geneid | 51719 |
---|---|
ensemblid | ENSG00000135932.12 |
hgncid | 20292 |
symbol | CAB39 |
name | calcium binding protein 39 |
refseq_nuc | NM_016289.4 |
refseq_prot | NP_057373.1 |
ensembl_nuc | ENST00000258418.10 |
ensembl_prot | ENSP00000258418.5 |
mane_status | MANE Select |
chr | chr2 |
start | 230712842 |
end | 230821075 |
strand | + |
ver | v1.2 |
region | chr2:230712842-230821075 |
region5000 | chr2:230707842-230826075 |
regionname0 | CAB39_chr2_230712842_230821075 |
regionname5000 | CAB39_chr2_230707842_230826075 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 341 | 340 | 84 | 68 | 142 | 14 | 30 | 112 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0002 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0003 | 0/0 | 341 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1026 | 335 | 83 | 68 | 138 | 14 | 30 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
c0002 | 0/0 | 1026 | 4 | 0 | 0 | 4 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
c0003 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
c0004 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
c0005 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2804 | 95 | 8 | 25 | 45 | 6 | 10 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0002 | 0/0 | 2804 | 36 | 2 | 7 | 22 | 1 | 4 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0003 | 0/0 | 2804 | 31 | 1 | 1 | 28 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0004 | 0/0 | 2804 | 23 | 3 | 6 | 7 | 2 | 5 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0005 | 0/1 | 2802 | 12 | 0 | 5 | 5 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0006 | 0/0 | 2804 | 10 | 1 | 4 | 4 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0007 | 0/0 | 2802 | 9 | 0 | 0 | 7 | 2 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0008 | 0/0 | 2802 | 7 | 0 | 2 | 5 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0009 | 0/0 | 2804 | 6 | 6 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0010 | 0/0 | 2804 | 6 | 5 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0011 | 0/0 | 2804 | 6 | 5 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0012 | 0/0 | 2804 | 6 | 5 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0013 | 0/0 | 2802 | 4 | 0 | 1 | 2 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0014 | 0/0 | 2802 | 4 | 0 | 1 | 3 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0015 | 0/0 | 2804 | 4 | 0 | 2 | 2 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0016 | 0/0 | 2804 | 4 | 0 | 0 | 4 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0017 | 0/0 | 2804 | 3 | 3 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0018 | 0/0 | 2804 | 3 | 2 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0019 | 0/0 | 2804 | 3 | 2 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0020 | 0/0 | 2804 | 3 | 3 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0021 | 0/0 | 2804 | 3 | 3 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0022 | 0/0 | 2802 | 2 | 0 | 0 | 2 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0023 | 0/0 | 2802 | 2 | 0 | 1 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0024 | 0/0 | 2802 | 2 | 1 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0025 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0026 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0027 | 0/0 | 2804 | 2 | 0 | 2 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0028 | 0/0 | 2804 | 2 | 1 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0029 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0030 | 0/0 | 2804 | 2 | 1 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0031 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0032 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0033 | 0/0 | 2804 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0034 | 0/0 | 2804 | 2 | 1 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0035 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0036 | 0/0 | 2804 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0037 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0038 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0039 | 0/0 | 2802 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0040 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0041 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0042 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0043 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0044 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0045 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0046 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0047 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0048 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0049 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0050 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0051 | 0/0 | 2804 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0052 | 0/0 | 2804 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0053 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0054 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0055 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0056 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0057 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0058 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0059 | 0/0 | 2804 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0060 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0061 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0062 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0063 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0064 | 0/0 | 2802 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0065 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0066 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0067 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0068 | 0/0 | 2804 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0069 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0070 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0071 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
t0072 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1026 | 335 | 83 | 68 | 138 | 14 | 30 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0002 | 0/0 | 1026 | 4 | 0 | 0 | 4 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0005 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0002c0004 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0003c0003 | 0/0 | 1026 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3829 | 91 | 8 | 25 | 41 | 6 | 10 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0002 | 0/0 | 3829 | 36 | 2 | 7 | 22 | 1 | 4 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0003 | 0/0 | 3829 | 31 | 1 | 1 | 28 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0004 | 0/0 | 3829 | 23 | 3 | 6 | 7 | 2 | 5 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0005 | 0/1 | 3827 | 12 | 0 | 5 | 5 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0006 | 0/0 | 3829 | 10 | 1 | 4 | 4 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0007 | 0/0 | 3827 | 9 | 0 | 0 | 7 | 2 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0008 | 0/0 | 3827 | 7 | 0 | 2 | 5 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0009 | 0/0 | 3829 | 6 | 6 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0010 | 0/0 | 3829 | 6 | 5 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0011 | 0/0 | 3829 | 6 | 5 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0012 | 0/0 | 3829 | 4 | 3 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0013 | 0/0 | 3827 | 4 | 0 | 1 | 2 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0014 | 0/0 | 3827 | 4 | 0 | 1 | 3 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0015 | 0/0 | 3829 | 4 | 0 | 2 | 2 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0016 | 0/0 | 3829 | 4 | 0 | 0 | 4 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0017 | 0/0 | 3829 | 3 | 3 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0018 | 0/0 | 3829 | 3 | 2 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0019 | 0/0 | 3829 | 3 | 2 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0020 | 0/0 | 3829 | 3 | 3 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0021 | 0/0 | 3829 | 3 | 3 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0022 | 0/0 | 3827 | 2 | 0 | 0 | 2 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0023 | 0/0 | 3827 | 2 | 0 | 1 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0024 | 0/0 | 3827 | 2 | 1 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0025 | 0/0 | 3829 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0026 | 0/0 | 3829 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0027 | 0/0 | 3829 | 2 | 0 | 2 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0028 | 0/0 | 3829 | 2 | 1 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0029 | 0/0 | 3829 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0030 | 0/0 | 3829 | 2 | 1 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0031 | 0/0 | 3829 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0032 | 0/0 | 3829 | 2 | 2 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0033 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0034 | 0/0 | 3829 | 2 | 1 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0035 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0036 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0037 | 0/0 | 3829 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0038 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0039 | 0/0 | 3827 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0040 | 0/0 | 3829 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0041 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0042 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0043 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0044 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0045 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0046 | 0/0 | 3829 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0047 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0048 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0049 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0050 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0051 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0052 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0053 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0054 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0055 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0056 | 0/0 | 3829 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0057 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0058 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0059 | 0/0 | 3829 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0060 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0061 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0062 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0063 | 0/0 | 3829 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0064 | 0/0 | 3827 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0065 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0066 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0067 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0068 | 0/0 | 3829 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0069 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0070 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0071 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0001t0072 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0002t0001 | 0/0 | 3829 | 4 | 0 | 0 | 4 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0001c0005t0012 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0002c0004t0033 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
a0003c0003t0012 | 0/0 | 3829 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | copy fasta | chr2 | 230707842 | 230826075 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0088 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0008g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0009g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0009g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0010g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0010g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0011g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0012g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0013g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0013g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0013g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0013g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0014g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0014g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0014g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0015g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0015g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0015g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0016g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0016g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0016g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0016g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0017g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0017g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0018g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0018g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0018g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0019g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0019g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0019g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0020g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0020g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0021g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0021g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0021g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0022g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0023g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0024g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0024g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0025g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0025g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0026g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0026g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0027g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0027g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0028g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0028g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0029g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0029g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0030g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0030g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0031g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0031g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0032g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0032g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0033g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0034g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0034g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0035g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0036g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0037g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0038g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0039g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0040g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0041g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0042g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0043g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0044g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0045g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0046g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0047g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0048g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0049g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0050g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0051g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0052g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0053g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0054g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0055g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0056g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0057g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0058g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0059g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0060g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0061g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0062g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0063g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0064g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0065g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0066g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0067g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0068g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0069g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0070g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0071g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0001t0072g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0001c0005t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0002c0004t0033g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
a0003c0003t0012g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00099 | hp2 | a0001 | c0001 | t0068 | g0199 | EUR | GBR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | GBR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | FIN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00423 | hp1 | a0001 | c0001 | t0013 | g0139 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00597 | hp1 | a0001 | c0001 | t0013 | g0124 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00639 | hp2 | a0001 | c0001 | t0019 | g0023 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00735 | hp1 | a0001 | c0001 | t0037 | g0019 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01069 | hp2 | a0001 | c0001 | t0015 | g0115 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0130 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01071 | hp1 | a0001 | c0001 | t0015 | g0114 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01106 | hp1 | a0001 | c0001 | t0040 | g0014 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0238 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0123 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01168 | hp1 | a0001 | c0001 | t0018 | g0243 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0201 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0196 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01243 | hp2 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01256 | hp1 | a0001 | c0001 | t0030 | g0232 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0194 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0251 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0195 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01261 | hp1 | a0001 | c0001 | t0039 | g0120 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0339 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01346 | hp1 | a0001 | c0001 | t0063 | g0193 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0334 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0138 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0103 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0307 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01433 | hp2 | a0001 | c0001 | t0014 | g0025 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0132 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0300 | EUR | IBS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01515 | hp2 | a0001 | c0001 | t0007 | g0121 | EUR | IBS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0122 | EUR | IBS | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01884 | hp1 | a0001 | c0001 | t0045 | g0005 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01884 | hp2 | a0001 | c0001 | t0034 | g0305 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01891 | hp2 | a0001 | c0001 | t0029 | g0304 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01934 | hp2 | a0001 | c0001 | t0008 | g0267 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01943 | hp2 | a0001 | c0001 | t0056 | g0247 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0072 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0191 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01981 | hp1 | a0001 | c0001 | t0027 | g0032 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02027 | hp2 | a0001 | c0001 | t0006 | g0197 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02055 | hp2 | a0001 | c0001 | t0031 | g0198 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0295 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02074 | hp1 | a0001 | c0001 | t0036 | g0333 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02129 | hp1 | a0001 | c0001 | t0052 | g0107 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0049 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02145 | hp2 | a0001 | c0001 | t0069 | g0167 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02148 | hp1 | a0001 | c0001 | t0023 | g0060 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | CDX | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02257 | hp1 | a0001 | c0001 | t0055 | g0136 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02257 | hp2 | a0001 | c0001 | t0066 | g0202 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02258 | hp1 | a0001 | c0001 | t0019 | g0022 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02280 | hp1 | a0001 | c0001 | t0031 | g0030 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02280 | hp2 | a0001 | c0001 | t0071 | g0177 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02293 | hp1 | a0001 | c0001 | t0027 | g0061 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02293 | hp2 | a0001 | c0001 | t0046 | g0311 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PEL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0161 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0316 | EAS | KHV | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02572 | hp1 | a0001 | c0001 | t0012 | g0173 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02615 | hp2 | a0001 | c0001 | t0070 | g0170 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02622 | hp2 | a0001 | c0001 | t0017 | g0007 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02630 | hp2 | a0003 | c0003 | t0012 | g0178 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0175 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02647 | hp2 | a0001 | c0001 | t0065 | g0031 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02717 | hp1 | a0001 | c0001 | t0047 | g0057 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0017 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0159 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0268 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02809 | hp1 | a0001 | c0001 | t0032 | g0322 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02809 | hp2 | a0001 | c0001 | t0017 | g0006 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0092 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02895 | hp2 | a0001 | c0001 | t0026 | g0012 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02897 | hp1 | a0001 | c0001 | t0021 | g0166 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02897 | hp2 | a0001 | c0001 | t0026 | g0011 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0047 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02922 | hp2 | a0001 | c0001 | t0012 | g0174 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02965 | hp1 | a0001 | c0001 | t0030 | g0233 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02965 | hp2 | a0001 | c0001 | t0021 | g0168 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02976 | hp1 | a0001 | c0001 | t0067 | g0206 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02976 | hp2 | a0001 | c0001 | t0041 | g0308 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03041 | hp1 | a0001 | c0001 | t0018 | g0240 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03041 | hp2 | a0001 | c0001 | t0021 | g0169 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0109 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03130 | hp1 | a0001 | c0001 | t0011 | g0050 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03139 | hp2 | a0001 | c0001 | t0025 | g0135 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03195 | hp1 | a0001 | c0001 | t0020 | g0204 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0241 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03209 | hp1 | a0001 | c0001 | t0058 | g0015 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0110 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0192 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03453 | hp1 | a0001 | c0001 | t0033 | g0172 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03453 | hp2 | a0001 | c0005 | t0012 | g0179 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03486 | hp1 | a0001 | c0001 | t0049 | g0239 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03486 | hp2 | a0001 | c0001 | t0028 | g0028 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03491 | hp2 | a0001 | c0001 | t0053 | g0089 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0162 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0319 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03516 | hp2 | a0001 | c0001 | t0060 | g0024 | AFR | ESN | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03540 | hp1 | a0001 | c0001 | t0017 | g0010 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03540 | hp2 | a0001 | c0001 | t0020 | g0205 | AFR | GWD | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0260 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03704 | hp2 | a0001 | c0001 | t0035 | g0097 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03710 | hp1 | a0001 | c0001 | t0034 | g0190 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03927 | hp1 | a0001 | c0001 | t0062 | g0200 | SAS | BEB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0329 | SAS | BEB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04115 | hp2 | a0001 | c0001 | t0050 | g0036 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0131 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04204 | hp2 | a0001 | c0001 | t0057 | g0116 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG04228 | hp2 | a0001 | c0001 | t0038 | g0282 | SAS | STU | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18522 | hp1 | a0001 | c0001 | t0043 | g0009 | AFR | YRI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0134 | AFR | YRI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18906 | hp1 | a0001 | c0001 | t0032 | g0323 | AFR | YRI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0242 | AFR | YRI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18947 | hp1 | a0001 | c0001 | t0016 | g0187 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18948 | hp1 | a0001 | c0001 | t0014 | g0150 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18952 | hp2 | a0001 | c0001 | t0015 | g0335 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0337 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18970 | hp1 | a0001 | c0001 | t0014 | g0145 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18971 | hp2 | a0001 | c0001 | t0007 | g0148 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18985 | hp2 | a0001 | c0001 | t0008 | g0045 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18991 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18992 | hp1 | a0001 | c0001 | t0016 | g0165 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18994 | hp1 | a0001 | c0001 | t0016 | g0184 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18998 | hp1 | a0001 | c0001 | t0059 | g0155 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19002 | hp1 | a0001 | c0001 | t0014 | g0151 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19002 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19004 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19007 | hp1 | a0001 | c0001 | t0015 | g0263 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19010 | hp2 | a0001 | c0001 | t0023 | g0281 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19030 | hp2 | a0001 | c0001 | t0042 | g0027 | AFR | LWK | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19055 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19055 | hp2 | a0001 | c0001 | t0008 | g0073 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19056 | hp1 | a0001 | c0001 | t0051 | g0067 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19058 | hp2 | a0001 | c0001 | t0022 | g0147 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0111 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19065 | hp1 | a0001 | c0001 | t0016 | g0185 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19068 | hp1 | a0001 | c0001 | t0028 | g0154 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19085 | hp1 | a0001 | c0001 | t0022 | g0146 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19087 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19240 | hp1 | a0001 | c0001 | t0020 | g0203 | AFR | YRI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0309 | AFR | YRI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20129 | hp1 | a0001 | c0001 | t0064 | g0183 | AFR | ASW | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20129 | hp2 | a0001 | c0001 | t0044 | g0133 | AFR | ASW | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0321 | EUR | TSI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20752 | hp2 | a0001 | c0001 | t0024 | g0129 | EUR | TSI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | TSI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20805 | hp2 | a0001 | c0001 | t0013 | g0127 | EUR | TSI | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02109 | hp1 | a0001 | c0001 | t0019 | g0021 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02486 | hp1 | a0001 | c0001 | t0048 | g0037 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02486 | hp2 | a0001 | c0001 | t0054 | g0137 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG02559 | hp2 | a0002 | c0004 | t0033 | g0171 | AFR | ACB | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0306 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0318 | AFR | MSL | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG06807 | hp1 | a0001 | c0001 | t0029 | g0002 | AFR | USA | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
HG06807 | hp2 | a0001 | c0001 | t0024 | g0125 | AFR | USA | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20300 | hp1 | a0001 | c0001 | t0072 | g0176 | AFR | USA | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA20300 | hp2 | a0001 | c0001 | t0061 | g0231 | AFR | USA | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | LWK | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | LWK | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0128 | REF | REF | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0088 | REF | REF | CAB39_chr2_230707842_230826075 | CAB39 | chr2 | 230707842 | 230826075 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230814050
|
T | A | 1 | a0003 | 1 | HG02630.hp2 | missense_variant&splice_region_variant | MODERATE | c.629T>A | p.Phe210Tyr | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/9 | 1061/3829 | 629/1026 | 210/341 | chr2 | 230814050 | ||
chr2:230818619
|
C | T | 1 | a0002 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.941C>T | p.Thr314Met | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1373/3829 | 941/1026 | 314/341 | chr2 | 230818619 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230790964
|
A | G | 1 | a0001c0005 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.207A>G | p.Gln69Gln | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/9 | 639/3829 | 207/1026 | 69/341 | chr2 | 230790964 | ||
chr2:230798819
|
G | A | 1 | a0001c0002 | 4 | NA18966.hp1 NA18993.hp2 NA19066.hp2 others(1): Show |
synonymous_variant | LOW | c.489G>A | p.Ser163Ser | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/9 | 921/3829 | 489/1026 | 163/341 | chr2 | 230798819 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230712868
|
G | C | 1 | a0001c0001t0035 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-406G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 47134 | chr2 | 230712868 | |||||
chr2:230712947
|
C | G | 24 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(21): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-327C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 47055 | chr2 | 230712947 | |||||
chr2:230712995
|
C | T | 4 | a0001c0001t0019a0001c0001t0030a0001c0001t0060others(1): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-279C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 47007 | chr2 | 230712995 | |||||
chr2:230713031
|
C | A | 2 | a0001c0001t0062a0001c0001t0063 | 2 | HG01346.hp1 HG03927.hp1 |
5_prime_UTR_variant | MODIFIER | c.-243C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 46971 | chr2 | 230713031 | |||||
chr2:230713042
|
C | G | 8 | a0001c0001t0012a0001c0001t0021a0001c0001t0069others(5): Show | 13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-232C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 46960 | chr2 | 230713042 | |||||
chr2:230713078
|
C | G | 1 | a0001c0001t0059 | 1 | NA18998.hp1 | 5_prime_UTR_variant | MODIFIER | c.-196C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 46924 | chr2 | 230713078 | |||||
chr2:230713082
|
G | A | 1 | a0001c0001t0036 | 1 | HG02074.hp1 | 5_prime_UTR_variant | MODIFIER | c.-192G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 46920 | chr2 | 230713082 | |||||
chr2:230713218
|
C | A | 1 | a0001c0001t0037 | 1 | HG00735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/9 | 46784 | chr2 | 230713218 | |||||
chr2:230759970
|
G | A | 1 | a0001c0001t0038 | 1 | HG04228.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/9 | 32 | chr2 | 230759970 | |||||
chr2:230818759
|
A | G | 1 | a0001c0001t0058 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 55 | chr2 | 230818759 | |||||
chr2:230818772
|
CTT | C | 10 | a0001c0001t0005a0001c0001t0007a0001c0001t0008others(7): Show | 44 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*69_*70delTT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 69 | chr2 | 230818772 | |||||
chr2:230818902
|
C | T | 1 | a0001c0001t0018 | 3 | HG01168.hp1 HG03041.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*198C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 198 | chr2 | 230818902 | |||||
chr2:230818906
|
C | G | 2 | a0001c0001t0024a0001c0001t0039 | 3 | HG01261.hp1 HG06807.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*202C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 202 | chr2 | 230818906 | |||||
chr2:230818942
|
G | A | 4 | a0001c0001t0020a0001c0001t0031a0001c0001t0065others(1): Show | 7 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*238G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 238 | chr2 | 230818942 | |||||
chr2:230818975
|
T | C | 1 | a0001c0001t0025 | 2 | HG03139.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*271T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 271 | chr2 | 230818975 | |||||
chr2:230819037
|
C | T | 1 | a0001c0001t0072 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*333C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 333 | chr2 | 230819037 | |||||
chr2:230819057
|
T | C | 11 | a0001c0001t0017a0001c0001t0019a0001c0001t0025others(8): Show | 17 | HG00639.hp2 HG01106.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*353T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 353 | chr2 | 230819057 | |||||
chr2:230819134
|
A | G | 29 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(26): Show | 107 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*430A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 430 | chr2 | 230819134 | |||||
chr2:230819150
|
G | T | 1 | a0001c0001t0027 | 2 | HG01981.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*446G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 446 | chr2 | 230819150 | |||||
chr2:230819184
|
G | A | 24 | a0001c0001t0004a0001c0001t0010a0001c0001t0013others(21): Show | 67 | HG00423.hp1 HG00597.hp1 HG00642.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*480G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 480 | chr2 | 230819184 | |||||
chr2:230819215
|
A | C | 12 | a0001c0001t0009a0001c0001t0011a0001c0001t0026others(9): Show | 24 | HG01243.hp2 HG01891.hp2 HG02451.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*511A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 511 | chr2 | 230819215 | |||||
chr2:230819279
|
A | C | 1 | a0001c0001t0060 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 575 | chr2 | 230819279 | |||||
chr2:230819279
|
A | G | 1 | a0001c0001t0053 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*575A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 575 | chr2 | 230819279 | |||||
chr2:230819332
|
T | C | 3 | a0001c0001t0019a0001c0001t0049a0001c0001t0060 | 5 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*628T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 628 | chr2 | 230819332 | |||||
chr2:230819452
|
A | C | 2 | a0001c0001t0030a0001c0001t0061 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*748A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 748 | chr2 | 230819452 | |||||
chr2:230819689
|
T | C | 3 | a0001c0001t0044a0001c0001t0054a0001c0001t0055 | 3 | HG02257.hp1 HG02486.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*985T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 985 | chr2 | 230819689 | |||||
chr2:230819772
|
A | G | 1 | a0001c0001t0052 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1068 | chr2 | 230819772 | |||||
chr2:230820074
|
T | C | 1 | a0001c0001t0050 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1370 | chr2 | 230820074 | |||||
chr2:230820213
|
G | A | 1 | a0001c0001t0022 | 2 | NA19058.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1509G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1509 | chr2 | 230820213 | |||||
chr2:230820243
|
T | C | 1 | a0001c0001t0018 | 3 | HG01168.hp1 HG03041.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1539T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1539 | chr2 | 230820243 | |||||
chr2:230820483
|
A | G | 28 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(25): Show | 105 | HG00423.hp1 HG00597.hp1 HG01069.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1779A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1779 | chr2 | 230820483 | |||||
chr2:230820490
|
T | C | 28 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(25): Show | 105 | HG00423.hp1 HG00597.hp1 HG01069.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*1786T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1786 | chr2 | 230820490 | |||||
chr2:230820522
|
G | A | 1 | a0001c0001t0056 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1818G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1818 | chr2 | 230820522 | |||||
chr2:230820590
|
C | G | 3 | a0001c0001t0020a0001c0001t0066a0001c0001t0067 | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1886C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 1886 | chr2 | 230820590 | |||||
chr2:230820719
|
A | G | 1 | a0001c0001t0051 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 2015 | chr2 | 230820719 | |||||
chr2:230821070
|
A | C | 1 | a0001c0001t0046 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2366A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 9/9 | 2366 | chr2 | 230821070 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:230713272
|
T | G | 14 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(11): Show | 14 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+42T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713272 | ||||||
chr2:230713423
|
C | T | 18 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0326others(15): Show | 18 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44+193C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713423 | ||||||
chr2:230713446
|
C | T | 2 | a0001c0001t0032g0322a0001c0001t0032g0323 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+216C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713446 | ||||||
chr2:230713498
|
C | T | 1 | a0001c0001t0004g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-44+268C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713498 | ||||||
chr2:230713502
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-44+272C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713502 | ||||||
chr2:230713511
|
T | C | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-44+281T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713511 | ||||||
chr2:230713563
|
G | A | 1 | a0001c0001t0037g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-44+333G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713563 | ||||||
chr2:230713713
|
C | T | 4 | a0001c0001t0001g0317a0001c0001t0001g0320a0001c0001t0009g0319others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+483C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713713 | ||||||
chr2:230713737
|
T | G | 1 | a0001c0001t0004g0020 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-44+507T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713737 | ||||||
chr2:230713752
|
C | G | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0002g0313others(1): Show | 4 | HG02027.hp1 HG02523.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+522C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713752 | ||||||
chr2:230713789
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-44+559G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713789 | ||||||
chr2:230713920
|
C | G | 1 | a0001c0001t0046g0311 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-44+690C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230713920 | ||||||
chr2:230714164
|
A | G | 1 | a0001c0001t0001g0310 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-44+934A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714164 | ||||||
chr2:230714201
|
A | C | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+971A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714201 | ||||||
chr2:230714210
|
G | T | 1 | a0001c0001t0005g0307 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-44+980G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714210 | ||||||
chr2:230714223
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44+993A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714223 | ||||||
chr2:230714291
|
T | A | 22 | a0001c0001t0001g0317a0001c0001t0001g0320a0001c0001t0001g0324others(19): Show | 22 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-44+1061T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714291 | ||||||
chr2:230714347
|
G | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+1117G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714347 | ||||||
chr2:230714354
|
A | G | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+1124A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714354 | ||||||
chr2:230714495
|
G | A | 1 | a0001c0001t0014g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-44+1265G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714495 | ||||||
chr2:230714536
|
A | G | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+1306A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714536 | ||||||
chr2:230714558
|
A | G | 87 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0001g0249others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-44+1328A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714558 | ||||||
chr2:230714745
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0028g0028others(1): Show | 4 | HG02818.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+1515T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714745 | ||||||
chr2:230714890
|
T | C | 1 | a0001c0001t0014g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-44+1660T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714890 | ||||||
chr2:230714966
|
T | C | 6 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0011g0309others(3): Show | 6 | HG02818.hp2 HG02976.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+1736T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230714966 | ||||||
chr2:230715113
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-44+1883T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715113 | ||||||
chr2:230715140
|
C | T | 21 | a0001c0001t0009g0008a0001c0001t0009g0017a0001c0001t0009g0018others(18): Show | 21 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+1910C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715140 | ||||||
chr2:230715222
|
T | C | 3 | a0001c0001t0006g0029a0001c0001t0031g0030a0001c0001t0065g0031 | 3 | HG02280.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-44+1992T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715222 | ||||||
chr2:230715359
|
C | G | 1 | a0001c0001t0012g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-44+2129C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715359 | ||||||
chr2:230715445
|
A | G | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-44+2215A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715445 | ||||||
chr2:230715524
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-44+2294A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715524 | ||||||
chr2:230715675
|
A | G | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-44+2445A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715675 | ||||||
chr2:230715750
|
C | T | 111 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(108): Show | 111 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(108): Show |
intron_variant | MODIFIER | c.-44+2520C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715750 | ||||||
chr2:230715753
|
A | G | 1 | a0001c0001t0003g0236 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-44+2523A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715753 | ||||||
chr2:230715879
|
T | G | 1 | a0001c0001t0027g0032 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-44+2649T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715879 | ||||||
chr2:230715943
|
C | T | 1 | a0001c0001t0018g0243 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-44+2713C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230715943 | ||||||
chr2:230716063
|
T | TA | 3 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0056g0247 | 3 | HG01943.hp2 HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-44+2833_-44+2834i others(3): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716063 | ||||||
chr2:230716100
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-44+2870T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716100 | ||||||
chr2:230716176
|
C | T | 1 | a0001c0001t0003g0235 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-44+2946C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716176 | ||||||
chr2:230716347
|
A | G | 1 | a0001c0001t0003g0234 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-44+3117A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716347 | ||||||
chr2:230716362
|
T | C | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.-44+3132T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716362 | ||||||
chr2:230716379
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01081.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-44+3149G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716379 | ||||||
chr2:230716413
|
C | G | 3 | a0001c0001t0001g0244a0001c0001t0004g0020a0001c0001t0004g0300 | 3 | HG01515.hp1 HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-44+3183C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716413 | ||||||
chr2:230716682
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+3452C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716682 | ||||||
chr2:230716794
|
G | C | 21 | a0001c0001t0009g0008a0001c0001t0009g0017a0001c0001t0009g0018others(18): Show | 21 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+3564G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716794 | ||||||
chr2:230716805
|
C | T | 3 | a0001c0001t0001g0320a0001c0001t0009g0319a0001c0001t0010g0318 | 3 | HG03130.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-44+3575C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230716805 | ||||||
chr2:230717195
|
G | A | 1 | a0001c0001t0016g0165 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-44+3965G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717195 | ||||||
chr2:230717284
|
G | A | 17 | a0001c0001t0012g0173a0001c0001t0012g0174a0001c0001t0012g0175others(14): Show | 17 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44+4054G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717284 | ||||||
chr2:230717426
|
C | T | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+4196C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717426 | ||||||
chr2:230717481
|
G | A | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.-44+4251G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717481 | ||||||
chr2:230717560
|
G | A | 15 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+4330G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717560 | ||||||
chr2:230717583
|
A | C | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-44+4353A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717583 | ||||||
chr2:230717614
|
C | T | 2 | a0001c0001t0019g0023a0001c0001t0060g0024 | 2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-44+4384C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717614 | ||||||
chr2:230717688
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+4458G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717688 | ||||||
chr2:230717698
|
C | G | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-44+4468C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717698 | ||||||
chr2:230717841
|
G | A | 13 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(10): Show | 13 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44+4611G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717841 | ||||||
chr2:230717892
|
G | A | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-44+4662G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717892 | ||||||
chr2:230717984
|
A | C | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-44+4754A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230717984 | ||||||
chr2:230718018
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0028g0028others(1): Show | 4 | HG02818.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+4788T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718018 | ||||||
chr2:230718082
|
T | C | 108 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(105): Show | 108 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(105): Show |
intron_variant | MODIFIER | c.-44+4852T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718082 | ||||||
chr2:230718174
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-44+4944C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718174 | ||||||
chr2:230718472
|
G | C | 4 | a0001c0001t0021g0166a0001c0001t0021g0168a0001c0001t0021g0169others(1): Show | 4 | HG02145.hp2 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5242G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718472 | ||||||
chr2:230718513
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5283A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718513 | ||||||
chr2:230718584
|
T | C | 1 | a0001c0001t0070g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+5354T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718584 | ||||||
chr2:230718875
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-44+5645T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230718875 | ||||||
chr2:230719067
|
T | C | 1 | a0001c0001t0005g0119 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-44+5837T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719067 | ||||||
chr2:230719445
|
C | G | 1 | a0001c0001t0037g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-44+6215C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719445 | ||||||
chr2:230719445
|
C | T | 21 | a0001c0001t0009g0008a0001c0001t0009g0017a0001c0001t0009g0018others(18): Show | 21 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+6215C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719445 | ||||||
chr2:230719620
|
G | T | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+6390G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719620 | ||||||
chr2:230719759
|
C | T | 13 | a0001c0001t0012g0173a0001c0001t0012g0174a0001c0001t0012g0175others(10): Show | 13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44+6529C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719759 | ||||||
chr2:230719981
|
A | G | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+6751A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719981 | ||||||
chr2:230719991
|
C | A | 18 | a0001c0001t0005g0123a0001c0001t0005g0126a0001c0001t0005g0128others(15): Show | 18 | HG00597.hp1 HG01070.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44+6761C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230719991 | ||||||
chr2:230720058
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-44+6828A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720058 | ||||||
chr2:230720162
|
G | A | 1 | a0001c0001t0050g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+6932G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720162 | ||||||
chr2:230720325
|
G | C | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+7095G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720325 | ||||||
chr2:230720344
|
T | C | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0048g0037others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+7114T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720344 | ||||||
chr2:230720368
|
G | A | 2 | a0001c0001t0004g0250a0001c0001t0004g0251 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-44+7138G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720368 | ||||||
chr2:230720474
|
C | T | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-44+7244C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720474 | ||||||
chr2:230720505
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-44+7275G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720505 | ||||||
chr2:230720539
|
G | C | 16 | a0001c0001t0005g0123a0001c0001t0005g0126a0001c0001t0005g0128others(13): Show | 16 | HG00597.hp1 HG01070.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+7309G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720539 | ||||||
chr2:230720607
|
A | G | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-44+7377A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720607 | ||||||
chr2:230720712
|
G | T | 1 | a0001c0001t0018g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-44+7482G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720712 | ||||||
chr2:230720957
|
T | C | 1 | a0001c0001t0041g0308 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+7727T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230720957 | ||||||
chr2:230721022
|
T | G | 1 | a0001c0001t0003g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-44+7792T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721022 | ||||||
chr2:230721023
|
G | T | 1 | a0001c0001t0003g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-44+7793G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721023 | ||||||
chr2:230721166
|
C | T | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-44+7936C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721166 | ||||||
chr2:230721324
|
A | G | 17 | a0001c0001t0005g0123a0001c0001t0005g0126a0001c0001t0005g0128others(14): Show | 17 | HG00597.hp1 HG01070.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-44+8094A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721324 | ||||||
chr2:230721341
|
G | T | 1 | a0001c0001t0032g0323 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+8111G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721341 | ||||||
chr2:230721396
|
G | A | 1 | a0001c0001t0002g0252 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-44+8166G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721396 | ||||||
chr2:230721591
|
A | G | 1 | a0001c0001t0004g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-44+8361A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721591 | ||||||
chr2:230721625
|
T | G | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+8395T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230721625 | ||||||
chr2:230722087
|
A | G | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+8857A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230722087 | ||||||
chr2:230722173
|
G | A | 15 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+8943G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230722173 | ||||||
chr2:230722393
|
G | A | 19 | a0001c0001t0005g0123a0001c0001t0005g0126a0001c0001t0005g0128others(16): Show | 19 | HG00597.hp1 HG01070.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44+9163G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230722393 | ||||||
chr2:230722571
|
T | C | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG00733.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-44+9341T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230722571 | ||||||
chr2:230722693
|
T | C | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-44+9463T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230722693 | ||||||
chr2:230722943
|
C | T | 9 | a0001c0001t0003g0180a0001c0001t0003g0221a0001c0001t0003g0222others(6): Show | 9 | NA18951.hp1 NA18952.hp1 NA18962.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+9713C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230722943 | ||||||
chr2:230723002
|
T | G | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+9772T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723002 | ||||||
chr2:230723058
|
A | G | 1 | a0001c0001t0003g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-44+9828A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723058 | ||||||
chr2:230723112
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-44+9882T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723112 | ||||||
chr2:230723394
|
G | T | 97 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(94): Show | 97 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(94): Show |
intron_variant | MODIFIER | c.-44+10164G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723394 | ||||||
chr2:230723484
|
T | C | 5 | a0001c0001t0001g0026a0001c0001t0011g0309a0001c0001t0028g0028others(2): Show | 5 | HG02818.hp2 HG02976.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+10254T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723484 | ||||||
chr2:230723572
|
C | G | 15 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(12): Show | 15 | HG02129.hp2 NA18943.hp1 NA18966.hp2 others(12): Show |
intron_variant | MODIFIER | c.-44+10342C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723572 | ||||||
chr2:230723585
|
C | T | 3 | a0001c0001t0015g0114a0001c0001t0015g0115a0001c0001t0057g0116 | 3 | HG01069.hp2 HG01071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-44+10355C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723585 | ||||||
chr2:230723667
|
C | T | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-44+10437C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723667 | ||||||
chr2:230723919
|
G | A | 26 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(23): Show | 26 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-44+10689G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230723919 | ||||||
chr2:230723930
|
A | AT | 8 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(5): Show | 8 | HG00639.hp2 HG01256.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+10701dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230723930 | |||||
chr2:230724171
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-44+10941C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724171 | ||||||
chr2:230724244
|
C | T | 2 | a0001c0001t0005g0131a0001c0001t0005g0132 | 2 | HG01496.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-44+11014C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724244 | ||||||
chr2:230724244
|
CA | C | 90 | a0001c0001t0001g0112a0001c0001t0002g0299a0001c0001t0003g0180others(87): Show | 90 | HG00099.hp2 HG00639.hp2 HG01109.hp2 others(87): Show |
intron_variant | MODIFIER | c.-44+11029delA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724244 | |||||
chr2:230724244
|
CAA | C | 17 | a0001c0001t0002g0306a0001c0001t0003g0227a0001c0001t0003g0235others(14): Show | 17 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-44+11028_-44+1102 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724244 | |||||
chr2:230724353
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-44+11123T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724353 | ||||||
chr2:230724410
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-44+11180G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724410 | ||||||
chr2:230724462
|
A | T | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-44+11232A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724462 | ||||||
chr2:230724480
|
G | A | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+11250G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724480 | ||||||
chr2:230724534
|
A | C | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-44+11304A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724534 | ||||||
chr2:230724677
|
C | T | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0048g0037others(2): Show | 5 | HG02257.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+11447C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724677 | ||||||
chr2:230724703
|
C | CA | 63 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(60): Show | 63 | HG00597.hp1 HG00642.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.-44+11492dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724703 | |||||
chr2:230724703
|
C | CAA | 8 | a0001c0001t0013g0139a0001c0001t0025g0135a0001c0001t0029g0304others(5): Show | 8 | HG00423.hp1 HG01261.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+11491_-44+1149 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724703 | |||||
chr2:230724703
|
C | CAAA | 14 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0011g0003others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+11490_-44+1149 others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724703 | |||||
chr2:230724703
|
CA | C | 9 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(6): Show | 9 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+11492delA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724703 | |||||
chr2:230724719
|
A | AC | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+11489_-44+1149 others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724719 | ||||||
chr2:230724743
|
C | T | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+11513C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724743 | ||||||
chr2:230724751
|
C | CT | 21 | a0001c0001t0001g0325a0001c0001t0001g0340a0001c0001t0001g0341others(18): Show | 21 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-44+11539dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724751 | |||||
chr2:230724751
|
CT | C | 25 | a0001c0001t0001g0026a0001c0001t0001g0157a0001c0001t0001g0326others(22): Show | 25 | HG00639.hp2 HG01256.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.-44+11539delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230724751 | |||||
chr2:230724844
|
G | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+11614G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724844 | ||||||
chr2:230724888
|
C | T | 19 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0288others(16): Show | 19 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44+11658C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724888 | ||||||
chr2:230724889
|
G | A | 15 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+11659G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230724889 | ||||||
chr2:230725030
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0002g0286 | 2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-44+11800C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725030 | ||||||
chr2:230725061
|
C | A | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+11831C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725061 | ||||||
chr2:230725158
|
G | A | 3 | a0001c0001t0016g0165a0001c0001t0016g0184a0001c0001t0016g0185 | 3 | NA18992.hp1 NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-44+11928G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725158 | ||||||
chr2:230725169
|
G | A | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+11939G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725169 | ||||||
chr2:230725193
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-44+11963C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725193 | ||||||
chr2:230725225
|
C | T | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+11995C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725225 | ||||||
chr2:230725300
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-44+12070T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725300 | ||||||
chr2:230725381
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-44+12151C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725381 | ||||||
chr2:230725397
|
T | A | 12 | a0001c0001t0001g0255a0001c0001t0001g0261a0001c0001t0001g0264others(9): Show | 12 | HG00408.hp1 HG01934.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+12167T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725397 | ||||||
chr2:230725470
|
C | T | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-44+12240C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725470 | ||||||
chr2:230725649
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-44+12419G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725649 | ||||||
chr2:230725695
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-44+12465T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725695 | ||||||
chr2:230725768
|
G | T | 1 | a0001c0001t0002g0285 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-44+12538G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725768 | ||||||
chr2:230725940
|
C | T | 8 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(5): Show | 8 | HG00639.hp2 HG01256.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+12710C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230725940 | ||||||
chr2:230726051
|
A | G | 1 | a0001c0001t0012g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-44+12821A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726051 | ||||||
chr2:230726066
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-44+12836T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726066 | ||||||
chr2:230726140
|
T | C | 14 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(11): Show | 14 | NA18947.hp1 NA18951.hp1 NA18952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+12910T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726140 | ||||||
chr2:230726170
|
AT | A | 16 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(13): Show | 16 | HG02129.hp2 NA18522.hp2 NA18943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+12951delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230726170 | |||||
chr2:230726338
|
AT | A | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+13119delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230726338 | |||||
chr2:230726488
|
A | G | 1 | a0001c0001t0052g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-44+13258A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726488 | ||||||
chr2:230726722
|
C | T | 1 | a0001c0001t0003g0236 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-44+13492C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726722 | ||||||
chr2:230726729
|
A | G | 45 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.-44+13499A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726729 | ||||||
chr2:230726925
|
G | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+13695G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230726925 | ||||||
chr2:230727007
|
G | C | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+13777G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727007 | ||||||
chr2:230727027
|
C | T | 3 | a0001c0001t0006g0029a0001c0001t0031g0030a0001c0001t0065g0031 | 3 | HG02280.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-44+13797C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727027 | ||||||
chr2:230727184
|
A | G | 4 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0028g0028others(1): Show | 4 | HG02818.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+13954A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727184 | ||||||
chr2:230727219
|
A | G | 1 | a0001c0001t0004g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-44+13989A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727219 | ||||||
chr2:230727225
|
A | C | 6 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0310others(3): Show | 6 | HG00423.hp2 HG00673.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+13995A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727225 | ||||||
chr2:230727231
|
TTAAA | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+14004_-44+1400 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727231 | |||||
chr2:230727363
|
C | CGT | 38 | a0001c0001t0001g0001a0001c0001t0001g0040a0001c0001t0001g0051others(35): Show | 39 | HG00140.hp1 HG00642.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.-44+14168_-44+1416 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGT | 21 | a0001c0001t0001g0095a0001c0001t0001g0098a0001c0001t0001g0099others(18): Show | 21 | HG00140.hp2 HG01069.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-44+14166_-44+1416 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGT | 9 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0106others(6): Show | 9 | HG01106.hp2 HG01361.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+14164_-44+1416 others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0011g0050others(5): Show | 8 | HG00733.hp1 HG01891.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+14162_-44+1416 others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGTG others(3): Show |
6 | a0001c0001t0011g0003a0001c0001t0018g0240a0001c0001t0018g0243others(3): Show | 6 | HG01168.hp1 HG01884.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+14160_-44+1416 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGTG others(5): Show |
6 | a0001c0001t0009g0241a0001c0001t0017g0006a0001c0001t0028g0028others(3): Show | 6 | HG01884.hp1 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+14158_-44+1416 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGTG others(7): Show |
3 | a0001c0001t0010g0013a0001c0001t0017g0007a0001c0001t0029g0002 | 3 | HG02615.hp1 HG02622.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-44+14156_-44+1416 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGTG others(9): Show |
5 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0017g0010others(2): Show | 5 | HG01106.hp1 HG03471.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+14154_-44+1416 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
C | CGTGTGTG others(11): Show |
2 | a0001c0001t0026g0011a0001c0001t0026g0012 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-44+14152_-44+1416 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
CGT | C | 84 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0038others(81): Show | 84 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.-44+14168_-44+1416 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
CGTGT | C | 36 | a0001c0001t0001g0317a0001c0001t0001g0324a0001c0001t0001g0326others(33): Show | 36 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44+14166_-44+1416 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
CGTGTGT | C | 23 | a0001c0001t0001g0327a0001c0001t0002g0054a0001c0001t0005g0119others(20): Show | 23 | HG00423.hp1 HG01109.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-44+14164_-44+1416 others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-44+14160_-44+1416 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0001g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-44+14158_-44+1416 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727363
|
CGTGTGTG others(11): Show |
C | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+14152_-44+1416 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727363 | |||||
chr2:230727398
|
G | GTGTGTGT others(11): Show |
3 | a0001c0001t0019g0021a0001c0001t0019g0023a0001c0001t0060g0024 | 3 | HG00639.hp2 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44+14169_-44+1417 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727398 | |||||
chr2:230727398
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0061g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-44+14169_-44+1417 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727398 | |||||
chr2:230727398
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0030g0232a0001c0001t0030g0233 | 2 | HG01256.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-44+14169_-44+1417 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727398 | |||||
chr2:230727398
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0019g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-44+14169_-44+1417 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727398 | |||||
chr2:230727400
|
A | G | 5 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0004others(2): Show | 5 | HG01243.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+14170A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727400 | ||||||
chr2:230727400
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-44+14170A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727400 | ||||||
chr2:230727402
|
T | A | 4 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0047others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+14172T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727402 | ||||||
chr2:230727410
|
C | T | 4 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0047others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+14180C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727410 | ||||||
chr2:230727416
|
C | CT | 9 | a0001c0001t0015g0114a0001c0001t0015g0115a0001c0001t0018g0240others(6): Show | 9 | HG01069.hp2 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44+14202dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230727416 | |||||
chr2:230727469
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-44+14239C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727469 | ||||||
chr2:230727471
|
G | A | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+14241G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727471 | ||||||
chr2:230727496
|
C | T | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+14266C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727496 | ||||||
chr2:230727517
|
T | C | 4 | a0001c0001t0032g0322a0001c0001t0032g0323a0001c0001t0033g0172others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+14287T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727517 | ||||||
chr2:230727669
|
C | T | 15 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+14439C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727669 | ||||||
chr2:230727748
|
G | A | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-44+14518G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727748 | ||||||
chr2:230727780
|
G | A | 34 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-44+14550G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727780 | ||||||
chr2:230727833
|
C | T | 1 | a0001c0001t0038g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-44+14603C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727833 | ||||||
chr2:230727974
|
C | T | 5 | a0001c0001t0002g0278a0001c0001t0002g0285a0001c0001t0002g0299others(2): Show | 5 | NA18939.hp2 NA18975.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+14744C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230727974 | ||||||
chr2:230728005
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+14775G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728005 | ||||||
chr2:230728097
|
G | C | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+14867G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728097 | ||||||
chr2:230728112
|
G | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-44+14882G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728112 | ||||||
chr2:230728134
|
C | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0266 | 2 | HG02523.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-44+14904C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728134 | ||||||
chr2:230728152
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0002g0056 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-44+14922T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728152 | ||||||
chr2:230728232
|
C | T | 1 | a0001c0001t0004g0294 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-44+15002C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728232 | ||||||
chr2:230728239
|
A | AAAAT | 44 | a0001c0001t0002g0338a0001c0001t0005g0119a0001c0001t0005g0123others(41): Show | 44 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-44+15033_-44+1503 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230728239 | |||||
chr2:230728239
|
A | AAAATAAA others(1): Show |
4 | a0001c0001t0007g0121a0001c0001t0007g0122a0001c0001t0039g0120others(1): Show | 4 | HG01261.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+15029_-44+1503 others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230728239 | |||||
chr2:230728239
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0019g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-44+15025_-44+1503 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230728239 | |||||
chr2:230728239
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0019g0021 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+15021_-44+1503 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230728239 | |||||
chr2:230728262
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-44+15032A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728262 | ||||||
chr2:230728317
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-44+15087C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728317 | ||||||
chr2:230728341
|
A | G | 21 | a0001c0001t0009g0008a0001c0001t0009g0017a0001c0001t0009g0018others(18): Show | 21 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+15111A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728341 | ||||||
chr2:230728350
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-44+15120A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728350 | ||||||
chr2:230728541
|
A | G | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-44+15311A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728541 | ||||||
chr2:230728577
|
T | C | 6 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0001g0163others(3): Show | 6 | HG00140.hp2 HG01069.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+15347T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728577 | ||||||
chr2:230728625
|
T | A | 6 | a0001c0001t0012g0173a0001c0001t0012g0174a0001c0001t0012g0175others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+15395T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728625 | ||||||
chr2:230728757
|
G | A | 1 | a0001c0001t0002g0313 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-44+15527G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728757 | ||||||
chr2:230728798
|
A | C | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+15568A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728798 | ||||||
chr2:230728884
|
A | T | 1 | a0001c0001t0028g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-44+15654A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728884 | ||||||
chr2:230728908
|
C | T | 3 | a0001c0001t0015g0114a0001c0001t0015g0115a0001c0001t0057g0116 | 3 | HG01069.hp2 HG01071.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-44+15678C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230728908 | ||||||
chr2:230729048
|
CAATT | C | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+15822_-44+1582 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230729048 | |||||
chr2:230729205
|
C | T | 4 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0047others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+15975C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729205 | ||||||
chr2:230729317
|
G | C | 2 | a0001c0001t0001g0102a0001c0001t0004g0103 | 2 | HG01106.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-44+16087G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729317 | ||||||
chr2:230729318
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0004g0020a0001c0001t0004g0300 | 3 | HG01515.hp1 HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-44+16088T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729318 | ||||||
chr2:230729374
|
A | G | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+16144A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729374 | ||||||
chr2:230729679
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-44+16449G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729679 | ||||||
chr2:230729922
|
A | G | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+16692A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729922 | ||||||
chr2:230729989
|
G | A | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+16759G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230729989 | ||||||
chr2:230730220
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-44+16990C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730220 | ||||||
chr2:230730265
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-44+17035C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730265 | ||||||
chr2:230730352
|
G | A | 1 | a0001c0001t0039g0120 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-44+17122G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730352 | ||||||
chr2:230730445
|
CT | C | 240 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0051others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.-44+17231delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230730445 | |||||
chr2:230730707
|
G | A | 1 | a0001c0002t0001g0059 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-44+17477G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730707 | ||||||
chr2:230730739
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+17509C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730739 | ||||||
chr2:230730767
|
T | C | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+17537T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730767 | ||||||
chr2:230730898
|
T | C | 3 | a0001c0001t0001g0320a0001c0001t0009g0319a0001c0001t0010g0318 | 3 | HG03130.hp2 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-44+17668T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730898 | ||||||
chr2:230730929
|
C | T | 23 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0051others(20): Show | 23 | HG00733.hp1 HG01069.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.-44+17699C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730929 | ||||||
chr2:230730945
|
A | G | 8 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(5): Show | 8 | HG00639.hp2 HG01256.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+17715A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230730945 | ||||||
chr2:230731113
|
A | C | 4 | a0001c0001t0005g0119a0001c0001t0005g0152a0001c0001t0005g0153others(1): Show | 4 | HG00423.hp1 NA18944.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+17883A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731113 | ||||||
chr2:230731235
|
C | A | 1 | a0001c0001t0036g0333 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-44+18005C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731235 | ||||||
chr2:230731289
|
G | A | 1 | a0001c0001t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-44+18059G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731289 | ||||||
chr2:230731357
|
T | G | 132 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(129): Show | 132 | HG00099.hp2 HG00597.hp1 HG00639.hp2 others(129): Show |
intron_variant | MODIFIER | c.-44+18127T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731357 | ||||||
chr2:230731463
|
T | C | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+18233T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731463 | ||||||
chr2:230731591
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+18361C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731591 | ||||||
chr2:230731592
|
G | A | 1 | a0001c0001t0004g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-44+18362G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731592 | ||||||
chr2:230731634
|
C | T | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-44+18404C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731634 | ||||||
chr2:230731673
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-44+18443A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731673 | ||||||
chr2:230731687
|
C | T | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-44+18457C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731687 | ||||||
chr2:230731735
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG02040.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-44+18505A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230731735 | ||||||
chr2:230732083
|
T | C | 1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-44+18853T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732083 | ||||||
chr2:230732106
|
G | T | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+18876G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732106 | ||||||
chr2:230732134
|
G | T | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+18904G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732134 | ||||||
chr2:230732167
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+18937C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732167 | ||||||
chr2:230732239
|
G | A | 36 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-44+19009G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732239 | ||||||
chr2:230732240
|
C | T | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+19010C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732240 | ||||||
chr2:230732267
|
G | A | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-44+19037G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732267 | ||||||
chr2:230732358
|
T | C | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-44+19128T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732358 | ||||||
chr2:230732381
|
C | T | 2 | a0001c0001t0001g0078a0001c0001t0001g0112 | 2 | NA18992.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-44+19151C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732381 | ||||||
chr2:230732437
|
C | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-44+19207C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732437 | ||||||
chr2:230732717
|
T | C | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+19487T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732717 | ||||||
chr2:230732745
|
G | T | 15 | a0001c0001t0009g0008a0001c0001t0010g0013a0001c0001t0011g0003others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+19515G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230732745 | ||||||
chr2:230733011
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0259 | 2 | NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-44+19781T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733011 | ||||||
chr2:230733148
|
G | A | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.-44+19918G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733148 | ||||||
chr2:230733183
|
A | G | 1 | a0001c0001t0003g0216 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-44+19953A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733183 | ||||||
chr2:230733233
|
A | G | 1 | a0001c0001t0070g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44+20003A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733233 | ||||||
chr2:230733303
|
C | A | 1 | a0001c0001t0047g0057 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-44+20073C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733303 | ||||||
chr2:230733306
|
C | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+20076C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733306 | ||||||
chr2:230733328
|
A | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+20098A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733328 | ||||||
chr2:230733358
|
G | A | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+20128G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733358 | ||||||
chr2:230733671
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-44+20441A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733671 | ||||||
chr2:230733763
|
C | A | 1 | a0001c0001t0004g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-44+20533C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230733763 | ||||||
chr2:230734142
|
T | C | 1 | a0001c0001t0014g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-44+20912T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734142 | ||||||
chr2:230734238
|
T | G | 2 | a0001c0001t0030g0232a0001c0001t0061g0231 | 2 | HG01256.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-44+21008T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734238 | ||||||
chr2:230734326
|
G | A | 36 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-44+21096G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734326 | ||||||
chr2:230734422
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+21192G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734422 | ||||||
chr2:230734427
|
G | A | 1 | a0001c0001t0016g0187 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-44+21197G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734427 | ||||||
chr2:230734567
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-44+21337C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734567 | ||||||
chr2:230734604
|
T | G | 1 | a0001c0001t0041g0308 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+21374T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734604 | ||||||
chr2:230734805
|
C | CT | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-44+21575_-44+2157 others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734805 | ||||||
chr2:230734932
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-44+21702C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230734932 | ||||||
chr2:230735198
|
G | A | 2 | a0001c0001t0002g0246a0001c0001t0004g0055 | 2 | HG01952.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-44+21968G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735198 | ||||||
chr2:230735316
|
G | C | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-44+22086G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735316 | ||||||
chr2:230735366
|
C | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0053a0001c0001t0001g0077others(3): Show | 6 | HG01981.hp2 HG02300.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+22136C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735366 | ||||||
chr2:230735387
|
G | T | 2 | a0001c0001t0033g0172a0002c0004t0033g0171 | 2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-44+22157G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735387 | ||||||
chr2:230735419
|
G | A | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-44+22189G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735419 | ||||||
chr2:230735451
|
G | A | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+22221G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735451 | ||||||
chr2:230735969
|
T | C | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+22739T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230735969 | ||||||
chr2:230736169
|
C | A | 1 | a0001c0001t0066g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-44+22939C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736169 | ||||||
chr2:230736318
|
G | A | 1 | a0001c0001t0029g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-44+23088G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736318 | ||||||
chr2:230736410
|
G | A | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-44+23180G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736410 | ||||||
chr2:230736412
|
C | T | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-44+23182C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736412 | ||||||
chr2:230736449
|
G | A | 2 | a0001c0001t0040g0014a0001c0001t0045g0005 | 2 | HG01106.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-44+23219G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736449 | ||||||
chr2:230736536
|
G | A | 1 | a0001c0001t0048g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-44+23306G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736536 | ||||||
chr2:230736871
|
A | G | 2 | a0001c0001t0011g0003a0001c0001t0011g0004 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-43-23088A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230736871 | ||||||
chr2:230737128
|
A | G | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-22831A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737128 | ||||||
chr2:230737149
|
A | G | 2 | a0001c0001t0014g0150a0001c0001t0014g0151 | 2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-43-22810A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737149 | ||||||
chr2:230737378
|
C | T | 2 | a0001c0001t0003g0215a0001c0001t0003g0219 | 2 | NA19084.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-43-22581C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737378 | ||||||
chr2:230737423
|
G | A | 340 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-43-22536G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737423 | ||||||
chr2:230737497
|
G | T | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-22462G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737497 | ||||||
chr2:230737572
|
C | T | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-22387C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737572 | ||||||
chr2:230737622
|
A | G | 1 | a0001c0001t0042g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-22337A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737622 | ||||||
chr2:230737667
|
A | G | 1 | a0001c0001t0005g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-43-22292A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737667 | ||||||
chr2:230737766
|
A | C | 1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43-22193A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737766 | ||||||
chr2:230737982
|
C | T | 1 | a0001c0001t0011g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-43-21977C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230737982 | ||||||
chr2:230738040
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-43-21919T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230738040 | ||||||
chr2:230738138
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-43-21821G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230738138 | ||||||
chr2:230738144
|
G | T | 2 | a0001c0001t0006g0196a0001c0001t0006g0201 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-43-21815G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230738144 | ||||||
chr2:230738468
|
G | C | 1 | a0001c0001t0053g0089 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-43-21491G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230738468 | ||||||
chr2:230739356
|
G | A | 1 | a0001c0001t0009g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-20603G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739356 | ||||||
chr2:230739380
|
G | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | NA19054.hp2 NA19058.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-43-20579G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739380 | ||||||
chr2:230739635
|
C | T | 10 | a0001c0001t0003g0191a0001c0001t0006g0192a0001c0001t0006g0194others(7): Show | 10 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-20324C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739635 | ||||||
chr2:230739722
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-43-20237G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739722 | ||||||
chr2:230739728
|
G | A | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-20231G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739728 | ||||||
chr2:230739820
|
A | G | 1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43-20139A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739820 | ||||||
chr2:230739839
|
G | A | 2 | a0001c0001t0001g0314a0001c0001t0002g0313 | 2 | NA18967.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-43-20120G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739839 | ||||||
chr2:230739920
|
A | G | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-20039A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739920 | ||||||
chr2:230739949
|
T | G | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-43-20010T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739949 | ||||||
chr2:230739983
|
T | C | 1 | a0001c0001t0071g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-43-19976T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230739983 | ||||||
chr2:230740011
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-19948G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230740011 | ||||||
chr2:230740468
|
C | A | 4 | a0001c0001t0001g0317a0001c0001t0001g0320a0001c0001t0009g0319others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-19491C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230740468 | ||||||
chr2:230740672
|
G | A | 1 | a0001c0001t0048g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-43-19287G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230740672 | ||||||
chr2:230740969
|
A | T | 2 | a0001c0001t0020g0205a0001c0001t0067g0206 | 2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-43-18990A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230740969 | ||||||
chr2:230741036
|
G | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-18923G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741036 | ||||||
chr2:230741117
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-18842G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741117 | ||||||
chr2:230741262
|
C | T | 1 | a0001c0001t0017g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-43-18697C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741262 | ||||||
chr2:230741368
|
G | A | 37 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(34): Show | 37 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.-43-18591G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741368 | ||||||
chr2:230741417
|
T | A | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-18542T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741417 | ||||||
chr2:230741484
|
A | G | 1 | a0001c0001t0007g0316 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-43-18475A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741484 | ||||||
chr2:230741642
|
T | A | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-18317T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741642 | ||||||
chr2:230741653
|
T | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-18306T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741653 | ||||||
chr2:230741659
|
C | T | 7 | a0001c0001t0001g0058a0001c0001t0001g0328a0001c0001t0001g0330others(4): Show | 7 | HG00558.hp1 HG02074.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-18300C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741659 | ||||||
chr2:230741822
|
A | G | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-43-18137A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230741822 | ||||||
chr2:230742155
|
T | TTTTG | 3 | a0001c0001t0004g0020a0001c0001t0010g0260a0001c0001t0043g0009 | 3 | HG03669.hp1 HG03669.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-43-17772_-43-1776 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230742155 | |||||
chr2:230742155
|
TTTTG | T | 137 | a0001c0001t0001g0038a0001c0001t0001g0051a0001c0001t0001g0053others(134): Show | 137 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-43-17772_-43-1776 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230742155 | |||||
chr2:230742155
|
TTTTGTTT others(5): Show |
T | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-17780_-43-1776 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230742155 | |||||
chr2:230742260
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-43-17699C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742260 | ||||||
chr2:230742276
|
G | A | 1 | a0001c0001t0012g0238 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-43-17683G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742276 | ||||||
chr2:230742392
|
G | A | 1 | a0001c0001t0014g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-43-17567G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742392 | ||||||
chr2:230742421
|
C | T | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-17538C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742421 | ||||||
chr2:230742558
|
C | CA | 28 | a0001c0001t0001g0041a0001c0001t0001g0244a0001c0001t0001g0265others(25): Show | 28 | HG01109.hp2 HG01168.hp1 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.-43-17382dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230742558 | |||||
chr2:230742558
|
CA | C | 10 | a0001c0001t0002g0299a0001c0001t0002g0303a0001c0001t0003g0236others(7): Show | 10 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-17382delA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230742558 | |||||
chr2:230742577
|
AT | A | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-17381delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742577 | ||||||
chr2:230742701
|
A | T | 1 | a0001c0001t0007g0316 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-43-17258A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742701 | ||||||
chr2:230742850
|
AG | A | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-43-17108delG | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742850 | ||||||
chr2:230742925
|
C | CT | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-17031dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230742925 | |||||
chr2:230742989
|
C | A | 108 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(105): Show | 108 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(105): Show |
intron_variant | MODIFIER | c.-43-16970C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230742989 | ||||||
chr2:230743260
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-43-16699G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743260 | ||||||
chr2:230743284
|
G | A | 1 | a0001c0001t0001g0340 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-43-16675G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743284 | ||||||
chr2:230743337
|
G | A | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-43-16622G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743337 | ||||||
chr2:230743339
|
C | T | 3 | a0001c0001t0002g0284a0001c0001t0025g0134a0001c0001t0025g0135 | 3 | HG03139.hp2 NA18522.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-43-16620C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743339 | ||||||
chr2:230743447
|
G | A | 1 | a0001c0001t0002g0090 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-43-16512G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743447 | ||||||
chr2:230743453
|
A | G | 1 | a0001c0001t0002g0339 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-43-16506A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743453 | ||||||
chr2:230743591
|
A | G | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-16368A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743591 | ||||||
chr2:230743844
|
T | C | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-43-16115T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743844 | ||||||
chr2:230743916
|
C | CT | 90 | a0001c0001t0001g0026a0001c0001t0001g0085a0001c0001t0001g0266others(87): Show | 90 | HG00099.hp2 HG01109.hp2 HG01168.hp1 others(87): Show |
intron_variant | MODIFIER | c.-43-16022dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230743916 | |||||
chr2:230743916
|
C | CTT | 7 | a0001c0001t0009g0241a0001c0001t0019g0021a0001c0001t0019g0022others(4): Show | 7 | HG01256.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-16023_-43-1602 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230743916 | |||||
chr2:230743916
|
C | T | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-16043C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743916 | ||||||
chr2:230743916
|
CT | C | 13 | a0001c0001t0001g0042a0001c0001t0001g0079a0001c0001t0001g0265others(10): Show | 13 | HG01515.hp1 HG01934.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-16022delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230743916 | |||||
chr2:230743937
|
T | A | 1 | a0001c0001t0004g0295 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-43-16022T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230743937 | ||||||
chr2:230744033
|
C | G | 1 | a0001c0001t0013g0139 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-43-15926C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744033 | ||||||
chr2:230744228
|
A | G | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-15731A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744228 | ||||||
chr2:230744357
|
G | A | 1 | a0001c0001t0005g0123 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-43-15602G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744357 | ||||||
chr2:230744362
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-43-15597C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744362 | ||||||
chr2:230744535
|
G | A | 96 | a0001c0001t0001g0026a0001c0001t0001g0081a0001c0001t0002g0306others(93): Show | 96 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(93): Show |
intron_variant | MODIFIER | c.-43-15424G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744535 | ||||||
chr2:230744565
|
T | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-15394T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744565 | ||||||
chr2:230744698
|
A | G | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-43-15261A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230744698 | ||||||
chr2:230745003
|
T | G | 1 | a0001c0001t0050g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-43-14956T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745003 | ||||||
chr2:230745015
|
A | G | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-14944A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745015 | ||||||
chr2:230745042
|
T | A | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43-14917T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745042 | ||||||
chr2:230745077
|
A | T | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43-14882A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745077 | ||||||
chr2:230745110
|
C | T | 3 | a0001c0001t0001g0297a0001c0001t0002g0296a0001c0001t0004g0295 | 3 | HG00423.hp2 HG00673.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-43-14849C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745110 | ||||||
chr2:230745264
|
G | A | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-14695G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745264 | ||||||
chr2:230745456
|
C | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-14503C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745456 | ||||||
chr2:230745642
|
C | T | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-14317C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745642 | ||||||
chr2:230745659
|
G | A | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43-14300G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745659 | ||||||
chr2:230745768
|
A | G | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-14191A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745768 | ||||||
chr2:230745784
|
G | A | 1 | a0001c0001t0009g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-14175G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745784 | ||||||
chr2:230745815
|
C | T | 1 | a0001c0001t0014g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-43-14144C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745815 | ||||||
chr2:230745816
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0061g0231 | 2 | HG00099.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-14143G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745816 | ||||||
chr2:230745867
|
C | T | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-43-14092C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745867 | ||||||
chr2:230745872
|
G | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-14087G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745872 | ||||||
chr2:230745916
|
G | T | 1 | a0001c0001t0001g0340 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-43-14043G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745916 | ||||||
chr2:230745948
|
T | A | 3 | a0001c0001t0020g0203a0001c0001t0034g0190a0001c0001t0068g0199 | 3 | HG00099.hp2 HG03710.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-14011T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745948 | ||||||
chr2:230745949
|
T | G | 1 | a0001c0001t0023g0281 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-43-14010T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230745949 | ||||||
chr2:230746279
|
G | A | 1 | a0001c0001t0027g0032 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-43-13680G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746279 | ||||||
chr2:230746342
|
G | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-13617G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746342 | ||||||
chr2:230746371
|
A | C | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-13588A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746371 | ||||||
chr2:230746385
|
C | CCAGTTTA others(21): Show |
1 | a0001c0001t0026g0011 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-43-13572_-43-1354 others(32): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230746385 | |||||
chr2:230746426
|
T | C | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-43-13533T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746426 | ||||||
chr2:230746467
|
T | G | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-43-13492T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746467 | ||||||
chr2:230746670
|
C | T | 1 | a0001c0001t0035g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-43-13289C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746670 | ||||||
chr2:230746966
|
A | G | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-12993A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230746966 | ||||||
chr2:230747078
|
A | C | 249 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0042others(246): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-43-12881A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230747078 | ||||||
chr2:230747140
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-43-12819G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230747140 | ||||||
chr2:230747185
|
A | G | 1 | a0001c0001t0050g0036 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-43-12774A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230747185 | ||||||
chr2:230747515
|
A | G | 152 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(149): Show | 152 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(149): Show |
intron_variant | MODIFIER | c.-43-12444A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230747515 | ||||||
chr2:230747939
|
G | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-12020G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230747939 | ||||||
chr2:230748222
|
A | G | 91 | a0001c0001t0002g0306a0001c0001t0003g0180a0001c0001t0003g0181others(88): Show | 91 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(88): Show |
intron_variant | MODIFIER | c.-43-11737A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748222 | ||||||
chr2:230748300
|
T | C | 340 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-43-11659T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748300 | ||||||
chr2:230748425
|
C | G | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-11534C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748425 | ||||||
chr2:230748426
|
G | A | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.-43-11533G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748426 | ||||||
chr2:230748612
|
C | T | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-11347C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748612 | ||||||
chr2:230748717
|
G | T | 1 | a0001c0001t0059g0155 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-43-11242G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748717 | ||||||
chr2:230748812
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-11147A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748812 | ||||||
chr2:230748813
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-11146G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748813 | ||||||
chr2:230748813
|
G | GA | 7 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0095others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-11127dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748813 | |||||
chr2:230748813
|
G | GAA | 10 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 10 | HG00733.hp1 HG01517.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-11128_-43-1112 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748813 | |||||
chr2:230748821
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-43-11138_-43-1113 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748821 | ||||||
chr2:230748823
|
A | T | 1 | a0001c0001t0001g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-43-11136A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748823 | ||||||
chr2:230748824
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0003g0214 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-43-11133_-43-1111 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748824 | |||||
chr2:230748825
|
A | AATATATA others(13): Show |
1 | a0001c0001t0002g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-43-11133_-43-1113 others(24): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748825 | |||||
chr2:230748825
|
A | T | 1 | a0001c0001t0001g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-43-11134A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748825 | ||||||
chr2:230748825
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0028g0028 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-43-11132_-43-1112 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748825 | |||||
chr2:230748825
|
AAAAAAAA others(7): Show |
A | 3 | a0001c0001t0016g0165a0001c0001t0016g0184a0001c0001t0016g0185 | 3 | NA18992.hp1 NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-43-11132_-43-1111 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748825 | |||||
chr2:230748825
|
AAAAAAAA others(9): Show |
A | 8 | a0001c0001t0003g0218a0001c0001t0012g0173a0001c0001t0012g0174others(5): Show | 8 | HG01109.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-11132_-43-1111 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748825 | |||||
chr2:230748826
|
AAAAAAAT others(4): Show |
A | 1 | a0001c0001t0001g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-43-11131_-43-1112 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748826 | |||||
chr2:230748826
|
AAAAAAAT others(6): Show |
A | 2 | a0001c0001t0003g0181a0001c0001t0003g0213 | 2 | HG02129.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-43-11131_-43-1111 others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748826 | |||||
chr2:230748826
|
AAAAAAAT others(8): Show |
A | 11 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(8): Show | 11 | NA18943.hp1 NA18966.hp2 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-11131_-43-1111 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748826 | |||||
chr2:230748826
|
AAAAAAAT others(10): Show |
A | 1 | a0001c0001t0006g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-43-11131_-43-1111 others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748826 | |||||
chr2:230748826
|
AAAAAAAT others(16): Show |
A | 1 | a0001c0001t0002g0334 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-43-11131_-43-1110 others(27): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748826 | |||||
chr2:230748827
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0292 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-43-11131_-43-1113 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748827 | |||||
chr2:230748827
|
A | AATATATA others(11): Show |
1 | a0001c0001t0007g0148 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-43-11131_-43-1113 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748827 | |||||
chr2:230748827
|
A | AATATATA others(15): Show |
1 | a0001c0001t0013g0139 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-43-11131_-43-1113 others(26): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748827 | |||||
chr2:230748827
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-43-11132_-43-1113 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748827 | ||||||
chr2:230748827
|
A | T | 3 | a0001c0001t0001g0325a0001c0001t0001g0332a0001c0001t0002g0329 | 3 | HG01361.hp1 HG03927.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-43-11132A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748827 | ||||||
chr2:230748827
|
AAAAAATA others(5): Show |
A | 4 | a0001c0001t0019g0023a0001c0001t0029g0304a0001c0001t0032g0322others(1): Show | 4 | HG00639.hp2 HG01891.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-11130_-43-1111 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748827 | |||||
chr2:230748827
|
AAAAAATA others(7): Show |
A | 6 | a0001c0001t0003g0219a0001c0001t0003g0230a0001c0001t0031g0198others(3): Show | 6 | HG02055.hp2 HG02559.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-11130_-43-1111 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748827 | |||||
chr2:230748827
|
AAAAAATA others(9): Show |
A | 9 | a0001c0001t0003g0207a0001c0001t0020g0203a0001c0001t0020g0204others(6): Show | 9 | HG00099.hp2 HG02257.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-11130_-43-1111 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748827 | |||||
chr2:230748828
|
AAAAATAT others(8): Show |
A | 6 | a0001c0001t0003g0180a0001c0001t0003g0226a0001c0001t0006g0194others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-11129_-43-1111 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748828 | |||||
chr2:230748828
|
AAAAATAT others(10): Show |
A | 2 | a0001c0001t0020g0205a0001c0001t0064g0183 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-43-11129_-43-1111 others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748828 | |||||
chr2:230748829
|
A | AAT | 5 | a0001c0001t0001g0001a0001c0001t0001g0317a0001c0001t0004g0055others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-11129_-43-1112 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | AATATATA others(3): Show |
2 | a0001c0001t0002g0034a0001c0001t0005g0119 | 2 | HG01943.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-43-11129_-43-1112 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | AATATATA others(5): Show |
6 | a0001c0001t0001g0289a0001c0001t0002g0296a0001c0001t0005g0143others(3): Show | 6 | HG00673.hp1 NA18972.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-11129_-43-1112 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | AATATATA others(7): Show |
3 | a0001c0001t0005g0149a0001c0001t0013g0127a0001c0001t0014g0145 | 3 | NA18970.hp1 NA18990.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-43-11129_-43-1112 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | AATATATA others(9): Show |
3 | a0001c0001t0001g0297a0001c0001t0005g0128a0001c0001t0007g0156 | 3 | HG00423.hp2 NA18991.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-43-11129_-43-1112 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | AATATATA others(11): Show |
1 | a0001c0001t0022g0146 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-43-11129_-43-1112 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0298 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-43-11129_-43-1112 others(26): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0058a0001c0001t0004g0117 | 2 | HG00642.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-43-11130_-43-1112 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0022g0147 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-43-11130_-43-1112 others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0059g0155 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-43-11130_-43-1112 others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0299a0001c0001t0014g0151a0001c0001t0028g0154 | 3 | NA19002.hp1 NA19003.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-43-11130_-43-1112 others(23): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0014g0150 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-43-11130_-43-1112 others(25): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-43-11130_-43-1112 others(27): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
A | T | 16 | a0001c0001t0001g0292a0001c0001t0001g0312a0001c0001t0001g0324others(13): Show | 16 | HG00408.hp2 HG00423.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-11130A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748829 | ||||||
chr2:230748829
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0042g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-43-11128_-43-1111 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
AAAATATA others(5): Show |
A | 6 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0006g0197others(3): Show | 6 | HG02027.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-11128_-43-1111 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
AAAATATA others(7): Show |
A | 10 | a0001c0001t0003g0182a0001c0001t0003g0189a0001c0001t0003g0222others(7): Show | 10 | HG02080.hp2 HG02145.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-11128_-43-1111 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
AAAATATA others(9): Show |
A | 9 | a0001c0001t0006g0192a0001c0001t0006g0196a0001c0001t0006g0201others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-11128_-43-1111 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
AAAATATA others(13): Show |
A | 1 | a0001c0001t0003g0191 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-43-11128_-43-1110 others(24): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748829
|
AAAATATA others(15): Show |
A | 1 | a0001c0001t0018g0243 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-43-11128_-43-1110 others(26): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748829 | |||||
chr2:230748830
|
AAATATAT others(8): Show |
A | 1 | a0001c0001t0003g0223 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1111 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748830 | |||||
chr2:230748830
|
AAATATAT others(14): Show |
A | 1 | a0001c0001t0018g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1110 others(25): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748830 | |||||
chr2:230748831
|
A | AAAAAAAA others(10): Show |
1 | a0001c0001t0009g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0009g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(24): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0025g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(25): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(3): Show |
1 | a0001c0001t0002g0270 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(7): Show |
2 | a0001c0001t0004g0250a0001c0001t0004g0251 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(9): Show |
2 | a0001c0001t0001g0266a0001c0001t0038g0282 | 2 | HG02523.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0256 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0255 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(6): Show |
1 | a0001c0001t0004g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(8): Show |
3 | a0001c0001t0002g0246a0001c0001t0002g0283a0001c0001t0002g0286 | 3 | HG00642.hp2 HG01952.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(10): Show |
1 | a0001c0001t0004g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(12): Show |
2 | a0001c0001t0002g0245a0001c0001t0002g0252 | 2 | HG01993.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(23): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(14): Show |
1 | a0001c0001t0004g0280 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(25): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAAAT others(18): Show |
1 | a0001c0001t0002g0257 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(29): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAATA others(3): Show |
2 | a0001c0001t0001g0272a0001c0001t0002g0271 | 2 | HG00597.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0002g0273 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAATA others(9): Show |
1 | a0001c0001t0056g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAAATA others(25): Show |
1 | a0001c0001t0002g0269 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(36): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAATAT others(4): Show |
1 | a0001c0001t0002g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAAT | 7 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0160others(4): Show | 7 | HG00140.hp2 HG01069.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0158 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAATATA others(9): Show |
2 | a0001c0001t0001g0261a0001c0001t0007g0141 | 2 | NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAATATA others(11): Show |
1 | a0001c0001t0001g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAAATATA others(13): Show |
1 | a0001c0001t0002g0274 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(24): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAATATAT others(4): Show |
3 | a0001c0001t0001g0041a0001c0001t0001g0244a0001c0001t0001g0340 | 3 | HG04199.hp1 HG04199.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-43-11127_-43-1112 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAATATAT others(8): Show |
1 | a0001c0001t0023g0281 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAATATAT others(12): Show |
1 | a0001c0001t0002g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(23): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAATATAT others(14): Show |
1 | a0001c0001t0001g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-43-11127_-43-1112 others(25): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AAT | 11 | a0001c0001t0001g0035a0001c0001t0001g0081a0001c0001t0001g0084others(8): Show | 11 | HG00597.hp1 HG01261.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-11092_-43-1109 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AATATATA others(3): Show |
1 | a0001c0001t0024g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43-11100_-43-1109 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AATATATA others(5): Show |
2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-43-11102_-43-1109 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AATATATA others(7): Show |
1 | a0001c0001t0004g0293 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-43-11104_-43-1109 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0249 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-43-11106_-43-1109 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AATATATA others(11): Show |
1 | a0001c0001t0004g0277 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-43-11108_-43-1109 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AATATATA others(19): Show |
2 | a0001c0001t0001g0290a0001c0001t0002g0262 | 2 | HG00099.hp1 HG00408.hp1 |
intron_variant | MODIFIER | c.-43-11116_-43-1109 others(30): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
A | AT | 4 | a0001c0001t0001g0069a0001c0001t0013g0130a0001c0001t0015g0114others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-11128_-43-1112 others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0005g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-43-11128_-43-1112 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-43-11128_-43-1112 others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0004g0294a0001c0001t0011g0309 | 2 | HG01255.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-43-11128_-43-1112 others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0004g0253a0001c0001t0034g0305 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-43-11128_-43-1112 others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0310a0001c0001t0002g0278 | 2 | NA19066.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-43-11128_-43-1112 others(23): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0004g0020a0001c0001t0010g0260 | 2 | HG03669.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-43-11128_-43-1112 others(29): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0291 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-43-11128_-43-1112 others(31): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
A | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0039others(68): Show | 72 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-43-11128A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748831 | ||||||
chr2:230748831
|
AATATATA others(7): Show |
A | 3 | a0001c0001t0003g0221a0001c0001t0015g0263a0001c0001t0030g0233 | 3 | HG02965.hp1 NA18993.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-43-11104_-43-1109 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748831
|
AATATATA others(15): Show |
A | 2 | a0001c0001t0009g0241a0001c0001t0018g0242 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-43-11112_-43-1109 others(26): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230748831 | |||||
chr2:230748832
|
AT | A | 6 | a0001c0001t0002g0306a0001c0001t0010g0013a0001c0001t0011g0004others(3): Show | 6 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-11126delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748832 | ||||||
chr2:230748832
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0030g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-43-11126_-43-1111 others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748832 | ||||||
chr2:230748832
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0061g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-43-11126_-43-1111 others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748832 | ||||||
chr2:230748833
|
T | A | 19 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0095others(16): Show | 19 | HG00558.hp2 HG01517.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.-43-11126T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748833 | ||||||
chr2:230748835
|
T | A | 10 | a0001c0001t0001g0043a0001c0001t0001g0095a0001c0001t0001g0098others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-11124T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748835 | ||||||
chr2:230748837
|
T | A | 4 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0047others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-11122T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748837 | ||||||
chr2:230748841
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-11118T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748841 | ||||||
chr2:230748843
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-11116T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748843 | ||||||
chr2:230748847
|
T | A | 1 | a0001c0001t0015g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-43-11112T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748847 | ||||||
chr2:230748849
|
T | A | 1 | a0001c0001t0015g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-43-11110T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748849 | ||||||
chr2:230748867
|
T | A | 2 | a0001c0001t0031g0198a0001c0001t0049g0239 | 2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-43-11092T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748867 | ||||||
chr2:230748993
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-10966C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230748993 | ||||||
chr2:230749007
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-10952G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749007 | ||||||
chr2:230749009
|
G | GT | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(19): Show | 22 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-43-10940dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230749009 | |||||
chr2:230749009
|
G | GTT | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-10941_-43-1094 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230749009 | |||||
chr2:230749111
|
C | T | 38 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(35): Show | 38 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-43-10848C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749111 | ||||||
chr2:230749218
|
A | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-10741A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749218 | ||||||
chr2:230749417
|
A | T | 1 | a0001c0001t0002g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-43-10542A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749417 | ||||||
chr2:230749490
|
A | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-10469A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749490 | ||||||
chr2:230749550
|
C | T | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-10409C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749550 | ||||||
chr2:230749613
|
C | A | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.-43-10346C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749613 | ||||||
chr2:230749678
|
G | T | 3 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0056g0247 | 3 | HG01943.hp2 HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-43-10281G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749678 | ||||||
chr2:230749849
|
T | G | 2 | a0001c0001t0003g0186a0001c0001t0003g0188 | 2 | NA18971.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-43-10110T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749849 | ||||||
chr2:230749874
|
T | G | 1 | a0001c0001t0003g0182 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-43-10085T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230749874 | ||||||
chr2:230750201
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-43-9758T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230750201 | ||||||
chr2:230750414
|
A | G | 1 | a0001c0001t0004g0321 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-43-9545A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230750414 | ||||||
chr2:230750512
|
A | T | 2 | a0001c0001t0022g0146a0001c0001t0022g0147 | 2 | NA19058.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-43-9447A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230750512 | ||||||
chr2:230750572
|
A | AT | 26 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(23): Show | 26 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.-43-9377dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230750572 | |||||
chr2:230750642
|
C | T | 1 | a0001c0001t0031g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-43-9317C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230750642 | ||||||
chr2:230750664
|
T | A | 10 | a0001c0001t0003g0191a0001c0001t0006g0192a0001c0001t0006g0194others(7): Show | 10 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-9295T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230750664 | ||||||
chr2:230751094
|
T | C | 1 | a0001c0001t0019g0021 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-43-8865T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230751094 | ||||||
chr2:230751231
|
C | T | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-8728C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230751231 | ||||||
chr2:230751433
|
G | A | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-43-8526G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230751433 | ||||||
chr2:230751754
|
G | A | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-43-8205G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230751754 | ||||||
chr2:230751868
|
A | G | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-43-8091A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230751868 | ||||||
chr2:230751949
|
G | A | 1 | a0001c0001t0003g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-43-8010G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230751949 | ||||||
chr2:230752029
|
A | AC | 67 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0038others(64): Show | 68 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-43-7916dupC | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752029 | |||||
chr2:230752029
|
A | ACC | 38 | a0001c0001t0001g0042a0001c0001t0001g0255a0001c0001t0001g0261others(35): Show | 38 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-43-7917_-43-7916d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752029 | |||||
chr2:230752029
|
A | ACCC | 21 | a0001c0001t0001g0026a0001c0001t0001g0249a0001c0001t0001g0266others(18): Show | 21 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-43-7918_-43-7916d others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752029 | |||||
chr2:230752029
|
AC | A | 67 | a0001c0001t0001g0016a0001c0001t0001g0074a0001c0001t0001g0075others(64): Show | 67 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(64): Show |
intron_variant | MODIFIER | c.-43-7916delC | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752029 | |||||
chr2:230752029
|
ACC | A | 15 | a0001c0001t0002g0306a0001c0001t0002g0313a0001c0001t0005g0149others(12): Show | 15 | HG01168.hp1 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43-7917_-43-7916d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752029 | |||||
chr2:230752029
|
ACCC | A | 14 | a0001c0001t0009g0008a0001c0001t0009g0018a0001c0001t0011g0003others(11): Show | 14 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43-7918_-43-7916d others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752029 | |||||
chr2:230752032
|
C | A | 1 | a0001c0001t0019g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-43-7927C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752032 | ||||||
chr2:230752040
|
C | G | 1 | a0001c0001t0003g0219 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-43-7919C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752040 | ||||||
chr2:230752044
|
A | C | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-7915A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752044 | ||||||
chr2:230752247
|
C | CA | 111 | a0001c0001t0001g0026a0001c0001t0001g0266a0001c0001t0002g0306others(108): Show | 111 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(108): Show |
intron_variant | MODIFIER | c.-43-7699dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230752247 | |||||
chr2:230752261
|
T | A | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-43-7698T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752261 | ||||||
chr2:230752562
|
G | A | 1 | a0001c0001t0006g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-43-7397G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752562 | ||||||
chr2:230752981
|
A | G | 8 | a0001c0001t0003g0191a0001c0001t0006g0192a0001c0001t0006g0194others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43-6978A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752981 | ||||||
chr2:230752993
|
T | A | 95 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(92): Show | 95 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(92): Show |
intron_variant | MODIFIER | c.-43-6966T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230752993 | ||||||
chr2:230753221
|
G | A | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-6738G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753221 | ||||||
chr2:230753366
|
C | T | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-6593C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753366 | ||||||
chr2:230753462
|
A | C | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-6497A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753462 | ||||||
chr2:230753511
|
T | A | 1 | a0001c0001t0029g0002 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-43-6448T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753511 | ||||||
chr2:230753618
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0004g0046 | 2 | NA18986.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-43-6341G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753618 | ||||||
chr2:230753679
|
G | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-43-6280G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753679 | ||||||
chr2:230753743
|
C | CA | 11 | a0001c0001t0001g0016a0001c0001t0001g0113a0001c0001t0001g0118others(8): Show | 11 | HG00280.hp1 HG00733.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-6200dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230753743 | |||||
chr2:230753743
|
CA | C | 79 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(76): Show | 79 | HG00099.hp2 HG01109.hp2 HG01168.hp1 others(76): Show |
intron_variant | MODIFIER | c.-43-6200delA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230753743 | |||||
chr2:230753755
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-43-6204A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753755 | ||||||
chr2:230753968
|
C | T | 1 | a0001c0001t0007g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-43-5991C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753968 | ||||||
chr2:230753994
|
A | G | 18 | a0001c0001t0001g0058a0001c0001t0001g0324a0001c0001t0001g0325others(15): Show | 18 | HG00558.hp1 HG00639.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-43-5965A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230753994 | ||||||
chr2:230754114
|
A | G | 1 | a0001c0001t0005g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-43-5845A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754114 | ||||||
chr2:230754117
|
C | G | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-5842C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754117 | ||||||
chr2:230754140
|
T | C | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-43-5819T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754140 | ||||||
chr2:230754227
|
A | G | 92 | a0001c0001t0002g0306a0001c0001t0003g0180a0001c0001t0003g0181others(89): Show | 92 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(89): Show |
intron_variant | MODIFIER | c.-43-5732A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754227 | ||||||
chr2:230754236
|
T | G | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-5723T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754236 | ||||||
chr2:230754294
|
C | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-5665C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754294 | ||||||
chr2:230754305
|
T | TTTCTTCC | 81 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0248others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.-43-5633_-43-5627d others(9): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754305 | |||||
chr2:230754320
|
TTCTTCCT others(13): Show |
T | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-5633_-43-5614d others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754320 | |||||
chr2:230754327
|
TTCTTCTT others(6): Show |
T | 79 | a0001c0001t0001g0026a0001c0001t0003g0180a0001c0001t0003g0181others(76): Show | 79 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(76): Show |
intron_variant | MODIFIER | c.-43-5609_-43-5597d others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754327 | |||||
chr2:230754374
|
C | CCTTCCCC others(11): Show |
7 | a0001c0001t0011g0309a0001c0001t0025g0134a0001c0001t0025g0135others(4): Show | 7 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-5580_-43-5579i others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754374 | |||||
chr2:230754380
|
T | C | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.-43-5579T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754380 | ||||||
chr2:230754380
|
T | TCTTCCCC others(11): Show |
1 | a0001c0001t0001g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-43-5557_-43-5540d others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754380 | |||||
chr2:230754384
|
C | CCCCTCCT others(29): Show |
1 | a0001c0001t0047g0057 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-43-5522_-43-5487d others(38): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754384 | |||||
chr2:230754402
|
C | CCCCTCCT others(29): Show |
36 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-43-5540_-43-5539i others(38): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754402 | |||||
chr2:230754402
|
C | T | 2 | a0001c0001t0001g0040a0001c0001t0050g0036 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-43-5557C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754402 | ||||||
chr2:230754420
|
T | C | 38 | a0001c0001t0001g0040a0001c0001t0005g0119a0001c0001t0005g0123others(35): Show | 38 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.-43-5539T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754420 | ||||||
chr2:230754420
|
T | TCCCTCCT others(11): Show |
3 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0037g0019 | 3 | HG00735.hp1 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-43-5521_-43-5504d others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754420 | |||||
chr2:230754438
|
C | T | 36 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-43-5521C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754438 | ||||||
chr2:230754438
|
CCCCTCCT others(11): Show |
C | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-5504_-43-5487d others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754438 | |||||
chr2:230754472
|
T | G | 2 | a0001c0001t0002g0252a0001c0001t0002g0269 | 2 | NA18973.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-43-5487T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754472 | ||||||
chr2:230754484
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-43-5475C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754484 | ||||||
chr2:230754498
|
C | T | 1 | a0001c0001t0002g0284 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-5461C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754498 | ||||||
chr2:230754543
|
C | T | 108 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(105): Show | 108 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(105): Show |
intron_variant | MODIFIER | c.-43-5416C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754543 | ||||||
chr2:230754582
|
G | A | 1 | a0001c0001t0038g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-43-5377G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754582 | ||||||
chr2:230754593
|
A | G | 1 | a0001c0001t0003g0235 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-43-5366A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754593 | ||||||
chr2:230754604
|
C | T | 41 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.-43-5355C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754604 | ||||||
chr2:230754665
|
C | T | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-5294C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754665 | ||||||
chr2:230754709
|
G | T | 5 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0020g0205others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-5250G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754709 | ||||||
chr2:230754744
|
C | T | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-5215C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754744 | ||||||
chr2:230754819
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-43-5140T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754819 | ||||||
chr2:230754820
|
A | T | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-43-5139A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754820 | ||||||
chr2:230754821
|
T | A | 1 | a0001c0001t0001g0328 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-43-5138T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754821 | ||||||
chr2:230754841
|
G | GC | 8 | a0001c0001t0001g0158a0001c0001t0001g0315a0001c0001t0002g0334others(5): Show | 8 | HG01358.hp1 HG01978.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-5115dupC | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230754841 | |||||
chr2:230754842
|
C | CA | 3 | a0001c0001t0001g0314a0001c0001t0005g0138a0001c0001t0009g0319 | 3 | HG01358.hp2 HG03516.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.-43-5117_-43-5116i others(3): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754842 | ||||||
chr2:230754894
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-5065G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230754894 | ||||||
chr2:230755231
|
G | A | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-43-4728G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230755231 | ||||||
chr2:230755489
|
A | G | 337 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(334): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-43-4470A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230755489 | ||||||
chr2:230755749
|
C | T | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-4210C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230755749 | ||||||
chr2:230755779
|
C | A | 1 | a0001c0001t0048g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-43-4180C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230755779 | ||||||
chr2:230755833
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-43-4126G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230755833 | ||||||
chr2:230755925
|
G | A | 3 | a0001c0001t0003g0180a0001c0001t0003g0223a0001c0001t0003g0226 | 3 | NA18997.hp1 NA19054.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-43-4034G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230755925 | ||||||
chr2:230756054
|
G | A | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.-43-3905G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756054 | ||||||
chr2:230756300
|
A | G | 1 | a0001c0001t0018g0240 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-43-3659A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756300 | ||||||
chr2:230756402
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-43-3557T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756402 | ||||||
chr2:230756521
|
G | A | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.-43-3438G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756521 | ||||||
chr2:230756626
|
A | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-43-3333A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756626 | ||||||
chr2:230756640
|
G | C | 1 | a0001c0001t0002g0105 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-43-3319G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756640 | ||||||
chr2:230756655
|
C | CTGTT | 16 | a0001c0001t0001g0289a0001c0001t0001g0291a0001c0001t0001g0297others(13): Show | 16 | HG00423.hp2 HG00642.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-3298_-43-3295d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756655 | |||||
chr2:230756655
|
CTGTT | C | 31 | a0001c0001t0005g0119a0001c0001t0005g0131a0001c0001t0005g0132others(28): Show | 31 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.-43-3298_-43-3295d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756655 | |||||
chr2:230756657
|
GTTTGTTT others(1): Show |
G | 24 | a0001c0001t0001g0026a0001c0001t0005g0123a0001c0001t0005g0126others(21): Show | 24 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-43-3298_-43-3291d others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756657 | |||||
chr2:230756657
|
GTTTGTTT others(5): Show |
G | 22 | a0001c0001t0002g0306a0001c0001t0003g0181a0001c0001t0003g0182others(19): Show | 22 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-43-3298_-43-3287d others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756657 | |||||
chr2:230756657
|
GTTTGTTT others(9): Show |
G | 69 | a0001c0001t0003g0180a0001c0001t0003g0186a0001c0001t0003g0188others(66): Show | 69 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(66): Show |
intron_variant | MODIFIER | c.-43-3298_-43-3283d others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756657 | |||||
chr2:230756661
|
G | A | 2 | a0001c0001t0007g0121a0001c0001t0049g0239 | 2 | HG01515.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-43-3298G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756661 | ||||||
chr2:230756661
|
G | GTTTA | 10 | a0001c0001t0001g0039a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 10 | HG01255.hp1 HG01257.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-43-3254_-43-3251d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756661 | |||||
chr2:230756661
|
GTTTA | G | 23 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0044others(20): Show | 23 | HG01069.hp1 HG01081.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-3254_-43-3251d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756661 | |||||
chr2:230756661
|
GTTTATTT others(5): Show |
G | 2 | a0001c0001t0001g0113a0001c0001t0004g0268 | 2 | HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.-43-3262_-43-3251d others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230756661 | |||||
chr2:230756665
|
A | G | 95 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0042others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-43-3294A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756665 | ||||||
chr2:230756669
|
A | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0042others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-43-3290A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756669 | ||||||
chr2:230756673
|
A | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0249a0001c0001t0001g0264others(8): Show | 11 | HG00280.hp2 HG01081.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-3286A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756673 | ||||||
chr2:230756677
|
A | G | 1 | a0001c0001t0010g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-43-3282A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756677 | ||||||
chr2:230756818
|
G | A | 6 | a0001c0001t0003g0207a0001c0001t0020g0203a0001c0001t0020g0204others(3): Show | 6 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-3141G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230756818 | ||||||
chr2:230757014
|
A | G | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43-2945A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757014 | ||||||
chr2:230757182
|
C | T | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-2777C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757182 | ||||||
chr2:230757270
|
A | T | 7 | a0001c0001t0012g0173a0001c0001t0012g0174a0001c0001t0012g0175others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-2689A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757270 | ||||||
chr2:230757304
|
G | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-43-2655G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757304 | ||||||
chr2:230757362
|
G | A | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-43-2597G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757362 | ||||||
chr2:230757428
|
C | A | 1 | a0001c0001t0021g0168 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-43-2531C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757428 | ||||||
chr2:230757569
|
G | A | 37 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(34): Show | 37 | HG02027.hp2 HG02080.hp2 HG02129.hp2 others(34): Show |
intron_variant | MODIFIER | c.-43-2390G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757569 | ||||||
chr2:230757813
|
C | G | 1 | a0001c0001t0004g0295 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-43-2146C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757813 | ||||||
chr2:230757851
|
A | G | 4 | a0001c0001t0013g0130a0001c0001t0024g0125a0001c0001t0024g0129others(1): Show | 4 | HG01070.hp2 HG01261.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-2108A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757851 | ||||||
chr2:230757938
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-43-2021T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757938 | ||||||
chr2:230757950
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-43-2009C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757950 | ||||||
chr2:230757994
|
A | G | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-1965A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230757994 | ||||||
chr2:230758056
|
T | G | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-1903T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758056 | ||||||
chr2:230758174
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-1785A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758174 | ||||||
chr2:230758260
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0004g0086 | 2 | HG02165.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.-43-1699G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758260 | ||||||
chr2:230758261
|
C | G | 7 | a0001c0001t0003g0180a0001c0001t0003g0222a0001c0001t0003g0223others(4): Show | 7 | NA18951.hp1 NA18952.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-1698C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758261 | ||||||
chr2:230758264
|
C | T | 1 | a0001c0001t0030g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-43-1695C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758264 | ||||||
chr2:230758290
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-43-1669G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758290 | ||||||
chr2:230758297
|
C | CA | 112 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.-43-1642dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230758297 | |||||
chr2:230758297
|
C | CAA | 23 | a0001c0001t0001g0026a0001c0001t0003g0182a0001c0001t0003g0188others(20): Show | 23 | HG01891.hp2 HG02027.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-1643_-43-1642d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 230758297 | |||||
chr2:230758587
|
G | A | 48 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(45): Show | 48 | HG01891.hp2 HG02027.hp2 HG02055.hp2 others(45): Show |
intron_variant | MODIFIER | c.-43-1372G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758587 | ||||||
chr2:230758594
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-43-1365C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758594 | ||||||
chr2:230758596
|
C | G | 1 | a0001c0001t0001g0289 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-43-1363C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758596 | ||||||
chr2:230758781
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0261a0001c0001t0001g0264others(4): Show | 7 | HG01934.hp1 HG02148.hp2 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-1178C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758781 | ||||||
chr2:230758840
|
C | T | 21 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0091others(18): Show | 21 | HG00733.hp1 HG01069.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.-43-1119C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230758840 | ||||||
chr2:230759170
|
A | G | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-789A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230759170 | ||||||
chr2:230759216
|
G | C | 2 | a0001c0001t0004g0253a0001c0001t0004g0254 | 2 | HG00733.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-43-743G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230759216 | ||||||
chr2:230759373
|
C | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-586C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230759373 | ||||||
chr2:230759398
|
A | G | 7 | a0001c0001t0003g0180a0001c0001t0003g0222a0001c0001t0003g0223others(4): Show | 7 | NA18951.hp1 NA18952.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-561A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230759398 | ||||||
chr2:230759587
|
T | C | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-372T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230759587 | ||||||
chr2:230759611
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-43-348C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 1/8 | chr2 | 230759611 | ||||||
chr2:230760186
|
C | G | 1 | a0001c0001t0014g0145 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.114+71C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760186 | ||||||
chr2:230760412
|
T | A | 1 | a0001c0001t0036g0333 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114+297T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760412 | ||||||
chr2:230760453
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+338A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760453 | ||||||
chr2:230760521
|
T | G | 5 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0020g0205others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+406T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760521 | ||||||
chr2:230760636
|
C | CT | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+523dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230760636 | |||||
chr2:230760644
|
A | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+529A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760644 | ||||||
chr2:230760657
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.114+542G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760657 | ||||||
chr2:230760658
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.114+543A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760658 | ||||||
chr2:230760709
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+594C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760709 | ||||||
chr2:230760721
|
C | T | 1 | a0001c0001t0061g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114+606C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760721 | ||||||
chr2:230760810
|
A | G | 1 | a0001c0001t0002g0252 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.114+695A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760810 | ||||||
chr2:230760833
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+718A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760833 | ||||||
chr2:230760834
|
G | A | 1 | a0001c0001t0009g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.114+719G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230760834 | ||||||
chr2:230761060
|
A | AT | 78 | a0001c0001t0001g0051a0001c0001t0001g0314a0001c0001t0002g0087others(75): Show | 78 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(75): Show |
intron_variant | MODIFIER | c.114+960dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230761060 | |||||
chr2:230761145
|
T | C | 1 | a0001c0001t0002g0270 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.114+1030T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230761145 | ||||||
chr2:230761159
|
G | C | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.114+1044G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230761159 | ||||||
chr2:230761273
|
A | G | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1158A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230761273 | ||||||
chr2:230761483
|
G | A | 1 | a0001c0001t0013g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.114+1368G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230761483 | ||||||
chr2:230761888
|
T | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+1773T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230761888 | ||||||
chr2:230761888
|
T | TTTG | 107 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(104): Show | 107 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.114+1806_114+1808d others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230761888 | |||||
chr2:230761888
|
T | TTTGTTG | 48 | a0001c0001t0002g0090a0001c0001t0003g0181a0001c0001t0003g0182others(45): Show | 48 | HG00642.hp1 HG01070.hp2 HG01261.hp1 others(45): Show |
intron_variant | MODIFIER | c.114+1803_114+1808d others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230761888 | |||||
chr2:230761888
|
TTTG | T | 23 | a0001c0001t0001g0042a0001c0001t0001g0102a0001c0001t0001g0264others(20): Show | 23 | HG01106.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.114+1806_114+1808d others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230761888 | |||||
chr2:230761888
|
TTTGTTGT others(2): Show |
T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0004g0280 | 3 | HG00280.hp2 HG01346.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.114+1800_114+1808d others(11): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230761888 | |||||
chr2:230761888
|
TTTGTTGT others(8): Show |
T | 1 | a0001c0001t0047g0057 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114+1794_114+1808d others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230761888 | |||||
chr2:230762108
|
A | G | 1 | a0001c0001t0035g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.114+1993A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762108 | ||||||
chr2:230762197
|
C | T | 1 | a0001c0001t0009g0241 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.114+2082C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762197 | ||||||
chr2:230762198
|
G | T | 2 | a0001c0001t0032g0322a0001c0001t0032g0323 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.114+2083G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762198 | ||||||
chr2:230762207
|
T | G | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.114+2092T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762207 | ||||||
chr2:230762319
|
A | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+2204A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762319 | ||||||
chr2:230762454
|
A | G | 1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114+2339A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762454 | ||||||
chr2:230762545
|
C | A | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.114+2430C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762545 | ||||||
chr2:230762573
|
G | T | 36 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(33): Show | 36 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.114+2458G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762573 | ||||||
chr2:230762974
|
C | G | 1 | a0001c0001t0001g0314 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.114+2859C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230762974 | ||||||
chr2:230763123
|
T | C | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.114+3008T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763123 | ||||||
chr2:230763205
|
C | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+3090C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763205 | ||||||
chr2:230763465
|
G | A | 2 | a0001c0001t0025g0134a0001c0001t0025g0135 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.114+3350G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763465 | ||||||
chr2:230763541
|
C | A | 2 | a0001c0001t0001g0053a0001c0001t0002g0056 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.114+3426C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763541 | ||||||
chr2:230763630
|
T | C | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+3515T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763630 | ||||||
chr2:230763897
|
G | A | 37 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(34): Show | 37 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.114+3782G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763897 | ||||||
chr2:230763916
|
G | C | 1 | a0001c0001t0010g0260 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.114+3801G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763916 | ||||||
chr2:230763930
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+3815T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230763930 | ||||||
chr2:230764120
|
A | C | 1 | a0001c0001t0002g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.114+4005A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764120 | ||||||
chr2:230764163
|
T | C | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.114+4048T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764163 | ||||||
chr2:230764188
|
A | G | 1 | a0001c0001t0017g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114+4073A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764188 | ||||||
chr2:230764350
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114+4235A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764350 | ||||||
chr2:230764645
|
G | T | 247 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0042others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.114+4530G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764645 | ||||||
chr2:230764699
|
A | C | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+4584A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764699 | ||||||
chr2:230764930
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.114+4815A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764930 | ||||||
chr2:230764950
|
T | C | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+4835T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764950 | ||||||
chr2:230764960
|
C | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+4845C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764960 | ||||||
chr2:230764988
|
C | CT | 6 | a0001c0001t0002g0068a0001c0001t0002g0313a0001c0001t0025g0134others(3): Show | 6 | HG02071.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+4882dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230764988 | |||||
chr2:230764993
|
T | C | 3 | a0001c0001t0016g0165a0001c0001t0016g0184a0001c0001t0016g0185 | 3 | NA18992.hp1 NA18994.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.114+4878T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230764993 | ||||||
chr2:230765221
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114+5106C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765221 | ||||||
chr2:230765301
|
G | A | 5 | a0001c0001t0005g0307a0001c0001t0013g0130a0001c0001t0024g0125others(2): Show | 5 | HG01070.hp2 HG01261.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+5186G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765301 | ||||||
chr2:230765562
|
G | T | 8 | a0001c0001t0005g0143a0001c0001t0007g0141a0001c0001t0007g0156others(5): Show | 8 | NA18948.hp1 NA18979.hp2 NA18991.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+5447G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765562 | ||||||
chr2:230765613
|
G | A | 21 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0091others(18): Show | 21 | HG00733.hp1 HG01069.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.114+5498G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765613 | ||||||
chr2:230765874
|
G | C | 1 | a0001c0001t0009g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.114+5759G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765874 | ||||||
chr2:230765888
|
A | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+5773A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765888 | ||||||
chr2:230765892
|
C | T | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+5777C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765892 | ||||||
chr2:230765916
|
G | GA | 36 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(33): Show | 36 | HG02027.hp2 HG02080.hp2 HG02129.hp2 others(33): Show |
intron_variant | MODIFIER | c.114+5806dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230765916 | |||||
chr2:230765958
|
C | G | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+5843C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765958 | ||||||
chr2:230765979
|
C | T | 149 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(146): Show | 149 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.114+5864C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765979 | ||||||
chr2:230765987
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+5872A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230765987 | ||||||
chr2:230766173
|
A | G | 1 | a0001c0001t0003g0221 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.114+6058A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766173 | ||||||
chr2:230766369
|
A | G | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.114+6254A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766369 | ||||||
chr2:230766682
|
C | A | 1 | a0001c0001t0002g0338 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.114+6567C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766682 | ||||||
chr2:230766780
|
G | A | 1 | a0001c0001t0005g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.114+6665G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766780 | ||||||
chr2:230766802
|
C | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+6687C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766802 | ||||||
chr2:230766885
|
A | G | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114+6770A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766885 | ||||||
chr2:230766940
|
A | G | 41 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.114+6825A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766940 | ||||||
chr2:230766974
|
A | G | 94 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0058others(91): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.114+6859A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230766974 | ||||||
chr2:230767027
|
G | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+6912G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230767027 | ||||||
chr2:230767349
|
A | T | 41 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(38): Show | 41 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.114+7234A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230767349 | ||||||
chr2:230767425
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.114+7310C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230767425 | ||||||
chr2:230767538
|
A | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.114+7423A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230767538 | ||||||
chr2:230767749
|
C | G | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.114+7634C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230767749 | ||||||
chr2:230767795
|
A | C | 1 | a0001c0001t0002g0090 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.114+7680A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230767795 | ||||||
chr2:230768253
|
G | C | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.114+8138G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230768253 | ||||||
chr2:230768286
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.114+8171C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230768286 | ||||||
chr2:230768656
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.114+8541A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230768656 | ||||||
chr2:230768660
|
A | G | 1 | a0001c0001t0005g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.114+8545A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230768660 | ||||||
chr2:230768763
|
A | C | 1 | a0001c0001t0001g0325 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.114+8648A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230768763 | ||||||
chr2:230768812
|
ATTAATTT others(6): Show |
A | 2 | a0001c0001t0034g0190a0001c0001t0068g0199 | 2 | HG00099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.114+8698_114+8710d others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230768812 | ||||||
chr2:230769029
|
T | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+8914T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769029 | ||||||
chr2:230769157
|
A | G | 11 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0078others(8): Show | 11 | HG01981.hp1 HG02293.hp1 NA18966.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+9042A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769157 | ||||||
chr2:230769398
|
T | C | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114+9283T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769398 | ||||||
chr2:230769607
|
A | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.114+9492A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769607 | ||||||
chr2:230769624
|
A | G | 1 | a0001c0001t0023g0281 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.114+9509A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769624 | ||||||
chr2:230769704
|
C | T | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.114+9589C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769704 | ||||||
chr2:230769818
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.114+9703A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230769818 | ||||||
chr2:230769824
|
C | CA | 7 | a0001c0001t0006g0197a0001c0001t0013g0130a0001c0001t0020g0205others(4): Show | 7 | HG01070.hp2 HG02027.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+9723dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230769824 | |||||
chr2:230770078
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.114+9963A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230770078 | ||||||
chr2:230770256
|
A | G | 11 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(8): Show | 11 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+10141A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230770256 | ||||||
chr2:230770784
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+10669A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230770784 | ||||||
chr2:230770836
|
A | G | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.114+10721A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230770836 | ||||||
chr2:230770927
|
C | G | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.114+10812C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230770927 | ||||||
chr2:230770935
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.114+10820A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230770935 | ||||||
chr2:230771099
|
A | T | 1 | a0001c0001t0017g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.114+10984A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771099 | ||||||
chr2:230771122
|
GATC | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.114+11011_114+1101 others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230771122 | |||||
chr2:230771184
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.114+11069C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771184 | ||||||
chr2:230771234
|
T | A | 14 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(11): Show | 14 | NA18947.hp1 NA18951.hp1 NA18952.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+11119T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771234 | ||||||
chr2:230771425
|
CAAAG | C | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+11311_114+1131 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771425 | ||||||
chr2:230771689
|
T | C | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+11574T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771689 | ||||||
chr2:230771716
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.114+11601C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771716 | ||||||
chr2:230771717
|
G | A | 1 | a0001c0001t0002g0303 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.114+11602G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771717 | ||||||
chr2:230771790
|
C | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+11675C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771790 | ||||||
chr2:230771925
|
A | G | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114+11810A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230771925 | ||||||
chr2:230772036
|
G | A | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.114+11921G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772036 | ||||||
chr2:230772412
|
G | A | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114+12297G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772412 | ||||||
chr2:230772421
|
C | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+12306C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772421 | ||||||
chr2:230772487
|
G | GT | 104 | a0001c0001t0001g0065a0001c0001t0001g0084a0001c0001t0001g0106others(101): Show | 104 | HG00099.hp2 HG00597.hp1 HG01106.hp1 others(101): Show |
intron_variant | MODIFIER | c.114+12387dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772487 | |||||
chr2:230772734
|
T | C | 274 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0040others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.114+12619T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772734 | ||||||
chr2:230772764
|
C | T | 1 | a0001c0001t0012g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.114+12649C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772764 | ||||||
chr2:230772979
|
C | CA | 13 | a0001c0001t0003g0180a0001c0001t0003g0191a0001c0001t0006g0192others(10): Show | 13 | HG00099.hp2 HG01169.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.114+12866dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772979 | |||||
chr2:230772979
|
C | CAA | 3 | a0001c0001t0003g0224a0001c0001t0034g0190a0001c0001t0063g0193 | 3 | HG01346.hp1 HG03710.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.114+12865_114+1286 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772979 | |||||
chr2:230772982
|
T | A | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.114+12867T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772982 | ||||||
chr2:230772982
|
T | TAA | 7 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+12887_114+1288 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772982 | |||||
chr2:230772982
|
T | TAAA | 21 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(18): Show | 21 | HG01168.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.114+12886_114+1288 others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772982 | |||||
chr2:230772982
|
TA | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(208): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.114+12888delA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772982 | |||||
chr2:230772982
|
TAA | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0079a0001c0001t0005g0153others(7): Show | 10 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+12887_114+1288 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230772982 | |||||
chr2:230772999
|
A | C | 1 | a0001c0001t0002g0334 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.114+12884A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230772999 | ||||||
chr2:230773004
|
C | T | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.114+12889C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773004 | ||||||
chr2:230773273
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+13158T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773273 | ||||||
chr2:230773298
|
G | GTA | 4 | a0001c0001t0001g0261a0001c0001t0002g0278a0001c0001t0002g0299others(1): Show | 4 | HG03486.hp1 NA19003.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+13199_114+1320 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773298 | |||||
chr2:230773298
|
GTA | G | 3 | a0001c0001t0009g0018a0001c0001t0018g0242a0001c0001t0055g0136 | 3 | HG02257.hp1 HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.114+13199_114+1320 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773298 | |||||
chr2:230773298
|
GTATA | G | 4 | a0001c0001t0009g0017a0001c0001t0009g0241a0001c0001t0018g0240others(1): Show | 4 | HG01168.hp1 HG02717.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+13197_114+1320 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773298 | |||||
chr2:230773300
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.114+13185A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773300 | ||||||
chr2:230773310
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0011g0309a0001c0001t0014g0145 | 2 | NA18970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.114+13196_114+1319 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773310 | |||||
chr2:230773310
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0041g0308 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114+13196_114+1319 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773310 | |||||
chr2:230773312
|
A | ATG | 3 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0312 | 3 | HG00733.hp1 HG02258.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.114+13198_114+1319 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | ATGTGTG | 3 | a0001c0001t0022g0146a0001c0001t0022g0147a0001c0001t0029g0002 | 3 | HG06807.hp1 NA19058.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.114+13198_114+1319 others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | ATGTGTGT others(3): Show |
9 | a0001c0001t0005g0126a0001c0001t0005g0128a0001c0001t0005g0138others(6): Show | 9 | HG00597.hp1 HG01175.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+13198_114+1319 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | ATGTGTGT others(5): Show |
10 | a0001c0001t0005g0119a0001c0001t0005g0143a0001c0001t0005g0149others(7): Show | 10 | HG00423.hp1 NA18944.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+13198_114+1319 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | ATGTGTGT others(7): Show |
3 | a0001c0001t0005g0152a0001c0001t0007g0140a0001c0001t0028g0154 | 3 | NA18986.hp2 NA19055.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.114+13198_114+1319 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | ATGTGTGT others(11): Show |
2 | a0001c0001t0005g0131a0001c0001t0007g0156 | 2 | HG04204.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.114+13198_114+1319 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0064g0183 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.114+13198_114+1319 others(24): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773312 | |||||
chr2:230773312
|
A | G | 5 | a0001c0001t0004g0048a0001c0001t0011g0050a0001c0001t0011g0309others(2): Show | 5 | HG02451.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+13197A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773312 | ||||||
chr2:230773314
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0048g0037others(1): Show | 4 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+13200_114+1320 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0026a0001c0001t0042g0027 | 2 | HG02818.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+13200_114+1320 others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATATGT others(1): Show |
5 | a0001c0001t0002g0090a0001c0001t0002g0245a0001c0001t0002g0246others(2): Show | 5 | HG01943.hp2 HG01952.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+13200_114+1320 others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATATGT others(5): Show |
2 | a0001c0001t0001g0106a0001c0001t0067g0206 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114+13200_114+1320 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATGTG | 39 | a0001c0001t0001g0042a0001c0001t0001g0164a0001c0001t0001g0255others(36): Show | 39 | HG01517.hp1 HG01934.hp1 HG02080.hp2 others(36): Show |
intron_variant | MODIFIER | c.114+13200_114+1320 others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATGTGT others(1): Show |
17 | a0001c0001t0001g0091a0001c0001t0001g0095a0001c0001t0001g0098others(14): Show | 17 | HG01891.hp2 HG01978.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.114+13200_114+1320 others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATGTGT others(3): Show |
8 | a0001c0001t0001g0104a0001c0001t0006g0197a0001c0001t0019g0022others(5): Show | 8 | HG00099.hp2 HG00639.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+13200_114+1320 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATGTGT others(5): Show |
6 | a0001c0001t0001g0326a0001c0001t0006g0192a0001c0001t0006g0195others(3): Show | 6 | HG01258.hp2 HG01496.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+13200_114+1320 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATGTGT others(7): Show |
3 | a0001c0001t0003g0207a0001c0001t0006g0194a0001c0001t0019g0021 | 3 | HG01256.hp2 HG02109.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.114+13200_114+1320 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATATGTGT others(9): Show |
2 | a0001c0001t0028g0028a0001c0001t0063g0193 | 2 | HG01346.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.114+13200_114+1320 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATG | 14 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0237others(11): Show | 14 | HG00099.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+13233_114+1323 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTG | 53 | a0001c0001t0001g0040a0001c0001t0001g0093a0001c0001t0001g0158others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.114+13231_114+1323 others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTGTG | 26 | a0001c0001t0001g0041a0001c0001t0001g0157a0001c0001t0001g0272others(23): Show | 26 | HG00597.hp2 HG00673.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.114+13229_114+1323 others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0002g0338a0001c0001t0012g0175a0001c0001t0013g0130others(6): Show | 9 | HG01070.hp2 HG02040.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+13227_114+1323 others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTGTGT others(3): Show |
12 | a0001c0001t0004g0321a0001c0001t0006g0196a0001c0001t0006g0201others(9): Show | 12 | HG01168.hp2 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.114+13225_114+1323 others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTGTGT others(5): Show |
5 | a0001c0001t0005g0132a0001c0001t0012g0238a0001c0001t0039g0120others(2): Show | 5 | HG01109.hp2 HG01261.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+13223_114+1323 others(16): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTGTGT others(7): Show |
3 | a0001c0001t0024g0125a0001c0001t0070g0170a0001c0005t0012g0179 | 3 | HG02615.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.114+13221_114+1323 others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0024g0129 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114+13219_114+1323 others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773314
|
A | G | 48 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0058others(45): Show | 48 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.114+13199A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773314 | ||||||
chr2:230773314
|
ATG | A | 4 | a0001c0001t0002g0068a0001c0001t0015g0114a0001c0001t0015g0115others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+13233_114+1323 others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230773314 | |||||
chr2:230773316
|
G | A | 6 | a0001c0001t0001g0102a0001c0001t0004g0103a0001c0001t0030g0232others(3): Show | 6 | HG01106.hp2 HG01256.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+13201G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773316 | ||||||
chr2:230773318
|
G | A | 1 | a0001c0001t0061g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114+13203G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773318 | ||||||
chr2:230773320
|
G | A | 1 | a0001c0001t0061g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114+13205G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773320 | ||||||
chr2:230773322
|
G | A | 1 | a0001c0001t0061g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114+13207G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773322 | ||||||
chr2:230773350
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.114+13235T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773350 | ||||||
chr2:230773425
|
T | C | 150 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.114+13310T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773425 | ||||||
chr2:230773561
|
C | T | 10 | a0001c0001t0001g0272a0001c0001t0002g0252a0001c0001t0002g0256others(7): Show | 10 | HG00597.hp2 HG00673.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+13446C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773561 | ||||||
chr2:230773768
|
G | A | 78 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(75): Show | 78 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(75): Show |
intron_variant | MODIFIER | c.114+13653G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773768 | ||||||
chr2:230773788
|
T | C | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.114+13673T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773788 | ||||||
chr2:230773820
|
A | G | 14 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(11): Show | 14 | NA18943.hp1 NA18966.hp2 NA18973.hp1 others(11): Show |
intron_variant | MODIFIER | c.114+13705A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773820 | ||||||
chr2:230773914
|
A | G | 150 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.114+13799A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230773914 | ||||||
chr2:230774051
|
G | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | NA19054.hp2 NA19058.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.114+13936G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774051 | ||||||
chr2:230774200
|
A | T | 1 | a0001c0001t0056g0247 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.114+14085A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774200 | ||||||
chr2:230774259
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0099a0001c0001t0001g0102others(4): Show | 8 | HG00140.hp2 HG00408.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+14144A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774259 | ||||||
chr2:230774462
|
G | C | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+14347G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774462 | ||||||
chr2:230774466
|
C | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.114+14351C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774466 | ||||||
chr2:230774621
|
C | G | 2 | a0001c0001t0007g0121a0001c0001t0007g0122 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.114+14506C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774621 | ||||||
chr2:230774657
|
A | G | 42 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(39): Show | 42 | HG01891.hp2 HG02027.hp2 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.114+14542A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774657 | ||||||
chr2:230774822
|
T | C | 1 | a0001c0001t0001g0330 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.114+14707T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230774822 | ||||||
chr2:230775189
|
C | A | 3 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0050 | 3 | HG02145.hp1 HG02451.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.114+15074C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230775189 | ||||||
chr2:230775305
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.114+15190G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230775305 | ||||||
chr2:230775395
|
C | G | 5 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0020g0205others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.114+15280C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230775395 | ||||||
chr2:230775660
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.115-15212A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230775660 | ||||||
chr2:230775680
|
ATTGGAG | A | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-15189_115-1518 others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230775680 | |||||
chr2:230776015
|
T | G | 3 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0016g0187 | 3 | NA18947.hp1 NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.115-14857T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776015 | ||||||
chr2:230776063
|
C | CA | 34 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.115-14807dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230776063 | |||||
chr2:230776069
|
A | G | 18 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(15): Show | 18 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.115-14803A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776069 | ||||||
chr2:230776121
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-14751A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776121 | ||||||
chr2:230776285
|
T | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.115-14587T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776285 | ||||||
chr2:230776310
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.115-14562A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776310 | ||||||
chr2:230776406
|
T | G | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.115-14466T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776406 | ||||||
chr2:230776542
|
C | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-14330C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776542 | ||||||
chr2:230776564
|
G | T | 1 | a0001c0001t0004g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.115-14308G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776564 | ||||||
chr2:230776700
|
TC | T | 225 | a0001c0001t0001g0026a0001c0001t0001g0042a0001c0001t0001g0058others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.115-14164delC | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230776700 | |||||
chr2:230776754
|
G | A | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.115-14118G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776754 | ||||||
chr2:230776755
|
A | G | 1 | a0001c0001t0031g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.115-14117A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776755 | ||||||
chr2:230776772
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-14100G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776772 | ||||||
chr2:230776784
|
G | A | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-14088G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776784 | ||||||
chr2:230776940
|
G | A | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115-13932G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776940 | ||||||
chr2:230776969
|
G | A | 1 | a0001c0001t0007g0316 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.115-13903G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230776969 | ||||||
chr2:230777097
|
A | G | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.115-13775A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777097 | ||||||
chr2:230777140
|
AATGATGT others(2): Show |
A | 148 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(145): Show | 148 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.115-13722_115-1371 others(13): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230777140 | |||||
chr2:230777358
|
T | G | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-13514T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777358 | ||||||
chr2:230777362
|
G | GT | 12 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0047others(9): Show | 12 | HG00597.hp1 HG01256.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-13497dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230777362 | |||||
chr2:230777362
|
G | T | 21 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(18): Show | 21 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-13510G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777362 | ||||||
chr2:230777362
|
GT | G | 8 | a0001c0001t0003g0191a0001c0001t0006g0192a0001c0001t0006g0194others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-13497delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230777362 | |||||
chr2:230777366
|
T | G | 68 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(65): Show | 68 | HG00099.hp2 HG01109.hp2 HG01891.hp2 others(65): Show |
intron_variant | MODIFIER | c.115-13506T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777366 | ||||||
chr2:230777442
|
T | C | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-13430T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777442 | ||||||
chr2:230777500
|
A | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0157a0001c0001t0001g0158others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.115-13372A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777500 | ||||||
chr2:230777756
|
G | A | 148 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(145): Show | 148 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.115-13116G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777756 | ||||||
chr2:230777826
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.115-13046G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777826 | ||||||
chr2:230777922
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.115-12950T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777922 | ||||||
chr2:230777972
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.115-12900A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230777972 | ||||||
chr2:230778422
|
T | C | 1 | a0001c0001t0004g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.115-12450T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778422 | ||||||
chr2:230778531
|
G | A | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-12341G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778531 | ||||||
chr2:230778573
|
T | C | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-12299T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778573 | ||||||
chr2:230778739
|
T | C | 1 | a0001c0001t0019g0021 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.115-12133T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778739 | ||||||
chr2:230778842
|
A | T | 1 | a0001c0001t0011g0004 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.115-12030A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778842 | ||||||
chr2:230778887
|
G | A | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115-11985G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778887 | ||||||
chr2:230778959
|
G | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-11913G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230778959 | ||||||
chr2:230779027
|
T | G | 1 | a0001c0001t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.115-11845T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779027 | ||||||
chr2:230779156
|
G | T | 79 | a0001c0001t0001g0026a0001c0001t0003g0180a0001c0001t0003g0181others(76): Show | 79 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(76): Show |
intron_variant | MODIFIER | c.115-11716G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779156 | ||||||
chr2:230779251
|
T | G | 150 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.115-11621T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779251 | ||||||
chr2:230779338
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115-11534C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779338 | ||||||
chr2:230779356
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-11516A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779356 | ||||||
chr2:230779437
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.115-11435G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779437 | ||||||
chr2:230779612
|
A | G | 5 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0020g0205others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-11260A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230779612 | ||||||
chr2:230780068
|
C | T | 2 | a0001c0001t0001g0033a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.115-10804C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780068 | ||||||
chr2:230780226
|
G | A | 1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.115-10646G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780226 | ||||||
chr2:230780482
|
C | G | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.115-10390C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780482 | ||||||
chr2:230780583
|
C | T | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.115-10289C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780583 | ||||||
chr2:230780589
|
A | G | 4 | a0001c0001t0032g0322a0001c0001t0032g0323a0001c0001t0033g0172others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-10283A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780589 | ||||||
chr2:230780702
|
A | G | 2 | a0001c0001t0001g0330a0001c0001t0004g0331 | 2 | NA18963.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.115-10170A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780702 | ||||||
chr2:230780907
|
C | T | 5 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0020g0205others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9965C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230780907 | ||||||
chr2:230781061
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.115-9811A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781061 | ||||||
chr2:230781074
|
T | C | 146 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(143): Show | 146 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.115-9798T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781074 | ||||||
chr2:230781080
|
C | CA | 64 | a0001c0001t0001g0043a0001c0001t0003g0189a0001c0001t0003g0191others(61): Show | 64 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(61): Show |
intron_variant | MODIFIER | c.115-9779dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230781080 | |||||
chr2:230781080
|
C | CAA | 14 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(11): Show | 14 | NA18947.hp1 NA18951.hp1 NA18952.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-9780_115-9779d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230781080 | |||||
chr2:230781224
|
G | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-9648G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781224 | ||||||
chr2:230781264
|
A | G | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-9608A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781264 | ||||||
chr2:230781396
|
A | G | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.115-9476A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781396 | ||||||
chr2:230781416
|
G | A | 5 | a0001c0001t0001g0157a0001c0001t0001g0160a0001c0001t0004g0159others(2): Show | 5 | HG01069.hp1 HG01993.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9456G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781416 | ||||||
chr2:230781432
|
C | T | 1 | a0001c0001t0019g0022 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.115-9440C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781432 | ||||||
chr2:230781461
|
T | C | 5 | a0001c0001t0004g0048a0001c0001t0010g0049a0001c0001t0011g0047others(2): Show | 5 | HG02145.hp1 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-9411T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781461 | ||||||
chr2:230781488
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.115-9384A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781488 | ||||||
chr2:230781575
|
C | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-9297C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781575 | ||||||
chr2:230781676
|
T | TA | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-9195dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230781676 | |||||
chr2:230781711
|
G | A | 1 | a0001c0001t0060g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.115-9161G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781711 | ||||||
chr2:230781812
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.115-9060T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781812 | ||||||
chr2:230781887
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115-8985C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781887 | ||||||
chr2:230781987
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01081.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.115-8885C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781987 | ||||||
chr2:230781988
|
C | G | 3 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0016g0187 | 3 | NA18947.hp1 NA18983.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.115-8884C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230781988 | ||||||
chr2:230782055
|
G | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-8817G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782055 | ||||||
chr2:230782064
|
C | T | 14 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(11): Show | 14 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.115-8808C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782064 | ||||||
chr2:230782238
|
A | G | 1 | a0001c0001t0001g0336 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.115-8634A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782238 | ||||||
chr2:230782262
|
C | A | 1 | a0001c0001t0008g0337 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.115-8610C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782262 | ||||||
chr2:230782341
|
T | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-8531T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782341 | ||||||
chr2:230782355
|
T | C | 1 | a0001c0001t0005g0131 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.115-8517T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782355 | ||||||
chr2:230782363
|
G | A | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115-8509G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782363 | ||||||
chr2:230782418
|
C | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-8454C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782418 | ||||||
chr2:230782653
|
A | T | 2 | a0001c0001t0001g0033a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.115-8219A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782653 | ||||||
chr2:230782789
|
G | GTTTC | 30 | a0001c0001t0001g0041a0001c0001t0001g0244a0001c0001t0001g0258others(27): Show | 30 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.115-8059_115-8056d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782789 | |||||
chr2:230782789
|
G | GTTTCTTT others(1): Show |
49 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0248others(46): Show | 49 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.115-8063_115-8056d others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782789 | |||||
chr2:230782789
|
G | GTTTCTTT others(5): Show |
1 | a0001c0001t0001g0264 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.115-8067_115-8056d others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782789 | |||||
chr2:230782789
|
GTTTCTTT others(1): Show |
G | 5 | a0001c0001t0001g0051a0001c0001t0002g0252a0001c0001t0002g0269others(2): Show | 5 | HG00597.hp2 HG02258.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-8063_115-8056d others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782789 | |||||
chr2:230782809
|
C | CT | 13 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(10): Show | 13 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.115-8060dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTT | 5 | a0001c0001t0003g0180a0001c0001t0003g0207a0001c0001t0012g0238others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-8061_115-8060d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTT | 5 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0243others(2): Show | 5 | HG01168.hp1 HG01256.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0006g0192a0001c0001t0006g0194a0001c0001t0006g0195others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0006g0196a0001c0001t0006g0201a0001c0001t0019g0021 | 3 | HG01168.hp2 HG01169.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.115-8060_115-8059i others(13): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0063g0193 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.115-8060_115-8059i others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0019g0023a0001c0001t0060g0024 | 2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-8060_115-8059i others(15): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0032g0322 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.115-8060_115-8059i others(18): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(10): Show |
11 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0212others(8): Show | 11 | NA18952.hp1 NA18966.hp2 NA18972.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(11): Show |
8 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0188others(5): Show | 8 | HG02080.hp2 NA18962.hp1 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(20): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(12): Show |
7 | a0001c0001t0003g0186a0001c0001t0003g0210a0001c0001t0003g0219others(4): Show | 7 | NA18947.hp1 NA18951.hp1 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(21): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(13): Show |
3 | a0001c0001t0003g0214a0001c0001t0003g0220a0001c0001t0003g0221 | 3 | NA18943.hp1 NA18993.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.115-8060_115-8059i others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0006g0197a0001c0001t0031g0198a0001c0001t0064g0183others(1): Show | 4 | HG02027.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(23): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(15): Show |
2 | a0001c0001t0012g0173a0003c0003t0012g0178 | 2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.115-8060_115-8059i others(24): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0021g0168a0001c0001t0071g0177a0001c0001t0072g0176others(1): Show | 4 | HG02280.hp2 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-8060_115-8059i others(25): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(18): Show |
2 | a0001c0001t0006g0211a0001c0001t0033g0172 | 2 | HG03453.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.115-8060_115-8059i others(27): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(20): Show |
3 | a0001c0001t0003g0213a0001c0001t0003g0227a0001c0001t0032g0323 | 3 | HG02129.hp2 NA18906.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.115-8060_115-8059i others(29): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(21): Show |
1 | a0002c0004t0033g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.115-8060_115-8059i others(30): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0228 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.115-8060_115-8059i others(32): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(26): Show |
1 | a0001c0001t0021g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.115-8060_115-8059i others(35): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0021g0166 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.115-8060_115-8059i others(36): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782809
|
C | CTTTTTTT others(41): Show |
1 | a0001c0001t0069g0167 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.115-8060_115-8059i others(50): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782809 | |||||
chr2:230782811
|
TTC | T | 28 | a0001c0001t0005g0119a0001c0001t0005g0126a0001c0001t0005g0132others(25): Show | 28 | HG00423.hp1 HG01070.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.115-8059_115-8058d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782811 | |||||
chr2:230782812
|
TC | T | 3 | a0001c0001t0005g0123a0001c0001t0005g0128a0001c0001t0005g0152 | 3 | HG01167.hp1 NA19055.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.115-8059delC | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782812 | ||||||
chr2:230782813
|
C | CT | 17 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0080others(14): Show | 17 | HG00408.hp2 HG01069.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.115-8040dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782813 | |||||
chr2:230782813
|
C | CTTTCTTT others(22): Show |
1 | a0001c0001t0009g0017 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.115-8056_115-8055i others(31): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782813 | |||||
chr2:230782813
|
C | CTTTCTTT others(28): Show |
1 | a0001c0001t0009g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.115-8056_115-8055i others(37): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782813 | |||||
chr2:230782813
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0016g0165 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.115-8040_115-8039i others(23): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782813 | |||||
chr2:230782813
|
C | T | 93 | a0001c0001t0002g0306a0001c0001t0003g0180a0001c0001t0003g0181others(90): Show | 93 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(90): Show |
intron_variant | MODIFIER | c.115-8059C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782813 | ||||||
chr2:230782941
|
T | C | 2 | a0001c0001t0007g0121a0001c0001t0007g0122 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.115-7931T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230782941 | ||||||
chr2:230782980
|
T | TTTTTTG | 81 | a0001c0001t0002g0306a0001c0001t0003g0180a0001c0001t0003g0181others(78): Show | 81 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(78): Show |
intron_variant | MODIFIER | c.115-7868_115-7863d others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782980 | |||||
chr2:230782980
|
T | TTTTTTGT others(5): Show |
45 | a0001c0001t0001g0026a0001c0001t0005g0119a0001c0001t0005g0123others(42): Show | 45 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.115-7874_115-7863d others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782980 | |||||
chr2:230782980
|
TTTTTTG | T | 15 | a0001c0001t0003g0208a0001c0001t0003g0209a0001c0001t0003g0210others(12): Show | 15 | HG02129.hp2 NA18943.hp1 NA18966.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-7868_115-7863d others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782980 | |||||
chr2:230782982
|
T | TTTTG | 3 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0066g0202 | 3 | HG02257.hp2 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.115-7886_115-7883d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230782982 | |||||
chr2:230783018
|
C | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-7854C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783018 | ||||||
chr2:230783122
|
C | T | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-7750C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783122 | ||||||
chr2:230783176
|
T | C | 1 | a0001c0001t0023g0281 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.115-7696T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783176 | ||||||
chr2:230783305
|
G | C | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-7567G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783305 | ||||||
chr2:230783407
|
G | A | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.115-7465G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783407 | ||||||
chr2:230783422
|
A | G | 1 | a0001c0001t0007g0141 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.115-7450A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783422 | ||||||
chr2:230783442
|
A | AGTTTT | 100 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0035others(97): Show | 101 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.115-7395_115-7391d others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
A | AGTTTTGT others(3): Show |
65 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0058others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.115-7400_115-7391d others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
A | AGTTTTGT others(8): Show |
70 | a0001c0001t0001g0042a0001c0001t0001g0255a0001c0001t0001g0258others(67): Show | 70 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.115-7405_115-7391d others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
A | AGTTTTGT others(13): Show |
15 | a0001c0001t0001g0261a0001c0001t0001g0266a0001c0001t0001g0287others(12): Show | 15 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-7410_115-7391d others(22): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
A | AGTTTTGT others(18): Show |
5 | a0001c0001t0001g0298a0001c0001t0001g0310a0001c0001t0001g0320others(2): Show | 5 | HG03130.hp2 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-7415_115-7391d others(27): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
AGTTTT | A | 66 | a0001c0001t0001g0026a0001c0001t0002g0096a0001c0001t0003g0180others(63): Show | 66 | HG01109.hp2 HG02027.hp2 HG02055.hp2 others(63): Show |
intron_variant | MODIFIER | c.115-7395_115-7391d others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
AGTTTTGT others(3): Show |
A | 1 | a0001c0001t0006g0029 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.115-7400_115-7391d others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783442
|
AGTTTTGT others(8): Show |
A | 10 | a0001c0001t0003g0191a0001c0001t0006g0192a0001c0001t0006g0194others(7): Show | 10 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.115-7405_115-7391d others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230783442 | |||||
chr2:230783525
|
G | A | 3 | a0001c0001t0003g0228a0001c0001t0003g0229a0001c0001t0003g0230 | 3 | HG02080.hp2 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.115-7347G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783525 | ||||||
chr2:230783562
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-7310C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230783562 | ||||||
chr2:230784162
|
G | A | 8 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(5): Show | 8 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-6710G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784162 | ||||||
chr2:230784211
|
G | A | 1 | a0001c0001t0037g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.115-6661G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784211 | ||||||
chr2:230784247
|
C | T | 1 | a0001c0001t0005g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.115-6625C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784247 | ||||||
chr2:230784365
|
G | T | 1 | a0001c0001t0003g0227 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.115-6507G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784365 | ||||||
chr2:230784467
|
T | C | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.115-6405T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784467 | ||||||
chr2:230784542
|
C | G | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.115-6330C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784542 | ||||||
chr2:230784550
|
A | G | 1 | a0001c0001t0025g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.115-6322A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784550 | ||||||
chr2:230784884
|
G | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-5988G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784884 | ||||||
chr2:230784937
|
C | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-5935C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230784937 | ||||||
chr2:230785116
|
T | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.115-5756T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785116 | ||||||
chr2:230785179
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.115-5693A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785179 | ||||||
chr2:230785372
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.115-5500C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785372 | ||||||
chr2:230785403
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.115-5469C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785403 | ||||||
chr2:230785574
|
A | C | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.115-5298A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785574 | ||||||
chr2:230785759
|
A | G | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5113A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785759 | ||||||
chr2:230785890
|
C | T | 1 | a0001c0001t0015g0335 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.115-4982C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785890 | ||||||
chr2:230785939
|
C | T | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.115-4933C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230785939 | ||||||
chr2:230786043
|
A | G | 1 | a0001c0001t0010g0260 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.115-4829A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786043 | ||||||
chr2:230786163
|
C | CA | 24 | a0001c0001t0001g0026a0001c0001t0001g0041a0001c0001t0001g0043others(21): Show | 24 | HG00639.hp2 HG00642.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.115-4684dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230786163 | |||||
chr2:230786163
|
CA | C | 15 | a0001c0001t0001g0164a0001c0001t0001g0298a0001c0001t0001g0302others(12): Show | 15 | HG01168.hp1 HG01517.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-4684delA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230786163 | |||||
chr2:230786163
|
CAAAAAAA others(1): Show |
C | 73 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(70): Show | 73 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(70): Show |
intron_variant | MODIFIER | c.115-4691_115-4684d others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230786163 | |||||
chr2:230786163
|
CAAAAAAA others(5): Show |
C | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.115-4695_115-4684d others(14): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230786163 | |||||
chr2:230786187
|
A | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.115-4685A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786187 | ||||||
chr2:230786211
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.115-4661C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786211 | ||||||
chr2:230786328
|
CCTGT | C | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.115-4541_115-4538d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230786328 | |||||
chr2:230786463
|
A | G | 1 | a0001c0001t0049g0239 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.115-4409A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786463 | ||||||
chr2:230786705
|
T | G | 150 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.115-4167T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786705 | ||||||
chr2:230786749
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.115-4123A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786749 | ||||||
chr2:230786970
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.115-3902A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786970 | ||||||
chr2:230786998
|
C | T | 1 | a0001c0001t0015g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.115-3874C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230786998 | ||||||
chr2:230787055
|
A | G | 1 | a0001c0001t0003g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.115-3817A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230787055 | ||||||
chr2:230787117
|
G | T | 247 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(244): Show | 248 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.115-3755G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230787117 | ||||||
chr2:230787280
|
A | G | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.115-3592A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230787280 | ||||||
chr2:230787364
|
GACAT | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-3502_115-3499d others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230787364 | |||||
chr2:230787493
|
G | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-3379G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230787493 | ||||||
chr2:230787516
|
C | T | 1 | a0001c0001t0031g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.115-3356C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230787516 | ||||||
chr2:230787641
|
C | A | 1 | a0001c0001t0003g0236 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.115-3231C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230787641 | ||||||
chr2:230788125
|
T | C | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.115-2747T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230788125 | ||||||
chr2:230788130
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.115-2742T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230788130 | ||||||
chr2:230788246
|
G | GT | 30 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0033others(27): Show | 30 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.115-2612dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230788246 | |||||
chr2:230788246
|
G | T | 1 | a0001c0001t0011g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.115-2626G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230788246 | ||||||
chr2:230788403
|
G | A | 37 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(34): Show | 37 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.115-2469G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230788403 | ||||||
chr2:230788467
|
A | G | 1 | a0001c0001t0004g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.115-2405A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230788467 | ||||||
chr2:230788664
|
T | C | 35 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(32): Show | 35 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.115-2208T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230788664 | ||||||
chr2:230789066
|
T | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-1806T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789066 | ||||||
chr2:230789225
|
G | GT | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-1640dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230789225 | |||||
chr2:230789329
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.115-1543A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789329 | ||||||
chr2:230789334
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-1538C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789334 | ||||||
chr2:230789521
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-1351G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789521 | ||||||
chr2:230789691
|
G | T | 2 | a0001c0001t0018g0240a0001c0001t0018g0243 | 2 | HG01168.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.115-1181G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789691 | ||||||
chr2:230789750
|
A | G | 1 | a0001c0001t0003g0213 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.115-1122A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789750 | ||||||
chr2:230789877
|
T | C | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-995T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789877 | ||||||
chr2:230789932
|
C | G | 2 | a0001c0001t0019g0023a0001c0001t0060g0024 | 2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.115-940C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789932 | ||||||
chr2:230789962
|
C | T | 1 | a0001c0001t0030g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.115-910C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789962 | ||||||
chr2:230789996
|
G | T | 1 | a0001c0001t0041g0308 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115-876G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230789996 | ||||||
chr2:230790004
|
G | C | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.115-868G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790004 | ||||||
chr2:230790163
|
G | A | 150 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.115-709G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790163 | ||||||
chr2:230790197
|
T | C | 108 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(105): Show | 108 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(105): Show |
intron_variant | MODIFIER | c.115-675T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790197 | ||||||
chr2:230790242
|
C | CA | 74 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0035others(71): Show | 75 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.115-618dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 230790242 | |||||
chr2:230790254
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.115-618A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790254 | ||||||
chr2:230790489
|
A | G | 3 | a0001c0001t0001g0325a0001c0001t0001g0341a0001c0001t0002g0339 | 3 | HG00639.hp1 HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.115-383A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790489 | ||||||
chr2:230790562
|
C | T | 4 | a0001c0001t0015g0114a0001c0001t0015g0115a0001c0001t0047g0057others(1): Show | 4 | HG01069.hp2 HG01071.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-310C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790562 | ||||||
chr2:230790837
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.115-35T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 2/8 | chr2 | 230790837 | ||||||
chr2:230791647
|
A | T | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.279+611A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230791647 | ||||||
chr2:230791677
|
G | A | 1 | a0001c0001t0028g0154 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.279+641G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230791677 | ||||||
chr2:230791746
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.279+710T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230791746 | ||||||
chr2:230791792
|
A | G | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.279+756A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230791792 | ||||||
chr2:230791886
|
C | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+850C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230791886 | ||||||
chr2:230791973
|
T | C | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+937T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230791973 | ||||||
chr2:230792006
|
T | C | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.279+970T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230792006 | ||||||
chr2:230792245
|
A | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.280-968A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230792245 | ||||||
chr2:230792323
|
C | T | 141 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0181others(138): Show | 141 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.280-890C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230792323 | ||||||
chr2:230792347
|
G | A | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.280-866G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230792347 | ||||||
chr2:230792402
|
G | A | 2 | a0001c0001t0012g0174a0001c0001t0012g0175 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.280-811G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230792402 | ||||||
chr2:230792693
|
G | T | 1 | a0001c0001t0004g0300 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.280-520G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230792693 | ||||||
chr2:230793179
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.280-34C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 3/8 | chr2 | 230793179 | ||||||
chr2:230793408
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.398+77C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230793408 | ||||||
chr2:230793488
|
T | C | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.398+157T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230793488 | ||||||
chr2:230793719
|
A | G | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.398+388A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230793719 | ||||||
chr2:230793774
|
A | G | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.398+443A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230793774 | ||||||
chr2:230793930
|
A | C | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.398+599A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230793930 | ||||||
chr2:230794054
|
T | A | 34 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.398+723T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794054 | ||||||
chr2:230794231
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.398+900A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794231 | ||||||
chr2:230794242
|
C | T | 4 | a0001c0001t0032g0322a0001c0001t0032g0323a0001c0001t0033g0172others(1): Show | 4 | HG02559.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+911C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794242 | ||||||
chr2:230794453
|
T | C | 40 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(37): Show | 40 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.398+1122T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794453 | ||||||
chr2:230794458
|
C | T | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.398+1127C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794458 | ||||||
chr2:230794543
|
T | G | 4 | a0001c0001t0001g0255a0001c0001t0002g0245a0001c0001t0002g0246others(1): Show | 4 | HG01943.hp2 HG01952.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+1212T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794543 | ||||||
chr2:230794564
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.398+1233G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794564 | ||||||
chr2:230794628
|
G | C | 4 | a0001c0001t0001g0255a0001c0001t0002g0245a0001c0001t0002g0246others(1): Show | 4 | HG01943.hp2 HG01952.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.398+1297G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794628 | ||||||
chr2:230794680
|
C | T | 12 | a0001c0001t0001g0042a0001c0001t0001g0255a0001c0001t0001g0261others(9): Show | 12 | HG00408.hp1 HG01934.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.398+1349C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794680 | ||||||
chr2:230794719
|
G | T | 2 | a0001c0001t0001g0085a0001c0001t0052g0107 | 2 | HG02083.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.398+1388G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794719 | ||||||
chr2:230794843
|
A | AC | 149 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(146): Show | 149 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.398+1513dupC | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230794843 | |||||
chr2:230794880
|
G | A | 2 | a0001c0001t0003g0228a0001c0001t0003g0230 | 2 | NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.398+1549G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794880 | ||||||
chr2:230794998
|
T | C | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.398+1667T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230794998 | ||||||
chr2:230795064
|
C | G | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.398+1733C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795064 | ||||||
chr2:230795224
|
C | T | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.398+1893C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795224 | ||||||
chr2:230795276
|
C | CA | 205 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(202): Show | 206 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.398+1959dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230795276 | |||||
chr2:230795276
|
C | CAA | 9 | a0001c0001t0010g0049a0001c0001t0019g0021a0001c0001t0019g0022others(6): Show | 9 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.398+1958_398+1959d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230795276 | |||||
chr2:230795330
|
C | G | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.398+1999C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795330 | ||||||
chr2:230795458
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.398+2127C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795458 | ||||||
chr2:230795516
|
G | A | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.398+2185G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795516 | ||||||
chr2:230795528
|
A | AG | 18 | a0001c0001t0005g0119a0001c0001t0005g0143a0001c0001t0005g0149others(15): Show | 18 | HG00423.hp1 NA18944.hp2 NA18948.hp1 others(15): Show |
intron_variant | MODIFIER | c.398+2203dupG | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230795528 | |||||
chr2:230795537
|
A | G | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.398+2206A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795537 | ||||||
chr2:230795825
|
T | G | 34 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.398+2494T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795825 | ||||||
chr2:230795843
|
AT | A | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.398+2522delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230795843 | |||||
chr2:230795888
|
G | T | 2 | a0001c0001t0032g0322a0001c0001t0032g0323 | 2 | HG02809.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.398+2557G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795888 | ||||||
chr2:230795903
|
G | A | 1 | a0001c0001t0006g0197 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.398+2572G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230795903 | ||||||
chr2:230796048
|
G | C | 149 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(146): Show | 149 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.399-2681G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230796048 | ||||||
chr2:230796278
|
G | A | 5 | a0001c0001t0020g0203a0001c0001t0020g0204a0001c0001t0020g0205others(2): Show | 5 | HG02257.hp2 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.399-2451G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230796278 | ||||||
chr2:230796389
|
C | T | 34 | a0001c0001t0005g0119a0001c0001t0005g0123a0001c0001t0005g0126others(31): Show | 34 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.399-2340C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230796389 | ||||||
chr2:230796404
|
GT | G | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.399-2323delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230796404 | |||||
chr2:230796446
|
G | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.399-2283G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230796446 | ||||||
chr2:230796515
|
C | G | 1 | a0001c0001t0003g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.399-2214C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230796515 | ||||||
chr2:230796542
|
A | G | 6 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.399-2187A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230796542 | ||||||
chr2:230797233
|
G | A | 340 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.399-1496G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797233 | ||||||
chr2:230797243
|
A | G | 1 | a0001c0001t0038g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.399-1486A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797243 | ||||||
chr2:230797597
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.399-1132C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797597 | ||||||
chr2:230797625
|
G | T | 4 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0054g0137others(1): Show | 4 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.399-1104G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797625 | ||||||
chr2:230797753
|
ACAGT | A | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.399-972_399-969del others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 230797753 | |||||
chr2:230797786
|
G | A | 12 | a0001c0001t0012g0173a0001c0001t0012g0174a0001c0001t0012g0175others(9): Show | 12 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.399-943G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797786 | ||||||
chr2:230797974
|
T | C | 1 | a0001c0001t0002g0245 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.399-755T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797974 | ||||||
chr2:230797989
|
G | C | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.399-740G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230797989 | ||||||
chr2:230798022
|
G | A | 1 | a0001c0001t0025g0134 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.399-707G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230798022 | ||||||
chr2:230798142
|
T | G | 1 | a0001c0001t0067g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.399-587T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230798142 | ||||||
chr2:230798512
|
C | T | 14 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(11): Show | 14 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.399-217C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230798512 | ||||||
chr2:230798644
|
G | A | 2 | a0001c0001t0034g0190a0001c0001t0068g0199 | 2 | HG00099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.399-85G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 4/8 | chr2 | 230798644 | ||||||
chr2:230799024
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.567+127A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799024 | ||||||
chr2:230799205
|
GT | G | 149 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(146): Show | 149 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.567+311delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230799205 | |||||
chr2:230799331
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+434A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799331 | ||||||
chr2:230799371
|
C | G | 1 | a0001c0001t0027g0032 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.567+474C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799371 | ||||||
chr2:230799387
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.567+490C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799387 | ||||||
chr2:230799641
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0084 | 2 | HG02074.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.567+744A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799641 | ||||||
chr2:230799812
|
G | A | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.567+915G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799812 | ||||||
chr2:230799978
|
C | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1081C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230799978 | ||||||
chr2:230799991
|
C | CA | 6 | a0001c0001t0001g0340a0001c0001t0011g0309a0001c0001t0034g0190others(3): Show | 6 | HG00099.hp2 HG02976.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.567+1108dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230799991 | |||||
chr2:230800044
|
C | T | 17 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(14): Show | 17 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.567+1147C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800044 | ||||||
chr2:230800059
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.567+1162G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800059 | ||||||
chr2:230800081
|
G | T | 1 | a0001c0001t0060g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.567+1184G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800081 | ||||||
chr2:230800082
|
A | T | 1 | a0001c0001t0060g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.567+1185A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800082 | ||||||
chr2:230800115
|
A | G | 1 | a0001c0001t0001g0340 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.567+1218A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800115 | ||||||
chr2:230800455
|
T | C | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+1558T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800455 | ||||||
chr2:230800539
|
C | T | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.567+1642C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230800539 | ||||||
chr2:230801090
|
A | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0035others(68): Show | 72 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.567+2193A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801090 | ||||||
chr2:230801231
|
T | C | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.567+2334T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801231 | ||||||
chr2:230801272
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.567+2375C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801272 | ||||||
chr2:230801317
|
C | G | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0049g0239others(2): Show | 5 | HG02257.hp1 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+2420C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801317 | ||||||
chr2:230801463
|
C | T | 1 | a0001c0001t0032g0322 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.567+2566C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801463 | ||||||
chr2:230801472
|
A | G | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.567+2575A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801472 | ||||||
chr2:230801674
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0004g0020a0001c0001t0004g0300 | 3 | HG01515.hp1 HG03669.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.567+2777C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801674 | ||||||
chr2:230801697
|
C | T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.567+2800C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801697 | ||||||
chr2:230801701
|
G | A | 42 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(39): Show | 42 | HG01891.hp2 HG02027.hp2 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.567+2804G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801701 | ||||||
chr2:230801730
|
G | C | 13 | a0001c0001t0012g0173a0001c0001t0012g0174a0001c0001t0012g0175others(10): Show | 13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.567+2833G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801730 | ||||||
chr2:230801808
|
G | A | 6 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.567+2911G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801808 | ||||||
chr2:230801818
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0052g0107 | 2 | HG02083.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.567+2921G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801818 | ||||||
chr2:230801826
|
T | G | 113 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(110): Show | 113 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(110): Show |
intron_variant | MODIFIER | c.567+2929T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230801826 | ||||||
chr2:230801867
|
T | TA | 30 | a0001c0001t0001g0066a0001c0001t0001g0272a0001c0001t0002g0296others(27): Show | 30 | HG00673.hp1 HG00673.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.567+2983dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230801867 | |||||
chr2:230801867
|
T | TAA | 74 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(71): Show | 74 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(71): Show |
intron_variant | MODIFIER | c.567+2982_567+2983d others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230801867 | |||||
chr2:230802095
|
A | C | 1 | a0001c0001t0005g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.567+3198A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802095 | ||||||
chr2:230802122
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.567+3225C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802122 | ||||||
chr2:230802212
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.567+3315C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802212 | ||||||
chr2:230802245
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.567+3348C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802245 | ||||||
chr2:230802508
|
G | A | 2 | a0001c0001t0015g0114a0001c0001t0015g0115 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.567+3611G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802508 | ||||||
chr2:230802512
|
G | GA | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+3615_567+3616i others(3): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802512 | ||||||
chr2:230802513
|
C | A | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.567+3616C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802513 | ||||||
chr2:230802584
|
C | T | 1 | a0001c0001t0014g0025 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.567+3687C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802584 | ||||||
chr2:230802653
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.567+3756T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802653 | ||||||
chr2:230802666
|
G | C | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.567+3769G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802666 | ||||||
chr2:230802773
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.567+3876G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230802773 | ||||||
chr2:230803089
|
T | G | 23 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(20): Show | 23 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.567+4192T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803089 | ||||||
chr2:230803099
|
A | G | 23 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(20): Show | 23 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.567+4202A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803099 | ||||||
chr2:230803126
|
G | A | 4 | a0001c0001t0010g0049a0001c0001t0011g0047a0001c0001t0011g0050others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+4229G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803126 | ||||||
chr2:230803202
|
A | G | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.567+4305A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803202 | ||||||
chr2:230803462
|
A | G | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.567+4565A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803462 | ||||||
chr2:230803625
|
C | G | 23 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(20): Show | 23 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.567+4728C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803625 | ||||||
chr2:230803653
|
T | C | 23 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(20): Show | 23 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.567+4756T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803653 | ||||||
chr2:230803682
|
G | A | 150 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(147): Show | 150 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(147): Show |
intron_variant | MODIFIER | c.567+4785G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803682 | ||||||
chr2:230803735
|
G | A | 8 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0025g0134others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.567+4838G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803735 | ||||||
chr2:230803748
|
G | A | 8 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0025g0134others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.567+4851G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803748 | ||||||
chr2:230803799
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.567+4902A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803799 | ||||||
chr2:230803931
|
G | A | 1 | a0001c0001t0010g0260 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.567+5034G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803931 | ||||||
chr2:230803947
|
C | T | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.567+5050C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803947 | ||||||
chr2:230803977
|
C | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5080C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803977 | ||||||
chr2:230803978
|
A | G | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5081A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803978 | ||||||
chr2:230803986
|
T | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5089T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803986 | ||||||
chr2:230803987
|
G | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5090G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803987 | ||||||
chr2:230803991
|
T | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5094T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803991 | ||||||
chr2:230803992
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5095C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803992 | ||||||
chr2:230803995
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5098A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803995 | ||||||
chr2:230803997
|
T | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5100T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803997 | ||||||
chr2:230803998
|
C | G | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5101C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803998 | ||||||
chr2:230803999
|
T | G | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5102T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230803999 | ||||||
chr2:230804003
|
A | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5106A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804003 | ||||||
chr2:230804006
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5109A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804006 | ||||||
chr2:230804007
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5110G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804007 | ||||||
chr2:230804018
|
C | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5121C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804018 | ||||||
chr2:230804074
|
G | A | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.567+5177G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804074 | ||||||
chr2:230804077
|
G | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5180G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804077 | ||||||
chr2:230804079
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5182C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804079 | ||||||
chr2:230804087
|
T | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5190T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804087 | ||||||
chr2:230804094
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.567+5197G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804094 | ||||||
chr2:230804099
|
C | T | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.567+5202C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804099 | ||||||
chr2:230804150
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.567+5253A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804150 | ||||||
chr2:230804180
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5283G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804180 | ||||||
chr2:230804212
|
A | G | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.567+5315A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804212 | ||||||
chr2:230804231
|
C | T | 1 | a0001c0001t0005g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.567+5334C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804231 | ||||||
chr2:230804256
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5359G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804256 | ||||||
chr2:230804269
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5372A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804269 | ||||||
chr2:230804303
|
G | GCCAACTA others(10): Show |
1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5406_567+5407i others(19): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804303 | ||||||
chr2:230804311
|
A | G | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.567+5414A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804311 | ||||||
chr2:230804319
|
C | G | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5422C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804319 | ||||||
chr2:230804323
|
T | G | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5426T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804323 | ||||||
chr2:230804330
|
A | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5433A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804330 | ||||||
chr2:230804340
|
G | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5443G>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804340 | ||||||
chr2:230804342
|
A | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5445A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804342 | ||||||
chr2:230804344
|
G | A | 3 | a0001c0001t0001g0312a0001c0001t0006g0211a0001c0001t0006g0217 | 3 | NA18950.hp1 NA18990.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.567+5447G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804344 | ||||||
chr2:230804380
|
A | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5483A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804380 | ||||||
chr2:230804389
|
AATAGATA others(3): Show |
A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5493_567+5502d others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804389 | ||||||
chr2:230804425
|
C | A | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5528C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804425 | ||||||
chr2:230804434
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5537A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804434 | ||||||
chr2:230804447
|
A | C | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5550A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804447 | ||||||
chr2:230804448
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.567+5551G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804448 | ||||||
chr2:230804459
|
C | A | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.567+5562C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804459 | ||||||
chr2:230804691
|
A | G | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(19): Show | 22 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.568-5572A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804691 | ||||||
chr2:230804730
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.568-5533T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804730 | ||||||
chr2:230804735
|
A | C | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.568-5528A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804735 | ||||||
chr2:230804957
|
C | T | 340 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.568-5306C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804957 | ||||||
chr2:230804999
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.568-5264A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230804999 | ||||||
chr2:230805068
|
T | TA | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.568-5189dupA | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230805068 | |||||
chr2:230805084
|
C | T | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.568-5179C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805084 | ||||||
chr2:230805138
|
G | A | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-5125G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805138 | ||||||
chr2:230805462
|
A | G | 7 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(4): Show | 7 | HG00639.hp2 HG01256.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.568-4801A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805462 | ||||||
chr2:230805506
|
A | G | 1 | a0001c0001t0029g0304 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.568-4757A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805506 | ||||||
chr2:230805557
|
T | C | 1 | a0001c0001t0015g0335 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.568-4706T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805557 | ||||||
chr2:230805622
|
AGTT | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.568-4635_568-4633d others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230805622 | |||||
chr2:230805632
|
C | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.568-4631C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805632 | ||||||
chr2:230805799
|
A | C | 24 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(21): Show | 24 | HG00639.hp2 HG01106.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.568-4464A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230805799 | ||||||
chr2:230806175
|
C | G | 16 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.568-4088C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806175 | ||||||
chr2:230806195
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.568-4068A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806195 | ||||||
chr2:230806214
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-4049A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806214 | ||||||
chr2:230806463
|
A | G | 62 | a0001c0001t0002g0306a0001c0001t0005g0119a0001c0001t0005g0123others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.568-3800A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806463 | ||||||
chr2:230806555
|
G | A | 2 | a0001c0001t0054g0137a0001c0001t0055g0136 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.568-3708G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806555 | ||||||
chr2:230806701
|
C | G | 62 | a0001c0001t0002g0306a0001c0001t0005g0119a0001c0001t0005g0123others(59): Show | 62 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.568-3562C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806701 | ||||||
chr2:230806874
|
C | G | 1 | a0001c0001t0004g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.568-3389C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806874 | ||||||
chr2:230806994
|
A | G | 1 | a0001c0001t0012g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.568-3269A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230806994 | ||||||
chr2:230807250
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0053others(19): Show | 22 | HG00733.hp1 HG01069.hp1 HG01517.hp1 others(19): Show |
intron_variant | MODIFIER | c.568-3013C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807250 | ||||||
chr2:230807375
|
G | T | 21 | a0001c0001t0001g0026a0001c0001t0001g0317a0001c0001t0002g0096others(18): Show | 21 | HG01168.hp1 HG01256.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.568-2888G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807375 | ||||||
chr2:230807412
|
C | G | 3 | a0001c0001t0003g0228a0001c0001t0003g0229a0001c0001t0003g0230 | 3 | HG02080.hp2 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.568-2851C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807412 | ||||||
chr2:230807415
|
C | G | 2 | a0001c0001t0009g0109a0001c0001t0010g0110 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.568-2848C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807415 | ||||||
chr2:230807758
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0002g0034 | 2 | HG01081.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.568-2505T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807758 | ||||||
chr2:230807857
|
C | T | 37 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0005g0119others(34): Show | 37 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.568-2406C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807857 | ||||||
chr2:230807887
|
A | G | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.568-2376A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230807887 | ||||||
chr2:230808011
|
T | G | 6 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0009g0241others(3): Show | 6 | HG01168.hp1 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-2252T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808011 | ||||||
chr2:230808038
|
G | A | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.568-2225G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808038 | ||||||
chr2:230808051
|
TTTTTC | T | 151 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.568-2187_568-2183d others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230808051 | |||||
chr2:230808051
|
TTTTTCTT others(3): Show |
T | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.568-2192_568-2183d others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230808051 | |||||
chr2:230808064
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.568-2199T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808064 | ||||||
chr2:230808334
|
G | A | 1 | a0001c0001t0031g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.568-1929G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808334 | ||||||
chr2:230808389
|
A | C | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.568-1874A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808389 | ||||||
chr2:230808397
|
T | C | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.568-1866T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808397 | ||||||
chr2:230808480
|
C | T | 1 | a0001c0001t0025g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.568-1783C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808480 | ||||||
chr2:230808510
|
A | G | 76 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(73): Show | 76 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(73): Show |
intron_variant | MODIFIER | c.568-1753A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808510 | ||||||
chr2:230808539
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.568-1724G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808539 | ||||||
chr2:230808616
|
C | CT | 27 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0017others(24): Show | 27 | HG01106.hp1 HG01168.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.568-1645dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 230808616 | |||||
chr2:230808689
|
T | A | 1 | a0001c0001t0020g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.568-1574T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808689 | ||||||
chr2:230808803
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.568-1460G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808803 | ||||||
chr2:230808985
|
C | T | 1 | a0001c0001t0024g0125 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.568-1278C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230808985 | ||||||
chr2:230809047
|
G | A | 1 | a0001c0001t0008g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.568-1216G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809047 | ||||||
chr2:230809156
|
C | G | 2 | a0001c0001t0001g0290a0001c0001t0004g0294 | 2 | HG00099.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.568-1107C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809156 | ||||||
chr2:230809198
|
C | G | 1 | a0001c0001t0041g0308 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.568-1065C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809198 | ||||||
chr2:230809262
|
G | A | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.568-1001G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809262 | ||||||
chr2:230809345
|
G | A | 1 | a0001c0001t0037g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.568-918G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809345 | ||||||
chr2:230809380
|
C | T | 1 | a0001c0001t0016g0187 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.568-883C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809380 | ||||||
chr2:230809537
|
G | A | 1 | a0001c0001t0005g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.568-726G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809537 | ||||||
chr2:230809865
|
C | T | 19 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0009g0008others(16): Show | 19 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.568-398C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230809865 | ||||||
chr2:230810106
|
T | G | 1 | a0001c0001t0013g0127 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.568-157T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 5/8 | chr2 | 230810106 | ||||||
chr2:230810578
|
T | C | 1 | a0001c0001t0002g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.627+256T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230810578 | ||||||
chr2:230810592
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.627+270G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230810592 | ||||||
chr2:230810617
|
C | T | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.627+295C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230810617 | ||||||
chr2:230810971
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.627+649A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230810971 | ||||||
chr2:230811061
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.627+739T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811061 | ||||||
chr2:230811326
|
C | G | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.627+1004C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811326 | ||||||
chr2:230811340
|
C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0002g0056others(2): Show | 5 | HG01981.hp2 HG02300.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.627+1018C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811340 | ||||||
chr2:230811351
|
C | T | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1029C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811351 | ||||||
chr2:230811422
|
T | C | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0237 | 3 | HG01070.hp1 HG01071.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.627+1100T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811422 | ||||||
chr2:230811696
|
G | A | 1 | a0001c0001t0052g0107 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.627+1374G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811696 | ||||||
chr2:230811824
|
C | G | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.627+1502C>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811824 | ||||||
chr2:230811977
|
G | A | 2 | a0001c0001t0024g0125a0001c0001t0024g0129 | 2 | HG06807.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.627+1655G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811977 | ||||||
chr2:230811982
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.627+1660A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811982 | ||||||
chr2:230811986
|
T | C | 1 | a0001c0001t0001g0340 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.627+1664T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230811986 | ||||||
chr2:230812028
|
A | G | 102 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(99): Show | 102 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(99): Show |
intron_variant | MODIFIER | c.627+1706A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812028 | ||||||
chr2:230812071
|
A | G | 109 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(106): Show | 109 | HG00099.hp2 HG00639.hp2 HG01106.hp1 others(106): Show |
intron_variant | MODIFIER | c.627+1749A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812071 | ||||||
chr2:230812228
|
G | A | 1 | a0001c0001t0009g0109 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.628-1821G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812228 | ||||||
chr2:230812676
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.628-1373A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812676 | ||||||
chr2:230812681
|
A | T | 340 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.628-1368A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812681 | ||||||
chr2:230812724
|
G | A | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1325G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812724 | ||||||
chr2:230812796
|
A | G | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-1253A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230812796 | ||||||
chr2:230813055
|
C | T | 4 | a0001c0001t0019g0021a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.628-994C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230813055 | ||||||
chr2:230813470
|
A | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(249): Show | 253 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.628-579A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230813470 | ||||||
chr2:230813650
|
C | T | 36 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(33): Show | 36 | HG02027.hp2 HG02080.hp2 HG02129.hp2 others(33): Show |
intron_variant | MODIFIER | c.628-399C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230813650 | ||||||
chr2:230813698
|
A | G | 75 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(72): Show | 75 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(72): Show |
intron_variant | MODIFIER | c.628-351A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230813698 | ||||||
chr2:230813771
|
T | C | 6 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-278T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | chr2 | 230813771 | ||||||
chr2:230813978
|
C | CT | 30 | a0001c0001t0001g0255a0001c0001t0001g0258a0001c0001t0001g0264others(27): Show | 30 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.628-37dupT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTT | 11 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0336others(8): Show | 11 | HG00558.hp1 HG00733.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.628-38_628-37dupTT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTT | 8 | a0001c0001t0002g0252a0001c0001t0002g0271a0001c0001t0002g0273others(5): Show | 8 | HG00597.hp2 HG02300.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.628-39_628-37dupTT others(1): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTT | 6 | a0001c0001t0001g0033a0001c0001t0001g0074a0001c0001t0001g0075others(3): Show | 6 | HG01081.hp1 NA18986.hp1 NA19054.hp2 others(3): Show |
intron_variant | MODIFIER | c.628-41_628-37dupTT others(3): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTT | 21 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0040others(18): Show | 21 | HG00735.hp1 HG01106.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.628-42_628-37dupTT others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT | 26 | a0001c0001t0001g0001a0001c0001t0001g0038a0001c0001t0001g0063others(23): Show | 27 | HG00280.hp1 HG00408.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.628-43_628-37dupTT others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(1): Show |
20 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0069others(17): Show | 20 | HG00140.hp2 HG00733.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.628-44_628-37dupTT others(6): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0065a0001c0001t0001g0160a0001c0001t0001g0237others(3): Show | 6 | HG01069.hp1 HG01255.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.628-45_628-37dupTT others(7): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0095others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.628-46_628-37dupTT others(8): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.628-47_628-37dupTT others(9): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0100a0001c0001t0002g0082a0001c0001t0010g0049 | 3 | HG00558.hp2 HG01070.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.628-48_628-37dupTT others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0093a0001c0001t0001g0113 | 2 | HG02080.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.628-49_628-37dupTT others(11): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0001g0101a0001c0001t0013g0130 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.628-50_628-37dupTT others(12): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CT | C | 24 | a0001c0001t0001g0249a0001c0001t0001g0297a0001c0001t0001g0320others(21): Show | 24 | HG00423.hp2 HG00639.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.628-37delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTT | C | 36 | a0001c0001t0001g0292a0001c0001t0001g0298a0001c0001t0001g0310others(33): Show | 36 | HG01243.hp2 HG01891.hp2 HG02027.hp2 others(33): Show |
intron_variant | MODIFIER | c.628-38_628-37delTT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTT | C | 30 | a0001c0001t0003g0191a0001c0001t0003g0210a0001c0001t0006g0192others(27): Show | 30 | HG00099.hp2 HG01106.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.628-39_628-37delTT others(1): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTT | C | 15 | a0001c0001t0006g0194a0001c0001t0006g0195a0001c0001t0006g0196others(12): Show | 15 | HG01168.hp2 HG01169.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.628-40_628-37delTT others(2): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTTT | C | 29 | a0001c0001t0005g0119a0001c0001t0005g0128a0001c0001t0005g0131others(26): Show | 29 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.628-41_628-37delTT others(3): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTTTT | C | 11 | a0001c0001t0005g0123a0001c0001t0005g0126a0001c0001t0005g0143others(8): Show | 11 | HG01167.hp1 HG01168.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.628-42_628-37delTT others(4): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTTTTT | C | 7 | a0001c0001t0001g0026a0001c0001t0009g0017a0001c0001t0009g0018others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-43_628-37delTT others(5): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0327a0001c0001t0004g0117 | 2 | HG00642.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.628-47_628-37delTT others(9): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0081a0001c0001t0001g0084 | 2 | HG02074.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.628-48_628-37delTT others(10): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230813978
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.628-55_628-37delTT others(17): Show |
CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 230813978 | |||||
chr2:230814235
|
G | A | 5 | a0001c0001t0008g0073a0001c0001t0019g0021a0001c0001t0019g0022others(2): Show | 5 | HG00639.hp2 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+121G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230814235 | ||||||
chr2:230814416
|
A | G | 4 | a0001c0001t0009g0241a0001c0001t0018g0240a0001c0001t0018g0242others(1): Show | 4 | HG01168.hp1 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+302A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230814416 | ||||||
chr2:230814486
|
A | T | 1 | a0001c0001t0004g0020 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.693+372A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230814486 | ||||||
chr2:230814509
|
G | A | 149 | a0001c0001t0001g0026a0001c0001t0002g0306a0001c0001t0003g0180others(146): Show | 149 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.693+395G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230814509 | ||||||
chr2:230814611
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.693+497C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230814611 | ||||||
chr2:230814829
|
G | T | 1 | a0001c0001t0017g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.693+715G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230814829 | ||||||
chr2:230815223
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.693+1109G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230815223 | ||||||
chr2:230815851
|
G | A | 15 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0010g0013others(12): Show | 15 | HG01106.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.693+1737G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230815851 | ||||||
chr2:230815961
|
C | T | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0290others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1793C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230815961 | ||||||
chr2:230815979
|
T | G | 340 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.694-1775T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230815979 | ||||||
chr2:230816006
|
G | T | 2 | a0001c0001t0001g0320a0001c0001t0009g0319 | 2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.694-1748G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816006 | ||||||
chr2:230816155
|
C | A | 1 | a0001c0001t0030g0232 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.694-1599C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816155 | ||||||
chr2:230816179
|
A | C | 1 | a0001c0001t0008g0267 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.694-1575A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816179 | ||||||
chr2:230816277
|
T | A | 1 | a0001c0001t0003g0180 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.694-1477T>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816277 | ||||||
chr2:230816336
|
T | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0237 | 3 | HG01070.hp1 HG01071.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.694-1418T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816336 | ||||||
chr2:230816350
|
G | A | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.694-1404G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816350 | ||||||
chr2:230816475
|
G | A | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.694-1279G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816475 | ||||||
chr2:230816586
|
A | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0035others(67): Show | 71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.694-1168A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816586 | ||||||
chr2:230816706
|
A | T | 1 | a0001c0001t0034g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.694-1048A>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816706 | ||||||
chr2:230816719
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.694-1035A>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816719 | ||||||
chr2:230816785
|
T | C | 2 | a0001c0001t0006g0196a0001c0001t0006g0201 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.694-969T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230816785 | ||||||
chr2:230817041
|
C | A | 113 | a0001c0001t0002g0306a0001c0001t0003g0180a0001c0001t0003g0181others(110): Show | 113 | HG00423.hp1 HG00597.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.694-713C>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817041 | ||||||
chr2:230817047
|
A | C | 22 | a0001c0001t0002g0306a0001c0001t0009g0008a0001c0001t0009g0241others(19): Show | 22 | HG01106.hp1 HG01243.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.694-707A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817047 | ||||||
chr2:230817067
|
A | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.694-687A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817067 | ||||||
chr2:230817268
|
A | C | 2 | a0001c0001t0011g0309a0001c0001t0041g0308 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.694-486A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817268 | ||||||
chr2:230817424
|
GT | G | 3 | a0001c0001t0009g0017a0001c0001t0009g0018a0001c0001t0034g0305 | 3 | HG01884.hp2 HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.694-327delT | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 230817424 | |||||
chr2:230817541
|
G | A | 1 | a0001c0001t0071g0177 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.694-213G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817541 | ||||||
chr2:230817546
|
C | T | 129 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0053others(126): Show | 129 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.694-208C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817546 | ||||||
chr2:230817548
|
T | C | 151 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0053others(148): Show | 151 | HG00099.hp2 HG00423.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.694-206T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817548 | ||||||
chr2:230817689
|
T | G | 1 | a0001c0001t0031g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.694-65T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 7/8 | chr2 | 230817689 | ||||||
chr2:230817943
|
G | A | 3 | a0001c0001t0001g0325a0001c0001t0001g0341a0001c0001t0002g0339 | 3 | HG00639.hp1 HG01261.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.837+46G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230817943 | ||||||
chr2:230818070
|
C | T | 1 | a0001c0001t0002g0279 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.837+173C>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818070 | ||||||
chr2:230818076
|
A | C | 1 | a0001c0001t0003g0227 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.837+179A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818076 | ||||||
chr2:230818082
|
T | C | 3 | a0001c0001t0030g0232a0001c0001t0030g0233a0001c0001t0061g0231 | 3 | HG01256.hp1 HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.837+185T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818082 | ||||||
chr2:230818223
|
T | C | 50 | a0001c0001t0002g0306a0001c0001t0005g0119a0001c0001t0005g0123others(47): Show | 50 | HG00423.hp1 HG00597.hp1 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.838-293T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818223 | ||||||
chr2:230818230
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0028g0028a0001c0001t0042g0027 | 3 | HG02818.hp2 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.838-286T>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818230 | ||||||
chr2:230818234
|
T | G | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.838-282T>G | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818234 | ||||||
chr2:230818238
|
G | T | 5 | a0001c0001t0025g0134a0001c0001t0025g0135a0001c0001t0034g0305others(2): Show | 5 | HG01884.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.838-278G>T | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818238 | ||||||
chr2:230818342
|
A | C | 1 | a0001c0001t0044g0133 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.838-174A>C | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818342 | ||||||
chr2:230818372
|
G | A | 1 | a0001c0001t0008g0111 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.838-144G>A | CAB39 | ENSG00000135932.12 | transcript | ENST00000258418.10 | protein_coding | 8/8 | chr2 | 230818372 |