geneid | 1373 |
---|---|
ensemblid | ENSG00000021826.18 |
hgncid | 2323 |
symbol | CPS1 |
name | carbamoyl-phosphate synthase 1 |
refseq_nuc | NM_001875.5 |
refseq_prot | NP_001866.2 |
ensembl_nuc | ENST00000233072.10 |
ensembl_prot | ENSP00000233072.5 |
mane_status | MANE Select |
chr | chr2 |
start | 210556599 |
end | 210679107 |
strand | + |
ver | v1.2 |
region | chr2:210556599-210679107 |
region5000 | chr2:210551599-210684107 |
regionname0 | CPS1_chr2_210556599_210679107 |
regionname5000 | CPS1_chr2_210551599_210684107 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1500 | 127 | 32 | 20 | 58 | 6 | 10 | 45 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002 | 1/0 | 1500 | 96 | 17 | 17 | 51 | 2 | 8 | 46 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003 | 0/0 | 1500 | 60 | 20 | 11 | 22 | 0 | 7 | 18 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004 | 0/0 | 1500 | 34 | 9 | 10 | 6 | 0 | 9 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0005 | 0/0 | 1500 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0006 | 0/0 | 1500 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0007 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0008 | 0/0 | 1500 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0009 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0010 | 0/0 | 1500 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0011 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0012 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0013 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0014 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0015 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0016 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0017 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0018 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0019 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 4503 | 115 | 30 | 18 | 51 | 6 | 9 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0002 | 1/0 | 4503 | 77 | 5 | 16 | 47 | 2 | 6 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0003 | 0/0 | 4503 | 52 | 19 | 9 | 18 | 0 | 6 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0004 | 0/0 | 4503 | 26 | 4 | 10 | 6 | 0 | 6 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0005 | 0/0 | 4503 | 12 | 5 | 1 | 4 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0006 | 0/0 | 4503 | 9 | 0 | 1 | 7 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0007 | 0/0 | 4503 | 8 | 5 | 0 | 0 | 0 | 3 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0008 | 0/0 | 4503 | 6 | 0 | 2 | 3 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0009 | 0/0 | 4503 | 4 | 4 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0010 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0011 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0012 | 0/0 | 4503 | 2 | 0 | 0 | 2 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0013 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0014 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0015 | 0/0 | 4503 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0016 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0017 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0018 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0019 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0020 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0021 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0022 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0023 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0024 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0025 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0026 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0027 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0028 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0029 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0030 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0031 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
c0032 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1258 | 69 | 10 | 4 | 52 | 1 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0002 | 0/0 | 1261 | 45 | 14 | 7 | 21 | 0 | 3 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0003 | 0/0 | 1258 | 44 | 12 | 3 | 26 | 1 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0004 | 0/0 | 1261 | 43 | 6 | 7 | 21 | 0 | 9 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0005 | 0/0 | 1258 | 39 | 8 | 13 | 11 | 0 | 7 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0006 | 0/0 | 1261 | 25 | 9 | 1 | 11 | 0 | 4 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0007 | 0/0 | 1261 | 21 | 11 | 6 | 0 | 3 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0008 | 0/0 | 1258 | 9 | 4 | 2 | 0 | 0 | 3 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0009 | 0/0 | 1261 | 8 | 7 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0010 | 0/0 | 1261 | 6 | 2 | 3 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0011 | 0/0 | 1258 | 5 | 2 | 2 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0012 | 0/0 | 1258 | 3 | 0 | 3 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0013 | 0/1 | 1261 | 3 | 0 | 1 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0014 | 0/0 | 1258 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0015 | 0/0 | 1258 | 2 | 0 | 0 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0016 | 0/0 | 1261 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0017 | 0/0 | 1261 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0018 | 0/0 | 1261 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0019 | 0/0 | 1261 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0020 | 0/0 | 1261 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0021 | 0/0 | 1258 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0022 | 0/0 | 1258 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0023 | 0/0 | 1258 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0024 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0025 | 0/0 | 1261 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0026 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0027 | 0/0 | 1249 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0028 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
t0029 | 0/0 | 1261 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4503 | 115 | 30 | 18 | 51 | 6 | 9 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0006 | 0/0 | 4503 | 9 | 0 | 1 | 7 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0024 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0028 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0029 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002 | 1/0 | 4503 | 77 | 5 | 16 | 47 | 2 | 6 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0005 | 0/0 | 4503 | 12 | 5 | 1 | 4 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0009 | 0/0 | 4503 | 4 | 4 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0013 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0021 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0003 | 0/0 | 4503 | 52 | 19 | 9 | 18 | 0 | 6 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0008 | 0/0 | 4503 | 6 | 0 | 2 | 3 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0018 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0025 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0004 | 0/0 | 4503 | 26 | 4 | 10 | 6 | 0 | 6 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0007 | 0/0 | 4503 | 8 | 5 | 0 | 0 | 0 | 3 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0005c0011 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0006c0010 | 0/0 | 4503 | 3 | 3 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0007c0014 | 0/0 | 4503 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0008c0015 | 0/0 | 4503 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0009c0030 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0009c0032 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0010c0012 | 0/0 | 4503 | 2 | 0 | 0 | 2 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0011c0017 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0012c0027 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0013c0026 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0014c0031 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0015c0022 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0016c0023 | 0/0 | 4503 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0017c0020 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0018c0019 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0019c0016 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5760 | 17 | 2 | 1 | 14 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0002 | 0/0 | 5763 | 17 | 2 | 0 | 13 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0003 | 0/0 | 5760 | 23 | 4 | 1 | 16 | 1 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0006 | 0/0 | 5763 | 15 | 3 | 1 | 8 | 0 | 3 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0007 | 0/0 | 5763 | 14 | 5 | 5 | 0 | 3 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0008 | 0/0 | 5760 | 3 | 2 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0009 | 0/0 | 5763 | 8 | 7 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0010 | 0/0 | 5763 | 5 | 1 | 3 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0011 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0013 | 0/1 | 5763 | 3 | 0 | 1 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0014 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0016 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0017 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0018 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0019 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0023 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0025 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0028 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0001t0029 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0006t0001 | 0/0 | 5760 | 3 | 0 | 1 | 2 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0006t0002 | 0/0 | 5763 | 2 | 0 | 0 | 2 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0006t0006 | 0/0 | 5763 | 4 | 0 | 0 | 3 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0024t0017 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0028t0024 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0001c0029t0007 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0001 | 1/0 | 5760 | 37 | 0 | 2 | 32 | 1 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0002 | 0/0 | 5763 | 12 | 0 | 6 | 5 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0003 | 0/0 | 5760 | 15 | 3 | 2 | 9 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0005 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0007 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0008 | 0/0 | 5760 | 3 | 1 | 1 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0011 | 0/0 | 5760 | 2 | 1 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0012 | 0/0 | 5760 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0015 | 0/0 | 5760 | 2 | 0 | 0 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0021 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0002t0022 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0005t0001 | 0/0 | 5760 | 3 | 0 | 0 | 3 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0005t0003 | 0/0 | 5760 | 5 | 4 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0005t0006 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0005t0008 | 0/0 | 5760 | 2 | 0 | 0 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0005t0012 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0009t0003 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0009t0006 | 0/0 | 5763 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0009t0007 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0013t0006 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0013t0007 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0002c0021t0002 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0003t0001 | 0/0 | 5760 | 3 | 3 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0003t0002 | 0/0 | 5763 | 6 | 6 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0003t0004 | 0/0 | 5763 | 28 | 6 | 3 | 14 | 0 | 5 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0003t0005 | 0/0 | 5760 | 14 | 3 | 6 | 4 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0003t0027 | 0/0 | 5751 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0008t0004 | 0/0 | 5763 | 5 | 0 | 1 | 3 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0008t0005 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0018t0002 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0003c0025t0004 | 0/0 | 5763 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0004t0002 | 0/0 | 5763 | 3 | 2 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0004t0004 | 0/0 | 5763 | 8 | 0 | 3 | 3 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0004t0005 | 0/0 | 5760 | 15 | 2 | 6 | 3 | 0 | 4 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0007t0001 | 0/0 | 5760 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0007t0004 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0004c0007t0005 | 0/0 | 5760 | 5 | 3 | 0 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0005c0011t0001 | 0/0 | 5760 | 3 | 3 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0006c0010t0008 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0006c0010t0010 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0006c0010t0014 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0007c0014t0007 | 0/0 | 5763 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0008c0015t0011 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0008c0015t0020 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0009c0030t0007 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0009c0032t0026 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0010c0012t0005 | 0/0 | 5760 | 2 | 0 | 0 | 2 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0011c0017t0005 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0012c0027t0016 | 0/0 | 5763 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0013c0026t0006 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0014c0031t0002 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0015c0022t0002 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0016c0023t0006 | 0/0 | 5763 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0017c0020t0011 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0018c0019t0001 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
a0019c0016t0002 | 0/0 | 5763 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | copy fasta | chr2 | 210551599 | 210684107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0006g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0009g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0010g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0010g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0013g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0016g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0017g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0018g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0019g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0023g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0025g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0028g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0001t0029g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0006g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0006t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0024t0017g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0028t0024g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0001c0029t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0007g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0008g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0011g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0012g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0015g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0015g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0021g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0002t0022g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0008g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0005t0012g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0009t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0009t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0009t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0009t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0013t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0013t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0002c0021t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0003t0027g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0008t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0008t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0008t0004g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0008t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0018t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0003c0025t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0004t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0004g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0005g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0004c0007t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0005c0011t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0005c0011t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0006c0010t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0006c0010t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0006c0010t0014g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0007c0014t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0007c0014t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0008c0015t0011g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0008c0015t0020g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0009c0030t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0009c0032t0026g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0010c0012t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0010c0012t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0011c0017t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0012c0027t0016g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0013c0026t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0014c0031t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0015c0022t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0016c0023t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0017c0020t0011g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0018c0019t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
a0019c0016t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0007 | g0057 | EUR | GBR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0131 | EUR | GBR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0305 | EUR | FIN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0170 | EUR | FIN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00408 | hp1 | a0003 | c0003 | t0004 | g0036 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00408 | hp2 | a0001 | c0006 | t0001 | g0109 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00438 | hp1 | a0003 | c0003 | t0005 | g0078 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00609 | hp1 | a0003 | c0003 | t0004 | g0041 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0245 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00621 | hp1 | a0004 | c0004 | t0004 | g0059 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | CHS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0318 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0327 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00733 | hp1 | a0001 | c0001 | t0010 | g0047 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00733 | hp2 | a0001 | c0001 | t0017 | g0322 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00735 | hp1 | a0001 | c0001 | t0010 | g0044 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00735 | hp2 | a0002 | c0002 | t0012 | g0005 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00738 | hp1 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00738 | hp2 | a0003 | c0003 | t0005 | g0097 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0254 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG00741 | hp2 | a0017 | c0020 | t0011 | g0173 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01069 | hp1 | a0002 | c0002 | t0007 | g0314 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0285 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01081 | hp1 | a0004 | c0004 | t0004 | g0027 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01081 | hp2 | a0004 | c0004 | t0005 | g0186 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01106 | hp1 | a0002 | c0002 | t0012 | g0005 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01106 | hp2 | a0003 | c0008 | t0005 | g0098 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01109 | hp2 | a0004 | c0004 | t0005 | g0143 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01167 | hp1 | a0003 | c0008 | t0004 | g0039 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01167 | hp2 | a0001 | c0001 | t0007 | g0307 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01168 | hp1 | a0008 | c0015 | t0020 | g0048 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01168 | hp2 | a0003 | c0003 | t0005 | g0114 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01169 | hp1 | a0003 | c0003 | t0005 | g0113 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0306 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0004 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0320 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01192 | hp2 | a0001 | c0001 | t0010 | g0303 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0056 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0248 | AMR | PUR | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01257 | hp1 | a0008 | c0015 | t0011 | g0130 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01257 | hp2 | a0004 | c0004 | t0005 | g0206 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01258 | hp1 | a0004 | c0004 | t0005 | g0205 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01258 | hp2 | a0012 | c0027 | t0016 | g0304 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01261 | hp1 | a0001 | c0001 | t0018 | g0053 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01261 | hp2 | a0002 | c0002 | t0008 | g0145 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01346 | hp1 | a0002 | c0002 | t0022 | g0189 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01346 | hp2 | a0003 | c0003 | t0004 | g0263 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01358 | hp1 | a0003 | c0003 | t0004 | g0052 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01358 | hp2 | a0004 | c0004 | t0004 | g0058 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01361 | hp1 | a0004 | c0004 | t0005 | g0227 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0096 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01433 | hp1 | a0001 | c0024 | t0017 | g0288 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0031 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01496 | hp1 | a0003 | c0003 | t0004 | g0050 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01496 | hp2 | a0002 | c0002 | t0021 | g0236 | AMR | CLM | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0046 | EUR | IBS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01516 | hp2 | a0001 | c0001 | t0013 | g0028 | EUR | IBS | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01884 | hp1 | a0002 | c0005 | t0003 | g0139 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01891 | hp2 | a0004 | c0007 | t0005 | g0158 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0321 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01934 | hp2 | a0003 | c0003 | t0005 | g0116 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01943 | hp1 | a0004 | c0004 | t0002 | g0317 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01943 | hp2 | a0001 | c0006 | t0001 | g0088 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01952 | hp1 | a0004 | c0004 | t0004 | g0315 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01952 | hp2 | a0003 | c0003 | t0005 | g0105 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0319 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG01993 | hp2 | a0003 | c0003 | t0005 | g0087 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02015 | hp2 | a0011 | c0017 | t0005 | g0203 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02040 | hp2 | a0004 | c0004 | t0004 | g0311 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02071 | hp1 | a0001 | c0006 | t0002 | g0296 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0148 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02129 | hp2 | a0004 | c0004 | t0004 | g0297 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02135 | hp1 | a0004 | c0004 | t0005 | g0182 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02145 | hp1 | a0001 | c0001 | t0009 | g0247 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02145 | hp2 | a0003 | c0003 | t0004 | g0260 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02165 | hp1 | a0001 | c0006 | t0002 | g0038 | EAS | CDX | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | CDX | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02257 | hp2 | a0002 | c0013 | t0006 | g0070 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02258 | hp1 | a0007 | c0014 | t0007 | g0061 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02258 | hp2 | a0003 | c0003 | t0004 | g0290 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02273 | hp1 | a0002 | c0005 | t0012 | g0169 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0313 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02280 | hp2 | a0006 | c0010 | t0014 | g0133 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02293 | hp1 | a0001 | c0001 | t0025 | g0043 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02300 | hp1 | a0004 | c0004 | t0005 | g0167 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0244 | AMR | PEL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02451 | hp1 | a0001 | c0028 | t0024 | g0067 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02451 | hp2 | a0003 | c0003 | t0005 | g0164 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02523 | hp1 | a0018 | c0019 | t0001 | g0110 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02523 | hp2 | a0003 | c0008 | t0004 | g0001 | EAS | KHV | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02572 | hp1 | a0003 | c0018 | t0002 | g0239 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02572 | hp2 | a0002 | c0009 | t0007 | g0069 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02602 | hp1 | a0002 | c0002 | t0008 | g0188 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02602 | hp2 | a0003 | c0003 | t0004 | g0300 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02615 | hp1 | a0003 | c0003 | t0002 | g0256 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02615 | hp2 | a0003 | c0003 | t0005 | g0123 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02622 | hp2 | a0004 | c0007 | t0005 | g0160 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0329 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02630 | hp2 | a0003 | c0003 | t0002 | g0240 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0127 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02647 | hp2 | a0002 | c0009 | t0006 | g0072 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02717 | hp2 | a0006 | c0010 | t0008 | g0137 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02723 | hp1 | a0004 | c0007 | t0001 | g0157 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02723 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0033 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02738 | hp2 | a0001 | c0006 | t0006 | g0276 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02809 | hp1 | a0016 | c0023 | t0006 | g0019 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02818 | hp1 | a0015 | c0022 | t0002 | g0018 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02886 | hp2 | a0003 | c0003 | t0004 | g0255 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02895 | hp1 | a0002 | c0005 | t0003 | g0136 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02895 | hp2 | a0004 | c0004 | t0002 | g0010 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02897 | hp2 | a0004 | c0004 | t0002 | g0011 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02922 | hp1 | a0002 | c0009 | t0006 | g0071 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02922 | hp2 | a0005 | c0011 | t0001 | g0252 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02965 | hp2 | a0002 | c0005 | t0003 | g0138 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0246 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02970 | hp2 | a0002 | c0002 | t0011 | g0140 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02976 | hp1 | a0003 | c0003 | t0004 | g0330 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02976 | hp2 | a0004 | c0007 | t0005 | g0159 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03017 | hp1 | a0004 | c0004 | t0004 | g0020 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03017 | hp2 | a0002 | c0005 | t0008 | g0134 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03041 | hp1 | a0009 | c0030 | t0007 | g0074 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03130 | hp2 | a0004 | c0007 | t0001 | g0152 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03139 | hp1 | a0003 | c0003 | t0002 | g0286 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0249 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03195 | hp1 | a0002 | c0013 | t0007 | g0073 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | ESN | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03209 | hp1 | a0003 | c0003 | t0004 | g0251 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03209 | hp2 | a0002 | c0009 | t0003 | g0155 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03225 | hp1 | a0014 | c0031 | t0002 | g0014 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03225 | hp2 | a0003 | c0003 | t0004 | g0259 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03239 | hp1 | a0004 | c0004 | t0005 | g0175 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03486 | hp1 | a0003 | c0003 | t0005 | g0118 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03486 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03490 | hp1 | a0004 | c0004 | t0005 | g0135 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0325 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03491 | hp1 | a0002 | c0005 | t0008 | g0237 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03492 | hp1 | a0004 | c0004 | t0004 | g0324 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03540 | hp1 | a0002 | c0021 | t0002 | g0281 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0241 | AFR | GWD | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03579 | hp1 | a0002 | c0002 | t0008 | g0142 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03579 | hp2 | a0005 | c0011 | t0001 | g0006 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03654 | hp1 | a0004 | c0007 | t0004 | g0323 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0295 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03704 | hp1 | a0001 | c0001 | t0007 | g0032 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03704 | hp2 | a0004 | c0004 | t0005 | g0082 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03710 | hp1 | a0004 | c0007 | t0005 | g0184 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03710 | hp2 | a0003 | c0003 | t0004 | g0279 | SAS | PJL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03831 | hp1 | a0002 | c0002 | t0015 | g0171 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03831 | hp2 | a0001 | c0001 | t0019 | g0049 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03834 | hp1 | a0004 | c0007 | t0005 | g0228 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03834 | hp2 | a0002 | c0002 | t0015 | g0084 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03942 | hp1 | a0003 | c0003 | t0004 | g0308 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0224 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0037 | SAS | STU | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG04115 | hp2 | a0004 | c0004 | t0005 | g0141 | SAS | STU | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0226 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG04184 | hp2 | a0003 | c0003 | t0004 | g0021 | SAS | BEB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG04199 | hp1 | a0003 | c0008 | t0004 | g0277 | SAS | STU | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG04199 | hp2 | a0003 | c0003 | t0004 | g0301 | SAS | STU | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18522 | hp1 | a0006 | c0010 | t0010 | g0287 | AFR | YRI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0283 | AFR | YRI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0165 | EAS | CHB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0261 | AFR | YRI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18906 | hp2 | a0001 | c0029 | t0007 | g0250 | AFR | YRI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18942 | hp2 | a0003 | c0003 | t0004 | g0298 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18945 | hp1 | a0010 | c0012 | t0005 | g0199 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18945 | hp2 | a0002 | c0005 | t0001 | g0192 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18946 | hp2 | a0003 | c0003 | t0005 | g0168 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18948 | hp1 | a0003 | c0003 | t0004 | g0265 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18951 | hp1 | a0001 | c0006 | t0006 | g0294 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18954 | hp2 | a0019 | c0016 | t0002 | g0268 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18956 | hp1 | a0003 | c0003 | t0005 | g0089 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18957 | hp1 | a0002 | c0002 | t0003 | g0210 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18962 | hp1 | a0002 | c0002 | t0003 | g0149 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18963 | hp2 | a0003 | c0003 | t0004 | g0051 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18965 | hp2 | a0003 | c0008 | t0004 | g0001 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0309 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18968 | hp1 | a0002 | c0002 | t0003 | g0204 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18972 | hp1 | a0001 | c0001 | t0006 | g0293 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18974 | hp1 | a0001 | c0001 | t0006 | g0023 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18978 | hp2 | a0003 | c0003 | t0004 | g0042 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18979 | hp1 | a0003 | c0003 | t0004 | g0274 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18982 | hp1 | a0001 | c0006 | t0006 | g0016 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18983 | hp1 | a0003 | c0003 | t0004 | g0262 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18990 | hp2 | a0003 | c0003 | t0005 | g0077 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18994 | hp2 | a0004 | c0004 | t0005 | g0220 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18995 | hp2 | a0003 | c0003 | t0004 | g0269 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18998 | hp1 | a0002 | c0005 | t0003 | g0212 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19001 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19001 | hp2 | a0003 | c0008 | t0004 | g0001 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19004 | hp1 | a0003 | c0003 | t0004 | g0025 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19004 | hp2 | a0003 | c0003 | t0004 | g0064 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19005 | hp1 | a0003 | c0003 | t0004 | g0022 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19005 | hp2 | a0002 | c0005 | t0001 | g0191 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19009 | hp1 | a0002 | c0002 | t0003 | g0217 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19030 | hp1 | a0005 | c0011 | t0001 | g0006 | AFR | LWK | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19030 | hp2 | a0002 | c0005 | t0006 | g0075 | AFR | LWK | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19043 | hp1 | a0013 | c0026 | t0006 | g0257 | AFR | LWK | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19043 | hp2 | a0002 | c0005 | t0003 | g0132 | AFR | LWK | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19054 | hp1 | a0001 | c0006 | t0001 | g0115 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19054 | hp2 | a0001 | c0006 | t0006 | g0292 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19056 | hp1 | a0002 | c0002 | t0005 | g0202 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19064 | hp1 | a0002 | c0002 | t0003 | g0015 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19067 | hp2 | a0010 | c0012 | t0005 | g0200 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19072 | hp1 | a0003 | c0003 | t0004 | g0299 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19077 | hp2 | a0004 | c0004 | t0005 | g0181 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19084 | hp1 | a0002 | c0005 | t0001 | g0180 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19087 | hp1 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19087 | hp2 | a0002 | c0002 | t0003 | g0218 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19090 | hp2 | a0003 | c0003 | t0004 | g0029 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19091 | hp1 | a0003 | c0025 | t0004 | g0270 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0280 | AFR | YRI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0331 | AFR | YRI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20129 | hp1 | a0001 | c0001 | t0023 | g0079 | AFR | ASW | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0153 | AFR | ASW | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20805 | hp1 | a0001 | c0001 | t0010 | g0045 | EUR | TSI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20805 | hp2 | a0002 | c0002 | t0011 | g0187 | EUR | TSI | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20905 | hp1 | a0001 | c0001 | t0029 | g0278 | SAS | GIH | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20905 | hp2 | a0003 | c0003 | t0005 | g0083 | SAS | GIH | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02109 | hp1 | a0003 | c0003 | t0002 | g0017 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02109 | hp2 | a0001 | c0001 | t0028 | g0243 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02486 | hp1 | a0003 | c0003 | t0027 | g0242 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0289 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02559 | hp1 | a0007 | c0014 | t0007 | g0062 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG02559 | hp2 | a0004 | c0004 | t0005 | g0151 | AFR | ACB | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03471 | hp1 | a0001 | c0001 | t0008 | g0119 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0144 | AFR | MSL | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0013 | AFR | USA | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0284 | AFR | USA | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20300 | hp1 | a0004 | c0004 | t0005 | g0225 | AFR | USA | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | USA | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA21309 | hp1 | a0009 | c0032 | t0026 | g0012 | AFR | LWK | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
NA21309 | hp2 | a0003 | c0003 | t0002 | g0060 | AFR | LWK | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0055 | REF | REF | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0146 | REF | REF | CPS1_chr2_210551599_210684107 | CPS1 | chr2 | 210551599 | 210684107 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:210576411
|
T | C | 1 | a0019 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.302T>C | p.Ile101Thr | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/38 | 437/5760 | 302/4503 | 101/1500 | chr2 | 210576411 | ||
chr2:210577488
|
G | A | 1 | a0011 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.449G>A | p.Gly150Glu | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/38 | 584/5760 | 449/4503 | 150/1500 | chr2 | 210577488 | ||
chr2:210591901
|
G | A | 1 | a0018 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1018G>A | p.Ala340Thr | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/38 | 1153/5760 | 1018/4503 | 340/1500 | chr2 | 210591901 | ||
chr2:210591913
|
A | G | 9 | a0001a0003a0005others(6): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): Show |
missense_variant | MODERATE | c.1030A>G | p.Thr344Ala | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/38 | 1165/5760 | 1030/4503 | 344/1500 | chr2 | 210591913 | ||
chr2:210591913
|
A | T | 2 | a0009a0014 | 3 | HG03041.hp1 HG03225.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1030A>T | p.Thr344Ser | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/38 | 1165/5760 | 1030/4503 | 344/1500 | chr2 | 210591913 | ||
chr2:210594557
|
C | A | 1 | a0007 | 2 | HG02258.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.1214C>A | p.Thr405Asn | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 12/38 | 1349/5760 | 1214/4503 | 405/1500 | chr2 | 210594557 | ||
chr2:210600635
|
A | T | 2 | a0015a0016 | 2 | HG02809.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.1630A>T | p.Thr544Ser | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/38 | 1765/5760 | 1630/4503 | 544/1500 | chr2 | 210600635 | ||
chr2:210637785
|
C | G | 1 | a0010 | 2 | NA18945.hp1 NA19067.hp2 |
missense_variant | MODERATE | c.2771C>G | p.Thr924Ser | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/38 | 2906/5760 | 2771/4503 | 924/1500 | chr2 | 210637785 | ||
chr2:210648491
|
G | A | 3 | a0005a0006a0013 | 7 | HG02280.hp2 HG02717.hp2 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.3355G>A | p.Ala1119Thr | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/38 | 3490/5760 | 3355/4503 | 1119/1500 | chr2 | 210648491 | ||
chr2:210674926
|
G | A | 2 | a0008a0017 | 3 | HG00741.hp2 HG01168.hp1 HG01257.hp1 |
missense_variant | MODERATE | c.4126G>A | p.Gly1376Ser | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 35/38 | 4261/5760 | 4126/4503 | 1376/1500 | chr2 | 210674926 | ||
chr2:210675783
|
C | A | 7 | a0003a0004a0005others(4): Show | 102 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(99): Show |
missense_variant | MODERATE | c.4217C>A | p.Thr1406Asn | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/38 | 4352/5760 | 4217/4503 | 1406/1500 | chr2 | 210675783 | ||
chr2:210677939
|
A | G | 1 | a0012 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.4457A>G | p.Lys1486Arg | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 4592/5760 | 4457/4503 | 1486/1500 | chr2 | 210677939 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:210577510
|
G | A | 1 | a0003c0018 | 1 | HG02572.hp1 | splice_region_variant&synonymous_variant | LOW | c.471G>A | p.Lys157Lys | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/38 | 606/5760 | 471/4503 | 157/1500 | chr2 | 210577510 | ||
chr2:210591915
|
C | T | 19 | a0001c0001a0001c0006a0001c0024others(16): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(198): Show |
synonymous_variant | LOW | c.1032C>T | p.Thr344Thr | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/38 | 1167/5760 | 1032/4503 | 344/1500 | chr2 | 210591915 | ||
chr2:210591951
|
C | G | 2 | a0002c0009a0002c0013 | 6 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
synonymous_variant | LOW | c.1068C>G | p.Val356Val | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/38 | 1203/5760 | 1068/4503 | 356/1500 | chr2 | 210591951 | ||
chr2:210608433
|
C | A | 1 | a0001c0024 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.2265C>A | p.Ser755Ser | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/38 | 2400/5760 | 2265/4503 | 755/1500 | chr2 | 210608433 | ||
chr2:210608433
|
C | T | 2 | a0002c0009a0002c0021 | 5 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.2265C>T | p.Ser755Ser | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/38 | 2400/5760 | 2265/4503 | 755/1500 | chr2 | 210608433 | ||
chr2:210612119
|
C | A | 1 | a0002c0009 | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.2394C>A | p.Val798Val | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/38 | 2529/5760 | 2394/4503 | 798/1500 | chr2 | 210612119 | ||
chr2:210616533
|
C | G | 22 | a0001c0001a0001c0028a0001c0029others(19): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
synonymous_variant | LOW | c.2679C>G | p.Gly893Gly | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/38 | 2814/5760 | 2679/4503 | 893/1500 | chr2 | 210616533 | ||
chr2:210637747
|
G | A | 1 | a0003c0025 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.2733G>A | p.Gly911Gly | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/38 | 2868/5760 | 2733/4503 | 911/1500 | chr2 | 210637747 | ||
chr2:210642557
|
G | C | 1 | a0009c0030 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.3033G>C | p.Val1011Val | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/38 | 3168/5760 | 3033/4503 | 1011/1500 | chr2 | 210642557 | ||
chr2:210668272
|
G | T | 1 | a0001c0029 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.4089G>T | p.Leu1363Leu | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/38 | 4224/5760 | 4089/4503 | 1363/1500 | chr2 | 210668272 | ||
chr2:210675826
|
C | G | 1 | a0001c0028 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.4260C>G | p.Leu1420Leu | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/38 | 4395/5760 | 4260/4503 | 1420/1500 | chr2 | 210675826 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:210556705
|
T | G | 3 | a0001c0001t0018a0001c0001t0019a0008c0015t0020 | 3 | HG01168.hp1 HG01261.hp1 HG03831.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/38 | chr2 | 210556705 | ||||||
chr2:210556728
|
A | ATCT | 46 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(43): Show | 164 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
5_prime_UTR_variant | MODIFIER | c.-4_-3insTTC | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/38 | 3 | INFO_REALIGN_3_PRIME | chr2 | 210556728 | ||||
chr2:210678299
|
T | A | 1 | a0001c0028t0024 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 314 | chr2 | 210678299 | |||||
chr2:210678331
|
T | C | 14 | a0001c0001t0016a0002c0002t0005a0003c0003t0004others(11): Show | 84 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*346T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 346 | chr2 | 210678331 | |||||
chr2:210678365
|
C | G | 11 | a0001c0001t0010a0001c0001t0011a0001c0001t0023others(8): Show | 17 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*380C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 380 | chr2 | 210678365 | |||||
chr2:210678423
|
T | G | 33 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(30): Show | 67 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*438T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 438 | chr2 | 210678423 | |||||
chr2:210678585
|
CTTTTCTT others(5): Show |
C | 1 | a0003c0003t0027 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611_*622delCTTTTT others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 611 | INFO_REALIGN_3_PRIME | chr2 | 210678585 | ||||
chr2:210678643
|
A | G | 2 | a0001c0001t0029a0002c0002t0015 | 3 | HG03831.hp1 HG03834.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*658A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 658 | chr2 | 210678643 | |||||
chr2:210678677
|
C | G | 16 | a0001c0001t0003a0001c0001t0006a0001c0001t0013others(13): Show | 76 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*692C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 692 | chr2 | 210678677 | |||||
chr2:210678739
|
T | G | 5 | a0001c0001t0009a0001c0001t0014a0001c0001t0029others(2): Show | 13 | HG01243.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*754T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 754 | chr2 | 210678739 | |||||
chr2:210678814
|
T | C | 4 | a0001c0001t0017a0001c0024t0017a0002c0002t0012others(1): Show | 5 | HG00733.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*829T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 829 | chr2 | 210678814 | |||||
chr2:210678834
|
A | G | 1 | a0009c0032t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 849 | chr2 | 210678834 | |||||
chr2:210678931
|
C | T | 2 | a0001c0001t0025a0002c0002t0021 | 2 | HG01496.hp2 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*946C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 38/38 | 946 | chr2 | 210678931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:210556983
|
G | A | 6 | a0001c0001t0007g0009a0001c0001t0007g0013a0004c0004t0002g0010others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+124G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210556983 | ||||||
chr2:210557143
|
T | C | 1 | a0002c0002t0003g0015 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.126+284T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210557143 | ||||||
chr2:210557180
|
T | G | 1 | a0001c0006t0006g0016 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.126+321T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210557180 | ||||||
chr2:210557609
|
A | C | 93 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(90): Show | 98 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.126+750A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210557609 | ||||||
chr2:210557736
|
T | C | 4 | a0003c0003t0002g0017a0004c0004t0004g0020a0015c0022t0002g0018others(1): Show | 4 | HG02109.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+877T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210557736 | ||||||
chr2:210557821
|
G | T | 4 | a0001c0001t0028g0243a0003c0003t0002g0240a0003c0003t0002g0241others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+962G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210557821 | ||||||
chr2:210557925
|
T | C | 1 | a0002c0002t0002g0244 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.126+1066T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210557925 | ||||||
chr2:210558080
|
A | G | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+1221A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210558080 | ||||||
chr2:210558362
|
A | G | 3 | a0001c0001t0006g0329a0001c0001t0006g0331a0003c0003t0004g0330 | 3 | HG02630.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.126+1503A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210558362 | ||||||
chr2:210558632
|
T | C | 1 | a0001c0001t0006g0245 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.126+1773T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210558632 | ||||||
chr2:210558659
|
C | T | 81 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(78): Show | 85 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.126+1800C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210558659 | ||||||
chr2:210559010
|
C | T | 1 | a0002c0002t0001g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.126+2151C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559010 | ||||||
chr2:210559053
|
G | A | 48 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0035others(45): Show | 48 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+2194G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559053 | ||||||
chr2:210559148
|
C | A | 6 | a0001c0001t0007g0009a0001c0001t0007g0013a0004c0004t0002g0010others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+2289C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559148 | ||||||
chr2:210559402
|
G | A | 1 | a0003c0003t0004g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.126+2543G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559402 | ||||||
chr2:210559409
|
T | C | 1 | a0002c0002t0003g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.126+2550T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559409 | ||||||
chr2:210559654
|
A | G | 1 | a0002c0005t0008g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.126+2795A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559654 | ||||||
chr2:210559674
|
G | A | 159 | a0001c0001t0002g0007a0001c0001t0002g0026a0001c0001t0002g0034others(156): Show | 163 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.126+2815G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559674 | ||||||
chr2:210559725
|
C | G | 3 | a0001c0001t0002g0068a0001c0001t0007g0066a0001c0028t0024g0067 | 3 | HG02451.hp1 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.126+2866C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559725 | ||||||
chr2:210559801
|
A | G | 1 | a0002c0002t0021g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126+2942A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559801 | ||||||
chr2:210559989
|
G | A | 1 | a0002c0002t0001g0076 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.126+3130G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210559989 | ||||||
chr2:210560013
|
A | G | 1 | a0002c0002t0002g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.126+3154A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560013 | ||||||
chr2:210560109
|
A | G | 3 | a0001c0001t0002g0063a0001c0001t0002g0065a0003c0003t0004g0064 | 3 | NA18992.hp2 NA19004.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.126+3250A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560109 | ||||||
chr2:210560138
|
A | C | 7 | a0001c0001t0001g0231a0001c0001t0003g0229a0001c0001t0003g0230others(4): Show | 7 | NA18952.hp2 NA18966.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+3279A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560138 | ||||||
chr2:210560148
|
A | G | 1 | a0001c0001t0016g0327 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.126+3289A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560148 | ||||||
chr2:210560156
|
T | C | 45 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0035others(42): Show | 45 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.126+3297T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560156 | ||||||
chr2:210560482
|
G | A | 6 | a0002c0009t0006g0071a0002c0009t0006g0072a0002c0009t0007g0069others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+3623G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560482 | ||||||
chr2:210560497
|
T | G | 3 | a0003c0003t0002g0017a0015c0022t0002g0018a0016c0023t0006g0019 | 3 | HG02109.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.126+3638T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560497 | ||||||
chr2:210560912
|
C | T | 2 | a0001c0001t0007g0013a0014c0031t0002g0014 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.126+4053C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560912 | ||||||
chr2:210560934
|
A | G | 1 | a0004c0007t0005g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.126+4075A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210560934 | ||||||
chr2:210561134
|
G | A | 2 | a0003c0003t0005g0077a0003c0003t0005g0078 | 2 | HG00438.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.126+4275G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210561134 | ||||||
chr2:210561236
|
A | G | 6 | a0001c0001t0007g0009a0001c0001t0007g0013a0004c0004t0002g0010others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+4377A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210561236 | ||||||
chr2:210561241
|
G | A | 3 | a0001c0001t0006g0329a0001c0001t0006g0331a0003c0003t0004g0330 | 3 | HG02630.hp1 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.126+4382G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210561241 | ||||||
chr2:210561836
|
T | G | 6 | a0002c0009t0006g0071a0002c0009t0006g0072a0002c0009t0007g0069others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+4977T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210561836 | ||||||
chr2:210561936
|
A | G | 92 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(89): Show | 97 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.126+5077A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210561936 | ||||||
chr2:210561983
|
A | G | 2 | a0015c0022t0002g0018a0016c0023t0006g0019 | 2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.126+5124A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210561983 | ||||||
chr2:210562250
|
A | G | 67 | a0002c0002t0001g0076a0002c0002t0001g0165a0002c0002t0001g0166others(64): Show | 68 | HG00323.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.126+5391A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562250 | ||||||
chr2:210562298
|
C | T | 3 | a0002c0002t0001g0226a0004c0004t0005g0225a0004c0004t0005g0227 | 3 | HG01361.hp1 HG04184.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+5439C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562298 | ||||||
chr2:210562380
|
T | G | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.126+5521T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562380 | ||||||
chr2:210562403
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+5544G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562403 | ||||||
chr2:210562429
|
T | G | 1 | a0001c0001t0007g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.126+5570T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562429 | ||||||
chr2:210562517
|
A | G | 82 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(79): Show | 86 | HG00323.hp1 HG00597.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.126+5658A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562517 | ||||||
chr2:210562547
|
A | G | 1 | a0002c0002t0001g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.126+5688A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562547 | ||||||
chr2:210562683
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0003g0162 | 2 | NA18981.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.126+5824A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562683 | ||||||
chr2:210562852
|
C | T | 148 | a0001c0001t0002g0007a0001c0001t0002g0026a0001c0001t0002g0034others(145): Show | 152 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.126+5993C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562852 | ||||||
chr2:210562868
|
G | GT | 10 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0003g0162others(7): Show | 10 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+6024dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210562868 | |||||
chr2:210562868
|
GT | G | 145 | a0001c0001t0002g0007a0001c0001t0002g0026a0001c0001t0002g0034others(142): Show | 149 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.126+6024delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210562868 | |||||
chr2:210562868
|
GTT | G | 7 | a0001c0001t0007g0258a0001c0001t0009g0261a0003c0003t0002g0256others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+6023_126+6024d others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210562868 | |||||
chr2:210562949
|
G | A | 3 | a0003c0003t0002g0017a0015c0022t0002g0018a0016c0023t0006g0019 | 3 | HG02109.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.126+6090G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210562949 | ||||||
chr2:210563040
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0003g0081a0002c0002t0001g0080 | 3 | NA18944.hp2 NA18949.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.126+6181T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563040 | ||||||
chr2:210563190
|
G | A | 1 | a0004c0004t0005g0082 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.126+6331G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563190 | ||||||
chr2:210563382
|
G | C | 2 | a0002c0002t0001g0165a0002c0002t0001g0166 | 2 | NA18612.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.126+6523G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563382 | ||||||
chr2:210563388
|
T | C | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+6529T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563388 | ||||||
chr2:210563475
|
G | A | 5 | a0001c0001t0009g0246a0001c0001t0028g0243a0003c0003t0002g0240others(2): Show | 5 | HG02109.hp2 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+6616G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563475 | ||||||
chr2:210563630
|
T | G | 48 | a0001c0001t0002g0026a0001c0001t0002g0034a0001c0001t0002g0035others(45): Show | 48 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.126+6771T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563630 | ||||||
chr2:210563673
|
T | C | 6 | a0001c0001t0007g0009a0001c0001t0007g0013a0004c0004t0002g0010others(3): Show | 6 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+6814T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563673 | ||||||
chr2:210563697
|
A | G | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+6838A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210563697 | ||||||
chr2:210564100
|
C | CCCTAAAA others(41): Show |
1 | a0002c0002t0002g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.126+7243_126+7244i others(50): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210564100 | |||||
chr2:210564125
|
AGAAATTT others(41): Show |
A | 1 | a0002c0002t0002g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.126+7267_126+7314d others(50): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564125 | ||||||
chr2:210564174
|
T | A | 1 | a0004c0004t0005g0167 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.126+7315T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564174 | ||||||
chr2:210564401
|
A | C | 6 | a0002c0009t0006g0071a0002c0009t0006g0072a0002c0009t0007g0069others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+7542A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564401 | ||||||
chr2:210564458
|
G | C | 1 | a0003c0003t0004g0022 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.126+7599G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564458 | ||||||
chr2:210564520
|
T | C | 1 | a0003c0003t0005g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+7661T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564520 | ||||||
chr2:210564524
|
T | C | 1 | a0003c0003t0005g0083 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+7665T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564524 | ||||||
chr2:210564608
|
C | T | 5 | a0002c0002t0001g0219a0002c0002t0001g0221a0002c0002t0001g0222others(2): Show | 5 | HG00621.hp1 NA18944.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+7749C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564608 | ||||||
chr2:210564623
|
G | A | 1 | a0002c0002t0015g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.126+7764G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564623 | ||||||
chr2:210564710
|
G | C | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+7851G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564710 | ||||||
chr2:210564791
|
G | A | 214 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(211): Show | 219 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.126+7932G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210564791 | ||||||
chr2:210565011
|
AATAAAAA others(9): Show |
A | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.126+8154_126+8169d others(18): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210565011 | |||||
chr2:210565015
|
A | AAAAT | 8 | a0001c0001t0007g0013a0003c0003t0002g0017a0004c0004t0002g0010others(5): Show | 8 | HG02109.hp1 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+8172_126+8175d others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210565015 | |||||
chr2:210565236
|
T | G | 208 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(205): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.127-8062T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565236 | ||||||
chr2:210565268
|
C | T | 135 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(132): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.127-8030C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565268 | ||||||
chr2:210565272
|
G | C | 1 | a0002c0005t0003g0132 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.127-8026G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565272 | ||||||
chr2:210565379
|
G | C | 213 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(210): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.127-7919G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565379 | ||||||
chr2:210565381
|
G | A | 20 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(17): Show | 21 | HG00558.hp1 HG00609.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-7917G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565381 | ||||||
chr2:210565439
|
T | C | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.127-7859T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565439 | ||||||
chr2:210565456
|
G | A | 2 | a0001c0001t0008g0119a0003c0003t0005g0118 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.127-7842G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565456 | ||||||
chr2:210565589
|
T | G | 1 | a0003c0003t0004g0279 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-7709T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565589 | ||||||
chr2:210565609
|
G | A | 206 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(203): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.127-7689G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565609 | ||||||
chr2:210565616
|
C | T | 4 | a0001c0001t0009g0246a0001c0001t0028g0243a0003c0003t0002g0241others(1): Show | 4 | HG02109.hp2 HG02486.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-7682C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565616 | ||||||
chr2:210565631
|
T | C | 1 | a0003c0003t0005g0168 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.127-7667T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565631 | ||||||
chr2:210565736
|
G | T | 4 | a0001c0001t0003g0129a0001c0001t0003g0131a0003c0003t0005g0083others(1): Show | 4 | HG00140.hp2 HG01257.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-7562G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565736 | ||||||
chr2:210565983
|
A | G | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.127-7315A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210565983 | ||||||
chr2:210566010
|
A | T | 2 | a0001c0001t0003g0128a0003c0003t0001g0127 | 2 | HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.127-7288A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566010 | ||||||
chr2:210566036
|
T | C | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.127-7262T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566036 | ||||||
chr2:210566060
|
T | C | 1 | a0001c0001t0007g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127-7238T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566060 | ||||||
chr2:210566258
|
C | T | 2 | a0002c0002t0003g0217a0002c0002t0003g0218 | 2 | NA19009.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.127-7040C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566258 | ||||||
chr2:210566278
|
G | T | 1 | a0002c0002t0001g0216 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.127-7020G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566278 | ||||||
chr2:210566283
|
G | T | 62 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(59): Show | 63 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-7015G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566283 | ||||||
chr2:210566314
|
G | T | 53 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.127-6984G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566314 | ||||||
chr2:210566350
|
C | T | 55 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(52): Show | 59 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.127-6948C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566350 | ||||||
chr2:210566670
|
C | T | 3 | a0001c0001t0029g0278a0001c0006t0006g0276a0003c0008t0004g0277 | 3 | HG02738.hp2 HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.127-6628C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566670 | ||||||
chr2:210566773
|
G | C | 64 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.127-6525G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566773 | ||||||
chr2:210566876
|
C | T | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-6422C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566876 | ||||||
chr2:210566959
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.127-6339G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210566959 | ||||||
chr2:210567153
|
G | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.127-6145G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567153 | ||||||
chr2:210567176
|
T | C | 1 | a0006c0010t0014g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.127-6122T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567176 | ||||||
chr2:210567196
|
A | T | 1 | a0001c0006t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.127-6102A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567196 | ||||||
chr2:210567285
|
T | G | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-6013T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567285 | ||||||
chr2:210567500
|
A | G | 1 | a0001c0001t0014g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-5798A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567500 | ||||||
chr2:210567553
|
T | C | 1 | a0001c0001t0013g0028 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.127-5745T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567553 | ||||||
chr2:210567614
|
G | A | 136 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(133): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.127-5684G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567614 | ||||||
chr2:210567892
|
G | A | 1 | a0002c0005t0012g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127-5406G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567892 | ||||||
chr2:210567955
|
A | G | 35 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(32): Show | 38 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-5343A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567955 | ||||||
chr2:210567982
|
C | T | 1 | a0004c0007t0001g0152 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127-5316C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210567982 | ||||||
chr2:210568017
|
C | T | 1 | a0004c0004t0005g0151 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-5281C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568017 | ||||||
chr2:210568355
|
T | C | 1 | a0003c0003t0004g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.127-4943T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568355 | ||||||
chr2:210568459
|
G | A | 1 | a0003c0003t0004g0255 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127-4839G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568459 | ||||||
chr2:210568521
|
G | A | 2 | a0003c0003t0002g0240a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.127-4777G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568521 | ||||||
chr2:210568547
|
T | C | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-4751T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568547 | ||||||
chr2:210568750
|
G | A | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-4548G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568750 | ||||||
chr2:210568973
|
A | G | 7 | a0001c0001t0007g0057a0001c0001t0007g0305a0001c0001t0007g0306others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-4325A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210568973 | ||||||
chr2:210569014
|
A | G | 139 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(136): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-4284A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210569014 | ||||||
chr2:210569066
|
A | G | 203 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(200): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.127-4232A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210569066 | ||||||
chr2:210569114
|
G | C | 5 | a0001c0001t0007g0249a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-4184G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210569114 | ||||||
chr2:210569120
|
G | A | 1 | a0004c0007t0004g0323 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-4178G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210569120 | ||||||
chr2:210569594
|
C | T | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.127-3704C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210569594 | ||||||
chr2:210569927
|
T | TGGACCTC others(16): Show |
9 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-3367_127-3345d others(25): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210569927 | |||||
chr2:210569980
|
A | G | 5 | a0001c0001t0007g0249a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-3318A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210569980 | ||||||
chr2:210570138
|
T | C | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-3160T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570138 | ||||||
chr2:210570285
|
C | T | 1 | a0001c0001t0009g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.127-3013C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570285 | ||||||
chr2:210570294
|
A | G | 2 | a0002c0002t0003g0217a0002c0002t0003g0218 | 2 | NA19009.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.127-3004A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570294 | ||||||
chr2:210570307
|
C | T | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-2991C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570307 | ||||||
chr2:210570597
|
A | G | 2 | a0003c0003t0002g0240a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.127-2701A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570597 | ||||||
chr2:210570755
|
AC | A | 53 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(50): Show | 54 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.127-2542delC | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570755 | ||||||
chr2:210570761
|
T | C | 203 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(200): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.127-2537T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570761 | ||||||
chr2:210570996
|
T | C | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0283others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-2302T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210570996 | ||||||
chr2:210571341
|
C | T | 139 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(136): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-1957C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571341 | ||||||
chr2:210571599
|
C | T | 6 | a0002c0002t0001g0219a0002c0002t0001g0221a0002c0002t0001g0222others(3): Show | 6 | HG00621.hp1 HG02109.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1699C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571599 | ||||||
chr2:210571617
|
T | A | 1 | a0001c0001t0002g0264 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.127-1681T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571617 | ||||||
chr2:210571710
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.127-1588A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571710 | ||||||
chr2:210571854
|
TTTGTGTG others(18): Show |
T | 1 | a0001c0001t0006g0030 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.127-1442_127-1418d others(27): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571854 | |||||
chr2:210571855
|
T | G | 2 | a0002c0005t0008g0134a0003c0003t0004g0029 | 2 | HG03017.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.127-1443T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571855 | ||||||
chr2:210571855
|
T | TTG | 21 | a0002c0002t0001g0165a0002c0002t0001g0207a0002c0002t0001g0208others(18): Show | 21 | HG01081.hp1 HG01257.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-1389_127-1388d others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
T | TTGTG | 9 | a0002c0002t0001g0166a0002c0002t0001g0215a0002c0002t0001g0221others(6): Show | 10 | HG00621.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-1391_127-1388d others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTG | T | 15 | a0002c0002t0001g0176a0002c0002t0001g0177a0002c0002t0001g0178others(12): Show | 15 | HG00621.hp2 HG01261.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-1389_127-1388d others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTG | T | 11 | a0002c0002t0001g0174a0002c0002t0002g0309a0002c0002t0002g0310others(8): Show | 12 | HG00741.hp2 HG01109.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-1391_127-1388d others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTG | T | 8 | a0002c0002t0001g0172a0002c0002t0001g0219a0002c0002t0002g0325others(5): Show | 8 | HG01358.hp2 HG02293.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-1393_127-1388d others(8): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(1): Show |
T | 8 | a0001c0001t0014g0153a0002c0002t0001g0170a0002c0005t0003g0136others(5): Show | 8 | HG00323.hp2 HG01884.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-1395_127-1388d others(10): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(3): Show |
T | 5 | a0004c0004t0005g0135a0004c0007t0001g0157a0004c0007t0005g0158others(2): Show | 5 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-1397_127-1388d others(12): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(5): Show |
T | 4 | a0002c0013t0007g0073a0007c0014t0007g0061a0007c0014t0007g0062others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1399_127-1388d others(14): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(7): Show |
T | 7 | a0001c0001t0002g0302a0002c0009t0003g0155a0002c0009t0006g0071others(4): Show | 7 | HG02135.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-1401_127-1388d others(16): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(9): Show |
T | 5 | a0001c0001t0001g0111a0001c0001t0003g0112a0003c0003t0005g0113others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1403_127-1388d others(18): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(11): Show |
T | 63 | a0001c0001t0001g0085a0001c0001t0001g0094a0001c0001t0001g0095others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.127-1405_127-1388d others(20): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(13): Show |
T | 56 | a0001c0001t0001g0086a0001c0001t0002g0007a0001c0001t0002g0264others(53): Show | 59 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.127-1407_127-1388d others(22): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(15): Show |
T | 35 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0068others(32): Show | 38 | HG01243.hp2 HG02109.hp2 HG02145.hp1 others(35): Show |
intron_variant | MODIFIER | c.127-1409_127-1388d others(24): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(19): Show |
T | 38 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(35): Show | 38 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.127-1413_127-1388d others(28): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571855
|
TTGTGTGT others(21): Show |
T | 2 | a0009c0032t0026g0012a0014c0031t0002g0014 | 2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-1415_127-1388d others(30): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571855 | |||||
chr2:210571856
|
TGTGTGTG others(16): Show |
T | 1 | a0003c0003t0004g0029 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.127-1441_127-1419d others(25): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571856 | ||||||
chr2:210571889
|
GTGTGTGT others(15): Show |
G | 1 | a0002c0002t0001g0223 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.127-1403_127-1382d others(24): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr2 | 210571889 | |||||
chr2:210571911
|
A | G | 6 | a0002c0002t0001g0211a0002c0002t0001g0213a0002c0002t0001g0214others(3): Show | 6 | NA18957.hp1 NA18971.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1387A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210571911 | ||||||
chr2:210572033
|
A | G | 1 | a0004c0007t0005g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127-1265A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572033 | ||||||
chr2:210572195
|
A | G | 2 | a0007c0014t0007g0061a0007c0014t0007g0062 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.127-1103A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572195 | ||||||
chr2:210572198
|
G | A | 1 | a0003c0003t0005g0089 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.127-1100G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572198 | ||||||
chr2:210572321
|
T | G | 199 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(196): Show | 205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.127-977T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572321 | ||||||
chr2:210572342
|
A | G | 1 | a0001c0001t0003g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.127-956A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572342 | ||||||
chr2:210572394
|
T | C | 1 | a0002c0005t0012g0169 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.127-904T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572394 | ||||||
chr2:210572411
|
A | C | 2 | a0002c0002t0003g0224a0004c0004t0005g0175 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.127-887A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572411 | ||||||
chr2:210572452
|
G | A | 1 | a0002c0021t0002g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-846G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572452 | ||||||
chr2:210572481
|
C | T | 1 | a0001c0006t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.127-817C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572481 | ||||||
chr2:210572663
|
C | G | 57 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.127-635C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572663 | ||||||
chr2:210572750
|
G | A | 10 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-548G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572750 | ||||||
chr2:210572773
|
G | T | 1 | a0002c0002t0002g0312 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.127-525G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572773 | ||||||
chr2:210572890
|
T | C | 217 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(214): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.127-408T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572890 | ||||||
chr2:210572985
|
A | G | 1 | a0001c0001t0007g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127-313A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210572985 | ||||||
chr2:210573035
|
T | G | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127-263T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210573035 | ||||||
chr2:210573121
|
A | G | 2 | a0003c0003t0005g0113a0003c0003t0005g0114 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.127-177A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210573121 | ||||||
chr2:210573200
|
G | T | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-98G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210573200 | ||||||
chr2:210573205
|
T | A | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.127-93T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 1/37 | chr2 | 210573205 | ||||||
chr2:210573422
|
T | C | 1 | a0001c0001t0007g0031 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.236+15T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573422 | ||||||
chr2:210573499
|
C | T | 1 | a0018c0019t0001g0110 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.236+92C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573499 | ||||||
chr2:210573672
|
G | A | 208 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(205): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.236+265G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573672 | ||||||
chr2:210573717
|
A | T | 1 | a0003c0003t0002g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.236+310A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573717 | ||||||
chr2:210573749
|
C | T | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.236+342C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573749 | ||||||
chr2:210573794
|
T | G | 3 | a0001c0001t0001g0161a0001c0001t0003g0162a0018c0019t0001g0110 | 3 | HG02523.hp1 NA18981.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.236+387T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573794 | ||||||
chr2:210573838
|
A | G | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.236+431A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573838 | ||||||
chr2:210573994
|
A | G | 2 | a0002c0002t0002g0325a0004c0004t0004g0324 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.236+587A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210573994 | ||||||
chr2:210574109
|
T | A | 1 | a0003c0003t0004g0265 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.236+702T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574109 | ||||||
chr2:210574123
|
A | G | 4 | a0004c0007t0001g0157a0004c0007t0005g0158a0004c0007t0005g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.236+716A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574123 | ||||||
chr2:210574162
|
TGAGTTCT others(17): Show |
T | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.236+756_236+779del others(24): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574162 | ||||||
chr2:210574300
|
A | G | 136 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(133): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.236+893A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574300 | ||||||
chr2:210574444
|
C | T | 1 | a0001c0001t0010g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.236+1037C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574444 | ||||||
chr2:210574511
|
A | G | 1 | a0002c0002t0003g0224 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.236+1104A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574511 | ||||||
chr2:210574574
|
C | T | 1 | a0002c0002t0001g0201 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.236+1167C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574574 | ||||||
chr2:210574587
|
T | A | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.236+1180T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574587 | ||||||
chr2:210574588
|
A | T | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.236+1181A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574588 | ||||||
chr2:210574612
|
A | G | 2 | a0003c0003t0002g0240a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.236+1205A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574612 | ||||||
chr2:210574656
|
G | T | 5 | a0001c0001t0007g0009a0007c0014t0007g0061a0007c0014t0007g0062others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.236+1249G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574656 | ||||||
chr2:210574860
|
A | T | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.236+1453A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574860 | ||||||
chr2:210574862
|
C | A | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.236+1455C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574862 | ||||||
chr2:210574863
|
A | ATAAATTA others(5): Show |
1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.236+1456_236+1457i others(14): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574863 | ||||||
chr2:210574875
|
GT | G | 207 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(204): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.237-1462delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210574875 | |||||
chr2:210574957
|
T | G | 1 | a0001c0001t0002g0291 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.237-1389T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210574957 | ||||||
chr2:210575030
|
C | T | 2 | a0004c0004t0002g0010a0004c0004t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.237-1316C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575030 | ||||||
chr2:210575201
|
G | C | 6 | a0001c0001t0003g0253a0001c0001t0028g0243a0003c0003t0002g0241others(3): Show | 7 | HG02109.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-1145G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575201 | ||||||
chr2:210575274
|
G | A | 2 | a0001c0001t0007g0066a0001c0028t0024g0067 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.237-1072G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575274 | ||||||
chr2:210575346
|
AT | A | 4 | a0002c0002t0001g0185a0002c0002t0001g0211a0002c0002t0001g0215others(1): Show | 4 | NA18956.hp2 NA18957.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-996delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575346 | |||||
chr2:210575516
|
G | GCA | 129 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(126): Show | 134 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.237-804_237-803dup others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575516 | |||||
chr2:210575516
|
G | GCACA | 7 | a0001c0001t0002g0291a0001c0001t0006g0033a0001c0006t0006g0276others(4): Show | 7 | HG02109.hp1 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.237-806_237-803dup others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575516 | |||||
chr2:210575516
|
G | GCACACA | 7 | a0001c0001t0007g0032a0002c0009t0003g0155a0002c0009t0006g0071others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.237-808_237-803dup others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575516 | |||||
chr2:210575516
|
GCA | G | 4 | a0003c0003t0002g0240a0003c0018t0002g0239a0007c0014t0007g0061others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.237-804_237-803del others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575516 | |||||
chr2:210575516
|
GCACA | G | 4 | a0002c0002t0001g0223a0002c0005t0006g0075a0004c0004t0002g0010others(1): Show | 4 | HG02895.hp2 HG02897.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.237-806_237-803del others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575516 | |||||
chr2:210575516
|
GCACACAC others(1): Show |
G | 57 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.237-810_237-803del others(8): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575516 | |||||
chr2:210575540
|
A | C | 2 | a0010c0012t0005g0199a0010c0012t0005g0200 | 2 | NA18945.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.237-806A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575540 | ||||||
chr2:210575680
|
C | A | 5 | a0001c0001t0007g0249a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.237-666C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575680 | ||||||
chr2:210575728
|
T | C | 1 | a0003c0003t0002g0256 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.237-618T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575728 | ||||||
chr2:210575769
|
TTGAG | T | 3 | a0001c0001t0006g0054a0001c0001t0013g0055a0001c0001t0013g0056 | 3 | HG01175.hp1 HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.237-575_237-572del others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr2 | 210575769 | |||||
chr2:210575815
|
A | G | 2 | a0001c0001t0008g0119a0003c0003t0005g0118 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.237-531A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210575815 | ||||||
chr2:210576137
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.237-209C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210576137 | ||||||
chr2:210576255
|
C | T | 5 | a0001c0001t0007g0009a0007c0014t0007g0061a0007c0014t0007g0062others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.237-91C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 2/37 | chr2 | 210576255 | ||||||
chr2:210576548
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.381+58T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210576548 | ||||||
chr2:210576587
|
C | T | 4 | a0001c0006t0001g0109a0001c0006t0001g0115a0003c0003t0005g0077others(1): Show | 4 | HG00408.hp2 HG00438.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+97C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210576587 | ||||||
chr2:210576699
|
A | G | 1 | a0001c0001t0007g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.381+209A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210576699 | ||||||
chr2:210576702
|
C | T | 11 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0003g0124others(8): Show | 12 | HG01109.hp1 HG02615.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+212C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210576702 | ||||||
chr2:210576703
|
G | A | 1 | a0001c0006t0006g0292 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.381+213G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210576703 | ||||||
chr2:210576880
|
G | A | 2 | a0007c0014t0007g0061a0007c0014t0007g0062 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.381+390G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210576880 | ||||||
chr2:210577226
|
C | T | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-195C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210577226 | ||||||
chr2:210577274
|
A | AT | 11 | a0001c0001t0003g0235a0002c0005t0003g0139a0002c0009t0003g0155others(8): Show | 11 | HG01884.hp1 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.382-134dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr2 | 210577274 | |||||
chr2:210577309
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.382-112T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210577309 | ||||||
chr2:210577329
|
A | G | 1 | a0001c0001t0003g0108 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.382-92A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 3/37 | chr2 | 210577329 | ||||||
chr2:210577582
|
C | T | 4 | a0004c0004t0004g0058a0004c0004t0005g0135a0004c0004t0005g0143others(1): Show | 4 | HG01109.hp2 HG01358.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+72C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210577582 | ||||||
chr2:210577717
|
T | C | 1 | a0002c0009t0007g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.471+207T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210577717 | ||||||
chr2:210577723
|
G | A | 2 | a0004c0004t0002g0010a0004c0004t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.471+213G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210577723 | ||||||
chr2:210577839
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.471+329T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210577839 | ||||||
chr2:210577942
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.471+432G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210577942 | ||||||
chr2:210578318
|
C | T | 1 | a0001c0001t0023g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.471+808C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578318 | ||||||
chr2:210578356
|
C | T | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.471+846C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578356 | ||||||
chr2:210578381
|
A | G | 2 | a0001c0001t0006g0331a0003c0003t0004g0330 | 2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.471+871A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578381 | ||||||
chr2:210578606
|
G | A | 1 | a0003c0003t0004g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.471+1096G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578606 | ||||||
chr2:210578745
|
A | G | 9 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(6): Show | 9 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-969A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578745 | ||||||
chr2:210578779
|
A | C | 9 | a0001c0001t0007g0057a0001c0001t0007g0305a0001c0001t0007g0306others(6): Show | 9 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-935A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578779 | ||||||
chr2:210578822
|
C | T | 2 | a0003c0003t0004g0300a0003c0003t0004g0301 | 2 | HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.472-892C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210578822 | ||||||
chr2:210579035
|
C | T | 1 | a0002c0002t0001g0198 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.472-679C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210579035 | ||||||
chr2:210579168
|
A | G | 3 | a0001c0001t0001g0086a0001c0006t0001g0088a0003c0003t0005g0087 | 3 | HG01943.hp2 HG01978.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.472-546A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 4/37 | chr2 | 210579168 | ||||||
chr2:210579809
|
G | GGT | 68 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(65): Show | 68 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.528+63_528+64dupTG | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr2 | 210579809 | |||||
chr2:210579809
|
G | GGTGT | 5 | a0001c0001t0001g0107a0001c0001t0001g0161a0001c0001t0003g0106others(2): Show | 5 | HG03041.hp1 NA18981.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+61_528+64dupTG others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr2 | 210579809 | |||||
chr2:210579966
|
T | C | 1 | a0002c0002t0005g0202 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.528+196T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210579966 | ||||||
chr2:210580434
|
A | G | 2 | a0003c0003t0002g0240a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.528+664A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580434 | ||||||
chr2:210580490
|
A | G | 7 | a0001c0001t0007g0057a0001c0001t0007g0305a0001c0001t0007g0306others(4): Show | 7 | HG00140.hp1 HG00323.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+720A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580490 | ||||||
chr2:210580532
|
T | A | 7 | a0001c0001t0007g0009a0003c0003t0002g0240a0003c0018t0002g0239others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.528+762T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580532 | ||||||
chr2:210580616
|
C | T | 4 | a0001c0001t0002g0264a0001c0001t0002g0275a0001c0001t0006g0245others(1): Show | 4 | HG00609.hp2 NA18612.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.528+846C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580616 | ||||||
chr2:210580637
|
G | A | 2 | a0007c0014t0007g0061a0007c0014t0007g0062 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.528+867G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580637 | ||||||
chr2:210580659
|
C | T | 3 | a0002c0002t0002g0325a0004c0004t0004g0324a0004c0007t0005g0160 | 3 | HG02622.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.528+889C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580659 | ||||||
chr2:210580858
|
C | CA | 63 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(60): Show | 66 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.528+1105dupA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr2 | 210580858 | |||||
chr2:210580858
|
CA | C | 18 | a0001c0001t0002g0063a0001c0001t0002g0065a0001c0001t0003g0121others(15): Show | 18 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.528+1105delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr2 | 210580858 | |||||
chr2:210580860
|
A | T | 1 | a0003c0003t0005g0105 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.528+1090A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580860 | ||||||
chr2:210580905
|
A | T | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.528+1135A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580905 | ||||||
chr2:210580906
|
T | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.528+1136T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210580906 | ||||||
chr2:210581397
|
C | T | 198 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(195): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.529-1220C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210581397 | ||||||
chr2:210581403
|
T | C | 10 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.529-1214T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210581403 | ||||||
chr2:210581496
|
G | A | 7 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(4): Show | 7 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.529-1121G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210581496 | ||||||
chr2:210581596
|
G | T | 1 | a0001c0029t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529-1021G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210581596 | ||||||
chr2:210581969
|
A | G | 1 | a0002c0005t0008g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.529-648A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210581969 | ||||||
chr2:210582111
|
A | G | 5 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(2): Show | 5 | HG02630.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.529-506A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210582111 | ||||||
chr2:210582274
|
C | G | 3 | a0001c0001t0028g0243a0003c0003t0002g0241a0003c0003t0027g0242 | 3 | HG02109.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.529-343C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210582274 | ||||||
chr2:210582318
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.529-299C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210582318 | ||||||
chr2:210582465
|
A | T | 2 | a0001c0001t0007g0258a0003c0003t0004g0259 | 2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.529-152A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 5/37 | chr2 | 210582465 | ||||||
chr2:210582855
|
C | T | 1 | a0002c0002t0002g0310 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.621+146C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210582855 | ||||||
chr2:210583001
|
A | C | 1 | a0003c0003t0004g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.621+292A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583001 | ||||||
chr2:210583226
|
A | T | 136 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(133): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.621+517A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583226 | ||||||
chr2:210583490
|
A | C | 2 | a0003c0003t0002g0240a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.621+781A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583490 | ||||||
chr2:210583900
|
G | A | 53 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.621+1191G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583900 | ||||||
chr2:210583935
|
C | A | 203 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(200): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.621+1226C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583935 | ||||||
chr2:210583959
|
G | A | 5 | a0001c0001t0007g0249a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+1250G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583959 | ||||||
chr2:210583969
|
A | T | 203 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(200): Show | 209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.621+1260A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210583969 | ||||||
chr2:210584076
|
A | G | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.621+1367A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210584076 | ||||||
chr2:210584239
|
C | T | 2 | a0003c0003t0002g0240a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.621+1530C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210584239 | ||||||
chr2:210584416
|
A | T | 1 | a0004c0007t0005g0160 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.621+1707A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210584416 | ||||||
chr2:210584548
|
G | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.621+1839G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210584548 | ||||||
chr2:210584937
|
C | T | 134 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(131): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.621+2228C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210584937 | ||||||
chr2:210585001
|
G | A | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.621+2292G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585001 | ||||||
chr2:210585185
|
T | C | 207 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(204): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.621+2476T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585185 | ||||||
chr2:210585226
|
T | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.621+2517T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585226 | ||||||
chr2:210585498
|
G | A | 2 | a0001c0001t0007g0066a0001c0028t0024g0067 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.622-2560G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585498 | ||||||
chr2:210585672
|
T | C | 207 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(204): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.622-2386T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585672 | ||||||
chr2:210585678
|
TAACA | T | 7 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0003g0124others(4): Show | 8 | HG02615.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.622-2379_622-2376d others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585678 | ||||||
chr2:210585744
|
G | T | 4 | a0004c0007t0001g0157a0004c0007t0005g0158a0004c0007t0005g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-2314G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585744 | ||||||
chr2:210585892
|
T | C | 11 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(8): Show | 11 | HG01943.hp2 HG01978.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.622-2166T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585892 | ||||||
chr2:210585986
|
G | A | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.622-2072G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210585986 | ||||||
chr2:210586126
|
C | T | 59 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0266others(56): Show | 62 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.622-1932C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210586126 | ||||||
chr2:210586345
|
TTTAAAAT others(235): Show |
T | 1 | a0003c0003t0004g0298 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.622-1708_622-1467d others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr2 | 210586345 | |||||
chr2:210586421
|
G | A | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.622-1637G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210586421 | ||||||
chr2:210586575
|
A | G | 2 | a0007c0014t0007g0061a0007c0014t0007g0062 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.622-1483A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210586575 | ||||||
chr2:210586611
|
T | C | 1 | a0001c0001t0003g0230 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.622-1447T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210586611 | ||||||
chr2:210586718
|
G | C | 3 | a0001c0001t0007g0009a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG01884.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.622-1340G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210586718 | ||||||
chr2:210586850
|
A | G | 1 | a0001c0001t0003g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.622-1208A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210586850 | ||||||
chr2:210587072
|
AT | A | 194 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.622-977delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr2 | 210587072 | |||||
chr2:210587226
|
C | G | 1 | a0003c0003t0004g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.622-832C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587226 | ||||||
chr2:210587374
|
A | T | 1 | a0002c0002t0002g0320 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.622-684A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587374 | ||||||
chr2:210587451
|
G | A | 132 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(129): Show | 138 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.622-607G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587451 | ||||||
chr2:210587472
|
C | A | 3 | a0001c0001t0003g0081a0001c0001t0003g0091a0001c0001t0003g0108 | 3 | NA18983.hp2 NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.622-586C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587472 | ||||||
chr2:210587563
|
CTT | C | 52 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.622-494_622-493del others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587563 | ||||||
chr2:210587566
|
A | T | 1 | a0001c0001t0006g0329 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.622-492A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587566 | ||||||
chr2:210587749
|
T | G | 4 | a0004c0007t0001g0157a0004c0007t0005g0158a0004c0007t0005g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-309T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587749 | ||||||
chr2:210587776
|
G | T | 1 | a0003c0003t0004g0298 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.622-282G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587776 | ||||||
chr2:210587874
|
TAC | T | 53 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(50): Show | 54 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.622-182_622-181del others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr2 | 210587874 | |||||
chr2:210587907
|
A | C | 1 | a0001c0001t0003g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.622-151A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587907 | ||||||
chr2:210587980
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.622-78T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 6/37 | chr2 | 210587980 | ||||||
chr2:210588296
|
A | C | 2 | a0007c0014t0007g0061a0007c0014t0007g0062 | 2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.711+149A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588296 | ||||||
chr2:210588313
|
A | G | 3 | a0009c0030t0007g0074a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG03041.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.711+166A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588313 | ||||||
chr2:210588426
|
T | A | 1 | a0003c0003t0004g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.711+279T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588426 | ||||||
chr2:210588536
|
C | A | 1 | a0002c0002t0015g0084 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.711+389C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588536 | ||||||
chr2:210588681
|
C | T | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+534C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588681 | ||||||
chr2:210588744
|
A | G | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.711+597A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588744 | ||||||
chr2:210588858
|
A | G | 3 | a0001c0001t0007g0066a0001c0028t0024g0067a0003c0018t0002g0239 | 3 | HG02451.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.711+711A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588858 | ||||||
chr2:210588890
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.711+743G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210588890 | ||||||
chr2:210589077
|
A | G | 212 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(209): Show | 218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.711+930A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210589077 | ||||||
chr2:210589115
|
G | T | 1 | a0016c0023t0006g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.711+968G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210589115 | ||||||
chr2:210589409
|
G | A | 125 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(122): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.712-697G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210589409 | ||||||
chr2:210589734
|
G | A | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.712-372G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210589734 | ||||||
chr2:210589948
|
C | T | 1 | a0001c0001t0018g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.712-158C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210589948 | ||||||
chr2:210590078
|
A | G | 1 | a0001c0001t0003g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.712-28A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 7/37 | chr2 | 210590078 | ||||||
chr2:210590276
|
G | C | 5 | a0001c0001t0007g0066a0001c0001t0014g0153a0001c0028t0024g0067others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+42G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590276 | ||||||
chr2:210590386
|
T | C | 5 | a0001c0001t0007g0066a0001c0001t0014g0153a0001c0028t0024g0067others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+152T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590386 | ||||||
chr2:210590440
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.840+206A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590440 | ||||||
chr2:210590557
|
A | G | 133 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(130): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.841-243A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590557 | ||||||
chr2:210590613
|
T | C | 2 | a0004c0004t0002g0010a0004c0004t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.841-187T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590613 | ||||||
chr2:210590618
|
T | C | 197 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(194): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.841-182T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590618 | ||||||
chr2:210590623
|
C | A | 1 | a0001c0001t0006g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.841-177C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590623 | ||||||
chr2:210590634
|
A | G | 1 | a0002c0005t0008g0237 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.841-166A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 8/37 | chr2 | 210590634 | ||||||
chr2:210590948
|
C | T | 1 | a0001c0001t0003g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.947+42C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210590948 | ||||||
chr2:210590990
|
T | C | 2 | a0002c0002t0011g0140a0004c0004t0005g0151 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.947+84T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210590990 | ||||||
chr2:210591041
|
A | AAAAT | 4 | a0002c0005t0008g0134a0004c0004t0004g0020a0007c0014t0007g0061others(1): Show | 4 | HG02258.hp1 HG02559.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.947+163_947+166dup others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr2 | 210591041 | |||||
chr2:210591041
|
A | AAAATAAA others(1): Show |
3 | a0009c0030t0007g0074a0009c0032t0026g0012a0014c0031t0002g0014 | 3 | HG03041.hp1 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.947+159_947+166dup others(8): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr2 | 210591041 | |||||
chr2:210591041
|
AAAAT | A | 6 | a0001c0006t0002g0038a0002c0005t0006g0075a0004c0007t0001g0157others(3): Show | 6 | HG01891.hp2 HG02165.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.947+163_947+166del others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr2 | 210591041 | |||||
chr2:210591229
|
A | G | 66 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(63): Show | 68 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.947+323A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210591229 | ||||||
chr2:210591397
|
C | T | 1 | a0004c0007t0005g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.948-434C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210591397 | ||||||
chr2:210591590
|
C | T | 2 | a0001c0001t0007g0254a0001c0024t0017g0288 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.948-241C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210591590 | ||||||
chr2:210591628
|
C | T | 1 | a0001c0001t0006g0037 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.948-203C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210591628 | ||||||
chr2:210591760
|
T | C | 1 | a0003c0008t0004g0039 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.948-71T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210591760 | ||||||
chr2:210591767
|
A | C | 3 | a0001c0001t0028g0243a0003c0003t0002g0241a0003c0003t0027g0242 | 3 | HG02109.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.948-64A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 9/37 | chr2 | 210591767 | ||||||
chr2:210592082
|
C | T | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1086+113C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/37 | chr2 | 210592082 | ||||||
chr2:210592175
|
C | T | 1 | a0004c0004t0005g0135 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1086+206C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/37 | chr2 | 210592175 | ||||||
chr2:210592225
|
G | C | 1 | a0002c0002t0005g0202 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1086+256G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/37 | chr2 | 210592225 | ||||||
chr2:210592537
|
C | T | 194 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1087-342C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/37 | chr2 | 210592537 | ||||||
chr2:210592732
|
A | G | 26 | a0002c0002t0001g0147a0002c0002t0001g0165a0002c0002t0001g0166others(23): Show | 26 | HG00438.hp2 HG00639.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1087-147A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 10/37 | chr2 | 210592732 | ||||||
chr2:210593019
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1164+63G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593019 | ||||||
chr2:210593055
|
A | G | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1164+99A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593055 | ||||||
chr2:210593182
|
G | A | 1 | a0009c0030t0007g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1164+226G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593182 | ||||||
chr2:210593182
|
G | T | 6 | a0001c0001t0003g0120a0001c0001t0007g0249a0001c0001t0009g0247others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1164+226G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593182 | ||||||
chr2:210593274
|
C | G | 15 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0003g0124others(12): Show | 17 | HG01109.hp1 HG01884.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1164+318C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593274 | ||||||
chr2:210593372
|
A | C | 1 | a0002c0009t0006g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1164+416A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593372 | ||||||
chr2:210593411
|
G | A | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1164+455G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593411 | ||||||
chr2:210593550
|
C | G | 2 | a0001c0001t0007g0249a0001c0029t0007g0250 | 2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1164+594C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593550 | ||||||
chr2:210593775
|
T | A | 3 | a0001c0001t0006g0293a0001c0006t0006g0294a0003c0008t0004g0001 | 5 | HG02523.hp2 NA18951.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-733T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593775 | ||||||
chr2:210593876
|
A | G | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1165-632A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210593876 | ||||||
chr2:210594067
|
C | A | 1 | a0003c0003t0004g0274 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1165-441C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210594067 | ||||||
chr2:210594115
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1165-393G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210594115 | ||||||
chr2:210594154
|
A | G | 7 | a0001c0001t0003g0120a0001c0001t0007g0249a0001c0001t0009g0247others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1165-354A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210594154 | ||||||
chr2:210594262
|
A | T | 1 | a0001c0001t0003g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1165-246A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210594262 | ||||||
chr2:210594381
|
C | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1165-127C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 11/37 | chr2 | 210594381 | ||||||
chr2:210595168
|
T | A | 2 | a0002c0002t0002g0325a0004c0004t0004g0324 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1264-319T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 12/37 | chr2 | 210595168 | ||||||
chr2:210595363
|
A | G | 1 | a0001c0001t0014g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1264-124A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 12/37 | chr2 | 210595363 | ||||||
chr2:210595589
|
G | A | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | splice_region_variant&intron_variant | LOW | c.1359+7G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210595589 | ||||||
chr2:210595702
|
A | C | 1 | a0003c0003t0004g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1359+120A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210595702 | ||||||
chr2:210595780
|
T | C | 1 | a0001c0001t0002g0264 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1359+198T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210595780 | ||||||
chr2:210595957
|
A | C | 1 | a0002c0002t0001g0080 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1359+375A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210595957 | ||||||
chr2:210595978
|
G | A | 194 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(191): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1359+396G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210595978 | ||||||
chr2:210596106
|
G | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1359+524G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210596106 | ||||||
chr2:210596140
|
A | G | 213 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(210): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1359+558A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210596140 | ||||||
chr2:210596277
|
A | T | 16 | a0002c0002t0001g0172a0002c0002t0001g0194a0002c0002t0001g0195others(13): Show | 16 | HG01257.hp2 HG01258.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.1359+695A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210596277 | ||||||
chr2:210596388
|
G | A | 125 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(122): Show | 131 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1359+806G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210596388 | ||||||
chr2:210596707
|
T | G | 2 | a0001c0001t0008g0119a0003c0003t0005g0118 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1359+1125T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210596707 | ||||||
chr2:210596890
|
T | C | 5 | a0001c0001t0008g0096a0003c0003t0005g0097a0003c0003t0005g0105others(2): Show | 5 | HG00738.hp2 HG01106.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1359+1308T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210596890 | ||||||
chr2:210597027
|
C | T | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1359+1445C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597027 | ||||||
chr2:210597084
|
G | A | 5 | a0007c0014t0007g0061a0007c0014t0007g0062a0009c0030t0007g0074others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1359+1502G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597084 | ||||||
chr2:210597156
|
T | A | 208 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(205): Show | 214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1359+1574T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597156 | ||||||
chr2:210597262
|
C | T | 1 | a0002c0002t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1359+1680C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597262 | ||||||
chr2:210597290
|
A | G | 1 | a0004c0004t0004g0058 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1359+1708A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597290 | ||||||
chr2:210597683
|
G | A | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1360-1689G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597683 | ||||||
chr2:210597823
|
C | CATATATA others(29): Show |
1 | a0002c0009t0007g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1360-1540_1360-153 others(40): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597823 | |||||
chr2:210597823
|
C | CATATATA others(37): Show |
2 | a0004c0004t0002g0010a0004c0004t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1360-1540_1360-153 others(48): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597823 | |||||
chr2:210597829
|
T | TATATATA others(67): Show |
1 | a0002c0009t0006g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1360-1540_1360-153 others(78): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597829 | |||||
chr2:210597829
|
T | TATATATA others(35): Show |
1 | a0002c0013t0006g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1360-1540_1360-153 others(46): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597829 | |||||
chr2:210597829
|
T | TATATATA others(39): Show |
1 | a0002c0013t0007g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1360-1540_1360-153 others(50): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597829 | |||||
chr2:210597829
|
T | TATATATA others(41): Show |
1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1360-1540_1360-153 others(52): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597829 | |||||
chr2:210597829
|
T | TATATATA others(43): Show |
1 | a0002c0009t0006g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1360-1540_1360-153 others(54): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210597829 | |||||
chr2:210597908
|
A | G | 1 | a0003c0003t0004g0052 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1360-1464A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210597908 | ||||||
chr2:210598075
|
C | A | 55 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(52): Show | 57 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1360-1297C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598075 | ||||||
chr2:210598090
|
T | TC | 62 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(59): Show | 62 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1360-1282_1360-128 others(5): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598090 | ||||||
chr2:210598492
|
G | A | 1 | a0003c0008t0004g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1360-880G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598492 | ||||||
chr2:210598504
|
G | C | 1 | a0001c0001t0001g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1360-868G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598504 | ||||||
chr2:210598540
|
GA | G | 127 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(124): Show | 133 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1360-823delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210598540 | |||||
chr2:210598549
|
A | AG | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360-819dupG | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | INFO_REALIGN_3_PRIME | chr2 | 210598549 | |||||
chr2:210598569
|
C | T | 1 | a0001c0001t0001g0161 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1360-803C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598569 | ||||||
chr2:210598611
|
C | T | 55 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(52): Show | 57 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1360-761C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598611 | ||||||
chr2:210598679
|
A | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0065a0003c0003t0004g0051others(1): Show | 4 | NA18963.hp2 NA18992.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360-693A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598679 | ||||||
chr2:210598773
|
C | T | 1 | a0001c0001t0003g0234 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1360-599C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598773 | ||||||
chr2:210598826
|
A | T | 9 | a0001c0001t0007g0057a0001c0001t0007g0305a0001c0001t0007g0306others(6): Show | 9 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360-546A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598826 | ||||||
chr2:210598892
|
C | T | 1 | a0002c0002t0001g0197 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1360-480C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598892 | ||||||
chr2:210598894
|
C | G | 3 | a0001c0001t0001g0104a0001c0001t0002g0026a0003c0003t0004g0025 | 3 | NA18974.hp2 NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1360-478C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598894 | ||||||
chr2:210598915
|
T | C | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360-457T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598915 | ||||||
chr2:210598935
|
C | T | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1360-437C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210598935 | ||||||
chr2:210599075
|
C | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360-297C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210599075 | ||||||
chr2:210599100
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1360-272G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210599100 | ||||||
chr2:210599142
|
G | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360-230G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210599142 | ||||||
chr2:210599262
|
G | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360-110G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210599262 | ||||||
chr2:210599361
|
G | C | 1 | a0003c0003t0004g0262 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1360-11G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 13/37 | chr2 | 210599361 | ||||||
chr2:210599719
|
T | C | 1 | a0003c0003t0002g0240 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1549+158T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210599719 | ||||||
chr2:210599820
|
A | G | 1 | a0011c0017t0005g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1549+259A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210599820 | ||||||
chr2:210599825
|
A | G | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1549+264A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210599825 | ||||||
chr2:210599829
|
C | T | 131 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(128): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1549+268C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210599829 | ||||||
chr2:210599854
|
A | G | 1 | a0002c0002t0002g0312 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1549+293A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210599854 | ||||||
chr2:210599880
|
T | C | 1 | a0002c0002t0003g0210 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1549+319T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210599880 | ||||||
chr2:210600005
|
T | A | 3 | a0001c0001t0001g0104a0001c0001t0002g0026a0003c0003t0004g0025 | 3 | NA18974.hp2 NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1549+444T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210600005 | ||||||
chr2:210600199
|
G | T | 5 | a0001c0001t0007g0249a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-356G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210600199 | ||||||
chr2:210600264
|
A | G | 5 | a0001c0001t0007g0066a0001c0001t0014g0153a0001c0028t0024g0067others(2): Show | 5 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1550-291A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210600264 | ||||||
chr2:210600389
|
G | A | 56 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(53): Show | 58 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1550-166G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210600389 | ||||||
chr2:210600420
|
C | T | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1550-135C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 14/37 | chr2 | 210600420 | ||||||
chr2:210601056
|
T | C | 210 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(207): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1707+344T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601056 | ||||||
chr2:210601227
|
T | G | 1 | a0001c0001t0002g0035 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1707+515T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601227 | ||||||
chr2:210601372
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1707+660T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601372 | ||||||
chr2:210601413
|
C | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1707+701C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601413 | ||||||
chr2:210601542
|
A | T | 3 | a0003c0003t0002g0017a0015c0022t0002g0018a0016c0023t0006g0019 | 3 | HG02109.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1708-660A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601542 | ||||||
chr2:210601654
|
T | C | 4 | a0004c0007t0001g0157a0004c0007t0005g0158a0004c0007t0005g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1708-548T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601654 | ||||||
chr2:210601866
|
G | A | 1 | a0003c0003t0004g0029 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1708-336G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601866 | ||||||
chr2:210601917
|
A | G | 2 | a0002c0002t0001g0190a0002c0002t0001g0198 | 2 | NA19010.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1708-285A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210601917 | ||||||
chr2:210602104
|
C | G | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1708-98C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210602104 | ||||||
chr2:210602105
|
A | T | 3 | a0001c0001t0003g0129a0003c0003t0005g0083a0008c0015t0011g0130 | 3 | HG01257.hp1 HG01891.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1708-97A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 15/37 | chr2 | 210602105 | ||||||
chr2:210602333
|
A | G | 1 | a0002c0002t0002g0319 | 1 | HG01978.hp2 | splice_region_variant&intron_variant | LOW | c.1836+3A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210602333 | ||||||
chr2:210602385
|
C | A | 1 | a0001c0001t0007g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1836+55C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210602385 | ||||||
chr2:210602824
|
A | G | 133 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(130): Show | 139 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1836+494A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210602824 | ||||||
chr2:210603096
|
C | T | 1 | a0001c0001t0009g0280 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1836+766C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210603096 | ||||||
chr2:210603195
|
A | T | 4 | a0001c0001t0007g0066a0001c0028t0024g0067a0003c0003t0002g0240others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1836+865A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210603195 | ||||||
chr2:210603537
|
T | C | 3 | a0001c0001t0006g0030a0001c0001t0006g0040a0003c0003t0004g0029 | 3 | HG00597.hp1 NA19087.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1836+1207T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210603537 | ||||||
chr2:210603564
|
T | C | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1836+1234T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210603564 | ||||||
chr2:210603795
|
T | A | 1 | a0003c0003t0004g0041 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1837-1307T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210603795 | ||||||
chr2:210603848
|
G | A | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1837-1254G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210603848 | ||||||
chr2:210604060
|
G | A | 1 | a0006c0010t0014g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1837-1042G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604060 | ||||||
chr2:210604166
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1837-936G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604166 | ||||||
chr2:210604186
|
C | T | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1837-916C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604186 | ||||||
chr2:210604217
|
T | A | 8 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(5): Show | 8 | HG02257.hp2 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837-885T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604217 | ||||||
chr2:210604399
|
A | G | 210 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(207): Show | 216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1837-703A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604399 | ||||||
chr2:210604466
|
T | G | 206 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(203): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.1837-636T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604466 | ||||||
chr2:210604707
|
A | G | 16 | a0002c0002t0001g0076a0002c0002t0001g0080a0002c0002t0001g0163others(13): Show | 16 | HG00558.hp1 NA18943.hp2 NA18944.hp2 others(13): Show |
intron_variant | MODIFIER | c.1837-395A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 16/37 | chr2 | 210604707 | ||||||
chr2:210605362
|
T | C | 76 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(73): Show | 76 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1981+116T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210605362 | ||||||
chr2:210605453
|
G | A | 3 | a0007c0014t0007g0061a0009c0030t0007g0074a0009c0032t0026g0012 | 3 | HG02258.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1981+207G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210605453 | ||||||
chr2:210605472
|
T | C | 11 | a0001c0001t0003g0121a0001c0001t0003g0129a0001c0001t0003g0131others(8): Show | 11 | HG00140.hp2 HG01175.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1981+226T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210605472 | ||||||
chr2:210605769
|
T | G | 93 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(90): Show | 93 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.1981+523T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210605769 | ||||||
chr2:210605990
|
C | A | 1 | a0001c0001t0001g0111 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1982-741C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210605990 | ||||||
chr2:210606058
|
A | G | 4 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1982-673A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606058 | ||||||
chr2:210606236
|
T | C | 75 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(72): Show | 75 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1982-495T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606236 | ||||||
chr2:210606268
|
G | A | 2 | a0001c0001t0003g0092a0001c0001t0006g0284 | 2 | HG06807.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1982-463G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606268 | ||||||
chr2:210606313
|
G | T | 20 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0272others(17): Show | 21 | HG00597.hp2 HG00609.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1982-418G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606313 | ||||||
chr2:210606347
|
G | A | 211 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(208): Show | 215 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.1982-384G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606347 | ||||||
chr2:210606444
|
G | C | 1 | a0007c0014t0007g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1982-287G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606444 | ||||||
chr2:210606515
|
A | T | 3 | a0001c0001t0014g0153a0001c0001t0028g0243a0003c0018t0002g0239 | 3 | HG02109.hp2 HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1982-216A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606515 | ||||||
chr2:210606638
|
T | C | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1982-93T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606638 | ||||||
chr2:210606665
|
G | T | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1982-66G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 17/37 | chr2 | 210606665 | ||||||
chr2:210606984
|
A | G | 1 | a0002c0002t0003g0204 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2192+43A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210606984 | ||||||
chr2:210607068
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2192+127A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607068 | ||||||
chr2:210607299
|
A | G | 1 | a0001c0001t0007g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2192+358A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607299 | ||||||
chr2:210607570
|
A | G | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(6): Show | 9 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2192+629A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607570 | ||||||
chr2:210607574
|
T | A | 1 | a0002c0013t0006g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2192+633T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607574 | ||||||
chr2:210607807
|
C | A | 5 | a0001c0001t0009g0247a0001c0001t0009g0248a0001c0001t0009g0280others(2): Show | 5 | HG01243.hp2 HG02145.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2193-554C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607807 | ||||||
chr2:210607886
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2193-475A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607886 | ||||||
chr2:210607994
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2193-367G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210607994 | ||||||
chr2:210608078
|
T | C | 4 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2193-283T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210608078 | ||||||
chr2:210608133
|
G | A | 1 | a0009c0032t0026g0012 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2193-228G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210608133 | ||||||
chr2:210608161
|
G | A | 8 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2193-200G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210608161 | ||||||
chr2:210608203
|
G | T | 1 | a0002c0013t0007g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2193-158G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210608203 | ||||||
chr2:210608346
|
G | T | 64 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(61): Show | 64 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2193-15G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 18/37 | chr2 | 210608346 | ||||||
chr2:210608577
|
T | G | 6 | a0001c0001t0003g0120a0001c0001t0009g0247a0001c0001t0009g0248others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2391+18T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210608577 | ||||||
chr2:210608579
|
C | T | 1 | a0001c0001t0007g0009 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2391+20C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210608579 | ||||||
chr2:210608683
|
T | A | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2391+124T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210608683 | ||||||
chr2:210608841
|
A | G | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2391+282A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210608841 | ||||||
chr2:210608845
|
A | T | 1 | a0004c0004t0004g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2391+286A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210608845 | ||||||
chr2:210609088
|
A | T | 1 | a0002c0002t0015g0171 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2391+529A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210609088 | ||||||
chr2:210609148
|
A | G | 1 | a0002c0002t0001g0178 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2391+589A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210609148 | ||||||
chr2:210609306
|
G | C | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2391+747G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210609306 | ||||||
chr2:210609523
|
A | G | 1 | a0002c0002t0003g0217 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2391+964A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210609523 | ||||||
chr2:210609671
|
C | T | 1 | a0002c0002t0008g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2391+1112C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210609671 | ||||||
chr2:210610259
|
A | G | 4 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2391+1700A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210610259 | ||||||
chr2:210610392
|
C | T | 1 | a0003c0008t0004g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2392-1725C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210610392 | ||||||
chr2:210610393
|
G | A | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2392-1724G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210610393 | ||||||
chr2:210610454
|
C | T | 1 | a0002c0002t0002g0318 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2392-1663C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210610454 | ||||||
chr2:210610819
|
A | G | 7 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2392-1298A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210610819 | ||||||
chr2:210610838
|
GT | G | 6 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2392-1269delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr2 | 210610838 | |||||
chr2:210610940
|
A | G | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(6): Show | 9 | HG02109.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2392-1177A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210610940 | ||||||
chr2:210611047
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2392-1070G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611047 | ||||||
chr2:210611122
|
A | C | 10 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(7): Show | 10 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2392-995A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611122 | ||||||
chr2:210611255
|
A | G | 1 | a0001c0001t0010g0303 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2392-862A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611255 | ||||||
chr2:210611264
|
A | T | 1 | a0001c0001t0006g0293 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2392-853A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611264 | ||||||
chr2:210611423
|
G | T | 7 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2392-694G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611423 | ||||||
chr2:210611547
|
AT | A | 63 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(60): Show | 63 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.2392-567delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr2 | 210611547 | |||||
chr2:210611570
|
C | T | 7 | a0002c0005t0003g0138a0002c0005t0003g0139a0002c0013t0006g0070others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2392-547C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611570 | ||||||
chr2:210611619
|
G | A | 4 | a0002c0002t0001g0190a0002c0002t0001g0198a0002c0002t0001g0209others(1): Show | 4 | NA18954.hp1 NA19010.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.2392-498G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611619 | ||||||
chr2:210611625
|
T | G | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2392-492T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611625 | ||||||
chr2:210611644
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0002g0026a0003c0003t0004g0025 | 3 | NA18974.hp2 NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2392-473G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | chr2 | 210611644 | ||||||
chr2:210611971
|
C | CT | 53 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0264others(50): Show | 55 | HG00597.hp2 HG00609.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.2392-133dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr2 | 210611971 | |||||
chr2:210611971
|
C | CTT | 60 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(57): Show | 62 | HG00140.hp2 HG00597.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.2392-134_2392-133d others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr2 | 210611971 | |||||
chr2:210611971
|
C | CTTT | 8 | a0001c0001t0007g0057a0001c0001t0016g0327a0001c0001t0017g0322others(5): Show | 8 | HG00140.hp1 HG00408.hp1 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.2392-135_2392-133d others(5): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr2 | 210611971 | |||||
chr2:210611971
|
CT | C | 69 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(66): Show | 69 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.2392-133delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr2 | 210611971 | |||||
chr2:210612494
|
A | G | 11 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(8): Show | 13 | HG02109.hp2 HG02258.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.2568+201A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210612494 | ||||||
chr2:210612562
|
C | G | 1 | a0003c0003t0004g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2568+269C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210612562 | ||||||
chr2:210612593
|
C | CTT | 4 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2568+300_2568+301i others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210612593 | ||||||
chr2:210612653
|
A | G | 1 | a0001c0024t0017g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2568+360A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210612653 | ||||||
chr2:210612697
|
T | C | 1 | a0004c0004t0005g0182 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2568+404T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210612697 | ||||||
chr2:210612875
|
C | A | 1 | a0001c0029t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2568+582C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210612875 | ||||||
chr2:210613138
|
G | A | 1 | a0001c0001t0016g0327 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2568+845G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613138 | ||||||
chr2:210613292
|
A | G | 2 | a0009c0030t0007g0074a0009c0032t0026g0012 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2568+999A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613292 | ||||||
chr2:210613345
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2568+1052G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613345 | ||||||
chr2:210613558
|
A | ATG | 14 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(11): Show | 14 | HG02109.hp2 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2568+1281_2568+128 others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr2 | 210613558 | |||||
chr2:210613642
|
A | C | 21 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0068others(18): Show | 23 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.2568+1349A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613642 | ||||||
chr2:210613704
|
G | A | 64 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(61): Show | 64 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.2568+1411G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613704 | ||||||
chr2:210613738
|
T | C | 4 | a0004c0007t0001g0157a0004c0007t0005g0158a0004c0007t0005g0159others(1): Show | 4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2568+1445T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613738 | ||||||
chr2:210613922
|
C | T | 2 | a0002c0013t0007g0073a0003c0003t0005g0164 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2568+1629C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210613922 | ||||||
chr2:210614193
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2568+1900G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210614193 | ||||||
chr2:210614248
|
T | A | 1 | a0002c0005t0003g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2568+1955T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210614248 | ||||||
chr2:210614295
|
A | G | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2568+2002A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210614295 | ||||||
chr2:210614473
|
A | C | 1 | a0007c0014t0007g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2569-1950A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210614473 | ||||||
chr2:210614885
|
G | A | 70 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.2569-1538G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210614885 | ||||||
chr2:210615027
|
G | GTA | 7 | a0001c0001t0003g0120a0001c0001t0009g0247a0001c0001t0009g0248others(4): Show | 7 | HG01243.hp2 HG01934.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-1381_2569-138 others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr2 | 210615027 | |||||
chr2:210615107
|
T | A | 1 | a0007c0014t0007g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2569-1316T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210615107 | ||||||
chr2:210615233
|
A | C | 6 | a0001c0001t0003g0120a0001c0001t0009g0247a0001c0001t0009g0248others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2569-1190A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210615233 | ||||||
chr2:210615374
|
C | T | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2569-1049C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210615374 | ||||||
chr2:210615649
|
T | C | 2 | a0002c0002t0003g0224a0004c0004t0005g0175 | 2 | HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2569-774T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210615649 | ||||||
chr2:210615967
|
G | A | 5 | a0001c0001t0008g0096a0001c0001t0028g0243a0003c0003t0005g0097others(2): Show | 5 | HG00738.hp2 HG01361.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569-456G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210615967 | ||||||
chr2:210616158
|
G | T | 1 | a0002c0002t0001g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2569-265G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210616158 | ||||||
chr2:210616309
|
A | G | 4 | a0001c0001t0008g0096a0003c0003t0005g0097a0003c0003t0005g0105others(1): Show | 4 | HG00738.hp2 HG01361.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2569-114A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 20/37 | chr2 | 210616309 | ||||||
chr2:210616713
|
A | T | 2 | a0002c0013t0007g0073a0003c0003t0005g0164 | 2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2687+172A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210616713 | ||||||
chr2:210616758
|
T | G | 1 | a0002c0002t0002g0321 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2687+217T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210616758 | ||||||
chr2:210616929
|
G | A | 8 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(5): Show | 8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2687+388G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210616929 | ||||||
chr2:210616990
|
C | T | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2687+449C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210616990 | ||||||
chr2:210617107
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2687+566C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617107 | ||||||
chr2:210617252
|
C | A | 5 | a0001c0001t0003g0120a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2687+711C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617252 | ||||||
chr2:210617436
|
G | T | 5 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2687+895G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617436 | ||||||
chr2:210617549
|
T | G | 1 | a0004c0004t0005g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2687+1008T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617549 | ||||||
chr2:210617572
|
A | C | 67 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(64): Show | 67 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.2687+1031A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617572 | ||||||
chr2:210617583
|
G | A | 1 | a0001c0006t0006g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2687+1042G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617583 | ||||||
chr2:210617676
|
G | C | 67 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(64): Show | 67 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.2687+1135G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617676 | ||||||
chr2:210617685
|
G | T | 1 | a0001c0001t0003g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2687+1144G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617685 | ||||||
chr2:210617774
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2687+1233T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210617774 | ||||||
chr2:210618221
|
G | C | 4 | a0001c0001t0007g0305a0001c0001t0007g0306a0001c0001t0007g0307others(1): Show | 4 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2687+1680G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618221 | ||||||
chr2:210618266
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2687+1725A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618266 | ||||||
chr2:210618486
|
C | G | 2 | a0004c0004t0005g0082a0004c0004t0005g0141 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2687+1945C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618486 | ||||||
chr2:210618643
|
A | C | 1 | a0001c0001t0009g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2687+2102A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618643 | ||||||
chr2:210618788
|
G | A | 1 | a0003c0003t0004g0042 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2687+2247G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618788 | ||||||
chr2:210618838
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2687+2297A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618838 | ||||||
chr2:210618984
|
G | T | 1 | a0002c0002t0003g0193 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2687+2443G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210618984 | ||||||
chr2:210619087
|
C | T | 4 | a0002c0002t0001g0219a0002c0002t0001g0221a0004c0004t0004g0059others(1): Show | 4 | HG00621.hp1 NA18994.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.2687+2546C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619087 | ||||||
chr2:210619098
|
T | TGTACTTT others(627): Show |
1 | a0001c0001t0006g0030 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2687+2566_2687+256 others(638): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210619098 | |||||
chr2:210619114
|
A | C | 1 | a0003c0003t0004g0251 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2687+2573A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619114 | ||||||
chr2:210619193
|
G | A | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2687+2652G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619193 | ||||||
chr2:210619253
|
G | A | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2687+2712G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619253 | ||||||
chr2:210619257
|
G | T | 1 | a0002c0002t0003g0002 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2687+2716G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619257 | ||||||
chr2:210619366
|
A | G | 5 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(2): Show | 5 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2687+2825A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619366 | ||||||
chr2:210619624
|
T | C | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2687+3083T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619624 | ||||||
chr2:210619747
|
A | G | 7 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2687+3206A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210619747 | ||||||
chr2:210620463
|
C | T | 44 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(41): Show | 44 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2687+3922C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210620463 | ||||||
chr2:210620683
|
T | G | 65 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(62): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.2687+4142T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210620683 | ||||||
chr2:210620747
|
G | T | 1 | a0011c0017t0005g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2687+4206G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210620747 | ||||||
chr2:210620752
|
T | A | 150 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(147): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2687+4211T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210620752 | ||||||
chr2:210620829
|
G | A | 1 | a0016c0023t0006g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2687+4288G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210620829 | ||||||
chr2:210621029
|
A | G | 1 | a0002c0009t0007g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2687+4488A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210621029 | ||||||
chr2:210621072
|
C | T | 1 | a0002c0002t0003g0193 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2687+4531C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210621072 | ||||||
chr2:210621123
|
A | G | 1 | a0001c0001t0003g0108 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2687+4582A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210621123 | ||||||
chr2:210621254
|
T | C | 2 | a0002c0002t0012g0005a0004c0004t0004g0027 | 3 | HG00735.hp2 HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2687+4713T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210621254 | ||||||
chr2:210621644
|
T | G | 77 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(74): Show | 77 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.2687+5103T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210621644 | ||||||
chr2:210621797
|
C | G | 1 | a0001c0001t0018g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2687+5256C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210621797 | ||||||
chr2:210622005
|
A | G | 1 | a0004c0004t0004g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2687+5464A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622005 | ||||||
chr2:210622144
|
G | A | 1 | a0004c0007t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2687+5603G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622144 | ||||||
chr2:210622270
|
C | A | 3 | a0001c0001t0009g0247a0001c0001t0009g0248a0001c0001t0009g0280 | 3 | HG01243.hp2 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2687+5729C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622270 | ||||||
chr2:210622552
|
G | C | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2687+6011G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622552 | ||||||
chr2:210622555
|
T | G | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2687+6014T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622555 | ||||||
chr2:210622616
|
T | C | 71 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2687+6075T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622616 | ||||||
chr2:210622670
|
A | G | 72 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(69): Show | 72 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.2687+6129A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622670 | ||||||
chr2:210622764
|
CT | C | 3 | a0002c0005t0001g0180a0002c0005t0001g0191a0002c0005t0001g0192 | 3 | NA18945.hp2 NA19005.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2687+6225delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210622764 | |||||
chr2:210622766
|
TA | T | 173 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(170): Show | 176 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.2687+6239delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210622766 | |||||
chr2:210622767
|
A | G | 3 | a0002c0005t0001g0180a0002c0005t0001g0191a0002c0005t0001g0192 | 3 | NA18945.hp2 NA19005.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2687+6226A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622767 | ||||||
chr2:210622770
|
A | C | 1 | a0009c0030t0007g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2687+6229A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622770 | ||||||
chr2:210622851
|
G | A | 1 | a0002c0005t0003g0212 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2687+6310G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622851 | ||||||
chr2:210622870
|
T | G | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2687+6329T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622870 | ||||||
chr2:210622889
|
G | GT | 6 | a0002c0002t0001g0185a0002c0009t0003g0155a0002c0009t0006g0071others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2687+6355dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210622889 | |||||
chr2:210622976
|
T | C | 1 | a0007c0014t0007g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2687+6435T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210622976 | ||||||
chr2:210623133
|
A | G | 38 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0272others(35): Show | 39 | HG00597.hp2 HG00609.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2687+6592A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210623133 | ||||||
chr2:210623324
|
A | G | 1 | a0003c0003t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2687+6783A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210623324 | ||||||
chr2:210623352
|
A | G | 2 | a0003c0003t0004g0260a0003c0003t0004g0290 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2687+6811A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210623352 | ||||||
chr2:210623366
|
G | A | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2687+6825G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210623366 | ||||||
chr2:210623426
|
G | GT | 13 | a0001c0001t0002g0326a0001c0001t0003g0120a0001c0001t0006g0030others(10): Show | 13 | HG00597.hp1 HG00597.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2687+6894dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210623426 | |||||
chr2:210623677
|
T | C | 1 | a0001c0001t0006g0284 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2687+7136T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210623677 | ||||||
chr2:210623959
|
C | A | 71 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2687+7418C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210623959 | ||||||
chr2:210624072
|
T | C | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2687+7531T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210624072 | ||||||
chr2:210624268
|
C | A | 1 | a0002c0002t0002g0313 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2687+7727C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210624268 | ||||||
chr2:210624379
|
T | G | 67 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(64): Show | 69 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.2687+7838T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210624379 | ||||||
chr2:210624484
|
T | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2687+7943T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210624484 | ||||||
chr2:210624543
|
A | G | 1 | a0001c0001t0002g0326 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2687+8002A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210624543 | ||||||
chr2:210624973
|
A | C | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2687+8432A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210624973 | ||||||
chr2:210625091
|
T | C | 79 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(76): Show | 79 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.2687+8550T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210625091 | ||||||
chr2:210625480
|
G | A | 1 | a0004c0004t0005g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2687+8939G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210625480 | ||||||
chr2:210625548
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0002g0026a0003c0003t0004g0025 | 3 | NA18974.hp2 NA18994.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2687+9007A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210625548 | ||||||
chr2:210625952
|
G | T | 20 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0272others(17): Show | 21 | HG00597.hp2 HG00609.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.2687+9411G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210625952 | ||||||
chr2:210625975
|
G | A | 1 | a0001c0001t0006g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2687+9434G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210625975 | ||||||
chr2:210626108
|
C | G | 1 | a0003c0003t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2687+9567C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626108 | ||||||
chr2:210626169
|
A | G | 2 | a0003c0003t0005g0113a0003c0003t0005g0114 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2687+9628A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626169 | ||||||
chr2:210626175
|
C | T | 1 | a0004c0004t0005g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2687+9634C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626175 | ||||||
chr2:210626296
|
T | G | 78 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0034others(75): Show | 80 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.2687+9755T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626296 | ||||||
chr2:210626431
|
T | G | 1 | a0001c0006t0006g0016 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2687+9890T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626431 | ||||||
chr2:210626451
|
G | T | 2 | a0009c0030t0007g0074a0009c0032t0026g0012 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2687+9910G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626451 | ||||||
chr2:210626636
|
C | T | 3 | a0001c0006t0001g0088a0002c0002t0003g0004a0002c0002t0003g0149 | 4 | HG00738.hp1 HG01175.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2687+10095C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626636 | ||||||
chr2:210626667
|
C | G | 1 | a0007c0014t0007g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2687+10126C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626667 | ||||||
chr2:210626740
|
G | A | 1 | a0001c0006t0006g0016 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2687+10199G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626740 | ||||||
chr2:210626862
|
T | G | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2687+10321T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210626862 | ||||||
chr2:210627054
|
G | A | 4 | a0001c0001t0009g0247a0001c0001t0009g0248a0001c0001t0009g0280others(1): Show | 4 | HG01243.hp2 HG02145.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2687+10513G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627054 | ||||||
chr2:210627141
|
G | A | 2 | a0009c0030t0007g0074a0009c0032t0026g0012 | 2 | HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2688-10561G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627141 | ||||||
chr2:210627154
|
G | T | 1 | a0004c0007t0004g0323 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2688-10548G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627154 | ||||||
chr2:210627368
|
A | G | 15 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(12): Show | 15 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2688-10334A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627368 | ||||||
chr2:210627447
|
C | T | 2 | a0001c0001t0014g0153a0003c0018t0002g0239 | 2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2688-10255C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627447 | ||||||
chr2:210627628
|
C | T | 15 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0003g0124others(12): Show | 17 | HG02257.hp1 HG02486.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.2688-10074C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627628 | ||||||
chr2:210627705
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2688-9997G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627705 | ||||||
chr2:210627988
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2688-9714G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210627988 | ||||||
chr2:210628007
|
G | A | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2688-9695G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210628007 | ||||||
chr2:210628077
|
A | G | 9 | a0001c0001t0028g0243a0002c0005t0003g0136a0002c0005t0003g0138others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2688-9625A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210628077 | ||||||
chr2:210628361
|
G | A | 17 | a0002c0002t0001g0207a0002c0002t0002g0309a0002c0002t0002g0310others(14): Show | 17 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2688-9341G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210628361 | ||||||
chr2:210628383
|
C | A | 120 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(117): Show | 120 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.2688-9319C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210628383 | ||||||
chr2:210628520
|
A | T | 1 | a0002c0002t0001g0221 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2688-9182A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210628520 | ||||||
chr2:210628914
|
T | C | 14 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(11): Show | 14 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2688-8788T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210628914 | ||||||
chr2:210629283
|
A | G | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2688-8419A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629283 | ||||||
chr2:210629286
|
A | G | 76 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(73): Show | 76 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.2688-8416A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629286 | ||||||
chr2:210629310
|
A | G | 1 | a0001c0001t0003g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2688-8392A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629310 | ||||||
chr2:210629354
|
G | A | 1 | a0002c0002t0003g0193 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2688-8348G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629354 | ||||||
chr2:210629463
|
T | C | 3 | a0002c0005t0006g0075a0002c0005t0008g0237a0003c0003t0004g0301 | 3 | HG03491.hp1 HG04199.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2688-8239T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629463 | ||||||
chr2:210629530
|
C | T | 3 | a0004c0004t0004g0311a0009c0030t0007g0074a0009c0032t0026g0012 | 3 | HG02040.hp2 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2688-8172C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629530 | ||||||
chr2:210629561
|
C | T | 4 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2688-8141C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629561 | ||||||
chr2:210629620
|
A | C | 1 | a0001c0001t0003g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2688-8082A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629620 | ||||||
chr2:210629741
|
G | A | 8 | a0001c0001t0001g0231a0001c0001t0003g0229a0001c0001t0003g0230others(5): Show | 8 | NA18952.hp2 NA18966.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.2688-7961G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629741 | ||||||
chr2:210629904
|
AT | A | 4 | a0001c0001t0007g0066a0001c0028t0024g0067a0003c0018t0002g0239others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2688-7796delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210629904 | |||||
chr2:210629905
|
T | A | 66 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2688-7797T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210629905 | ||||||
chr2:210630057
|
A | G | 1 | a0001c0001t0002g0026 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2688-7645A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630057 | ||||||
chr2:210630092
|
C | CA | 57 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(54): Show | 57 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.2688-7598dupA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210630092 | |||||
chr2:210630095
|
A | AC | 4 | a0002c0009t0003g0155a0002c0009t0006g0071a0002c0009t0006g0072others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2688-7607_2688-760 others(5): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630095 | ||||||
chr2:210630096
|
A | AC | 3 | a0001c0001t0006g0030a0001c0001t0006g0295a0001c0001t0018g0053 | 3 | HG00597.hp1 HG01261.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2688-7606_2688-760 others(5): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630096 | ||||||
chr2:210630096
|
A | C | 1 | a0002c0013t0007g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2688-7606A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630096 | ||||||
chr2:210630097
|
A | C | 75 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(72): Show | 75 | HG00323.hp1 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2688-7605A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630097 | ||||||
chr2:210630105
|
C | A | 1 | a0004c0004t0005g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2688-7597C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630105 | ||||||
chr2:210630170
|
C | T | 1 | a0001c0001t0003g0106 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2688-7532C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630170 | ||||||
chr2:210630386
|
T | C | 137 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(134): Show | 137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.2688-7316T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630386 | ||||||
chr2:210630597
|
G | T | 3 | a0001c0001t0018g0053a0001c0001t0019g0049a0008c0015t0020g0048 | 3 | HG01168.hp1 HG01261.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2688-7105G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630597 | ||||||
chr2:210630863
|
C | T | 55 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(52): Show | 55 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2688-6839C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210630863 | ||||||
chr2:210631020
|
G | GT | 6 | a0001c0001t0002g0291a0001c0001t0003g0253a0001c0001t0007g0249others(3): Show | 6 | HG00621.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2688-6666dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210631020 | |||||
chr2:210631020
|
GT | G | 126 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(123): Show | 127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2688-6666delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210631020 | |||||
chr2:210631021
|
T | G | 3 | a0001c0001t0028g0243a0003c0018t0002g0239a0004c0007t0005g0228 | 3 | HG02109.hp2 HG02572.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2688-6681T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210631021 | ||||||
chr2:210631022
|
T | G | 119 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(116): Show | 119 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.2688-6680T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210631022 | ||||||
chr2:210631096
|
C | A | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2688-6606C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210631096 | ||||||
chr2:210631361
|
G | A | 1 | a0003c0003t0005g0116 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2688-6341G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210631361 | ||||||
chr2:210631758
|
C | T | 1 | a0002c0009t0006g0071 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2688-5944C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210631758 | ||||||
chr2:210631809
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2688-5893G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210631809 | ||||||
chr2:210632690
|
A | G | 1 | a0001c0001t0006g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2688-5012A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210632690 | ||||||
chr2:210632691
|
T | C | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2688-5011T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210632691 | ||||||
chr2:210632974
|
C | T | 1 | a0002c0002t0001g0209 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2688-4728C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210632974 | ||||||
chr2:210633608
|
T | A | 56 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(53): Show | 56 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2688-4094T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210633608 | ||||||
chr2:210633699
|
C | A | 56 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(53): Show | 56 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2688-4003C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210633699 | ||||||
chr2:210633719
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2688-3983A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210633719 | ||||||
chr2:210633975
|
T | C | 16 | a0001c0001t0007g0066a0001c0001t0007g0305a0001c0001t0007g0306others(13): Show | 16 | HG00323.hp1 HG00733.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.2688-3727T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210633975 | ||||||
chr2:210634025
|
C | A | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2688-3677C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634025 | ||||||
chr2:210634026
|
G | A | 17 | a0001c0006t0001g0109a0001c0006t0006g0292a0002c0002t0001g0076others(14): Show | 17 | HG00408.hp2 HG00558.hp1 NA18943.hp2 others(14): Show |
intron_variant | MODIFIER | c.2688-3676G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634026 | ||||||
chr2:210634062
|
G | A | 2 | a0003c0003t0002g0017a0003c0003t0002g0060 | 2 | HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2688-3640G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634062 | ||||||
chr2:210634115
|
A | G | 2 | a0001c0001t0007g0066a0001c0028t0024g0067 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2688-3587A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634115 | ||||||
chr2:210634188
|
T | C | 24 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(21): Show | 24 | HG00323.hp1 HG00733.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.2688-3514T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634188 | ||||||
chr2:210634206
|
G | A | 1 | a0003c0008t0004g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2688-3496G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634206 | ||||||
chr2:210634255
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2688-3447T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634255 | ||||||
chr2:210634298
|
C | T | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2688-3404C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634298 | ||||||
chr2:210634322
|
C | T | 36 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0272others(33): Show | 37 | HG00597.hp2 HG00609.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.2688-3380C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634322 | ||||||
chr2:210634324
|
G | A | 1 | a0002c0005t0003g0212 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2688-3378G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634324 | ||||||
chr2:210634434
|
GA | G | 19 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(16): Show | 19 | HG00323.hp1 HG00733.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.2688-3258delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr2 | 210634434 | |||||
chr2:210634512
|
A | G | 1 | a0004c0007t0005g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2688-3190A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634512 | ||||||
chr2:210634540
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2688-3162G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634540 | ||||||
chr2:210634643
|
A | G | 79 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.2688-3059A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634643 | ||||||
chr2:210634670
|
T | A | 79 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.2688-3032T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634670 | ||||||
chr2:210634680
|
G | T | 54 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(51): Show | 57 | HG00597.hp2 HG00609.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.2688-3022G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210634680 | ||||||
chr2:210635005
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2688-2697G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635005 | ||||||
chr2:210635032
|
C | T | 1 | a0001c0001t0007g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2688-2670C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635032 | ||||||
chr2:210635043
|
A | C | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2688-2659A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635043 | ||||||
chr2:210635141
|
C | T | 2 | a0004c0004t0005g0082a0004c0004t0005g0141 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2688-2561C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635141 | ||||||
chr2:210635234
|
C | T | 1 | a0007c0014t0007g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2688-2468C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635234 | ||||||
chr2:210635235
|
A | G | 79 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.2688-2467A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635235 | ||||||
chr2:210635255
|
A | C | 79 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.2688-2447A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635255 | ||||||
chr2:210635349
|
A | G | 5 | a0002c0002t0001g0190a0002c0002t0001g0198a0002c0002t0001g0209others(2): Show | 5 | NA18954.hp1 NA18954.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.2688-2353A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635349 | ||||||
chr2:210635453
|
A | G | 1 | a0002c0002t0002g0312 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2688-2249A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635453 | ||||||
chr2:210635602
|
A | G | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2688-2100A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635602 | ||||||
chr2:210635626
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2688-2076G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635626 | ||||||
chr2:210635921
|
AGGGAAAT others(4): Show |
A | 5 | a0001c0001t0007g0057a0001c0001t0016g0327a0004c0007t0004g0323others(2): Show | 5 | HG00140.hp1 HG00639.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2688-1780_2688-177 others(15): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210635921 | ||||||
chr2:210636116
|
A | G | 19 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0013others(16): Show | 19 | HG00323.hp1 HG00733.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.2688-1586A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636116 | ||||||
chr2:210636163
|
A | T | 74 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(71): Show | 74 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2688-1539A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636163 | ||||||
chr2:210636469
|
T | G | 3 | a0001c0001t0008g0096a0003c0003t0005g0105a0003c0003t0005g0116 | 3 | HG01361.hp2 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2688-1233T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636469 | ||||||
chr2:210636478
|
A | G | 75 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(72): Show | 75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.2688-1224A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636478 | ||||||
chr2:210636599
|
A | G | 1 | a0004c0007t0001g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2688-1103A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636599 | ||||||
chr2:210636600
|
C | T | 1 | a0003c0003t0002g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2688-1102C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636600 | ||||||
chr2:210636609
|
G | T | 66 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(63): Show | 66 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2688-1093G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636609 | ||||||
chr2:210636633
|
G | A | 2 | a0001c0029t0007g0250a0015c0022t0002g0018 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2688-1069G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636633 | ||||||
chr2:210636713
|
A | G | 41 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0272others(38): Show | 42 | HG00597.hp2 HG00609.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2688-989A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636713 | ||||||
chr2:210636818
|
T | C | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2688-884T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636818 | ||||||
chr2:210636877
|
G | A | 49 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(46): Show | 49 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.2688-825G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636877 | ||||||
chr2:210636880
|
G | C | 2 | a0010c0012t0005g0199a0010c0012t0005g0200 | 2 | NA18945.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.2688-822G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636880 | ||||||
chr2:210636918
|
A | G | 1 | a0001c0001t0014g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2688-784A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636918 | ||||||
chr2:210636998
|
T | G | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2688-704T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210636998 | ||||||
chr2:210637187
|
A | G | 1 | a0001c0001t0002g0302 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2688-515A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210637187 | ||||||
chr2:210637323
|
T | A | 88 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(85): Show | 92 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2688-379T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210637323 | ||||||
chr2:210637407
|
G | A | 88 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(85): Show | 92 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2688-295G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210637407 | ||||||
chr2:210637502
|
T | C | 1 | a0002c0005t0003g0212 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2688-200T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210637502 | ||||||
chr2:210637560
|
G | A | 1 | a0011c0017t0005g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2688-142G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210637560 | ||||||
chr2:210637619
|
T | C | 1 | a0001c0001t0010g0303 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2688-83T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 21/37 | chr2 | 210637619 | ||||||
chr2:210637870
|
C | T | 1 | a0002c0002t0001g0214 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2829+27C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210637870 | ||||||
chr2:210637891
|
T | A | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2829+48T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210637891 | ||||||
chr2:210637951
|
G | A | 1 | a0002c0002t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2829+108G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210637951 | ||||||
chr2:210638104
|
A | G | 6 | a0001c0001t0007g0009a0001c0001t0009g0261a0003c0003t0002g0256others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2829+261A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638104 | ||||||
chr2:210638114
|
T | G | 1 | a0003c0003t0004g0298 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2829+271T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638114 | ||||||
chr2:210638289
|
G | C | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2829+446G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638289 | ||||||
chr2:210638361
|
C | T | 2 | a0002c0002t0003g0002a0002c0021t0002g0281 | 3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2829+518C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638361 | ||||||
chr2:210638386
|
T | G | 3 | a0001c0001t0008g0096a0003c0003t0005g0105a0003c0003t0005g0116 | 3 | HG01361.hp2 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2829+543T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638386 | ||||||
chr2:210638391
|
A | AT | 9 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(6): Show | 9 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2829+556dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr2 | 210638391 | |||||
chr2:210638525
|
T | G | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2830-625T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638525 | ||||||
chr2:210638526
|
T | A | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2830-624T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638526 | ||||||
chr2:210638588
|
C | G | 18 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2830-562C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638588 | ||||||
chr2:210638599
|
G | A | 84 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(81): Show | 87 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2830-551G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638599 | ||||||
chr2:210638675
|
A | T | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2830-475A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638675 | ||||||
chr2:210638690
|
C | T | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2830-460C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638690 | ||||||
chr2:210638697
|
C | A | 1 | a0002c0002t0001g0219 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2830-453C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638697 | ||||||
chr2:210638747
|
C | A | 1 | a0002c0002t0001g0213 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2830-403C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638747 | ||||||
chr2:210638777
|
C | G | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2830-373C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638777 | ||||||
chr2:210638832
|
G | T | 84 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(81): Show | 87 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2830-318G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638832 | ||||||
chr2:210638897
|
G | A | 1 | a0001c0001t0003g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2830-253G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638897 | ||||||
chr2:210638991
|
C | G | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2830-159C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210638991 | ||||||
chr2:210639012
|
C | T | 87 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(84): Show | 91 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.2830-138C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210639012 | ||||||
chr2:210639067
|
T | G | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2830-83T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210639067 | ||||||
chr2:210639132
|
A | G | 3 | a0001c0001t0008g0096a0003c0003t0005g0105a0003c0003t0005g0116 | 3 | HG01361.hp2 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2830-18A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 22/37 | chr2 | 210639132 | ||||||
chr2:210639341
|
G | A | 84 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(81): Show | 87 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.2895+126G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639341 | ||||||
chr2:210639350
|
C | T | 86 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(83): Show | 90 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.2895+135C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639350 | ||||||
chr2:210639351
|
G | A | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2895+136G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639351 | ||||||
chr2:210639378
|
C | T | 1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2895+163C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639378 | ||||||
chr2:210639474
|
C | T | 48 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0063others(45): Show | 48 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2895+259C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639474 | ||||||
chr2:210639537
|
G | A | 2 | a0001c0029t0007g0250a0015c0022t0002g0018 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2895+322G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639537 | ||||||
chr2:210639591
|
C | A | 95 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(92): Show | 99 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.2895+376C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639591 | ||||||
chr2:210639600
|
C | A | 89 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(86): Show | 92 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.2895+385C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639600 | ||||||
chr2:210639614
|
G | A | 1 | a0001c0001t0007g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2896-382G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639614 | ||||||
chr2:210639618
|
C | CA | 65 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0122others(62): Show | 67 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2896-352dupA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr2 | 210639618 | |||||
chr2:210639618
|
C | CAA | 45 | a0001c0001t0001g0126a0001c0001t0002g0007a0001c0001t0002g0264others(42): Show | 46 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2896-353_2896-352d others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr2 | 210639618 | |||||
chr2:210639618
|
C | CAAA | 10 | a0001c0001t0002g0272a0001c0001t0002g0302a0001c0001t0003g0112others(7): Show | 10 | HG01069.hp2 HG01952.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.2896-354_2896-352d others(5): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr2 | 210639618 | |||||
chr2:210639618
|
CA | C | 7 | a0001c0001t0003g0103a0001c0029t0007g0250a0002c0002t0001g0178others(4): Show | 7 | HG00408.hp1 HG01257.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.2896-352delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr2 | 210639618 | |||||
chr2:210639648
|
A | C | 96 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(93): Show | 99 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.2896-348A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639648 | ||||||
chr2:210639651
|
A | G | 4 | a0002c0002t0002g0325a0003c0008t0004g0039a0003c0008t0005g0098others(1): Show | 4 | HG01106.hp2 HG01109.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.2896-345A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639651 | ||||||
chr2:210639733
|
A | G | 3 | a0002c0002t0003g0224a0002c0002t0015g0171a0004c0004t0005g0175 | 3 | HG03239.hp1 HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2896-263A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639733 | ||||||
chr2:210639740
|
A | G | 4 | a0001c0001t0007g0057a0001c0001t0016g0327a0001c0001t0028g0243others(1): Show | 4 | HG00140.hp1 HG00639.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2896-256A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 23/37 | chr2 | 210639740 | ||||||
chr2:210640395
|
G | A | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2959+336G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210640395 | ||||||
chr2:210640748
|
A | G | 1 | a0002c0005t0003g0212 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2959+689A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210640748 | ||||||
chr2:210641363
|
C | T | 3 | a0001c0001t0009g0247a0001c0001t0009g0248a0001c0001t0009g0280 | 3 | HG01243.hp2 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2960-1121C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641363 | ||||||
chr2:210641401
|
C | T | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2960-1083C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641401 | ||||||
chr2:210641456
|
T | C | 7 | a0001c0001t0002g0282a0001c0001t0008g0096a0001c0001t0009g0008others(4): Show | 8 | HG01361.hp2 HG01934.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2960-1028T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641456 | ||||||
chr2:210641457
|
G | A | 1 | a0002c0002t0008g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2960-1027G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641457 | ||||||
chr2:210641485
|
C | T | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2960-999C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641485 | ||||||
chr2:210641536
|
T | C | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2960-948T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641536 | ||||||
chr2:210641587
|
T | C | 86 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(83): Show | 89 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.2960-897T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641587 | ||||||
chr2:210641762
|
A | G | 87 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(84): Show | 90 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.2960-722A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641762 | ||||||
chr2:210641778
|
G | A | 1 | a0001c0001t0007g0057 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2960-706G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641778 | ||||||
chr2:210641780
|
G | A | 86 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(83): Show | 89 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.2960-704G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210641780 | ||||||
chr2:210642318
|
A | G | 3 | a0001c0001t0008g0096a0003c0003t0005g0105a0003c0003t0005g0116 | 3 | HG01361.hp2 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2960-166A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 24/37 | chr2 | 210642318 | ||||||
chr2:210642829
|
A | G | 1 | a0001c0001t0028g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3141+164A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210642829 | ||||||
chr2:210643056
|
T | A | 18 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.3141+391T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643056 | ||||||
chr2:210643104
|
A | G | 1 | a0002c0002t0001g0214 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3141+439A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643104 | ||||||
chr2:210643424
|
G | A | 17 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(14): Show | 17 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3141+759G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643424 | ||||||
chr2:210643470
|
C | G | 83 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(80): Show | 86 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.3141+805C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643470 | ||||||
chr2:210643514
|
C | A | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3141+849C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643514 | ||||||
chr2:210643529
|
A | G | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3141+864A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643529 | ||||||
chr2:210643535
|
C | T | 4 | a0001c0001t0002g0282a0001c0001t0009g0008a0001c0001t0009g0246others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3141+870C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643535 | ||||||
chr2:210643536
|
G | A | 1 | a0004c0004t0005g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3141+871G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643536 | ||||||
chr2:210643563
|
G | A | 89 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(86): Show | 93 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.3141+898G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643563 | ||||||
chr2:210643755
|
T | A | 3 | a0001c0001t0008g0096a0003c0003t0005g0105a0003c0003t0005g0116 | 3 | HG01361.hp2 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.3141+1090T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643755 | ||||||
chr2:210643802
|
C | T | 2 | a0001c0029t0007g0250a0015c0022t0002g0018 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3141+1137C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643802 | ||||||
chr2:210643811
|
A | G | 1 | a0003c0003t0005g0078 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3141+1146A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643811 | ||||||
chr2:210643846
|
G | C | 89 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(86): Show | 93 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.3141+1181G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643846 | ||||||
chr2:210643854
|
C | G | 18 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.3141+1189C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210643854 | ||||||
chr2:210644220
|
T | C | 1 | a0003c0003t0004g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3141+1555T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644220 | ||||||
chr2:210644276
|
C | A | 80 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(77): Show | 83 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.3141+1611C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644276 | ||||||
chr2:210644416
|
A | G | 1 | a0001c0006t0001g0115 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.3141+1751A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644416 | ||||||
chr2:210644462
|
A | C | 6 | a0001c0001t0007g0031a0001c0001t0007g0046a0001c0001t0010g0044others(3): Show | 6 | HG00733.hp1 HG00735.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.3141+1797A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644462 | ||||||
chr2:210644501
|
T | C | 1 | a0001c0001t0014g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3141+1836T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644501 | ||||||
chr2:210644567
|
A | C | 2 | a0001c0001t0013g0055a0001c0001t0013g0056 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.3141+1902A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644567 | ||||||
chr2:210644794
|
G | GTATGACT others(16): Show |
2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3141+2130_3141+213 others(27): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr2 | 210644794 | |||||
chr2:210644807
|
C | G | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3141+2142C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644807 | ||||||
chr2:210644859
|
A | G | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3141+2194A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210644859 | ||||||
chr2:210644893
|
ATTAATGG others(12): Show |
A | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3141+2245_3141+226 others(23): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr2 | 210644893 | |||||
chr2:210645095
|
G | T | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3141+2430G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645095 | ||||||
chr2:210645150
|
T | C | 1 | a0001c0001t0014g0153 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3141+2485T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645150 | ||||||
chr2:210645205
|
A | T | 90 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(87): Show | 93 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.3141+2540A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645205 | ||||||
chr2:210645280
|
C | T | 1 | a0001c0001t0003g0131 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3142-2583C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645280 | ||||||
chr2:210645281
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3142-2582G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645281 | ||||||
chr2:210645285
|
A | G | 5 | a0001c0001t0003g0120a0001c0001t0009g0247a0001c0001t0009g0248others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.3142-2578A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645285 | ||||||
chr2:210645517
|
G | A | 2 | a0007c0014t0007g0061a0014c0031t0002g0014 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3142-2346G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645517 | ||||||
chr2:210645568
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3142-2295G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645568 | ||||||
chr2:210645574
|
C | T | 3 | a0001c0001t0007g0258a0003c0003t0004g0259a0007c0014t0007g0062 | 3 | HG02280.hp1 HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3142-2289C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645574 | ||||||
chr2:210645605
|
G | T | 1 | a0009c0030t0007g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3142-2258G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645605 | ||||||
chr2:210645609
|
C | G | 1 | a0001c0001t0006g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3142-2254C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645609 | ||||||
chr2:210645638
|
C | T | 39 | a0001c0001t0002g0007a0001c0001t0002g0264a0001c0001t0002g0272others(36): Show | 40 | HG00597.hp2 HG00609.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.3142-2225C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645638 | ||||||
chr2:210645749
|
C | T | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3142-2114C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645749 | ||||||
chr2:210645804
|
T | C | 152 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0002g0007others(149): Show | 156 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.3142-2059T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645804 | ||||||
chr2:210645970
|
T | C | 1 | a0001c0001t0006g0295 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3142-1893T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210645970 | ||||||
chr2:210646474
|
C | G | 3 | a0001c0001t0007g0057a0001c0001t0016g0327a0004c0007t0004g0323 | 3 | HG00140.hp1 HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3142-1389C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210646474 | ||||||
chr2:210646727
|
C | T | 2 | a0001c0001t0008g0125a0009c0030t0007g0074 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3142-1136C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210646727 | ||||||
chr2:210646775
|
G | C | 263 | a0001c0001t0001g0095a0001c0001t0001g0100a0001c0001t0001g0122others(260): Show | 271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.3142-1088G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210646775 | ||||||
chr2:210646800
|
G | A | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.3142-1063G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210646800 | ||||||
chr2:210646842
|
C | T | 6 | a0002c0009t0006g0071a0002c0009t0006g0072a0002c0013t0006g0070others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.3142-1021C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210646842 | ||||||
chr2:210646867
|
TCTCACGC others(9): Show |
T | 8 | a0002c0005t0003g0132a0002c0009t0003g0155a0002c0009t0006g0071others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.3142-990_3142-975d others(18): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr2 | 210646867 | |||||
chr2:210646935
|
AT | A | 11 | a0001c0001t0001g0099a0001c0001t0006g0024a0001c0001t0008g0125others(8): Show | 12 | HG00408.hp2 HG00558.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.3142-917delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr2 | 210646935 | |||||
chr2:210647054
|
G | A | 313 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(310): Show | 322 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.3142-809G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647054 | ||||||
chr2:210647169
|
G | C | 2 | a0002c0005t0006g0075a0014c0031t0002g0014 | 2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3142-694G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647169 | ||||||
chr2:210647445
|
A | T | 83 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(80): Show | 85 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.3142-418A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647445 | ||||||
chr2:210647460
|
A | G | 1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3142-403A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647460 | ||||||
chr2:210647648
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3142-215G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647648 | ||||||
chr2:210647713
|
G | A | 45 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(42): Show | 46 | HG01884.hp2 HG02135.hp2 HG02145.hp2 others(43): Show |
intron_variant | MODIFIER | c.3142-150G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647713 | ||||||
chr2:210647744
|
G | C | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0008g0125others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3142-119G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 25/37 | chr2 | 210647744 | ||||||
chr2:210648343
|
C | T | 2 | a0001c0001t0007g0254a0001c0001t0025g0043 | 2 | HG00741.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.3337-130C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 26/37 | chr2 | 210648343 | ||||||
chr2:210648394
|
C | T | 330 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(327): Show | 339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.3337-79C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 26/37 | chr2 | 210648394 | ||||||
chr2:210648669
|
A | G | 2 | a0001c0001t0003g0124a0001c0001t0003g0253 | 2 | HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3404+129A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210648669 | ||||||
chr2:210648691
|
A | G | 4 | a0001c0001t0009g0008a0001c0001t0009g0246a0001c0001t0009g0283others(1): Show | 5 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3404+151A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210648691 | ||||||
chr2:210648824
|
C | T | 56 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(53): Show | 57 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.3404+284C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210648824 | ||||||
chr2:210648961
|
C | A | 323 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(320): Show | 332 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.3404+421C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210648961 | ||||||
chr2:210649045
|
A | T | 1 | a0003c0003t0001g0003 | 2 | HG02717.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.3404+505A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649045 | ||||||
chr2:210649105
|
C | A | 1 | a0007c0014t0007g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3404+565C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649105 | ||||||
chr2:210649474
|
C | T | 44 | a0001c0001t0001g0100a0001c0001t0003g0129a0001c0001t0006g0030others(41): Show | 44 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.3405-889C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649474 | ||||||
chr2:210649768
|
A | G | 89 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(86): Show | 91 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.3405-595A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649768 | ||||||
chr2:210649811
|
T | G | 1 | a0003c0003t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3405-552T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649811 | ||||||
chr2:210649839
|
G | A | 61 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(58): Show | 63 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.3405-524G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649839 | ||||||
chr2:210649912
|
G | A | 1 | a0001c0024t0017g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3405-451G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210649912 | ||||||
chr2:210650093
|
A | G | 1 | a0001c0001t0007g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3405-270A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210650093 | ||||||
chr2:210650235
|
A | G | 2 | a0003c0003t0005g0077a0003c0003t0005g0078 | 2 | HG00438.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.3405-128A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210650235 | ||||||
chr2:210650271
|
G | T | 64 | a0001c0001t0001g0100a0001c0001t0003g0129a0001c0001t0006g0030others(61): Show | 66 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.3405-92G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210650271 | ||||||
chr2:210650334
|
A | T | 139 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(136): Show | 142 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.3405-29A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 27/37 | chr2 | 210650334 | ||||||
chr2:210650526
|
C | A | 2 | a0003c0003t0004g0255a0003c0003t0004g0330 | 2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3480+88C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210650526 | ||||||
chr2:210650878
|
C | CT | 219 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(216): Show | 226 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.3480+441dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chr2 | 210650878 | |||||
chr2:210650889
|
T | C | 6 | a0001c0001t0003g0128a0001c0001t0007g0013a0001c0001t0011g0150others(3): Show | 6 | HG00639.hp2 HG01109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.3480+451T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210650889 | ||||||
chr2:210651166
|
G | A | 1 | a0001c0001t0007g0254 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3480+728G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651166 | ||||||
chr2:210651467
|
C | T | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3480+1029C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651467 | ||||||
chr2:210651475
|
G | T | 1 | a0001c0001t0003g0103 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3480+1037G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651475 | ||||||
chr2:210651494
|
C | T | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3480+1056C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651494 | ||||||
chr2:210651529
|
G | A | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3480+1091G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651529 | ||||||
chr2:210651559
|
A | G | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3480+1121A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651559 | ||||||
chr2:210651587
|
G | A | 7 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.3480+1149G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651587 | ||||||
chr2:210651662
|
G | A | 1 | a0003c0018t0002g0239 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3480+1224G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651662 | ||||||
chr2:210651780
|
C | T | 27 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(24): Show | 27 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.3480+1342C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651780 | ||||||
chr2:210651818
|
T | C | 7 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(4): Show | 7 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.3480+1380T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651818 | ||||||
chr2:210651857
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3480+1419G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651857 | ||||||
chr2:210651887
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3480+1449G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651887 | ||||||
chr2:210651901
|
A | G | 47 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(44): Show | 49 | HG00733.hp2 HG01069.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.3480+1463A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651901 | ||||||
chr2:210651906
|
C | T | 57 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.3480+1468C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210651906 | ||||||
chr2:210652146
|
T | C | 47 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(44): Show | 49 | HG00733.hp2 HG01069.hp2 HG01168.hp2 others(46): Show |
intron_variant | MODIFIER | c.3480+1708T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210652146 | ||||||
chr2:210652699
|
T | G | 106 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(103): Show | 111 | HG00609.hp2 HG00733.hp2 HG01069.hp2 others(108): Show |
intron_variant | MODIFIER | c.3481-1326T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210652699 | ||||||
chr2:210652717
|
G | T | 1 | a0002c0002t0001g0170 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3481-1308G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210652717 | ||||||
chr2:210652747
|
A | G | 2 | a0002c0009t0007g0069a0002c0013t0007g0073 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3481-1278A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210652747 | ||||||
chr2:210653216
|
G | T | 1 | a0001c0001t0003g0092 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.3481-809G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653216 | ||||||
chr2:210653353
|
A | G | 2 | a0001c0001t0007g0013a0001c0001t0011g0150 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3481-672A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653353 | ||||||
chr2:210653627
|
G | C | 1 | a0004c0004t0005g0220 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3481-398G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653627 | ||||||
chr2:210653750
|
C | T | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3481-275C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653750 | ||||||
chr2:210653772
|
C | A | 3 | a0004c0007t0005g0158a0004c0007t0005g0159a0004c0007t0005g0160 | 3 | HG01891.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3481-253C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653772 | ||||||
chr2:210653793
|
G | T | 7 | a0003c0003t0001g0003a0003c0003t0002g0286a0004c0007t0005g0158others(4): Show | 9 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3481-232G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653793 | ||||||
chr2:210653843
|
A | G | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3481-182A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653843 | ||||||
chr2:210653875
|
A | C | 2 | a0001c0001t0007g0066a0001c0028t0024g0067 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.3481-150A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653875 | ||||||
chr2:210653945
|
T | C | 1 | a0002c0002t0001g0176 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3481-80T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653945 | ||||||
chr2:210653998
|
C | T | 1 | a0001c0006t0006g0292 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3481-27C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210653998 | ||||||
chr2:210654000
|
G | A | 1 | a0002c0002t0011g0187 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3481-25G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210654000 | ||||||
chr2:210654017
|
C | T | 1 | a0003c0003t0004g0050 | 1 | HG01496.hp1 | splice_region_variant&intron_variant | LOW | c.3481-8C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210654017 | ||||||
chr2:210654018
|
G | A | 2 | a0001c0006t0006g0276a0002c0002t0015g0084 | 2 | HG02738.hp2 HG03834.hp2 |
splice_region_variant&intron_variant | LOW | c.3481-7G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 28/37 | chr2 | 210654018 | ||||||
chr2:210654138
|
T | G | 1 | a0001c0001t0016g0327 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3558+36T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654138 | ||||||
chr2:210654140
|
C | G | 1 | a0003c0003t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3558+38C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654140 | ||||||
chr2:210654268
|
G | A | 1 | a0004c0004t0005g0175 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3558+166G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654268 | ||||||
chr2:210654308
|
A | C | 7 | a0003c0003t0001g0003a0003c0003t0002g0286a0004c0007t0005g0158others(4): Show | 9 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3558+206A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654308 | ||||||
chr2:210654580
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3558+478A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654580 | ||||||
chr2:210654638
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3558+536A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654638 | ||||||
chr2:210654643
|
G | A | 9 | a0001c0001t0002g0034a0002c0002t0001g0207a0002c0002t0001g0209others(6): Show | 9 | NA18948.hp2 NA18966.hp2 NA18992.hp1 others(6): Show |
intron_variant | MODIFIER | c.3558+541G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654643 | ||||||
chr2:210654802
|
A | G | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3558+700A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210654802 | ||||||
chr2:210655075
|
CTTT | C | 23 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(20): Show | 23 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.3558+979_3558+981d others(5): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chr2 | 210655075 | |||||
chr2:210655189
|
C | T | 2 | a0001c0001t0006g0329a0001c0001t0006g0331 | 2 | HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3558+1087C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210655189 | ||||||
chr2:210655231
|
G | A | 3 | a0002c0005t0003g0136a0002c0005t0003g0138a0002c0005t0003g0139 | 3 | HG01884.hp1 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.3558+1129G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210655231 | ||||||
chr2:210655524
|
TG | T | 50 | a0001c0001t0001g0100a0001c0001t0003g0129a0001c0001t0006g0030others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.3559-997delG | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chr2 | 210655524 | |||||
chr2:210655671
|
T | C | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3559-854T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210655671 | ||||||
chr2:210655872
|
C | A | 1 | a0002c0002t0001g0216 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3559-653C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210655872 | ||||||
chr2:210655971
|
A | C | 2 | a0004c0004t0002g0010a0004c0004t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3559-554A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210655971 | ||||||
chr2:210656064
|
T | C | 27 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(24): Show | 27 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.3559-461T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210656064 | ||||||
chr2:210656133
|
C | T | 1 | a0001c0001t0006g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3559-392C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210656133 | ||||||
chr2:210656351
|
C | G | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3559-174C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | chr2 | 210656351 | ||||||
chr2:210656503
|
CT | C | 321 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(318): Show | 330 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(327): Show |
splice_region_variant&intron_variant | LOW | c.3559-7delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chr2 | 210656503 | |||||
chr2:210656665
|
A | C | 1 | a0002c0002t0003g0144 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3666+33A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210656665 | ||||||
chr2:210656693
|
G | GT | 61 | a0001c0001t0003g0108a0001c0001t0006g0037a0001c0001t0006g0284others(58): Show | 64 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.3666+77dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr2 | 210656693 | |||||
chr2:210656693
|
G | GTT | 9 | a0002c0002t0003g0218a0002c0005t0006g0075a0003c0003t0001g0003others(6): Show | 11 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3666+76_3666+77dup others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr2 | 210656693 | |||||
chr2:210656693
|
GT | G | 12 | a0001c0001t0003g0120a0001c0001t0006g0329a0001c0001t0006g0331others(9): Show | 12 | HG01243.hp2 HG01943.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3666+77delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr2 | 210656693 | |||||
chr2:210656698
|
T | C | 3 | a0001c0001t0008g0096a0003c0003t0005g0105a0003c0003t0005g0116 | 3 | HG01361.hp2 HG01934.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.3666+66T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210656698 | ||||||
chr2:210656765
|
C | G | 1 | a0004c0007t0004g0323 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3666+133C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210656765 | ||||||
chr2:210656889
|
G | A | 2 | a0003c0003t0002g0017a0003c0003t0002g0256 | 2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3666+257G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210656889 | ||||||
chr2:210656954
|
G | C | 27 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(24): Show | 27 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.3666+322G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210656954 | ||||||
chr2:210657052
|
T | G | 2 | a0003c0003t0002g0241a0004c0004t0005g0181 | 2 | HG03540.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.3666+420T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657052 | ||||||
chr2:210657198
|
T | C | 324 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(321): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.3666+566T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657198 | ||||||
chr2:210657310
|
C | CT | 13 | a0001c0001t0007g0249a0001c0006t0002g0296a0002c0002t0003g0217others(10): Show | 15 | HG02071.hp1 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.3666+695dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr2 | 210657310 | |||||
chr2:210657334
|
G | T | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3666+702G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657334 | ||||||
chr2:210657368
|
T | C | 1 | a0003c0003t0005g0087 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3666+736T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657368 | ||||||
chr2:210657502
|
G | C | 1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3666+870G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657502 | ||||||
chr2:210657732
|
C | T | 11 | a0001c0001t0007g0009a0001c0001t0007g0258a0001c0001t0009g0261others(8): Show | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.3667-867C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657732 | ||||||
chr2:210657763
|
T | A | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3667-836T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657763 | ||||||
chr2:210657819
|
G | A | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3667-780G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657819 | ||||||
chr2:210657827
|
GA | G | 5 | a0001c0001t0009g0008a0001c0001t0009g0246a0001c0001t0009g0283others(2): Show | 6 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3667-766delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr2 | 210657827 | |||||
chr2:210657882
|
T | C | 1 | a0001c0001t0002g0007 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3667-717T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657882 | ||||||
chr2:210657974
|
T | C | 1 | a0001c0001t0003g0108 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3667-625T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210657974 | ||||||
chr2:210658165
|
C | T | 330 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(327): Show | 339 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.3667-434C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210658165 | ||||||
chr2:210658288
|
C | T | 2 | a0002c0009t0007g0069a0002c0013t0007g0073 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3667-311C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210658288 | ||||||
chr2:210658439
|
A | G | 218 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(215): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.3667-160A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 30/37 | chr2 | 210658439 | ||||||
chr2:210658733
|
C | T | 50 | a0001c0001t0001g0100a0001c0001t0003g0129a0001c0001t0006g0030others(47): Show | 50 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.3756+45C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210658733 | ||||||
chr2:210658846
|
T | C | 2 | a0002c0009t0007g0069a0002c0013t0007g0073 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3756+158T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210658846 | ||||||
chr2:210658945
|
C | G | 14 | a0001c0001t0001g0231a0001c0001t0003g0112a0001c0001t0003g0229others(11): Show | 14 | HG02165.hp2 NA18942.hp2 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.3756+257C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210658945 | ||||||
chr2:210658991
|
T | TAAATGGA others(5): Show |
1 | a0002c0002t0001g0207 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3756+304_3756+315d others(14): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | INFO_REALIGN_3_PRIME | chr2 | 210658991 | |||||
chr2:210659276
|
C | A | 2 | a0001c0001t0008g0125a0009c0030t0007g0074 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3756+588C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210659276 | ||||||
chr2:210659298
|
G | A | 1 | a0001c0001t0003g0129 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3756+610G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210659298 | ||||||
chr2:210659472
|
C | A | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0008g0125others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3756+784C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210659472 | ||||||
chr2:210659604
|
A | C | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0008g0125others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3757-881A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210659604 | ||||||
chr2:210660429
|
A | T | 2 | a0002c0002t0001g0211a0002c0002t0001g0215 | 2 | NA18990.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.3757-56A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 31/37 | chr2 | 210660429 | ||||||
chr2:210660696
|
A | G | 2 | a0001c0001t0016g0327a0004c0007t0004g0323 | 2 | HG00639.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3927+41A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210660696 | ||||||
chr2:210660804
|
T | C | 1 | a0003c0003t0004g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3927+149T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210660804 | ||||||
chr2:210660833
|
T | C | 1 | a0002c0002t0003g0224 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3927+178T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210660833 | ||||||
chr2:210660860
|
C | T | 6 | a0001c0001t0007g0009a0001c0001t0009g0261a0003c0003t0004g0255others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3927+205C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210660860 | ||||||
chr2:210660961
|
T | C | 3 | a0004c0007t0005g0158a0004c0007t0005g0159a0004c0007t0005g0160 | 3 | HG01891.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3927+306T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210660961 | ||||||
chr2:210661040
|
G | A | 61 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(58): Show | 63 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.3927+385G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661040 | ||||||
chr2:210661153
|
C | T | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0008g0125others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3927+498C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661153 | ||||||
chr2:210661189
|
A | C | 35 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(32): Show | 36 | HG00609.hp2 HG01516.hp2 HG02135.hp2 others(33): Show |
intron_variant | MODIFIER | c.3927+534A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661189 | ||||||
chr2:210661191
|
C | A | 149 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(146): Show | 150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.3927+536C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661191 | ||||||
chr2:210661250
|
C | T | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3927+595C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661250 | ||||||
chr2:210661402
|
A | G | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3927+747A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661402 | ||||||
chr2:210661471
|
C | T | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3927+816C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661471 | ||||||
chr2:210661472
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3927+817G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661472 | ||||||
chr2:210661542
|
A | G | 2 | a0003c0003t0002g0286a0005c0011t0001g0252 | 2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.3927+887A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661542 | ||||||
chr2:210661663
|
C | T | 1 | a0001c0028t0024g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3927+1008C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661663 | ||||||
chr2:210661856
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3927+1201T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661856 | ||||||
chr2:210661903
|
C | CT | 64 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(61): Show | 65 | HG00609.hp2 HG00733.hp2 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.3928-1200dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chr2 | 210661903 | |||||
chr2:210661903
|
CT | C | 84 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(81): Show | 90 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.3928-1200delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chr2 | 210661903 | |||||
chr2:210661934
|
C | T | 1 | a0001c0029t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3928-1189C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661934 | ||||||
chr2:210661945
|
A | G | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3928-1178A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210661945 | ||||||
chr2:210662030
|
A | G | 1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3928-1093A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662030 | ||||||
chr2:210662115
|
C | T | 1 | a0003c0003t0004g0274 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3928-1008C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662115 | ||||||
chr2:210662167
|
C | T | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3928-956C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662167 | ||||||
chr2:210662198
|
A | T | 59 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(56): Show | 64 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.3928-925A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662198 | ||||||
chr2:210662592
|
C | T | 2 | a0003c0003t0004g0052a0004c0004t0004g0315 | 2 | HG01358.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.3928-531C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662592 | ||||||
chr2:210662840
|
A | G | 4 | a0001c0006t0002g0296a0002c0002t0001g0213a0002c0002t0001g0214others(1): Show | 6 | HG02071.hp1 HG02523.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3928-283A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662840 | ||||||
chr2:210662873
|
C | T | 1 | a0016c0023t0006g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3928-250C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210662873 | ||||||
chr2:210662992
|
A | AT | 59 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(56): Show | 64 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.3928-125dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chr2 | 210662992 | |||||
chr2:210663103
|
GT | G | 287 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(284): Show | 294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
splice_region_variant&intron_variant | LOW | c.3928-8delT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chr2 | 210663103 | |||||
chr2:210663103
|
GTT | G | 7 | a0003c0003t0001g0003a0003c0003t0002g0286a0004c0007t0005g0158others(4): Show | 9 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.3928-9_3928-8delTT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chr2 | 210663103 | |||||
chr2:210663108
|
T | C | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3928-15T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 32/37 | chr2 | 210663108 | ||||||
chr2:210663277
|
T | C | 5 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(2): Show | 5 | HG01081.hp2 HG01361.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.4002+80T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663277 | ||||||
chr2:210663355
|
C | T | 4 | a0001c0006t0002g0038a0002c0002t0001g0165a0002c0002t0001g0166others(1): Show | 4 | HG02135.hp1 HG02165.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+158C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663355 | ||||||
chr2:210663411
|
T | C | 1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4002+214T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663411 | ||||||
chr2:210663477
|
T | C | 4 | a0001c0001t0002g0264a0001c0001t0002g0275a0001c0001t0006g0245others(1): Show | 4 | HG00609.hp2 NA18612.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+280T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663477 | ||||||
chr2:210663483
|
G | T | 1 | a0003c0003t0004g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4002+286G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663483 | ||||||
chr2:210663585
|
A | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+388A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663585 | ||||||
chr2:210663672
|
TC | T | 57 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(54): Show | 62 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.4002+477delC | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210663672 | |||||
chr2:210663705
|
G | A | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4002+508G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663705 | ||||||
chr2:210663788
|
A | G | 3 | a0001c0001t0003g0120a0002c0009t0006g0071a0002c0009t0006g0072 | 3 | HG02647.hp2 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4002+591A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663788 | ||||||
chr2:210663789
|
G | C | 1 | a0012c0027t0016g0304 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4002+592G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663789 | ||||||
chr2:210663903
|
C | T | 1 | a0001c0001t0006g0245 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4002+706C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663903 | ||||||
chr2:210663952
|
A | T | 1 | a0002c0002t0001g0207 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.4002+755A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663952 | ||||||
chr2:210663962
|
A | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+765A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663962 | ||||||
chr2:210663982
|
T | C | 1 | a0002c0002t0001g0166 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4002+785T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663982 | ||||||
chr2:210663985
|
A | C | 44 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(41): Show | 45 | HG00609.hp2 HG01243.hp2 HG01516.hp2 others(42): Show |
intron_variant | MODIFIER | c.4002+788A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210663985 | ||||||
chr2:210664150
|
A | G | 1 | a0004c0004t0004g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4002+953A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664150 | ||||||
chr2:210664163
|
A | C | 1 | a0002c0002t0001g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4002+966A>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664163 | ||||||
chr2:210664184
|
A | G | 6 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(3): Show | 6 | HG01081.hp2 HG01361.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.4002+987A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664184 | ||||||
chr2:210664257
|
A | G | 5 | a0001c0001t0006g0040a0002c0002t0001g0177a0003c0003t0004g0029others(2): Show | 5 | HG00621.hp2 NA18945.hp1 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.4002+1060A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664257 | ||||||
chr2:210664355
|
A | G | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4002+1158A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664355 | ||||||
chr2:210664370
|
G | A | 1 | a0001c0001t0008g0096 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4002+1173G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664370 | ||||||
chr2:210664397
|
C | T | 60 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(57): Show | 65 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.4002+1200C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664397 | ||||||
chr2:210664428
|
T | C | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+1231T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664428 | ||||||
chr2:210664493
|
C | T | 151 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.4002+1296C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664493 | ||||||
chr2:210664500
|
C | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+1303C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664500 | ||||||
chr2:210664514
|
T | G | 2 | a0004c0004t0002g0010a0004c0004t0002g0011 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4002+1317T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664514 | ||||||
chr2:210664558
|
C | T | 1 | a0001c0001t0003g0230 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4002+1361C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664558 | ||||||
chr2:210664572
|
C | T | 1 | a0001c0001t0002g0264 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.4002+1375C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664572 | ||||||
chr2:210664598
|
A | T | 5 | a0004c0007t0001g0157a0006c0010t0008g0137a0006c0010t0010g0287others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4002+1401A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664598 | ||||||
chr2:210664604
|
C | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+1407C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664604 | ||||||
chr2:210664605
|
G | A | 2 | a0004c0004t0005g0205a0004c0004t0005g0206 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.4002+1408G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664605 | ||||||
chr2:210664644
|
G | A | 5 | a0004c0007t0001g0157a0006c0010t0008g0137a0006c0010t0010g0287others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4002+1447G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664644 | ||||||
chr2:210664654
|
G | C | 217 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(214): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.4002+1457G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664654 | ||||||
chr2:210664791
|
G | A | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4002+1594G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664791 | ||||||
chr2:210664816
|
A | G | 1 | a0001c0001t0003g0120 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4002+1619A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664816 | ||||||
chr2:210664831
|
G | A | 1 | a0002c0009t0006g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4002+1634G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664831 | ||||||
chr2:210664870
|
A | G | 2 | a0001c0001t0017g0322a0004c0007t0005g0184 | 2 | HG00733.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.4002+1673A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664870 | ||||||
chr2:210664879
|
T | A | 1 | a0006c0010t0014g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4002+1682T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210664879 | ||||||
chr2:210665042
|
T | C | 1 | a0002c0005t0008g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4002+1845T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665042 | ||||||
chr2:210665086
|
T | C | 2 | a0002c0009t0007g0069a0002c0013t0007g0073 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4002+1889T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665086 | ||||||
chr2:210665126
|
C | T | 52 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(49): Show | 57 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.4002+1929C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665126 | ||||||
chr2:210665219
|
T | G | 1 | a0001c0001t0007g0305 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4002+2022T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665219 | ||||||
chr2:210665259
|
G | A | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+2062G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665259 | ||||||
chr2:210665377
|
A | G | 1 | a0003c0003t0002g0060 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4002+2180A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665377 | ||||||
chr2:210665466
|
C | T | 56 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(53): Show | 57 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.4002+2269C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665466 | ||||||
chr2:210665474
|
C | A | 1 | a0001c0001t0007g0066 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4002+2277C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665474 | ||||||
chr2:210665474
|
C | G | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4002+2277C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665474 | ||||||
chr2:210665477
|
C | A | 3 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0007g0066 | 3 | HG02630.hp1 HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4002+2280C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665477 | ||||||
chr2:210665510
|
A | G | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+2313A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665510 | ||||||
chr2:210665549
|
C | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+2352C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665549 | ||||||
chr2:210665553
|
C | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4002+2356C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665553 | ||||||
chr2:210665572
|
G | A | 1 | a0001c0001t0007g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4002+2375G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665572 | ||||||
chr2:210665595
|
A | G | 8 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(5): Show | 8 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.4002+2398A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665595 | ||||||
chr2:210665639
|
T | C | 27 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(24): Show | 27 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.4002+2442T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665639 | ||||||
chr2:210665690
|
A | G | 7 | a0001c0001t0008g0096a0002c0002t0021g0236a0002c0009t0006g0071others(4): Show | 7 | HG01081.hp2 HG01361.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.4002+2493A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665690 | ||||||
chr2:210665735
|
T | A | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4003-2451T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665735 | ||||||
chr2:210665774
|
C | T | 23 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(20): Show | 23 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4003-2412C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665774 | ||||||
chr2:210665775
|
G | A | 8 | a0001c0001t0002g0068a0003c0003t0001g0003a0003c0003t0002g0286others(5): Show | 10 | HG01891.hp2 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.4003-2411G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665775 | ||||||
chr2:210665776
|
T | C | 11 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0001g0003others(8): Show | 13 | HG01361.hp2 HG01496.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.4003-2410T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665776 | ||||||
chr2:210665787
|
C | T | 61 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0101others(58): Show | 63 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.4003-2399C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665787 | ||||||
chr2:210665895
|
G | C | 324 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(321): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.4003-2291G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665895 | ||||||
chr2:210665903
|
T | C | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4003-2283T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665903 | ||||||
chr2:210665947
|
G | A | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4003-2239G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665947 | ||||||
chr2:210665973
|
C | T | 5 | a0004c0007t0001g0157a0006c0010t0008g0137a0006c0010t0010g0287others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4003-2213C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210665973 | ||||||
chr2:210666146
|
A | G | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4003-2040A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666146 | ||||||
chr2:210666190
|
A | G | 1 | a0001c0006t0002g0296 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4003-1996A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666190 | ||||||
chr2:210666305
|
T | C | 28 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(25): Show | 28 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.4003-1881T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666305 | ||||||
chr2:210666346
|
C | G | 33 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(30): Show | 34 | HG00609.hp2 HG01516.hp2 HG02135.hp2 others(31): Show |
intron_variant | MODIFIER | c.4003-1840C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666346 | ||||||
chr2:210666348
|
A | G | 59 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(56): Show | 64 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.4003-1838A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666348 | ||||||
chr2:210666376
|
G | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4003-1810G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666376 | ||||||
chr2:210666466
|
C | T | 4 | a0006c0010t0008g0137a0006c0010t0010g0287a0006c0010t0014g0133others(1): Show | 4 | HG02280.hp2 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4003-1720C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666466 | ||||||
chr2:210666490
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.4003-1696A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666490 | ||||||
chr2:210666503
|
A | G | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4003-1683A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666503 | ||||||
chr2:210666537
|
C | G | 1 | a0014c0031t0002g0014 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4003-1649C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666537 | ||||||
chr2:210666541
|
G | A | 1 | a0003c0003t0004g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4003-1645G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666541 | ||||||
chr2:210666565
|
A | G | 1 | a0015c0022t0002g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4003-1621A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666565 | ||||||
chr2:210666586
|
C | G | 7 | a0003c0003t0001g0003a0003c0003t0002g0286a0004c0007t0005g0158others(4): Show | 9 | HG01891.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.4003-1600C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666586 | ||||||
chr2:210666670
|
C | T | 79 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(76): Show | 80 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.4003-1516C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666670 | ||||||
chr2:210666710
|
C | T | 2 | a0001c0001t0003g0090a0002c0002t0001g0147 | 2 | NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.4003-1476C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666710 | ||||||
chr2:210666867
|
A | G | 1 | a0001c0001t0010g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4003-1319A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666867 | ||||||
chr2:210666871
|
C | T | 1 | a0001c0001t0010g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4003-1315C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666871 | ||||||
chr2:210666979
|
T | C | 22 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(19): Show | 25 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.4003-1207T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210666979 | ||||||
chr2:210667058
|
G | T | 2 | a0001c0001t0008g0125a0009c0030t0007g0074 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4003-1128G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667058 | ||||||
chr2:210667066
|
A | T | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4003-1120A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667066 | ||||||
chr2:210667087
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4003-1099C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667087 | ||||||
chr2:210667123
|
CTGTT | C | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4003-1059_4003-105 others(8): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210667123 | |||||
chr2:210667226
|
G | A | 1 | a0001c0001t0007g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4003-960G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667226 | ||||||
chr2:210667312
|
T | C | 1 | a0001c0001t0003g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4003-874T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667312 | ||||||
chr2:210667323
|
T | G | 1 | a0002c0002t0021g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4003-863T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667323 | ||||||
chr2:210667417
|
C | G | 1 | a0002c0002t0001g0219 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4003-769C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667417 | ||||||
chr2:210667675
|
G | T | 1 | a0002c0002t0021g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4003-511G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667675 | ||||||
chr2:210667724
|
C | T | 1 | a0003c0003t0005g0123 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4003-462C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667724 | ||||||
chr2:210667809
|
A | T | 1 | a0002c0009t0003g0155 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4003-377A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667809 | ||||||
chr2:210667878
|
C | A | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4003-308C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667878 | ||||||
chr2:210667907
|
G | C | 1 | a0004c0004t0005g0220 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4003-279G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667907 | ||||||
chr2:210667979
|
C | T | 81 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(78): Show | 82 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.4003-207C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210667979 | ||||||
chr2:210668071
|
C | T | 1 | a0004c0004t0005g0143 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4003-115C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | chr2 | 210668071 | ||||||
chr2:210668076
|
A | ATG | 144 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0100others(141): Show | 149 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.4003-82_4003-81dup others(2): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210668076 | |||||
chr2:210668076
|
A | ATGTG | 91 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(88): Show | 91 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.4003-84_4003-81dup others(4): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210668076 | |||||
chr2:210668076
|
A | ATGTGTG | 10 | a0001c0001t0008g0096a0001c0006t0001g0088a0002c0002t0003g0224others(7): Show | 12 | HG01361.hp2 HG01934.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.4003-86_4003-81dup others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210668076 | |||||
chr2:210668076
|
A | ATGTGTGT others(1): Show |
11 | a0001c0001t0007g0249a0002c0002t0001g0172a0002c0002t0002g0244others(8): Show | 12 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.4003-88_4003-81dup others(8): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210668076 | |||||
chr2:210668076
|
ATGTGTGT others(9): Show |
A | 1 | a0003c0003t0004g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4003-96_4003-81del others(16): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr2 | 210668076 | |||||
chr2:210668312
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4101+28C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668312 | ||||||
chr2:210668314
|
A | G | 1 | a0002c0002t0001g0178 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4101+30A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668314 | ||||||
chr2:210668346
|
A | G | 322 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(319): Show | 331 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.4101+62A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668346 | ||||||
chr2:210668472
|
C | T | 1 | a0011c0017t0005g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4101+188C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668472 | ||||||
chr2:210668473
|
G | A | 1 | a0002c0002t0003g0149 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4101+189G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668473 | ||||||
chr2:210668540
|
G | C | 1 | a0004c0004t0004g0059 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4101+256G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668540 | ||||||
chr2:210668541
|
C | T | 1 | a0002c0005t0006g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4101+257C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668541 | ||||||
chr2:210668723
|
A | G | 1 | a0003c0003t0005g0164 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4101+439A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668723 | ||||||
chr2:210668917
|
C | A | 1 | a0001c0029t0007g0250 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4101+633C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668917 | ||||||
chr2:210668995
|
G | C | 1 | a0001c0001t0003g0235 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.4101+711G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210668995 | ||||||
chr2:210669384
|
G | T | 5 | a0004c0007t0001g0157a0006c0010t0008g0137a0006c0010t0010g0287others(2): Show | 5 | HG02280.hp2 HG02717.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.4101+1100G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669384 | ||||||
chr2:210669392
|
A | G | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4101+1108A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669392 | ||||||
chr2:210669430
|
G | T | 3 | a0002c0002t0002g0309a0002c0002t0002g0316a0002c0002t0002g0328 | 3 | NA18966.hp2 NA19060.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.4101+1146G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669430 | ||||||
chr2:210669584
|
T | G | 4 | a0002c0002t0001g0208a0004c0004t0005g0167a0004c0004t0005g0205others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.4101+1300T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669584 | ||||||
chr2:210669611
|
C | G | 94 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 95 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.4101+1327C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669611 | ||||||
chr2:210669679
|
G | A | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4101+1395G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669679 | ||||||
chr2:210669693
|
C | A | 20 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(17): Show | 23 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.4101+1409C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669693 | ||||||
chr2:210669733
|
G | A | 23 | a0001c0001t0010g0303a0001c0001t0017g0322a0001c0006t0006g0016others(20): Show | 23 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.4101+1449G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210669733 | ||||||
chr2:210670122
|
T | C | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4101+1838T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670122 | ||||||
chr2:210670234
|
G | A | 56 | a0001c0001t0006g0284a0001c0001t0007g0249a0001c0001t0007g0285others(53): Show | 61 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.4101+1950G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670234 | ||||||
chr2:210670492
|
A | AT | 161 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(158): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.4101+2209dupT | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr2 | 210670492 | |||||
chr2:210670554
|
C | T | 51 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(48): Show | 56 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.4101+2270C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670554 | ||||||
chr2:210670830
|
A | G | 5 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.4101+2546A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670830 | ||||||
chr2:210670838
|
G | A | 2 | a0003c0003t0001g0127a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4101+2554G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670838 | ||||||
chr2:210670958
|
T | C | 60 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0231others(57): Show | 61 | HG00609.hp2 HG00733.hp2 HG01168.hp2 others(58): Show |
intron_variant | MODIFIER | c.4101+2674T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670958 | ||||||
chr2:210670959
|
A | G | 2 | a0001c0001t0003g0124a0001c0001t0003g0253 | 2 | HG02257.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4101+2675A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670959 | ||||||
chr2:210670987
|
A | G | 1 | a0002c0002t0011g0187 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4101+2703A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670987 | ||||||
chr2:210670995
|
G | A | 2 | a0003c0003t0004g0260a0003c0003t0004g0290 | 2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4101+2711G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210670995 | ||||||
chr2:210671057
|
G | A | 2 | a0002c0002t0011g0140a0004c0004t0005g0151 | 2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4101+2773G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671057 | ||||||
chr2:210671133
|
T | A | 5 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.4101+2849T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671133 | ||||||
chr2:210671207
|
T | C | 162 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(159): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.4101+2923T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671207 | ||||||
chr2:210671239
|
C | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4101+2955C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671239 | ||||||
chr2:210671332
|
C | A | 7 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0009g0247others(4): Show | 7 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4101+3048C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671332 | ||||||
chr2:210671540
|
C | G | 19 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(16): Show | 22 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.4101+3256C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671540 | ||||||
chr2:210671545
|
G | A | 61 | a0001c0001t0001g0100a0001c0001t0003g0129a0001c0001t0006g0030others(58): Show | 61 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.4101+3261G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671545 | ||||||
chr2:210671636
|
A | G | 5 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.4102-3266A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671636 | ||||||
chr2:210671668
|
A | G | 24 | a0001c0001t0006g0284a0001c0001t0007g0285a0001c0001t0008g0119others(21): Show | 27 | HG00735.hp2 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.4102-3234A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671668 | ||||||
chr2:210671799
|
C | T | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4102-3103C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671799 | ||||||
chr2:210671998
|
C | A | 4 | a0001c0001t0008g0096a0002c0002t0021g0236a0003c0003t0005g0105others(1): Show | 4 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.4102-2904C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210671998 | ||||||
chr2:210672065
|
A | G | 6 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(3): Show | 6 | HG01081.hp2 HG01361.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.4102-2837A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672065 | ||||||
chr2:210672108
|
G | C | 5 | a0001c0001t0007g0249a0001c0001t0008g0096a0002c0002t0021g0236others(2): Show | 5 | HG01361.hp2 HG01496.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.4102-2794G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672108 | ||||||
chr2:210672122
|
A | G | 97 | a0001c0001t0001g0086a0001c0001t0001g0094a0001c0001t0001g0095others(94): Show | 98 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.4102-2780A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672122 | ||||||
chr2:210672154
|
G | A | 1 | a0002c0002t0021g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4102-2748G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672154 | ||||||
chr2:210672187
|
G | A | 1 | a0001c0001t0006g0293 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.4102-2715G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672187 | ||||||
chr2:210672226
|
T | C | 1 | a0002c0013t0007g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4102-2676T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672226 | ||||||
chr2:210672267
|
C | T | 9 | a0001c0001t0006g0329a0001c0001t0006g0331a0001c0001t0008g0125others(6): Show | 9 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.4102-2635C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672267 | ||||||
chr2:210672341
|
G | A | 1 | a0001c0001t0025g0043 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.4102-2561G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672341 | ||||||
chr2:210672375
|
G | A | 1 | a0002c0002t0001g0222 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4102-2527G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672375 | ||||||
chr2:210672380
|
G | T | 5 | a0001c0001t0009g0008a0001c0001t0009g0246a0001c0001t0009g0283others(2): Show | 6 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.4102-2522G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672380 | ||||||
chr2:210672541
|
A | G | 1 | a0001c0001t0007g0285 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4102-2361A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672541 | ||||||
chr2:210672709
|
G | A | 1 | a0002c0002t0001g0176 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4102-2193G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672709 | ||||||
chr2:210672738
|
C | T | 1 | a0003c0003t0004g0259 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4102-2164C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672738 | ||||||
chr2:210672740
|
T | C | 2 | a0003c0003t0001g0127a0003c0018t0002g0239 | 2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.4102-2162T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672740 | ||||||
chr2:210672919
|
C | T | 1 | a0001c0001t0007g0249 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4102-1983C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210672919 | ||||||
chr2:210673019
|
G | T | 1 | a0001c0001t0013g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4102-1883G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673019 | ||||||
chr2:210673079
|
T | C | 2 | a0003c0003t0002g0060a0003c0003t0004g0259 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4102-1823T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673079 | ||||||
chr2:210673245
|
G | A | 1 | a0001c0006t0006g0276 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4102-1657G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673245 | ||||||
chr2:210673489
|
A | G | 324 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(321): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.4102-1413A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673489 | ||||||
chr2:210673731
|
A | G | 8 | a0001c0001t0006g0037a0001c0001t0007g0031a0001c0001t0007g0046others(5): Show | 8 | HG00733.hp1 HG00735.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.4102-1171A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673731 | ||||||
chr2:210673778
|
ACTCATAC others(4): Show |
A | 1 | a0001c0001t0009g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4102-1123_4102-111 others(15): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673778 | ||||||
chr2:210673834
|
T | G | 3 | a0001c0001t0006g0329a0001c0001t0006g0331a0003c0003t0005g0164 | 3 | HG02451.hp2 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.4102-1068T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673834 | ||||||
chr2:210673856
|
A | G | 1 | a0004c0007t0005g0184 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4102-1046A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673856 | ||||||
chr2:210673867
|
C | T | 1 | a0002c0002t0003g0149 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4102-1035C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210673867 | ||||||
chr2:210674011
|
A | G | 1 | a0001c0001t0006g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4102-891A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674011 | ||||||
chr2:210674077
|
A | G | 9 | a0001c0001t0009g0008a0001c0001t0009g0246a0001c0001t0009g0247others(6): Show | 10 | HG01243.hp2 HG02145.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4102-825A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674077 | ||||||
chr2:210674141
|
A | G | 1 | a0002c0002t0021g0236 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4102-761A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674141 | ||||||
chr2:210674329
|
T | C | 1 | a0001c0001t0006g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4102-573T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674329 | ||||||
chr2:210674339
|
G | A | 1 | a0001c0001t0006g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4102-563G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674339 | ||||||
chr2:210674341
|
T | C | 1 | a0001c0001t0006g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4102-561T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674341 | ||||||
chr2:210674343
|
G | C | 1 | a0001c0001t0006g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4102-559G>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674343 | ||||||
chr2:210674357
|
C | T | 1 | a0001c0001t0006g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4102-545C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674357 | ||||||
chr2:210674368
|
G | A | 1 | a0001c0001t0003g0230 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4102-534G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674368 | ||||||
chr2:210674426
|
G | A | 63 | a0001c0001t0003g0121a0001c0001t0003g0131a0001c0001t0006g0037others(60): Show | 66 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.4102-476G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674426 | ||||||
chr2:210674449
|
A | G | 2 | a0001c0001t0007g0258a0007c0014t0007g0062 | 2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.4102-453A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674449 | ||||||
chr2:210674471
|
CA | C | 11 | a0001c0001t0007g0249a0001c0001t0008g0119a0001c0001t0009g0008others(8): Show | 12 | HG01243.hp2 HG02145.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.4102-420delA | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr2 | 210674471 | |||||
chr2:210674479
|
AAAACC | A | 56 | a0001c0001t0003g0081a0001c0001t0003g0091a0001c0001t0003g0092others(53): Show | 56 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.4102-419_4102-415d others(7): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr2 | 210674479 | |||||
chr2:210674480
|
AAACC | A | 16 | a0001c0001t0002g0326a0001c0001t0003g0106a0001c0001t0007g0009others(13): Show | 16 | HG00597.hp2 HG01167.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.4102-419_4102-416d others(6): Show |
CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr2 | 210674480 | |||||
chr2:210674547
|
T | C | 15 | a0001c0001t0002g0068a0001c0001t0007g0009a0001c0001t0007g0066others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.4102-355T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674547 | ||||||
chr2:210674560
|
G | A | 21 | a0001c0001t0003g0129a0001c0001t0006g0040a0001c0001t0008g0125others(18): Show | 22 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.4102-342G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674560 | ||||||
chr2:210674560
|
G | T | 1 | a0001c0001t0006g0284 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4102-342G>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674560 | ||||||
chr2:210674578
|
C | T | 150 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(147): Show | 154 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.4102-324C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674578 | ||||||
chr2:210674639
|
A | G | 315 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(312): Show | 321 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.4102-263A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674639 | ||||||
chr2:210674804
|
T | C | 1 | a0002c0002t0001g0238 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4102-98T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 34/37 | chr2 | 210674804 | ||||||
chr2:210675259
|
A | T | 1 | a0004c0004t0004g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4161+298A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 35/37 | chr2 | 210675259 | ||||||
chr2:210675540
|
T | A | 3 | a0004c0004t0002g0010a0004c0004t0002g0011a0004c0007t0001g0157 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4162-188T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 35/37 | chr2 | 210675540 | ||||||
chr2:210675880
|
G | A | 1 | a0002c0002t0001g0183 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.4274+40G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210675880 | ||||||
chr2:210676029
|
T | A | 1 | a0003c0003t0005g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4274+189T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676029 | ||||||
chr2:210676139
|
T | G | 94 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0094others(91): Show | 95 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.4274+299T>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676139 | ||||||
chr2:210676202
|
T | C | 4 | a0001c0001t0017g0322a0001c0024t0017g0288a0002c0002t0012g0005others(1): Show | 5 | HG00733.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4274+362T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676202 | ||||||
chr2:210676250
|
A | G | 15 | a0001c0001t0010g0044a0001c0001t0010g0045a0001c0001t0010g0047others(12): Show | 15 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.4274+410A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676250 | ||||||
chr2:210676340
|
C | A | 15 | a0001c0001t0010g0044a0001c0001t0010g0045a0001c0001t0010g0047others(12): Show | 15 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.4274+500C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676340 | ||||||
chr2:210676441
|
G | A | 14 | a0001c0001t0010g0044a0001c0001t0010g0045a0001c0001t0010g0047others(11): Show | 14 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.4275-566G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676441 | ||||||
chr2:210676744
|
T | C | 1 | a0003c0003t0027g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4275-263T>C | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676744 | ||||||
chr2:210676788
|
C | T | 1 | a0001c0028t0024g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4275-219C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676788 | ||||||
chr2:210676898
|
C | T | 2 | a0003c0003t0004g0263a0004c0004t0002g0317 | 2 | HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.4275-109C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676898 | ||||||
chr2:210676997
|
A | G | 1 | a0001c0001t0013g0028 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4275-10A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 36/37 | chr2 | 210676997 | ||||||
chr2:210677140
|
T | A | 3 | a0001c0001t0029g0278a0002c0002t0015g0084a0002c0002t0015g0171 | 3 | HG03831.hp1 HG03834.hp2 NA20905.hp1 |
splice_region_variant&intron_variant | LOW | c.4404+4T>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677140 | ||||||
chr2:210677367
|
C | G | 3 | a0001c0001t0009g0247a0001c0001t0009g0248a0001c0001t0009g0280 | 3 | HG01243.hp2 HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4404+231C>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677367 | ||||||
chr2:210677497
|
G | A | 4 | a0001c0001t0017g0322a0001c0024t0017g0288a0002c0002t0012g0005others(1): Show | 5 | HG00733.hp2 HG00735.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.4404+361G>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677497 | ||||||
chr2:210677675
|
C | T | 3 | a0001c0001t0029g0278a0002c0002t0015g0084a0002c0002t0015g0171 | 3 | HG03831.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.4405-212C>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677675 | ||||||
chr2:210677689
|
C | A | 3 | a0001c0001t0029g0278a0002c0002t0015g0084a0002c0002t0015g0171 | 3 | HG03831.hp1 HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.4405-198C>A | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677689 | ||||||
chr2:210677755
|
A | T | 4 | a0003c0003t0004g0260a0003c0003t0004g0290a0003c0003t0004g0330others(1): Show | 4 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.4405-132A>T | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677755 | ||||||
chr2:210677801
|
A | G | 14 | a0001c0001t0010g0044a0001c0001t0010g0045a0001c0001t0010g0047others(11): Show | 14 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.4405-86A>G | CPS1 | ENSG00000021826.18 | transcript | ENST00000233072.10 | protein_coding | 37/37 | chr2 | 210677801 |