chr2:48441581
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.57+571G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441581 | ||||||
chr2:48441607
|
C | A | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.57+597C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441607 | ||||||
chr2:48441649
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.57+639A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441649 | ||||||
chr2:48441701
|
G | T | 12 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(9): Show | 12 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+691G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441701 | ||||||
chr2:48441718
|
A | T | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.57+708A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441718 | ||||||
chr2:48441809
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.57+799A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48441809 | ||||||
chr2:48442024
|
T | C | 1 | a0001c0005t0030g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57+1014T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442024 | ||||||
chr2:48442025
|
A | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+1015A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442025 | ||||||
chr2:48442129
|
G | A | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1119G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442129 | ||||||
chr2:48442131
|
G | A | 1 | a0001c0001t0003g0016 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.57+1121G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442131 | ||||||
chr2:48442234
|
A | G | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.57+1224A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442234 | ||||||
chr2:48442387
|
A | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+1377A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442387 | ||||||
chr2:48442826
|
C | G | 1 | a0001c0001t0002g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.57+1816C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442826 | ||||||
chr2:48442828
|
A | G | 1 | a0001c0001t0001g0309 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.57+1818A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442828 | ||||||
chr2:48442836
|
A | G | 13 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(10): Show | 13 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1826A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48442836 | ||||||
chr2:48443032
|
G | A | 28 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+2022G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443032 | ||||||
chr2:48443067
|
T | A | 30 | a0001c0001t0010g0018a0001c0001t0017g0326a0001c0001t0017g0330others(27): Show | 30 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.57+2057T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443067 | ||||||
chr2:48443159
|
C | T | 2 | a0001c0001t0002g0307a0001c0002t0002g0306 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.57+2149C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443159 | ||||||
chr2:48443227
|
C | A | 13 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(10): Show | 13 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+2217C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443227 | ||||||
chr2:48443387
|
A | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+2377A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443387 | ||||||
chr2:48443485
|
C | G | 22 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0002g0305others(19): Show | 22 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.57+2475C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443485 | ||||||
chr2:48443512
|
A | C | 1 | a0001c0001t0002g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.57+2502A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443512 | ||||||
chr2:48443682
|
G | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+2672G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443682 | ||||||
chr2:48443751
|
A | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+2741A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443751 | ||||||
chr2:48443851
|
TC | T | 31 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0006others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.57+2842delC | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443851 | ||||||
chr2:48443863
|
A | G | 28 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+2853A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443863 | ||||||
chr2:48443880
|
G | T | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+2870G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48443880 | ||||||
chr2:48444048
|
A | AAAAC | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+3040_57+3041ins others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48444048 | |||||
chr2:48444051
|
C | A | 34 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.57+3041C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444051 | ||||||
chr2:48444126
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.57+3116G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444126 | ||||||
chr2:48444175
|
G | A | 20 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(17): Show | 20 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+3165G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444175 | ||||||
chr2:48444341
|
C | G | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG00621.hp2 HG02040.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+3331C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444341 | ||||||
chr2:48444390
|
A | G | 4 | a0001c0001t0004g0279a0001c0001t0004g0280a0001c0001t0015g0282others(1): Show | 4 | HG01099.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+3380A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444390 | ||||||
chr2:48444517
|
G | T | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG00621.hp2 HG02040.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+3507G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444517 | ||||||
chr2:48444541
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0003g0021 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.57+3531G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444541 | ||||||
chr2:48444627
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0160others(97): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.57+3617A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444627 | ||||||
chr2:48444709
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0160others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.57+3699A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444709 | ||||||
chr2:48444908
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0003g0021 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.57+3898A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444908 | ||||||
chr2:48444908
|
A | T | 20 | a0001c0001t0002g0305a0001c0001t0013g0284a0001c0001t0013g0285others(17): Show | 20 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.57+3898A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444908 | ||||||
chr2:48444939
|
T | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | HG01167.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.57+3929T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48444939 | ||||||
chr2:48445081
|
A | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+4071A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445081 | ||||||
chr2:48445135
|
C | CT | 101 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0162others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.57+4146dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48445135 | |||||
chr2:48445135
|
CT | C | 28 | a0001c0001t0003g0254a0001c0001t0004g0338a0001c0001t0005g0022others(25): Show | 28 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+4146delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48445135 | |||||
chr2:48445135
|
CTT | C | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+4145_57+4146del others(2): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48445135 | |||||
chr2:48445228
|
A | G | 28 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+4218A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445228 | ||||||
chr2:48445234
|
G | C | 28 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.57+4224G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445234 | ||||||
chr2:48445272
|
C | T | 29 | a0001c0001t0004g0338a0001c0001t0004g0347a0001c0001t0004g0349others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.57+4262C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445272 | ||||||
chr2:48445289
|
A | G | 1 | a0001c0007t0031g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.57+4279A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445289 | ||||||
chr2:48445390
|
C | G | 1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.57+4380C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445390 | ||||||
chr2:48445480
|
A | C | 1 | a0001c0005t0019g0014 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.57+4470A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445480 | ||||||
chr2:48445521
|
G | A | 13 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(10): Show | 13 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+4511G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445521 | ||||||
chr2:48445545
|
G | A | 2 | a0001c0001t0032g0255a0001c0001t0032g0256 | 2 | NA18962.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.57+4535G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445545 | ||||||
chr2:48445577
|
C | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+4567C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445577 | ||||||
chr2:48445652
|
A | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.57+4642A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445652 | ||||||
chr2:48445768
|
C | G | 2 | a0001c0003t0028g0334a0001c0003t0028g0335 | 2 | HG01884.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.57+4758C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445768 | ||||||
chr2:48445794
|
CT | C | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+4785delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445794 | ||||||
chr2:48445819
|
C | A | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.57+4809C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445819 | ||||||
chr2:48445995
|
A | C | 2 | a0001c0003t0035g0332a0001c0003t0035g0333 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.57+4985A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48445995 | ||||||
chr2:48446057
|
A | G | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG00621.hp2 HG02040.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-4951A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446057 | ||||||
chr2:48446100
|
TGTCAAAA others(3): Show |
T | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.58-4904_58-4895del others(10): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48446100 | |||||
chr2:48446185
|
A | T | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG00621.hp2 HG02040.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-4823A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446185 | ||||||
chr2:48446189
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.58-4819A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446189 | ||||||
chr2:48446305
|
C | T | 2 | a0001c0001t0002g0307a0001c0002t0002g0306 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.58-4703C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446305 | ||||||
chr2:48446566
|
A | G | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-4442A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446566 | ||||||
chr2:48446876
|
G | C | 37 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(34): Show | 37 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.58-4132G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446876 | ||||||
chr2:48446878
|
G | C | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-4130G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446878 | ||||||
chr2:48446893
|
T | C | 35 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(32): Show | 35 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.58-4115T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48446893 | ||||||
chr2:48447208
|
G | T | 2 | a0001c0001t0032g0255a0001c0001t0032g0256 | 2 | NA18962.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.58-3800G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447208 | ||||||
chr2:48447209
|
A | T | 2 | a0001c0001t0032g0255a0001c0001t0032g0256 | 2 | NA18962.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.58-3799A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447209 | ||||||
chr2:48447235
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0026 | 2 | NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.58-3773G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447235 | ||||||
chr2:48447352
|
T | A | 28 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.58-3656T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447352 | ||||||
chr2:48447493
|
G | T | 1 | a0001c0001t0004g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.58-3515G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447493 | ||||||
chr2:48447587
|
A | G | 1 | a0001c0001t0007g0278 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.58-3421A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447587 | ||||||
chr2:48447620
|
G | T | 2 | a0001c0001t0002g0150a0001c0001t0023g0149 | 2 | HG00323.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.58-3388G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447620 | ||||||
chr2:48447726
|
A | C | 1 | a0001c0005t0019g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.58-3282A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447726 | ||||||
chr2:48447751
|
C | G | 1 | a0001c0003t0028g0335 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.58-3257C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447751 | ||||||
chr2:48447807
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.58-3201G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447807 | ||||||
chr2:48447820
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-3188C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447820 | ||||||
chr2:48447864
|
C | A | 1 | a0001c0001t0008g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-3144C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447864 | ||||||
chr2:48447874
|
C | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-3134C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447874 | ||||||
chr2:48447907
|
A | G | 6 | a0001c0001t0004g0366a0001c0001t0004g0367a0001c0001t0004g0368others(3): Show | 6 | HG01952.hp1 HG01975.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-3101A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447907 | ||||||
chr2:48447978
|
TA | T | 13 | a0001c0001t0004g0338a0001c0001t0004g0364a0001c0001t0004g0365others(10): Show | 13 | HG01099.hp2 HG01952.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-3020delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48447978 | |||||
chr2:48447983
|
A | G | 13 | a0001c0001t0017g0326a0001c0001t0017g0330a0001c0001t0017g0331others(10): Show | 13 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-3025A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48447983 | ||||||
chr2:48448074
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.58-2934A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448074 | ||||||
chr2:48448149
|
T | C | 1 | a0001c0001t0002g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.58-2859T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448149 | ||||||
chr2:48448316
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0012g0245 | 2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.58-2692A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448316 | ||||||
chr2:48448395
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.58-2613C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448395 | ||||||
chr2:48448483
|
A | G | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-2525A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448483 | ||||||
chr2:48448522
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.58-2486C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448522 | ||||||
chr2:48448582
|
GAAATAAA others(22): Show |
G | 170 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.58-2412_58-2384del others(29): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48448582 | |||||
chr2:48448592
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-2416C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448592 | ||||||
chr2:48448606
|
T | A | 1 | a0001c0001t0006g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.58-2402T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448606 | ||||||
chr2:48448698
|
A | G | 6 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-2310A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448698 | ||||||
chr2:48448980
|
G | C | 1 | a0001c0005t0030g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.58-2028G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48448980 | ||||||
chr2:48449070
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-1938T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449070 | ||||||
chr2:48449392
|
C | A | 1 | a0001c0001t0001g0148 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.58-1616C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449392 | ||||||
chr2:48449477
|
T | C | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-1531T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449477 | ||||||
chr2:48449683
|
G | C | 27 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.58-1325G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449683 | ||||||
chr2:48449710
|
T | G | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-1298T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449710 | ||||||
chr2:48449762
|
AT | A | 6 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0002g0079others(3): Show | 6 | HG02886.hp2 HG03453.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-1232delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48449762 | |||||
chr2:48449792
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.58-1216A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449792 | ||||||
chr2:48449807
|
T | C | 27 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.58-1201T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449807 | ||||||
chr2:48449846
|
G | T | 1 | a0001c0001t0033g0343 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58-1162G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449846 | ||||||
chr2:48449860
|
G | T | 1 | a0001c0001t0008g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-1148G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449860 | ||||||
chr2:48449923
|
T | C | 1 | a0001c0001t0007g0082 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.58-1085T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48449923 | ||||||
chr2:48450031
|
A | C | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-977A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48450031 | ||||||
chr2:48450104
|
G | T | 1 | a0001c0002t0001g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.58-904G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48450104 | ||||||
chr2:48450152
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-856C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48450152 | ||||||
chr2:48450775
|
A | AT | 9 | a0001c0001t0001g0253a0001c0001t0003g0254a0001c0004t0009g0312others(6): Show | 9 | HG00280.hp1 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-221dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr2 | 48450775 | |||||
chr2:48450788
|
A | T | 1 | a0001c0002t0048g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.58-220A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 1/21 | chr2 | 48450788 | ||||||
chr2:48451183
|
C | T | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+107C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48451183 | ||||||
chr2:48451283
|
A | T | 1 | a0001c0001t0050g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.126+207A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48451283 | ||||||
chr2:48451520
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.126+444T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48451520 | ||||||
chr2:48451582
|
G | A | 2 | a0001c0004t0009g0312a0001c0004t0009g0313 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.126+506G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48451582 | ||||||
chr2:48451791
|
CTT | C | 7 | a0001c0001t0017g0326a0001c0003t0035g0332a0001c0003t0035g0333others(4): Show | 7 | HG01069.hp1 HG01243.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+717_126+718del others(2): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr2 | 48451791 | |||||
chr2:48451806
|
A | G | 1 | a0001c0013t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.126+730A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48451806 | ||||||
chr2:48451844
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0007g0243 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.126+768C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48451844 | ||||||
chr2:48452182
|
G | A | 1 | a0001c0001t0006g0083 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.126+1106G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452182 | ||||||
chr2:48452276
|
C | A | 1 | a0001c0001t0002g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.126+1200C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452276 | ||||||
chr2:48452295
|
A | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+1219A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452295 | ||||||
chr2:48452359
|
A | C | 30 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+1283A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452359 | ||||||
chr2:48452384
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+1308C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452384 | ||||||
chr2:48452676
|
A | C | 34 | a0001c0001t0006g0139a0001c0001t0013g0284a0001c0001t0013g0285others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.126+1600A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452676 | ||||||
chr2:48452700
|
C | A | 311 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(308): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.126+1624C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452700 | ||||||
chr2:48452715
|
T | A | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.126+1639T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452715 | ||||||
chr2:48452718
|
A | G | 1 | a0001c0001t0022g0359 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.126+1642A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452718 | ||||||
chr2:48452796
|
C | G | 33 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+1720C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452796 | ||||||
chr2:48452824
|
A | G | 1 | a0001c0001t0006g0241 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+1748A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452824 | ||||||
chr2:48452876
|
C | A | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-1719C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48452876 | ||||||
chr2:48452954
|
C | CT | 6 | a0001c0001t0001g0239a0001c0001t0004g0358a0001c0001t0005g0069others(3): Show | 6 | HG02071.hp1 HG02738.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1624dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr2 | 48452954 | |||||
chr2:48452954
|
CT | C | 8 | a0001c0001t0004g0338a0001c0004t0009g0312a0001c0004t0009g0313others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-1624delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr2 | 48452954 | |||||
chr2:48453107
|
C | T | 19 | a0001c0001t0002g0020a0001c0001t0002g0079a0001c0001t0002g0080others(16): Show | 19 | HG01074.hp2 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-1488C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453107 | ||||||
chr2:48453252
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0007g0243 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-1343C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453252 | ||||||
chr2:48453253
|
C | T | 1 | a0001c0001t0010g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.127-1342C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453253 | ||||||
chr2:48453275
|
T | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.127-1320T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453275 | ||||||
chr2:48453284
|
C | G | 2 | a0001c0001t0001g0244a0001c0001t0007g0243 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-1311C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453284 | ||||||
chr2:48453341
|
A | G | 1 | a0004c0010t0018g0327 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-1254A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453341 | ||||||
chr2:48453399
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0007g0243 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-1196C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453399 | ||||||
chr2:48453551
|
A | T | 1 | a0001c0001t0001g0237 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.127-1044A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453551 | ||||||
chr2:48453573
|
A | G | 1 | a0001c0007t0031g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-1022A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453573 | ||||||
chr2:48453692
|
A | G | 2 | a0001c0001t0006g0139a0001c0003t0045g0159 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.127-903A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453692 | ||||||
chr2:48453760
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.127-835A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48453760 | ||||||
chr2:48454022
|
G | T | 2 | a0001c0001t0001g0244a0001c0001t0007g0243 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.127-573G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48454022 | ||||||
chr2:48454033
|
TGGATCAC others(4): Show |
T | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-559_127-549del others(11): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr2 | 48454033 | |||||
chr2:48454095
|
C | T | 1 | a0001c0003t0028g0334 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.127-500C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48454095 | ||||||
chr2:48454197
|
G | A | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127-398G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48454197 | ||||||
chr2:48454222
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-373C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | chr2 | 48454222 | ||||||
chr2:48454263
|
A | AAAAT | 17 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.127-307_127-304dup others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr2 | 48454263 | |||||
chr2:48454263
|
A | AAAATAAA others(1): Show |
7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-311_127-304dup others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr2 | 48454263 | |||||
chr2:48454764
|
T | C | 1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.273+23T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454764 | ||||||
chr2:48454779
|
G | A | 3 | a0001c0001t0013g0285a0001c0001t0027g0286a0001c0001t0027g0287 | 3 | HG00735.hp2 HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.273+38G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454779 | ||||||
chr2:48454858
|
G | C | 35 | a0001c0001t0004g0338a0001c0001t0004g0347a0001c0001t0004g0349others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.273+117G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454858 | ||||||
chr2:48454868
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.273+127C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454868 | ||||||
chr2:48454920
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0003g0021 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.273+179A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454920 | ||||||
chr2:48454937
|
C | G | 5 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+196C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454937 | ||||||
chr2:48454977
|
A | G | 1 | a0001c0001t0006g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.273+236A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48454977 | ||||||
chr2:48455124
|
C | T | 4 | a0001c0001t0006g0139a0001c0003t0034g0152a0001c0003t0034g0153others(1): Show | 4 | HG03225.hp2 HG03453.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+383C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455124 | ||||||
chr2:48455133
|
C | T | 2 | a0001c0001t0006g0139a0001c0003t0045g0159 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.273+392C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455133 | ||||||
chr2:48455142
|
A | AT | 56 | a0001c0001t0001g0019a0001c0001t0001g0174a0001c0001t0001g0176others(53): Show | 56 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.273+424dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48455142 | |||||
chr2:48455142
|
A | ATT | 8 | a0001c0001t0001g0170a0001c0001t0001g0230a0001c0001t0001g0231others(5): Show | 8 | HG00408.hp2 HG01952.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+423_273+424dup others(2): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48455142 | |||||
chr2:48455142
|
AT | A | 52 | a0001c0001t0001g0084a0001c0001t0003g0016a0001c0001t0003g0033others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.273+424delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48455142 | |||||
chr2:48455227
|
A | G | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+486A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455227 | ||||||
chr2:48455295
|
T | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.273+554T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455295 | ||||||
chr2:48455374
|
T | C | 28 | a0001c0001t0006g0139a0001c0001t0017g0326a0001c0001t0020g0340others(25): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.273+633T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455374 | ||||||
chr2:48455381
|
G | T | 6 | a0001c0001t0017g0326a0001c0001t0020g0340a0001c0001t0039g0339others(3): Show | 6 | HG01069.hp1 HG03239.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+640G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455381 | ||||||
chr2:48455423
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.273+682C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455423 | ||||||
chr2:48455424
|
T | G | 1 | a0001c0001t0001g0201 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.273+683T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455424 | ||||||
chr2:48455445
|
G | A | 5 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0239others(2): Show | 5 | HG02071.hp1 HG03710.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+704G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455445 | ||||||
chr2:48455567
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.273+826T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455567 | ||||||
chr2:48455606
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+865C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455606 | ||||||
chr2:48455630
|
A | C | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.273+889A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455630 | ||||||
chr2:48455679
|
G | T | 2 | a0001c0001t0001g0244a0001c0001t0007g0243 | 2 | HG00140.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.273+938G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455679 | ||||||
chr2:48455771
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.273+1030T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455771 | ||||||
chr2:48455866
|
T | A | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.273+1125T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455866 | ||||||
chr2:48455886
|
C | T | 17 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0013g0284others(14): Show | 17 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.273+1145C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455886 | ||||||
chr2:48455913
|
G | A | 2 | a0001c0001t0002g0257a0001c0001t0040g0274 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.273+1172G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455913 | ||||||
chr2:48455937
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.273+1196C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455937 | ||||||
chr2:48455979
|
C | G | 12 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+1238C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455979 | ||||||
chr2:48455985
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.273+1244G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48455985 | ||||||
chr2:48456014
|
C | CA | 9 | a0001c0001t0001g0248a0001c0001t0003g0062a0001c0001t0004g0135others(6): Show | 9 | NA18974.hp2 NA18995.hp1 NA19006.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+1295dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456014 | |||||
chr2:48456034
|
AAAT | A | 29 | a0001c0001t0001g0273a0001c0001t0004g0371a0001c0001t0008g0272others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+1295_273+1297d others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456034 | |||||
chr2:48456035
|
AAT | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0084a0001c0001t0001g0097others(243): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.273+1296_273+1297d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456035 | |||||
chr2:48456036
|
AT | A | 18 | a0001c0001t0001g0019a0001c0001t0001g0166a0001c0001t0001g0178others(15): Show | 18 | HG00741.hp2 HG01109.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.273+1296delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456036 | ||||||
chr2:48456037
|
T | A | 3 | a0001c0001t0002g0277a0001c0003t0034g0152a0001c0003t0034g0153 | 3 | HG02738.hp1 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.273+1296T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456037 | ||||||
chr2:48456054
|
C | G | 1 | a0001c0003t0028g0335 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.273+1313C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456054 | ||||||
chr2:48456080
|
T | C | 1 | a0001c0004t0009g0314 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.273+1339T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456080 | ||||||
chr2:48456184
|
T | C | 34 | a0001c0001t0006g0139a0001c0001t0013g0284a0001c0001t0013g0285others(31): Show | 34 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.273+1443T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456184 | ||||||
chr2:48456252
|
C | CT | 16 | a0001c0001t0006g0139a0001c0001t0017g0326a0001c0003t0045g0159others(13): Show | 16 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.273+1526dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456252 | |||||
chr2:48456252
|
C | CTT | 14 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(11): Show | 14 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+1525_273+1526d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456252 | |||||
chr2:48456252
|
C | CTTTTT | 6 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+1522_273+1526d others(7): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456252 | |||||
chr2:48456252
|
CT | C | 7 | a0001c0001t0001g0175a0001c0001t0003g0033a0001c0001t0004g0366others(4): Show | 7 | HG01975.hp2 HG02735.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+1526delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48456252 | |||||
chr2:48456320
|
A | G | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+1579A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456320 | ||||||
chr2:48456607
|
A | C | 57 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.274-1519A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456607 | ||||||
chr2:48456621
|
A | G | 17 | a0001c0001t0017g0326a0001c0001t0020g0340a0001c0001t0039g0339others(14): Show | 17 | HG00738.hp1 HG01069.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-1505A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456621 | ||||||
chr2:48456662
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0003g0021 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.274-1464A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456662 | ||||||
chr2:48456674
|
C | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.274-1452C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456674 | ||||||
chr2:48456727
|
T | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.274-1399T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456727 | ||||||
chr2:48456788
|
C | T | 9 | a0001c0001t0017g0326a0001c0001t0020g0340a0001c0001t0039g0339others(6): Show | 9 | HG01069.hp1 HG01243.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-1338C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456788 | ||||||
chr2:48456818
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.274-1308C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456818 | ||||||
chr2:48456829
|
G | T | 3 | a0001c0001t0004g0338a0001c0001t0004g0364a0001c0001t0016g0363 | 3 | NA18956.hp1 NA18963.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.274-1297G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456829 | ||||||
chr2:48456920
|
T | C | 30 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.274-1206T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48456920 | ||||||
chr2:48457051
|
C | CA | 35 | a0001c0001t0001g0230a0001c0001t0006g0139a0001c0001t0013g0284others(32): Show | 35 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.274-1064dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr2 | 48457051 | |||||
chr2:48457180
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0006g0202a0001c0001t0007g0203 | 3 | NA18979.hp1 NA18989.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.274-946G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457180 | ||||||
chr2:48457214
|
C | G | 1 | a0001c0001t0047g0164 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.274-912C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457214 | ||||||
chr2:48457391
|
G | T | 1 | a0001c0001t0012g0229 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.274-735G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457391 | ||||||
chr2:48457407
|
A | G | 1 | a0003c0008t0018g0325 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.274-719A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457407 | ||||||
chr2:48457407
|
A | T | 1 | a0001c0002t0001g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.274-719A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457407 | ||||||
chr2:48457422
|
G | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.274-704G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457422 | ||||||
chr2:48457572
|
A | T | 1 | a0001c0001t0017g0326 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.274-554A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457572 | ||||||
chr2:48457646
|
C | G | 22 | a0001c0001t0001g0104a0001c0001t0002g0006a0001c0001t0004g0279others(19): Show | 22 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.274-480C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457646 | ||||||
chr2:48457657
|
A | G | 17 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(14): Show | 17 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.274-469A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457657 | ||||||
chr2:48457685
|
G | T | 1 | a0001c0001t0002g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274-441G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457685 | ||||||
chr2:48457753
|
A | G | 1 | a0001c0001t0005g0061 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.274-373A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457753 | ||||||
chr2:48457779
|
A | T | 1 | a0002c0006t0003g0322 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.274-347A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457779 | ||||||
chr2:48457944
|
C | T | 1 | a0001c0001t0026g0200 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.274-182C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 3/21 | chr2 | 48457944 | ||||||
chr2:48458278
|
T | C | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+51T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48458278 | ||||||
chr2:48458579
|
C | CT | 15 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.375+368dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr2 | 48458579 | |||||
chr2:48458579
|
C | CTTT | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+366_375+368dup others(3): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr2 | 48458579 | |||||
chr2:48458579
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.375+352C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48458579 | ||||||
chr2:48458579
|
CT | C | 10 | a0001c0001t0001g0247a0001c0001t0002g0105a0001c0001t0004g0279others(7): Show | 10 | HG01099.hp1 HG01175.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.375+368delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr2 | 48458579 | |||||
chr2:48458819
|
G | C | 2 | a0001c0001t0007g0125a0001c0001t0007g0126 | 2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.375+592G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48458819 | ||||||
chr2:48458943
|
T | G | 2 | a0001c0001t0002g0122a0001c0001t0002g0258 | 2 | HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.375+716T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48458943 | ||||||
chr2:48458952
|
C | T | 13 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(10): Show | 13 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.375+725C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48458952 | ||||||
chr2:48459014
|
C | T | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.376-740C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459014 | ||||||
chr2:48459017
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.376-737G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459017 | ||||||
chr2:48459065
|
C | G | 6 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0059others(3): Show | 6 | HG02080.hp1 NA18949.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.376-689C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459065 | ||||||
chr2:48459071
|
G | A | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.376-683G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459071 | ||||||
chr2:48459091
|
C | CA | 47 | a0001c0001t0001g0019a0001c0001t0001g0239a0001c0001t0001g0259others(44): Show | 47 | HG00280.hp1 HG00621.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.376-642dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr2 | 48459091 | |||||
chr2:48459091
|
CA | C | 10 | a0001c0001t0001g0104a0001c0001t0001g0228a0001c0001t0002g0311others(7): Show | 10 | HG00408.hp1 HG02109.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.376-642delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr2 | 48459091 | |||||
chr2:48459171
|
G | A | 145 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0113others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.376-583G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459171 | ||||||
chr2:48459178
|
A | AAC | 34 | a0001c0001t0001g0104a0001c0001t0002g0006a0001c0001t0002g0105others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.376-558_376-557dup others(2): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr2 | 48459178 | |||||
chr2:48459352
|
T | A | 1 | a0001c0001t0003g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.376-402T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459352 | ||||||
chr2:48459382
|
T | C | 1 | a0001c0001t0020g0342 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.376-372T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459382 | ||||||
chr2:48459556
|
T | A | 131 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0113others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.376-198T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 4/21 | chr2 | 48459556 | ||||||
chr2:48459981
|
A | T | 15 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+63A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 5/21 | chr2 | 48459981 | ||||||
chr2:48459996
|
G | C | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+78G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 5/21 | chr2 | 48459996 | ||||||
chr2:48460197
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0010g0168 | 2 | NA18949.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.599+44C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460197 | ||||||
chr2:48460378
|
A | G | 1 | a0001c0003t0028g0334 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.599+225A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460378 | ||||||
chr2:48460381
|
G | A | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.599+228G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460381 | ||||||
chr2:48460418
|
G | C | 47 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(44): Show | 47 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.599+265G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460418 | ||||||
chr2:48460519
|
A | G | 2 | a0001c0001t0007g0082a0001c0001t0043g0119 | 2 | HG00438.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.599+366A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460519 | ||||||
chr2:48460529
|
C | T | 1 | a0001c0001t0010g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.599+376C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460529 | ||||||
chr2:48460579
|
A | G | 2 | a0001c0001t0006g0139a0001c0003t0045g0159 | 2 | HG03453.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.599+426A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460579 | ||||||
chr2:48460677
|
A | G | 1 | a0001c0001t0008g0085 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.600-461A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460677 | ||||||
chr2:48460685
|
C | G | 1 | a0001c0001t0008g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.600-453C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460685 | ||||||
chr2:48460718
|
A | G | 26 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(23): Show | 26 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.600-420A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460718 | ||||||
chr2:48460724
|
A | ATTACCAG others(5): Show |
16 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.600-414_600-413ins others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460724 | ||||||
chr2:48460724
|
A | ATTATCAG others(5): Show |
10 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0005t0019g0010others(7): Show | 10 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.600-414_600-413ins others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460724 | ||||||
chr2:48460815
|
A | C | 2 | a0001c0001t0003g0025a0001c0001t0003g0026 | 2 | NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.600-323A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460815 | ||||||
chr2:48460976
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.600-162G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48460976 | ||||||
chr2:48461119
|
A | AT | 7 | a0001c0001t0001g0195a0001c0001t0001g0235a0001c0001t0001g0247others(4): Show | 7 | HG01109.hp1 HG02080.hp2 NA19006.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.600-5dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr2 | 48461119 | |||||
chr2:48461125
|
T | G | 1 | a0001c0001t0015g0344 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.600-13T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 6/21 | chr2 | 48461125 | ||||||
chr2:48461324
|
A | C | 14 | a0001c0001t0002g0305a0001c0002t0001g0296a0001c0002t0002g0294others(11): Show | 14 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.694+92A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461324 | ||||||
chr2:48461427
|
C | T | 24 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(21): Show | 24 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+195C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461427 | ||||||
chr2:48461496
|
A | G | 50 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.694+264A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461496 | ||||||
chr2:48461664
|
T | C | 1 | a0001c0001t0010g0168 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.694+432T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461664 | ||||||
chr2:48461702
|
C | T | 1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.694+470C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461702 | ||||||
chr2:48461810
|
CT | C | 10 | a0001c0001t0006g0002a0001c0001t0006g0083a0001c0001t0006g0123others(7): Show | 10 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.694+580delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr2 | 48461810 | |||||
chr2:48461905
|
T | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(317): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.694+673T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461905 | ||||||
chr2:48461914
|
A | G | 31 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(28): Show | 31 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.694+682A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48461914 | ||||||
chr2:48462090
|
T | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+858T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462090 | ||||||
chr2:48462338
|
C | G | 31 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(28): Show | 31 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.694+1106C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462338 | ||||||
chr2:48462493
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.694+1261G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462493 | ||||||
chr2:48462497
|
G | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(78): Show | 81 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.694+1265G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462497 | ||||||
chr2:48462664
|
G | T | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0236 | 3 | NA18945.hp2 NA18979.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.694+1432G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462664 | ||||||
chr2:48462769
|
A | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.694+1537A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462769 | ||||||
chr2:48462790
|
C | G | 18 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.694+1558C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462790 | ||||||
chr2:48462876
|
C | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.694+1644C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48462876 | ||||||
chr2:48463063
|
C | G | 44 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0122others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.694+1831C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463063 | ||||||
chr2:48463076
|
G | T | 1 | a0001c0001t0006g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.694+1844G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463076 | ||||||
chr2:48463091
|
A | G | 1 | a0001c0002t0048g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.695-1846A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463091 | ||||||
chr2:48463138
|
C | G | 32 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0122others(29): Show | 32 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.695-1799C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463138 | ||||||
chr2:48463271
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.695-1666T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463271 | ||||||
chr2:48463356
|
C | T | 3 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0329 | 3 | HG01891.hp2 HG02451.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.695-1581C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463356 | ||||||
chr2:48463362
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.695-1575G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463362 | ||||||
chr2:48463457
|
T | G | 163 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(160): Show | 163 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.695-1480T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463457 | ||||||
chr2:48463544
|
T | G | 1 | a0001c0005t0030g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695-1393T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463544 | ||||||
chr2:48463578
|
C | T | 1 | a0001c0001t0008g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.695-1359C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463578 | ||||||
chr2:48463764
|
G | A | 1 | a0001c0001t0029g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.695-1173G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463764 | ||||||
chr2:48463834
|
G | T | 1 | a0001c0005t0030g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.695-1103G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463834 | ||||||
chr2:48463960
|
TGGGATAG others(5): Show |
T | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0002t0001g0107 | 3 | HG02602.hp1 HG03492.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.695-976_695-965del others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463960 | ||||||
chr2:48463995
|
G | A | 2 | a0001c0005t0019g0010a0001c0005t0030g0011 | 2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.695-942G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48463995 | ||||||
chr2:48464072
|
C | T | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-865C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464072 | ||||||
chr2:48464180
|
G | A | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-757G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464180 | ||||||
chr2:48464594
|
G | T | 10 | a0001c0001t0006g0002a0001c0001t0006g0083a0001c0001t0006g0123others(7): Show | 10 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.695-343G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464594 | ||||||
chr2:48464609
|
G | A | 1 | a0001c0003t0028g0334 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.695-328G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464609 | ||||||
chr2:48464634
|
C | T | 5 | a0001c0001t0014g0099a0001c0001t0014g0100a0001c0001t0014g0101others(2): Show | 5 | HG01433.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.695-303C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464634 | ||||||
chr2:48464658
|
C | T | 44 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0122others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.695-279C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464658 | ||||||
chr2:48464915
|
G | A | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.695-22G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 7/21 | chr2 | 48464915 | ||||||
chr2:48465071
|
C | G | 1 | a0001c0001t0002g0147 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.747+82C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 8/21 | chr2 | 48465071 | ||||||
chr2:48465190
|
C | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.747+201C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 8/21 | chr2 | 48465190 | ||||||
chr2:48465765
|
A | G | 13 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.897+123A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48465765 | ||||||
chr2:48465983
|
G | A | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.897+341G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48465983 | ||||||
chr2:48466071
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.897+429A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466071 | ||||||
chr2:48466086
|
C | T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+444C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466086 | ||||||
chr2:48466141
|
G | A | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.897+499G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466141 | ||||||
chr2:48466209
|
G | GT | 6 | a0001c0001t0001g0222a0001c0001t0002g0277a0001c0001t0005g0023others(3): Show | 6 | HG02738.hp1 HG03927.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.897+579dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48466209 | |||||
chr2:48466357
|
G | A | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+715G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466357 | ||||||
chr2:48466370
|
C | G | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.897+728C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466370 | ||||||
chr2:48466387
|
T | C | 1 | a0001c0001t0012g0245 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.897+745T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466387 | ||||||
chr2:48466439
|
C | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.897+797C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466439 | ||||||
chr2:48466890
|
A | C | 1 | a0001c0001t0004g0354 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.897+1248A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48466890 | ||||||
chr2:48467151
|
T | G | 1 | a0001c0013t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.897+1509T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467151 | ||||||
chr2:48467284
|
G | A | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.897+1642G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467284 | ||||||
chr2:48467376
|
G | A | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.897+1734G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467376 | ||||||
chr2:48467512
|
C | A | 4 | a0001c0001t0014g0099a0001c0001t0014g0100a0001c0001t0014g0101others(1): Show | 4 | HG01433.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+1870C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467512 | ||||||
chr2:48467651
|
T | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.897+2009T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467651 | ||||||
chr2:48467670
|
G | A | 1 | a0001c0001t0010g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.897+2028G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467670 | ||||||
chr2:48467701
|
A | G | 1 | a0001c0001t0010g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.897+2059A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467701 | ||||||
chr2:48467848
|
G | A | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.897+2206G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467848 | ||||||
chr2:48467969
|
T | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.897+2327T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467969 | ||||||
chr2:48467990
|
G | A | 1 | a0001c0001t0002g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.897+2348G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48467990 | ||||||
chr2:48468061
|
T | C | 2 | a0001c0003t0028g0334a0001c0003t0028g0335 | 2 | HG01884.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.897+2419T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468061 | ||||||
chr2:48468195
|
C | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.897+2553C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468195 | ||||||
chr2:48468244
|
G | T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.897+2602G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468244 | ||||||
chr2:48468452
|
A | G | 2 | a0001c0004t0009g0314a0001c0004t0009g0318 | 2 | HG01070.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.898-2635A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468452 | ||||||
chr2:48468454
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.898-2633A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468454 | ||||||
chr2:48468556
|
T | C | 168 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0113others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.898-2531T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468556 | ||||||
chr2:48468579
|
G | A | 1 | a0003c0008t0018g0324 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.898-2508G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468579 | ||||||
chr2:48468584
|
G | A | 1 | a0001c0001t0003g0062 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.898-2503G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468584 | ||||||
chr2:48468600
|
C | A | 3 | a0001c0001t0006g0071a0001c0001t0006g0072a0001c0001t0006g0157 | 3 | HG02615.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.898-2487C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468600 | ||||||
chr2:48468659
|
A | C | 1 | a0001c0001t0007g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.898-2428A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468659 | ||||||
chr2:48468711
|
G | A | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.898-2376G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468711 | ||||||
chr2:48468825
|
A | ATGTGTGT others(3): Show |
1 | a0001c0001t0027g0287 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.898-2259_898-2258i others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468825 | |||||
chr2:48468826
|
T | C | 4 | a0001c0001t0014g0099a0001c0001t0014g0100a0001c0001t0014g0101others(1): Show | 4 | HG01433.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-2261T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468826 | ||||||
chr2:48468829
|
A | ATG | 15 | a0001c0001t0001g0182a0001c0001t0002g0073a0001c0001t0002g0074others(12): Show | 15 | HG00544.hp2 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.898-2230_898-2229d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTG | 31 | a0001c0001t0002g0020a0001c0001t0002g0204a0001c0001t0004g0086others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.898-2232_898-2229d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTGTAT others(3): Show |
4 | a0001c0001t0004g0279a0001c0001t0004g0280a0001c0001t0015g0282others(1): Show | 4 | HG01099.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-2253_898-2252i others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTGTG | 88 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.898-2234_898-2229d others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTGTGT others(1): Show |
83 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.898-2236_898-2229d others(10): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTGTGT others(3): Show |
46 | a0001c0001t0001g0104a0001c0001t0001g0118a0001c0001t0001g0148others(43): Show | 46 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.898-2238_898-2229d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTGTGT others(5): Show |
4 | a0001c0001t0003g0143a0001c0001t0017g0330a0001c0001t0017g0331others(1): Show | 4 | HG01891.hp2 HG02083.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-2240_898-2229d others(14): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0029g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.898-2242_898-2229d others(16): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468829
|
A | G | 3 | a0001c0001t0001g0177a0001c0001t0004g0352a0001c0001t0027g0287 | 3 | HG02004.hp2 HG02056.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.898-2258A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468829 | ||||||
chr2:48468829
|
ATG | A | 28 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(25): Show | 28 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.898-2230_898-2229d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48468829 | |||||
chr2:48468855
|
G | A | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-2232G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468855 | ||||||
chr2:48468861
|
G | A | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-2226G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468861 | ||||||
chr2:48468865
|
A | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-2222A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48468865 | ||||||
chr2:48469261
|
T | TTGTGTG | 7 | a0001c0001t0001g0084a0001c0001t0002g0094a0001c0001t0002g0095others(4): Show | 7 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-1796_898-1791d others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469261 | |||||
chr2:48469261
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0007g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.898-1802_898-1791d others(14): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469261 | |||||
chr2:48469261
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG00735.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.898-1804_898-1791d others(16): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469261 | |||||
chr2:48469261
|
TTG | T | 23 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(20): Show | 23 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.898-1792_898-1791d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469261 | |||||
chr2:48469261
|
TTGTG | T | 10 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0075others(7): Show | 10 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.898-1794_898-1791d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469261 | |||||
chr2:48469261
|
TTGTGTGT others(11): Show |
T | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.898-1808_898-1791d others(20): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469261 | |||||
chr2:48469262
|
TG | T | 5 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-1824delG | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469262 | ||||||
chr2:48469287
|
GTGTGTGT others(3): Show |
G | 14 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0128others(11): Show | 14 | HG01074.hp2 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.898-1796_898-1787d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469287 | |||||
chr2:48469289
|
GTGTGTGT others(1): Show |
G | 87 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(84): Show | 87 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.898-1794_898-1787d others(10): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469289 | |||||
chr2:48469291
|
GTGTGTA | G | 98 | a0001c0001t0001g0104a0001c0001t0001g0175a0001c0001t0001g0177others(95): Show | 98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.898-1792_898-1787d others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469291 | |||||
chr2:48469293
|
GTGTA | G | 48 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(45): Show | 48 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.898-1788_898-1785d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469293 | |||||
chr2:48469293
|
GTGTATGT others(3): Show |
G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.898-1792_898-1783d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469293 | |||||
chr2:48469295
|
GTA | G | 9 | a0001c0001t0002g0105a0001c0001t0002g0307a0001c0001t0008g0120others(6): Show | 9 | HG00738.hp2 HG01978.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.898-1790_898-1789d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469295 | |||||
chr2:48469295
|
GTATGTA | G | 3 | a0001c0001t0008g0134a0001c0001t0008g0336a0001c0003t0044g0308 | 3 | NA18522.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.898-1788_898-1783d others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469295 | |||||
chr2:48469297
|
A | G | 24 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(21): Show | 24 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.898-1790A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469297 | ||||||
chr2:48469297
|
ATG | A | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-1788_898-1787d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469297 | |||||
chr2:48469301
|
A | G | 12 | a0001c0001t0006g0139a0001c0001t0025g0093a0001c0003t0028g0334others(9): Show | 12 | HG00738.hp1 HG01109.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.898-1786A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469301 | ||||||
chr2:48469302
|
TATATATA others(5): Show |
T | 1 | a0001c0007t0031g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.898-1783_898-1772d others(14): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469302 | |||||
chr2:48469304
|
TATATACA others(3): Show |
T | 7 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(4): Show | 7 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.898-1781_898-1772d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469304 | |||||
chr2:48469308
|
T | C | 2 | a0001c0002t0002g0301a0001c0002t0002g0302 | 2 | HG00738.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.898-1779T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469308 | ||||||
chr2:48469315
|
ACACACAT others(27): Show |
A | 1 | a0001c0002t0002g0302 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.898-1769_898-1736d others(36): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469315 | |||||
chr2:48469317
|
ACACATAT others(25): Show |
A | 8 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(5): Show | 8 | HG01978.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1767_898-1736d others(34): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469317 | |||||
chr2:48469319
|
ACATATAT others(23): Show |
A | 289 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0112others(286): Show | 289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.898-1710_898-1681d others(32): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469319 | |||||
chr2:48469320
|
C | T | 18 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(15): Show | 18 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.898-1767C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469320 | ||||||
chr2:48469320
|
CATATATA others(25): Show |
C | 2 | a0001c0001t0015g0362a0001c0001t0022g0360 | 2 | HG01099.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.898-1757_898-1726d others(34): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469320 | |||||
chr2:48469322
|
T | C | 9 | a0001c0001t0001g0165a0001c0005t0019g0010a0001c0005t0019g0013others(6): Show | 9 | HG00738.hp1 HG01109.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.898-1765T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469322 | ||||||
chr2:48469332
|
GAGCATAT others(8): Show |
G | 1 | a0001c0001t0020g0342 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.898-1740_898-1726d others(17): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469332 | |||||
chr2:48469335
|
CAT | C | 14 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(11): Show | 14 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.898-1740_898-1739d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469335 | |||||
chr2:48469337
|
TATATATA others(21): Show |
T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-1738_898-1711d others(30): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469337 | |||||
chr2:48469352
|
T | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01167.hp2 HG01975.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.898-1735T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469352 | ||||||
chr2:48469360
|
T | G | 2 | a0001c0001t0001g0171a0001c0001t0004g0137 | 2 | HG00423.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.898-1727T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469360 | ||||||
chr2:48469362
|
GAGCATAT others(8): Show |
G | 1 | a0001c0001t0020g0342 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.898-1710_898-1696d others(17): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469362 | |||||
chr2:48469366
|
A | G | 1 | a0001c0014t0022g0350 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.898-1721A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469366 | ||||||
chr2:48469375
|
T | TAGAG | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-1711_898-1710i others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469375 | |||||
chr2:48469375
|
T | TAGAGAG | 4 | a0001c0001t0001g0165a0001c0001t0003g0007a0001c0002t0006g0111others(1): Show | 4 | HG01978.hp2 HG04115.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-1711_898-1710i others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469375 | |||||
chr2:48469375
|
TATAGCAT others(25): Show |
T | 17 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(14): Show | 17 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.898-1710_898-1679d others(34): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469375 | |||||
chr2:48469375
|
TATAGCAT others(27): Show |
T | 1 | a0007c0012t0007g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.898-1710_898-1677d others(36): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469375 | |||||
chr2:48469377
|
T | G | 15 | a0001c0001t0001g0165a0001c0001t0003g0007a0001c0001t0013g0284others(12): Show | 15 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.898-1710T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469377 | ||||||
chr2:48469377
|
TAGCATAT others(23): Show |
T | 22 | a0001c0001t0001g0104a0001c0001t0001g0290a0001c0001t0001g0291others(19): Show | 22 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.898-1707_898-1678d others(32): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469377 | |||||
chr2:48469379
|
GCATATAT others(38): Show |
G | 3 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288 | 3 | HG00323.hp2 HG00642.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.898-1707_898-1663d others(47): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469379 | ||||||
chr2:48469379
|
GCATATAT others(57): Show |
G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1707_898-1644d others(66): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469379 | ||||||
chr2:48469390
|
T | G | 2 | a0001c0001t0013g0289a0001c0001t0027g0286 | 2 | HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.898-1697T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469390 | ||||||
chr2:48469405
|
TAG | T | 8 | a0001c0001t0003g0007a0001c0003t0041g0081a0001c0004t0009g0312others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1673_898-1672d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469405 | |||||
chr2:48469407
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.898-1680G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469407 | ||||||
chr2:48469414
|
A | C | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.898-1673A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469414 | ||||||
chr2:48469415
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.898-1672G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469415 | ||||||
chr2:48469416
|
C | CAT | 3 | a0001c0001t0013g0289a0001c0001t0027g0286a0001c0002t0006g0111 | 3 | HG00735.hp2 HG01981.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.898-1661_898-1660d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469416 | |||||
chr2:48469416
|
C | CATATATA others(14): Show |
1 | a0001c0001t0001g0165 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.898-1660_898-1659i others(23): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469416 | |||||
chr2:48469416
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.898-1671C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469416 | ||||||
chr2:48469416
|
CATATATA others(48): Show |
C | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.898-1659_898-1605d others(57): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469416 | |||||
chr2:48469426
|
T | G | 3 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288 | 3 | HG00323.hp2 HG00642.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.898-1661T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469426 | ||||||
chr2:48469428
|
GAGCATAT others(8): Show |
G | 14 | a0001c0001t0027g0287a0001c0002t0001g0296a0001c0002t0002g0294others(11): Show | 14 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.898-1656_898-1642d others(17): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469428 | |||||
chr2:48469431
|
CAT | C | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-1644_898-1643d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469431 | |||||
chr2:48469433
|
TATATATA others(48): Show |
T | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-1642_898-1588d others(57): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469433 | |||||
chr2:48469441
|
TATAGAGA others(4): Show |
T | 1 | a0001c0003t0041g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.898-1642_898-1632d others(13): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469441 | |||||
chr2:48469443
|
T | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.898-1644T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469443 | ||||||
chr2:48469445
|
G | T | 3 | a0001c0001t0013g0289a0001c0001t0027g0286a0001c0002t0006g0111 | 3 | HG00735.hp2 HG01981.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.898-1642G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469445 | ||||||
chr2:48469447
|
G | T | 4 | a0001c0001t0003g0007a0001c0001t0013g0289a0001c0001t0027g0286others(1): Show | 4 | HG00735.hp2 HG01981.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.898-1640G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469447 | ||||||
chr2:48469452
|
CAT | C | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.898-1623_898-1622d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469452 | |||||
chr2:48469456
|
TATATATA others(6): Show |
T | 1 | a0001c0002t0006g0111 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.898-1621_898-1609d others(15): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469456 | |||||
chr2:48469456
|
TATATATA others(25): Show |
T | 2 | a0001c0001t0013g0289a0001c0001t0027g0286 | 2 | HG00735.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.898-1621_898-1590d others(34): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469456 | |||||
chr2:48469458
|
TATATATA others(4): Show |
T | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.898-1621_898-1611d others(13): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469458 | |||||
chr2:48469464
|
T | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1623T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469464 | ||||||
chr2:48469469
|
C | CAT | 226 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0104others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.898-1604_898-1603d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469469 | |||||
chr2:48469469
|
C | CATAT | 6 | a0001c0001t0013g0284a0001c0002t0002g0300a0001c0002t0002g0301others(3): Show | 6 | HG00323.hp2 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.898-1606_898-1603d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469469 | |||||
chr2:48469469
|
CATATATA others(39): Show |
C | 1 | a0001c0001t0050g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.898-1602_898-1557d others(48): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469469 | |||||
chr2:48469469
|
CATATATA others(41): Show |
C | 15 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.898-1602_898-1555d others(50): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469469 | |||||
chr2:48469481
|
T | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1606T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469481 | ||||||
chr2:48469483
|
T | G | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1604T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469483 | ||||||
chr2:48469485
|
G | T | 5 | a0001c0001t0005g0032a0001c0001t0032g0255a0001c0001t0032g0256others(2): Show | 5 | HG02083.hp1 NA18962.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-1602G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469485 | ||||||
chr2:48469488
|
C | A | 13 | a0001c0001t0005g0032a0001c0001t0032g0255a0001c0001t0032g0256others(10): Show | 13 | HG00738.hp1 HG01109.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.898-1599C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469488 | ||||||
chr2:48469488
|
C | CAT | 76 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(73): Show | 76 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.898-1583_898-1582d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469488 | |||||
chr2:48469488
|
C | CATAT | 112 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.898-1585_898-1582d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469488 | |||||
chr2:48469489
|
A | G | 13 | a0001c0001t0005g0032a0001c0001t0032g0255a0001c0001t0032g0256others(10): Show | 13 | HG00738.hp1 HG01109.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.898-1598A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469489 | ||||||
chr2:48469490
|
T | C | 13 | a0001c0001t0005g0032a0001c0001t0032g0255a0001c0001t0032g0256others(10): Show | 13 | HG00738.hp1 HG01109.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.898-1597T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469490 | ||||||
chr2:48469500
|
T | G | 2 | a0001c0001t0001g0180a0001c0001t0001g0228 | 2 | NA18960.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.898-1587T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469500 | ||||||
chr2:48469502
|
T | G | 29 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0174others(26): Show | 29 | HG00544.hp1 HG01074.hp1 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.898-1585T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469502 | ||||||
chr2:48469504
|
T | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.898-1583T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469504 | ||||||
chr2:48469506
|
G | T | 25 | a0001c0001t0002g0074a0001c0001t0002g0076a0001c0001t0002g0077others(22): Show | 25 | HG01243.hp1 HG02056.hp2 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.898-1581G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469506 | ||||||
chr2:48469507
|
AG | A | 23 | a0001c0001t0002g0074a0001c0001t0002g0076a0001c0001t0002g0077others(20): Show | 23 | HG01243.hp1 HG02056.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.898-1579delG | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469507 | ||||||
chr2:48469508
|
G | GA | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0239 | 3 | HG02071.hp1 NA19058.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.898-1579_898-1578i others(3): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469508 | ||||||
chr2:48469509
|
C | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.898-1578C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469509 | ||||||
chr2:48469509
|
C | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0239 | 3 | HG02071.hp1 NA19058.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.898-1578C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469509 | ||||||
chr2:48469509
|
C | T | 23 | a0001c0001t0002g0074a0001c0001t0002g0076a0001c0001t0002g0077others(20): Show | 23 | HG01243.hp1 HG02056.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.898-1578C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469509 | ||||||
chr2:48469509
|
CATAT | C | 170 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0113others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.898-1554_898-1551d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469509 | |||||
chr2:48469509
|
CATATAT | C | 6 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.898-1556_898-1551d others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469509 | |||||
chr2:48469509
|
CATATATA others(3): Show |
C | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-1560_898-1551d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469509 | |||||
chr2:48469510
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(76): Show | 79 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.898-1577A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469510 | ||||||
chr2:48469511
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.898-1576T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469511 | ||||||
chr2:48469511
|
T | C | 2 | a0001c0001t0005g0042a0001c0001t0033g0043 | 2 | NA18939.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.898-1576T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469511 | ||||||
chr2:48469511
|
T | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0239 | 3 | HG02071.hp1 NA19058.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.898-1576T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469511 | ||||||
chr2:48469512
|
A | AG | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0239 | 3 | HG02071.hp1 NA19058.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.898-1575_898-1574i others(3): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469512 | ||||||
chr2:48469512
|
A | AGAG | 11 | a0001c0001t0002g0074a0001c0001t0002g0077a0001c0001t0004g0352others(8): Show | 11 | HG01243.hp1 HG02056.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.898-1575_898-1574i others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469512 | ||||||
chr2:48469512
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.898-1575A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469512 | ||||||
chr2:48469513
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(88): Show | 91 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.898-1574T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469513 | ||||||
chr2:48469513
|
T | G | 1 | a0001c0003t0035g0333 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.898-1574T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469513 | ||||||
chr2:48469513
|
T | TAGAGC | 11 | a0001c0001t0002g0076a0001c0001t0004g0349a0001c0001t0007g0121others(8): Show | 11 | HG03540.hp2 NA18522.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.898-1573_898-1572i others(7): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469513 | |||||
chr2:48469515
|
T | C | 1 | a0001c0003t0035g0333 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.898-1572T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469515 | ||||||
chr2:48469525
|
T | G | 5 | a0001c0001t0003g0007a0001c0002t0002g0300a0003c0008t0018g0324others(2): Show | 5 | HG01106.hp1 HG03239.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.898-1562T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469525 | ||||||
chr2:48469527
|
T | G | 32 | a0001c0001t0002g0070a0001c0001t0002g0079a0001c0001t0002g0080others(29): Show | 32 | HG00738.hp2 HG01069.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.898-1560T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469527 | ||||||
chr2:48469529
|
T | G | 202 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0113others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.898-1558T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469529 | ||||||
chr2:48469531
|
T | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0104others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.898-1556T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469531 | ||||||
chr2:48469533
|
T | G | 294 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0104others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.898-1554T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469533 | ||||||
chr2:48469535
|
T | G | 326 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0104others(323): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.898-1552T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469535 | ||||||
chr2:48469535
|
T | TAG | 4 | a0001c0001t0003g0198a0001c0001t0005g0023a0001c0001t0005g0027others(1): Show | 4 | NA19003.hp2 NA19064.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.898-1549_898-1548d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469535 | |||||
chr2:48469552
|
T | G | 16 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0178others(13): Show | 16 | HG01167.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.898-1535T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469552 | ||||||
chr2:48469554
|
G | T | 47 | a0001c0001t0001g0233a0001c0001t0001g0248a0001c0001t0001g0252others(44): Show | 47 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.898-1533G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469554 | ||||||
chr2:48469556
|
G | T | 3 | a0001c0001t0002g0283a0001c0003t0041g0081a0001c0005t0019g0013 | 3 | HG01109.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.898-1531G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469556 | ||||||
chr2:48469567
|
C | CAT | 135 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(132): Show | 135 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.898-1503_898-1502d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469567 | |||||
chr2:48469567
|
C | CATAT | 41 | a0001c0001t0001g0104a0001c0001t0001g0290a0001c0001t0001g0291others(38): Show | 41 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.898-1505_898-1502d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469567 | |||||
chr2:48469567
|
C | CATATATA others(3): Show |
1 | a0001c0001t0008g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.898-1511_898-1502d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48469567 | |||||
chr2:48469944
|
T | A | 1 | a0001c0001t0001g0210 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.898-1143T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48469944 | ||||||
chr2:48470117
|
A | G | 1 | a0001c0001t0010g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.898-970A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470117 | ||||||
chr2:48470125
|
G | C | 1 | a0001c0001t0010g0115 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.898-962G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470125 | ||||||
chr2:48470155
|
T | A | 9 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.898-932T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470155 | ||||||
chr2:48470266
|
A | C | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.898-821A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470266 | ||||||
chr2:48470354
|
C | G | 7 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(4): Show | 7 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.898-733C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470354 | ||||||
chr2:48470491
|
G | A | 1 | a0001c0002t0007g0293 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.898-596G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470491 | ||||||
chr2:48470519
|
C | CA | 28 | a0001c0001t0001g0176a0001c0001t0001g0180a0001c0001t0001g0182others(25): Show | 28 | HG00280.hp1 HG00597.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.898-552dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr2 | 48470519 | |||||
chr2:48470543
|
G | A | 37 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(34): Show | 37 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.898-544G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470543 | ||||||
chr2:48470621
|
A | G | 3 | a0001c0001t0040g0274a0001c0004t0009g0312a0001c0004t0009g0313 | 3 | HG01516.hp2 HG01517.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.898-466A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470621 | ||||||
chr2:48470655
|
C | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.898-432C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470655 | ||||||
chr2:48470825
|
C | A | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.898-262C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470825 | ||||||
chr2:48470897
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0074 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.898-190C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48470897 | ||||||
chr2:48471016
|
T | A | 1 | a0001c0001t0013g0284 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.898-71T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 9/21 | chr2 | 48471016 | ||||||
chr2:48471466
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1088+99C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471466 | ||||||
chr2:48471469
|
A | G | 2 | a0001c0003t0028g0334a0001c0003t0028g0335 | 2 | HG01884.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1088+102A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471469 | ||||||
chr2:48471512
|
A | G | 2 | a0001c0001t0007g0125a0001c0001t0007g0126 | 2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1088+145A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471512 | ||||||
chr2:48471754
|
T | C | 1 | a0001c0001t0020g0340 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1088+387T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471754 | ||||||
chr2:48471765
|
C | A | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088+398C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471765 | ||||||
chr2:48471867
|
A | C | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1088+500A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471867 | ||||||
chr2:48471881
|
T | C | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1088+514T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471881 | ||||||
chr2:48471989
|
C | A | 1 | a0001c0001t0001g0309 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1088+622C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471989 | ||||||
chr2:48471999
|
G | A | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+632G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48471999 | ||||||
chr2:48472026
|
A | G | 37 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(34): Show | 37 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1088+659A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472026 | ||||||
chr2:48472068
|
C | T | 10 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02055.hp1 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1088+701C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472068 | ||||||
chr2:48472239
|
C | CA | 36 | a0001c0001t0001g0176a0001c0001t0001g0195a0001c0001t0001g0210others(33): Show | 36 | HG00438.hp1 HG01175.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1088+901dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48472239 | |||||
chr2:48472239
|
CA | C | 41 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0148others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1088+901delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48472239 | |||||
chr2:48472239
|
CAA | C | 134 | a0001c0001t0001g0098a0001c0001t0001g0104a0001c0001t0001g0112others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1088+900_1088+901d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48472239 | |||||
chr2:48472239
|
CAAA | C | 6 | a0001c0001t0002g0074a0001c0001t0010g0109a0001c0003t0034g0152others(3): Show | 6 | HG02723.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1088+899_1088+901d others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48472239 | |||||
chr2:48472239
|
CAAAA | C | 11 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0075others(8): Show | 11 | HG00738.hp1 HG01109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1088+898_1088+901d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48472239 | |||||
chr2:48472287
|
G | A | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1088+920G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472287 | ||||||
chr2:48472302
|
T | C | 1 | a0001c0001t0002g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1088+935T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472302 | ||||||
chr2:48472607
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1088+1240C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472607 | ||||||
chr2:48472616
|
A | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088+1249A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472616 | ||||||
chr2:48472620
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0006g0001a0001c0001t0006g0181others(2): Show | 5 | HG01123.hp1 HG01192.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1088+1253C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472620 | ||||||
chr2:48472778
|
T | C | 12 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(9): Show | 12 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1088+1411T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472778 | ||||||
chr2:48472828
|
G | C | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1088+1461G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48472828 | ||||||
chr2:48472935
|
T | TA | 92 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(89): Show | 92 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1088+1582dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48472935 | |||||
chr2:48473003
|
TA | T | 10 | a0001c0001t0001g0319a0001c0001t0003g0039a0001c0001t0003g0059others(7): Show | 10 | HG00639.hp1 HG02258.hp1 HG03831.hp2 others(7): Show |
intron_variant | MODIFIER | c.1088+1651delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr2 | 48473003 | |||||
chr2:48473274
|
A | G | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1089-1409A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48473274 | ||||||
chr2:48473542
|
T | C | 1 | a0001c0001t0037g0268 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1089-1141T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48473542 | ||||||
chr2:48473669
|
A | C | 4 | a0001c0001t0014g0099a0001c0001t0014g0100a0001c0001t0014g0101others(1): Show | 4 | HG01433.hp2 HG02818.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-1014A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48473669 | ||||||
chr2:48473763
|
T | C | 1 | a0003c0008t0018g0324 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1089-920T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48473763 | ||||||
chr2:48473887
|
G | A | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1089-796G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48473887 | ||||||
chr2:48473996
|
A | G | 1 | a0001c0001t0020g0342 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1089-687A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48473996 | ||||||
chr2:48474108
|
C | G | 2 | a0001c0001t0002g0122a0001c0001t0002g0258 | 2 | HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1089-575C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474108 | ||||||
chr2:48474180
|
C | T | 1 | a0001c0001t0017g0326 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1089-503C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474180 | ||||||
chr2:48474243
|
C | T | 3 | a0003c0008t0018g0324a0003c0008t0018g0325a0004c0010t0018g0327 | 3 | HG03239.hp2 HG03516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1089-440C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474243 | ||||||
chr2:48474355
|
T | C | 12 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(9): Show | 12 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1089-328T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474355 | ||||||
chr2:48474384
|
A | T | 1 | a0001c0001t0006g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1089-299A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474384 | ||||||
chr2:48474482
|
G | A | 1 | a0001c0001t0002g0337 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1089-201G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474482 | ||||||
chr2:48474517
|
G | T | 1 | a0001c0001t0002g0277 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1089-166G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 11/21 | chr2 | 48474517 | ||||||
chr2:48474916
|
A | T | 1 | a0001c0001t0011g0263 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1225+97A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48474916 | ||||||
chr2:48475043
|
T | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(86): Show | 89 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1225+224T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475043 | ||||||
chr2:48475163
|
G | C | 3 | a0003c0008t0018g0324a0003c0008t0018g0325a0004c0010t0018g0327 | 3 | HG03239.hp2 HG03516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1225+344G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475163 | ||||||
chr2:48475260
|
G | A | 1 | a0001c0001t0004g0371 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1225+441G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475260 | ||||||
chr2:48475273
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1225+454A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475273 | ||||||
chr2:48475307
|
C | T | 7 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(4): Show | 7 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+488C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475307 | ||||||
chr2:48475323
|
A | C | 3 | a0001c0001t0013g0285a0001c0001t0027g0286a0001c0001t0027g0287 | 3 | HG00735.hp2 HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1225+504A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475323 | ||||||
chr2:48475496
|
G | A | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1225+677G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475496 | ||||||
chr2:48475498
|
A | G | 2 | a0001c0001t0004g0135a0001c0001t0004g0138 | 2 | NA19067.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1225+679A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475498 | ||||||
chr2:48475763
|
C | T | 1 | a0001c0002t0048g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1225+944C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475763 | ||||||
chr2:48475861
|
T | C | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(8): Show | 11 | HG00280.hp1 HG01070.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1225+1042T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475861 | ||||||
chr2:48475873
|
T | A | 1 | a0001c0001t0007g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1225+1054T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475873 | ||||||
chr2:48475975
|
T | A | 9 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(6): Show | 9 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1225+1156T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48475975 | ||||||
chr2:48476029
|
C | T | 2 | a0001c0001t0007g0227a0001c0001t0010g0168 | 2 | NA18949.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1225+1210C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48476029 | ||||||
chr2:48476217
|
C | A | 4 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(1): Show | 4 | HG01891.hp2 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+1398C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48476217 | ||||||
chr2:48476255
|
G | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1225+1436G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48476255 | ||||||
chr2:48476289
|
A | G | 1 | a0001c0001t0010g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1225+1470A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48476289 | ||||||
chr2:48476305
|
G | C | 3 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0051g0038 | 3 | HG00597.hp2 NA18977.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1225+1486G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48476305 | ||||||
chr2:48477109
|
T | C | 1 | a0001c0001t0051g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1225+2290T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477109 | ||||||
chr2:48477116
|
A | AT | 26 | a0001c0001t0001g0097a0001c0001t0001g0190a0001c0001t0001g0252others(23): Show | 26 | HG00280.hp2 HG00438.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1225+2321dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477116 | |||||
chr2:48477116
|
A | ATT | 76 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(73): Show | 76 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1225+2320_1225+232 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477116 | |||||
chr2:48477116
|
A | ATTT | 8 | a0001c0001t0001g0206a0001c0001t0001g0236a0001c0001t0001g0246others(5): Show | 8 | HG01175.hp2 HG01192.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1225+2319_1225+232 others(7): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477116 | |||||
chr2:48477116
|
AT | A | 7 | a0001c0001t0002g0150a0001c0001t0003g0026a0001c0001t0003g0067others(4): Show | 7 | HG00323.hp1 HG01515.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1225+2321delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477116 | |||||
chr2:48477451
|
C | T | 1 | a0001c0001t0047g0164 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1226-2473C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477451 | ||||||
chr2:48477576
|
A | C | 1 | a0001c0001t0003g0154 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1226-2348A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477576 | ||||||
chr2:48477580
|
C | G | 14 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(11): Show | 14 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1226-2344C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477580 | ||||||
chr2:48477654
|
G | A | 1 | a0001c0002t0001g0197 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1226-2270G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477654 | ||||||
chr2:48477667
|
C | CT | 89 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(86): Show | 89 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1226-2242dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477667 | |||||
chr2:48477667
|
CT | C | 7 | a0001c0001t0003g0067a0001c0001t0047g0164a0001c0003t0028g0334others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1226-2242delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477667 | |||||
chr2:48477667
|
CTT | C | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1226-2243_1226-224 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr2 | 48477667 | |||||
chr2:48477705
|
G | C | 1 | a0001c0001t0050g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1226-2219G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477705 | ||||||
chr2:48477752
|
T | C | 13 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(10): Show | 13 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1226-2172T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477752 | ||||||
chr2:48477838
|
C | T | 1 | a0001c0002t0002g0294 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1226-2086C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477838 | ||||||
chr2:48477954
|
G | T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226-1970G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48477954 | ||||||
chr2:48478079
|
T | C | 1 | a0001c0001t0025g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1226-1845T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478079 | ||||||
chr2:48478180
|
C | T | 1 | a0003c0008t0018g0325 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1226-1744C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478180 | ||||||
chr2:48478271
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1226-1653A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478271 | ||||||
chr2:48478302
|
C | G | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-1622C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478302 | ||||||
chr2:48478406
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0337 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-1518C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478406 | ||||||
chr2:48478740
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1226-1184C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478740 | ||||||
chr2:48478744
|
G | A | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1226-1180G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478744 | ||||||
chr2:48478753
|
A | G | 15 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(12): Show | 15 | HG00280.hp1 HG00738.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1226-1171A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478753 | ||||||
chr2:48478792
|
T | C | 5 | a0001c0001t0014g0099a0001c0001t0014g0100a0001c0001t0014g0101others(2): Show | 5 | HG01433.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226-1132T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478792 | ||||||
chr2:48478907
|
G | T | 3 | a0003c0008t0018g0324a0003c0008t0018g0325a0004c0010t0018g0327 | 3 | HG03239.hp2 HG03516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1226-1017G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478907 | ||||||
chr2:48478919
|
C | A | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1226-1005C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48478919 | ||||||
chr2:48479004
|
G | T | 8 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(5): Show | 8 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1226-920G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479004 | ||||||
chr2:48479116
|
C | T | 2 | a0001c0004t0009g0314a0001c0004t0009g0318 | 2 | HG01070.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1226-808C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479116 | ||||||
chr2:48479146
|
A | T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1226-778A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479146 | ||||||
chr2:48479270
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1226-654C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479270 | ||||||
chr2:48479302
|
G | A | 1 | a0001c0001t0006g0202 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1226-622G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479302 | ||||||
chr2:48479313
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0337 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1226-611C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479313 | ||||||
chr2:48479341
|
A | C | 1 | a0001c0001t0003g0037 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1226-583A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479341 | ||||||
chr2:48479790
|
G | A | 3 | a0001c0001t0013g0285a0001c0001t0027g0286a0001c0001t0027g0287 | 3 | HG00735.hp2 HG02004.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1226-134G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479790 | ||||||
chr2:48479804
|
A | G | 2 | a0001c0001t0006g0189a0001c0001t0007g0188 | 2 | HG02132.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1226-120A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479804 | ||||||
chr2:48479846
|
T | A | 1 | a0001c0001t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1226-78T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 12/21 | chr2 | 48479846 | ||||||
chr2:48480248
|
G | A | 3 | a0003c0008t0018g0324a0003c0008t0018g0325a0004c0010t0018g0327 | 3 | HG03239.hp2 HG03516.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1318+232G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48480248 | ||||||
chr2:48480411
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1318+395A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48480411 | ||||||
chr2:48480600
|
G | A | 5 | a0001c0001t0017g0326a0001c0003t0028g0334a0001c0003t0035g0332others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318+584G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48480600 | ||||||
chr2:48480702
|
G | C | 15 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.1318+686G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48480702 | ||||||
chr2:48480713
|
C | G | 17 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(14): Show | 17 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1318+697C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48480713 | ||||||
chr2:48480739
|
A | G | 1 | a0001c0001t0005g0047 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1318+723A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48480739 | ||||||
chr2:48481186
|
G | C | 1 | a0001c0001t0001g0186 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1318+1170G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481186 | ||||||
chr2:48481207
|
T | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1318+1191T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481207 | ||||||
chr2:48481458
|
A | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1318+1442A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481458 | ||||||
chr2:48481506
|
G | C | 7 | a0001c0001t0007g0269a0001c0001t0008g0264a0001c0001t0008g0265others(4): Show | 7 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.1318+1490G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481506 | ||||||
chr2:48481706
|
G | A | 12 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328others(9): Show | 12 | HG00738.hp1 HG01109.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1318+1690G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481706 | ||||||
chr2:48481712
|
A | G | 1 | a0001c0001t0007g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1318+1696A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481712 | ||||||
chr2:48481753
|
A | C | 6 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1318+1737A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481753 | ||||||
chr2:48481753
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(82): Show | 85 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1318+1737A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481753 | ||||||
chr2:48481869
|
T | A | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1318+1853T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481869 | ||||||
chr2:48481942
|
A | T | 1 | a0001c0001t0012g0229 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1318+1926A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48481942 | ||||||
chr2:48482062
|
C | A | 1 | a0001c0003t0041g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1318+2046C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482062 | ||||||
chr2:48482109
|
C | T | 1 | a0001c0001t0008g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1318+2093C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482109 | ||||||
chr2:48482176
|
A | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1318+2160A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482176 | ||||||
chr2:48482334
|
G | T | 1 | a0001c0001t0002g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1318+2318G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482334 | ||||||
chr2:48482527
|
T | C | 2 | a0001c0001t0004g0351a0001c0001t0004g0352 | 2 | HG02056.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1318+2511T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482527 | ||||||
chr2:48482614
|
A | C | 15 | a0001c0001t0002g0147a0001c0001t0002g0337a0001c0001t0006g0002others(12): Show | 15 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1318+2598A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482614 | ||||||
chr2:48482643
|
C | CTGT | 6 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(3): Show | 6 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1318+2629_1318+263 others(7): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48482643 | |||||
chr2:48482645
|
G | GT | 122 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(119): Show | 122 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1318+2647dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48482645 | |||||
chr2:48482719
|
A | G | 1 | a0001c0001t0012g0270 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1318+2703A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482719 | ||||||
chr2:48482745
|
A | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1318+2729A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482745 | ||||||
chr2:48482770
|
CT | C | 39 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(36): Show | 39 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1318+2762delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48482770 | |||||
chr2:48482809
|
T | C | 1 | a0001c0001t0010g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1318+2793T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482809 | ||||||
chr2:48482849
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1318+2833G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482849 | ||||||
chr2:48482885
|
A | C | 1 | a0001c0001t0005g0030 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1318+2869A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482885 | ||||||
chr2:48482916
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1318+2900C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48482916 | ||||||
chr2:48483117
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0002g0095others(1): Show | 4 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1318+3101C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483117 | ||||||
chr2:48483195
|
C | CT | 214 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(211): Show | 214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1318+3203dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48483195 | |||||
chr2:48483195
|
C | CTT | 38 | a0001c0001t0001g0176a0001c0001t0001g0193a0001c0001t0001g0201others(35): Show | 38 | HG01106.hp1 HG01106.hp2 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.1318+3202_1318+320 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48483195 | |||||
chr2:48483195
|
C | CTTTT | 19 | a0001c0001t0001g0112a0001c0001t0001g0117a0001c0001t0001g0148others(16): Show | 19 | HG00099.hp2 HG00323.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1318+3200_1318+320 others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48483195 | |||||
chr2:48483195
|
C | CTTTTT | 8 | a0001c0001t0001g0118a0001c0001t0002g0105a0001c0001t0002g0116others(5): Show | 8 | HG00438.hp2 HG01358.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1318+3199_1318+320 others(9): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48483195 | |||||
chr2:48483400
|
C | T | 25 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(22): Show | 25 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.1319-3231C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483400 | ||||||
chr2:48483442
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1319-3189C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483442 | ||||||
chr2:48483451
|
G | T | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1319-3180G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483451 | ||||||
chr2:48483567
|
G | A | 29 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(26): Show | 29 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.1319-3064G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483567 | ||||||
chr2:48483654
|
T | G | 1 | a0001c0001t0052g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1319-2977T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483654 | ||||||
chr2:48483719
|
C | T | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1319-2912C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483719 | ||||||
chr2:48483812
|
A | G | 12 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0182others(9): Show | 12 | NA18942.hp2 NA18968.hp1 NA18970.hp1 others(9): Show |
intron_variant | MODIFIER | c.1319-2819A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483812 | ||||||
chr2:48483879
|
G | A | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1319-2752G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483879 | ||||||
chr2:48483991
|
T | C | 1 | a0001c0014t0022g0350 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1319-2640T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483991 | ||||||
chr2:48483998
|
C | G | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1319-2633C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48483998 | ||||||
chr2:48484004
|
A | G | 1 | a0001c0013t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1319-2627A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484004 | ||||||
chr2:48484053
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0003g0041 | 2 | HG00621.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.1319-2578G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484053 | ||||||
chr2:48484180
|
G | A | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1319-2451G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484180 | ||||||
chr2:48484361
|
A | G | 2 | a0001c0001t0007g0269a0006c0011t0001g0103 | 2 | HG00099.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1319-2270A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484361 | ||||||
chr2:48484384
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1319-2247G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484384 | ||||||
chr2:48484514
|
CT | C | 7 | a0001c0001t0001g0206a0001c0001t0001g0209a0001c0001t0001g0228others(4): Show | 7 | HG00408.hp1 HG01175.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-2098delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48484514 | |||||
chr2:48484514
|
CTT | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(252): Show | 255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1319-2099_1319-209 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48484514 | |||||
chr2:48484621
|
A | G | 1 | a0003c0008t0018g0324 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1319-2010A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484621 | ||||||
chr2:48484765
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1319-1866G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484765 | ||||||
chr2:48484783
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1319-1848T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484783 | ||||||
chr2:48484825
|
A | T | 1 | a0001c0001t0003g0057 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1319-1806A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484825 | ||||||
chr2:48484860
|
A | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-1771A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484860 | ||||||
chr2:48484902
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0007g0096 | 3 | HG00735.hp1 HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1319-1729A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484902 | ||||||
chr2:48484975
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1319-1656T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48484975 | ||||||
chr2:48485029
|
A | AG | 290 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1319-1602_1319-160 others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485029 | ||||||
chr2:48485061
|
G | C | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1319-1570G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485061 | ||||||
chr2:48485097
|
T | C | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1319-1534T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485097 | ||||||
chr2:48485112
|
A | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1319-1519A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485112 | ||||||
chr2:48485228
|
G | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.1319-1403G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485228 | ||||||
chr2:48485307
|
TA | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(89): Show | 92 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1319-1313delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48485307 | |||||
chr2:48485410
|
G | C | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1319-1221G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485410 | ||||||
chr2:48485540
|
C | G | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1319-1091C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485540 | ||||||
chr2:48485677
|
T | C | 3 | a0001c0001t0002g0147a0001c0001t0002g0337a0001c0001t0003g0007 | 3 | HG02055.hp1 HG03098.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1319-954T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485677 | ||||||
chr2:48485784
|
A | G | 1 | a0001c0001t0049g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1319-847A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485784 | ||||||
chr2:48485823
|
T | G | 32 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1319-808T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485823 | ||||||
chr2:48485862
|
T | TTAACTAA others(19): Show |
2 | a0001c0001t0003g0198a0001c0003t0045g0159 | 2 | HG03453.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1319-714_1319-689d others(28): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48485862 | |||||
chr2:48485862
|
TTAACTAA others(19): Show |
T | 287 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.1319-714_1319-689d others(28): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr2 | 48485862 | |||||
chr2:48485967
|
T | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-664T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48485967 | ||||||
chr2:48486081
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0003g0021 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1319-550A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486081 | ||||||
chr2:48486094
|
G | A | 1 | a0001c0001t0006g0157 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1319-537G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486094 | ||||||
chr2:48486120
|
C | G | 2 | a0001c0001t0002g0307a0001c0001t0015g0344 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1319-511C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486120 | ||||||
chr2:48486201
|
C | T | 17 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(14): Show | 17 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1319-430C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486201 | ||||||
chr2:48486363
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02602.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1319-268A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486363 | ||||||
chr2:48486484
|
C | T | 17 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(14): Show | 17 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1319-147C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486484 | ||||||
chr2:48486590
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1319-41T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 13/21 | chr2 | 48486590 | ||||||
chr2:48486801
|
A | G | 11 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0128others(8): Show | 11 | HG01074.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+43A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48486801 | ||||||
chr2:48486833
|
G | C | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+75G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48486833 | ||||||
chr2:48486990
|
G | T | 1 | a0001c0001t0002g0310 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1446+232G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48486990 | ||||||
chr2:48487150
|
A | G | 4 | a0001c0001t0003g0037a0001c0001t0003g0050a0001c0007t0031g0009others(1): Show | 4 | HG01993.hp1 HG02273.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+392A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487150 | ||||||
chr2:48487170
|
G | C | 14 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(11): Show | 14 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1446+412G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487170 | ||||||
chr2:48487188
|
C | T | 1 | a0001c0002t0002g0299 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1446+430C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487188 | ||||||
chr2:48487290
|
G | A | 12 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(9): Show | 12 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1446+532G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487290 | ||||||
chr2:48487355
|
G | A | 14 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(11): Show | 14 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.1446+597G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487355 | ||||||
chr2:48487448
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1446+690C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487448 | ||||||
chr2:48487564
|
A | C | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02040.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1446+806A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487564 | ||||||
chr2:48487657
|
T | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(294): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1446+899T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487657 | ||||||
chr2:48487710
|
G | A | 1 | a0001c0001t0004g0338 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1446+952G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487710 | ||||||
chr2:48487760
|
C | CA | 21 | a0001c0001t0001g0104a0001c0001t0001g0223a0001c0001t0002g0204others(18): Show | 21 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.1446+1020dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr2 | 48487760 | |||||
chr2:48487760
|
CA | C | 6 | a0001c0001t0001g0219a0001c0001t0002g0094a0001c0001t0003g0062others(3): Show | 6 | HG01257.hp2 NA18962.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1446+1020delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr2 | 48487760 | |||||
chr2:48487799
|
T | G | 36 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(33): Show | 36 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1446+1041T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487799 | ||||||
chr2:48487910
|
G | A | 1 | a0001c0001t0007g0005 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1446+1152G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48487910 | ||||||
chr2:48488033
|
A | G | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1446+1275A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488033 | ||||||
chr2:48488135
|
C | T | 3 | a0001c0001t0011g0167a0001c0001t0011g0225a0001c0001t0011g0226 | 3 | NA18943.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1446+1377C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488135 | ||||||
chr2:48488142
|
T | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1446+1384T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488142 | ||||||
chr2:48488143
|
A | G | 17 | a0001c0001t0004g0086a0001c0001t0004g0347a0001c0001t0004g0349others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1446+1385A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488143 | ||||||
chr2:48488266
|
C | T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+1508C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488266 | ||||||
chr2:48488273
|
C | T | 1 | a0001c0001t0020g0341 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1446+1515C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488273 | ||||||
chr2:48488293
|
A | G | 1 | a0001c0003t0044g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1446+1535A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488293 | ||||||
chr2:48488344
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1446+1586T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488344 | ||||||
chr2:48488667
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1446+1909C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488667 | ||||||
chr2:48488921
|
T | C | 3 | a0001c0001t0005g0042a0001c0001t0005g0045a0001c0001t0033g0043 | 3 | NA18939.hp2 NA18941.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1447-2097T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488921 | ||||||
chr2:48488976
|
CTA | C | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-2035_1447-203 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr2 | 48488976 | |||||
chr2:48488982
|
A | G | 1 | a0001c0001t0007g0227 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1447-2036A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488982 | ||||||
chr2:48488988
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0193 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1447-2030C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48488988 | ||||||
chr2:48489074
|
C | T | 1 | a0001c0001t0006g0169 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1447-1944C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489074 | ||||||
chr2:48489344
|
T | C | 1 | a0002c0006t0003g0320 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1447-1674T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489344 | ||||||
chr2:48489367
|
G | A | 1 | a0001c0001t0051g0038 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1447-1651G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489367 | ||||||
chr2:48489480
|
A | C | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-1538A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489480 | ||||||
chr2:48489517
|
A | G | 1 | a0001c0007t0031g0009 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1447-1501A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489517 | ||||||
chr2:48489532
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.1447-1486G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489532 | ||||||
chr2:48489664
|
G | A | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1447-1354G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489664 | ||||||
chr2:48489683
|
G | T | 250 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0097others(247): Show | 250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.1447-1335G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489683 | ||||||
chr2:48489739
|
G | C | 153 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.1447-1279G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489739 | ||||||
chr2:48489740
|
T | C | 1 | a0001c0001t0006g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1447-1278T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489740 | ||||||
chr2:48489873
|
G | A | 26 | a0001c0001t0013g0284a0001c0001t0013g0285a0001c0001t0013g0288others(23): Show | 26 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1447-1145G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489873 | ||||||
chr2:48489881
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1447-1137T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489881 | ||||||
chr2:48489881
|
T | C | 3 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0051g0038 | 3 | HG00597.hp2 NA18977.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1447-1137T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48489881 | ||||||
chr2:48490176
|
G | A | 83 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1447-842G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490176 | ||||||
chr2:48490218
|
CA | C | 133 | a0001c0001t0001g0104a0001c0001t0001g0290a0001c0001t0001g0291others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1447-779delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr2 | 48490218 | |||||
chr2:48490218
|
CAA | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0112others(133): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1447-780_1447-779d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr2 | 48490218 | |||||
chr2:48490218
|
CAAAAAAA others(3): Show |
C | 15 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(12): Show | 15 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1447-788_1447-779d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr2 | 48490218 | |||||
chr2:48490331
|
G | T | 12 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(9): Show | 12 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1447-687G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490331 | ||||||
chr2:48490512
|
C | A | 2 | a0001c0001t0008g0134a0001c0001t0008g0336 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1447-506C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490512 | ||||||
chr2:48490591
|
A | G | 194 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(191): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1447-427A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490591 | ||||||
chr2:48490605
|
C | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1447-413C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490605 | ||||||
chr2:48490607
|
A | G | 1 | a0001c0003t0028g0334 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1447-411A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490607 | ||||||
chr2:48490668
|
G | A | 291 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1447-350G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490668 | ||||||
chr2:48490864
|
C | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(80): Show | 83 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.1447-154C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490864 | ||||||
chr2:48490962
|
T | G | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1447-56T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 14/21 | chr2 | 48490962 | ||||||
chr2:48491222
|
C | G | 1 | a0001c0001t0004g0354 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1599+52C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48491222 | ||||||
chr2:48491299
|
G | T | 4 | a0001c0002t0001g0296a0001c0002t0002g0294a0001c0002t0002g0295others(1): Show | 4 | HG00140.hp1 HG01167.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1599+129G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48491299 | ||||||
chr2:48491387
|
G | C | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1599+217G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48491387 | ||||||
chr2:48491535
|
G | A | 2 | a0001c0001t0002g0105a0001c0001t0002g0106 | 2 | HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1599+365G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48491535 | ||||||
chr2:48491539
|
CA | C | 37 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1599+378delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48491539 | |||||
chr2:48491548
|
A | G | 249 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(246): Show | 249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.1599+378A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48491548 | ||||||
chr2:48491550
|
A | G | 37 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(34): Show | 37 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1599+380A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48491550 | ||||||
chr2:48491557
|
AAAG | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(245): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1599+389_1599+391d others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48491557 | |||||
chr2:48492248
|
C | T | 1 | a0001c0001t0043g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1599+1078C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48492248 | ||||||
chr2:48492292
|
ATTT | A | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1599+1125_1599+112 others(7): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48492292 | |||||
chr2:48492388
|
A | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+1218A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48492388 | ||||||
chr2:48492597
|
T | C | 11 | a0001c0001t0002g0020a0001c0001t0003g0021a0001c0001t0013g0284others(8): Show | 11 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1599+1427T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48492597 | ||||||
chr2:48492654
|
G | A | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1599+1484G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48492654 | ||||||
chr2:48492721
|
C | T | 1 | a0001c0001t0012g0199 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1599+1551C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48492721 | ||||||
chr2:48492987
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1599+1817A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48492987 | ||||||
chr2:48493011
|
C | CT | 67 | a0001c0001t0001g0019a0001c0001t0001g0098a0001c0001t0001g0112others(64): Show | 67 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1599+1864dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48493011 | |||||
chr2:48493011
|
C | CTT | 7 | a0001c0001t0003g0143a0001c0001t0007g0082a0001c0001t0007g0121others(4): Show | 7 | HG00438.hp2 HG02723.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1599+1863_1599+186 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48493011 | |||||
chr2:48493011
|
CT | C | 6 | a0001c0001t0001g0084a0001c0001t0002g0006a0001c0001t0002g0094others(3): Show | 6 | HG00639.hp2 HG01123.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1599+1864delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48493011 | |||||
chr2:48493196
|
G | A | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1599+2026G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493196 | ||||||
chr2:48493308
|
C | T | 1 | a0001c0001t0010g0238 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1599+2138C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493308 | ||||||
chr2:48493375
|
T | C | 7 | a0001c0001t0007g0003a0001c0001t0007g0004a0001c0001t0007g0005others(4): Show | 7 | HG02451.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1599+2205T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493375 | ||||||
chr2:48493384
|
G | A | 4 | a0001c0001t0007g0125a0001c0001t0007g0126a0001c0001t0007g0127others(1): Show | 4 | HG02451.hp2 HG02970.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1599+2214G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493384 | ||||||
chr2:48493433
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1600-2246G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493433 | ||||||
chr2:48493492
|
G | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1600-2187G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493492 | ||||||
chr2:48493597
|
CATAA | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(245): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.1600-2071_1600-206 others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48493597 | |||||
chr2:48493772
|
A | G | 2 | a0001c0001t0008g0265a0001c0001t0008g0266 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1600-1907A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493772 | ||||||
chr2:48493848
|
T | A | 3 | a0001c0001t0007g0121a0001c0001t0032g0255a0001c0001t0032g0256 | 3 | NA18962.hp1 NA19074.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1600-1831T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493848 | ||||||
chr2:48493848
|
T | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1600-1831T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493848 | ||||||
chr2:48493883
|
C | T | 1 | a0001c0002t0002g0306 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1600-1796C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48493883 | ||||||
chr2:48494058
|
C | CA | 127 | a0001c0001t0001g0001a0001c0001t0001g0098a0001c0001t0001g0104others(124): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1600-1598dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494058 | |||||
chr2:48494058
|
C | CAA | 28 | a0001c0001t0001g0148a0001c0001t0001g0178a0001c0001t0001g0180others(25): Show | 28 | HG00099.hp2 HG00438.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1600-1599_1600-159 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494058 | |||||
chr2:48494058
|
CA | C | 94 | a0001c0001t0001g0019a0001c0001t0001g0176a0001c0001t0001g0190others(91): Show | 94 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1600-1598delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494058 | |||||
chr2:48494169
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1600-1510G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48494169 | ||||||
chr2:48494208
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1600-1471C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48494208 | ||||||
chr2:48494239
|
C | CA | 12 | a0001c0001t0001g0163a0001c0001t0001g0253a0001c0001t0003g0037others(9): Show | 12 | HG01993.hp1 HG02071.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1600-1401dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CA | C | 26 | a0001c0001t0001g0160a0001c0001t0001g0249a0001c0001t0003g0025others(23): Show | 26 | HG00423.hp1 HG00544.hp2 HG01975.hp1 others(23): Show |
intron_variant | MODIFIER | c.1600-1401delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(1): Show |
C | 19 | a0001c0001t0001g0183a0001c0001t0001g0231a0001c0001t0001g0239others(16): Show | 19 | HG01192.hp2 HG01884.hp1 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.1600-1408_1600-140 others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(2): Show |
C | 100 | a0001c0001t0001g0001a0001c0001t0001g0098a0001c0001t0001g0166others(97): Show | 100 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.1600-1409_1600-140 others(13): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(3): Show |
C | 106 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0097others(103): Show | 106 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1600-1410_1600-140 others(14): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(4): Show |
C | 36 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(33): Show | 36 | HG00140.hp1 HG00597.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.1600-1411_1600-140 others(15): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0150a0001c0001t0029g0328 | 2 | HG00323.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1600-1412_1600-140 others(16): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0003g0016a0001c0001t0025g0161 | 2 | NA18988.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1600-1417_1600-140 others(21): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(12): Show |
C | 24 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0122others(21): Show | 24 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1600-1419_1600-140 others(23): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494239
|
CAAAAAAA others(15): Show |
C | 1 | a0001c0005t0030g0011 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1600-1422_1600-140 others(26): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494239 | |||||
chr2:48494411
|
TTTTA | T | 213 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0097others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1600-1240_1600-123 others(8): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr2 | 48494411 | |||||
chr2:48494604
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1600-1075C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48494604 | ||||||
chr2:48494782
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(285): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.1600-897A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48494782 | ||||||
chr2:48494926
|
C | A | 1 | a0001c0001t0002g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1600-753C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48494926 | ||||||
chr2:48494972
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1600-707C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48494972 | ||||||
chr2:48495132
|
A | G | 1 | a0002c0006t0003g0322 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1600-547A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495132 | ||||||
chr2:48495262
|
G | A | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1600-417G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495262 | ||||||
chr2:48495364
|
C | T | 1 | a0001c0001t0002g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1600-315C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495364 | ||||||
chr2:48495435
|
C | T | 34 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(31): Show | 34 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1600-244C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495435 | ||||||
chr2:48495493
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0258 | 2 | HG00741.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1600-186C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495493 | ||||||
chr2:48495531
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0242 | 2 | HG01074.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1600-148G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495531 | ||||||
chr2:48495539
|
G | A | 6 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(3): Show | 6 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1600-140G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495539 | ||||||
chr2:48495595
|
G | A | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1600-84G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495595 | ||||||
chr2:48495616
|
T | C | 158 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0097others(155): Show | 158 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1600-63T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495616 | ||||||
chr2:48495668
|
T | G | 3 | a0001c0005t0019g0013a0001c0005t0019g0014a0001c0005t0036g0012 | 3 | HG00738.hp1 HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1600-11T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 15/21 | chr2 | 48495668 | ||||||
chr2:48495855
|
G | C | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1692+84G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48495855 | ||||||
chr2:48495905
|
A | C | 1 | a0001c0003t0028g0335 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1692+134A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48495905 | ||||||
chr2:48495927
|
T | G | 5 | a0001c0001t0007g0003a0001c0001t0007g0004a0001c0001t0007g0005others(2): Show | 5 | HG02647.hp1 HG02896.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1692+156T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48495927 | ||||||
chr2:48495965
|
G | A | 2 | a0001c0001t0002g0257a0001c0001t0040g0274 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1692+194G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48495965 | ||||||
chr2:48496044
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1692+273G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496044 | ||||||
chr2:48496081
|
G | T | 32 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(29): Show | 32 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.1692+310G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496081 | ||||||
chr2:48496206
|
G | C | 2 | a0001c0001t0003g0155a0001c0001t0003g0156 | 2 | HG02040.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1692+435G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496206 | ||||||
chr2:48496215
|
GA | G | 5 | a0001c0001t0006g0087a0001c0001t0006g0088a0001c0001t0006g0090others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692+454delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48496215 | |||||
chr2:48496226
|
T | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02486.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1692+455T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496226 | ||||||
chr2:48496257
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0002g0094 | 2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1692+486G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496257 | ||||||
chr2:48496377
|
C | A | 38 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(35): Show | 38 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1692+606C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496377 | ||||||
chr2:48496400
|
C | T | 9 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(6): Show | 9 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1692+629C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496400 | ||||||
chr2:48496413
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1692+642G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496413 | ||||||
chr2:48496470
|
G | GT | 40 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(37): Show | 40 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1692+714dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48496470 | |||||
chr2:48496470
|
GT | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(239): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.1692+714delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48496470 | |||||
chr2:48496528
|
T | C | 45 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1692+757T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496528 | ||||||
chr2:48496598
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1692+827G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496598 | ||||||
chr2:48496660
|
G | C | 1 | a0001c0001t0005g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1692+889G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496660 | ||||||
chr2:48496665
|
G | A | 1 | a0001c0001t0007g0276 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1692+894G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496665 | ||||||
chr2:48496708
|
T | TC | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1692+941dupC | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48496708 | |||||
chr2:48496726
|
CAAAGTGC others(10): Show |
C | 1 | a0001c0001t0004g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1692+956_1692+972d others(19): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496726 | ||||||
chr2:48496793
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1692+1022C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496793 | ||||||
chr2:48496820
|
T | A | 1 | a0001c0001t0007g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1692+1049T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496820 | ||||||
chr2:48496835
|
C | T | 1 | a0001c0001t0004g0338 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1692+1064C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496835 | ||||||
chr2:48496893
|
G | C | 160 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0097others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1692+1122G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496893 | ||||||
chr2:48496935
|
G | C | 1 | a0001c0001t0006g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1692+1164G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496935 | ||||||
chr2:48496936
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1692+1165C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48496936 | ||||||
chr2:48497070
|
A | G | 35 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(32): Show | 35 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.1692+1299A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497070 | ||||||
chr2:48497273
|
A | G | 1 | a0001c0001t0001g0319 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1693-1220A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497273 | ||||||
chr2:48497366
|
C | G | 37 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(34): Show | 37 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1693-1127C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497366 | ||||||
chr2:48497432
|
C | G | 2 | a0001c0001t0004g0135a0001c0001t0004g0138 | 2 | NA19067.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1693-1061C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497432 | ||||||
chr2:48497603
|
A | T | 160 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0097others(157): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1693-890A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497603 | ||||||
chr2:48497615
|
A | G | 3 | a0001c0003t0045g0159a0001c0007t0031g0009a0001c0007t0031g0015 | 3 | HG02717.hp1 HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1693-878A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497615 | ||||||
chr2:48497649
|
C | G | 1 | a0001c0001t0005g0030 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1693-844C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497649 | ||||||
chr2:48497651
|
A | AT | 19 | a0001c0001t0001g0223a0001c0001t0001g0239a0001c0001t0002g0073others(16): Show | 19 | HG02071.hp1 HG02258.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.1693-825dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48497651 | |||||
chr2:48497651
|
AT | A | 7 | a0001c0001t0001g0160a0001c0001t0006g0221a0001c0003t0034g0152others(4): Show | 7 | HG01975.hp1 HG02717.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693-825delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48497651 | |||||
chr2:48497774
|
C | T | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1693-719C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497774 | ||||||
chr2:48497776
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1693-717C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497776 | ||||||
chr2:48497893
|
A | C | 5 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0002g0094others(2): Show | 5 | HG00639.hp2 HG00735.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693-600A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497893 | ||||||
chr2:48497897
|
C | T | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1693-596C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497897 | ||||||
chr2:48497943
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1693-550G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48497943 | ||||||
chr2:48498186
|
A | G | 33 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1693-307A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498186 | ||||||
chr2:48498268
|
T | G | 54 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(51): Show | 54 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1693-225T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498268 | ||||||
chr2:48498276
|
G | GT | 131 | a0001c0001t0001g0001a0001c0001t0001g0084a0001c0001t0001g0097others(128): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1693-206dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr2 | 48498276 | |||||
chr2:48498292
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1693-201C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498292 | ||||||
chr2:48498322
|
G | C | 1 | a0001c0001t0029g0329 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1693-171G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498322 | ||||||
chr2:48498424
|
G | A | 12 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(9): Show | 12 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1693-69G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498424 | ||||||
chr2:48498428
|
G | C | 1 | a0001c0003t0028g0334 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1693-65G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498428 | ||||||
chr2:48498471
|
C | T | 145 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0097others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1693-22C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 16/21 | chr2 | 48498471 | ||||||
chr2:48498772
|
T | G | 3 | a0001c0001t0017g0330a0001c0001t0017g0331a0001c0001t0029g0328 | 3 | HG01891.hp2 HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1935+37T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48498772 | ||||||
chr2:48498793
|
C | G | 1 | a0003c0008t0018g0324 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1935+58C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48498793 | ||||||
chr2:48499132
|
T | G | 1 | a0001c0001t0004g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1935+397T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499132 | ||||||
chr2:48499220
|
T | A | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+485T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499220 | ||||||
chr2:48499553
|
G | C | 294 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1935+818G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499553 | ||||||
chr2:48499604
|
A | G | 1 | a0001c0001t0006g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1935+869A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499604 | ||||||
chr2:48499614
|
C | A | 8 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(5): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+879C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499614 | ||||||
chr2:48499623
|
C | T | 5 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+888C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499623 | ||||||
chr2:48499647
|
A | C | 3 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0012g0261 | 3 | HG00741.hp1 HG01070.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1935+912A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499647 | ||||||
chr2:48499654
|
G | A | 5 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159others(2): Show | 5 | HG02717.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+919G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499654 | ||||||
chr2:48499708
|
A | T | 8 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(5): Show | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+973A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48499708 | ||||||
chr2:48500141
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1935+1406C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500141 | ||||||
chr2:48500384
|
T | G | 1 | a0001c0001t0007g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1935+1649T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500384 | ||||||
chr2:48500401
|
C | T | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1935+1666C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500401 | ||||||
chr2:48500423
|
A | G | 1 | a0001c0001t0004g0369 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1935+1688A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500423 | ||||||
chr2:48500489
|
A | G | 9 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(6): Show | 9 | HG02258.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1935+1754A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500489 | ||||||
chr2:48500523
|
A | G | 1 | a0001c0001t0029g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1935+1788A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500523 | ||||||
chr2:48500841
|
G | A | 1 | a0001c0001t0052g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1935+2106G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500841 | ||||||
chr2:48500850
|
A | T | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1935+2115A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500850 | ||||||
chr2:48500873
|
C | T | 1 | a0001c0001t0015g0344 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1935+2138C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500873 | ||||||
chr2:48500877
|
C | G | 1 | a0001c0003t0044g0308 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1935+2142C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500877 | ||||||
chr2:48500911
|
C | CA | 41 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(38): Show | 41 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1935+2185dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48500911 | |||||
chr2:48500921
|
C | A | 295 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1935+2186C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500921 | ||||||
chr2:48500922
|
C | A | 2 | a0001c0001t0002g0147a0001c0001t0002g0337 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1935+2187C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48500922 | ||||||
chr2:48501086
|
G | A | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1935+2351G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501086 | ||||||
chr2:48501171
|
A | G | 33 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0117others(30): Show | 33 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1935+2436A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501171 | ||||||
chr2:48501269
|
G | T | 1 | a0001c0001t0001g0319 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1935+2534G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501269 | ||||||
chr2:48501382
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1935+2647C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501382 | ||||||
chr2:48501402
|
G | A | 4 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0007t0031g0009others(1): Show | 4 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+2667G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501402 | ||||||
chr2:48501475
|
A | G | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1935+2740A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501475 | ||||||
chr2:48501624
|
A | G | 1 | a0001c0001t0004g0354 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1935+2889A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501624 | ||||||
chr2:48501665
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1935+2930C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501665 | ||||||
chr2:48501843
|
C | G | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1935+3108C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501843 | ||||||
chr2:48501928
|
G | A | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0239others(1): Show | 4 | HG02071.hp1 NA18747.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1935+3193G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501928 | ||||||
chr2:48501986
|
A | G | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1935+3251A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48501986 | ||||||
chr2:48502026
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0235 | 2 | NA18991.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1935+3291A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502026 | ||||||
chr2:48502168
|
C | G | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1936-3396C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502168 | ||||||
chr2:48502388
|
G | T | 1 | a0001c0001t0026g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1936-3176G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502388 | ||||||
chr2:48502400
|
T | TAAAAAGA others(317): Show |
1 | a0001c0003t0034g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1936-3156_1936-315 others(328): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502400 | |||||
chr2:48502400
|
T | TAAAAAGA others(318): Show |
1 | a0001c0003t0034g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1936-3156_1936-315 others(329): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502400 | |||||
chr2:48502400
|
T | TAAAAAGA others(297): Show |
1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1936-3156_1936-315 others(308): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502400 | |||||
chr2:48502400
|
T | TAAAAAGA others(301): Show |
5 | a0001c0003t0028g0334a0001c0003t0035g0332a0001c0003t0035g0333others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-3156_1936-315 others(312): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502400 | |||||
chr2:48502400
|
T | TAAAAAGA others(302): Show |
1 | a0001c0003t0028g0335 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1936-3156_1936-315 others(313): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502400 | |||||
chr2:48502462
|
C | A | 1 | a0001c0001t0003g0198 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1936-3102C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502462 | ||||||
chr2:48502615
|
G | A | 9 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1936-2949G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502615 | ||||||
chr2:48502671
|
C | G | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1936-2893C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502671 | ||||||
chr2:48502676
|
C | CT | 117 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0166others(114): Show | 117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1936-2866dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502676 | |||||
chr2:48502676
|
C | CTT | 9 | a0001c0001t0001g0175a0001c0001t0001g0236a0001c0001t0002g0196others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1936-2867_1936-286 others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48502676 | |||||
chr2:48502680
|
T | C | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1936-2884T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502680 | ||||||
chr2:48502712
|
G | A | 50 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(47): Show | 50 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1936-2852G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502712 | ||||||
chr2:48502773
|
C | T | 1 | a0001c0001t0027g0287 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1936-2791C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502773 | ||||||
chr2:48502781
|
C | T | 2 | a0001c0001t0008g0085a0001c0001t0010g0115 | 2 | HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1936-2783C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502781 | ||||||
chr2:48502805
|
C | G | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-2759C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502805 | ||||||
chr2:48502817
|
A | G | 1 | a0001c0003t0035g0332 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1936-2747A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502817 | ||||||
chr2:48502870
|
C | T | 3 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0045g0159 | 3 | HG03225.hp2 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1936-2694C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502870 | ||||||
chr2:48502882
|
T | G | 18 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1936-2682T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502882 | ||||||
chr2:48502887
|
A | G | 8 | a0001c0001t0001g0166a0001c0001t0001g0207a0001c0001t0001g0235others(5): Show | 8 | HG01074.hp1 HG01952.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1936-2677A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502887 | ||||||
chr2:48502987
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1936-2577T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48502987 | ||||||
chr2:48503015
|
G | A | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1936-2549G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503015 | ||||||
chr2:48503129
|
A | G | 1 | a0001c0001t0002g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1936-2435A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503129 | ||||||
chr2:48503160
|
A | T | 7 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936-2404A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503160 | ||||||
chr2:48503272
|
T | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1936-2292T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503272 | ||||||
chr2:48503342
|
T | A | 1 | a0001c0001t0026g0063 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1936-2222T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503342 | ||||||
chr2:48503364
|
C | T | 1 | a0001c0001t0040g0274 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1936-2200C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503364 | ||||||
chr2:48503372
|
A | G | 1 | a0001c0001t0026g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1936-2192A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503372 | ||||||
chr2:48503435
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0235 | 2 | NA18991.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1936-2129T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503435 | ||||||
chr2:48503527
|
T | C | 9 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1936-2037T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503527 | ||||||
chr2:48503607
|
A | G | 1 | a0001c0002t0002g0299 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1936-1957A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503607 | ||||||
chr2:48503743
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1936-1821C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503743 | ||||||
chr2:48503744
|
G | A | 1 | a0001c0003t0028g0334 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1936-1820G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503744 | ||||||
chr2:48503810
|
G | A | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-1754G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503810 | ||||||
chr2:48503840
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1936-1724C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503840 | ||||||
chr2:48503908
|
G | A | 5 | a0001c0005t0019g0010a0001c0005t0019g0013a0001c0005t0019g0014others(2): Show | 5 | HG00738.hp1 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1936-1656G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503908 | ||||||
chr2:48503946
|
A | G | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG00621.hp2 HG02040.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1936-1618A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503946 | ||||||
chr2:48503952
|
C | CA | 305 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1936-1596dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48503952 | |||||
chr2:48503974
|
C | G | 7 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936-1590C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48503974 | ||||||
chr2:48504148
|
T | G | 1 | a0001c0001t0043g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1936-1416T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504148 | ||||||
chr2:48504253
|
C | T | 1 | a0001c0001t0005g0048 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1936-1311C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504253 | ||||||
chr2:48504407
|
G | C | 18 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.1936-1157G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504407 | ||||||
chr2:48504510
|
G | A | 1 | a0001c0001t0004g0354 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1936-1054G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504510 | ||||||
chr2:48504523
|
C | A | 3 | a0002c0006t0003g0320a0002c0006t0003g0321a0002c0006t0003g0322 | 3 | HG02615.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1936-1041C>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504523 | ||||||
chr2:48504534
|
G | A | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936-1030G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504534 | ||||||
chr2:48504566
|
G | A | 137 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0104others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.1936-998G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504566 | ||||||
chr2:48504596
|
G | A | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1936-968G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504596 | ||||||
chr2:48504642
|
GAAAC | G | 13 | a0001c0002t0001g0296a0001c0002t0002g0294a0001c0002t0002g0295others(10): Show | 13 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1936-910_1936-907d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48504642 | |||||
chr2:48504654
|
C | CA | 8 | a0001c0001t0016g0363a0001c0004t0009g0312a0001c0004t0009g0313others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1936-901dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr2 | 48504654 | |||||
chr2:48504658
|
A | C | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-906A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504658 | ||||||
chr2:48504797
|
G | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1936-767G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504797 | ||||||
chr2:48504860
|
G | C | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1936-704G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48504860 | ||||||
chr2:48505276
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1936-288C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48505276 | ||||||
chr2:48505391
|
A | T | 1 | a0001c0001t0002g0074 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1936-173A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48505391 | ||||||
chr2:48505394
|
C | G | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-170C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48505394 | ||||||
chr2:48505472
|
G | A | 2 | a0001c0001t0017g0330a0001c0001t0017g0331 | 2 | HG01891.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1936-92G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48505472 | ||||||
chr2:48505496
|
A | G | 1 | a0001c0001t0004g0365 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1936-68A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48505496 | ||||||
chr2:48505531
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0007g0243others(1): Show | 4 | HG00140.hp2 HG01106.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-33C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 17/21 | chr2 | 48505531 | ||||||
chr2:48505640
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | NA18943.hp1 NA18944.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1968+44G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48505640 | ||||||
chr2:48505672
|
C | G | 3 | a0001c0001t0011g0167a0001c0001t0011g0225a0001c0001t0011g0226 | 3 | NA18943.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1968+76C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48505672 | ||||||
chr2:48505759
|
A | G | 1 | a0001c0001t0007g0121 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1968+163A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48505759 | ||||||
chr2:48505805
|
A | G | 207 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.1968+209A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48505805 | ||||||
chr2:48506005
|
C | G | 1 | a0001c0001t0004g0349 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1968+409C>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506005 | ||||||
chr2:48506168
|
T | C | 14 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1968+572T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506168 | ||||||
chr2:48506186
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1968+590C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506186 | ||||||
chr2:48506239
|
G | A | 10 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1968+643G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506239 | ||||||
chr2:48506496
|
T | C | 12 | a0001c0001t0006g0002a0001c0001t0006g0083a0001c0001t0006g0123others(9): Show | 12 | HG01243.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1969-773T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506496 | ||||||
chr2:48506672
|
G | A | 1 | a0001c0001t0007g0269 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1969-597G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506672 | ||||||
chr2:48506693
|
C | T | 1 | a0001c0001t0002g0116 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1969-576C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506693 | ||||||
chr2:48506697
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1969-572G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506697 | ||||||
chr2:48506798
|
T | G | 1 | a0001c0001t0015g0362 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1969-471T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506798 | ||||||
chr2:48506806
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0201 | 2 | NA18990.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1969-463C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506806 | ||||||
chr2:48506944
|
C | CA | 9 | a0001c0001t0001g0201a0001c0001t0002g0196a0001c0001t0003g0060others(6): Show | 9 | HG01192.hp2 HG02080.hp2 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1969-305dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr2 | 48506944 | |||||
chr2:48506944
|
CA | C | 197 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1969-305delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr2 | 48506944 | |||||
chr2:48506944
|
CAA | C | 8 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0003t0035g0332others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1969-306_1969-305d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr2 | 48506944 | |||||
chr2:48506949
|
A | G | 2 | a0001c0001t0003g0025a0001c0001t0003g0026 | 2 | NA18962.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1969-320A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | chr2 | 48506949 | ||||||
chr2:48507192
|
C | CT | 11 | a0001c0001t0001g0180a0001c0001t0004g0352a0001c0001t0006g0241others(8): Show | 11 | HG00280.hp1 HG00408.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.1969-60dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr2 | 48507192 | |||||
chr2:48507192
|
CT | C | 27 | a0001c0001t0001g0291a0001c0001t0002g0020a0001c0001t0002g0070others(24): Show | 27 | HG01069.hp1 HG01069.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.1969-60delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr2 | 48507192 | |||||
chr2:48507437
|
G | A | 371 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(368): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.2085+52G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507437 | ||||||
chr2:48507459
|
A | C | 18 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2085+74A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507459 | ||||||
chr2:48507524
|
C | T | 4 | a0001c0002t0002g0300a0001c0002t0002g0301a0001c0002t0002g0302others(1): Show | 4 | HG00738.hp2 HG01106.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2085+139C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507524 | ||||||
chr2:48507586
|
A | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2085+201A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507586 | ||||||
chr2:48507634
|
T | C | 171 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(168): Show | 171 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.2085+249T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507634 | ||||||
chr2:48507668
|
G | A | 1 | a0001c0001t0008g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2085+283G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507668 | ||||||
chr2:48507708
|
T | G | 1 | a0007c0012t0007g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2085+323T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507708 | ||||||
chr2:48507749
|
C | CT | 58 | a0001c0001t0001g0084a0001c0001t0001g0160a0001c0001t0001g0162others(55): Show | 58 | HG00558.hp2 HG00639.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2085+398dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
C | CTT | 61 | a0001c0001t0001g0148a0001c0001t0001g0163a0001c0001t0001g0165others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.2085+397_2085+398d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
C | CTTT | 48 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0290others(45): Show | 48 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.2085+396_2085+398d others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
C | CTTTT | 15 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0003g0143others(12): Show | 15 | HG00735.hp2 HG01243.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2085+395_2085+398d others(6): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
CT | C | 45 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0170others(42): Show | 45 | HG00544.hp1 HG01074.hp2 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.2085+398delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
CTT | C | 41 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0174others(38): Show | 41 | HG00280.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.2085+397_2085+398d others(4): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
CTTT | C | 8 | a0001c0001t0001g0273a0001c0001t0002g0122a0001c0001t0002g0257others(5): Show | 8 | HG00099.hp2 HG00741.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.2085+396_2085+398d others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0005g0047 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2085+389_2085+398d others(12): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
CTTTTTTT others(8): Show |
C | 10 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2085+384_2085+398d others(17): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507749
|
CTTTTTTT others(10): Show |
C | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2085+382_2085+398d others(19): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48507749 | |||||
chr2:48507829
|
G | A | 1 | a0001c0001t0005g0048 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2085+444G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507829 | ||||||
chr2:48507846
|
A | T | 1 | a0001c0001t0037g0268 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2085+461A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507846 | ||||||
chr2:48507900
|
G | C | 1 | a0001c0001t0016g0361 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2085+515G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507900 | ||||||
chr2:48507914
|
C | T | 5 | a0001c0001t0005g0029a0001c0001t0005g0036a0001c0001t0005g0044others(2): Show | 5 | NA18945.hp1 NA18998.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2085+529C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48507914 | ||||||
chr2:48508078
|
T | TA | 10 | a0001c0001t0002g0196a0001c0001t0003g0060a0001c0003t0028g0334others(7): Show | 10 | HG01243.hp1 HG01884.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.2085+708dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48508078 | |||||
chr2:48508078
|
TA | T | 6 | a0001c0001t0001g0259a0001c0001t0001g0273a0001c0001t0002g0213others(3): Show | 6 | HG00741.hp1 HG01070.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2085+708delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr2 | 48508078 | |||||
chr2:48508116
|
T | G | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2085+731T>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508116 | ||||||
chr2:48508200
|
T | C | 1 | a0001c0004t0009g0317 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2085+815T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508200 | ||||||
chr2:48508348
|
T | C | 9 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2085+963T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508348 | ||||||
chr2:48508397
|
A | T | 2 | a0001c0001t0002g0020a0001c0001t0003g0021 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2085+1012A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508397 | ||||||
chr2:48508549
|
G | A | 1 | a0001c0001t0006g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2085+1164G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508549 | ||||||
chr2:48508550
|
G | C | 9 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2085+1165G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508550 | ||||||
chr2:48508800
|
A | C | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2086-1215A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508800 | ||||||
chr2:48508828
|
T | C | 1 | a0001c0001t0027g0286 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2086-1187T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508828 | ||||||
chr2:48508854
|
A | G | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2086-1161A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508854 | ||||||
chr2:48508940
|
G | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2086-1075G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48508940 | ||||||
chr2:48509045
|
A | G | 11 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2086-970A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509045 | ||||||
chr2:48509153
|
A | G | 2 | a0001c0001t0005g0027a0001c0001t0005g0028 | 2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2086-862A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509153 | ||||||
chr2:48509533
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2086-482C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509533 | ||||||
chr2:48509629
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2086-386C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509629 | ||||||
chr2:48509700
|
G | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0104others(31): Show | 34 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.2086-315G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509700 | ||||||
chr2:48509705
|
A | C | 9 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2086-310A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509705 | ||||||
chr2:48509862
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2086-153T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509862 | ||||||
chr2:48509953
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2086-62C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509953 | ||||||
chr2:48509976
|
G | A | 4 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0007t0031g0009others(1): Show | 4 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2086-39G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 19/21 | chr2 | 48509976 | ||||||
chr2:48510182
|
T | C | 9 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(6): Show | 9 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2184+69T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510182 | ||||||
chr2:48510392
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2184+279A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510392 | ||||||
chr2:48510404
|
G | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2184+291G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510404 | ||||||
chr2:48510424
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2184+311G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510424 | ||||||
chr2:48510431
|
G | T | 222 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.2184+318G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510431 | ||||||
chr2:48510457
|
G | T | 18 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2184+344G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510457 | ||||||
chr2:48510459
|
A | G | 1 | a0001c0002t0048g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2184+346A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510459 | ||||||
chr2:48510678
|
A | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2184+565A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510678 | ||||||
chr2:48510721
|
G | A | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2184+608G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510721 | ||||||
chr2:48510756
|
A | G | 2 | a0001c0001t0013g0284a0001c0001t0013g0288 | 2 | HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.2185-584A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510756 | ||||||
chr2:48510847
|
C | T | 4 | a0001c0003t0034g0152a0001c0003t0034g0153a0001c0007t0031g0009others(1): Show | 4 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2185-493C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510847 | ||||||
chr2:48510899
|
T | C | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2185-441T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510899 | ||||||
chr2:48510903
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2185-437T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510903 | ||||||
chr2:48510912
|
G | A | 18 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2185-428G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510912 | ||||||
chr2:48510985
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2185-355C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48510985 | ||||||
chr2:48511073
|
G | A | 1 | a0001c0001t0033g0343 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2185-267G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48511073 | ||||||
chr2:48511232
|
G | T | 7 | a0001c0004t0009g0312a0001c0004t0009g0313a0001c0004t0009g0314others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.2185-108G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48511232 | ||||||
chr2:48511249
|
C | T | 26 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0259others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.2185-91C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 20/21 | chr2 | 48511249 | ||||||
chr2:48511548
|
G | C | 226 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2313+80G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48511548 | ||||||
chr2:48511586
|
G | A | 1 | a0001c0001t0008g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2313+118G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48511586 | ||||||
chr2:48511698
|
C | CA | 12 | a0001c0001t0001g0182a0001c0001t0002g0070a0001c0001t0003g0033others(9): Show | 12 | HG02080.hp1 HG02135.hp2 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.2313+245dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48511698 | |||||
chr2:48511707
|
A | G | 1 | a0001c0003t0045g0159 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2313+239A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48511707 | ||||||
chr2:48511762
|
T | C | 1 | a0001c0001t0002g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2313+294T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48511762 | ||||||
chr2:48511832
|
C | T | 1 | a0001c0001t0017g0331 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2313+364C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48511832 | ||||||
chr2:48511878
|
G | GA | 7 | a0001c0001t0001g0182a0001c0003t0028g0334a0001c0003t0028g0335others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2313+420dupA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48511878 | |||||
chr2:48512093
|
G | A | 16 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(13): Show | 16 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2313+625G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512093 | ||||||
chr2:48512140
|
A | T | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313+672A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512140 | ||||||
chr2:48512162
|
T | C | 6 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0059others(3): Show | 6 | HG02080.hp1 NA18949.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313+694T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512162 | ||||||
chr2:48512329
|
G | A | 1 | a0001c0001t0003g0007 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2313+861G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512329 | ||||||
chr2:48512349
|
GGGCTCAC others(183): Show |
G | 7 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(4): Show | 7 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2313+886_2313+1075 others(3): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48512349 | |||||
chr2:48512384
|
T | C | 290 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.2313+916T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512384 | ||||||
chr2:48512499
|
C | T | 1 | a0001c0001t0052g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2313+1031C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512499 | ||||||
chr2:48512529
|
G | GAAGAAAC others(310): Show |
1 | a0001c0003t0034g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2313+1074_2313+107 others(321): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48512529 | |||||
chr2:48512529
|
G | GAAGAAAC others(311): Show |
1 | a0001c0003t0034g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2313+1074_2313+107 others(322): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48512529 | |||||
chr2:48512558
|
G | C | 1 | a0001c0001t0002g0116 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2313+1090G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512558 | ||||||
chr2:48512647
|
A | G | 48 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0117others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.2313+1179A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512647 | ||||||
chr2:48512824
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2313+1356C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512824 | ||||||
chr2:48512828
|
CA | C | 48 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0117others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.2313+1361delA | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512828 | ||||||
chr2:48512829
|
A | G | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2313+1361A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512829 | ||||||
chr2:48512869
|
T | C | 50 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0112others(47): Show | 50 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2313+1401T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48512869 | ||||||
chr2:48513047
|
G | T | 16 | a0001c0001t0001g0104a0001c0001t0002g0006a0001c0001t0004g0279others(13): Show | 16 | HG00099.hp1 HG00639.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.2313+1579G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513047 | ||||||
chr2:48513056
|
A | G | 145 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0290others(142): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.2313+1588A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513056 | ||||||
chr2:48513371
|
A | AT | 43 | a0001c0001t0001g0084a0001c0001t0001g0098a0001c0001t0001g0112others(40): Show | 43 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.2314-1330dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48513371 | |||||
chr2:48513524
|
G | A | 6 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(3): Show | 6 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.2314-1191G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513524 | ||||||
chr2:48513588
|
A | G | 1 | a0001c0013t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2314-1127A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513588 | ||||||
chr2:48513627
|
G | T | 18 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0034g0152others(15): Show | 18 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2314-1088G>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513627 | ||||||
chr2:48513705
|
G | C | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2314-1010G>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513705 | ||||||
chr2:48513775
|
A | G | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2314-940A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513775 | ||||||
chr2:48513847
|
C | T | 1 | a0001c0001t0007g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2314-868C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48513847 | ||||||
chr2:48514062
|
C | T | 2 | a0001c0007t0031g0009a0001c0007t0031g0015 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2314-653C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514062 | ||||||
chr2:48514073
|
C | CT | 34 | a0001c0001t0001g0201a0001c0001t0001g0206a0001c0001t0001g0244others(31): Show | 34 | HG00140.hp2 HG00438.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.2314-619dupT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48514073 | |||||
chr2:48514073
|
CT | C | 49 | a0001c0001t0001g0098a0001c0001t0001g0112a0001c0001t0001g0117others(46): Show | 49 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.2314-619delT | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48514073 | |||||
chr2:48514107
|
CTTG | C | 212 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(209): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.2314-604_2314-602d others(5): Show |
PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr2 | 48514107 | |||||
chr2:48514124
|
C | T | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2314-591C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514124 | ||||||
chr2:48514146
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2314-569C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514146 | ||||||
chr2:48514147
|
G | A | 10 | a0001c0001t0002g0070a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02258.hp2 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2314-568G>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514147 | ||||||
chr2:48514171
|
C | T | 1 | a0001c0001t0004g0347 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2314-544C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514171 | ||||||
chr2:48514246
|
C | T | 14 | a0001c0003t0028g0334a0001c0003t0028g0335a0001c0003t0035g0332others(11): Show | 14 | HG00280.hp1 HG01070.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2314-469C>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514246 | ||||||
chr2:48514251
|
A | T | 1 | a0001c0001t0003g0026 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2314-464A>T | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514251 | ||||||
chr2:48514456
|
T | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0084others(293): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2314-259T>A | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514456 | ||||||
chr2:48514617
|
A | C | 2 | a0001c0003t0034g0152a0001c0003t0034g0153 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2314-98A>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514617 | ||||||
chr2:48514657
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0193 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2314-58A>G | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514657 | ||||||
chr2:48514689
|
T | C | 13 | a0001c0001t0002g0020a0001c0001t0002g0079a0001c0001t0002g0080others(10): Show | 13 | HG01074.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2314-26T>C | PPP1R21 | ENSG00000162869.16 | transcript | ENST00000294952.13 | protein_coding | 21/21 | chr2 | 48514689 |