geneid | 257062 |
---|---|
ensemblid | ENSG00000174898.16 |
hgncid | 28598 |
symbol | CATSPERD |
name | cation channel sperm associated auxiliary subunit delta |
refseq_nuc | NM_152784.4 |
refseq_prot | NP_689997.3 |
ensembl_nuc | ENST00000381624.4 |
ensembl_prot | ENSP00000371037.3 |
mane_status | MANE Select |
chr | chr19 |
start | 5720637 |
end | 5778734 |
strand | + |
ver | v1.2 |
region | chr19:5720637-5778734 |
region5000 | chr19:5715637-5783734 |
regionname0 | CATSPERD_chr19_5720637_5778734 |
regionname5000 | CATSPERD_chr19_5715637_5783734 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 798 | 98 | 38 | 32 | 6 | 8 | 13 | 5 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002 | 0/1 | 798 | 80 | 1 | 26 | 37 | 2 | 13 | 28 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003 | 0/0 | 798 | 55 | 15 | 6 | 24 | 2 | 8 | 11 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004 | 0/0 | 798 | 47 | 1 | 3 | 40 | 0 | 3 | 31 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0005 | 0/0 | 798 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0006 | 0/0 | 798 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0007 | 0/0 | 798 | 3 | 0 | 2 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0008 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0009 | 0/0 | 798 | 3 | 0 | 0 | 0 | 2 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0010 | 0/0 | 798 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0011 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0012 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0013 | 0/0 | 798 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0014 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0015 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0016 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0017 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0018 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0019 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0020 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0021 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0022 | 0/0 | 798 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0023 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0024 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0025 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0026 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0027 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0028 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0029 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0030 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0031 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0032 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0033 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0034 | 0/0 | 798 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2397 | 93 | 37 | 30 | 5 | 8 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0002 | 0/1 | 2397 | 77 | 1 | 25 | 36 | 2 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0003 | 0/0 | 2397 | 45 | 1 | 3 | 38 | 0 | 3 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0004 | 0/0 | 2397 | 42 | 14 | 6 | 14 | 1 | 7 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0005 | 0/0 | 2397 | 10 | 0 | 0 | 9 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0006 | 0/0 | 2397 | 7 | 6 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0007 | 0/0 | 2397 | 5 | 5 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0008 | 0/0 | 2397 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0009 | 0/0 | 2397 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0010 | 0/0 | 2397 | 3 | 0 | 2 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0011 | 0/0 | 2397 | 3 | 2 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0012 | 0/0 | 2397 | 3 | 0 | 0 | 0 | 2 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0013 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0014 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0015 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0016 | 0/0 | 2397 | 2 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0017 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0018 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0019 | 0/0 | 2397 | 2 | 0 | 1 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0020 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0021 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0022 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0023 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0024 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0025 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0026 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0027 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0028 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0029 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0030 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0031 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0032 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0033 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0034 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0035 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0036 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0037 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0038 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0039 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0040 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0041 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0042 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0043 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0044 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0045 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0046 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
c0047 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
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 | 1/1 | 160 | 307 | 75 | 64 | 108 | 14 | 44 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
t0002 | 0/0 | 160 | 16 | 16 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
t0003 | 0/0 | 160 | 10 | 0 | 6 | 4 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
t0004 | 0/0 | 160 | 2 | 1 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
t0005 | 0/0 | 160 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2397 | 93 | 37 | 30 | 5 | 8 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0016 | 0/0 | 2397 | 2 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0034 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0040 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0045 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0002 | 0/1 | 2397 | 77 | 1 | 25 | 36 | 2 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0019 | 0/0 | 2397 | 2 | 0 | 1 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0027 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0004 | 0/0 | 2397 | 42 | 14 | 6 | 14 | 1 | 7 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0005 | 0/0 | 2397 | 10 | 0 | 0 | 9 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0037 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0041 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0043 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0003 | 0/0 | 2397 | 45 | 1 | 3 | 38 | 0 | 3 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0042 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0044 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0005c0006 | 0/0 | 2397 | 7 | 6 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0006c0007 | 0/0 | 2397 | 5 | 5 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0007c0010 | 0/0 | 2397 | 3 | 0 | 2 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0008c0009 | 0/0 | 2397 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0009c0012 | 0/0 | 2397 | 3 | 0 | 0 | 0 | 2 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0010c0011 | 0/0 | 2397 | 3 | 2 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0011c0008 | 0/0 | 2397 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0012c0015 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0013c0030 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0013c0031 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0014c0017 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0015c0018 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0016c0013 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0017c0014 | 0/0 | 2397 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0018c0020 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0019c0022 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0020c0021 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0021c0023 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0022c0025 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0023c0026 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0024c0035 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0025c0032 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0026c0033 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0027c0036 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0028c0029 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0029c0039 | 0/0 | 2397 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0030c0038 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0031c0028 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0032c0024 | 0/0 | 2397 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0033c0047 | 0/0 | 2397 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0034c0046 | 0/0 | 2397 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2556 | 82 | 28 | 28 | 5 | 8 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0001t0002 | 0/0 | 2556 | 8 | 8 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0001t0004 | 0/0 | 2556 | 2 | 1 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0001t0005 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0016t0001 | 0/0 | 2556 | 2 | 0 | 1 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0034t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0040t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0001c0045t0001 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0002t0001 | 0/1 | 2556 | 73 | 1 | 21 | 36 | 2 | 12 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0002t0003 | 0/0 | 2556 | 4 | 0 | 4 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0019t0001 | 0/0 | 2556 | 2 | 0 | 1 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0002c0027t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0004t0001 | 0/0 | 2556 | 41 | 14 | 5 | 14 | 1 | 7 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0004t0003 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0005t0001 | 0/0 | 2556 | 10 | 0 | 0 | 9 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0037t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0041t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0003c0043t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0003t0001 | 0/0 | 2556 | 40 | 1 | 2 | 34 | 0 | 3 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0003t0003 | 0/0 | 2556 | 5 | 0 | 1 | 4 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0042t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0004c0044t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0005c0006t0001 | 0/0 | 2556 | 7 | 6 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0006c0007t0001 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0006c0007t0002 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0007c0010t0001 | 0/0 | 2556 | 3 | 0 | 2 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0008c0009t0001 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0009c0012t0001 | 0/0 | 2556 | 3 | 0 | 0 | 0 | 2 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0010c0011t0001 | 0/0 | 2556 | 3 | 2 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0011c0008t0001 | 0/0 | 2556 | 3 | 3 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0012c0015t0001 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0013c0030t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0013c0031t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0014c0017t0002 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0015c0018t0001 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0016c0013t0001 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0017c0014t0002 | 0/0 | 2556 | 2 | 2 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0018c0020t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0019c0022t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0020c0021t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0021c0023t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0022c0025t0001 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0023c0026t0002 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0024c0035t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0025c0032t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0026c0033t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0027c0036t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0028c0029t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0029c0039t0001 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0030c0038t0002 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0031c0028t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0032c0024t0001 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0033c0047t0001 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
a0034c0046t0001 | 0/0 | 2556 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | copy fasta | chr19 | 5715637 | 5783734 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0016t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0016t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0034t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0040t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0001c0045t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0092 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0019t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0019t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0002c0027t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0004t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0005t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0037t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0041t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0003c0043t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0003t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0042t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0004c0044t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0005c0006t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0006c0007t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0007c0010t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0007c0010t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0007c0010t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0008c0009t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0008c0009t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0008c0009t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0009c0012t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0009c0012t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0009c0012t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0010c0011t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0010c0011t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0010c0011t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0011c0008t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0011c0008t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0011c0008t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0012c0015t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0012c0015t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0013c0030t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0013c0031t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0014c0017t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0014c0017t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0015c0018t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0015c0018t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0016c0013t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0016c0013t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0017c0014t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0017c0014t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0018c0020t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0019c0022t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0020c0021t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0021c0023t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0022c0025t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0023c0026t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0024c0035t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0025c0032t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0026c0033t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0027c0036t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0028c0029t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0029c0039t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0030c0038t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0031c0028t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0032c0024t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0033c0047t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
a0034c0046t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0004 | t0001 | g0281 | EUR | GBR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00280 | hp2 | a0003 | c0037 | t0001 | g0203 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0068 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0250 | EUR | FIN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00438 | hp1 | a0003 | c0004 | t0001 | g0109 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00438 | hp2 | a0004 | c0003 | t0001 | g0307 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00544 | hp1 | a0003 | c0004 | t0001 | g0294 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00544 | hp2 | a0004 | c0003 | t0001 | g0117 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00609 | hp1 | a0003 | c0004 | t0001 | g0324 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00609 | hp2 | a0003 | c0005 | t0001 | g0269 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00621 | hp1 | a0004 | c0003 | t0003 | g0047 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00621 | hp2 | a0013 | c0030 | t0001 | g0295 | EAS | CHS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00642 | hp1 | a0022 | c0025 | t0001 | g0146 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0238 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG00741 | hp2 | a0034 | c0046 | t0001 | g0005 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01074 | hp2 | a0003 | c0004 | t0001 | g0094 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01081 | hp2 | a0003 | c0004 | t0001 | g0260 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0327 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01168 | hp1 | a0003 | c0004 | t0001 | g0098 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01169 | hp2 | a0003 | c0004 | t0001 | g0096 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01243 | hp2 | a0001 | c0045 | t0001 | g0151 | AMR | PUR | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0072 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01258 | hp1 | a0003 | c0004 | t0001 | g0246 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01258 | hp2 | a0002 | c0002 | t0003 | g0070 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0286 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01346 | hp1 | a0002 | c0019 | t0001 | g0332 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0142 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0236 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01496 | hp2 | a0003 | c0004 | t0003 | g0083 | AMR | CLM | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01515 | hp1 | a0009 | c0012 | t0001 | g0156 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01517 | hp2 | a0009 | c0012 | t0001 | g0153 | EUR | IBS | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01884 | hp2 | a0005 | c0006 | t0001 | g0206 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01928 | hp1 | a0004 | c0003 | t0001 | g0274 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0081 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01934 | hp1 | a0005 | c0006 | t0001 | g0207 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01934 | hp2 | a0001 | c0016 | t0001 | g0126 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01952 | hp1 | a0002 | c0002 | t0003 | g0138 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01952 | hp2 | a0007 | c0010 | t0001 | g0027 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01975 | hp1 | a0004 | c0003 | t0003 | g0131 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG01993 | hp2 | a0007 | c0010 | t0001 | g0026 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0119 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02015 | hp1 | a0003 | c0004 | t0001 | g0262 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02027 | hp1 | a0003 | c0041 | t0001 | g0329 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02027 | hp2 | a0004 | c0003 | t0001 | g0242 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02040 | hp1 | a0004 | c0003 | t0001 | g0313 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02040 | hp2 | a0003 | c0005 | t0001 | g0239 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0061 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02056 | hp1 | a0004 | c0003 | t0001 | g0144 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02071 | hp2 | a0003 | c0004 | t0001 | g0244 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02074 | hp1 | a0003 | c0004 | t0001 | g0322 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02074 | hp2 | a0013 | c0031 | t0001 | g0036 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02083 | hp1 | a0003 | c0004 | t0001 | g0323 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02083 | hp2 | a0003 | c0004 | t0001 | g0290 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02129 | hp2 | a0004 | c0003 | t0001 | g0272 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02135 | hp2 | a0004 | c0003 | t0001 | g0079 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0150 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02148 | hp2 | a0004 | c0003 | t0001 | g0247 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02155 | hp1 | a0003 | c0005 | t0001 | g0325 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02155 | hp2 | a0004 | c0003 | t0001 | g0042 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02165 | hp1 | a0003 | c0005 | t0001 | g0306 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | CDX | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02258 | hp1 | a0005 | c0006 | t0001 | g0219 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0271 | AMR | PEL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02451 | hp1 | a0030 | c0038 | t0002 | g0317 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02451 | hp2 | a0027 | c0036 | t0001 | g0297 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02572 | hp1 | a0006 | c0007 | t0001 | g0034 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02572 | hp2 | a0003 | c0004 | t0001 | g0230 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02615 | hp1 | a0008 | c0009 | t0001 | g0016 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02615 | hp2 | a0003 | c0043 | t0001 | g0233 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02622 | hp1 | a0005 | c0006 | t0001 | g0217 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02630 | hp1 | a0033 | c0047 | t0001 | g0004 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02698 | hp1 | a0009 | c0012 | t0001 | g0159 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02717 | hp1 | a0005 | c0006 | t0001 | g0198 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02717 | hp2 | a0003 | c0004 | t0001 | g0222 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02735 | hp1 | a0021 | c0023 | t0001 | g0052 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02735 | hp2 | a0026 | c0033 | t0001 | g0301 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02809 | hp1 | a0011 | c0008 | t0001 | g0012 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02809 | hp2 | a0016 | c0013 | t0001 | g0015 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02818 | hp1 | a0019 | c0022 | t0001 | g0028 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0333 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0123 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02895 | hp1 | a0008 | c0009 | t0001 | g0032 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02895 | hp2 | a0003 | c0004 | t0001 | g0022 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0106 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02896 | hp2 | a0014 | c0017 | t0002 | g0223 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02897 | hp1 | a0014 | c0017 | t0002 | g0224 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02897 | hp2 | a0003 | c0004 | t0001 | g0314 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02922 | hp1 | a0017 | c0014 | t0002 | g0011 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02965 | hp1 | a0025 | c0032 | t0001 | g0334 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02965 | hp2 | a0006 | c0007 | t0002 | g0031 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02970 | hp1 | a0010 | c0011 | t0001 | g0003 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02970 | hp2 | a0011 | c0008 | t0001 | g0014 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02976 | hp1 | a0003 | c0004 | t0001 | g0058 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03041 | hp2 | a0011 | c0008 | t0001 | g0010 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03098 | hp1 | a0008 | c0009 | t0001 | g0008 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0076 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03130 | hp2 | a0012 | c0015 | t0001 | g0125 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03139 | hp1 | a0017 | c0014 | t0002 | g0013 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0149 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03195 | hp2 | a0006 | c0007 | t0001 | g0025 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03209 | hp1 | a0015 | c0018 | t0001 | g0308 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03209 | hp2 | a0003 | c0004 | t0001 | g0129 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03225 | hp2 | a0015 | c0018 | t0001 | g0309 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03239 | hp1 | a0003 | c0004 | t0001 | g0196 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03239 | hp2 | a0004 | c0003 | t0001 | g0087 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03486 | hp2 | a0018 | c0020 | t0001 | g0018 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03491 | hp2 | a0003 | c0004 | t0001 | g0108 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03516 | hp2 | a0023 | c0026 | t0002 | g0335 | AFR | ESN | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03579 | hp1 | a0016 | c0013 | t0001 | g0009 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03579 | hp2 | a0003 | c0004 | t0001 | g0336 | AFR | MSL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03654 | hp1 | a0029 | c0039 | t0001 | g0140 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03654 | hp2 | a0024 | c0035 | t0001 | g0152 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03669 | hp1 | a0020 | c0021 | t0001 | g0019 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03669 | hp2 | a0003 | c0004 | t0001 | g0199 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0097 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03710 | hp2 | a0003 | c0004 | t0001 | g0158 | SAS | PJL | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03831 | hp1 | a0002 | c0027 | t0001 | g0237 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03831 | hp2 | a0003 | c0004 | t0001 | g0040 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03834 | hp1 | a0004 | c0003 | t0001 | g0243 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03834 | hp2 | a0001 | c0016 | t0001 | g0167 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03927 | hp1 | a0003 | c0004 | t0001 | g0303 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0182 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04184 | hp1 | a0004 | c0003 | t0001 | g0319 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04199 | hp1 | a0010 | c0011 | t0001 | g0315 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0200 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0073 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0050 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG04228 | hp2 | a0003 | c0005 | t0001 | g0214 | SAS | STU | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18522 | hp1 | a0012 | c0015 | t0001 | g0122 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18522 | hp2 | a0005 | c0006 | t0001 | g0213 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18942 | hp2 | a0004 | c0003 | t0001 | g0179 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18943 | hp1 | a0003 | c0005 | t0001 | g0254 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18943 | hp2 | a0002 | c0019 | t0001 | g0330 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0257 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18944 | hp2 | a0003 | c0004 | t0001 | g0188 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18946 | hp1 | a0004 | c0042 | t0001 | g0316 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18946 | hp2 | a0004 | c0003 | t0001 | g0321 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18952 | hp2 | a0004 | c0003 | t0001 | g0248 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18954 | hp2 | a0004 | c0003 | t0001 | g0302 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18960 | hp1 | a0004 | c0003 | t0001 | g0080 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18963 | hp1 | a0004 | c0003 | t0001 | g0282 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18966 | hp1 | a0003 | c0005 | t0001 | g0253 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18967 | hp1 | a0003 | c0005 | t0001 | g0300 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18967 | hp2 | a0007 | c0010 | t0001 | g0029 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0278 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18969 | hp1 | a0028 | c0029 | t0001 | g0264 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18969 | hp2 | a0004 | c0003 | t0001 | g0169 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18971 | hp2 | a0003 | c0004 | t0001 | g0095 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18972 | hp1 | a0004 | c0003 | t0001 | g0218 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18972 | hp2 | a0003 | c0004 | t0001 | g0287 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18974 | hp1 | a0004 | c0003 | t0003 | g0053 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18983 | hp1 | a0004 | c0003 | t0001 | g0110 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18986 | hp1 | a0004 | c0003 | t0001 | g0104 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18986 | hp2 | a0004 | c0003 | t0001 | g0275 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18990 | hp2 | a0004 | c0003 | t0001 | g0245 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18998 | hp1 | a0004 | c0003 | t0001 | g0293 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18999 | hp1 | a0004 | c0044 | t0001 | g0211 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA18999 | hp2 | a0001 | c0040 | t0001 | g0331 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19002 | hp2 | a0004 | c0003 | t0001 | g0267 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19007 | hp1 | a0032 | c0024 | t0001 | g0204 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19007 | hp2 | a0003 | c0005 | t0001 | g0249 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19011 | hp1 | a0003 | c0004 | t0001 | g0192 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19011 | hp2 | a0003 | c0004 | t0001 | g0328 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19012 | hp1 | a0004 | c0003 | t0001 | g0183 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19012 | hp2 | a0004 | c0003 | t0001 | g0174 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19043 | hp2 | a0004 | c0003 | t0001 | g0202 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0326 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19060 | hp2 | a0003 | c0004 | t0001 | g0216 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19065 | hp1 | a0004 | c0003 | t0001 | g0252 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19065 | hp2 | a0004 | c0003 | t0003 | g0071 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19066 | hp1 | a0004 | c0003 | t0001 | g0132 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19074 | hp1 | a0004 | c0003 | t0001 | g0172 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19074 | hp2 | a0004 | c0003 | t0003 | g0075 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19077 | hp2 | a0004 | c0003 | t0001 | g0168 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19078 | hp1 | a0004 | c0003 | t0001 | g0035 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19078 | hp2 | a0004 | c0003 | t0001 | g0320 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19079 | hp1 | a0004 | c0003 | t0001 | g0141 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19089 | hp2 | a0004 | c0003 | t0001 | g0240 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19090 | hp1 | a0004 | c0003 | t0001 | g0048 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19090 | hp2 | a0004 | c0003 | t0001 | g0241 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19091 | hp1 | a0003 | c0005 | t0001 | g0185 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19240 | hp1 | a0006 | c0007 | t0002 | g0030 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20905 | hp1 | a0003 | c0004 | t0001 | g0178 | SAS | GIH | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02109 | hp1 | a0001 | c0034 | t0001 | g0023 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02109 | hp2 | a0003 | c0004 | t0001 | g0148 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02486 | hp2 | a0006 | c0007 | t0001 | g0017 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG02559 | hp2 | a0005 | c0006 | t0001 | g0212 | AFR | ACB | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG06807 | hp1 | a0010 | c0011 | t0001 | g0002 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
NA21309 | hp2 | a0031 | c0028 | t0001 | g0130 | AFR | LWK | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0092 | REF | REF | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | CATSPERD_chr19_5715637_5783734 | CATSPERD | chr19 | 5715637 | 5783734 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720763
|
C | G | 2 | a0033a0034 | 2 | HG00741.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.26C>G | p.Ala9Gly | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | 127/2556 | 26/2397 | 9/798 | chr19 | 5720763 | ||
chr19:5727298
|
C | T | 1 | a0005 | 7 | HG01884.hp2 HG01934.hp1 HG02258.hp1 others(4): Show |
missense_variant | MODERATE | c.157C>T | p.Arg53Cys | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/22 | 258/2556 | 157/2397 | 53/798 | chr19 | 5727298 | ||
chr19:5733859
|
G | A | 3 | a0011a0016a0017 | 7 | HG02809.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
missense_variant | MODERATE | c.280G>A | p.Gly94Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 381/2556 | 280/2397 | 94/798 | chr19 | 5733859 | ||
chr19:5733863
|
T | C | 8 | a0006a0007a0008others(5): Show | 16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
missense_variant | MODERATE | c.284T>C | p.Val95Ala | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 385/2556 | 284/2397 | 95/798 | chr19 | 5733863 | ||
chr19:5733893
|
G | C | 1 | a0021 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.314G>C | p.Gly105Ala | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 415/2556 | 314/2397 | 105/798 | chr19 | 5733893 | ||
chr19:5744488
|
T | C | 9 | a0006a0008a0010others(6): Show | 17 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
missense_variant | MODERATE | c.635T>C | p.Met212Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/22 | 736/2556 | 635/2397 | 212/798 | chr19 | 5744488 | ||
chr19:5746013
|
G | C | 1 | a0022 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.758G>C | p.Gly253Ala | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/22 | 859/2556 | 758/2397 | 253/798 | chr19 | 5746013 | ||
chr19:5748177
|
G | A | 1 | a0023 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.826G>A | p.Val276Ile | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/22 | 927/2556 | 826/2397 | 276/798 | chr19 | 5748177 | ||
chr19:5749115
|
G | A | 1 | a0031 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.919G>A | p.Ala307Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/22 | 1020/2556 | 919/2397 | 307/798 | chr19 | 5749115 | ||
chr19:5749160
|
A | G | 10 | a0006a0008a0010others(7): Show | 18 | HG00741.hp2 HG02451.hp1 HG02486.hp2 others(15): Show |
missense_variant | MODERATE | c.964A>G | p.Ile322Val | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/22 | 1065/2556 | 964/2397 | 322/798 | chr19 | 5749160 | ||
chr19:5751791
|
A | G | 1 | a0015 | 2 | HG03209.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.1132A>G | p.Met378Val | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/22 | 1233/2556 | 1132/2397 | 378/798 | chr19 | 5751791 | ||
chr19:5751792
|
T | C | 1 | a0028 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1133T>C | p.Met378Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/22 | 1234/2556 | 1133/2397 | 378/798 | chr19 | 5751792 | ||
chr19:5754216
|
C | T | 3 | a0014a0017a0027 | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
missense_variant | MODERATE | c.1249C>T | p.Pro417Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/22 | 1350/2556 | 1249/2397 | 417/798 | chr19 | 5754216 | ||
chr19:5772812
|
G | C | 1 | a0009 | 3 | HG01515.hp1 HG01517.hp2 HG02698.hp1 |
missense_variant | MODERATE | c.1788G>C | p.Glu596Asp | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/22 | 1889/2556 | 1788/2397 | 596/798 | chr19 | 5772812 | ||
chr19:5772886
|
C | T | 4 | a0004a0019a0024others(1): Show | 50 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(47): Show |
missense_variant | MODERATE | c.1862C>T | p.Ser621Leu | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/22 | 1963/2556 | 1862/2397 | 621/798 | chr19 | 5772886 | ||
chr19:5772939
|
G | A | 6 | a0002a0007a0013others(3): Show | 88 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
missense_variant | MODERATE | c.1915G>A | p.Gly639Arg | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/22 | 2016/2556 | 1915/2397 | 639/798 | chr19 | 5772939 | ||
chr19:5776239
|
C | T | 1 | a0026 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.2020C>T | p.Arg674Trp | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2121/2556 | 2020/2397 | 674/798 | chr19 | 5776239 | ||
chr19:5776298
|
C | G | 1 | a0024 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2079C>G | p.Ile693Met | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2180/2556 | 2079/2397 | 693/798 | chr19 | 5776298 | ||
chr19:5778506
|
A | T | 15 | a0003a0004a0008others(12): Show | 120 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(117): Show |
missense_variant | MODERATE | c.2227A>T | p.Thr743Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2328/2556 | 2227/2397 | 743/798 | chr19 | 5778506 | ||
chr19:5778522
|
G | A | 1 | a0012 | 2 | HG03130.hp2 NA18522.hp1 |
missense_variant | MODERATE | c.2243G>A | p.Arg748His | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2344/2556 | 2243/2397 | 748/798 | chr19 | 5778522 | ||
chr19:5778543
|
T | C | 1 | a0025 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.2264T>C | p.Ile755Thr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2365/2556 | 2264/2397 | 755/798 | chr19 | 5778543 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720785
|
G | T | 1 | a0001c0045 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.48G>T | p.Pro16Pro | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | 149/2556 | 48/2397 | 16/798 | chr19 | 5720785 | ||
chr19:5729899
|
C | T | 1 | a0001c0045 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.231C>T | p.Asn77Asn | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/22 | 332/2556 | 231/2397 | 77/798 | chr19 | 5729899 | ||
chr19:5733897
|
G | C | 8 | a0006c0007a0007c0010a0008c0009others(5): Show | 16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
synonymous_variant | LOW | c.318G>C | p.Ser106Ser | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/22 | 419/2556 | 318/2397 | 106/798 | chr19 | 5733897 | ||
chr19:5745996
|
C | T | 1 | a0004c0044 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.741C>T | p.Ile247Ile | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/22 | 842/2556 | 741/2397 | 247/798 | chr19 | 5745996 | ||
chr19:5746002
|
C | T | 1 | a0003c0043 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.747C>T | p.Pro249Pro | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/22 | 848/2556 | 747/2397 | 249/798 | chr19 | 5746002 | ||
chr19:5748167
|
C | G | 4 | a0001c0040a0002c0019a0003c0041others(1): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
synonymous_variant | LOW | c.816C>G | p.Leu272Leu | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/22 | 917/2556 | 816/2397 | 272/798 | chr19 | 5748167 | ||
chr19:5748182
|
G | A | 1 | a0002c0027 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.831G>A | p.Arg277Arg | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/22 | 932/2556 | 831/2397 | 277/798 | chr19 | 5748182 | ||
chr19:5751661
|
C | T | 1 | a0003c0037 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.1002C>T | p.Tyr334Tyr | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/22 | 1103/2556 | 1002/2397 | 334/798 | chr19 | 5751661 | ||
chr19:5776190
|
C | T | 1 | a0001c0016 | 2 | HG01934.hp2 HG03834.hp2 |
synonymous_variant | LOW | c.1971C>T | p.Asn657Asn | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2072/2556 | 1971/2397 | 657/798 | chr19 | 5776190 | ||
chr19:5776238
|
C | G | 1 | a0001c0034 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2019C>G | p.Gly673Gly | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/22 | 2120/2556 | 2019/2397 | 673/798 | chr19 | 5776238 | ||
chr19:5778586
|
C | G | 2 | a0003c0005a0013c0031 | 11 | HG00609.hp2 HG02040.hp2 HG02074.hp2 others(8): Show |
synonymous_variant | LOW | c.2307C>G | p.Val769Val | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 2408/2556 | 2307/2397 | 769/798 | chr19 | 5778586 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720692
|
C | G | 3 | a0002c0002t0003a0003c0004t0003a0004c0003t0003 | 10 | HG00621.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | chr19 | 5720692 | ||||||
chr19:5720713
|
G | C | 1 | a0001c0001t0004 | 2 | HG01109.hp2 HG02896.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/22 | chr19 | 5720713 | ||||||
chr19:5778680
|
C | T | 1 | a0001c0001t0005 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 4 | chr19 | 5778680 | |||||
chr19:5778681
|
G | A | 6 | a0001c0001t0002a0006c0007t0002a0014c0017t0002others(3): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 22/22 | 5 | chr19 | 5778681 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:5720843
|
G | A | 3 | a0001c0001t0001g0001a0010c0011t0001g0002a0010c0011t0001g0003 | 3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.71+35G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720843 | ||||||
chr19:5720962
|
C | T | 1 | a0003c0004t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.71+154C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720962 | ||||||
chr19:5720968
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.71+160C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720968 | ||||||
chr19:5720996
|
C | T | 4 | a0001c0001t0001g0001a0010c0011t0001g0002a0010c0011t0001g0003others(1): Show | 4 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+188C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5720996 | ||||||
chr19:5720999
|
C | CT | 23 | a0001c0001t0001g0001a0001c0001t0001g0318a0001c0040t0001g0331others(20): Show | 23 | HG00609.hp1 HG01099.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.71+208dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5720999 | |||||
chr19:5720999
|
CT | C | 29 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(26): Show | 29 | HG01952.hp2 HG01993.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+208delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5720999 | |||||
chr19:5721007
|
T | A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+199T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721007 | ||||||
chr19:5721037
|
C | T | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(26): Show | 29 | HG01952.hp2 HG01993.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.71+229C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721037 | ||||||
chr19:5721045
|
C | T | 1 | a0004c0003t0001g0313 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.71+237C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721045 | ||||||
chr19:5721059
|
C | T | 7 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0002g0311others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+251C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721059 | ||||||
chr19:5721222
|
C | G | 4 | a0001c0001t0001g0001a0010c0011t0001g0002a0010c0011t0001g0003others(1): Show | 4 | HG02257.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71+414C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721222 | ||||||
chr19:5721280
|
G | C | 1 | a0004c0003t0001g0035 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.71+472G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721280 | ||||||
chr19:5721281
|
C | G | 1 | a0004c0003t0001g0035 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.71+473C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721281 | ||||||
chr19:5721552
|
T | A | 1 | a0004c0042t0001g0316 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.71+744T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721552 | ||||||
chr19:5721832
|
T | A | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71+1024T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721832 | ||||||
chr19:5721878
|
A | G | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.71+1070A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5721878 | ||||||
chr19:5721985
|
G | GA | 16 | a0001c0001t0001g0001a0002c0002t0001g0037a0004c0003t0001g0035others(13): Show | 16 | HG02074.hp2 HG02257.hp1 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.71+1192dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5721985 | |||||
chr19:5721985
|
GA | G | 9 | a0001c0001t0001g0304a0002c0002t0001g0305a0003c0004t0001g0303others(6): Show | 9 | HG00438.hp2 HG00741.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.71+1192delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5721985 | |||||
chr19:5722164
|
C | G | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71+1356C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722164 | ||||||
chr19:5722278
|
C | A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+1470C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722278 | ||||||
chr19:5722304
|
G | A | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.71+1496G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722304 | ||||||
chr19:5722324
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(121): Show | 124 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.71+1516T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722324 | ||||||
chr19:5722351
|
G | A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71+1543G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722351 | ||||||
chr19:5722392
|
C | A | 40 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(37): Show | 40 | HG00741.hp2 HG01243.hp2 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.71+1584C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722392 | ||||||
chr19:5722396
|
C | T | 1 | a0025c0032t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.71+1588C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722396 | ||||||
chr19:5722400
|
C | T | 7 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0002g0311others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.71+1592C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722400 | ||||||
chr19:5722413
|
G | A | 1 | a0024c0035t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.71+1605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722413 | ||||||
chr19:5722423
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(318): Show | 321 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(318): Show |
intron_variant | MODIFIER | c.71+1615C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722423 | ||||||
chr19:5722428
|
T | A | 7 | a0001c0001t0001g0170a0002c0002t0001g0171a0002c0002t0001g0173others(4): Show | 7 | HG02523.hp2 NA18960.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.71+1620T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722428 | ||||||
chr19:5722458
|
A | C | 34 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(31): Show | 34 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.71+1650A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722458 | ||||||
chr19:5722518
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.71+1710G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722518 | ||||||
chr19:5722648
|
A | G | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.71+1840A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722648 | ||||||
chr19:5722730
|
AC | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(231): Show | 234 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.71+1933delC | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5722730 | |||||
chr19:5722733
|
C | A | 1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.71+1925C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722733 | ||||||
chr19:5722734
|
C | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0016t0001g0167 | 3 | HG03491.hp1 HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.71+1926C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722734 | ||||||
chr19:5722736
|
C | G | 1 | a0001c0001t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.71+1928C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722736 | ||||||
chr19:5722738
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.71+1930C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722738 | ||||||
chr19:5722905
|
T | A | 1 | a0025c0032t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72-1903T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5722905 | ||||||
chr19:5722919
|
GGGCTCAC others(1504): Show |
G | 2 | a0002c0002t0001g0049a0002c0002t0001g0050 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.72-1868_72-358del | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5722919 | |||||
chr19:5723018
|
C | T | 1 | a0025c0032t0001g0334 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.72-1790C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723018 | ||||||
chr19:5723117
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.72-1691G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723117 | ||||||
chr19:5723186
|
C | CA | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.72-1608dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723186 | |||||
chr19:5723226
|
T | C | 39 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(36): Show | 39 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.72-1582T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723226 | ||||||
chr19:5723288
|
C | A | 35 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(32): Show | 35 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(32): Show |
intron_variant | MODIFIER | c.72-1520C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723288 | ||||||
chr19:5723370
|
T | C | 307 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(304): Show | 307 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(304): Show |
intron_variant | MODIFIER | c.72-1438T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723370 | ||||||
chr19:5723387
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.72-1421C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723387 | ||||||
chr19:5723403
|
G | A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.72-1405G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723403 | ||||||
chr19:5723458
|
A | AT | 64 | a0001c0001t0001g0128a0001c0001t0001g0133a0001c0001t0001g0134others(61): Show | 64 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.72-1326dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | |||||
chr19:5723458
|
A | ATT | 13 | a0001c0001t0001g0177a0001c0001t0001g0210a0001c0001t0001g0220others(10): Show | 13 | HG01261.hp1 HG01358.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.72-1327_72-1326dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | |||||
chr19:5723458
|
AT | A | 85 | a0001c0001t0001g0170a0001c0001t0001g0225a0001c0001t0001g0255others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.72-1326delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | |||||
chr19:5723458
|
ATT | A | 25 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(22): Show | 25 | HG01346.hp1 HG01496.hp1 HG01952.hp2 others(22): Show |
intron_variant | MODIFIER | c.72-1327_72-1326del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | |||||
chr19:5723458
|
ATTT | A | 6 | a0002c0019t0001g0330a0003c0041t0001g0329a0004c0042t0001g0316others(3): Show | 6 | HG02027.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.72-1328_72-1326del others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723458 | |||||
chr19:5723496
|
G | A | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.72-1312G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723496 | ||||||
chr19:5723572
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.72-1236C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723572 | ||||||
chr19:5723576
|
T | C | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.72-1232T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723576 | ||||||
chr19:5723782
|
G | GT | 27 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0002g0024others(24): Show | 27 | HG01261.hp2 HG01346.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.72-1015dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723782 | |||||
chr19:5723782
|
G | GTT | 8 | a0001c0001t0001g0033a0006c0007t0001g0017a0006c0007t0001g0034others(5): Show | 8 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.72-1016_72-1015dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr19 | 5723782 | |||||
chr19:5723788
|
T | G | 5 | a0002c0027t0001g0237a0003c0004t0001g0322a0003c0004t0001g0323others(2): Show | 5 | HG00609.hp1 HG02074.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.72-1020T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723788 | ||||||
chr19:5723819
|
C | T | 1 | a0001c0016t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.72-989C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723819 | ||||||
chr19:5723926
|
G | A | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.72-882G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5723926 | ||||||
chr19:5724029
|
G | A | 4 | a0006c0007t0001g0034a0006c0007t0002g0030a0006c0007t0002g0031others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.72-779G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724029 | ||||||
chr19:5724248
|
A | G | 2 | a0003c0004t0001g0324a0003c0005t0001g0325 | 2 | HG00609.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.72-560A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724248 | ||||||
chr19:5724251
|
T | C | 81 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(78): Show | 81 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.72-557T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724251 | ||||||
chr19:5724308
|
C | A | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.72-500C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724308 | ||||||
chr19:5724529
|
C | T | 34 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(31): Show | 34 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(31): Show |
intron_variant | MODIFIER | c.72-279C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724529 | ||||||
chr19:5724596
|
G | A | 3 | a0006c0007t0002g0030a0006c0007t0002g0031a0008c0009t0001g0032 | 3 | HG02895.hp1 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.72-212G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 1/21 | chr19 | 5724596 | ||||||
chr19:5725127
|
G | T | 2 | a0001c0001t0001g0285a0002c0002t0001g0327 | 2 | HG01099.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.126+265G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725127 | ||||||
chr19:5725146
|
C | G | 2 | a0002c0002t0001g0283a0002c0002t0001g0284 | 2 | HG01361.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.126+284C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725146 | ||||||
chr19:5725482
|
G | A | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+620G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725482 | ||||||
chr19:5725582
|
T | C | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+720T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725582 | ||||||
chr19:5725704
|
C | T | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+842C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725704 | ||||||
chr19:5725705
|
A | C | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+843A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725705 | ||||||
chr19:5725712
|
C | T | 1 | a0004c0042t0001g0316 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.126+850C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725712 | ||||||
chr19:5725880
|
G | A | 1 | a0006c0007t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.126+1018G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725880 | ||||||
chr19:5725890
|
A | G | 1 | a0002c0002t0001g0299 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.126+1028A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725890 | ||||||
chr19:5725981
|
A | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(37): Show | 40 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.126+1119A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5725981 | ||||||
chr19:5726008
|
C | G | 4 | a0002c0002t0001g0298a0003c0004t0001g0328a0004c0003t0001g0282others(1): Show | 4 | HG02135.hp1 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1146C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726008 | ||||||
chr19:5726036
|
G | A | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.126+1174G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726036 | ||||||
chr19:5726060
|
A | AT | 6 | a0001c0001t0001g0164a0002c0019t0001g0330a0004c0003t0001g0144others(3): Show | 6 | HG00741.hp2 HG01175.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1192dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr19 | 5726060 | |||||
chr19:5726099
|
T | A | 1 | a0002c0002t0001g0184 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.127-1169T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726099 | ||||||
chr19:5726637
|
C | G | 2 | a0001c0001t0001g0102a0003c0004t0001g0040 | 2 | HG01346.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.127-631C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726637 | ||||||
chr19:5726662
|
G | A | 1 | a0002c0002t0001g0326 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.127-606G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726662 | ||||||
chr19:5726816
|
G | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(257): Show | 260 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.127-452G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726816 | ||||||
chr19:5726932
|
G | A | 87 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0255others(84): Show | 87 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.127-336G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5726932 | ||||||
chr19:5727064
|
G | A | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-204G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5727064 | ||||||
chr19:5727067
|
C | T | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.127-201C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5727067 | ||||||
chr19:5727068
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.127-200G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 2/21 | chr19 | 5727068 | ||||||
chr19:5727370
|
A | C | 1 | a0003c0004t0001g0281 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.203+26A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727370 | ||||||
chr19:5727403
|
C | CT | 121 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(118): Show | 121 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(118): Show |
intron_variant | MODIFIER | c.203+59_203+60insT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727403 | ||||||
chr19:5727757
|
G | A | 28 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(25): Show | 28 | HG01952.hp2 HG01993.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.203+413G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727757 | ||||||
chr19:5727806
|
C | T | 1 | a0001c0001t0002g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.203+462C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5727806 | ||||||
chr19:5728038
|
C | CAAA | 67 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(64): Show | 67 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.203+709_203+711dup others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | |||||
chr19:5728038
|
C | CAAAA | 9 | a0001c0001t0001g0054a0001c0001t0001g0055a0002c0002t0001g0056others(6): Show | 9 | HG00642.hp1 HG01175.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.203+708_203+711dup others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | |||||
chr19:5728038
|
CA | C | 197 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0101others(194): Show | 197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.203+711delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | |||||
chr19:5728038
|
CAA | C | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(26): Show | 29 | HG01346.hp1 HG01952.hp2 HG01993.hp2 others(26): Show |
intron_variant | MODIFIER | c.203+710_203+711del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728038 | |||||
chr19:5728085
|
C | T | 5 | a0007c0010t0001g0026a0007c0010t0001g0027a0007c0010t0001g0029others(2): Show | 5 | HG01952.hp2 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+741C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728085 | ||||||
chr19:5728125
|
C | T | 7 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0002g0311others(4): Show | 7 | HG02145.hp2 HG02886.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.203+781C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728125 | ||||||
chr19:5728218
|
C | T | 1 | a0003c0005t0001g0306 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.203+874C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728218 | ||||||
chr19:5728238
|
G | GTCCCAGC others(3): Show |
1 | a0004c0003t0003g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.203+897_203+906dup others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728238 | |||||
chr19:5728290
|
G | A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.203+946G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728290 | ||||||
chr19:5728313
|
G | A | 1 | a0003c0005t0001g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.203+969G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728313 | ||||||
chr19:5728344
|
G | A | 2 | a0002c0002t0001g0139a0023c0026t0002g0335 | 2 | HG02056.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.203+1000G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728344 | ||||||
chr19:5728356
|
C | CA | 16 | a0001c0001t0001g0164a0001c0040t0001g0331a0002c0002t0001g0186others(13): Show | 16 | HG01175.hp2 HG01346.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.203+1030dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728356 | |||||
chr19:5728356
|
CA | C | 88 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(85): Show | 88 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.203+1030delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728356 | |||||
chr19:5728364
|
A | G | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.203+1020A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728364 | ||||||
chr19:5728369
|
AAAAAAGA others(5): Show |
A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.203+1030_203+1041d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728369 | |||||
chr19:5728371
|
A | G | 4 | a0002c0002t0001g0298a0003c0004t0001g0328a0004c0003t0001g0282others(1): Show | 4 | HG02135.hp1 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+1027A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728371 | ||||||
chr19:5728653
|
G | A | 4 | a0001c0001t0001g0288a0002c0002t0001g0238a0002c0002t0001g0289others(1): Show | 4 | HG00642.hp2 HG01070.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.204-1219G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5728653 | ||||||
chr19:5728705
|
C | CT | 72 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(69): Show | 72 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.204-1156dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728705 | |||||
chr19:5728705
|
C | CTT | 10 | a0001c0001t0001g0051a0001c0001t0001g0054a0002c0002t0001g0057others(7): Show | 10 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.204-1157_204-1156d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5728705 | |||||
chr19:5729004
|
A | ATC | 8 | a0001c0001t0001g0225a0001c0001t0001g0229a0001c0001t0001g0231others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.204-852_204-851dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5729004 | |||||
chr19:5729101
|
C | CT | 6 | a0001c0001t0001g0208a0001c0001t0001g0221a0001c0016t0001g0126others(3): Show | 6 | HG00741.hp1 HG01358.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.204-760dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr19 | 5729101 | |||||
chr19:5729147
|
G | A | 2 | a0002c0002t0001g0066a0003c0004t0001g0244 | 2 | HG02071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.204-725G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729147 | ||||||
chr19:5729231
|
G | A | 1 | a0004c0003t0001g0245 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.204-641G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729231 | ||||||
chr19:5729402
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.204-470T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729402 | ||||||
chr19:5729482
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.204-390A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 3/21 | chr19 | 5729482 | ||||||
chr19:5730327
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(116): Show | 119 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.276+383A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730327 | ||||||
chr19:5730341
|
G | A | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276+397G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730341 | ||||||
chr19:5730399
|
C | T | 1 | a0012c0015t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.276+455C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730399 | ||||||
chr19:5730498
|
G | A | 1 | a0002c0002t0001g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.276+554G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730498 | ||||||
chr19:5730561
|
A | AAAATAAA others(6): Show |
1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276+624_276+625ins others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | |||||
chr19:5730561
|
A | AAAATAAA others(1): Show |
37 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(34): Show | 37 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(34): Show |
intron_variant | MODIFIER | c.276+628_276+635dup others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | |||||
chr19:5730561
|
A | AAAATAAA others(5): Show |
210 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0046others(207): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.276+624_276+635dup others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | |||||
chr19:5730561
|
A | AAAATAAA others(9): Show |
3 | a0001c0001t0001g0189a0002c0002t0001g0190a0003c0004t0001g0246 | 3 | HG00738.hp2 HG01258.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.276+620_276+635dup others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | |||||
chr19:5730561
|
A | AAAATAAA others(13): Show |
2 | a0002c0002t0001g0187a0003c0004t0001g0188 | 2 | NA18944.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.276+635_276+636ins others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5730561 | |||||
chr19:5730715
|
T | C | 1 | a0003c0004t0001g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.276+771T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730715 | ||||||
chr19:5730878
|
G | A | 1 | a0004c0003t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.276+934G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730878 | ||||||
chr19:5730953
|
A | G | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.276+1009A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730953 | ||||||
chr19:5730984
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.276+1040C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5730984 | ||||||
chr19:5731058
|
C | T | 16 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(13): Show | 16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.276+1114C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731058 | ||||||
chr19:5731079
|
G | A | 91 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0255others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.276+1135G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731079 | ||||||
chr19:5731091
|
C | CA | 11 | a0001c0001t0001g0128a0001c0001t0001g0162a0001c0001t0001g0164others(8): Show | 11 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+1164dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731091 | |||||
chr19:5731091
|
CA | C | 12 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0093others(9): Show | 12 | HG00280.hp1 HG01070.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.276+1164delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731091 | |||||
chr19:5731117
|
C | T | 1 | a0010c0011t0001g0315 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.276+1173C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731117 | ||||||
chr19:5731217
|
C | A | 2 | a0001c0001t0004g0105a0001c0001t0004g0106 | 2 | HG01109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.276+1273C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731217 | ||||||
chr19:5731330
|
AGTGTGGT others(1): Show |
A | 79 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(76): Show | 79 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.276+1406_276+1413d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731330 | |||||
chr19:5731460
|
T | A | 2 | a0003c0005t0001g0249a0004c0003t0001g0248 | 2 | NA18952.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.276+1516T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731460 | ||||||
chr19:5731519
|
A | G | 1 | a0002c0002t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.276+1575A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731519 | ||||||
chr19:5731549
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.276+1605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731549 | ||||||
chr19:5731560
|
G | GT | 102 | a0001c0001t0001g0045a0001c0001t0001g0112a0001c0001t0001g0113others(99): Show | 102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.276+1642dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTT | 55 | a0001c0001t0001g0191a0001c0001t0001g0208a0001c0001t0001g0220others(52): Show | 55 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.276+1641_276+1642d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTT | 11 | a0001c0040t0001g0331a0002c0002t0001g0289a0002c0002t0001g0326others(8): Show | 11 | HG01070.hp1 HG01346.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.276+1640_276+1642d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTT | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(12): Show | 15 | HG01993.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.276+1639_276+1642d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTT | 7 | a0001c0001t0001g0001a0006c0007t0001g0034a0007c0010t0001g0027others(4): Show | 7 | HG01952.hp2 HG02257.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.276+1638_276+1642d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTT | 8 | a0011c0008t0001g0012a0016c0013t0001g0009a0016c0013t0001g0015others(5): Show | 8 | HG02809.hp1 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.276+1637_276+1642d others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT | 22 | a0001c0001t0001g0055a0001c0001t0001g0067a0001c0001t0001g0074others(19): Show | 22 | HG00323.hp1 HG00642.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.276+1636_276+1642d others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT others(1): Show |
31 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(28): Show | 31 | HG00621.hp1 HG01071.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.276+1635_276+1642d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT others(2): Show |
6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0304others(3): Show | 6 | HG01106.hp1 HG01168.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1634_276+1642d others(11): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT others(3): Show |
7 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0135others(4): Show | 7 | HG01070.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+1633_276+1642d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT others(4): Show |
7 | a0001c0001t0001g0054a0001c0001t0001g0063a0001c0001t0001g0099others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.276+1632_276+1642d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT others(5): Show |
5 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0136others(2): Show | 5 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.276+1631_276+1642d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
G | GTTTTTTT others(6): Show |
2 | a0002c0002t0001g0092a0004c0003t0001g0319 | 2 | HG04184.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.276+1630_276+1642d others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731560
|
GTTTTTTT others(4): Show |
G | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.276+1632_276+1642d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5731560 | |||||
chr19:5731611
|
C | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(76): Show | 79 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.276+1667C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731611 | ||||||
chr19:5731616
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.276+1672C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731616 | ||||||
chr19:5731636
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(20): Show | 23 | HG01346.hp1 HG02027.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.276+1692C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731636 | ||||||
chr19:5731644
|
C | T | 2 | a0003c0004t0001g0148a0003c0004t0001g0149 | 2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.276+1700C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731644 | ||||||
chr19:5731657
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.276+1713G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731657 | ||||||
chr19:5731720
|
C | T | 1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.276+1776C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731720 | ||||||
chr19:5731731
|
G | A | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.276+1787G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731731 | ||||||
chr19:5731750
|
T | C | 1 | a0004c0003t0001g0282 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.276+1806T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5731750 | ||||||
chr19:5732274
|
G | T | 1 | a0021c0023t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.277-1582G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732274 | ||||||
chr19:5732381
|
A | T | 1 | a0004c0044t0001g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.277-1475A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732381 | ||||||
chr19:5732455
|
C | T | 1 | a0001c0016t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.277-1401C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732455 | ||||||
chr19:5732464
|
ACT | A | 79 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(76): Show | 79 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.277-1389_277-1388d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5732464 | |||||
chr19:5732493
|
C | T | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-1363C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732493 | ||||||
chr19:5732494
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.277-1362G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732494 | ||||||
chr19:5732552
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277-1304C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732552 | ||||||
chr19:5732686
|
T | G | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.277-1170T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732686 | ||||||
chr19:5732968
|
T | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(262): Show | 265 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.277-888T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732968 | ||||||
chr19:5732972
|
C | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(21): Show | 24 | HG01243.hp2 HG01346.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.277-884C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5732972 | ||||||
chr19:5732983
|
G | GT | 8 | a0001c0001t0001g0225a0001c0001t0001g0229a0001c0001t0001g0231others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-865dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5732983 | |||||
chr19:5733070
|
C | G | 16 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(13): Show | 16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.277-786C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733070 | ||||||
chr19:5733305
|
C | CTCTTTCT others(17): Show |
1 | a0001c0001t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.277-550_277-549ins others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733305 | |||||
chr19:5733305
|
C | CTCTTTCT others(25): Show |
1 | a0001c0001t0001g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.277-550_277-549ins others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733305 | |||||
chr19:5733305
|
C | CTCTTTCT others(29): Show |
2 | a0003c0004t0001g0022a0003c0004t0001g0314 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.277-550_277-549ins others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733305 | |||||
chr19:5733307
|
T | C | 4 | a0001c0001t0001g0020a0001c0001t0001g0021a0003c0004t0001g0022others(1): Show | 4 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-549T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733307 | ||||||
chr19:5733307
|
T | TCTTTCTT others(34): Show |
1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.277-549_277-548ins others(41): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733307 | ||||||
chr19:5733307
|
T | TTTCTTTC others(44): Show |
1 | a0001c0001t0002g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.277-547_277-546ins others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(13): Show |
3 | a0001c0001t0001g0001a0010c0011t0001g0002a0010c0011t0001g0003 | 3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.277-540_277-521dup others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(17): Show |
2 | a0011c0008t0001g0010a0011c0008t0001g0014 | 2 | HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.277-544_277-521dup others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(21): Show |
1 | a0016c0013t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.277-548_277-521dup others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(25): Show |
3 | a0011c0008t0001g0012a0016c0013t0001g0015a0017c0014t0002g0011 | 3 | HG02809.hp1 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.277-521_277-520ins others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(29): Show |
1 | a0017c0014t0002g0013 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.277-521_277-520ins others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(37): Show |
1 | a0001c0001t0001g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.277-521_277-520ins others(44): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733307
|
T | TTTTCTTT others(41): Show |
1 | a0001c0034t0001g0023 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.277-521_277-520ins others(48): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733307 | |||||
chr19:5733326
|
T | C | 6 | a0006c0007t0001g0017a0006c0007t0001g0034a0006c0007t0002g0030others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-530T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733326 | ||||||
chr19:5733332
|
T | C | 81 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(78): Show | 81 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.277-524T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733332 | ||||||
chr19:5733335
|
C | CTTTCCTT others(1): Show |
3 | a0001c0045t0001g0151a0018c0020t0001g0018a0027c0036t0001g0297 | 3 | HG01243.hp2 HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.277-521_277-520ins others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733335 | ||||||
chr19:5733335
|
C | CTTTCTTT others(5): Show |
1 | a0002c0002t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.277-521_277-520ins others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733335 | ||||||
chr19:5733335
|
C | T | 81 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(78): Show | 81 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.277-521C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733335 | ||||||
chr19:5733347
|
T | C | 89 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(86): Show | 89 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.277-509T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733347 | ||||||
chr19:5733347
|
T | TCTTC | 156 | a0001c0001t0001g0041a0001c0001t0001g0045a0001c0001t0001g0046others(153): Show | 156 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.277-499_277-496dup others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733347 | |||||
chr19:5733347
|
TCTTCCTT others(9): Show |
T | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-491_277-476del others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733347 | |||||
chr19:5733349
|
TTCCTTCC others(5): Show |
T | 1 | a0003c0005t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.277-495_277-484del others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733349 | |||||
chr19:5733387
|
G | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(264): Show | 267 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.277-469G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | chr19 | 5733387 | ||||||
chr19:5733407
|
CTCCT | C | 39 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0191others(36): Show | 39 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.277-428_277-425del others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733407 | |||||
chr19:5733432
|
CCTTT | C | 17 | a0002c0002t0001g0250a0006c0007t0001g0017a0006c0007t0001g0025others(14): Show | 17 | HG00323.hp2 HG00741.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.277-409_277-406del others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr19 | 5733432 | |||||
chr19:5734057
|
T | C | 1 | a0013c0031t0001g0036 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.391+87T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734057 | ||||||
chr19:5734228
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(76): Show | 79 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.391+258T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734228 | ||||||
chr19:5734579
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.391+609G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734579 | ||||||
chr19:5734638
|
C | CA | 51 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(48): Show | 51 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.391+681dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5734638 | |||||
chr19:5734692
|
C | T | 1 | a0003c0037t0001g0203 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.391+722C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734692 | ||||||
chr19:5734718
|
C | T | 20 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(17): Show | 20 | HG01346.hp1 HG02027.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.391+748C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734718 | ||||||
chr19:5734744
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.391+774G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734744 | ||||||
chr19:5734800
|
T | TA | 10 | a0001c0001t0001g0060a0001c0001t0001g0102a0001c0001t0001g0227others(7): Show | 10 | HG01346.hp2 HG01433.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.391+845dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5734800 | |||||
chr19:5734800
|
TA | T | 6 | a0001c0001t0001g0086a0004c0003t0003g0075a0006c0007t0001g0034others(3): Show | 6 | HG02572.hp1 HG02895.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+845delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5734800 | |||||
chr19:5734805
|
A | T | 5 | a0001c0001t0001g0268a0002c0002t0001g0279a0003c0004t0001g0290others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+835A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734805 | ||||||
chr19:5734815
|
A | G | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.391+845A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734815 | ||||||
chr19:5734944
|
C | T | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.391+974C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5734944 | ||||||
chr19:5735287
|
G | A | 1 | a0016c0013t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.391+1317G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735287 | ||||||
chr19:5735352
|
C | T | 2 | a0002c0002t0001g0181a0002c0002t0001g0266 | 2 | NA18995.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.391+1382C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735352 | ||||||
chr19:5735373
|
C | T | 4 | a0002c0002t0001g0043a0002c0002t0001g0118a0002c0002t0001g0119others(1): Show | 4 | HG01074.hp1 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+1403C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735373 | ||||||
chr19:5735421
|
C | A | 1 | a0002c0002t0001g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391+1451C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735421 | ||||||
chr19:5735477
|
A | AT | 11 | a0001c0001t0001g0090a0001c0001t0001g0135a0001c0001t0001g0162others(8): Show | 11 | HG01070.hp2 HG01192.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+1523dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735477 | |||||
chr19:5735477
|
AT | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(91): Show | 94 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+1523delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735477 | |||||
chr19:5735505
|
G | C | 50 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(47): Show | 50 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.391+1535G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735505 | ||||||
chr19:5735550
|
G | A | 39 | a0001c0001t0001g0177a0001c0001t0001g0189a0001c0001t0001g0191others(36): Show | 39 | HG00280.hp2 HG00609.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.391+1580G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735550 | ||||||
chr19:5735606
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(116): Show | 119 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.392-1532A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735606 | ||||||
chr19:5735607
|
G | GGACTACA others(9): Show |
1 | a0004c0003t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.392-1530_392-1515d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735607 | |||||
chr19:5735720
|
A | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(262): Show | 265 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.392-1418A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735720 | ||||||
chr19:5735768
|
C | T | 1 | a0004c0003t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.392-1370C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735768 | ||||||
chr19:5735774
|
A | AT | 13 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0111others(10): Show | 13 | HG00735.hp2 HG01433.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.392-1344dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735774 | |||||
chr19:5735774
|
AT | A | 192 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(189): Show | 192 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.392-1344delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735774 | |||||
chr19:5735774
|
ATT | A | 8 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0101others(5): Show | 8 | HG01069.hp1 HG01168.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-1345_392-1344d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr19 | 5735774 | |||||
chr19:5735844
|
G | A | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.392-1294G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735844 | ||||||
chr19:5735873
|
T | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(36): Show | 39 | HG00741.hp2 HG01346.hp1 HG01952.hp2 others(36): Show |
intron_variant | MODIFIER | c.392-1265T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735873 | ||||||
chr19:5735874
|
G | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0034t0001g0023others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-1264G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735874 | ||||||
chr19:5735940
|
C | T | 2 | a0010c0011t0001g0002a0010c0011t0001g0003 | 2 | HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.392-1198C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5735940 | ||||||
chr19:5736029
|
A | G | 82 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(79): Show | 82 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.392-1109A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736029 | ||||||
chr19:5736052
|
C | T | 2 | a0002c0002t0001g0049a0002c0002t0001g0050 | 2 | HG03704.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.392-1086C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736052 | ||||||
chr19:5736063
|
C | T | 1 | a0003c0005t0001g0214 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.392-1075C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736063 | ||||||
chr19:5736139
|
C | T | 5 | a0007c0010t0001g0026a0007c0010t0001g0027a0007c0010t0001g0029others(2): Show | 5 | HG01952.hp2 HG01993.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-999C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736139 | ||||||
chr19:5736318
|
A | T | 1 | a0002c0002t0001g0068 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.392-820A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736318 | ||||||
chr19:5736361
|
C | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(76): Show | 79 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.392-777C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736361 | ||||||
chr19:5736362
|
G | A | 2 | a0003c0005t0001g0239a0003c0005t0001g0253 | 2 | HG02040.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.392-776G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736362 | ||||||
chr19:5736444
|
C | T | 1 | a0011c0008t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.392-694C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736444 | ||||||
chr19:5736533
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.392-605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736533 | ||||||
chr19:5736538
|
G | A | 1 | a0002c0019t0001g0332 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.392-600G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736538 | ||||||
chr19:5736697
|
A | G | 2 | a0002c0002t0001g0277a0028c0029t0001g0264 | 2 | NA18969.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.392-441A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736697 | ||||||
chr19:5736720
|
G | A | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-418G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736720 | ||||||
chr19:5736828
|
T | G | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.392-310T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736828 | ||||||
chr19:5736857
|
A | T | 1 | a0002c0002t0001g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.392-281A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736857 | ||||||
chr19:5736908
|
T | C | 16 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(13): Show | 16 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.392-230T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736908 | ||||||
chr19:5736933
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-205T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736933 | ||||||
chr19:5736980
|
C | A | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.392-158C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5736980 | ||||||
chr19:5737124
|
T | C | 1 | a0011c0008t0001g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.392-14T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 5/21 | chr19 | 5737124 | ||||||
chr19:5737492
|
A | G | 1 | a0004c0003t0001g0035 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.459+287A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737492 | ||||||
chr19:5737524
|
T | C | 9 | a0002c0002t0001g0069a0002c0002t0001g0085a0004c0003t0001g0079others(6): Show | 9 | HG01952.hp2 HG01993.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+319T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737524 | ||||||
chr19:5737536
|
AAGACTCT others(3): Show |
A | 1 | a0002c0002t0003g0138 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.459+333_459+342del others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737536 | |||||
chr19:5737540
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.459+335C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737540 | ||||||
chr19:5737546
|
CA | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(226): Show | 229 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.459+362delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737546 | |||||
chr19:5737557
|
A | G | 1 | a0003c0004t0001g0022 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.459+352A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737557 | ||||||
chr19:5737836
|
G | A | 13 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(10): Show | 13 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+631G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737836 | ||||||
chr19:5737850
|
C | CA | 22 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(19): Show | 22 | HG00140.hp1 HG00741.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+659dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737850 | |||||
chr19:5737850
|
CA | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0084others(6): Show | 9 | HG01070.hp2 HG01074.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+659delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5737850 | |||||
chr19:5737871
|
A | C | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.459+666A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737871 | ||||||
chr19:5737982
|
C | T | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(12): Show | 15 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.459+777C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5737982 | ||||||
chr19:5738070
|
C | A | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.459+865C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738070 | ||||||
chr19:5738071
|
C | A | 1 | a0001c0001t0001g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.459+866C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738071 | ||||||
chr19:5738110
|
C | T | 2 | a0002c0002t0001g0263a0004c0003t0001g0293 | 2 | HG00408.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.459+905C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738110 | ||||||
chr19:5738266
|
G | C | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-1060G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738266 | ||||||
chr19:5738267
|
C | G | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-1059C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738267 | ||||||
chr19:5738352
|
C | CA | 6 | a0001c0001t0001g0113a0002c0002t0001g0238a0002c0002t0001g0270others(3): Show | 6 | HG00642.hp2 HG01070.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-956dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5738352 | |||||
chr19:5738352
|
CA | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(83): Show | 86 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.460-956delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5738352 | |||||
chr19:5738352
|
CAA | C | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(27): Show | 30 | HG00741.hp2 HG01243.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-957_460-956del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5738352 | |||||
chr19:5738367
|
A | G | 1 | a0002c0002t0001g0305 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.460-959A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738367 | ||||||
chr19:5738462
|
G | A | 1 | a0001c0045t0001g0151 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.460-864G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738462 | ||||||
chr19:5738474
|
G | C | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.460-852G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738474 | ||||||
chr19:5738497
|
A | C | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-829A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738497 | ||||||
chr19:5738590
|
C | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.460-736C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738590 | ||||||
chr19:5738623
|
A | C | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-703A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738623 | ||||||
chr19:5738624
|
C | A | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-702C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738624 | ||||||
chr19:5738669
|
C | T | 1 | a0005c0006t0001g0219 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.460-657C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738669 | ||||||
chr19:5738740
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.460-586C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738740 | ||||||
chr19:5738767
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(101): Show | 104 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(101): Show |
intron_variant | MODIFIER | c.460-559G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738767 | ||||||
chr19:5738775
|
C | T | 3 | a0001c0001t0001g0001a0010c0011t0001g0002a0010c0011t0001g0003 | 3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.460-551C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738775 | ||||||
chr19:5738777
|
T | A | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-549T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738777 | ||||||
chr19:5738783
|
C | A | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-543C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738783 | ||||||
chr19:5738970
|
C | G | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-356C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738970 | ||||||
chr19:5738971
|
G | C | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.460-355G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738971 | ||||||
chr19:5738991
|
G | T | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.460-335G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5738991 | ||||||
chr19:5739101
|
G | A | 92 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0255others(89): Show | 92 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.460-225G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5739101 | ||||||
chr19:5739106
|
C | CTGCCTGC others(13): Show |
1 | a0001c0001t0001g0074 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.460-219_460-200dup others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5739106 | |||||
chr19:5739157
|
A | G | 1 | a0003c0004t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.460-169A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5739157 | ||||||
chr19:5739306
|
T | C | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.460-20T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | chr19 | 5739306 | ||||||
chr19:5739309
|
C | CT | 15 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(12): Show | 15 | HG00621.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.460-5dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr19 | 5739309 | |||||
chr19:5739630
|
G | C | 3 | a0003c0005t0001g0185a0003c0005t0001g0249a0004c0003t0001g0248 | 3 | NA18952.hp2 NA19007.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.573+191G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739630 | ||||||
chr19:5739683
|
AT | A | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+245delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739683 | ||||||
chr19:5739842
|
A | AAAAAAAA others(7): Show |
6 | a0001c0001t0001g0304a0001c0045t0001g0151a0004c0003t0001g0302others(3): Show | 6 | HG00741.hp2 HG01192.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+414_573+415ins others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5739842 | |||||
chr19:5739842
|
A | AAAAAAAA others(6): Show |
110 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(107): Show | 110 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.573+414_573+415ins others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5739842 | |||||
chr19:5739842
|
A | AAAAAAAA others(5): Show |
4 | a0001c0001t0001g0086a0001c0001t0001g0090a0002c0002t0001g0049others(1): Show | 4 | HG01433.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+404_573+415dup others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5739842 | |||||
chr19:5739918
|
TTAGAGAC others(3): Show |
T | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.573+480_573+489del others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739918 | ||||||
chr19:5739930
|
AG | A | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0034t0001g0023others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+492delG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739930 | ||||||
chr19:5739955
|
C | T | 1 | a0002c0002t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.573+516C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5739955 | ||||||
chr19:5740019
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.573+580C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740019 | ||||||
chr19:5740027
|
A | T | 2 | a0001c0001t0002g0296a0027c0036t0001g0297 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.573+588A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740027 | ||||||
chr19:5740098
|
A | G | 1 | a0003c0004t0001g0178 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.573+659A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740098 | ||||||
chr19:5740482
|
G | A | 2 | a0033c0047t0001g0004a0034c0046t0001g0005 | 2 | HG00741.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.573+1043G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740482 | ||||||
chr19:5740575
|
G | A | 1 | a0018c0020t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573+1136G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740575 | ||||||
chr19:5740582
|
C | T | 1 | a0018c0020t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573+1143C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740582 | ||||||
chr19:5740617
|
A | C | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+1178A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740617 | ||||||
chr19:5740680
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.573+1241C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740680 | ||||||
chr19:5740762
|
C | CA | 35 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0099others(32): Show | 35 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.573+1347dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5740762 | |||||
chr19:5740762
|
CA | C | 24 | a0001c0001t0001g0077a0001c0001t0001g0229a0001c0040t0001g0331others(21): Show | 24 | HG00323.hp1 HG00408.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.573+1347delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5740762 | |||||
chr19:5740793
|
G | A | 1 | a0029c0039t0001g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.573+1354G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740793 | ||||||
chr19:5740902
|
C | A | 1 | a0006c0007t0001g0017 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573+1463C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740902 | ||||||
chr19:5740942
|
G | A | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+1503G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5740942 | ||||||
chr19:5741042
|
GCCATTGC others(27): Show |
G | 106 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(103): Show | 106 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.573+1606_573+1639d others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741042 | |||||
chr19:5741118
|
C | A | 1 | a0004c0003t0001g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.573+1679C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741118 | ||||||
chr19:5741153
|
C | CA | 15 | a0006c0007t0001g0025a0006c0007t0001g0034a0006c0007t0002g0030others(12): Show | 15 | HG00741.hp2 HG01952.hp2 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.573+1715dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741153 | |||||
chr19:5741273
|
A | G | 4 | a0002c0002t0001g0263a0004c0003t0001g0035a0004c0003t0001g0275others(1): Show | 4 | HG00408.hp2 NA18986.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.573+1834A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741273 | ||||||
chr19:5741630
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.573+2191A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741630 | ||||||
chr19:5741740
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+2301C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741740 | ||||||
chr19:5741741
|
G | C | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+2302G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741741 | ||||||
chr19:5741785
|
C | CCGGGGGG others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.573+2346_573+2347i others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741785 | ||||||
chr19:5741785
|
C | CG | 69 | a0001c0001t0001g0112a0001c0001t0001g0157a0001c0001t0001g0164others(66): Show | 69 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.573+2359dupG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGG | 42 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0121others(39): Show | 42 | HG00140.hp1 HG00408.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.573+2358_573+2359d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGG | 39 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0143others(36): Show | 39 | HG00609.hp1 HG00738.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.573+2357_573+2359d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(4): Show |
5 | a0001c0001t0001g0054a0001c0001t0001g0090a0002c0002t0001g0050others(2): Show | 5 | HG01433.hp2 HG02293.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+2349_573+2359d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(5): Show |
9 | a0001c0001t0001g0063a0001c0001t0001g0136a0002c0002t0001g0068others(6): Show | 9 | HG00323.hp1 HG00621.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+2348_573+2359d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(6): Show |
14 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0001g0093others(11): Show | 14 | HG00741.hp2 HG01928.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.573+2347_573+2359d others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(7): Show |
6 | a0001c0001t0001g0078a0001c0001t0001g0128a0001c0001t0001g0134others(3): Show | 6 | HG00642.hp1 HG01071.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(8): Show |
11 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0060others(8): Show | 11 | HG01069.hp2 HG01258.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(9): Show |
3 | a0001c0001t0001g0039a0003c0004t0001g0061a0004c0003t0003g0075 | 3 | HG02055.hp1 NA19074.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.573+2359_573+2360i others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(10): Show |
6 | a0001c0001t0002g0059a0002c0002t0001g0085a0002c0002t0001g0097others(3): Show | 6 | HG02055.hp2 HG02486.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(11): Show |
8 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0133others(5): Show | 8 | HG01071.hp1 HG01346.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+2359_573+2360i others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(12): Show |
1 | a0001c0001t0001g0089 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(13): Show |
3 | a0001c0001t0001g0084a0002c0002t0001g0127a0013c0031t0001g0036 | 3 | HG02074.hp2 HG03492.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.573+2359_573+2360i others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(93): Show |
1 | a0001c0001t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.573+2359_573+2360i others(102): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | CGGGGGGG others(8): Show |
1 | a0033c0047t0001g0004 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741785 | |||||
chr19:5741785
|
C | T | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.573+2346C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741785 | ||||||
chr19:5741786
|
G | A | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+2347G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741786 | ||||||
chr19:5741788
|
G | A | 2 | a0002c0002t0001g0278a0002c0002t0001g0286 | 2 | HG01261.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.573+2349G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741788 | ||||||
chr19:5741789
|
GGGGGGGG others(3): Show |
G | 2 | a0002c0002t0001g0073a0002c0002t0001g0182 | 2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.573+2353_573+2362d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741789 | |||||
chr19:5741792
|
G | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.573+2353G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741792 | ||||||
chr19:5741793
|
G | GGGGGGGG others(15): Show |
1 | a0019c0022t0001g0028 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741793 | |||||
chr19:5741793
|
G | GGGGGGGG others(14): Show |
1 | a0020c0021t0001g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.573+2359_573+2360i others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741793 | |||||
chr19:5741794
|
G | GC | 5 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0002g0024others(2): Show | 5 | HG02109.hp1 HG02486.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+2355_573+2356i others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741794 | ||||||
chr19:5741794
|
G | GGGGTGGG others(14): Show |
2 | a0006c0007t0002g0030a0006c0007t0002g0031 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.573+2358_573+2359i others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741794 | |||||
chr19:5741794
|
G | GGGTGGGG others(13): Show |
1 | a0008c0009t0001g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.573+2357_573+2358i others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741794 | |||||
chr19:5741796
|
GGGT | G | 61 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(58): Show | 61 | HG00323.hp1 HG00621.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+2362_573+2364d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741796 | |||||
chr19:5741799
|
T | A | 1 | a0002c0002t0003g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.573+2360T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741799 | ||||||
chr19:5741799
|
T | C | 160 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(157): Show | 160 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.573+2360T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741799 | ||||||
chr19:5741799
|
T | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0045a0001c0001t0001g0046others(31): Show | 34 | HG00280.hp1 HG00735.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.573+2360T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741799 | ||||||
chr19:5741799
|
T | TGGGGGGG others(17): Show |
1 | a0006c0007t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573+2362_573+2363i others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741799 | |||||
chr19:5741800
|
G | GGGGGGGG others(5): Show |
2 | a0001c0001t0005g0142a0012c0015t0001g0125 | 2 | HG01433.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.573+2362_573+2363i others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741800 | |||||
chr19:5741800
|
G | GGGGGGGG others(4): Show |
2 | a0001c0001t0001g0045a0012c0015t0001g0122 | 2 | HG00280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.573+2362_573+2363i others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741800 | |||||
chr19:5741800
|
G | GGGGGGGG others(3): Show |
2 | a0001c0001t0001g0046a0003c0004t0001g0123 | 2 | HG02886.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.573+2362_573+2363i others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741800 | |||||
chr19:5741800
|
G | T | 1 | a0001c0001t0001g0124 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.573+2361G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741800 | ||||||
chr19:5741801
|
G | GGGGGGGG others(4): Show |
1 | a0001c0001t0001g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.573+2362_573+2363i others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741801 | ||||||
chr19:5741802
|
T | G | 14 | a0004c0042t0001g0316a0006c0007t0001g0017a0006c0007t0001g0025others(11): Show | 14 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.573+2363T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741802 | ||||||
chr19:5741802
|
T | TGGGGGGT others(8): Show |
1 | a0018c0020t0001g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.573+2364_573+2365i others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5741802 | |||||
chr19:5741925
|
T | G | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+2486T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741925 | ||||||
chr19:5741977
|
A | G | 3 | a0001c0001t0001g0001a0010c0011t0001g0002a0010c0011t0001g0003 | 3 | HG02257.hp1 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.574-2450A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5741977 | ||||||
chr19:5742010
|
T | A | 2 | a0004c0003t0003g0053a0004c0003t0003g0075 | 2 | NA18974.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.574-2417T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742010 | ||||||
chr19:5742058
|
C | CA | 5 | a0001c0001t0001g0137a0001c0001t0001g0164a0001c0001t0001g0208others(2): Show | 5 | HG00735.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-2361dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742058 | |||||
chr19:5742096
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.574-2331T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742096 | ||||||
chr19:5742127
|
TGCGTGTG others(3): Show |
T | 1 | a0002c0002t0001g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.574-2291_574-2282d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742127 | |||||
chr19:5742129
|
C | T | 1 | a0003c0004t0001g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.574-2298C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742129 | ||||||
chr19:5742150
|
GTGTGAAC others(23): Show |
G | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-2262_574-2233d others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742150 | |||||
chr19:5742157
|
CGT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(89): Show | 92 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.574-2262_574-2261d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742157 | |||||
chr19:5742165
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.574-2262T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742165 | ||||||
chr19:5742167
|
CGT | C | 46 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(43): Show | 46 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.574-2253_574-2252d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742167 | |||||
chr19:5742168
|
G | T | 1 | a0001c0001t0001g0304 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.574-2259G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742168 | ||||||
chr19:5742169
|
T | C | 3 | a0006c0007t0002g0030a0006c0007t0002g0031a0008c0009t0001g0032 | 3 | HG02895.hp1 HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.574-2258T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742169 | ||||||
chr19:5742208
|
GCATGTGT others(3): Show |
G | 107 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(104): Show | 107 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.574-2209_574-2200d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742208 | |||||
chr19:5742218
|
A | G | 1 | a0002c0002t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2209A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742218 | ||||||
chr19:5742220
|
A | G | 1 | a0002c0002t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2207A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742220 | ||||||
chr19:5742228
|
G | A | 1 | a0002c0002t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2199G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742228 | ||||||
chr19:5742232
|
G | A | 1 | a0002c0002t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2195G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742232 | ||||||
chr19:5742241
|
T | A | 1 | a0002c0002t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-2186T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742241 | ||||||
chr19:5742241
|
T | C | 13 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(10): Show | 13 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-2186T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742241 | ||||||
chr19:5742287
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-2140T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742287 | ||||||
chr19:5742289
|
C | CGT | 111 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.574-2133_574-2132d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742289 | |||||
chr19:5742289
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.574-2138C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742289 | ||||||
chr19:5742306
|
ATG | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(92): Show | 95 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.574-2112_574-2111d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742306 | |||||
chr19:5742306
|
ATGTG | A | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-2114_574-2111d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742306 | |||||
chr19:5742315
|
T | G | 91 | a0001c0001t0001g0170a0001c0001t0001g0175a0001c0001t0001g0255others(88): Show | 91 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.574-2112T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742315 | ||||||
chr19:5742323
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.574-2104C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742323 | ||||||
chr19:5742330
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0221 | 2 | HG00741.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.574-2097A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742330 | ||||||
chr19:5742339
|
CAT | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(90): Show | 93 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.574-2087_574-2086d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742339 | ||||||
chr19:5742340
|
A | G | 34 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(31): Show | 34 | HG00741.hp2 HG01243.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.574-2087A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742340 | ||||||
chr19:5742395
|
G | A | 1 | a0002c0002t0001g0326 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.574-2032G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742395 | ||||||
chr19:5742419
|
C | T | 2 | a0001c0001t0002g0296a0027c0036t0001g0297 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.574-2008C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742419 | ||||||
chr19:5742548
|
G | A | 47 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.574-1879G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742548 | ||||||
chr19:5742568
|
G | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(88): Show | 91 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.574-1859G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742568 | ||||||
chr19:5742587
|
G | C | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.574-1840G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742587 | ||||||
chr19:5742588
|
C | G | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.574-1839C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742588 | ||||||
chr19:5742601
|
G | A | 14 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0033others(11): Show | 14 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.574-1826G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742601 | ||||||
chr19:5742636
|
G | A | 88 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(85): Show | 88 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.574-1791G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742636 | ||||||
chr19:5742743
|
C | T | 1 | a0004c0003t0001g0293 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.574-1684C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742743 | ||||||
chr19:5742796
|
GA | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0304a0001c0001t0002g0059 | 3 | HG01192.hp2 HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.574-1626delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5742796 | |||||
chr19:5742797
|
A | G | 1 | a0003c0004t0003g0083 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.574-1630A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742797 | ||||||
chr19:5742807
|
G | T | 2 | a0009c0012t0001g0153a0009c0012t0001g0156 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.574-1620G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742807 | ||||||
chr19:5742943
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.574-1484C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742943 | ||||||
chr19:5742998
|
G | T | 93 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(90): Show | 93 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.574-1429G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5742998 | ||||||
chr19:5743000
|
G | T | 1 | a0002c0002t0001g0127 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.574-1427G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743000 | ||||||
chr19:5743085
|
C | T | 1 | a0004c0003t0001g0302 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.574-1342C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743085 | ||||||
chr19:5743183
|
A | G | 1 | a0003c0004t0001g0303 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.574-1244A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743183 | ||||||
chr19:5743234
|
C | T | 1 | a0004c0003t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.574-1193C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743234 | ||||||
chr19:5743317
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.574-1110G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743317 | ||||||
chr19:5743435
|
T | TA | 4 | a0001c0001t0001g0045a0001c0001t0002g0059a0001c0001t0005g0142others(1): Show | 4 | HG00280.hp1 HG01433.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-985dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743435 | |||||
chr19:5743445
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(266): Show | 269 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.574-982G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743445 | ||||||
chr19:5743450
|
T | C | 17 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(14): Show | 17 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.574-977T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743450 | ||||||
chr19:5743548
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.574-879G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743548 | ||||||
chr19:5743606
|
G | A | 2 | a0001c0001t0001g0060a0004c0003t0001g0087 | 2 | HG02647.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.574-821G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743606 | ||||||
chr19:5743606
|
G | GAAAAAA | 21 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0063others(18): Show | 21 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.574-819_574-814dup others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743606 | |||||
chr19:5743606
|
G | GAAAAAAA | 224 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(221): Show | 224 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.574-820_574-814dup others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743606 | |||||
chr19:5743606
|
G | GAAAAAAA others(1): Show |
19 | a0001c0001t0001g0001a0004c0003t0003g0071a0006c0007t0001g0025others(16): Show | 19 | HG00741.hp2 HG02257.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.574-814_574-813ins others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743606 | |||||
chr19:5743614
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.574-813G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743614 | ||||||
chr19:5743648
|
G | GTC | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(119): Show | 122 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.574-763_574-762dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743648 | |||||
chr19:5743654
|
C | T | 6 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(3): Show | 6 | HG01346.hp1 HG02027.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-773C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743654 | ||||||
chr19:5743658
|
C | T | 2 | a0001c0001t0002g0226a0003c0043t0001g0233 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.574-769C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743658 | ||||||
chr19:5743667
|
CCTCTCTC others(19): Show |
C | 2 | a0001c0001t0002g0147a0022c0025t0001g0146 | 2 | HG00642.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.574-745_574-720del others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743667 | |||||
chr19:5743677
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(89): Show | 92 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.574-750T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743677 | ||||||
chr19:5743683
|
C | CCTCT | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-723_574-720dup others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743683 | |||||
chr19:5743683
|
CCTCTCTC others(1): Show |
C | 90 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(87): Show | 90 | HG00323.hp1 HG00621.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.574-727_574-720del others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743683 | |||||
chr19:5743694
|
CTCTCTCT others(7): Show |
C | 3 | a0001c0001t0001g0045a0001c0001t0001g0128a0001c0001t0005g0142 | 3 | HG00280.hp1 HG01433.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.574-727_574-714del others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743694 | |||||
chr19:5743702
|
C | CTCTCTCT others(3): Show |
1 | a0006c0007t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.574-720_574-719ins others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743702 | |||||
chr19:5743702
|
C | CTCTCTG | 11 | a0006c0007t0001g0017a0008c0009t0001g0008a0008c0009t0001g0016others(8): Show | 11 | HG00741.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-700_574-695dup others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743702 | |||||
chr19:5743740
|
TG | T | 141 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(138): Show | 141 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.574-684delG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5743740 | |||||
chr19:5743797
|
C | T | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(94): Show | 97 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.574-630C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743797 | ||||||
chr19:5743813
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(89): Show | 92 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.574-614A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743813 | ||||||
chr19:5743863
|
C | T | 1 | a0002c0002t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.574-564C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5743863 | ||||||
chr19:5744073
|
G | A | 1 | a0002c0002t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.574-354G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744073 | ||||||
chr19:5744140
|
C | T | 1 | a0002c0002t0001g0197 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.574-287C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744140 | ||||||
chr19:5744171
|
G | A | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574-256G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744171 | ||||||
chr19:5744227
|
G | A | 1 | a0005c0006t0001g0206 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-200G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | chr19 | 5744227 | ||||||
chr19:5744347
|
TTAGA | T | 3 | a0003c0004t0001g0148a0003c0004t0001g0149a0003c0004t0001g0150 | 3 | HG02109.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.574-77_574-74delGA others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr19 | 5744347 | |||||
chr19:5744579
|
G | A | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.657+69G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744579 | ||||||
chr19:5744748
|
G | A | 5 | a0001c0040t0001g0331a0002c0019t0001g0330a0002c0019t0001g0332others(2): Show | 5 | HG01346.hp1 HG02027.hp1 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.657+238G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744748 | ||||||
chr19:5744815
|
G | A | 1 | a0002c0002t0001g0200 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.657+305G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744815 | ||||||
chr19:5744865
|
G | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(155): Show | 158 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.657+355G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744865 | ||||||
chr19:5744889
|
C | T | 1 | a0006c0007t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.657+379C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744889 | ||||||
chr19:5744903
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(110): Show | 113 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.657+393G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5744903 | ||||||
chr19:5745036
|
G | A | 2 | a0017c0014t0002g0011a0017c0014t0002g0013 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.657+526G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745036 | ||||||
chr19:5745056
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.657+546C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745056 | ||||||
chr19:5745201
|
G | T | 155 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0041others(152): Show | 155 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.657+691G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745201 | ||||||
chr19:5745242
|
C | T | 1 | a0004c0003t0001g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.658-671C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745242 | ||||||
chr19:5745247
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0033others(93): Show | 96 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.658-666G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745247 | ||||||
chr19:5745255
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.658-658G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745255 | ||||||
chr19:5745308
|
C | T | 9 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0134others(6): Show | 9 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-605C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745308 | ||||||
chr19:5745337
|
G | A | 2 | a0005c0006t0001g0207a0005c0006t0001g0212 | 2 | HG01934.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.658-576G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745337 | ||||||
chr19:5745493
|
C | T | 2 | a0001c0001t0001g0318a0030c0038t0002g0317 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.658-420C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745493 | ||||||
chr19:5745621
|
AAAAATAA others(3): Show |
A | 2 | a0001c0001t0001g0033a0001c0001t0002g0024 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.658-273_658-264del others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr19 | 5745621 | |||||
chr19:5745653
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0033others(98): Show | 101 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.658-260T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745653 | ||||||
chr19:5745683
|
G | A | 17 | a0006c0007t0001g0017a0006c0007t0001g0025a0006c0007t0001g0034others(14): Show | 17 | HG00741.hp2 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.658-230G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745683 | ||||||
chr19:5745753
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0033others(98): Show | 101 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.658-160G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745753 | ||||||
chr19:5745774
|
AG | A | 10 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0232others(7): Show | 10 | HG02572.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.658-138delG | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745774 | ||||||
chr19:5745814
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 4 | HG02258.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-99C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745814 | ||||||
chr19:5745821
|
C | T | 1 | a0031c0028t0001g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.658-92C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 8/21 | chr19 | 5745821 | ||||||
chr19:5746110
|
C | CA | 136 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(133): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.808+48dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746110 | |||||
chr19:5746120
|
G | A | 3 | a0001c0001t0001g0143a0001c0001t0004g0105a0001c0001t0004g0106 | 3 | HG01109.hp2 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.808+57G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746120 | ||||||
chr19:5746436
|
C | CT | 103 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0033others(100): Show | 103 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.808+383dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746436 | |||||
chr19:5746516
|
CCTCCCGG others(12): Show |
C | 1 | a0002c0002t0001g0181 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.808+457_808+475del others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746516 | |||||
chr19:5746551
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.808+488C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746551 | ||||||
chr19:5746589
|
C | T | 1 | a0002c0002t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.808+526C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746589 | ||||||
chr19:5746779
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.808+716T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746779 | ||||||
chr19:5746810
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.808+747T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746810 | ||||||
chr19:5746811
|
C | CT | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(261): Show | 264 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.808+758dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5746811 | |||||
chr19:5746811
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.808+748C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746811 | ||||||
chr19:5746848
|
C | T | 136 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(133): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.808+785C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746848 | ||||||
chr19:5746849
|
G | A | 1 | a0012c0015t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.808+786G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746849 | ||||||
chr19:5746871
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.808+808T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5746871 | ||||||
chr19:5747169
|
C | CT | 29 | a0001c0001t0001g0121a0001c0001t0001g0195a0001c0001t0001g0285others(26): Show | 29 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.809-970dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747169 | |||||
chr19:5747169
|
CT | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(94): Show | 97 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.809-970delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747169 | |||||
chr19:5747214
|
C | T | 1 | a0002c0002t0001g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.809-946C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747214 | ||||||
chr19:5747321
|
G | A | 1 | a0002c0019t0001g0332 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.809-839G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747321 | ||||||
chr19:5747543
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.809-617C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747543 | ||||||
chr19:5747610
|
CT | C | 14 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0165others(11): Show | 14 | HG00438.hp2 HG00609.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.809-530delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747610 | |||||
chr19:5747610
|
CTT | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(250): Show | 253 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.809-531_809-530del others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr19 | 5747610 | |||||
chr19:5747651
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.809-509C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747651 | ||||||
chr19:5747814
|
G | T | 140 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(137): Show | 140 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.809-346G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747814 | ||||||
chr19:5747819
|
C | T | 1 | a0004c0003t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.809-341C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747819 | ||||||
chr19:5747820
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.809-340C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747820 | ||||||
chr19:5747901
|
C | T | 1 | a0002c0002t0001g0201 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.809-259C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747901 | ||||||
chr19:5747960
|
C | T | 1 | a0003c0004t0001g0322 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.809-200C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5747960 | ||||||
chr19:5748037
|
C | T | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.809-123C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5748037 | ||||||
chr19:5748115
|
C | G | 10 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0062others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.809-45C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 9/21 | chr19 | 5748115 | ||||||
chr19:5748373
|
G | C | 1 | a0004c0003t0001g0319 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.904+118G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748373 | ||||||
chr19:5748397
|
G | A | 6 | a0011c0008t0001g0012a0011c0008t0001g0014a0016c0013t0001g0009others(3): Show | 6 | HG02809.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.904+142G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748397 | ||||||
chr19:5748429
|
G | A | 136 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(133): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.904+174G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748429 | ||||||
chr19:5748612
|
C | G | 1 | a0004c0003t0001g0218 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.904+357C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5748612 | ||||||
chr19:5748623
|
C | CA | 97 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0041others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.904+387dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748623 | |||||
chr19:5748623
|
C | CAA | 8 | a0001c0001t0001g0055a0001c0001t0001g0318a0001c0040t0001g0331others(5): Show | 8 | HG01346.hp1 HG02559.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.904+386_904+387dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748623 | |||||
chr19:5748623
|
CA | C | 12 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0086others(9): Show | 12 | HG00438.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.904+387delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748623 | |||||
chr19:5748728
|
C | CT | 28 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0021others(25): Show | 28 | HG00741.hp2 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.905-353dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748728 | |||||
chr19:5748728
|
C | CTT | 212 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0038others(209): Show | 212 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.905-354_905-353dup others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748728 | |||||
chr19:5748728
|
C | CTTT | 28 | a0001c0001t0001g0060a0001c0001t0001g0078a0001c0001t0001g0089others(25): Show | 28 | HG00621.hp2 HG00642.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.905-355_905-353dup others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr19 | 5748728 | |||||
chr19:5749059
|
C | T | 136 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0111others(133): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.905-42C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5749059 | ||||||
chr19:5749062
|
C | A | 1 | a0004c0003t0001g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.905-39C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 10/21 | chr19 | 5749062 | ||||||
chr19:5749271
|
C | T | 1 | a0012c0015t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.987+88C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749271 | ||||||
chr19:5749286
|
G | T | 1 | a0029c0039t0001g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.987+103G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749286 | ||||||
chr19:5749399
|
G | T | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.987+216G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749399 | ||||||
chr19:5749497
|
G | C | 1 | a0002c0002t0001g0057 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.987+314G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749497 | ||||||
chr19:5749573
|
G | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(24): Show | 27 | HG00741.hp2 HG01346.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.987+390G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749573 | ||||||
chr19:5749803
|
A | AT | 131 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0101others(128): Show | 131 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.987+638dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5749803 | |||||
chr19:5749843
|
G | A | 1 | a0003c0005t0001g0300 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.987+660G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749843 | ||||||
chr19:5749975
|
T | C | 1 | a0004c0003t0001g0141 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.987+792T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749975 | ||||||
chr19:5749976
|
G | A | 1 | a0004c0003t0001g0179 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.987+793G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5749976 | ||||||
chr19:5750084
|
G | A | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.987+901G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750084 | ||||||
chr19:5750176
|
T | C | 3 | a0001c0001t0001g0124a0004c0003t0001g0242a0011c0008t0001g0012 | 3 | HG01169.hp1 HG02027.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.987+993T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750176 | ||||||
chr19:5750187
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.987+1004G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750187 | ||||||
chr19:5750204
|
C | T | 1 | a0002c0002t0001g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.987+1021C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750204 | ||||||
chr19:5750210
|
T | A | 1 | a0002c0002t0001g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.987+1027T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750210 | ||||||
chr19:5750215
|
A | G | 2 | a0002c0002t0001g0139a0003c0004t0001g0324 | 2 | HG00609.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.987+1032A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750215 | ||||||
chr19:5750219
|
T | C | 1 | a0003c0004t0001g0324 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.987+1036T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750219 | ||||||
chr19:5750223
|
C | T | 3 | a0001c0001t0001g0189a0002c0002t0001g0292a0004c0003t0001g0274 | 3 | HG00738.hp2 HG01928.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.987+1040C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750223 | ||||||
chr19:5750234
|
T | G | 1 | a0002c0002t0001g0292 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.987+1051T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750234 | ||||||
chr19:5750246
|
T | A | 18 | a0001c0001t0001g0157a0001c0001t0001g0170a0001c0001t0001g0255others(15): Show | 18 | HG00140.hp2 HG00544.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.987+1063T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750246 | ||||||
chr19:5750260
|
A | G | 12 | a0001c0001t0001g0093a0001c0001t0001g0228a0001c0001t0002g0226others(9): Show | 12 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+1077A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750260 | ||||||
chr19:5750264
|
C | T | 1 | a0003c0004t0001g0323 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.987+1081C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750264 | ||||||
chr19:5750265
|
G | A | 1 | a0004c0003t0001g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.987+1082G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750265 | ||||||
chr19:5750274
|
C | T | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987+1091C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750274 | ||||||
chr19:5750275
|
C | G | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987+1092C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750275 | ||||||
chr19:5750276
|
G | A | 7 | a0001c0001t0001g0143a0001c0001t0004g0105a0003c0004t0001g0148others(4): Show | 7 | HG01109.hp2 HG02109.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1093G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750276 | ||||||
chr19:5750312
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.987+1129C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750312 | ||||||
chr19:5750374
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.987+1191C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750374 | ||||||
chr19:5750399
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.987+1216A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750399 | ||||||
chr19:5750420
|
T | C | 2 | a0002c0002t0001g0049a0003c0004t0001g0323 | 2 | HG02083.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.988-1227T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750420 | ||||||
chr19:5750450
|
C | CA | 33 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0055others(30): Show | 33 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.988-1174dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
C | CAA | 176 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0051others(173): Show | 176 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.988-1175_988-1174d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
C | CAAA | 30 | a0001c0001t0001g0020a0001c0001t0001g0082a0001c0001t0001g0154others(27): Show | 30 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.988-1176_988-1174d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
C | CAAAA | 8 | a0002c0002t0001g0256a0003c0004t0001g0287a0004c0003t0001g0117others(5): Show | 8 | HG00544.hp2 HG02027.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1177_988-1174d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
C | CAAAAAAA others(7): Show |
1 | a0003c0004t0001g0196 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.988-1187_988-1174d others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
C | CAAAAAAA others(9): Show |
1 | a0003c0004t0001g0199 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.988-1189_988-1174d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
C | CAAAAAAA others(25): Show |
1 | a0002c0002t0001g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.988-1174_988-1173i others(34): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750450
|
CA | C | 19 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0001g0099others(16): Show | 19 | HG00735.hp1 HG01109.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.988-1174delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5750450 | |||||
chr19:5750475
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0229a0011c0008t0001g0012others(2): Show | 5 | HG00741.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1172G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750475 | ||||||
chr19:5750689
|
C | T | 5 | a0001c0001t0002g0296a0003c0043t0001g0233a0006c0007t0001g0034others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-958C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750689 | ||||||
chr19:5750702
|
T | A | 10 | a0001c0001t0001g0001a0001c0001t0001g0137a0001c0001t0001g0175others(7): Show | 10 | HG00735.hp1 HG02257.hp1 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.988-945T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750702 | ||||||
chr19:5750741
|
A | G | 1 | a0004c0003t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.988-906A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750741 | ||||||
chr19:5750742
|
G | A | 1 | a0004c0003t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.988-905G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750742 | ||||||
chr19:5750829
|
C | T | 4 | a0001c0001t0001g0038a0001c0001t0001g0074a0001c0001t0001g0133others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-818C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750829 | ||||||
chr19:5750835
|
C | T | 11 | a0001c0001t0001g0137a0001c0001t0001g0175a0002c0002t0001g0049others(8): Show | 11 | HG00735.hp1 HG02027.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-812C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750835 | ||||||
chr19:5750882
|
T | C | 16 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0062others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.988-765T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750882 | ||||||
chr19:5750936
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.988-711C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5750936 | ||||||
chr19:5751069
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(243): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.988-578C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751069 | ||||||
chr19:5751141
|
T | C | 1 | a0003c0004t0001g0287 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.988-506T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751141 | ||||||
chr19:5751142
|
G | T | 1 | a0003c0004t0001g0287 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.988-505G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751142 | ||||||
chr19:5751151
|
T | C | 1 | a0002c0002t0001g0197 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.988-496T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751151 | ||||||
chr19:5751192
|
C | T | 1 | a0006c0007t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.988-455C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751192 | ||||||
chr19:5751197
|
CAAAA | C | 10 | a0001c0001t0001g0063a0003c0004t0001g0022a0003c0004t0001g0314others(7): Show | 10 | HG02486.hp2 HG02572.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.988-408_988-405del others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-412_988-405del others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(5): Show |
C | 2 | a0006c0007t0002g0031a0030c0038t0002g0317 | 2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.988-416_988-405del others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0001g0100a0008c0009t0001g0016 | 2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.988-420_988-405del others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(10): Show |
C | 8 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0001g0099others(5): Show | 8 | HG01109.hp2 HG01361.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.988-421_988-405del others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(11): Show |
C | 1 | a0003c0004t0001g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.988-422_988-405del others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(12): Show |
C | 8 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0062others(5): Show | 8 | HG01884.hp1 HG02165.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-423_988-405del others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(13): Show |
C | 40 | a0001c0001t0001g0089a0001c0001t0001g0162a0001c0001t0001g0220others(37): Show | 40 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.988-424_988-405del others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(14): Show |
C | 144 | a0001c0001t0001g0038a0001c0001t0001g0065a0001c0001t0001g0067others(141): Show | 144 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.988-425_988-405del others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(15): Show |
C | 17 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0137others(14): Show | 17 | HG00735.hp1 HG01169.hp2 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.988-426_988-405del others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(16): Show |
C | 2 | a0001c0001t0002g0296a0003c0043t0001g0233 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.988-427_988-405del others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(18): Show |
C | 5 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0312others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-429_988-405del others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(19): Show |
C | 1 | a0001c0001t0004g0106 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.988-430_988-405del others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(20): Show |
C | 4 | a0001c0001t0001g0143a0003c0004t0001g0148a0003c0004t0001g0149others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-431_988-405del others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(21): Show |
C | 4 | a0001c0001t0001g0170a0001c0001t0001g0194a0001c0001t0001g0208others(1): Show | 4 | HG00741.hp1 HG02559.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-432_988-405del others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751197
|
CAAAAAAA others(22): Show |
C | 52 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0033others(49): Show | 52 | HG00280.hp1 HG00280.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.988-433_988-405del others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751197 | |||||
chr19:5751300
|
G | A | 1 | a0004c0003t0001g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.988-347G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751300 | ||||||
chr19:5751321
|
G | C | 5 | a0002c0002t0001g0263a0004c0003t0001g0035a0004c0003t0001g0110others(2): Show | 5 | HG00408.hp2 NA18983.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-326G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751321 | ||||||
chr19:5751419
|
A | T | 190 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0051others(187): Show | 190 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.988-228A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751419 | ||||||
chr19:5751451
|
G | A | 2 | a0001c0001t0002g0296a0003c0043t0001g0233 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.988-196G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751451 | ||||||
chr19:5751512
|
A | C | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.988-135A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751512 | ||||||
chr19:5751520
|
T | C | 1 | a0003c0004t0001g0336 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.988-127T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | chr19 | 5751520 | ||||||
chr19:5751531
|
C | CA | 12 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0163others(9): Show | 12 | HG02109.hp1 HG02148.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.988-79dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
C | CAAAAAAA others(4): Show |
1 | a0003c0043t0001g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.988-89_988-79dupAA others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.988-94_988-79dupAA others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CA | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0090others(8): Show | 11 | HG00738.hp1 HG01168.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-79delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAA | C | 6 | a0001c0001t0001g0082a0001c0001t0001g0162a0001c0001t0001g0268others(3): Show | 6 | HG01192.hp1 HG02071.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.988-81_988-79delAA others(1): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAA | C | 58 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0065others(55): Show | 58 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.988-82_988-79delAA others(2): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAA | C | 118 | a0001c0001t0001g0067a0001c0001t0001g0074a0001c0001t0001g0084others(115): Show | 118 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.988-83_988-79delAA others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAA | C | 8 | a0001c0001t0001g0038a0001c0001t0001g0145a0001c0001t0001g0265others(5): Show | 8 | HG00408.hp1 HG01255.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.988-84_988-79delAA others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0001g0154a0001c0001t0002g0024a0002c0002t0001g0049others(1): Show | 4 | HG01255.hp1 HG02027.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-89_988-79delAA others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAAA others(5): Show |
C | 18 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0001g0099others(15): Show | 18 | HG00735.hp1 HG01109.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.988-90_988-79delAA others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAAA others(6): Show |
C | 15 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0062others(12): Show | 15 | HG01106.hp2 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.988-91_988-79delAA others(11): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAAA others(7): Show |
C | 47 | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0033others(44): Show | 47 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.988-92_988-79delAA others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0088a0001c0001t0002g0226a0005c0006t0001g0207 | 3 | HG01934.hp1 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.988-93_988-79delAA others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751531
|
CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0001g0225a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-94_988-79delAA others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr19 | 5751531 | |||||
chr19:5751900
|
C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0062others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1164+77C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5751900 | ||||||
chr19:5751980
|
T | C | 2 | a0001c0001t0002g0296a0003c0043t0001g0233 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1164+157T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5751980 | ||||||
chr19:5751997
|
C | CA | 7 | a0001c0001t0001g0088a0001c0001t0001g0225a0001c0001t0001g0231others(4): Show | 7 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+183dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5751997 | |||||
chr19:5752006
|
A | T | 3 | a0001c0001t0001g0318a0006c0007t0002g0031a0030c0038t0002g0317 | 3 | HG02451.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1164+183A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752006 | ||||||
chr19:5752007
|
T | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0288 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1164+184T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752007 | ||||||
chr19:5752202
|
C | T | 7 | a0001c0001t0001g0088a0001c0001t0001g0225a0001c0001t0001g0231others(4): Show | 7 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1164+379C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752202 | ||||||
chr19:5752203
|
G | A | 2 | a0001c0001t0001g0143a0001c0001t0004g0106 | 2 | HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1164+380G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752203 | ||||||
chr19:5752239
|
G | T | 2 | a0001c0001t0002g0296a0003c0043t0001g0233 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1164+416G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752239 | ||||||
chr19:5752303
|
C | T | 1 | a0002c0002t0001g0173 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1164+480C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752303 | ||||||
chr19:5752420
|
G | C | 3 | a0001c0001t0001g0318a0006c0007t0002g0031a0030c0038t0002g0317 | 3 | HG02451.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1164+597G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752420 | ||||||
chr19:5752428
|
G | A | 2 | a0001c0001t0002g0296a0003c0043t0001g0233 | 2 | HG01891.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1164+605G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752428 | ||||||
chr19:5752582
|
G | A | 1 | a0006c0007t0002g0031 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1164+759G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752582 | ||||||
chr19:5752624
|
A | G | 1 | a0003c0005t0001g0306 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1164+801A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752624 | ||||||
chr19:5752660
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0001g0099others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1164+837C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752660 | ||||||
chr19:5752762
|
T | C | 14 | a0001c0001t0001g0137a0001c0001t0001g0175a0001c0001t0002g0226others(11): Show | 14 | HG00735.hp1 HG02027.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1164+939T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752762 | ||||||
chr19:5752794
|
G | A | 4 | a0001c0001t0001g0195a0002c0002t0001g0235a0002c0002t0001g0298others(1): Show | 4 | HG02135.hp1 HG03490.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1164+971G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752794 | ||||||
chr19:5752908
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1164+1085A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5752908 | ||||||
chr19:5753007
|
G | A | 12 | a0001c0001t0001g0088a0001c0001t0001g0225a0001c0001t0001g0231others(9): Show | 12 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1165-1125G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753007 | ||||||
chr19:5753027
|
C | CA | 16 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0155others(13): Show | 16 | HG00642.hp2 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.1165-1088dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753027 | |||||
chr19:5753027
|
CA | C | 33 | a0001c0001t0001g0054a0001c0001t0001g0060a0001c0001t0001g0062others(30): Show | 33 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1165-1088delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753027 | |||||
chr19:5753105
|
C | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(265): Show | 268 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1165-1027C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753105 | ||||||
chr19:5753280
|
G | T | 2 | a0003c0005t0001g0185a0003c0005t0001g0249 | 2 | NA19007.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1165-852G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753280 | ||||||
chr19:5753281
|
G | C | 3 | a0003c0004t0001g0148a0003c0004t0001g0149a0003c0004t0001g0150 | 3 | HG02109.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1165-851G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753281 | ||||||
chr19:5753291
|
T | C | 28 | a0001c0001t0001g0020a0001c0001t0001g0063a0001c0001t0001g0220others(25): Show | 28 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1165-841T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753291 | ||||||
chr19:5753298
|
C | T | 1 | a0003c0004t0001g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165-834C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753298 | ||||||
chr19:5753300
|
C | G | 1 | a0003c0004t0001g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165-832C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753300 | ||||||
chr19:5753314
|
G | A | 1 | a0003c0005t0001g0300 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1165-818G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753314 | ||||||
chr19:5753335
|
T | C | 117 | a0001c0001t0001g0020a0001c0001t0001g0038a0001c0001t0001g0054others(114): Show | 117 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1165-797T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753335 | ||||||
chr19:5753363
|
T | A | 83 | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0001g0063others(80): Show | 83 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.1165-769T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753363 | ||||||
chr19:5753364
|
T | G | 75 | a0001c0001t0001g0020a0001c0001t0001g0074a0001c0001t0001g0084others(72): Show | 75 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1165-768T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753364 | ||||||
chr19:5753371
|
T | TAA | 3 | a0002c0002t0001g0193a0002c0002t0001g0197a0002c0002t0001g0215 | 3 | NA18963.hp2 NA18971.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1165-760_1165-759d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753371 | |||||
chr19:5753394
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1165-738C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753394 | ||||||
chr19:5753423
|
G | A | 4 | a0001c0001t0001g0312a0001c0001t0001g0318a0001c0001t0002g0107others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1165-709G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753423 | ||||||
chr19:5753434
|
C | T | 1 | a0002c0002t0003g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1165-698C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753434 | ||||||
chr19:5753518
|
C | T | 1 | a0004c0044t0001g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1165-614C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753518 | ||||||
chr19:5753529
|
C | T | 1 | a0003c0004t0001g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1165-603C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753529 | ||||||
chr19:5753567
|
A | G | 5 | a0001c0001t0001g0062a0003c0004t0001g0148a0003c0004t0001g0149others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-565A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753567 | ||||||
chr19:5753594
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1165-538C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753594 | ||||||
chr19:5753595
|
G | A | 3 | a0004c0003t0001g0320a0004c0003t0003g0053a0004c0003t0003g0075 | 3 | NA18974.hp1 NA19074.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1165-537G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753595 | ||||||
chr19:5753626
|
T | G | 5 | a0002c0002t0001g0205a0002c0002t0001g0209a0003c0004t0001g0188others(2): Show | 5 | HG01081.hp2 HG01496.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-506T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753626 | ||||||
chr19:5753683
|
A | T | 2 | a0002c0002t0001g0238a0002c0002t0001g0289 | 2 | HG00642.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1165-449A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753683 | ||||||
chr19:5753698
|
G | T | 3 | a0001c0001t0001g0020a0001c0034t0001g0023a0008c0009t0001g0032 | 3 | HG02109.hp1 HG02895.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1165-434G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753698 | ||||||
chr19:5753706
|
T | TA | 6 | a0001c0001t0001g0055a0001c0001t0001g0078a0002c0002t0001g0236others(3): Show | 6 | HG01496.hp1 HG02559.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165-414dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753706 | |||||
chr19:5753730
|
G | A | 1 | a0002c0002t0001g0278 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1165-402G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753730 | ||||||
chr19:5753859
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0312a0001c0001t0001g0318others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1165-273C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753859 | ||||||
chr19:5753872
|
C | CA | 12 | a0001c0001t0001g0055a0001c0001t0001g0078a0001c0001t0001g0225others(9): Show | 12 | HG01884.hp1 HG02074.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1165-250dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr19 | 5753872 | |||||
chr19:5753910
|
C | T | 1 | a0002c0002t0001g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1165-222C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753910 | ||||||
chr19:5753911
|
G | A | 1 | a0002c0002t0001g0270 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1165-221G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753911 | ||||||
chr19:5753947
|
G | A | 1 | a0002c0002t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1165-185G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5753947 | ||||||
chr19:5754090
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1165-42A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 12/21 | chr19 | 5754090 | ||||||
chr19:5754267
|
T | C | 1 | a0003c0004t0001g0188 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1278+22T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754267 | ||||||
chr19:5754375
|
T | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0067 | 3 | HG01255.hp2 HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1278+130T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754375 | ||||||
chr19:5754393
|
C | CT | 21 | a0001c0001t0001g0021a0001c0001t0001g0067a0001c0001t0001g0082others(18): Show | 21 | HG00438.hp1 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1278+171dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | |||||
chr19:5754393
|
C | CTT | 131 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(128): Show | 131 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1278+170_1278+171d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | |||||
chr19:5754393
|
C | CTTT | 34 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0086others(31): Show | 34 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1278+169_1278+171d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | |||||
chr19:5754393
|
CT | C | 25 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0078others(22): Show | 25 | HG01884.hp2 HG01934.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1278+171delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754393 | |||||
chr19:5754421
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1278+176C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754421 | ||||||
chr19:5754430
|
G | A | 2 | a0001c0001t0001g0067a0003c0004t0001g0333 | 2 | HG01257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1278+185G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754430 | ||||||
chr19:5754459
|
C | T | 1 | a0002c0002t0001g0069 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1278+214C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754459 | ||||||
chr19:5754460
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1278+215G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754460 | ||||||
chr19:5754562
|
C | A | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1278+317C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754562 | ||||||
chr19:5754629
|
C | G | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+384C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754629 | ||||||
chr19:5754650
|
G | A | 3 | a0001c0001t0001g0124a0003c0004t0001g0324a0003c0041t0001g0329 | 3 | HG00609.hp1 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1278+405G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754650 | ||||||
chr19:5754716
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0134a0001c0001t0001g0135others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+471C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754716 | ||||||
chr19:5754725
|
G | T | 1 | a0003c0004t0001g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1278+480G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754725 | ||||||
chr19:5754759
|
T | A | 1 | a0003c0004t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1278+514T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754759 | ||||||
chr19:5754788
|
G | A | 1 | a0003c0037t0001g0203 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1278+543G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754788 | ||||||
chr19:5754828
|
C | G | 3 | a0001c0001t0001g0063a0001c0001t0002g0024a0006c0007t0002g0030 | 3 | HG02976.hp2 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1278+583C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5754828 | ||||||
chr19:5754847
|
C | CT | 85 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0089others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1278+617dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5754847 | |||||
chr19:5755144
|
C | T | 1 | a0004c0003t0001g0240 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1278+899C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755144 | ||||||
chr19:5755199
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0155a0001c0001t0001g0160 | 3 | HG00738.hp1 HG01243.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1278+954C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755199 | ||||||
chr19:5755386
|
G | A | 3 | a0001c0001t0002g0147a0006c0007t0002g0031a0030c0038t0002g0317 | 3 | HG02257.hp2 HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1278+1141G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755386 | ||||||
chr19:5755458
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(231): Show | 234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1278+1213A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755458 | ||||||
chr19:5755635
|
T | C | 1 | a0003c0004t0001g0222 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1278+1390T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755635 | ||||||
chr19:5755714
|
G | A | 1 | a0003c0004t0001g0230 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1278+1469G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755714 | ||||||
chr19:5755773
|
C | CAATA | 37 | a0001c0001t0001g0033a0001c0001t0001g0039a0001c0001t0001g0063others(34): Show | 37 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1278+1551_1278+155 others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5755773 | |||||
chr19:5755869
|
A | C | 1 | a0004c0003t0001g0079 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1278+1624A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755869 | ||||||
chr19:5755919
|
T | G | 1 | a0002c0002t0001g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1278+1674T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5755919 | ||||||
chr19:5756009
|
G | A | 1 | a0003c0004t0003g0083 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1278+1764G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756009 | ||||||
chr19:5756132
|
T | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0078a0003c0004t0001g0058others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-1711T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756132 | ||||||
chr19:5756187
|
G | A | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1279-1656G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756187 | ||||||
chr19:5756284
|
G | GA | 172 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(169): Show | 172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1279-1548dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5756284 | |||||
chr19:5756379
|
G | A | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-1464G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756379 | ||||||
chr19:5756440
|
C | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1279-1403C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756440 | ||||||
chr19:5756493
|
A | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0229a0001c0001t0001g0318others(4): Show | 7 | HG00741.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1279-1350A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756493 | ||||||
chr19:5756555
|
C | T | 2 | a0001c0001t0002g0064a0006c0007t0001g0025 | 2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1279-1288C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756555 | ||||||
chr19:5756559
|
T | A | 1 | a0001c0001t0001g0312 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1279-1284T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756559 | ||||||
chr19:5756634
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0137a0001c0001t0001g0165others(3): Show | 6 | HG00642.hp1 HG00735.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1209G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756634 | ||||||
chr19:5756654
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0078a0003c0004t0001g0058others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-1189G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756654 | ||||||
chr19:5756748
|
C | T | 1 | a0003c0004t0001g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1279-1095C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756748 | ||||||
chr19:5756865
|
C | T | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-978C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756865 | ||||||
chr19:5756950
|
A | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0229a0001c0001t0001g0318others(4): Show | 7 | HG00741.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1279-893A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756950 | ||||||
chr19:5756978
|
G | A | 4 | a0002c0002t0001g0057a0002c0002t0001g0073a0002c0002t0001g0097others(1): Show | 4 | HG00323.hp2 HG01175.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-865G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5756978 | ||||||
chr19:5757084
|
T | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0078a0003c0004t0001g0058others(2): Show | 5 | HG02559.hp1 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-759T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757084 | ||||||
chr19:5757097
|
A | G | 1 | a0016c0013t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1279-746A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757097 | ||||||
chr19:5757119
|
G | A | 2 | a0008c0009t0001g0032a0023c0026t0002g0335 | 2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1279-724G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757119 | ||||||
chr19:5757259
|
G | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(236): Show | 239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1279-584G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757259 | ||||||
chr19:5757297
|
CT | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(284): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.1279-529delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757297 | |||||
chr19:5757297
|
CTT | C | 32 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0044others(29): Show | 32 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1279-530_1279-529d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757297 | |||||
chr19:5757525
|
G | A | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1279-318G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757525 | ||||||
chr19:5757547
|
T | C | 1 | a0016c0013t0001g0009 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279-296T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757547 | ||||||
chr19:5757581
|
G | A | 8 | a0001c0001t0001g0062a0003c0004t0001g0148a0003c0004t0001g0149others(5): Show | 8 | HG02109.hp2 HG02622.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279-262G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757581 | ||||||
chr19:5757599
|
A | AT | 8 | a0001c0001t0001g0054a0003c0004t0001g0061a0003c0004t0001g0129others(5): Show | 8 | HG02055.hp1 HG02451.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1279-222dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | |||||
chr19:5757599
|
AT | A | 88 | a0001c0001t0001g0045a0001c0001t0001g0078a0001c0001t0001g0088others(85): Show | 88 | HG00280.hp1 HG00438.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.1279-222delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | |||||
chr19:5757599
|
ATT | A | 202 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(199): Show | 202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.1279-223_1279-222d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | |||||
chr19:5757599
|
ATTT | A | 9 | a0001c0001t0001g0065a0001c0001t0002g0147a0002c0002t0001g0056others(6): Show | 9 | HG01258.hp2 HG01517.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279-224_1279-222d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | |||||
chr19:5757599
|
ATTTTTTT others(3): Show |
A | 1 | a0007c0010t0001g0029 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1279-231_1279-222d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr19 | 5757599 | |||||
chr19:5757656
|
G | A | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-187G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757656 | ||||||
chr19:5757706
|
G | C | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-137G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757706 | ||||||
chr19:5757793
|
G | A | 2 | a0017c0014t0002g0011a0017c0014t0002g0013 | 2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1279-50G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 13/21 | chr19 | 5757793 | ||||||
chr19:5758171
|
G | A | 1 | a0003c0004t0001g0287 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1368+239G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758171 | ||||||
chr19:5758261
|
G | A | 8 | a0002c0002t0001g0043a0002c0002t0001g0068a0002c0002t0001g0236others(5): Show | 8 | HG00323.hp1 HG01261.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368+329G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758261 | ||||||
chr19:5758454
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0229a0001c0001t0001g0318others(3): Show | 6 | HG00741.hp2 HG02572.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368+522G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758454 | ||||||
chr19:5758545
|
T | C | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1369-541T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758545 | ||||||
chr19:5758573
|
C | CA | 18 | a0001c0001t0001g0062a0001c0001t0001g0143a0001c0001t0002g0107others(15): Show | 18 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1369-493dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758573 | |||||
chr19:5758573
|
CA | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(251): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1369-493delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758573 | |||||
chr19:5758573
|
CAA | C | 11 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0007others(8): Show | 11 | HG00642.hp2 HG01081.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1369-494_1369-493d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758573 | |||||
chr19:5758599
|
C | T | 1 | a0024c0035t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1369-487C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758599 | ||||||
chr19:5758658
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1369-428G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758658 | ||||||
chr19:5758692
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1369-394G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758692 | ||||||
chr19:5758730
|
G | A | 10 | a0001c0001t0001g0054a0001c0001t0001g0225a0003c0004t0001g0061others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1369-356G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | chr19 | 5758730 | ||||||
chr19:5758758
|
GA | G | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1369-320delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758758 | |||||
chr19:5758923
|
C | CA | 32 | a0001c0001t0001g0038a0001c0001t0001g0055a0001c0001t0001g0078others(29): Show | 32 | HG00621.hp2 HG00741.hp1 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.1369-140dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758923 | |||||
chr19:5758923
|
CA | C | 19 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0054others(16): Show | 19 | HG00280.hp1 HG01099.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1369-140delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr19 | 5758923 | |||||
chr19:5759220
|
T | G | 250 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(247): Show | 250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1427+76T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759220 | ||||||
chr19:5759247
|
C | A | 1 | a0004c0003t0001g0319 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1427+103C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759247 | ||||||
chr19:5759259
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0310 | 2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1427+115G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759259 | ||||||
chr19:5759372
|
G | T | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1427+228G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759372 | ||||||
chr19:5759380
|
G | A | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1427+236G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759380 | ||||||
chr19:5759390
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1427+246C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759390 | ||||||
chr19:5759405
|
A | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(212): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1427+261A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759405 | ||||||
chr19:5759407
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1427+263A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759407 | ||||||
chr19:5759480
|
G | T | 15 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(12): Show | 15 | HG02109.hp2 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1427+336G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759480 | ||||||
chr19:5759552
|
T | A | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+408T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759552 | ||||||
chr19:5759566
|
CA | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1427+441delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5759566 | |||||
chr19:5759572
|
A | C | 1 | a0001c0001t0001g0090 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1427+428A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759572 | ||||||
chr19:5759611
|
G | A | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+467G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759611 | ||||||
chr19:5759737
|
G | A | 1 | a0002c0002t0001g0270 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1427+593G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759737 | ||||||
chr19:5759747
|
T | C | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+603T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759747 | ||||||
chr19:5759801
|
C | T | 3 | a0001c0001t0002g0024a0006c0007t0002g0030a0023c0026t0002g0335 | 3 | HG02976.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1427+657C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759801 | ||||||
chr19:5759814
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1427+670A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759814 | ||||||
chr19:5759927
|
A | T | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+783A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759927 | ||||||
chr19:5759950
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1427+806G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5759950 | ||||||
chr19:5760000
|
G | A | 2 | a0001c0001t0002g0296a0010c0011t0001g0003 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1427+856G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760000 | ||||||
chr19:5760073
|
C | CA | 189 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0038others(186): Show | 189 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1427+953dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760073 | |||||
chr19:5760073
|
C | CAA | 49 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(46): Show | 49 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1427+952_1427+953d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760073 | |||||
chr19:5760102
|
G | A | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1427+958G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760102 | ||||||
chr19:5760170
|
G | A | 1 | a0024c0035t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1427+1026G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760170 | ||||||
chr19:5760173
|
G | A | 52 | a0001c0001t0001g0001a0002c0002t0001g0044a0002c0002t0001g0092others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1427+1029G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760173 | ||||||
chr19:5760323
|
C | T | 11 | a0001c0001t0002g0059a0003c0004t0001g0022a0003c0004t0001g0148others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1427+1179C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760323 | ||||||
chr19:5760398
|
C | CA | 115 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0039others(112): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.1427+1268dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760398 | |||||
chr19:5760398
|
C | CAA | 16 | a0002c0002t0001g0050a0002c0002t0001g0056a0002c0002t0001g0085others(13): Show | 16 | HG00438.hp2 HG00544.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1427+1267_1427+126 others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760398 | |||||
chr19:5760398
|
CA | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0100a0001c0001t0002g0024others(50): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.1427+1268delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760398 | |||||
chr19:5760415
|
A | G | 1 | a0008c0009t0001g0016 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1427+1271A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760415 | ||||||
chr19:5760471
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1427+1327C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760471 | ||||||
chr19:5760472
|
T | A | 52 | a0001c0001t0001g0001a0002c0002t0001g0044a0002c0002t0001g0092others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1427+1328T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760472 | ||||||
chr19:5760477
|
G | A | 1 | a0003c0004t0001g0303 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1427+1333G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760477 | ||||||
chr19:5760486
|
C | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+1342C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760486 | ||||||
chr19:5760530
|
A | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(241): Show | 244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1427+1386A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760530 | ||||||
chr19:5760619
|
GGACCAAG others(4): Show |
G | 1 | a0004c0003t0003g0053 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1427+1476_1427+148 others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760619 | ||||||
chr19:5760767
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1427+1623G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760767 | ||||||
chr19:5760797
|
T | G | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1427+1653T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760797 | ||||||
chr19:5760916
|
G | A | 1 | a0002c0002t0001g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1427+1772G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5760916 | ||||||
chr19:5760939
|
CA | C | 12 | a0001c0001t0001g0165a0003c0004t0001g0022a0003c0004t0001g0148others(9): Show | 12 | HG02074.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1427+1809delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5760939 | |||||
chr19:5761006
|
C | G | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1427+1862C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761006 | ||||||
chr19:5761042
|
GT | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(206): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1427+1909delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761042 | |||||
chr19:5761333
|
C | T | 5 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428-1882C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761333 | ||||||
chr19:5761345
|
G | A | 52 | a0001c0001t0001g0001a0002c0002t0001g0044a0002c0002t0001g0092others(49): Show | 52 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1428-1870G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761345 | ||||||
chr19:5761416
|
A | AATGG | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1428-1774_1428-177 others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761416 | |||||
chr19:5761416
|
AATGGATG others(1): Show |
A | 3 | a0004c0003t0001g0079a0004c0003t0001g0272a0004c0003t0001g0302 | 3 | HG02129.hp2 HG02135.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1428-1778_1428-177 others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761416 | |||||
chr19:5761441
|
A | ATGGATGG others(5): Show |
5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428-1771_1428-177 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761441 | |||||
chr19:5761445
|
C | A | 30 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0062others(27): Show | 30 | HG01884.hp1 HG01891.hp2 HG01934.hp1 others(27): Show |
intron_variant | MODIFIER | c.1428-1770C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761445 | ||||||
chr19:5761463
|
G | GGCTGGAT others(148): Show |
222 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(219): Show | 222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1428-1750_1428-159 others(159): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761463 | |||||
chr19:5761463
|
G | GGCTGGAT others(303): Show |
2 | a0001c0001t0002g0296a0010c0011t0001g0003 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1428-1596_1428-159 others(314): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761463 | |||||
chr19:5761463
|
G | GGCTGGCT others(148): Show |
13 | a0002c0002t0001g0044a0002c0002t0001g0115a0002c0002t0001g0127others(10): Show | 13 | HG00408.hp1 HG01099.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1428-1747_1428-174 others(159): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761463 | |||||
chr19:5761469
|
A | C | 1 | a0002c0002t0001g0251 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1428-1746A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761469 | ||||||
chr19:5761703
|
C | CT | 33 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0062others(30): Show | 33 | HG00609.hp2 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1428-1498dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5761703 | |||||
chr19:5761783
|
A | G | 1 | a0002c0002t0001g0085 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1428-1432A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761783 | ||||||
chr19:5761791
|
C | T | 21 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0062others(18): Show | 21 | HG01884.hp1 HG01934.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1428-1424C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761791 | ||||||
chr19:5761822
|
C | T | 1 | a0027c0036t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1428-1393C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761822 | ||||||
chr19:5761913
|
T | G | 10 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1428-1302T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761913 | ||||||
chr19:5761937
|
C | T | 75 | a0001c0001t0001g0089a0001c0001t0001g0134a0001c0001t0001g0135others(72): Show | 75 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1428-1278C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761937 | ||||||
chr19:5761989
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1428-1226T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761989 | ||||||
chr19:5761990
|
G | A | 1 | a0006c0007t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1428-1225G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5761990 | ||||||
chr19:5762041
|
C | CATATATA others(5): Show |
1 | a0001c0001t0001g0045 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1428-1167_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762041 | |||||
chr19:5762041
|
C | CATATATA others(7): Show |
1 | a0001c0001t0005g0142 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1428-1169_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762041 | |||||
chr19:5762041
|
C | CATATATA others(9): Show |
3 | a0004c0003t0001g0110a0004c0003t0001g0245a0004c0003t0001g0248 | 3 | NA18952.hp2 NA18983.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.1428-1171_1428-115 others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762041 | |||||
chr19:5762048
|
ATATATAT others(5): Show |
A | 3 | a0014c0017t0002g0223a0017c0014t0002g0011a0017c0014t0002g0013 | 3 | HG02896.hp2 HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1428-1165_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762048 | |||||
chr19:5762048
|
ATATATAT others(6): Show |
A | 2 | a0014c0017t0002g0224a0027c0036t0001g0297 | 2 | HG02451.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1428-1165_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762048 | |||||
chr19:5762056
|
A | AT | 4 | a0002c0002t0001g0007a0002c0002t0001g0069a0003c0004t0001g0076others(1): Show | 4 | HG02155.hp1 HG02523.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1158dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762056 | |||||
chr19:5762056
|
A | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0155a0001c0001t0001g0160others(2): Show | 5 | HG00738.hp1 HG01243.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-1159A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762056 | ||||||
chr19:5762057
|
TA | T | 5 | a0002c0002t0001g0279a0002c0002t0001g0291a0004c0003t0001g0080others(2): Show | 5 | HG02129.hp1 NA18960.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-1157delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762057 | ||||||
chr19:5762058
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(6): Show |
5 | a0002c0002t0001g0234a0002c0002t0001g0261a0003c0004t0001g0222others(2): Show | 5 | HG00408.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(10): Show |
2 | a0004c0003t0001g0274a0031c0028t0001g0130 | 2 | HG01928.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(52): Show |
1 | a0001c0001t0001g0265 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(63): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(40): Show |
1 | a0032c0024t0001g0204 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(40): Show |
1 | a0001c0001t0001g0124 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(45): Show |
1 | a0001c0016t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(56): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0084a0001c0001t0001g0086 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(46): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0162 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(48): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(40): Show |
1 | a0001c0016t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(51): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(33): Show |
2 | a0001c0001t0001g0006a0004c0003t0001g0179 | 2 | NA18942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(44): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(34): Show |
1 | a0003c0004t0001g0040 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(45): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0001g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(47): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0051 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(38): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0001g0038 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(39): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0065 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(45): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(35): Show |
1 | a0003c0037t0001g0203 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(46): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(25): Show |
1 | a0004c0003t0001g0218 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0133 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(42): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(22): Show |
1 | a0003c0004t0001g0323 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0062 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(38): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(40): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(30): Show |
2 | a0001c0001t0001g0067a0003c0004t0001g0178 | 2 | HG01257.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(41): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0002g0024 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(35): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(25): Show |
1 | a0003c0004t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(36): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(33): Show |
1 | a0002c0002t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(44): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(21): Show |
1 | a0002c0027t0001g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(22): Show |
2 | a0002c0002t0001g0037a0004c0003t0001g0117 | 2 | HG00544.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0102a0002c0002t0001g0298 | 2 | HG01346.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(34): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(24): Show |
2 | a0002c0002t0001g0235a0006c0007t0002g0030 | 2 | HG03490.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(35): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(30): Show |
2 | a0001c0001t0001g0208a0003c0004t0001g0022 | 2 | HG00741.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(41): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0304a0002c0002t0001g0209a0002c0002t0001g0259 | 3 | HG01192.hp2 HG02273.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(20): Show |
1 | a0004c0044t0001g0211 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(21): Show |
2 | a0002c0002t0001g0186a0005c0006t0001g0213 | 2 | HG03942.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(22): Show |
2 | a0001c0001t0001g0268a0013c0031t0001g0036 | 2 | HG02071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(29): Show |
1 | a0003c0004t0001g0314 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(40): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0093a0001c0001t0001g0099a0016c0013t0001g0009 | 3 | HG02818.hp2 HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
8 | a0001c0001t0001g0039a0001c0001t0001g0121a0002c0002t0001g0050others(5): Show | 8 | HG01175.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(18): Show |
7 | a0001c0001t0001g0137a0001c0001t0001g0220a0001c0001t0001g0255others(4): Show | 7 | HG00735.hp1 HG03239.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0177a0003c0004t0001g0149a0003c0004t0001g0158 | 3 | HG02683.hp1 HG03195.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(20): Show |
4 | a0002c0002t0001g0205a0002c0002t0001g0270a0004c0003t0001g0313others(1): Show | 4 | HG02040.hp1 NA18954.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0285 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(22): Show |
1 | a0002c0002t0001g0139 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0077a0011c0008t0001g0010a0015c0018t0001g0309 | 3 | HG03041.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0145 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0089a0002c0002t0001g0184 | 2 | HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
8 | a0002c0002t0001g0049a0002c0002t0001g0073a0002c0002t0001g0116others(5): Show | 8 | HG00438.hp2 HG01109.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(18): Show |
6 | a0001c0001t0001g0170a0002c0002t0001g0056a0002c0002t0001g0097others(3): Show | 6 | HG00642.hp1 HG02027.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(19): Show |
2 | a0002c0002t0001g0187a0003c0004t0001g0199 | 2 | HG03669.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(20): Show |
1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0033a0005c0006t0001g0207 | 2 | HG01934.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(10): Show |
2 | a0003c0005t0001g0269a0004c0003t0001g0320 | 2 | HG00609.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0296 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(13): Show |
1 | a0010c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(14): Show |
2 | a0006c0007t0001g0025a0033c0047t0001g0004 | 2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(15): Show |
2 | a0005c0006t0001g0217a0015c0018t0001g0308 | 2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0002g0064a0001c0001t0002g0311 | 2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
12 | a0002c0002t0001g0114a0002c0002t0001g0119a0002c0002t0001g0120others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0135a0002c0002t0001g0289a0002c0002t0003g0081others(1): Show | 4 | HG01070.hp1 HG01070.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0134 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(8): Show |
1 | a0003c0005t0001g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(9): Show |
2 | a0004c0003t0003g0053a0004c0003t0003g0075 | 2 | NA18974.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(10): Show |
1 | a0009c0012t0001g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0021 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(15): Show |
1 | a0003c0004t0001g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(16): Show |
3 | a0003c0004t0001g0260a0003c0004t0003g0083a0010c0011t0001g0315 | 3 | HG01081.hp2 HG01496.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
4 | a0002c0002t0001g0043a0002c0002t0001g0066a0002c0002t0001g0068others(1): Show | 4 | HG00323.hp1 HG01975.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(18): Show |
4 | a0002c0002t0001g0103a0002c0002t0001g0286a0002c0002t0001g0305others(1): Show | 4 | HG01261.hp2 HG01358.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0002g0147a0003c0004t0001g0336a0007c0010t0001g0026 | 3 | HG01993.hp2 HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(6): Show |
8 | a0001c0001t0001g0001a0002c0002t0001g0180a0002c0002t0001g0251others(5): Show | 8 | HG01069.hp1 HG01258.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(7): Show |
4 | a0003c0004t0001g0287a0003c0004t0001g0303a0003c0004t0001g0333others(1): Show | 4 | HG02886.hp1 HG03486.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(10): Show |
2 | a0009c0012t0001g0153a0009c0012t0001g0156 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0228a0001c0001t0001g0312 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(15): Show |
2 | a0005c0006t0001g0212a0029c0039t0001g0140 | 2 | HG02559.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0082a0002c0002t0001g0266 | 2 | HG03486.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
1 | a0011c0008t0001g0012 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(3): Show |
2 | a0006c0007t0002g0031a0030c0038t0002g0317 | 2 | HG02451.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0002g0226 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(15): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(5): Show |
2 | a0003c0004t0001g0098a0026c0033t0001g0301 | 2 | HG01168.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(16): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(6): Show |
11 | a0002c0002t0001g0044a0002c0002t0001g0115a0002c0002t0001g0127others(8): Show | 11 | HG01074.hp2 HG01099.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(7): Show |
11 | a0002c0002t0001g0283a0003c0004t0001g0192a0003c0004t0001g0216others(8): Show | 11 | HG00544.hp1 HG00621.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(8): Show |
2 | a0003c0004t0001g0058a0003c0005t0001g0300 | 2 | HG02976.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(17): Show |
1 | a0002c0002t0001g0236 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(6): Show |
4 | a0001c0001t0001g0154a0001c0001t0001g0231a0003c0004t0001g0281others(1): Show | 4 | HG00140.hp1 HG01255.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(7): Show |
1 | a0003c0005t0001g0249 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0055a0003c0004t0001g0324 | 2 | HG00609.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATTT others(6): Show |
3 | a0001c0001t0001g0318a0003c0004t0001g0230a0023c0026t0002g0335 | 3 | HG02572.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATTATA others(21): Show |
1 | a0004c0003t0001g0321 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATTTTT others(6): Show |
2 | a0001c0001t0001g0060a0001c0001t0001g0310 | 2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(17): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | ATATTTTT others(7): Show |
2 | a0001c0001t0001g0229a0034c0046t0001g0005 | 2 | HG00741.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762058 | |||||
chr19:5762058
|
A | T | 55 | a0001c0001t0001g0041a0001c0001t0001g0090a0001c0001t0001g0101others(52): Show | 55 | HG00408.hp2 HG00621.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1428-1157A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762058 | ||||||
chr19:5762059
|
T | TATATATA others(8): Show |
5 | a0001c0001t0001g0046a0001c0001t0001g0136a0001c0001t0001g0194others(2): Show | 5 | HG01106.hp2 HG01261.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1428-1156_1428-115 others(19): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762059 | ||||||
chr19:5762059
|
T | TATATATA others(10): Show |
1 | a0012c0015t0001g0125 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(21): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762059 | ||||||
chr19:5762059
|
T | TATATATA others(12): Show |
1 | a0001c0001t0001g0221 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1428-1156_1428-115 others(23): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762059 | ||||||
chr19:5762060
|
T | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0128a0001c0001t0001g0232 | 3 | HG00280.hp1 HG01891.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1428-1155T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762060 | ||||||
chr19:5762061
|
T | A | 8 | a0001c0001t0001g0046a0001c0001t0001g0136a0001c0001t0001g0194others(5): Show | 8 | HG01106.hp2 HG01261.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1428-1154T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762061 | ||||||
chr19:5762063
|
T | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0136a0001c0001t0001g0194others(4): Show | 7 | HG01106.hp2 HG01261.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1428-1152T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762063 | ||||||
chr19:5762103
|
G | T | 1 | a0002c0002t0001g0277 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1428-1112G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762103 | ||||||
chr19:5762422
|
A | G | 1 | a0001c0016t0001g0167 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1428-793A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762422 | ||||||
chr19:5762533
|
T | C | 1 | a0002c0002t0001g0182 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1428-682T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762533 | ||||||
chr19:5762617
|
G | GTGGA | 5 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0112others(2): Show | 5 | HG01168.hp2 HG02004.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428-572_1428-569d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr19 | 5762617 | |||||
chr19:5762817
|
T | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1428-398T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762817 | ||||||
chr19:5762858
|
G | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1428-357G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5762858 | ||||||
chr19:5763203
|
G | A | 1 | a0003c0043t0001g0233 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1428-12G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 15/21 | chr19 | 5763203 | ||||||
chr19:5763318
|
C | T | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1506+25C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5763318 | ||||||
chr19:5763761
|
C | T | 1 | a0001c0001t0004g0105 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1506+468C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5763761 | ||||||
chr19:5763847
|
C | CTTTT | 10 | a0001c0001t0002g0311a0003c0004t0001g0022a0003c0004t0001g0148others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+569_1506+572d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTT | 21 | a0001c0001t0001g0021a0001c0001t0001g0033a0001c0001t0001g0062others(18): Show | 21 | HG01884.hp1 HG01891.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.1506+568_1506+572d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(1): Show |
27 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0051others(24): Show | 27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1506+565_1506+572d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(2): Show |
11 | a0001c0001t0001g0065a0001c0001t0001g0164a0001c0001t0001g0170others(8): Show | 11 | HG00741.hp1 HG01175.hp2 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.1506+564_1506+572d others(11): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(3): Show |
42 | a0001c0001t0001g0020a0001c0001t0001g0089a0001c0001t0001g0134others(39): Show | 42 | HG00408.hp1 HG00544.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1506+563_1506+572d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(4): Show |
26 | a0001c0001t0001g0001a0001c0001t0001g0055a0001c0001t0001g0060others(23): Show | 26 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1506+562_1506+572d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(5): Show |
6 | a0003c0004t0001g0216a0003c0004t0001g0230a0003c0004t0001g0281others(3): Show | 6 | HG00140.hp1 HG02027.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+561_1506+572d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(13): Show |
1 | a0002c0002t0001g0259 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(15): Show |
1 | a0002c0002t0001g0205 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1506+572_1506+573i others(24): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(16): Show |
1 | a0002c0002t0001g0209 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1506+572_1506+573i others(25): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(17): Show |
1 | a0002c0002t0001g0270 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(26): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(18): Show |
1 | a0002c0002t0003g0072 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1506+572_1506+573i others(27): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(19): Show |
15 | a0001c0001t0005g0142a0002c0002t0001g0037a0002c0002t0001g0049others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(28): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(20): Show |
39 | a0001c0001t0001g0045a0001c0001t0001g0194a0001c0001t0001g0195others(36): Show | 39 | HG00280.hp1 HG00544.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(29): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(21): Show |
19 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0136others(16): Show | 19 | HG00438.hp1 HG00438.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(30): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(22): Show |
5 | a0001c0001t0001g0137a0001c0001t0001g0165a0002c0002t0001g0238others(2): Show | 5 | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(31): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(23): Show |
2 | a0001c0001t0001g0166a0001c0001t0002g0059 | 2 | HG02055.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1506+572_1506+573i others(32): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(24): Show |
5 | a0002c0002t0001g0103a0002c0002t0001g0116a0002c0002t0001g0197others(2): Show | 5 | HG01109.hp1 HG01358.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506+572_1506+573i others(33): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0304 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(35): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763847
|
C | CTTTTTTT others(30): Show |
1 | a0031c0028t0001g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1506+572_1506+573i others(39): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5763847 | |||||
chr19:5763911
|
G | C | 6 | a0002c0002t0001g0085a0004c0003t0001g0104a0004c0003t0001g0117others(3): Show | 6 | HG00438.hp2 HG00544.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+618G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5763911 | ||||||
chr19:5764029
|
AGAAGAAA others(4): Show |
A | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1506+738_1506+748d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764029 | |||||
chr19:5764039
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(236): Show | 239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1506+746G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764039 | ||||||
chr19:5764041
|
G | T | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1506+748G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764041 | ||||||
chr19:5764092
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0078a0003c0004t0001g0058others(1): Show | 4 | HG02559.hp1 HG02976.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+799G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764092 | ||||||
chr19:5764101
|
GGCCTCCC others(78): Show |
G | 2 | a0002c0002t0001g0180a0004c0003t0001g0240 | 2 | NA18942.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1506+829_1506+913d others(87): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764101 | |||||
chr19:5764228
|
C | G | 6 | a0002c0002t0001g0173a0002c0002t0001g0263a0002c0002t0001g0279others(3): Show | 6 | HG00408.hp2 HG02129.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506+935C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764228 | ||||||
chr19:5764235
|
A | AT | 10 | a0001c0001t0001g0020a0001c0001t0001g0170a0001c0001t0001g0229others(7): Show | 10 | HG00741.hp2 HG02965.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.1506+955dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764235 | |||||
chr19:5764235
|
A | ATT | 223 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(220): Show | 223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1506+954_1506+955d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764235 | |||||
chr19:5764235
|
A | ATTT | 7 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(4): Show | 7 | HG01358.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1506+953_1506+955d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5764235 | |||||
chr19:5764379
|
G | A | 240 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(237): Show | 240 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.1506+1086G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764379 | ||||||
chr19:5764425
|
T | C | 237 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(234): Show | 237 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1506+1132T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764425 | ||||||
chr19:5764460
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1506+1167C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764460 | ||||||
chr19:5764461
|
G | A | 76 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0136others(73): Show | 76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1506+1168G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764461 | ||||||
chr19:5764461
|
G | C | 1 | a0004c0003t0001g0320 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1506+1168G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764461 | ||||||
chr19:5764464
|
T | C | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(239): Show | 242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.1506+1171T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764464 | ||||||
chr19:5764547
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0038others(186): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1506+1254G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764547 | ||||||
chr19:5764647
|
A | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1506+1354A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764647 | ||||||
chr19:5764657
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1506+1364T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764657 | ||||||
chr19:5764690
|
C | T | 10 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1506+1397C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764690 | ||||||
chr19:5764739
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0001g0137others(4): Show | 7 | HG00735.hp1 HG01192.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-1364G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764739 | ||||||
chr19:5764751
|
T | A | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1507-1352T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764751 | ||||||
chr19:5764862
|
G | A | 1 | a0003c0004t0001g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1507-1241G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5764862 | ||||||
chr19:5765071
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(243): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1507-1032T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765071 | ||||||
chr19:5765091
|
T | C | 1 | a0002c0002t0001g0201 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1507-1012T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765091 | ||||||
chr19:5765205
|
G | A | 1 | a0003c0005t0001g0300 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1507-898G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765205 | ||||||
chr19:5765225
|
C | T | 5 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1507-878C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765225 | ||||||
chr19:5765283
|
A | G | 1 | a0003c0005t0001g0254 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1507-820A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765283 | ||||||
chr19:5765353
|
GCTCT | G | 5 | a0001c0001t0001g0020a0001c0001t0001g0229a0001c0001t0001g0231others(2): Show | 5 | HG00741.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-745_1507-742d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765353 | |||||
chr19:5765401
|
GATTTATT others(9): Show |
G | 3 | a0002c0002t0001g0205a0002c0002t0001g0209a0002c0002t0001g0270 | 3 | NA18954.hp1 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1507-698_1507-683d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765401 | |||||
chr19:5765405
|
T | TATTC | 5 | a0001c0001t0001g0101a0002c0002t0001g0190a0003c0004t0001g0108others(2): Show | 5 | HG01168.hp2 HG03209.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-651_1507-648d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | |||||
chr19:5765405
|
TATTC | T | 45 | a0001c0001t0001g0128a0001c0001t0001g0143a0001c0001t0001g0175others(42): Show | 45 | HG00408.hp2 HG00621.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1507-651_1507-648d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | |||||
chr19:5765405
|
TATTCATT others(1): Show |
T | 16 | a0001c0001t0001g0033a0001c0001t0001g0062a0001c0001t0001g0082others(13): Show | 16 | HG00438.hp2 HG01099.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1507-655_1507-648d others(10): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | |||||
chr19:5765405
|
TATTCATT others(5): Show |
T | 53 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0038others(50): Show | 53 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.1507-659_1507-648d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | |||||
chr19:5765405
|
TATTCATT others(9): Show |
T | 164 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0039others(161): Show | 164 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1507-663_1507-648d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | |||||
chr19:5765405
|
TATTCATT others(13): Show |
T | 7 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(4): Show | 7 | HG02015.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1507-667_1507-648d others(22): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr19 | 5765405 | |||||
chr19:5765417
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1507-686C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765417 | ||||||
chr19:5765421
|
C | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0077a0001c0001t0001g0093others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1507-682C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765421 | ||||||
chr19:5765425
|
C | T | 21 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0229others(18): Show | 21 | HG00741.hp2 HG01934.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1507-678C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765425 | ||||||
chr19:5765446
|
A | T | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1507-657A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765446 | ||||||
chr19:5765466
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1507-637G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765466 | ||||||
chr19:5765518
|
A | G | 2 | a0001c0001t0002g0024a0006c0007t0002g0030 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1507-585A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765518 | ||||||
chr19:5765641
|
G | A | 2 | a0001c0001t0002g0024a0006c0007t0002g0030 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1507-462G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765641 | ||||||
chr19:5765684
|
C | T | 5 | a0002c0002t0001g0173a0002c0002t0001g0263a0004c0003t0001g0035others(2): Show | 5 | HG00408.hp2 NA18960.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1507-419C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765684 | ||||||
chr19:5765701
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(231): Show | 234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1507-402A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765701 | ||||||
chr19:5765709
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(231): Show | 234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1507-394A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765709 | ||||||
chr19:5765760
|
T | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(315): Show | 318 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(315): Show |
intron_variant | MODIFIER | c.1507-343T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765760 | ||||||
chr19:5765858
|
G | A | 53 | a0001c0001t0001g0175a0001c0001t0001g0288a0002c0002t0001g0007others(50): Show | 53 | HG00408.hp2 HG00621.hp1 HG01952.hp2 others(50): Show |
intron_variant | MODIFIER | c.1507-245G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765858 | ||||||
chr19:5765867
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1507-236C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5765867 | ||||||
chr19:5766024
|
T | C | 6 | a0002c0002t0001g0085a0004c0003t0001g0104a0004c0003t0001g0117others(3): Show | 6 | HG00438.hp2 HG00544.hp2 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1507-79T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5766024 | ||||||
chr19:5766079
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(229): Show | 232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1507-24T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 16/21 | chr19 | 5766079 | ||||||
chr19:5766288
|
T | TA | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1559+133_1559+134i others(3): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766288 | ||||||
chr19:5766289
|
G | A | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1559+134G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766289 | ||||||
chr19:5766289
|
G | GA | 7 | a0001c0001t0001g0067a0001c0001t0001g0089a0001c0001t0001g0145others(4): Show | 7 | HG01106.hp1 HG01257.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1559+150dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766289 | |||||
chr19:5766289
|
G | GAA | 200 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(197): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1559+149_1559+150d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766289 | |||||
chr19:5766289
|
G | GAAA | 23 | a0001c0001t0001g0195a0001c0001t0001g0208a0001c0001t0002g0296others(20): Show | 23 | HG00438.hp2 HG00544.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1559+148_1559+150d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766289 | |||||
chr19:5766311
|
C | T | 1 | a0031c0028t0001g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1559+156C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766311 | ||||||
chr19:5766312
|
G | A | 2 | a0001c0001t0002g0296a0010c0011t0001g0003 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1559+157G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766312 | ||||||
chr19:5766336
|
G | A | 2 | a0001c0001t0002g0024a0006c0007t0002g0030 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1559+181G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766336 | ||||||
chr19:5766349
|
G | C | 1 | a0010c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1559+194G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766349 | ||||||
chr19:5766459
|
GA | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1559+318delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766459 | |||||
chr19:5766574
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1559+419C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766574 | ||||||
chr19:5766579
|
AT | A | 88 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046others(85): Show | 88 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.1559+427delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766579 | |||||
chr19:5766697
|
AT | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(229): Show | 232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.1559+555delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5766697 | |||||
chr19:5766743
|
A | C | 1 | a0002c0027t0001g0237 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1559+588A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766743 | ||||||
chr19:5766931
|
G | T | 2 | a0003c0004t0001g0222a0003c0043t0001g0233 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1559+776G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5766931 | ||||||
chr19:5767141
|
C | T | 1 | a0020c0021t0001g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1559+986C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767141 | ||||||
chr19:5767174
|
G | A | 1 | a0002c0002t0001g0277 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1560-994G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767174 | ||||||
chr19:5767224
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1560-944G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767224 | ||||||
chr19:5767253
|
C | T | 3 | a0009c0012t0001g0153a0009c0012t0001g0156a0009c0012t0001g0159 | 3 | HG01515.hp1 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1560-915C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767253 | ||||||
chr19:5767289
|
C | G | 5 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1560-879C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767289 | ||||||
chr19:5767316
|
C | CA | 191 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0038others(188): Show | 191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1560-834dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767316 | |||||
chr19:5767316
|
C | CAA | 44 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0033others(41): Show | 44 | HG00741.hp1 HG01081.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.1560-835_1560-834d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767316 | |||||
chr19:5767321
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1560-847A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767321 | ||||||
chr19:5767339
|
G | T | 1 | a0002c0002t0001g0186 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1560-829G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767339 | ||||||
chr19:5767413
|
G | GT | 8 | a0001c0001t0001g0090a0001c0001t0002g0226a0002c0002t0001g0044others(5): Show | 8 | HG00544.hp2 HG01175.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.1560-742dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767413 | |||||
chr19:5767413
|
GT | G | 17 | a0001c0001t0002g0059a0003c0004t0001g0022a0003c0004t0001g0148others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1560-742delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767413 | |||||
chr19:5767449
|
T | G | 1 | a0002c0002t0001g0263 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1560-719T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767449 | ||||||
chr19:5767484
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1560-684T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767484 | ||||||
chr19:5767494
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1560-674A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767494 | ||||||
chr19:5767574
|
G | A | 36 | a0002c0002t0001g0044a0002c0002t0001g0092a0002c0002t0001g0115others(33): Show | 36 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.1560-594G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767574 | ||||||
chr19:5767588
|
T | C | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1560-580T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767588 | ||||||
chr19:5767631
|
C | T | 11 | a0002c0002t0001g0127a0003c0004t0001g0022a0003c0004t0001g0148others(8): Show | 11 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1560-537C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767631 | ||||||
chr19:5767709
|
G | A | 19 | a0002c0002t0001g0037a0002c0002t0001g0056a0002c0002t0001g0114others(16): Show | 19 | HG00438.hp1 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1560-459G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767709 | ||||||
chr19:5767763
|
C | A | 3 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280 | 3 | HG01934.hp2 HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1560-405C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767763 | ||||||
chr19:5767765
|
CTTTT | C | 10 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1560-400_1560-397d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767765 | |||||
chr19:5767781
|
ATTATT | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(238): Show | 241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1560-378_1560-374d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr19 | 5767781 | |||||
chr19:5767786
|
T | A | 2 | a0003c0004t0001g0022a0003c0004t0001g0314 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1560-382T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767786 | ||||||
chr19:5767857
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(243): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1560-311T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767857 | ||||||
chr19:5767943
|
C | G | 9 | a0001c0001t0001g0020a0001c0001t0001g0060a0001c0001t0001g0229others(6): Show | 9 | HG00741.hp2 HG02145.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1560-225C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767943 | ||||||
chr19:5767987
|
G | A | 1 | a0007c0010t0001g0026 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1560-181G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 17/21 | chr19 | 5767987 | ||||||
chr19:5768291
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1634+49G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768291 | ||||||
chr19:5768320
|
T | TTTTA | 215 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(212): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1634+101_1634+104d others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5768320 | |||||
chr19:5768320
|
T | TTTTATTT others(1): Show |
23 | a0001c0001t0001g0020a0001c0001t0001g0055a0001c0001t0001g0060others(20): Show | 23 | HG00741.hp2 HG02109.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1634+97_1634+104du others(9): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5768320 | |||||
chr19:5768320
|
T | TTTTATTT others(5): Show |
8 | a0001c0001t0002g0107a0001c0001t0002g0147a0001c0001t0002g0226others(5): Show | 8 | HG01934.hp2 HG02015.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1634+93_1634+104du others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5768320 | |||||
chr19:5768384
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(240): Show | 243 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1634+142T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768384 | ||||||
chr19:5768406
|
G | A | 10 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634+164G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768406 | ||||||
chr19:5768438
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1634+196A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768438 | ||||||
chr19:5768449
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1634+207G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768449 | ||||||
chr19:5768601
|
G | A | 1 | a0006c0007t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1634+359G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768601 | ||||||
chr19:5768697
|
G | A | 1 | a0022c0025t0001g0146 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1634+455G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768697 | ||||||
chr19:5768702
|
T | C | 1 | a0003c0004t0001g0323 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1634+460T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768702 | ||||||
chr19:5768807
|
C | G | 1 | a0002c0002t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1634+565C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768807 | ||||||
chr19:5768807
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1634+565C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768807 | ||||||
chr19:5768883
|
T | C | 2 | a0001c0001t0002g0024a0006c0007t0002g0030 | 2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1634+641T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768883 | ||||||
chr19:5768920
|
G | A | 239 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(236): Show | 239 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1634+678G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5768920 | ||||||
chr19:5769000
|
G | A | 1 | a0004c0003t0001g0169 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1634+758G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769000 | ||||||
chr19:5769046
|
C | T | 2 | a0002c0002t0001g0184a0002c0002t0001g0201 | 2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1634+804C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769046 | ||||||
chr19:5769086
|
A | G | 3 | a0001c0001t0002g0296a0001c0001t0002g0311a0010c0011t0001g0003 | 3 | HG01891.hp2 HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1634+844A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769086 | ||||||
chr19:5769150
|
T | G | 10 | a0001c0001t0002g0059a0003c0004t0001g0022a0003c0004t0001g0148others(7): Show | 10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634+908T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769150 | ||||||
chr19:5769162
|
A | AAG | 13 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0067others(10): Show | 13 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1634+935_1634+936d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5769162 | |||||
chr19:5769293
|
CA | C | 6 | a0002c0002t0001g0279a0003c0004t0001g0058a0003c0004t0001g0096others(3): Show | 6 | HG01169.hp2 HG02129.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+1072delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5769293 | |||||
chr19:5769314
|
A | AT | 25 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0060others(22): Show | 25 | HG00741.hp2 HG01099.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.1634+1072_1634+107 others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769314 | ||||||
chr19:5769314
|
A | T | 232 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0033others(229): Show | 232 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.1634+1072A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769314 | ||||||
chr19:5769329
|
G | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0227a0001c0001t0001g0228others(2): Show | 5 | HG02280.hp2 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1634+1087G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769329 | ||||||
chr19:5769376
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1634+1134T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769376 | ||||||
chr19:5769385
|
A | C | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1634+1143A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769385 | ||||||
chr19:5769433
|
C | A | 16 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0063others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1634+1191C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769433 | ||||||
chr19:5769435
|
G | A | 2 | a0002c0002t0001g0049a0002c0002t0001g0066 | 2 | HG03704.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1634+1193G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769435 | ||||||
chr19:5769572
|
C | T | 1 | a0006c0007t0001g0034 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1634+1330C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769572 | ||||||
chr19:5769574
|
C | T | 1 | a0002c0002t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1634+1332C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769574 | ||||||
chr19:5769672
|
G | A | 1 | a0004c0003t0001g0282 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1635-1272G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769672 | ||||||
chr19:5769705
|
G | A | 9 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-1239G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769705 | ||||||
chr19:5769860
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(296): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1635-1084A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769860 | ||||||
chr19:5769914
|
T | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(296): Show | 299 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.1635-1030T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769914 | ||||||
chr19:5769963
|
C | T | 1 | a0001c0016t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1635-981C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5769963 | ||||||
chr19:5770076
|
G | A | 2 | a0001c0001t0001g0231a0025c0032t0001g0334 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1635-868G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770076 | ||||||
chr19:5770088
|
C | CA | 13 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0285others(10): Show | 13 | HG01175.hp2 HG01433.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1635-839dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5770088 | |||||
chr19:5770112
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1635-832A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770112 | ||||||
chr19:5770168
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1635-776C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770168 | ||||||
chr19:5770190
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1635-754G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770190 | ||||||
chr19:5770235
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1635-709C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770235 | ||||||
chr19:5770258
|
A | T | 9 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1635-686A>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770258 | ||||||
chr19:5770430
|
C | CA | 26 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0163others(23): Show | 26 | HG00140.hp1 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1635-498dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5770430 | |||||
chr19:5770430
|
C | CAA | 7 | a0001c0001t0001g0090a0001c0016t0001g0126a0001c0016t0001g0167others(4): Show | 7 | HG01433.hp2 HG01934.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-499_1635-498d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr19 | 5770430 | |||||
chr19:5770459
|
G | A | 1 | a0002c0002t0001g0187 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1635-485G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770459 | ||||||
chr19:5770536
|
T | A | 3 | a0009c0012t0001g0153a0009c0012t0001g0156a0009c0012t0001g0159 | 3 | HG01515.hp1 HG01517.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1635-408T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770536 | ||||||
chr19:5770598
|
C | A | 14 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0063others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1635-346C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770598 | ||||||
chr19:5770651
|
C | T | 3 | a0004c0003t0001g0183a0004c0003t0001g0241a0004c0003t0001g0267 | 3 | NA19002.hp2 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1635-293C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770651 | ||||||
chr19:5770652
|
G | A | 32 | a0001c0001t0001g0088a0001c0001t0001g0100a0001c0001t0001g0128others(29): Show | 32 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1635-292G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770652 | ||||||
chr19:5770713
|
G | A | 1 | a0003c0005t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1635-231G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770713 | ||||||
chr19:5770720
|
G | A | 4 | a0001c0016t0001g0126a0001c0016t0001g0167a0002c0002t0001g0280others(1): Show | 4 | HG01934.hp2 HG02015.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-224G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770720 | ||||||
chr19:5770751
|
A | G | 6 | a0001c0001t0001g0045a0001c0001t0001g0089a0001c0001t0001g0134others(3): Show | 6 | HG00280.hp1 HG00642.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.1635-193A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 18/21 | chr19 | 5770751 | ||||||
chr19:5771114
|
G | A | 5 | a0001c0001t0002g0311a0001c0016t0001g0126a0001c0016t0001g0167others(2): Show | 5 | HG01934.hp2 HG02015.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1763+42G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771114 | ||||||
chr19:5771165
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0060others(9): Show | 12 | HG00741.hp2 HG01891.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1763+93C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771165 | ||||||
chr19:5771177
|
A | G | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1763+105A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771177 | ||||||
chr19:5771206
|
G | T | 1 | a0004c0003t0001g0243 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1763+134G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771206 | ||||||
chr19:5771223
|
A | G | 1 | a0010c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+151A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771223 | ||||||
chr19:5771229
|
C | T | 1 | a0002c0002t0001g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1763+157C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771229 | ||||||
chr19:5771303
|
C | T | 2 | a0002c0002t0001g0184a0002c0002t0001g0201 | 2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1763+231C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771303 | ||||||
chr19:5771440
|
G | A | 51 | a0002c0002t0001g0277a0002c0002t0001g0326a0004c0003t0001g0035others(48): Show | 51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1763+368G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771440 | ||||||
chr19:5771480
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1763+408C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771480 | ||||||
chr19:5771557
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1763+485C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771557 | ||||||
chr19:5771583
|
C | CT | 22 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0090others(19): Show | 22 | HG01175.hp1 HG01433.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1763+527dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5771583 | |||||
chr19:5771583
|
CT | C | 10 | a0001c0001t0001g0164a0001c0001t0002g0311a0002c0002t0001g0068others(7): Show | 10 | HG00323.hp1 HG01175.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.1763+527delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5771583 | |||||
chr19:5771603
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1763+531C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771603 | ||||||
chr19:5771690
|
C | T | 1 | a0010c0011t0001g0003 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1763+618C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771690 | ||||||
chr19:5771717
|
C | T | 1 | a0023c0026t0002g0335 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1763+645C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771717 | ||||||
chr19:5771905
|
A | C | 1 | a0004c0003t0001g0252 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1763+833A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5771905 | ||||||
chr19:5772044
|
CCTTTT | C | 3 | a0001c0001t0001g0077a0001c0001t0001g0093a0001c0001t0001g0099 | 3 | HG02818.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1764-743_1764-739d others(7): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772044 | ||||||
chr19:5772052
|
C | CT | 11 | a0002c0002t0001g0235a0003c0004t0001g0022a0003c0004t0001g0108others(8): Show | 11 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1764-723dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772052 | |||||
chr19:5772052
|
CT | C | 12 | a0001c0001t0001g0021a0001c0001t0001g0054a0001c0001t0001g0063others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1764-723delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772052 | |||||
chr19:5772101
|
C | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(277): Show | 280 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.1764-687C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772101 | ||||||
chr19:5772214
|
A | AT | 100 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0046others(97): Show | 100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1764-543dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
A | ATT | 45 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0082others(42): Show | 45 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1764-544_1764-543d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
A | ATTT | 12 | a0001c0001t0001g0038a0001c0001t0001g0175a0001c0001t0001g0177others(9): Show | 12 | HG00642.hp1 HG01109.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.1764-545_1764-543d others(5): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
A | ATTTTTT | 7 | a0001c0001t0002g0064a0002c0002t0001g0092a0003c0004t0001g0148others(4): Show | 7 | HG01884.hp1 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1764-548_1764-543d others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
AT | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0054a0001c0001t0001g0060others(17): Show | 20 | HG00140.hp1 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1764-543delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
ATT | A | 24 | a0001c0001t0001g0063a0001c0001t0001g0100a0001c0001t0001g0128others(21): Show | 24 | HG00280.hp2 HG00544.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1764-544_1764-543d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0041a0001c0001t0001g0101a0001c0001t0001g0112others(3): Show | 6 | HG01168.hp2 HG02004.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1764-552_1764-543d others(12): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
ATTTTTTT others(4): Show |
A | 10 | a0001c0001t0001g0099a0004c0003t0001g0110a0004c0003t0001g0241others(7): Show | 10 | HG01928.hp1 HG02027.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1764-553_1764-543d others(13): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
ATTTTTTT others(5): Show |
A | 39 | a0004c0003t0001g0035a0004c0003t0001g0042a0004c0003t0001g0048others(36): Show | 39 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1764-554_1764-543d others(14): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772214
|
ATTTTTTT others(9): Show |
A | 2 | a0003c0004t0001g0109a0003c0004t0001g0323 | 2 | HG00438.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1764-558_1764-543d others(18): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr19 | 5772214 | |||||
chr19:5772239
|
T | G | 1 | a0004c0003t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1764-549T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772239 | ||||||
chr19:5772259
|
G | A | 1 | a0001c0001t0002g0147 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1764-529G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772259 | ||||||
chr19:5772284
|
G | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0038a0001c0001t0001g0046others(27): Show | 30 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1764-504G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772284 | ||||||
chr19:5772313
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(279): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1764-475T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772313 | ||||||
chr19:5772314
|
G | A | 51 | a0004c0003t0001g0035a0004c0003t0001g0042a0004c0003t0001g0048others(48): Show | 51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1764-474G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772314 | ||||||
chr19:5772328
|
C | T | 51 | a0001c0001t0001g0051a0004c0003t0001g0035a0004c0003t0001g0042others(48): Show | 51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1764-460C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772328 | ||||||
chr19:5772352
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(13): Show | 16 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1764-436C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772352 | ||||||
chr19:5772365
|
T | C | 15 | a0004c0003t0001g0104a0004c0003t0001g0110a0004c0003t0001g0117others(12): Show | 15 | HG00438.hp2 HG00544.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.1764-423T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772365 | ||||||
chr19:5772375
|
C | A | 1 | a0002c0002t0001g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1764-413C>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772375 | ||||||
chr19:5772389
|
G | T | 3 | a0003c0004t0001g0058a0003c0004t0001g0333a0018c0020t0001g0018 | 3 | HG02886.hp1 HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1764-399G>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772389 | ||||||
chr19:5772448
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1764-340C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772448 | ||||||
chr19:5772474
|
G | A | 1 | a0006c0007t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1764-314G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772474 | ||||||
chr19:5772516
|
C | T | 2 | a0001c0001t0002g0064a0006c0007t0001g0034 | 2 | HG01884.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1764-272C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772516 | ||||||
chr19:5772729
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1764-59C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 19/21 | chr19 | 5772729 | ||||||
chr19:5773177
|
G | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(279): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1941+212G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773177 | ||||||
chr19:5773221
|
G | A | 2 | a0002c0002t0001g0215a0002c0002t0001g0250 | 2 | HG00323.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1941+256G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773221 | ||||||
chr19:5773328
|
T | C | 12 | a0001c0016t0001g0126a0001c0016t0001g0167a0003c0004t0001g0022others(9): Show | 12 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1941+363T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773328 | ||||||
chr19:5773466
|
A | G | 8 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0229others(5): Show | 8 | HG00741.hp2 HG02257.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1941+501A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773466 | ||||||
chr19:5773582
|
G | A | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1941+617G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773582 | ||||||
chr19:5773678
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(279): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1941+713A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773678 | ||||||
chr19:5773693
|
CT | C | 200 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0038others(197): Show | 200 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1941+745delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773693 | |||||
chr19:5773693
|
CTT | C | 28 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(25): Show | 28 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1941+744_1941+745d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773693 | |||||
chr19:5773773
|
T | C | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1941+808T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773773 | ||||||
chr19:5773774
|
C | T | 1 | a0002c0002t0001g0235 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1941+809C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773774 | ||||||
chr19:5773884
|
C | T | 1 | a0004c0003t0001g0042 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1941+919C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5773884 | ||||||
chr19:5773968
|
C | CT | 201 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0038others(198): Show | 201 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1941+1020dupT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773968 | |||||
chr19:5773968
|
C | CTT | 12 | a0001c0001t0001g0154a0001c0001t0001g0164a0001c0001t0001g0191others(9): Show | 12 | HG01175.hp2 HG01255.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.1941+1019_1941+102 others(6): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773968 | |||||
chr19:5773968
|
CT | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(46): Show | 49 | HG00280.hp2 HG00544.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1941+1020delT | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5773968 | |||||
chr19:5774029
|
G | A | 1 | a0004c0003t0003g0071 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1941+1064G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774029 | ||||||
chr19:5774129
|
G | C | 1 | a0027c0036t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1941+1164G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774129 | ||||||
chr19:5774209
|
G | A | 2 | a0001c0016t0001g0126a0001c0016t0001g0167 | 2 | HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1941+1244G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774209 | ||||||
chr19:5774223
|
C | T | 1 | a0002c0002t0001g0092 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1941+1258C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774223 | ||||||
chr19:5774366
|
T | G | 1 | a0002c0002t0001g0097 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1941+1401T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774366 | ||||||
chr19:5774603
|
C | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(23): Show | 26 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1942-1558C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774603 | ||||||
chr19:5774613
|
T | C | 314 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(311): Show | 314 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(311): Show |
intron_variant | MODIFIER | c.1942-1548T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774613 | ||||||
chr19:5774675
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(12): Show | 15 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-1486C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774675 | ||||||
chr19:5774715
|
AAAAT | A | 11 | a0001c0016t0001g0126a0001c0016t0001g0167a0003c0004t0001g0022others(8): Show | 11 | HG01934.hp2 HG02109.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1942-1434_1942-143 others(8): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5774715 | |||||
chr19:5774932
|
G | A | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(12): Show | 15 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-1229G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5774932 | ||||||
chr19:5775303
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0160 | 2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1942-858G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775303 | ||||||
chr19:5775326
|
G | C | 58 | a0003c0004t0001g0040a0003c0004t0001g0058a0003c0004t0001g0061others(55): Show | 58 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1942-835G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775326 | ||||||
chr19:5775481
|
C | CA | 15 | a0001c0001t0001g0128a0001c0001t0001g0134a0001c0001t0001g0135others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1942-662dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775481 | |||||
chr19:5775481
|
CA | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0020others(126): Show | 129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1942-662delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775481 | |||||
chr19:5775481
|
CAA | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0227a0001c0001t0001g0228others(11): Show | 14 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1942-663_1942-662d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775481 | |||||
chr19:5775523
|
C | T | 1 | a0031c0028t0001g0130 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1942-638C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775523 | ||||||
chr19:5775598
|
G | A | 148 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0077others(145): Show | 148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1942-563G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775598 | ||||||
chr19:5775599
|
A | C | 111 | a0003c0004t0001g0040a0003c0004t0001g0058a0003c0004t0001g0061others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1942-562A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775599 | ||||||
chr19:5775624
|
G | A | 1 | a0003c0004t0001g0287 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1942-537G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775624 | ||||||
chr19:5775648
|
C | CA | 99 | a0002c0027t0001g0237a0003c0004t0001g0040a0003c0004t0001g0061others(96): Show | 99 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1942-494dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775648 | |||||
chr19:5775648
|
C | CAA | 41 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0077others(38): Show | 41 | HG01515.hp1 HG01517.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1942-495_1942-494d others(4): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775648 | |||||
chr19:5775648
|
CA | C | 20 | a0001c0001t0002g0064a0001c0001t0004g0106a0001c0016t0001g0126others(17): Show | 20 | HG00323.hp1 HG01884.hp1 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.1942-494delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr19 | 5775648 | |||||
chr19:5775664
|
A | G | 2 | a0001c0016t0001g0126a0001c0016t0001g0167 | 2 | HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1942-497A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775664 | ||||||
chr19:5775699
|
G | A | 1 | a0004c0003t0001g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1942-462G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775699 | ||||||
chr19:5775827
|
C | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(12): Show | 15 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-334C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775827 | ||||||
chr19:5775835
|
G | A | 9 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1942-326G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775835 | ||||||
chr19:5775900
|
C | G | 6 | a0001c0001t0002g0059a0001c0001t0002g0107a0001c0001t0002g0147others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1942-261C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775900 | ||||||
chr19:5775926
|
C | T | 2 | a0002c0002t0001g0182a0002c0002t0001g0200 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1942-235C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5775926 | ||||||
chr19:5776038
|
G | C | 1 | a0003c0005t0001g0185 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1942-123G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5776038 | ||||||
chr19:5776052
|
C | T | 110 | a0003c0004t0001g0040a0003c0004t0001g0058a0003c0004t0001g0061others(107): Show | 110 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1942-109C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5776052 | ||||||
chr19:5776089
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1942-72G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 20/21 | chr19 | 5776089 | ||||||
chr19:5776360
|
C | T | 4 | a0003c0004t0001g0058a0003c0004t0001g0333a0018c0020t0001g0018others(1): Show | 4 | HG02886.hp1 HG02976.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2096+45C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776360 | ||||||
chr19:5776380
|
T | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0001g0093others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096+65T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776380 | ||||||
chr19:5776383
|
G | A | 1 | a0001c0016t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2096+68G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776383 | ||||||
chr19:5776416
|
C | T | 55 | a0003c0004t0001g0058a0003c0004t0001g0333a0004c0003t0001g0035others(52): Show | 55 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2096+101C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776416 | ||||||
chr19:5776423
|
C | T | 1 | a0027c0036t0001g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2096+108C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776423 | ||||||
chr19:5776432
|
C | G | 3 | a0001c0001t0002g0064a0001c0016t0001g0126a0001c0016t0001g0167 | 3 | HG01884.hp1 HG01934.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2096+117C>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776432 | ||||||
chr19:5776482
|
T | A | 1 | a0003c0004t0001g0108 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2096+167T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776482 | ||||||
chr19:5776548
|
G | A | 1 | a0010c0011t0001g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2096+233G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776548 | ||||||
chr19:5776788
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2096+473C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776788 | ||||||
chr19:5776837
|
C | T | 6 | a0001c0001t0002g0059a0001c0001t0002g0107a0001c0001t0002g0147others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096+522C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776837 | ||||||
chr19:5776870
|
T | G | 51 | a0004c0003t0001g0035a0004c0003t0001g0042a0004c0003t0001g0048others(48): Show | 51 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.2096+555T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776870 | ||||||
chr19:5776877
|
C | CA | 27 | a0001c0001t0001g0164a0001c0001t0002g0059a0001c0001t0002g0064others(24): Show | 27 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.2096+579dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5776877 | |||||
chr19:5776877
|
CA | C | 18 | a0001c0001t0001g0021a0001c0001t0001g0227a0001c0001t0001g0228others(15): Show | 18 | HG01109.hp2 HG01169.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2096+579delA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5776877 | |||||
chr19:5776935
|
C | T | 10 | a0004c0003t0001g0110a0004c0003t0001g0132a0004c0003t0001g0240others(7): Show | 10 | HG01928.hp1 NA18952.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.2096+620C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776935 | ||||||
chr19:5776947
|
A | G | 14 | a0003c0004t0001g0095a0003c0004t0001g0109a0003c0004t0001g0188others(11): Show | 14 | HG00438.hp1 HG00609.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.2096+632A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776947 | ||||||
chr19:5776954
|
A | G | 6 | a0001c0001t0002g0059a0001c0001t0002g0107a0001c0001t0002g0147others(3): Show | 6 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2096+639A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776954 | ||||||
chr19:5776958
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0229others(4): Show | 7 | HG00741.hp2 HG02257.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2096+643T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5776958 | ||||||
chr19:5777120
|
A | C | 4 | a0014c0017t0002g0223a0014c0017t0002g0224a0017c0014t0002g0011others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2096+805A>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777120 | ||||||
chr19:5777223
|
T | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0001g0093others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096+908T>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777223 | ||||||
chr19:5777226
|
T | TGCCTTCT others(11): Show |
5 | a0003c0004t0001g0192a0003c0004t0001g0216a0003c0004t0001g0287others(2): Show | 5 | HG00609.hp1 HG02027.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.2096+912_2096+929d others(20): Show |
CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5777226 | |||||
chr19:5777265
|
G | A | 2 | a0001c0001t0001g0033a0005c0006t0001g0207 | 2 | HG01934.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2096+950G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777265 | ||||||
chr19:5777304
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2096+989T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777304 | ||||||
chr19:5777312
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(174): Show | 177 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.2096+997A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777312 | ||||||
chr19:5777404
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0020a0001c0001t0001g0021others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.2097-972T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777404 | ||||||
chr19:5777463
|
G | C | 1 | a0002c0002t0001g0176 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2097-913G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777463 | ||||||
chr19:5777559
|
G | C | 9 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2097-817G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777559 | ||||||
chr19:5777614
|
A | G | 9 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(6): Show | 9 | HG02109.hp2 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2097-762A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777614 | ||||||
chr19:5777767
|
C | T | 1 | a0004c0003t0001g0282 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2097-609C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777767 | ||||||
chr19:5777856
|
T | C | 113 | a0001c0001t0002g0064a0003c0004t0001g0040a0003c0004t0001g0058others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2097-520T>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5777856 | ||||||
chr19:5778058
|
T | G | 1 | a0002c0002t0001g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2097-318T>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778058 | ||||||
chr19:5778066
|
C | T | 8 | a0003c0004t0001g0022a0003c0004t0001g0148a0003c0004t0001g0149others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.2097-310C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778066 | ||||||
chr19:5778115
|
G | A | 5 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0001g0093others(2): Show | 5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2097-261G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778115 | ||||||
chr19:5778139
|
G | C | 16 | a0001c0001t0002g0024a0001c0001t0002g0059a0001c0001t0002g0064others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2097-237G>C | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778139 | ||||||
chr19:5778156
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2097-220G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778156 | ||||||
chr19:5778196
|
G | A | 23 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0077others(20): Show | 23 | HG01515.hp1 HG01517.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.2097-180G>A | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778196 | ||||||
chr19:5778207
|
C | CA | 105 | a0001c0001t0001g0021a0001c0001t0001g0055a0001c0001t0001g0060others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2097-152dupA | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr19 | 5778207 | |||||
chr19:5778331
|
C | T | 1 | a0001c0001t0002g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2097-45C>T | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778331 | ||||||
chr19:5778333
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2097-43A>G | CATSPERD | ENSG00000174898.16 | transcript | ENST00000381624.4 | protein_coding | 21/21 | chr19 | 5778333 |