geneid | 388795 |
---|---|
ensemblid | ENSG00000215529.13 |
hgncid | 34532 |
symbol | EFCAB8 |
name | EF-hand calcium binding domain 8 |
refseq_nuc | NM_001143967.2 |
refseq_prot | NP_001137439.1 |
ensembl_nuc | ENST00000400522.9 |
ensembl_prot | ENSP00000383366.5 |
mane_status | MANE Select |
chr | chr20 |
start | 32858923 |
end | 32961845 |
strand | + |
ver | v1.2 |
region | chr20:32858923-32961845 |
region5000 | chr20:32853923-32966845 |
regionname0 | EFCAB8_chr20_32858923_32961845 |
regionname5000 | EFCAB8_chr20_32853923_32966845 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1288 | 75 | 11 | 20 | 30 | 2 | 11 | 23 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002 | 0/0 | 1288 | 58 | 30 | 2 | 17 | 1 | 8 | 16 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0003 | 0/0 | 1288 | 15 | 5 | 1 | 9 | 0 | 0 | 7 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0004 | 0/0 | 964 | 14 | 1 | 4 | 1 | 4 | 4 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005 | 0/0 | 148 | 13 | 5 | 1 | 6 | 0 | 1 | 5 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0006 | 0/0 | 1288 | 12 | 0 | 10 | 0 | 0 | 2 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007 | 0/0 | 1288 | 9 | 6 | 0 | 3 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0008 | 0/0 | 964 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009 | 0/0 | 1288 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0010 | 0/0 | 1288 | 5 | 2 | 0 | 2 | 0 | 1 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0011 | 0/0 | 964 | 5 | 0 | 4 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0012 | 0/0 | 1288 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0013 | 0/0 | 1288 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0014 | 0/0 | 1288 | 3 | 0 | 0 | 2 | 1 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0015 | 0/0 | 1288 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0016 | 0/0 | 1288 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0017 | 0/0 | 1288 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0018 | 0/0 | 1288 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0019 | 0/1 | 1288 | 3 | 0 | 0 | 0 | 1 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0020 | 0/0 | 1288 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0021 | 0/0 | 1288 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0022 | 0/0 | 1288 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0023 | 0/0 | 1288 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0024 | 0/0 | 1288 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0025 | 0/0 | 1288 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0026 | 0/0 | 1288 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0027 | 0/0 | 964 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0028 | 0/0 | 1288 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0029 | 0/0 | 148 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0030 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0031 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0032 | 0/0 | 964 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0033 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0034 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0035 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0036 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0037 | 0/0 | 964 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0038 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0039 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0040 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0041 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0042 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0043 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0044 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0045 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0046 | 0/0 | 1288 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0047 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0048 | 0/0 | 1288 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0049 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0050 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0051 | 0/0 | 1288 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3867 | 73 | 11 | 19 | 29 | 2 | 11 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0002 | 0/0 | 3867 | 50 | 24 | 2 | 17 | 1 | 6 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0003 | 0/0 | 3867 | 15 | 5 | 1 | 9 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0004 | 0/0 | 3867 | 14 | 1 | 4 | 1 | 4 | 4 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0005 | 0/0 | 3867 | 12 | 0 | 10 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0006 | 0/0 | 3867 | 7 | 4 | 0 | 3 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0007 | 0/0 | 3867 | 6 | 0 | 2 | 0 | 1 | 3 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0008 | 0/0 | 3868 | 5 | 1 | 0 | 3 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0009 | 0/0 | 3867 | 5 | 2 | 0 | 2 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0010 | 0/0 | 3867 | 5 | 0 | 4 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0011 | 0/0 | 3867 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0012 | 0/0 | 3867 | 4 | 0 | 3 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0013 | 0/0 | 3868 | 3 | 2 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0014 | 0/0 | 3867 | 3 | 0 | 0 | 2 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0015 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0016 | 0/1 | 3867 | 3 | 0 | 0 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0017 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0018 | 0/0 | 3867 | 3 | 1 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0019 | 0/0 | 3867 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0020 | 0/0 | 3867 | 3 | 0 | 2 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0021 | 0/0 | 3867 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0022 | 0/0 | 3867 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0023 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0024 | 0/0 | 3867 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0025 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0026 | 0/0 | 3867 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0027 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0028 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0029 | 0/0 | 3867 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0030 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0031 | 0/0 | 3867 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0032 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0033 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0034 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0035 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0036 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0037 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0038 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0039 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0040 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0041 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0042 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0043 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0044 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0045 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0046 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0047 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0048 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0049 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0050 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0051 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0052 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0053 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0054 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0055 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0056 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0057 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0058 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0059 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0060 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0061 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0062 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0063 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0064 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0065 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0066 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0067 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
c0068 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 331 | 129 | 46 | 28 | 37 | 4 | 12 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0002 | 0/0 | 331 | 56 | 5 | 3 | 35 | 3 | 10 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0003 | 0/0 | 331 | 46 | 11 | 18 | 2 | 3 | 12 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0004 | 0/0 | 331 | 28 | 16 | 6 | 5 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0005 | 0/0 | 331 | 11 | 7 | 2 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0006 | 0/0 | 331 | 8 | 0 | 6 | 1 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0007 | 0/0 | 331 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0008 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
t0009 | 0/0 | 331 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
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 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3867 | 73 | 11 | 19 | 29 | 2 | 11 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0052 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0056 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0002 | 0/0 | 3867 | 50 | 24 | 2 | 17 | 1 | 6 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0011 | 0/0 | 3867 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0022 | 0/0 | 3867 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0042 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0046 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0003c0003 | 0/0 | 3867 | 15 | 5 | 1 | 9 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0004c0004 | 0/0 | 3867 | 14 | 1 | 4 | 1 | 4 | 4 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0008 | 0/0 | 3868 | 5 | 1 | 0 | 3 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0013 | 0/0 | 3868 | 3 | 2 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0033 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0034 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0035 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0036 | 0/0 | 3868 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0037 | 0/0 | 3868 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0006c0005 | 0/0 | 3867 | 12 | 0 | 10 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007c0006 | 0/0 | 3867 | 7 | 4 | 0 | 3 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007c0030 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0008c0007 | 0/0 | 3867 | 6 | 0 | 2 | 0 | 1 | 3 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009c0015 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009c0023 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009c0041 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0010c0009 | 0/0 | 3867 | 5 | 2 | 0 | 2 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0011c0010 | 0/0 | 3867 | 5 | 0 | 4 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0012c0012 | 0/0 | 3867 | 4 | 0 | 3 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0013c0020 | 0/0 | 3867 | 3 | 0 | 2 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0014c0014 | 0/0 | 3867 | 3 | 0 | 0 | 2 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0015c0019 | 0/0 | 3867 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0016c0018 | 0/0 | 3867 | 3 | 1 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0017c0017 | 0/0 | 3867 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0018c0026 | 0/0 | 3867 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0018c0051 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0019c0016 | 0/1 | 3867 | 3 | 0 | 0 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0020c0032 | 0/0 | 3867 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0021c0061 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0021c0062 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0022c0031 | 0/0 | 3867 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0023c0028 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0024c0024 | 0/0 | 3867 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0025c0025 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0026c0027 | 0/0 | 3867 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0027c0029 | 0/0 | 3867 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0028c0021 | 0/0 | 3867 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0029c0059 | 0/0 | 3868 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0030c0063 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0031c0060 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0032c0064 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0033c0065 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0034c0040 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0035c0038 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0036c0039 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0037c0057 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0038c0047 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0039c0048 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0040c0049 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0041c0050 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0042c0043 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0043c0045 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0044c0044 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0045c0054 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0046c0053 | 0/0 | 3867 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0047c0055 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0048c0058 | 0/0 | 3867 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0049c0066 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0050c0068 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0051c0067 | 0/0 | 3867 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4197 | 64 | 8 | 18 | 25 | 2 | 10 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0001t0002 | 0/0 | 4197 | 4 | 0 | 0 | 3 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0001t0004 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0001t0005 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0001t0009 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0052t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0001c0056t0001 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0002t0001 | 0/0 | 4197 | 18 | 15 | 2 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0002t0002 | 0/0 | 4197 | 24 | 1 | 0 | 16 | 1 | 6 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0002t0003 | 0/0 | 4197 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0002t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0011t0001 | 0/0 | 4197 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0022t0002 | 0/0 | 4197 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0042t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0002c0046t0003 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0003c0003t0001 | 0/0 | 4197 | 11 | 3 | 1 | 7 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0003c0003t0002 | 0/0 | 4197 | 4 | 2 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0004c0004t0001 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0004c0004t0003 | 0/0 | 4197 | 13 | 1 | 4 | 1 | 3 | 4 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0008t0001 | 0/0 | 4198 | 3 | 1 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0008t0002 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0008t0004 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0013t0001 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0013t0002 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0013t0004 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0033t0008 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0034t0002 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0035t0001 | 0/0 | 4198 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0036t0004 | 0/0 | 4198 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0005c0037t0004 | 0/0 | 4198 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0006c0005t0003 | 0/0 | 4197 | 11 | 0 | 9 | 0 | 0 | 2 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0006c0005t0006 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007c0006t0001 | 0/0 | 4197 | 4 | 2 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007c0006t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007c0006t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0007c0030t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0008c0007t0003 | 0/0 | 4197 | 3 | 0 | 0 | 0 | 0 | 3 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0008c0007t0006 | 0/0 | 4197 | 3 | 0 | 2 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009c0015t0001 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009c0023t0001 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0009c0041t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0010c0009t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0010c0009t0004 | 0/0 | 4197 | 3 | 1 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0010c0009t0005 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0011c0010t0003 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0011c0010t0006 | 0/0 | 4197 | 4 | 0 | 3 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0012c0012t0004 | 0/0 | 4197 | 4 | 0 | 3 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0013c0020t0003 | 0/0 | 4197 | 3 | 0 | 2 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0014c0014t0002 | 0/0 | 4197 | 3 | 0 | 0 | 2 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0015c0019t0005 | 0/0 | 4197 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0016c0018t0004 | 0/0 | 4197 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0016c0018t0005 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0017c0017t0007 | 0/0 | 4197 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0018c0026t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0018c0026t0003 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0018c0051t0003 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0019c0016t0001 | 0/1 | 4197 | 3 | 0 | 0 | 0 | 1 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0020c0032t0004 | 0/0 | 4197 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0021c0061t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0021c0062t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0022c0031t0002 | 0/0 | 4197 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0023c0028t0002 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0023c0028t0005 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0024c0024t0005 | 0/0 | 4197 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0025c0025t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0025c0025t0002 | 0/0 | 4197 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0026c0027t0003 | 0/0 | 4197 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0027c0029t0003 | 0/0 | 4197 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0028c0021t0002 | 0/0 | 4197 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0029c0059t0003 | 0/0 | 4198 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0030c0063t0004 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0031c0060t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0032c0064t0003 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0033c0065t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0034c0040t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0035c0038t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0036c0039t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0037c0057t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0038c0047t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0039c0048t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0040c0049t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0041c0050t0002 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0042c0043t0001 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0043c0045t0007 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0044c0044t0002 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0045c0054t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0046c0053t0002 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0047c0055t0001 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0048c0058t0002 | 0/0 | 4197 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0049c0066t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0050c0068t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
a0051c0067t0004 | 0/0 | 4197 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | copy fasta | chr20 | 32853923 | 32966845 |
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 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0001t0009g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0052t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0001c0056t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0011t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0022t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0022t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0042t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0002c0046t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0003c0003t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0004c0004t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0008t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0013t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0013t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0013t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0033t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0034t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0035t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0036t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0005c0037t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0006c0005t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0006t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0030t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0007c0030t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0008c0007t0006g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0015t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0015t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0015t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0023t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0023t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0009c0041t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0009t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0009t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0009t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0009t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0010c0009t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0010t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0010t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0010t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0010t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0011c0010t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0012c0012t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0013c0020t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0013c0020t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0013c0020t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0014c0014t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0014c0014t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0014c0014t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0015c0019t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0015c0019t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0015c0019t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0016c0018t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0016c0018t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0016c0018t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0017c0017t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0017c0017t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0017c0017t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0018c0026t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0018c0026t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0018c0051t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0019c0016t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0019c0016t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0019c0016t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0020c0032t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0020c0032t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0021c0061t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0021c0062t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0022c0031t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0022c0031t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0023c0028t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0023c0028t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0024c0024t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0024c0024t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0025c0025t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0025c0025t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0026c0027t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0026c0027t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0027c0029t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0027c0029t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0028c0021t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0028c0021t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0029c0059t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0030c0063t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0031c0060t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0032c0064t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0033c0065t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0034c0040t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0035c0038t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0036c0039t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0037c0057t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0038c0047t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0039c0048t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0040c0049t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0041c0050t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0042c0043t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0043c0045t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0044c0044t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0045c0054t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0046c0053t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0047c0055t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0048c0058t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0049c0066t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0050c0068t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
a0051c0067t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0019 | c0016 | t0001 | g0178 | EUR | GBR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00280 | hp1 | a0004 | c0004 | t0001 | g0089 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00280 | hp2 | a0004 | c0004 | t0003 | g0077 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00323 | hp1 | a0025 | c0025 | t0002 | g0019 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0145 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00621 | hp2 | a0046 | c0053 | t0002 | g0029 | EAS | CHS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00639 | hp1 | a0042 | c0043 | t0001 | g0184 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00639 | hp2 | a0006 | c0005 | t0003 | g0065 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00642 | hp1 | a0032 | c0064 | t0003 | g0083 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00733 | hp1 | a0008 | c0007 | t0006 | g0013 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00733 | hp2 | a0031 | c0060 | t0001 | g0079 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00741 | hp1 | a0015 | c0019 | t0005 | g0232 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG00741 | hp2 | a0004 | c0004 | t0003 | g0084 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01070 | hp1 | a0006 | c0005 | t0003 | g0078 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0114 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01071 | hp1 | a0006 | c0005 | t0003 | g0076 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01071 | hp2 | a0001 | c0052 | t0001 | g0185 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01081 | hp1 | a0033 | c0065 | t0001 | g0060 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01081 | hp2 | a0006 | c0005 | t0003 | g0237 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01099 | hp1 | a0013 | c0020 | t0003 | g0080 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01099 | hp2 | a0021 | c0062 | t0001 | g0072 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01109 | hp2 | a0018 | c0026 | t0001 | g0283 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01167 | hp1 | a0016 | c0018 | t0004 | g0192 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01167 | hp2 | a0022 | c0031 | t0002 | g0196 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01168 | hp1 | a0008 | c0007 | t0006 | g0016 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01169 | hp2 | a0016 | c0018 | t0004 | g0147 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01175 | hp1 | a0006 | c0005 | t0003 | g0064 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01192 | hp1 | a0013 | c0020 | t0003 | g0090 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01243 | hp1 | a0030 | c0063 | t0004 | g0081 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01243 | hp2 | a0022 | c0031 | t0002 | g0230 | AMR | PUR | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01255 | hp2 | a0004 | c0004 | t0003 | g0066 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01257 | hp1 | a0006 | c0005 | t0006 | g0020 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01261 | hp1 | a0011 | c0010 | t0006 | g0010 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01261 | hp2 | a0048 | c0058 | t0002 | g0257 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01346 | hp1 | a0024 | c0024 | t0005 | g0041 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01358 | hp2 | a0003 | c0003 | t0001 | g0279 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01361 | hp1 | a0006 | c0005 | t0003 | g0082 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01433 | hp1 | a0012 | c0012 | t0004 | g0108 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01496 | hp1 | a0004 | c0004 | t0003 | g0059 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01515 | hp1 | a0014 | c0014 | t0002 | g0014 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01515 | hp2 | a0008 | c0007 | t0006 | g0044 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01516 | hp1 | a0004 | c0004 | t0003 | g0069 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01516 | hp2 | a0004 | c0004 | t0003 | g0253 | EUR | IBS | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01884 | hp2 | a0015 | c0019 | t0005 | g0219 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01891 | hp1 | a0017 | c0017 | t0007 | g0227 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01891 | hp2 | a0020 | c0032 | t0004 | g0277 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01943 | hp2 | a0011 | c0010 | t0006 | g0009 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01975 | hp2 | a0029 | c0059 | t0003 | g0071 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01981 | hp2 | a0012 | c0012 | t0004 | g0094 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01993 | hp2 | a0006 | c0005 | t0003 | g0070 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02027 | hp1 | a0005 | c0008 | t0002 | g0050 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02027 | hp2 | a0007 | c0006 | t0001 | g0179 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02040 | hp2 | a0038 | c0047 | t0002 | g0035 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02055 | hp1 | a0044 | c0044 | t0002 | g0202 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02055 | hp2 | a0005 | c0008 | t0001 | g0002 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0210 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02083 | hp2 | a0007 | c0006 | t0001 | g0182 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02129 | hp2 | a0039 | c0048 | t0002 | g0032 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | KHV | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02145 | hp1 | a0017 | c0017 | t0007 | g0228 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02145 | hp2 | a0002 | c0002 | t0003 | g0263 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02148 | hp1 | a0006 | c0005 | t0003 | g0074 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02148 | hp2 | a0012 | c0012 | t0004 | g0109 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02257 | hp2 | a0025 | c0025 | t0001 | g0193 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02280 | hp1 | a0002 | c0002 | t0003 | g0265 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0282 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02293 | hp1 | a0011 | c0010 | t0003 | g0141 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02300 | hp1 | a0006 | c0005 | t0003 | g0067 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02300 | hp2 | a0011 | c0010 | t0006 | g0049 | AMR | PEL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0275 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0221 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02572 | hp1 | a0009 | c0015 | t0001 | g0112 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02572 | hp2 | a0015 | c0019 | t0005 | g0231 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02602 | hp2 | a0026 | c0027 | t0003 | g0126 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02615 | hp1 | a0002 | c0011 | t0001 | g0244 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0269 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02622 | hp1 | a0003 | c0003 | t0002 | g0136 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02630 | hp1 | a0002 | c0002 | t0004 | g0102 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02630 | hp2 | a0010 | c0009 | t0004 | g0250 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02683 | hp1 | a0010 | c0009 | t0005 | g0007 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02683 | hp2 | a0004 | c0004 | t0003 | g0087 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02717 | hp1 | a0009 | c0015 | t0001 | g0098 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0262 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02738 | hp2 | a0008 | c0007 | t0003 | g0194 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0225 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02818 | hp1 | a0010 | c0009 | t0001 | g0248 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02818 | hp2 | a0040 | c0049 | t0001 | g0197 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02886 | hp1 | a0002 | c0002 | t0004 | g0101 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02886 | hp2 | a0009 | c0023 | t0001 | g0125 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0274 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0256 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02922 | hp1 | a0007 | c0006 | t0004 | g0142 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02922 | hp2 | a0051 | c0067 | t0004 | g0191 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0264 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02965 | hp2 | a0002 | c0011 | t0001 | g0245 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02970 | hp1 | a0020 | c0032 | t0004 | g0062 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02970 | hp2 | a0005 | c0013 | t0001 | g0200 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02976 | hp1 | a0002 | c0046 | t0003 | g0233 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02976 | hp2 | a0021 | c0061 | t0001 | g0238 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03017 | hp2 | a0008 | c0007 | t0003 | g0281 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03041 | hp2 | a0007 | c0006 | t0004 | g0199 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03098 | hp1 | a0007 | c0030 | t0004 | g0127 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03098 | hp2 | a0041 | c0050 | t0002 | g0218 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03130 | hp1 | a0023 | c0028 | t0005 | g0258 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03130 | hp2 | a0018 | c0026 | t0003 | g0226 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03139 | hp2 | a0002 | c0011 | t0001 | g0100 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03209 | hp2 | a0016 | c0018 | t0005 | g0229 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0276 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03225 | hp2 | a0007 | c0006 | t0001 | g0236 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03239 | hp1 | a0006 | c0005 | t0003 | g0075 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03453 | hp1 | a0017 | c0017 | t0007 | g0217 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0130 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03491 | hp2 | a0004 | c0004 | t0003 | g0058 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03492 | hp1 | a0013 | c0020 | t0003 | g0254 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03516 | hp1 | a0047 | c0055 | t0001 | g0278 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03516 | hp2 | a0045 | c0054 | t0004 | g0099 | AFR | ESN | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0223 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03579 | hp2 | a0002 | c0042 | t0001 | g0198 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03654 | hp1 | a0023 | c0028 | t0002 | g0018 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03654 | hp2 | a0002 | c0022 | t0002 | g0015 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03669 | hp1 | a0002 | c0022 | t0002 | g0008 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03688 | hp1 | a0027 | c0029 | t0003 | g0239 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0047 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0045 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03831 | hp2 | a0004 | c0004 | t0003 | g0086 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03834 | hp1 | a0024 | c0024 | t0005 | g0111 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0110 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03927 | hp2 | a0008 | c0007 | t0003 | g0280 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04115 | hp1 | a0005 | c0008 | t0001 | g0063 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0134 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04184 | hp1 | a0019 | c0016 | t0001 | g0143 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04184 | hp2 | a0006 | c0005 | t0003 | g0091 | SAS | BEB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0012 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04199 | hp2 | a0004 | c0004 | t0003 | g0189 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | STU | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18522 | hp1 | a0007 | c0006 | t0001 | g0247 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18522 | hp2 | a0037 | c0057 | t0004 | g0249 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18906 | hp1 | a0007 | c0030 | t0004 | g0266 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18906 | hp2 | a0009 | c0041 | t0001 | g0251 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18950 | hp2 | a0036 | c0039 | t0002 | g0043 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18951 | hp2 | a0004 | c0004 | t0003 | g0068 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18952 | hp1 | a0027 | c0029 | t0003 | g0117 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18952 | hp2 | a0001 | c0056 | t0001 | g0121 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18953 | hp1 | a0005 | c0013 | t0002 | g0024 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18959 | hp1 | a0005 | c0034 | t0002 | g0031 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18961 | hp1 | a0005 | c0008 | t0001 | g0214 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18966 | hp1 | a0010 | c0009 | t0004 | g0120 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18968 | hp2 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18979 | hp2 | a0014 | c0014 | t0002 | g0040 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18986 | hp1 | a0028 | c0021 | t0002 | g0011 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18992 | hp1 | a0034 | c0040 | t0002 | g0259 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18997 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18998 | hp1 | a0005 | c0037 | t0004 | g0183 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA18998 | hp2 | a0007 | c0006 | t0002 | g0026 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19007 | hp2 | a0010 | c0009 | t0004 | g0122 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19011 | hp2 | a0035 | c0038 | t0002 | g0260 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19030 | hp1 | a0026 | c0027 | t0003 | g0092 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19030 | hp2 | a0005 | c0033 | t0008 | g0113 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19043 | hp1 | a0009 | c0023 | t0001 | g0222 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19060 | hp2 | a0028 | c0021 | t0002 | g0037 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0201 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19068 | hp1 | a0003 | c0003 | t0002 | g0005 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19068 | hp2 | a0005 | c0008 | t0004 | g0205 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19081 | hp1 | a0014 | c0014 | t0002 | g0042 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19081 | hp2 | a0011 | c0010 | t0006 | g0030 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19085 | hp1 | a0003 | c0003 | t0001 | g0123 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | YRI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20129 | hp1 | a0050 | c0068 | t0004 | g0216 | AFR | ASW | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20129 | hp2 | a0004 | c0004 | t0003 | g0073 | AFR | ASW | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0017 | EUR | TSI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20805 | hp2 | a0012 | c0012 | t0004 | g0195 | EUR | TSI | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01123 | hp1 | a0004 | c0004 | t0003 | g0085 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG01123 | hp2 | a0005 | c0035 | t0001 | g0095 | AMR | CLM | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02109 | hp1 | a0005 | c0013 | t0004 | g0097 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02109 | hp2 | a0049 | c0066 | t0004 | g0107 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02486 | hp1 | a0003 | c0003 | t0002 | g0135 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG02486 | hp2 | a0002 | c0011 | t0001 | g0246 | AFR | ACB | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03471 | hp1 | a0005 | c0036 | t0004 | g0180 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG03471 | hp2 | a0043 | c0045 | t0007 | g0133 | AFR | MSL | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | USA | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA21309 | hp1 | a0018 | c0051 | t0003 | g0224 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
NA21309 | hp2 | a0009 | c0015 | t0001 | g0096 | AFR | LWK | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
homoSapiens_chm13v2 | hp1 | a0019 | c0016 | t0001 | g0177 | REF | REF | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0149 | REF | REF | EFCAB8_chr20_32853923_32966845 | EFCAB8 | chr20 | 32853923 | 32966845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32867732
|
A | G | 2 | a0050a0051 | 2 | HG02922.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.193A>G | p.Ile65Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/27 | 287/4197 | 193/3867 | 65/1288 | chr20 | 32867732 | ||
chr20:32875928
|
C | G | 1 | a0049 | 1 | HG02109.hp2 | missense_variant&splice_region_variant | MODERATE | c.211C>G | p.Leu71Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/27 | 305/4197 | 211/3867 | 71/1288 | chr20 | 32875928 | ||
chr20:32878728
|
C | T | 10 | a0004a0006a0013others(7): Show | 38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
missense_variant | MODERATE | c.352C>T | p.Arg118Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/27 | 446/4197 | 352/3867 | 118/1288 | chr20 | 32878728 | ||
chr20:32878768
|
A | AC | 2 | a0005a0029 | 14 | HG01123.hp2 HG01975.hp2 HG02027.hp1 others(11): Show |
frameshift_variant | HIGH | c.394dupC | p.Arg132fs | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/27 | 489/4197 | 395/3867 | 132/1288 | INFO_REALIGN_3_PRIME | chr20 | 32878768 | |
chr20:32892246
|
G | C | 4 | a0014a0034a0035others(1): Show | 6 | HG01515.hp1 NA18950.hp2 NA18979.hp2 others(3): Show |
missense_variant | MODERATE | c.707G>C | p.Arg236Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/27 | 801/4197 | 707/3867 | 236/1288 | chr20 | 32892246 | ||
chr20:32893184
|
C | T | 1 | a0048 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.769C>T | p.His257Tyr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/27 | 863/4197 | 769/3867 | 257/1288 | chr20 | 32893184 | ||
chr20:32893271
|
C | T | 6 | a0015a0016a0017others(3): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
missense_variant | MODERATE | c.856C>T | p.Arg286Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/27 | 950/4197 | 856/3867 | 286/1288 | chr20 | 32893271 | ||
chr20:32898568
|
G | A | 1 | a0028 | 2 | NA18986.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.1033G>A | p.Glu345Lys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/27 | 1127/4197 | 1033/3867 | 345/1288 | chr20 | 32898568 | ||
chr20:32906576
|
G | A | 42 | a0002a0003a0004others(39): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
missense_variant | MODERATE | c.1103G>A | p.Arg368His | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 12/27 | 1197/4197 | 1103/3867 | 368/1288 | chr20 | 32906576 | ||
chr20:32908386
|
A | G | 1 | a0012 | 4 | HG01433.hp1 HG01981.hp2 HG02148.hp2 others(1): Show |
missense_variant | MODERATE | c.1420A>G | p.Asn474Asp | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/27 | 1514/4197 | 1420/3867 | 474/1288 | chr20 | 32908386 | ||
chr20:32909876
|
G | T | 7 | a0010a0015a0020others(4): Show | 15 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
missense_variant | MODERATE | c.1502G>T | p.Arg501Met | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/27 | 1596/4197 | 1502/3867 | 501/1288 | chr20 | 32909876 | ||
chr20:32911501
|
G | A | 1 | a0009 | 6 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
missense_variant | MODERATE | c.1579G>A | p.Gly527Ser | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/27 | 1673/4197 | 1579/3867 | 527/1288 | chr20 | 32911501 | ||
chr20:32917383
|
C | T | 3 | a0006a0026a0032 | 15 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(12): Show |
missense_variant | MODERATE | c.1939C>T | p.Arg647Trp | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 2033/4197 | 1939/3867 | 647/1288 | chr20 | 32917383 | ||
chr20:32917483
|
C | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2039C>A | p.Pro680His | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 2133/4197 | 2039/3867 | 680/1288 | chr20 | 32917483 | ||
chr20:32917486
|
C | T | 32 | a0002a0004a0005others(29): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
missense_variant | MODERATE | c.2042C>T | p.Ser681Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 2136/4197 | 2042/3867 | 681/1288 | chr20 | 32917486 | ||
chr20:32918434
|
A | G | 1 | a0037 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.2134A>G | p.Thr712Ala | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/27 | 2228/4197 | 2134/3867 | 712/1288 | chr20 | 32918434 | ||
chr20:32920085
|
C | G | 1 | a0022 | 2 | HG01167.hp2 HG01243.hp2 |
missense_variant | MODERATE | c.2282C>G | p.Ser761Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/27 | 2376/4197 | 2282/3867 | 761/1288 | chr20 | 32920085 | ||
chr20:32930423
|
G | A | 1 | a0019 | 3 | HG00099.hp1 HG04184.hp1 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.2438G>A | p.Arg813His | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/27 | 2532/4197 | 2438/3867 | 813/1288 | chr20 | 32930423 | ||
chr20:32930492
|
A | G | 12 | a0005a0006a0013others(9): Show | 30 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
missense_variant | MODERATE | c.2507A>G | p.Glu836Gly | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/27 | 2601/4197 | 2507/3867 | 836/1288 | chr20 | 32930492 | ||
chr20:32930534
|
A | G | 2 | a0036a0039 | 2 | HG02129.hp2 NA18950.hp2 |
missense_variant | MODERATE | c.2549A>G | p.Asn850Ser | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/27 | 2643/4197 | 2549/3867 | 850/1288 | chr20 | 32930534 | ||
chr20:32943738
|
C | T | 8 | a0004a0005a0008others(5): Show | 31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
stop_gained | HIGH | c.2893C>T | p.Gln965* | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/27 | 2987/4197 | 2893/3867 | 965/1288 | chr20 | 32943738 | ||
chr20:32958472
|
C | T | 1 | a0050 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.3011C>T | p.Pro1004Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/27 | 3105/4197 | 3011/3867 | 1004/1288 | chr20 | 32958472 | ||
chr20:32959800
|
G | A | 1 | a0038 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.3112G>A | p.Ala1038Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 25/27 | 3206/4197 | 3112/3867 | 1038/1288 | chr20 | 32959800 | ||
chr20:32959816
|
G | A | 1 | a0040 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.3128G>A | p.Arg1043Gln | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 25/27 | 3222/4197 | 3128/3867 | 1043/1288 | chr20 | 32959816 | ||
chr20:32961238
|
A | G | 3 | a0005a0025a0041 | 4 | HG00323.hp1 HG01123.hp2 HG02257.hp2 others(1): Show |
missense_variant | MODERATE | c.3496A>G | p.Ile1166Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3590/4197 | 3496/3867 | 1166/1288 | chr20 | 32961238 | ||
chr20:32961241
|
C | T | 3 | a0005a0017a0043 | 5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
missense_variant | MODERATE | c.3499C>T | p.Arg1167Cys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3593/4197 | 3499/3867 | 1167/1288 | chr20 | 32961241 | ||
chr20:32961299
|
T | C | 1 | a0042 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.3557T>C | p.Leu1186Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3651/4197 | 3557/3867 | 1186/1288 | chr20 | 32961299 | ||
chr20:32961301
|
G | A | 1 | a0046 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.3559G>A | p.Asp1187Asn | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3653/4197 | 3559/3867 | 1187/1288 | chr20 | 32961301 | ||
chr20:32961317
|
C | T | 4 | a0012a0024a0030others(1): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
missense_variant | MODERATE | c.3575C>T | p.Thr1192Met | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3669/4197 | 3575/3867 | 1192/1288 | chr20 | 32961317 | ||
chr20:32961466
|
T | C | 2 | a0005a0045 | 2 | HG03471.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.3724T>C | p.Ser1242Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3818/4197 | 3724/3867 | 1242/1288 | chr20 | 32961466 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32896486
|
T | C | 3 | a0002c0042a0009c0015a0009c0041 | 5 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(2): Show |
synonymous_variant | LOW | c.916T>C | p.Leu306Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/27 | 1010/4197 | 916/3867 | 306/1288 | chr20 | 32896486 | ||
chr20:32898549
|
A | T | 1 | a0037c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1014A>T | p.Val338Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/27 | 1108/4197 | 1014/3867 | 338/1288 | chr20 | 32898549 | ||
chr20:32906868
|
C | T | 1 | a0037c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1182C>T | p.Ile394Ile | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/27 | 1276/4197 | 1182/3867 | 394/1288 | chr20 | 32906868 | ||
chr20:32906872
|
C | T | 1 | a0048c0058 | 1 | HG01261.hp2 | synonymous_variant | LOW | c.1186C>T | p.Leu396Leu | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/27 | 1280/4197 | 1186/3867 | 396/1288 | chr20 | 32906872 | ||
chr20:32911500
|
C | A | 1 | a0002c0022 | 2 | HG03654.hp2 HG03669.hp1 |
synonymous_variant | LOW | c.1578C>A | p.Arg526Arg | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/27 | 1672/4197 | 1578/3867 | 526/1288 | chr20 | 32911500 | ||
chr20:32911584
|
C | T | 1 | a0002c0042 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1662C>T | p.Thr554Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/27 | 1756/4197 | 1662/3867 | 554/1288 | chr20 | 32911584 | ||
chr20:32917319
|
A | G | 1 | a0037c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1875A>G | p.Pro625Pro | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 1969/4197 | 1875/3867 | 625/1288 | chr20 | 32917319 | ||
chr20:32917346
|
C | G | 1 | a0037c0057 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1902C>G | p.Thr634Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/27 | 1996/4197 | 1902/3867 | 634/1288 | chr20 | 32917346 | ||
chr20:32918415
|
T | C | 1 | a0002c0046 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.2115T>C | p.Tyr705Tyr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/27 | 2209/4197 | 2115/3867 | 705/1288 | chr20 | 32918415 | ||
chr20:32918445
|
C | G | 1 | a0001c0056 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.2145C>G | p.Thr715Thr | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/27 | 2239/4197 | 2145/3867 | 715/1288 | chr20 | 32918445 | ||
chr20:32920209
|
G | A | 1 | a0001c0052 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.2406G>A | p.Val802Val | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/27 | 2500/4197 | 2406/3867 | 802/1288 | chr20 | 32920209 | ||
chr20:32931204
|
A | G | 1 | a0009c0041 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2658A>G | p.Ala886Ala | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/27 | 2752/4197 | 2658/3867 | 886/1288 | chr20 | 32931204 | ||
chr20:32959874
|
C | T | 1 | a0018c0051 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.3186C>T | p.Asp1062Asp | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 25/27 | 3280/4197 | 3186/3867 | 1062/1288 | chr20 | 32959874 | ||
chr20:32960092
|
G | A | 3 | a0002c0011a0007c0030a0021c0061 | 7 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.3324G>A | p.Lys1108Lys | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/27 | 3418/4197 | 3324/3867 | 1108/1288 | chr20 | 32960092 | ||
chr20:32961141
|
G | A | 2 | a0009c0015a0009c0023 | 5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.3399G>A | p.Ser1133Ser | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 3493/4197 | 3399/3867 | 1133/1288 | chr20 | 32961141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32858936
|
G | C | 33 | a0001c0001t0002a0001c0001t0005a0002c0002t0002others(30): Show | 79 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/27 | 4857 | chr20 | 32858936 | |||||
chr20:32961618
|
G | A | 16 | a0002c0002t0003a0002c0046t0003a0004c0004t0003others(13): Show | 54 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*9G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 9 | chr20 | 32961618 | |||||
chr20:32961759
|
C | T | 1 | a0001c0001t0009 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 150 | chr20 | 32961759 | |||||
chr20:32961778
|
T | G | 40 | a0001c0001t0004a0001c0001t0005a0002c0002t0003others(37): Show | 93 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*169T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 169 | chr20 | 32961778 | |||||
chr20:32961827
|
G | A | 3 | a0005c0033t0008a0017c0017t0007a0043c0045t0007 | 5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*218G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 27/27 | 218 | chr20 | 32961827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:32859052
|
A | G | 22 | a0002c0002t0001g0261a0002c0002t0001g0264a0002c0002t0001g0267others(19): Show | 22 | HG01358.hp2 HG01361.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-11+46A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859052 | ||||||
chr20:32859052
|
A | T | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+46A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859052 | ||||||
chr20:32859085
|
G | T | 2 | a0034c0040t0002g0259a0035c0038t0002g0260 | 2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-11+79G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859085 | ||||||
chr20:32859099
|
C | T | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+93C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859099 | ||||||
chr20:32859518
|
CTG | C | 4 | a0001c0001t0005g0255a0001c0001t0005g0256a0023c0028t0005g0258others(1): Show | 4 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+514_-11+515del others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32859518 | |||||
chr20:32859562
|
A | G | 5 | a0003c0003t0001g0279a0003c0003t0001g0282a0008c0007t0003g0280others(2): Show | 5 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+556A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859562 | ||||||
chr20:32859763
|
A | G | 1 | a0013c0020t0003g0254 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-11+757A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859763 | ||||||
chr20:32859774
|
C | T | 1 | a0004c0004t0003g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-11+768C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859774 | ||||||
chr20:32859796
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-11+790A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859796 | ||||||
chr20:32859797
|
TAC | T | 8 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+793_-11+794del others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32859797 | |||||
chr20:32859836
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-11+830A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859836 | ||||||
chr20:32859887
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-11+881C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859887 | ||||||
chr20:32859891
|
C | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.-11+885C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859891 | ||||||
chr20:32859942
|
T | C | 1 | a0005c0008t0001g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-11+936T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32859942 | ||||||
chr20:32860033
|
G | A | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-11+1027G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860033 | ||||||
chr20:32860153
|
C | T | 1 | a0027c0029t0003g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-11+1147C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860153 | ||||||
chr20:32860313
|
C | CA | 57 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(54): Show | 57 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-11+1316dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860313 | |||||
chr20:32860322
|
A | C | 1 | a0021c0061t0001g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-11+1316A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860322 | ||||||
chr20:32860339
|
A | C | 1 | a0006c0005t0003g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-11+1333A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860339 | ||||||
chr20:32860469
|
T | A | 8 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+1463T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860469 | ||||||
chr20:32860479
|
G | A | 4 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1473G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860479 | ||||||
chr20:32860493
|
C | CAT | 3 | a0002c0002t0002g0003a0002c0002t0002g0004a0003c0003t0002g0005 | 3 | NA18946.hp2 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-11+1487_-11+1488i others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860493 | ||||||
chr20:32860493
|
C | CT | 33 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(30): Show | 33 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-11+1518dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
C | CTTTT | 10 | a0001c0001t0005g0220a0002c0002t0001g0221a0002c0002t0001g0225others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+1515_-11+1518d others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
C | CTTTTT | 10 | a0002c0002t0001g0234a0002c0002t0001g0235a0002c0046t0003g0233others(7): Show | 10 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-11+1514_-11+1518d others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CT | C | 43 | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(40): Show | 44 | HG00099.hp2 HG00642.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.-11+1518delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTT | C | 16 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(13): Show | 16 | HG01433.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-11+1517_-11+1518d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTT | C | 10 | a0002c0002t0001g0093a0002c0011t0001g0244a0002c0011t0001g0245others(7): Show | 10 | HG01123.hp2 HG01981.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+1516_-11+1518d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0022t0002g0008a0026c0027t0003g0092 | 2 | HG03669.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-11+1508_-11+1518d others(13): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTTTTTT others(5): Show |
C | 2 | a0002c0002t0002g0006a0010c0009t0005g0007 | 2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-11+1507_-11+1518d others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTTTTTT others(6): Show |
C | 1 | a0006c0005t0003g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-11+1506_-11+1518d others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTTTTTT others(7): Show |
C | 36 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0242others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-11+1505_-11+1518d others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTTTTTT others(8): Show |
C | 1 | a0004c0004t0003g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-11+1504_-11+1518d others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860493
|
CTTTTTTT others(11): Show |
C | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-11+1501_-11+1518d others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32860493 | |||||
chr20:32860718
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-11+1712T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860718 | ||||||
chr20:32860735
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-11+1729T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860735 | ||||||
chr20:32860842
|
A | G | 42 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(39): Show | 42 | HG00423.hp1 HG00621.hp2 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.-11+1836A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860842 | ||||||
chr20:32860890
|
C | T | 38 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0242others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-11+1884C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860890 | ||||||
chr20:32860966
|
C | G | 1 | a0013c0020t0003g0090 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-11+1960C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32860966 | ||||||
chr20:32861043
|
G | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(65): Show | 68 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-11+2037G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861043 | ||||||
chr20:32861101
|
T | G | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-11+2095T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861101 | ||||||
chr20:32861102
|
C | T | 7 | a0008c0007t0006g0044a0014c0014t0002g0040a0014c0014t0002g0042others(4): Show | 7 | HG01346.hp1 HG01515.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+2096C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861102 | ||||||
chr20:32861105
|
T | A | 2 | a0009c0041t0001g0251a0010c0009t0001g0248 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-11+2099T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861105 | ||||||
chr20:32861189
|
C | G | 1 | a0006c0005t0006g0020 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-11+2183C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861189 | ||||||
chr20:32861313
|
A | G | 1 | a0003c0003t0001g0201 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-11+2307A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861313 | ||||||
chr20:32861319
|
G | A | 13 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0003g0262others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-11+2313G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861319 | ||||||
chr20:32861384
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(194): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.-11+2378A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861384 | ||||||
chr20:32861491
|
G | A | 16 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(13): Show | 17 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-2292G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861491 | ||||||
chr20:32861579
|
G | A | 6 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(3): Show | 6 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2204G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861579 | ||||||
chr20:32861580
|
C | T | 37 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0242others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-10-2203C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861580 | ||||||
chr20:32861702
|
C | T | 16 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(13): Show | 17 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-10-2081C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861702 | ||||||
chr20:32861726
|
C | G | 3 | a0012c0012t0004g0108a0012c0012t0004g0109a0012c0012t0004g0195 | 3 | HG01433.hp1 HG02148.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-10-2057C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861726 | ||||||
chr20:32861897
|
A | G | 5 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0004g0101others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1886A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861897 | ||||||
chr20:32861919
|
CTT | C | 79 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(76): Show | 79 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10-1863_-10-1862d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861919 | ||||||
chr20:32861933
|
T | G | 5 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0004g0101others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1850T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32861933 | ||||||
chr20:32862040
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01346.hp2 HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-10-1743T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862040 | ||||||
chr20:32862065
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-10-1718C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862065 | ||||||
chr20:32862066
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-10-1717T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862066 | ||||||
chr20:32862134
|
C | CT | 15 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0003g0262others(12): Show | 15 | HG01167.hp1 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-10-1635dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32862134 | |||||
chr20:32862134
|
CT | C | 10 | a0001c0001t0001g0203a0002c0002t0001g0119a0002c0002t0001g0128others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10-1635delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32862134 | |||||
chr20:32862139
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-10-1644T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862139 | ||||||
chr20:32862230
|
A | G | 4 | a0002c0002t0001g0128a0002c0002t0001g0129a0003c0003t0001g0130others(1): Show | 4 | HG03098.hp1 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-1553A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862230 | ||||||
chr20:32862240
|
C | G | 1 | a0004c0004t0001g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-10-1543C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862240 | ||||||
chr20:32862245
|
C | T | 10 | a0002c0002t0001g0221a0002c0002t0001g0225a0002c0002t0001g0234others(7): Show | 10 | HG02451.hp2 HG02809.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1538C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862245 | ||||||
chr20:32862487
|
CT | C | 6 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(3): Show | 6 | HG01123.hp2 HG01433.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1294delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32862487 | |||||
chr20:32862723
|
G | C | 1 | a0002c0002t0003g0265 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-10-1060G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862723 | ||||||
chr20:32862732
|
A | G | 13 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0003g0262others(10): Show | 13 | HG02109.hp1 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-10-1051A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862732 | ||||||
chr20:32862840
|
G | A | 1 | a0010c0009t0004g0120 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-10-943G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862840 | ||||||
chr20:32862858
|
G | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(196): Show | 200 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-10-925G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862858 | ||||||
chr20:32862919
|
C | T | 1 | a0010c0009t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-10-864C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32862919 | ||||||
chr20:32863011
|
AT | A | 155 | a0001c0001t0001g0061a0001c0001t0001g0243a0001c0001t0002g0027others(152): Show | 155 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-10-759delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32863011 | |||||
chr20:32863011
|
ATT | A | 13 | a0002c0002t0001g0221a0002c0002t0001g0225a0002c0002t0001g0234others(10): Show | 13 | HG02451.hp2 HG02809.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.-10-760_-10-759del others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr20 | 32863011 | |||||
chr20:32863111
|
C | G | 1 | a0035c0038t0002g0260 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-10-672C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863111 | ||||||
chr20:32863216
|
A | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(192): Show | 196 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.-10-567A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863216 | ||||||
chr20:32863231
|
G | A | 1 | a0016c0018t0005g0229 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-10-552G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863231 | ||||||
chr20:32863233
|
T | G | 1 | a0002c0002t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-10-550T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863233 | ||||||
chr20:32863290
|
C | T | 1 | a0049c0066t0004g0107 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-10-493C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863290 | ||||||
chr20:32863437
|
C | G | 4 | a0002c0002t0003g0262a0002c0002t0003g0263a0002c0011t0001g0100others(1): Show | 4 | HG02145.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-346C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863437 | ||||||
chr20:32863544
|
T | A | 96 | a0001c0001t0001g0243a0001c0001t0002g0027a0001c0001t0002g0052others(93): Show | 96 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.-10-239T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863544 | ||||||
chr20:32863545
|
C | A | 96 | a0001c0001t0001g0243a0001c0001t0002g0027a0001c0001t0002g0052others(93): Show | 96 | HG00423.hp1 HG00621.hp2 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.-10-238C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863545 | ||||||
chr20:32863567
|
G | A | 2 | a0020c0032t0004g0062a0020c0032t0004g0277 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-10-216G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863567 | ||||||
chr20:32863758
|
A | T | 1 | a0004c0004t0003g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-10-25A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 1/26 | chr20 | 32863758 | ||||||
chr20:32863874
|
A | G | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42+40A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32863874 | ||||||
chr20:32863982
|
AT | A | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+160delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32863982 | |||||
chr20:32864322
|
A | G | 1 | a0002c0022t0002g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.42+488A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864322 | ||||||
chr20:32864336
|
C | G | 2 | a0008c0007t0003g0194a0026c0027t0003g0126 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.42+502C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864336 | ||||||
chr20:32864487
|
T | G | 2 | a0003c0003t0001g0130a0007c0030t0004g0127 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.42+653T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864487 | ||||||
chr20:32864488
|
G | A | 1 | a0005c0033t0008g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42+654G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864488 | ||||||
chr20:32864641
|
T | C | 4 | a0002c0002t0001g0221a0002c0002t0001g0234a0002c0002t0001g0235others(1): Show | 4 | HG02451.hp2 HG03195.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+807T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864641 | ||||||
chr20:32864756
|
T | C | 2 | a0010c0009t0004g0250a0037c0057t0004g0249 | 2 | HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.42+922T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864756 | ||||||
chr20:32864893
|
T | G | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42+1059T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864893 | ||||||
chr20:32864942
|
C | G | 2 | a0003c0003t0002g0135a0003c0003t0002g0136 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.42+1108C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864942 | ||||||
chr20:32864997
|
C | T | 1 | a0002c0002t0001g0190 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.42+1163C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32864997 | ||||||
chr20:32865119
|
A | G | 11 | a0001c0001t0005g0220a0015c0019t0005g0219a0015c0019t0005g0231others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+1285A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865119 | ||||||
chr20:32865150
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(56): Show | 60 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.42+1316C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865150 | ||||||
chr20:32865220
|
T | C | 7 | a0002c0002t0001g0261a0002c0011t0001g0100a0003c0003t0001g0279others(4): Show | 7 | HG01358.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.42+1386T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865220 | ||||||
chr20:32865319
|
AC | A | 193 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(190): Show | 194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.42+1486delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865319 | ||||||
chr20:32865390
|
G | C | 1 | a0007c0006t0004g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42+1556G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865390 | ||||||
chr20:32865669
|
C | T | 1 | a0050c0068t0004g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.42+1835C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865669 | ||||||
chr20:32865719
|
A | G | 13 | a0001c0001t0005g0220a0009c0041t0001g0251a0010c0009t0001g0248others(10): Show | 13 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.43-1863A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865719 | ||||||
chr20:32865761
|
G | A | 1 | a0002c0022t0002g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43-1821G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865761 | ||||||
chr20:32865794
|
C | CA | 45 | a0001c0001t0001g0106a0001c0001t0001g0131a0001c0001t0001g0204others(42): Show | 45 | HG00423.hp1 HG00621.hp2 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.43-1771dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32865794 | |||||
chr20:32865827
|
G | A | 2 | a0005c0035t0001g0095a0049c0066t0004g0107 | 2 | HG01123.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.43-1755G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32865827 | ||||||
chr20:32866102
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.43-1480G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866102 | ||||||
chr20:32866256
|
G | A | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.43-1326G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866256 | ||||||
chr20:32866303
|
A | G | 13 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(10): Show | 13 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.43-1279A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866303 | ||||||
chr20:32866357
|
G | A | 1 | a0043c0045t0007g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-1225G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866357 | ||||||
chr20:32866724
|
TCTTC | T | 6 | a0002c0002t0002g0012a0002c0002t0002g0045a0002c0002t0002g0046others(3): Show | 6 | HG01358.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-836_43-833delTT others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32866724 | |||||
chr20:32866778
|
TTCTTCCT others(26): Show |
T | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-781_43-749delCT others(31): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32866778 | |||||
chr20:32866851
|
T | TTCTCTCT others(36): Show |
1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.43-708_43-666dupCT others(41): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr20 | 32866851 | |||||
chr20:32866934
|
T | G | 1 | a0002c0002t0003g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.43-648T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866934 | ||||||
chr20:32866946
|
C | G | 2 | a0004c0004t0003g0086a0004c0004t0003g0087 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.43-636C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32866946 | ||||||
chr20:32867160
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.43-422T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32867160 | ||||||
chr20:32867195
|
T | C | 1 | a0006c0005t0003g0064 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43-387T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32867195 | ||||||
chr20:32867275
|
T | C | 3 | a0002c0002t0001g0261a0010c0009t0004g0250a0037c0057t0004g0249 | 3 | HG01884.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.43-307T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 2/26 | chr20 | 32867275 | ||||||
chr20:32867761
|
G | A | 1 | a0007c0006t0004g0199 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.208+14G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32867761 | ||||||
chr20:32867821
|
G | A | 1 | a0021c0061t0001g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.208+74G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32867821 | ||||||
chr20:32867964
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(53): Show | 57 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.208+217G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32867964 | ||||||
chr20:32868015
|
C | CT | 10 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0139others(7): Show | 10 | HG00639.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+278dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32868015 | |||||
chr20:32868169
|
C | T | 1 | a0009c0041t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208+422C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868169 | ||||||
chr20:32868299
|
C | T | 1 | a0003c0003t0002g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.208+552C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868299 | ||||||
chr20:32868362
|
C | G | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.208+615C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868362 | ||||||
chr20:32868691
|
A | C | 1 | a0046c0053t0002g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.208+944A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868691 | ||||||
chr20:32868921
|
G | A | 5 | a0002c0002t0002g0006a0002c0022t0002g0015a0008c0007t0006g0013others(2): Show | 5 | HG00733.hp1 HG01515.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.208+1174G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868921 | ||||||
chr20:32868953
|
C | T | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.208+1206C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32868953 | ||||||
chr20:32869046
|
C | A | 1 | a0005c0008t0004g0205 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.208+1299C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869046 | ||||||
chr20:32869196
|
A | G | 1 | a0024c0024t0005g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.208+1449A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869196 | ||||||
chr20:32869239
|
A | AT | 7 | a0001c0001t0002g0052a0002c0002t0002g0051a0005c0033t0008g0113others(4): Show | 7 | HG00423.hp1 HG01081.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+1507dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32869239 | |||||
chr20:32869344
|
T | C | 1 | a0002c0002t0002g0012 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.208+1597T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869344 | ||||||
chr20:32869424
|
C | A | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+1677C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869424 | ||||||
chr20:32869461
|
C | G | 4 | a0002c0002t0002g0012a0002c0002t0002g0045a0002c0002t0002g0046others(1): Show | 4 | HG02257.hp1 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+1714C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869461 | ||||||
chr20:32869487
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(164): Show | 168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.208+1740T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869487 | ||||||
chr20:32869531
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(70): Show | 74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.208+1784T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869531 | ||||||
chr20:32869570
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01346.hp2 HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.208+1823C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869570 | ||||||
chr20:32869732
|
C | CT | 12 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0001g0128others(9): Show | 12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1986dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32869732 | |||||
chr20:32869734
|
G | A | 12 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0001g0128others(9): Show | 12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1987G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869734 | ||||||
chr20:32869735
|
T | A | 12 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0001g0128others(9): Show | 12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.208+1988T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869735 | ||||||
chr20:32869902
|
C | T | 1 | a0007c0006t0001g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.208+2155C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32869902 | ||||||
chr20:32870081
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.208+2334T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870081 | ||||||
chr20:32870159
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.208+2412T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870159 | ||||||
chr20:32870230
|
A | G | 7 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+2483A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870230 | ||||||
chr20:32870289
|
T | C | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.208+2542T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870289 | ||||||
chr20:32870343
|
C | T | 5 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(2): Show | 5 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+2596C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870343 | ||||||
chr20:32870405
|
T | G | 2 | a0002c0011t0001g0244a0007c0006t0001g0247 | 2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.208+2658T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870405 | ||||||
chr20:32870487
|
T | C | 2 | a0002c0002t0001g0190a0042c0043t0001g0184 | 2 | HG00639.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.208+2740T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870487 | ||||||
chr20:32870710
|
C | T | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+2963C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870710 | ||||||
chr20:32870781
|
C | T | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.208+3034C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870781 | ||||||
chr20:32870859
|
CTT | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(63): Show | 67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.208+3125_208+3126d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32870859 | |||||
chr20:32870886
|
T | G | 2 | a0003c0003t0001g0279a0003c0003t0001g0282 | 2 | HG01358.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.208+3139T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870886 | ||||||
chr20:32870910
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.208+3163G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870910 | ||||||
chr20:32870927
|
C | T | 2 | a0015c0019t0005g0231a0015c0019t0005g0232 | 2 | HG00741.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.208+3180C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870927 | ||||||
chr20:32870933
|
A | C | 4 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3186A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870933 | ||||||
chr20:32870967
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+3220G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32870967 | ||||||
chr20:32871097
|
C | T | 14 | a0002c0002t0002g0006a0002c0002t0002g0012a0002c0002t0002g0017others(11): Show | 14 | HG00323.hp1 HG00733.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+3350C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871097 | ||||||
chr20:32871105
|
G | A | 1 | a0013c0020t0003g0254 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.208+3358G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871105 | ||||||
chr20:32871117
|
TCTGGGAT others(3062): Show |
T | 1 | a0009c0015t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208+3379_209-1732d others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32871117 | |||||
chr20:32871226
|
A | G | 11 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0001g0128others(8): Show | 11 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.208+3479A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871226 | ||||||
chr20:32871234
|
C | T | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.208+3487C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871234 | ||||||
chr20:32871317
|
A | G | 38 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.208+3570A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871317 | ||||||
chr20:32871320
|
G | A | 3 | a0002c0002t0002g0012a0002c0002t0002g0045a0002c0002t0002g0047 | 3 | HG03688.hp2 HG03831.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.208+3573G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871320 | ||||||
chr20:32871496
|
T | A | 1 | a0001c0052t0001g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.208+3749T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871496 | ||||||
chr20:32871517
|
A | G | 1 | a0008c0007t0003g0281 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.208+3770A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871517 | ||||||
chr20:32871554
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.208+3807C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871554 | ||||||
chr20:32871729
|
G | A | 76 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(73): Show | 76 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.208+3982G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871729 | ||||||
chr20:32871747
|
C | T | 4 | a0002c0042t0001g0198a0002c0046t0003g0233a0005c0013t0001g0200others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+4000C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871747 | ||||||
chr20:32871756
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+4009C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871756 | ||||||
chr20:32871915
|
G | A | 6 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(3): Show | 6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-4011G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871915 | ||||||
chr20:32871940
|
G | A | 1 | a0005c0008t0004g0205 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.209-3986G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871940 | ||||||
chr20:32871960
|
G | A | 1 | a0008c0007t0003g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.209-3966G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32871960 | ||||||
chr20:32872116
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.209-3810A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872116 | ||||||
chr20:32872240
|
C | T | 1 | a0007c0030t0004g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.209-3686C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872240 | ||||||
chr20:32872270
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-3656G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872270 | ||||||
chr20:32872357
|
C | T | 1 | a0002c0002t0002g0038 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.209-3569C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872357 | ||||||
chr20:32872398
|
G | A | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-3528G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872398 | ||||||
chr20:32872438
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-3488A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872438 | ||||||
chr20:32872495
|
G | A | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-3431G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872495 | ||||||
chr20:32872496
|
A | G | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-3430A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872496 | ||||||
chr20:32872515
|
C | T | 11 | a0001c0001t0005g0220a0015c0019t0005g0219a0015c0019t0005g0231others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-3411C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872515 | ||||||
chr20:32872781
|
G | A | 38 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(35): Show | 38 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.209-3145G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872781 | ||||||
chr20:32872792
|
T | TCAAAAA | 16 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0221others(13): Show | 16 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-3122_209-3117d others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32872792 | |||||
chr20:32872866
|
C | T | 1 | a0005c0033t0008g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-3060C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872866 | ||||||
chr20:32872912
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-3014C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872912 | ||||||
chr20:32872964
|
C | T | 2 | a0002c0042t0001g0198a0002c0046t0003g0233 | 2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.209-2962C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872964 | ||||||
chr20:32872965
|
G | T | 3 | a0005c0013t0004g0097a0009c0015t0001g0098a0009c0015t0001g0112 | 3 | HG02109.hp1 HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.209-2961G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32872965 | ||||||
chr20:32873276
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-2650T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873276 | ||||||
chr20:32873462
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.209-2464A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873462 | ||||||
chr20:32873478
|
C | A | 1 | a0002c0002t0002g0028 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.209-2448C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873478 | ||||||
chr20:32873809
|
C | CA | 51 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(48): Show | 52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.209-2117_209-2116i others(3): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873809 | ||||||
chr20:32873809
|
C | CAA | 7 | a0002c0002t0001g0119a0002c0002t0001g0261a0004c0004t0003g0066others(4): Show | 7 | HG00639.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-2117_209-2116i others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873809 | ||||||
chr20:32873810
|
C | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(71): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.209-2116C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873810 | ||||||
chr20:32873982
|
G | T | 1 | a0044c0044t0002g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.209-1944G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32873982 | ||||||
chr20:32874111
|
C | T | 1 | a0009c0023t0001g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.209-1815C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874111 | ||||||
chr20:32874379
|
C | T | 11 | a0001c0001t0005g0220a0015c0019t0005g0219a0015c0019t0005g0231others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-1547C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874379 | ||||||
chr20:32874392
|
T | A | 1 | a0001c0001t0001g0103 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.209-1534T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874392 | ||||||
chr20:32874398
|
A | G | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-1528A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874398 | ||||||
chr20:32874556
|
T | G | 1 | a0002c0002t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.209-1370T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874556 | ||||||
chr20:32874976
|
T | G | 16 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0221others(13): Show | 16 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-950T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32874976 | ||||||
chr20:32875120
|
G | A | 6 | a0001c0001t0005g0255a0001c0001t0005g0256a0007c0006t0001g0236others(3): Show | 6 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.209-806G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875120 | ||||||
chr20:32875208
|
G | C | 1 | a0002c0002t0003g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.209-718G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875208 | ||||||
chr20:32875263
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.209-663G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875263 | ||||||
chr20:32875265
|
G | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(63): Show | 67 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.209-661G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875265 | ||||||
chr20:32875350
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | NA18962.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.209-576G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875350 | ||||||
chr20:32875418
|
G | A | 1 | a0022c0031t0002g0196 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.209-508G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875418 | ||||||
chr20:32875446
|
G | T | 11 | a0001c0001t0005g0220a0015c0019t0005g0219a0015c0019t0005g0231others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-480G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875446 | ||||||
chr20:32875478
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-448T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875478 | ||||||
chr20:32875502
|
G | GT | 14 | a0001c0001t0001g0103a0002c0022t0002g0015a0005c0008t0001g0002others(11): Show | 14 | HG00741.hp1 HG02027.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.209-406dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(3): Show |
4 | a0012c0012t0004g0094a0012c0012t0004g0195a0024c0024t0005g0041others(1): Show | 4 | HG01346.hp1 HG01981.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-415_209-406dup others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(4): Show |
1 | a0012c0012t0004g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.209-416_209-406dup others(11): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(5): Show |
1 | a0006c0005t0003g0067 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.209-417_209-406dup others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(10): Show |
1 | a0002c0011t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.209-422_209-406dup others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(12): Show |
12 | a0004c0004t0001g0089a0004c0004t0003g0068a0004c0004t0003g0069others(9): Show | 12 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(13): Show |
18 | a0001c0001t0001g0240a0003c0003t0001g0279a0003c0003t0001g0282others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(14): Show |
12 | a0001c0001t0001g0001a0001c0001t0001g0241a0004c0004t0003g0066others(9): Show | 13 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(15): Show |
11 | a0002c0002t0001g0119a0003c0003t0001g0201a0004c0004t0003g0058others(8): Show | 11 | HG00741.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-406_209-405ins others(22): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(16): Show |
2 | a0004c0004t0003g0085a0025c0025t0001g0193 | 2 | HG01123.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.209-406_209-405ins others(23): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(18): Show |
1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.209-406_209-405ins others(25): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(20): Show |
1 | a0003c0003t0001g0123 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.209-406_209-405ins others(27): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
G | GTTTTTTT others(21): Show |
1 | a0001c0001t0001g0124 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.209-406_209-405ins others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875502
|
GT | G | 12 | a0001c0001t0001g0106a0002c0002t0001g0267a0002c0002t0001g0268others(9): Show | 12 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.209-406delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr20 | 32875502 | |||||
chr20:32875585
|
A | G | 16 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0221others(13): Show | 16 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.209-341A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875585 | ||||||
chr20:32875590
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-336T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875590 | ||||||
chr20:32875640
|
G | T | 1 | a0015c0019t0005g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.209-286G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875640 | ||||||
chr20:32875654
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.209-272A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875654 | ||||||
chr20:32875760
|
C | A | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.209-166C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 3/26 | chr20 | 32875760 | ||||||
chr20:32876245
|
C | T | 1 | a0023c0028t0005g0258 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.327+201C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876245 | ||||||
chr20:32876261
|
G | A | 4 | a0002c0042t0001g0198a0002c0046t0003g0233a0005c0013t0001g0200others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+217G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876261 | ||||||
chr20:32876295
|
C | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.327+251C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876295 | ||||||
chr20:32876422
|
GTTACA | G | 4 | a0002c0042t0001g0198a0002c0046t0003g0233a0005c0013t0001g0200others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+380_327+384del others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32876422 | |||||
chr20:32876571
|
A | G | 2 | a0001c0001t0002g0057a0005c0008t0002g0050 | 2 | HG02027.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.327+527A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876571 | ||||||
chr20:32876642
|
A | G | 1 | a0026c0027t0003g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327+598A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876642 | ||||||
chr20:32876661
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.327+617G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876661 | ||||||
chr20:32876688
|
C | T | 5 | a0001c0001t0001g0175a0001c0001t0001g0176a0019c0016t0001g0143others(2): Show | 5 | HG00099.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+644C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876688 | ||||||
chr20:32876702
|
C | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(10): Show | 14 | HG00099.hp2 HG00642.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+658C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876702 | ||||||
chr20:32876914
|
GCTGAGAT others(3): Show |
G | 1 | a0003c0003t0002g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.327+871_327+880del others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32876914 | ||||||
chr20:32877079
|
C | T | 2 | a0020c0032t0004g0062a0020c0032t0004g0277 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+1035C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877079 | ||||||
chr20:32877114
|
C | T | 3 | a0002c0002t0001g0261a0010c0009t0004g0250a0037c0057t0004g0249 | 3 | HG01884.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.327+1070C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877114 | ||||||
chr20:32877199
|
A | C | 11 | a0001c0001t0001g0106a0001c0001t0001g0140a0002c0002t0001g0093others(8): Show | 11 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+1155A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877199 | ||||||
chr20:32877203
|
C | A | 45 | a0001c0001t0001g0146a0001c0001t0005g0255a0001c0001t0005g0256others(42): Show | 45 | HG00621.hp1 HG01109.hp2 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.327+1159C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877203 | ||||||
chr20:32877207
|
C | CT | 18 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0002g0027others(15): Show | 18 | HG01109.hp2 HG01261.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.327+1182dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | |||||
chr20:32877207
|
C | CTTTT | 13 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(10): Show | 14 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.327+1179_327+1182d others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | |||||
chr20:32877207
|
C | CTTTTT | 32 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0066others(29): Show | 32 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.327+1178_327+1182d others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | |||||
chr20:32877207
|
CT | C | 8 | a0001c0001t0001g0148a0001c0001t0001g0175a0001c0001t0001g0215others(5): Show | 8 | HG01168.hp2 HG01169.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+1182delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32877207 | |||||
chr20:32877211
|
T | C | 12 | a0001c0001t0001g0243a0002c0002t0001g0093a0002c0002t0001g0128others(9): Show | 12 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.327+1167T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877211 | ||||||
chr20:32877247
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0242 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.327+1203C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877247 | ||||||
chr20:32877532
|
A | G | 3 | a0002c0002t0001g0261a0010c0009t0004g0250a0037c0057t0004g0249 | 3 | HG01884.hp1 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.328-1172A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877532 | ||||||
chr20:32877568
|
G | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-1136G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877568 | ||||||
chr20:32877644
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-1060T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877644 | ||||||
chr20:32877888
|
C | G | 2 | a0014c0014t0002g0042a0036c0039t0002g0043 | 2 | NA18950.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.328-816C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877888 | ||||||
chr20:32877914
|
C | T | 18 | a0004c0004t0003g0069a0004c0004t0003g0077a0006c0005t0003g0064others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.328-790C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32877914 | ||||||
chr20:32878098
|
T | G | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-606T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878098 | ||||||
chr20:32878126
|
A | G | 88 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(85): Show | 88 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.328-578A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878126 | ||||||
chr20:32878389
|
C | T | 11 | a0001c0001t0005g0220a0015c0019t0005g0219a0015c0019t0005g0231others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.328-315C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878389 | ||||||
chr20:32878407
|
AC | A | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-295delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32878407 | |||||
chr20:32878476
|
G | C | 1 | a0010c0009t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.328-228G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878476 | ||||||
chr20:32878508
|
C | CT | 77 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0146others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.328-176dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr20 | 32878508 | |||||
chr20:32878541
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-163C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878541 | ||||||
chr20:32878556
|
G | A | 1 | a0004c0004t0003g0085 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.328-148G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878556 | ||||||
chr20:32878558
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-146C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878558 | ||||||
chr20:32878579
|
G | A | 1 | a0004c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.328-125G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878579 | ||||||
chr20:32878581
|
A | G | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.328-123A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878581 | ||||||
chr20:32878619
|
G | A | 1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.328-85G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 4/26 | chr20 | 32878619 | ||||||
chr20:32878846
|
C | A | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+39C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32878846 | ||||||
chr20:32878995
|
G | A | 1 | a0039c0048t0002g0032 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.431+188G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32878995 | ||||||
chr20:32879013
|
A | T | 1 | a0003c0003t0002g0021 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.431+206A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879013 | ||||||
chr20:32879194
|
G | C | 4 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+387G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879194 | ||||||
chr20:32879308
|
G | A | 14 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0221others(11): Show | 14 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.431+501G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879308 | ||||||
chr20:32879409
|
C | T | 1 | a0002c0002t0002g0028 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.431+602C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879409 | ||||||
chr20:32879569
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0206others(162): Show | 166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.431+762T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879569 | ||||||
chr20:32879570
|
G | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+763G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879570 | ||||||
chr20:32879614
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.431+807A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879614 | ||||||
chr20:32879617
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+810C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879617 | ||||||
chr20:32879670
|
C | T | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+863C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879670 | ||||||
chr20:32879745
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+938T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32879745 | ||||||
chr20:32880005
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(54): Show | 58 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.431+1198C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880005 | ||||||
chr20:32880186
|
T | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(159): Show | 163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.431+1379T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880186 | ||||||
chr20:32880188
|
A | C | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.431+1381A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880188 | ||||||
chr20:32880272
|
C | CT | 73 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(70): Show | 74 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.431+1479dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32880272 | |||||
chr20:32880272
|
CT | C | 12 | a0001c0001t0005g0220a0010c0009t0001g0248a0015c0019t0005g0219others(9): Show | 12 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.431+1479delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32880272 | |||||
chr20:32880307
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.431+1500T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880307 | ||||||
chr20:32880413
|
C | T | 2 | a0003c0003t0001g0130a0007c0030t0004g0127 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.431+1606C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880413 | ||||||
chr20:32880636
|
A | T | 1 | a0033c0065t0001g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431+1829A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880636 | ||||||
chr20:32880720
|
C | T | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+1913C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32880720 | ||||||
chr20:32880898
|
C | CAT | 56 | a0001c0001t0002g0027a0001c0001t0002g0052a0001c0001t0002g0057others(53): Show | 56 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.431+2103_431+2104d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32880898 | |||||
chr20:32881069
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.431+2262G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881069 | ||||||
chr20:32881126
|
G | A | 3 | a0017c0017t0007g0217a0017c0017t0007g0227a0017c0017t0007g0228 | 3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.431+2319G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881126 | ||||||
chr20:32881446
|
T | G | 1 | a0005c0037t0004g0183 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.431+2639T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881446 | ||||||
chr20:32881685
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.431+2878A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881685 | ||||||
chr20:32881740
|
G | A | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(4): Show | 7 | HG01123.hp2 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.431+2933G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881740 | ||||||
chr20:32881769
|
G | A | 2 | a0013c0020t0003g0090a0031c0060t0001g0079 | 2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.431+2962G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881769 | ||||||
chr20:32881771
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(57): Show | 61 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.431+2964G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881771 | ||||||
chr20:32881864
|
C | T | 11 | a0001c0001t0005g0220a0015c0019t0005g0219a0015c0019t0005g0231others(8): Show | 11 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.431+3057C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881864 | ||||||
chr20:32881881
|
A | G | 4 | a0001c0001t0001g0212a0003c0003t0001g0145a0003c0003t0001g0172others(1): Show | 4 | HG00621.hp1 NA18947.hp2 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.431+3074A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32881881 | ||||||
chr20:32882401
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.432-3104C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882401 | ||||||
chr20:32882596
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(148): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.432-2909C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882596 | ||||||
chr20:32882607
|
A | G | 92 | a0001c0001t0001g0171a0001c0001t0002g0027a0001c0001t0002g0052others(89): Show | 92 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.432-2898A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882607 | ||||||
chr20:32882669
|
C | T | 1 | a0026c0027t0003g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432-2836C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882669 | ||||||
chr20:32882678
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(48): Show | 52 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.432-2827G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882678 | ||||||
chr20:32882686
|
G | A | 1 | a0010c0009t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.432-2819G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882686 | ||||||
chr20:32882901
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.432-2604T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882901 | ||||||
chr20:32882974
|
C | G | 7 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(4): Show | 7 | HG01109.hp2 HG02486.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.432-2531C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32882974 | ||||||
chr20:32883031
|
G | A | 1 | a0007c0006t0001g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.432-2474G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883031 | ||||||
chr20:32883200
|
C | A | 6 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(3): Show | 6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-2305C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883200 | ||||||
chr20:32883206
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.432-2299C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883206 | ||||||
chr20:32883251
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(139): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.432-2254G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883251 | ||||||
chr20:32883252
|
T | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432-2253T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883252 | ||||||
chr20:32883495
|
A | G | 1 | a0004c0004t0003g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.432-2010A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883495 | ||||||
chr20:32883507
|
T | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(161): Show | 165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.432-1998T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883507 | ||||||
chr20:32883751
|
C | T | 49 | a0001c0001t0002g0057a0002c0002t0002g0003a0002c0002t0002g0004others(46): Show | 49 | HG00323.hp1 HG00733.hp1 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.432-1754C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883751 | ||||||
chr20:32883752
|
G | A | 4 | a0002c0042t0001g0198a0002c0046t0003g0233a0005c0013t0001g0200others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-1753G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883752 | ||||||
chr20:32883899
|
C | T | 6 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(3): Show | 6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.432-1606C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32883899 | ||||||
chr20:32884058
|
C | G | 68 | a0001c0001t0002g0057a0001c0001t0005g0220a0002c0002t0002g0003others(65): Show | 68 | HG00323.hp1 HG00733.hp1 HG00741.hp1 others(65): Show |
intron_variant | MODIFIER | c.432-1447C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884058 | ||||||
chr20:32884376
|
C | T | 1 | a0002c0002t0002g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.432-1129C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884376 | ||||||
chr20:32884626
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(148): Show | 152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.432-879T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884626 | ||||||
chr20:32884630
|
G | A | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-875G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884630 | ||||||
chr20:32884657
|
G | A | 1 | a0004c0004t0003g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.432-848G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884657 | ||||||
chr20:32884659
|
C | T | 6 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.432-846C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884659 | ||||||
chr20:32884686
|
C | G | 1 | a0009c0023t0001g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.432-819C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884686 | ||||||
chr20:32884949
|
G | A | 1 | a0027c0029t0003g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.432-556G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32884949 | ||||||
chr20:32885138
|
TC | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(131): Show | 135 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.432-365delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32885138 | |||||
chr20:32885182
|
C | T | 13 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0002g0036others(10): Show | 13 | HG02040.hp2 HG02129.hp2 NA18944.hp1 others(10): Show |
intron_variant | MODIFIER | c.432-323C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885182 | ||||||
chr20:32885207
|
G | A | 12 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(9): Show | 12 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.432-298G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885207 | ||||||
chr20:32885374
|
A | G | 144 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0103others(141): Show | 144 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.432-131A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885374 | ||||||
chr20:32885376
|
G | T | 128 | a0001c0001t0001g0061a0001c0001t0001g0088a0001c0001t0001g0103others(125): Show | 128 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.432-129G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885376 | ||||||
chr20:32885379
|
C | CGTGCGTG others(3): Show |
1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.432-117_432-116ins others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | INFO_REALIGN_3_PRIME | chr20 | 32885379 | |||||
chr20:32885394
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.432-111C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 5/26 | chr20 | 32885394 | ||||||
chr20:32885677
|
G | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0153a0001c0001t0001g0206others(154): Show | 158 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.567+37G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885677 | ||||||
chr20:32885750
|
G | T | 17 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0221others(14): Show | 17 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(14): Show |
intron_variant | MODIFIER | c.567+110G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885750 | ||||||
chr20:32885852
|
C | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(146): Show | 150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.567+212C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885852 | ||||||
chr20:32885860
|
G | A | 1 | a0010c0009t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.567+220G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885860 | ||||||
chr20:32885941
|
T | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.567+301T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32885941 | ||||||
chr20:32886061
|
T | C | 2 | a0005c0013t0004g0097a0018c0026t0001g0283 | 2 | HG01109.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.567+421T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886061 | ||||||
chr20:32886097
|
C | A | 1 | a0007c0006t0001g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.567+457C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886097 | ||||||
chr20:32886196
|
T | G | 36 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.567+556T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886196 | ||||||
chr20:32886204
|
G | A | 1 | a0002c0042t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.567+564G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886204 | ||||||
chr20:32886348
|
T | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.567+708T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886348 | ||||||
chr20:32886378
|
G | A | 20 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(17): Show | 20 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.567+738G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886378 | ||||||
chr20:32886387
|
G | A | 1 | a0051c0067t0004g0191 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.567+747G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886387 | ||||||
chr20:32886524
|
C | T | 3 | a0017c0017t0007g0217a0017c0017t0007g0227a0017c0017t0007g0228 | 3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.567+884C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886524 | ||||||
chr20:32886581
|
C | G | 2 | a0008c0007t0003g0194a0026c0027t0003g0126 | 2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.567+941C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886581 | ||||||
chr20:32886641
|
A | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(138): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.567+1001A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886641 | ||||||
chr20:32886773
|
G | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(193): Show | 197 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.567+1133G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886773 | ||||||
chr20:32886803
|
C | T | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.567+1163C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886803 | ||||||
chr20:32886860
|
C | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(138): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.567+1220C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886860 | ||||||
chr20:32886964
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(140): Show | 144 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.567+1324A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32886964 | ||||||
chr20:32887065
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(138): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.567+1425A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887065 | ||||||
chr20:32887109
|
G | C | 1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.567+1469G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887109 | ||||||
chr20:32887110
|
T | C | 1 | a0008c0007t0006g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.567+1470T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887110 | ||||||
chr20:32887294
|
C | T | 1 | a0005c0008t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.567+1654C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887294 | ||||||
chr20:32887311
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.567+1671C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887311 | ||||||
chr20:32887440
|
G | A | 1 | a0001c0052t0001g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.567+1800G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887440 | ||||||
chr20:32887449
|
C | A | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.567+1809C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887449 | ||||||
chr20:32887484
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.568-1817G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887484 | ||||||
chr20:32887500
|
C | T | 1 | a0002c0002t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.568-1801C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887500 | ||||||
chr20:32887684
|
A | G | 2 | a0002c0002t0001g0261a0007c0006t0001g0247 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.568-1617A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887684 | ||||||
chr20:32887768
|
C | T | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1533C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887768 | ||||||
chr20:32887880
|
C | T | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1421C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887880 | ||||||
chr20:32887894
|
A | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1407A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32887894 | ||||||
chr20:32888051
|
A | G | 17 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(14): Show | 17 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.568-1250A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888051 | ||||||
chr20:32888070
|
C | CT | 62 | a0001c0001t0001g0124a0001c0001t0002g0027a0001c0001t0002g0052others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.568-1220dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr20 | 32888070 | |||||
chr20:32888118
|
G | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1183G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888118 | ||||||
chr20:32888148
|
C | T | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1153C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888148 | ||||||
chr20:32888155
|
C | T | 1 | a0007c0030t0004g0266 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.568-1146C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888155 | ||||||
chr20:32888173
|
T | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1128T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888173 | ||||||
chr20:32888189
|
A | G | 8 | a0001c0001t0005g0255a0001c0001t0005g0256a0003c0003t0001g0130others(5): Show | 8 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-1112A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888189 | ||||||
chr20:32888219
|
G | A | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-1082G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888219 | ||||||
chr20:32888223
|
C | A | 1 | a0002c0002t0002g0022 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.568-1078C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888223 | ||||||
chr20:32888331
|
T | A | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-970T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888331 | ||||||
chr20:32888836
|
G | T | 1 | a0001c0001t0001g0215 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.568-465G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888836 | ||||||
chr20:32888858
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(139): Show | 143 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.568-443T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888858 | ||||||
chr20:32888866
|
T | C | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568-435T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888866 | ||||||
chr20:32888895
|
T | C | 7 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0109others(4): Show | 7 | HG01123.hp2 HG01243.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.568-406T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888895 | ||||||
chr20:32888958
|
T | G | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-343T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888958 | ||||||
chr20:32888960
|
T | G | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.568-341T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32888960 | ||||||
chr20:32889022
|
C | T | 8 | a0001c0001t0005g0255a0001c0001t0005g0256a0003c0003t0001g0130others(5): Show | 8 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-279C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32889022 | ||||||
chr20:32889035
|
C | A | 8 | a0001c0001t0005g0255a0001c0001t0005g0256a0003c0003t0001g0130others(5): Show | 8 | HG01261.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-266C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 6/26 | chr20 | 32889035 | ||||||
chr20:32889436
|
T | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+30T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889436 | ||||||
chr20:32889535
|
A | C | 5 | a0003c0003t0001g0279a0003c0003t0001g0282a0008c0007t0003g0280others(2): Show | 5 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+129A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889535 | ||||||
chr20:32889569
|
G | A | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+163G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889569 | ||||||
chr20:32889580
|
G | A | 1 | a0035c0038t0002g0260 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.673+174G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889580 | ||||||
chr20:32889591
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(128): Show | 132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.673+185G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889591 | ||||||
chr20:32889696
|
A | G | 2 | a0007c0006t0004g0142a0007c0030t0004g0266 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.673+290A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889696 | ||||||
chr20:32889724
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.673+318G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889724 | ||||||
chr20:32889727
|
T | C | 8 | a0005c0035t0001g0095a0012c0012t0004g0094a0012c0012t0004g0108others(5): Show | 8 | HG01123.hp2 HG01243.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.673+321T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889727 | ||||||
chr20:32889752
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0240others(126): Show | 130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.673+346A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889752 | ||||||
chr20:32889794
|
G | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(124): Show | 128 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.673+388G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889794 | ||||||
chr20:32889915
|
T | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+509T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889915 | ||||||
chr20:32889949
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(130): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.673+543T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889949 | ||||||
chr20:32889955
|
C | T | 2 | a0002c0002t0003g0275a0002c0002t0003g0276 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.673+549C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889955 | ||||||
chr20:32889986
|
G | A | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.673+580G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32889986 | ||||||
chr20:32890000
|
TA | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.673+613delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32890000 | |||||
chr20:32890002
|
A | T | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.673+596A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890002 | ||||||
chr20:32890003
|
A | T | 1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.673+597A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890003 | ||||||
chr20:32890167
|
A | G | 2 | a0002c0002t0001g0261a0007c0006t0001g0247 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.673+761A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890167 | ||||||
chr20:32890175
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(71): Show | 75 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.673+769C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890175 | ||||||
chr20:32890220
|
C | T | 7 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(4): Show | 7 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+814C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890220 | ||||||
chr20:32890241
|
GTGCTGTG others(3): Show |
G | 7 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(4): Show | 7 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+838_673+847del others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32890241 | |||||
chr20:32890488
|
G | C | 1 | a0002c0011t0001g0244 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.673+1082G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890488 | ||||||
chr20:32890494
|
A | AACCTCCA others(2): Show |
143 | a0001c0001t0001g0124a0001c0001t0002g0027a0001c0001t0002g0052others(140): Show | 143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.673+1089_673+1090i others(11): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32890494 | |||||
chr20:32890647
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0106others(214): Show | 218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.673+1241A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890647 | ||||||
chr20:32890658
|
T | C | 43 | a0001c0001t0001g0106a0001c0001t0001g0146a0001c0001t0001g0170others(40): Show | 43 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+1252T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890658 | ||||||
chr20:32890880
|
G | T | 38 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(35): Show | 38 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.674-1333G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890880 | ||||||
chr20:32890932
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.674-1281A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32890932 | ||||||
chr20:32891169
|
G | A | 7 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(4): Show | 7 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-1044G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891169 | ||||||
chr20:32891178
|
C | T | 3 | a0017c0017t0007g0217a0017c0017t0007g0227a0017c0017t0007g0228 | 3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.674-1035C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891178 | ||||||
chr20:32891203
|
G | A | 35 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.674-1010G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891203 | ||||||
chr20:32891217
|
C | T | 104 | a0001c0001t0002g0057a0001c0001t0005g0255a0001c0001t0005g0256others(101): Show | 104 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.674-996C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891217 | ||||||
chr20:32891277
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0002g0057a0001c0001t0005g0255others(102): Show | 106 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.674-936A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891277 | ||||||
chr20:32891300
|
T | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.674-913T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891300 | ||||||
chr20:32891325
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-888C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891325 | ||||||
chr20:32891547
|
A | G | 1 | a0023c0028t0002g0018 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.674-666A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891547 | ||||||
chr20:32891640
|
G | A | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-573G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891640 | ||||||
chr20:32891650
|
G | A | 4 | a0002c0002t0001g0093a0002c0002t0004g0101a0002c0002t0004g0102others(1): Show | 4 | HG02630.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-563G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891650 | ||||||
chr20:32891660
|
A | T | 1 | a0005c0035t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.674-553A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891660 | ||||||
chr20:32891762
|
A | G | 148 | a0001c0001t0001g0124a0001c0001t0001g0240a0001c0001t0001g0241others(145): Show | 148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.674-451A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891762 | ||||||
chr20:32891808
|
G | A | 1 | a0007c0006t0001g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.674-405G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891808 | ||||||
chr20:32891827
|
G | GT | 10 | a0001c0001t0001g0061a0012c0012t0004g0094a0012c0012t0004g0108others(7): Show | 10 | HG00621.hp2 HG01243.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.674-371dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32891827 | |||||
chr20:32891827
|
GT | G | 50 | a0001c0001t0001g0170a0004c0004t0001g0089a0004c0004t0003g0058others(47): Show | 50 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.674-371delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | INFO_REALIGN_3_PRIME | chr20 | 32891827 | |||||
chr20:32891922
|
A | G | 147 | a0001c0001t0001g0124a0001c0001t0001g0240a0001c0001t0001g0241others(144): Show | 147 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.674-291A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32891922 | ||||||
chr20:32892073
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.674-140C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32892073 | ||||||
chr20:32892137
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.674-76A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 7/26 | chr20 | 32892137 | ||||||
chr20:32892831
|
C | CT | 8 | a0001c0001t0001g0124a0001c0001t0001g0146a0002c0002t0002g0025others(5): Show | 8 | HG01109.hp2 HG01175.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.759-327dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr20 | 32892831 | |||||
chr20:32892831
|
CT | C | 15 | a0001c0001t0005g0255a0002c0002t0001g0234a0003c0003t0001g0282others(12): Show | 15 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.759-327delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr20 | 32892831 | |||||
chr20:32892847
|
T | C | 1 | a0002c0002t0001g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759-327T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892847 | ||||||
chr20:32892848
|
C | CT | 14 | a0002c0002t0001g0268a0002c0002t0001g0269a0002c0002t0001g0270others(11): Show | 14 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.759-318dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | INFO_REALIGN_3_PRIME | chr20 | 32892848 | |||||
chr20:32892848
|
C | T | 1 | a0002c0002t0001g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.759-326C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892848 | ||||||
chr20:32892959
|
G | A | 1 | a0004c0004t0003g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.759-215G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892959 | ||||||
chr20:32892982
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0240a0001c0001t0001g0241others(136): Show | 140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.759-192T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892982 | ||||||
chr20:32892989
|
C | T | 1 | a0002c0002t0003g0263 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.759-185C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32892989 | ||||||
chr20:32893032
|
G | A | 3 | a0005c0035t0001g0095a0009c0023t0001g0125a0025c0025t0001g0193 | 3 | HG01123.hp2 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.759-142G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893032 | ||||||
chr20:32893130
|
C | T | 57 | a0001c0001t0002g0057a0002c0002t0002g0003a0002c0002t0002g0004others(54): Show | 57 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.759-44C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893130 | ||||||
chr20:32893132
|
C | T | 49 | a0002c0002t0001g0261a0004c0004t0001g0089a0004c0004t0003g0058others(46): Show | 49 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.759-42C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893132 | ||||||
chr20:32893155
|
C | T | 139 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0057others(136): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.759-19C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 8/26 | chr20 | 32893155 | ||||||
chr20:32893470
|
G | A | 59 | a0001c0001t0002g0057a0002c0002t0002g0003a0002c0002t0002g0004others(56): Show | 59 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(56): Show |
intron_variant | MODIFIER | c.883+172G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893470 | ||||||
chr20:32893721
|
G | A | 55 | a0001c0001t0002g0057a0002c0002t0002g0003a0002c0002t0002g0004others(52): Show | 55 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.883+423G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893721 | ||||||
chr20:32893767
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.883+469C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893767 | ||||||
chr20:32893844
|
C | T | 1 | a0002c0002t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.883+546C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893844 | ||||||
chr20:32893845
|
G | A | 3 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112 | 3 | HG02572.hp1 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.883+547G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32893845 | ||||||
chr20:32894059
|
G | A | 1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883+761G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894059 | ||||||
chr20:32894078
|
C | T | 26 | a0001c0001t0001g0206a0001c0001t0001g0211a0001c0001t0001g0240others(23): Show | 26 | HG00099.hp2 HG00642.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+780C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894078 | ||||||
chr20:32894091
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.883+793C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894091 | ||||||
chr20:32894213
|
A | G | 55 | a0001c0001t0002g0057a0002c0002t0002g0003a0002c0002t0002g0004others(52): Show | 55 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.883+915A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894213 | ||||||
chr20:32894295
|
T | C | 137 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0057others(134): Show | 137 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.883+997T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894295 | ||||||
chr20:32894295
|
T | G | 1 | a0009c0023t0001g0125 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+997T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894295 | ||||||
chr20:32894328
|
G | A | 36 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.883+1030G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894328 | ||||||
chr20:32894386
|
G | A | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.883+1088G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894386 | ||||||
chr20:32894489
|
A | G | 88 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0057others(85): Show | 88 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.883+1191A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894489 | ||||||
chr20:32894619
|
T | C | 179 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0057others(176): Show | 179 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.883+1321T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894619 | ||||||
chr20:32894746
|
G | A | 1 | a0017c0017t0007g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.883+1448G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894746 | ||||||
chr20:32894820
|
T | C | 1 | a0004c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.883+1522T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32894820 | ||||||
chr20:32895106
|
C | T | 54 | a0001c0001t0002g0057a0002c0002t0002g0003a0002c0002t0002g0004others(51): Show | 54 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(51): Show |
intron_variant | MODIFIER | c.884-1348C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895106 | ||||||
chr20:32895148
|
C | T | 14 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(11): Show | 14 | HG02451.hp2 HG02630.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.884-1306C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895148 | ||||||
chr20:32895313
|
A | AT | 13 | a0001c0001t0001g0163a0001c0001t0001g0211a0002c0002t0001g0267others(10): Show | 13 | HG01109.hp1 HG01358.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.884-1119dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | |||||
chr20:32895313
|
A | ATT | 16 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(13): Show | 16 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-1120_884-1119d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | |||||
chr20:32895313
|
AT | A | 66 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0148others(63): Show | 66 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(63): Show |
intron_variant | MODIFIER | c.884-1119delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | |||||
chr20:32895313
|
ATT | A | 48 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(45): Show | 48 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.884-1120_884-1119d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895313 | |||||
chr20:32895364
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.884-1090G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895364 | ||||||
chr20:32895571
|
C | CT | 21 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(18): Show | 21 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.884-880dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895571 | |||||
chr20:32895571
|
C | CTT | 6 | a0003c0003t0001g0123a0003c0003t0001g0164a0003c0003t0001g0201others(3): Show | 6 | HG01981.hp2 NA18966.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.884-881_884-880dup others(2): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | INFO_REALIGN_3_PRIME | chr20 | 32895571 | |||||
chr20:32895575
|
C | T | 29 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(26): Show | 29 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.884-879C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895575 | ||||||
chr20:32895579
|
T | C | 1 | a0044c0044t0002g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.884-875T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895579 | ||||||
chr20:32895608
|
A | G | 173 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0057others(170): Show | 173 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.884-846A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895608 | ||||||
chr20:32895633
|
G | A | 2 | a0010c0009t0004g0250a0023c0028t0005g0258 | 2 | HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.884-821G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895633 | ||||||
chr20:32895672
|
AG | A | 8 | a0004c0004t0003g0059a0004c0004t0003g0066a0004c0004t0003g0068others(5): Show | 8 | HG00741.hp2 HG01255.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-781delG | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895672 | ||||||
chr20:32895732
|
C | T | 1 | a0004c0004t0003g0085 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.884-722C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895732 | ||||||
chr20:32895847
|
A | C | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-607A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895847 | ||||||
chr20:32895861
|
G | A | 6 | a0002c0002t0001g0119a0003c0003t0001g0123a0003c0003t0001g0164others(3): Show | 6 | NA18966.hp1 NA19007.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.884-593G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895861 | ||||||
chr20:32895900
|
G | T | 89 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0002g0057others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.884-554G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32895900 | ||||||
chr20:32896174
|
C | T | 68 | a0001c0001t0002g0057a0002c0002t0001g0261a0002c0002t0002g0003others(65): Show | 68 | HG00323.hp1 HG00733.hp1 HG01099.hp2 others(65): Show |
intron_variant | MODIFIER | c.884-280C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896174 | ||||||
chr20:32896283
|
G | A | 3 | a0007c0006t0001g0236a0007c0006t0001g0247a0007c0006t0004g0199 | 3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.884-171G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896283 | ||||||
chr20:32896289
|
C | T | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.884-165C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896289 | ||||||
chr20:32896380
|
C | T | 13 | a0015c0019t0005g0219a0015c0019t0005g0231a0015c0019t0005g0232others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.884-74C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 9/26 | chr20 | 32896380 | ||||||
chr20:32896611
|
T | A | 36 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(33): Show | 36 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.957+84T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896611 | ||||||
chr20:32896713
|
G | A | 1 | a0026c0027t0003g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.957+186G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896713 | ||||||
chr20:32896765
|
G | T | 13 | a0015c0019t0005g0219a0015c0019t0005g0231a0015c0019t0005g0232others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+238G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896765 | ||||||
chr20:32896941
|
G | A | 13 | a0015c0019t0005g0219a0015c0019t0005g0231a0015c0019t0005g0232others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+414G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32896941 | ||||||
chr20:32897137
|
T | C | 1 | a0005c0035t0001g0095 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.957+610T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897137 | ||||||
chr20:32897302
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.957+775G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897302 | ||||||
chr20:32897308
|
G | A | 13 | a0015c0019t0005g0219a0015c0019t0005g0231a0015c0019t0005g0232others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.957+781G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897308 | ||||||
chr20:32897344
|
C | A | 13 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(10): Show | 13 | HG01361.hp2 HG02145.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.957+817C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897344 | ||||||
chr20:32897348
|
G | A | 22 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(19): Show | 22 | HG00099.hp2 HG00642.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.957+821G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897348 | ||||||
chr20:32897430
|
C | T | 1 | a0004c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.957+903C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897430 | ||||||
chr20:32897434
|
A | G | 5 | a0015c0019t0005g0231a0015c0019t0005g0232a0016c0018t0005g0229others(2): Show | 5 | HG00741.hp1 HG01167.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+907A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897434 | ||||||
chr20:32897439
|
C | CT | 62 | a0001c0001t0001g0153a0001c0001t0002g0057a0002c0002t0002g0003others(59): Show | 62 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.957+929dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr20 | 32897439 | |||||
chr20:32897439
|
CT | C | 12 | a0001c0001t0001g0124a0001c0001t0001g0186a0001c0001t0002g0027others(9): Show | 12 | HG00423.hp1 HG00621.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.957+929delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | INFO_REALIGN_3_PRIME | chr20 | 32897439 | |||||
chr20:32897473
|
T | G | 60 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.957+946T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897473 | ||||||
chr20:32897526
|
T | G | 1 | a0015c0019t0005g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.958-967T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897526 | ||||||
chr20:32897529
|
A | G | 2 | a0003c0003t0001g0172a0003c0003t0001g0173 | 2 | NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.958-964A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897529 | ||||||
chr20:32897591
|
A | C | 2 | a0002c0046t0003g0233a0040c0049t0001g0197 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.958-902A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897591 | ||||||
chr20:32897770
|
G | A | 6 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(3): Show | 6 | HG01358.hp2 HG02280.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.958-723G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897770 | ||||||
chr20:32897811
|
G | C | 2 | a0003c0003t0001g0130a0007c0030t0004g0127 | 2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.958-682G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897811 | ||||||
chr20:32897814
|
A | G | 3 | a0006c0005t0003g0064a0006c0005t0003g0067a0006c0005t0003g0074 | 3 | HG01175.hp1 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.958-679A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32897814 | ||||||
chr20:32898034
|
C | A | 169 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0093others(166): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.958-459C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898034 | ||||||
chr20:32898035
|
G | A | 1 | a0001c0052t0001g0185 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.958-458G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898035 | ||||||
chr20:32898052
|
A | G | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.958-441A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898052 | ||||||
chr20:32898154
|
A | G | 3 | a0007c0006t0001g0236a0007c0006t0001g0247a0007c0006t0004g0199 | 3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.958-339A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898154 | ||||||
chr20:32898206
|
G | A | 13 | a0015c0019t0005g0219a0015c0019t0005g0231a0015c0019t0005g0232others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.958-287G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898206 | ||||||
chr20:32898221
|
C | T | 1 | a0048c0058t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.958-272C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898221 | ||||||
chr20:32898245
|
C | T | 150 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(147): Show | 150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.958-248C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898245 | ||||||
chr20:32898263
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.958-230A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898263 | ||||||
chr20:32898400
|
A | G | 150 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(147): Show | 150 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.958-93A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 10/26 | chr20 | 32898400 | ||||||
chr20:32898657
|
G | A | 1 | a0009c0015t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1088+34G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32898657 | ||||||
chr20:32898753
|
T | C | 64 | a0001c0001t0001g0240a0001c0001t0001g0241a0002c0002t0001g0119others(61): Show | 64 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.1088+130T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32898753 | ||||||
chr20:32898802
|
C | T | 13 | a0002c0002t0001g0261a0003c0003t0001g0130a0007c0030t0004g0127others(10): Show | 13 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1088+179C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32898802 | ||||||
chr20:32899022
|
A | G | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+399A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899022 | ||||||
chr20:32899107
|
C | G | 1 | a0035c0038t0002g0260 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1088+484C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899107 | ||||||
chr20:32899107
|
C | T | 1 | a0018c0051t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1088+484C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899107 | ||||||
chr20:32899162
|
G | A | 2 | a0002c0011t0001g0100a0041c0050t0002g0218 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1088+539G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899162 | ||||||
chr20:32899229
|
C | CAAT | 24 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(21): Show | 24 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1088+631_1088+633d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32899229 | |||||
chr20:32899229
|
CAAT | C | 81 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(78): Show | 81 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1088+631_1088+633d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32899229 | |||||
chr20:32899266
|
G | A | 1 | a0048c0058t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088+643G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899266 | ||||||
chr20:32899297
|
C | T | 3 | a0002c0046t0003g0233a0018c0026t0001g0283a0040c0049t0001g0197 | 3 | HG01109.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1088+674C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899297 | ||||||
chr20:32899338
|
G | A | 1 | a0004c0004t0003g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1088+715G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899338 | ||||||
chr20:32899404
|
C | CA | 76 | a0002c0002t0001g0190a0002c0002t0001g0267a0002c0002t0001g0268others(73): Show | 76 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.1088+798dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32899404 | |||||
chr20:32899417
|
A | G | 14 | a0002c0002t0001g0119a0002c0002t0001g0261a0003c0003t0001g0123others(11): Show | 14 | HG01109.hp2 HG01123.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1088+794A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899417 | ||||||
chr20:32899423
|
A | G | 1 | a0002c0002t0004g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1088+800A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899423 | ||||||
chr20:32899622
|
T | C | 2 | a0002c0011t0001g0100a0041c0050t0002g0218 | 2 | HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1088+999T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899622 | ||||||
chr20:32899637
|
C | T | 1 | a0015c0019t0005g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1088+1014C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899637 | ||||||
chr20:32899735
|
C | T | 33 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1088+1112C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32899735 | ||||||
chr20:32900415
|
C | G | 4 | a0004c0004t0003g0077a0006c0005t0003g0076a0006c0005t0003g0078others(1): Show | 4 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088+1792C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900415 | ||||||
chr20:32900517
|
T | C | 163 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1088+1894T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900517 | ||||||
chr20:32900555
|
A | C | 1 | a0021c0062t0001g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1088+1932A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900555 | ||||||
chr20:32900590
|
C | T | 80 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(77): Show | 80 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1088+1967C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900590 | ||||||
chr20:32900615
|
G | A | 1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1088+1992G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900615 | ||||||
chr20:32900654
|
C | T | 12 | a0002c0002t0003g0275a0002c0002t0003g0276a0015c0019t0005g0219others(9): Show | 12 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1088+2031C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900654 | ||||||
chr20:32900660
|
G | A | 33 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1088+2037G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900660 | ||||||
chr20:32900790
|
G | A | 3 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246 | 3 | HG02486.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1088+2167G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900790 | ||||||
chr20:32900848
|
G | C | 104 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(101): Show | 104 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.1088+2225G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900848 | ||||||
chr20:32900859
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1088+2236T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900859 | ||||||
chr20:32900991
|
C | T | 54 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(51): Show | 54 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1088+2368C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32900991 | ||||||
chr20:32901102
|
G | A | 1 | a0002c0002t0003g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1088+2479G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901102 | ||||||
chr20:32901174
|
T | A | 1 | a0004c0004t0003g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1088+2551T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901174 | ||||||
chr20:32901182
|
G | C | 12 | a0002c0002t0003g0275a0002c0002t0003g0276a0015c0019t0005g0219others(9): Show | 12 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1088+2559G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901182 | ||||||
chr20:32901488
|
TCCTGATG others(64): Show |
T | 3 | a0017c0017t0007g0217a0017c0017t0007g0227a0017c0017t0007g0228 | 3 | HG01891.hp1 HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1088+2869_1088+293 others(75): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32901488 | |||||
chr20:32901521
|
C | T | 1 | a0003c0003t0002g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1088+2898C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901521 | ||||||
chr20:32901573
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1088+2950A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901573 | ||||||
chr20:32901837
|
G | A | 2 | a0002c0002t0002g0110a0002c0002t0002g0134 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1088+3214G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901837 | ||||||
chr20:32901908
|
C | G | 170 | a0001c0001t0001g0213a0002c0002t0001g0093a0002c0002t0001g0119others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1088+3285C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901908 | ||||||
chr20:32901929
|
G | A | 3 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0264 | 3 | HG02965.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1088+3306G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901929 | ||||||
chr20:32901931
|
C | G | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088+3308C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901931 | ||||||
chr20:32901958
|
T | C | 2 | a0003c0003t0002g0135a0003c0003t0002g0136 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1088+3335T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901958 | ||||||
chr20:32901966
|
G | A | 1 | a0021c0061t0001g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1088+3343G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32901966 | ||||||
chr20:32902101
|
G | A | 1 | a0002c0002t0002g0022 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1088+3478G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902101 | ||||||
chr20:32902124
|
A | G | 8 | a0002c0011t0001g0100a0003c0003t0001g0279a0003c0003t0001g0282others(5): Show | 8 | HG01358.hp2 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1088+3501A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902124 | ||||||
chr20:32902164
|
G | A | 1 | a0001c0056t0001g0121 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1088+3541G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902164 | ||||||
chr20:32902293
|
G | A | 1 | a0002c0002t0001g0268 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1088+3670G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902293 | ||||||
chr20:32902328
|
G | C | 11 | a0002c0002t0001g0119a0003c0003t0001g0123a0003c0003t0001g0164others(8): Show | 11 | HG01123.hp2 HG02257.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1088+3705G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902328 | ||||||
chr20:32902358
|
G | T | 1 | a0040c0049t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1088+3735G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902358 | ||||||
chr20:32902411
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1088+3788G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902411 | ||||||
chr20:32902419
|
GACAGAGC others(10): Show |
G | 1 | a0003c0003t0001g0173 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1088+3797_1088+381 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902419 | ||||||
chr20:32902458
|
C | A | 1 | a0048c0058t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088+3835C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902458 | ||||||
chr20:32902493
|
T | C | 1 | a0048c0058t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1088+3870T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902493 | ||||||
chr20:32902766
|
C | T | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-3796C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902766 | ||||||
chr20:32902818
|
T | C | 169 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1089-3744T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902818 | ||||||
chr20:32902828
|
C | T | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-3734C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902828 | ||||||
chr20:32902878
|
G | A | 2 | a0050c0068t0004g0216a0051c0067t0004g0191 | 2 | HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1089-3684G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902878 | ||||||
chr20:32902922
|
C | T | 1 | a0010c0009t0004g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1089-3640C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32902922 | ||||||
chr20:32903172
|
C | T | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1089-3390C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903172 | ||||||
chr20:32903279
|
C | T | 1 | a0014c0014t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1089-3283C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903279 | ||||||
chr20:32903305
|
A | C | 1 | a0003c0003t0001g0173 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-3257A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903305 | ||||||
chr20:32903353
|
C | T | 3 | a0001c0001t0005g0220a0005c0036t0004g0180a0045c0054t0004g0099 | 3 | HG03471.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1089-3209C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903353 | ||||||
chr20:32903368
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1089-3194C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903368 | ||||||
chr20:32903433
|
C | T | 1 | a0011c0010t0006g0049 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1089-3129C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903433 | ||||||
chr20:32903495
|
G | C | 34 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1089-3067G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903495 | ||||||
chr20:32903551
|
G | A | 1 | a0010c0009t0001g0248 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1089-3011G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903551 | ||||||
chr20:32903605
|
C | T | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-2957C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903605 | ||||||
chr20:32903712
|
G | C | 2 | a0002c0011t0001g0245a0002c0011t0001g0246 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1089-2850G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903712 | ||||||
chr20:32903785
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1089-2777A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903785 | ||||||
chr20:32903813
|
A | G | 4 | a0004c0004t0003g0077a0006c0005t0003g0076a0006c0005t0003g0078others(1): Show | 4 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089-2749A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903813 | ||||||
chr20:32903933
|
C | T | 1 | a0014c0014t0002g0040 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1089-2629C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32903933 | ||||||
chr20:32904019
|
G | T | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-2543G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904019 | ||||||
chr20:32904166
|
A | T | 1 | a0003c0003t0001g0173 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-2396A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904166 | ||||||
chr20:32904318
|
G | T | 13 | a0002c0002t0001g0119a0002c0002t0001g0261a0003c0003t0001g0123others(10): Show | 13 | HG01123.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1089-2244G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904318 | ||||||
chr20:32904375
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0242 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1089-2187A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904375 | ||||||
chr20:32904567
|
G | A | 169 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(166): Show | 169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.1089-1995G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904567 | ||||||
chr20:32904603
|
C | CT | 25 | a0001c0001t0001g0106a0002c0002t0001g0119a0002c0002t0001g0268others(22): Show | 25 | HG01243.hp1 HG01346.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1089-1938dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32904603 | |||||
chr20:32904603
|
CT | C | 102 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0144others(99): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1089-1938delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32904603 | |||||
chr20:32904629
|
C | CG | 3 | a0002c0002t0001g0119a0007c0030t0004g0127a0011c0010t0006g0030 | 3 | HG03098.hp1 NA19058.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1089-1931dupG | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32904629 | |||||
chr20:32904635
|
C | G | 1 | a0002c0002t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1089-1927C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904635 | ||||||
chr20:32904636
|
G | C | 69 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(66): Show | 69 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1089-1926G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904636 | ||||||
chr20:32904642
|
G | A | 1 | a0002c0002t0003g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1089-1920G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904642 | ||||||
chr20:32904712
|
C | T | 1 | a0009c0023t0001g0222 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1089-1850C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904712 | ||||||
chr20:32904713
|
A | G | 170 | a0001c0001t0001g0001a0002c0002t0001g0093a0002c0002t0001g0119others(167): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1089-1849A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904713 | ||||||
chr20:32904815
|
C | T | 1 | a0002c0002t0002g0033 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1089-1747C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904815 | ||||||
chr20:32904847
|
G | T | 1 | a0002c0002t0002g0033 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1089-1715G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904847 | ||||||
chr20:32904869
|
C | T | 2 | a0014c0014t0002g0042a0036c0039t0002g0043 | 2 | NA18950.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1089-1693C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904869 | ||||||
chr20:32904906
|
C | T | 1 | a0008c0007t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1089-1656C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904906 | ||||||
chr20:32904941
|
A | T | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-1621A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904941 | ||||||
chr20:32904965
|
G | A | 1 | a0008c0007t0003g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1089-1597G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32904965 | ||||||
chr20:32905137
|
C | T | 3 | a0001c0001t0005g0220a0005c0036t0004g0180a0045c0054t0004g0099 | 3 | HG03471.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1089-1425C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905137 | ||||||
chr20:32905439
|
T | C | 1 | a0048c0058t0002g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1089-1123T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905439 | ||||||
chr20:32905444
|
C | T | 1 | a0003c0003t0001g0173 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-1118C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905444 | ||||||
chr20:32905445
|
T | C | 1 | a0003c0003t0001g0173 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-1117T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905445 | ||||||
chr20:32905614
|
G | A | 58 | a0002c0002t0001g0190a0002c0011t0001g0100a0002c0042t0001g0198others(55): Show | 58 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1089-948G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905614 | ||||||
chr20:32905637
|
G | C | 1 | a0007c0006t0001g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1089-925G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905637 | ||||||
chr20:32905759
|
C | CAA | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-790_1089-789d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905759
|
C | CAAAAAAA others(6): Show |
32 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(29): Show | 32 | HG01168.hp1 HG01243.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.1089-801_1089-789d others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905759
|
C | CAAAAAAA others(7): Show |
63 | a0002c0002t0001g0269a0002c0002t0001g0270a0002c0002t0001g0271others(60): Show | 63 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1089-802_1089-789d others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905759
|
C | CAAAAAAA others(8): Show |
45 | a0002c0002t0001g0190a0002c0002t0001g0261a0002c0002t0001g0267others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1089-789_1089-788i others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905759
|
C | CAAAAAAA others(9): Show |
17 | a0002c0002t0001g0119a0003c0003t0001g0164a0004c0004t0003g0084others(14): Show | 17 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1089-789_1089-788i others(18): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905759
|
C | CAAAAAAA others(10): Show |
3 | a0003c0003t0001g0123a0003c0003t0001g0201a0009c0023t0001g0125 | 3 | HG02886.hp2 NA19064.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1089-789_1089-788i others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905759
|
C | CAAAAAAA others(11): Show |
2 | a0005c0035t0001g0095a0025c0025t0001g0193 | 2 | HG01123.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1089-789_1089-788i others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr20 | 32905759 | |||||
chr20:32905793
|
G | A | 1 | a0004c0004t0003g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1089-769G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905793 | ||||||
chr20:32905802
|
T | C | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-760T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905802 | ||||||
chr20:32905911
|
A | G | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089-651A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905911 | ||||||
chr20:32905960
|
T | A | 1 | a0003c0003t0001g0173 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1089-602T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32905960 | ||||||
chr20:32906202
|
C | T | 9 | a0015c0019t0005g0219a0015c0019t0005g0231a0015c0019t0005g0232others(6): Show | 9 | HG00741.hp1 HG01167.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1089-360C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32906202 | ||||||
chr20:32906354
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1089-208C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32906354 | ||||||
chr20:32906558
|
G | A | 1 | a0002c0002t0002g0047 | 1 | HG03688.hp2 | splice_region_variant&intron_variant | LOW | c.1089-4G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 11/26 | chr20 | 32906558 | ||||||
chr20:32907109
|
G | C | 54 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0006others(51): Show | 54 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1308+115G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907109 | ||||||
chr20:32907119
|
G | A | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+125G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907119 | ||||||
chr20:32907148
|
C | T | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+154C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907148 | ||||||
chr20:32907157
|
T | C | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+163T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907157 | ||||||
chr20:32907350
|
G | A | 6 | a0002c0042t0001g0198a0009c0015t0001g0096a0009c0015t0001g0098others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1308+356G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907350 | ||||||
chr20:32907375
|
G | A | 1 | a0013c0020t0003g0254 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1308+381G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907375 | ||||||
chr20:32907441
|
C | A | 1 | a0001c0001t0002g0027 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1308+447C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907441 | ||||||
chr20:32907519
|
G | A | 1 | a0002c0002t0002g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1308+525G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907519 | ||||||
chr20:32907796
|
C | G | 39 | a0002c0002t0001g0190a0002c0042t0001g0198a0004c0004t0001g0089others(36): Show | 39 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1309-479C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907796 | ||||||
chr20:32907904
|
G | T | 6 | a0002c0002t0001g0119a0003c0003t0001g0123a0003c0003t0001g0164others(3): Show | 6 | NA18966.hp1 NA19007.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.1309-371G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32907904 | ||||||
chr20:32908167
|
C | T | 1 | a0043c0045t0007g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1309-108C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908167 | ||||||
chr20:32908171
|
C | T | 33 | a0002c0002t0001g0190a0004c0004t0001g0089a0004c0004t0003g0058others(30): Show | 33 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1309-104C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908171 | ||||||
chr20:32908202
|
C | T | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1309-73C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908202 | ||||||
chr20:32908257
|
C | G | 16 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(13): Show | 16 | HG01261.hp2 HG01361.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1309-18C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 13/26 | chr20 | 32908257 | ||||||
chr20:32908528
|
C | T | 10 | a0002c0002t0001g0119a0003c0003t0001g0123a0003c0003t0001g0164others(7): Show | 10 | HG01123.hp2 HG02257.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.1446+116C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908528 | ||||||
chr20:32908602
|
G | T | 1 | a0007c0030t0004g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1446+190G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908602 | ||||||
chr20:32908691
|
G | A | 2 | a0002c0002t0002g0110a0002c0002t0002g0134 | 2 | HG03834.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1446+279G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908691 | ||||||
chr20:32908864
|
G | A | 1 | a0014c0014t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1446+452G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908864 | ||||||
chr20:32908996
|
G | T | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1446+584G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32908996 | ||||||
chr20:32909012
|
G | T | 5 | a0002c0002t0001g0119a0005c0013t0004g0097a0009c0041t0001g0251others(2): Show | 5 | HG01109.hp2 HG02109.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+600G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909012 | ||||||
chr20:32909094
|
G | A | 147 | a0001c0001t0001g0171a0001c0001t0005g0220a0002c0002t0001g0119others(144): Show | 147 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1446+682G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909094 | ||||||
chr20:32909125
|
C | T | 37 | a0002c0002t0001g0190a0002c0002t0002g0006a0002c0002t0002g0012others(34): Show | 37 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1447-696C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909125 | ||||||
chr20:32909221
|
G | C | 3 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246 | 3 | HG02486.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1447-600G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909221 | ||||||
chr20:32909465
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1447-356A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909465 | ||||||
chr20:32909515
|
G | A | 1 | a0040c0049t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1447-306G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909515 | ||||||
chr20:32909562
|
G | A | 19 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(16): Show | 19 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.1447-259G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909562 | ||||||
chr20:32909577
|
C | CTTGGAA | 7 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0264others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1447-241_1447-236d others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr20 | 32909577 | |||||
chr20:32909606
|
G | T | 1 | a0004c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1447-215G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909606 | ||||||
chr20:32909719
|
C | T | 5 | a0012c0012t0004g0094a0024c0024t0005g0041a0024c0024t0005g0111others(2): Show | 5 | HG01243.hp1 HG01346.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-102C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909719 | ||||||
chr20:32909783
|
C | G | 1 | a0002c0002t0002g0022 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1447-38C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 14/26 | chr20 | 32909783 | ||||||
chr20:32910071
|
G | A | 2 | a0016c0018t0004g0147a0016c0018t0004g0192 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1557+140G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910071 | ||||||
chr20:32910141
|
C | T | 1 | a0018c0051t0003g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1557+210C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910141 | ||||||
chr20:32910149
|
A | G | 1 | a0008c0007t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1557+218A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910149 | ||||||
chr20:32910205
|
C | T | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+274C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910205 | ||||||
chr20:32910214
|
G | C | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1557+283G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910214 | ||||||
chr20:32910226
|
T | G | 3 | a0037c0057t0004g0249a0047c0055t0001g0278a0048c0058t0002g0257 | 3 | HG01261.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1557+295T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910226 | ||||||
chr20:32910354
|
C | A | 146 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(143): Show | 146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1557+423C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910354 | ||||||
chr20:32910654
|
A | G | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1557+723A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910654 | ||||||
chr20:32910738
|
C | CT | 42 | a0001c0001t0001g0104a0001c0001t0001g0148a0001c0001t0001g0161others(39): Show | 42 | HG00423.hp1 HG00741.hp1 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.1558-720dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | |||||
chr20:32910738
|
C | CTT | 55 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(52): Show | 55 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1558-721_1558-720d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | |||||
chr20:32910738
|
C | CTTT | 10 | a0002c0002t0001g0273a0002c0002t0004g0102a0003c0003t0002g0135others(7): Show | 10 | HG00323.hp1 HG01123.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1558-722_1558-720d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | |||||
chr20:32910738
|
CT | C | 12 | a0001c0001t0001g0088a0001c0001t0001g0154a0001c0001t0001g0242others(9): Show | 12 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1558-720delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | |||||
chr20:32910738
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0042t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1558-731_1558-720d others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | INFO_REALIGN_3_PRIME | chr20 | 32910738 | |||||
chr20:32910771
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1558-709C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910771 | ||||||
chr20:32910780
|
G | A | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1558-700G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910780 | ||||||
chr20:32910792
|
G | A | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1558-688G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910792 | ||||||
chr20:32910841
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1558-639G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32910841 | ||||||
chr20:32911013
|
C | T | 32 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(29): Show | 32 | HG00639.hp2 HG00642.hp1 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.1558-467C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911013 | ||||||
chr20:32911020
|
G | A | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1558-460G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911020 | ||||||
chr20:32911164
|
C | T | 4 | a0004c0004t0003g0085a0037c0057t0004g0249a0047c0055t0001g0278others(1): Show | 4 | HG01123.hp1 HG01261.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1558-316C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911164 | ||||||
chr20:32911385
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1558-95T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911385 | ||||||
chr20:32911393
|
G | T | 3 | a0037c0057t0004g0249a0047c0055t0001g0278a0048c0058t0002g0257 | 3 | HG01261.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1558-87G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 15/26 | chr20 | 32911393 | ||||||
chr20:32911739
|
C | T | 1 | a0002c0042t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1785+32C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32911739 | ||||||
chr20:32911769
|
T | A | 3 | a0037c0057t0004g0249a0047c0055t0001g0278a0048c0058t0002g0257 | 3 | HG01261.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1785+62T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32911769 | ||||||
chr20:32911897
|
G | A | 3 | a0002c0002t0001g0221a0002c0002t0001g0234a0002c0002t0001g0235 | 3 | HG02451.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1785+190G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32911897 | ||||||
chr20:32912000
|
A | G | 4 | a0002c0002t0003g0262a0002c0002t0003g0263a0002c0002t0003g0265others(1): Show | 4 | HG02145.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785+293A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912000 | ||||||
chr20:32912004
|
G | A | 1 | a0004c0004t0003g0253 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1785+297G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912004 | ||||||
chr20:32912147
|
G | A | 2 | a0009c0015t0001g0098a0009c0015t0001g0112 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1785+440G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912147 | ||||||
chr20:32912301
|
C | T | 12 | a0002c0002t0003g0275a0002c0002t0003g0276a0002c0011t0001g0100others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1786-493C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912301 | ||||||
chr20:32912386
|
C | T | 2 | a0002c0011t0001g0245a0002c0011t0001g0246 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1786-408C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912386 | ||||||
chr20:32912398
|
C | T | 2 | a0022c0031t0002g0196a0022c0031t0002g0230 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1786-396C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912398 | ||||||
chr20:32912430
|
C | CA | 27 | a0001c0001t0002g0137a0003c0003t0001g0145a0003c0003t0001g0172others(24): Show | 27 | HG00621.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1786-349dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr20 | 32912430 | |||||
chr20:32912444
|
AAG | A | 74 | a0002c0002t0001g0119a0002c0002t0001g0190a0002c0002t0002g0003others(71): Show | 74 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1786-348_1786-347d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | INFO_REALIGN_3_PRIME | chr20 | 32912444 | |||||
chr20:32912445
|
AG | A | 63 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(60): Show | 63 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(60): Show |
intron_variant | MODIFIER | c.1786-348delG | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912445 | ||||||
chr20:32912446
|
G | A | 33 | a0002c0011t0001g0100a0002c0042t0001g0198a0005c0013t0001g0200others(30): Show | 33 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1786-348G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912446 | ||||||
chr20:32912449
|
G | A | 145 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(142): Show | 145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1786-345G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912449 | ||||||
chr20:32912572
|
A | G | 1 | a0002c0042t0001g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1786-222A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912572 | ||||||
chr20:32912613
|
C | G | 2 | a0004c0004t0003g0069a0029c0059t0003g0071 | 2 | HG01516.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1786-181C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912613 | ||||||
chr20:32912755
|
G | A | 1 | a0040c0049t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1786-39G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 16/26 | chr20 | 32912755 | ||||||
chr20:32912918
|
C | T | 3 | a0015c0019t0005g0219a0050c0068t0004g0216a0051c0067t0004g0191 | 3 | HG01884.hp2 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1856+54C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32912918 | ||||||
chr20:32913016
|
C | A | 1 | a0007c0006t0004g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1856+152C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913016 | ||||||
chr20:32913018
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1856+154T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913018 | ||||||
chr20:32913314
|
A | C | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1856+450A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913314 | ||||||
chr20:32913365
|
G | T | 1 | a0015c0019t0005g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1856+501G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913365 | ||||||
chr20:32913473
|
G | A | 1 | a0030c0063t0004g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1856+609G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913473 | ||||||
chr20:32913479
|
A | G | 48 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(45): Show | 48 | HG00323.hp1 HG01123.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.1856+615A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913479 | ||||||
chr20:32913573
|
C | G | 3 | a0001c0001t0004g0048a0003c0003t0001g0123a0005c0008t0004g0205 | 3 | NA18968.hp1 NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1856+709C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913573 | ||||||
chr20:32913678
|
AAATGCCC others(27): Show |
A | 34 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(31): Show | 34 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1856+816_1856+849d others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32913678 | |||||
chr20:32913998
|
G | T | 1 | a0004c0004t0003g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1856+1134G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32913998 | ||||||
chr20:32914255
|
T | C | 2 | a0008c0007t0006g0013a0008c0007t0006g0044 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1856+1391T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914255 | ||||||
chr20:32914336
|
G | A | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1856+1472G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914336 | ||||||
chr20:32914526
|
A | C | 74 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(71): Show | 74 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1856+1662A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914526 | ||||||
chr20:32914553
|
G | C | 166 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(163): Show | 166 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1856+1689G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914553 | ||||||
chr20:32914591
|
A | C | 1 | a0044c0044t0002g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1856+1727A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914591 | ||||||
chr20:32914601
|
G | A | 6 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1856+1737G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914601 | ||||||
chr20:32914751
|
A | C | 163 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.1856+1887A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32914751 | ||||||
chr20:32914900
|
A | AT | 34 | a0002c0002t0003g0275a0002c0002t0003g0276a0002c0011t0001g0100others(31): Show | 34 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1856+2046dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32914900 | |||||
chr20:32914900
|
A | ATT | 14 | a0010c0009t0001g0248a0010c0009t0004g0120a0010c0009t0004g0122others(11): Show | 14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1856+2045_1856+204 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32914900 | |||||
chr20:32915076
|
A | T | 157 | a0001c0001t0001g0115a0001c0001t0001g0168a0002c0002t0001g0093others(154): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1856+2212A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915076 | ||||||
chr20:32915077
|
T | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0163a0001c0001t0009g0114 | 3 | HG01070.hp2 NA18951.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1856+2213T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915077 | ||||||
chr20:32915158
|
C | T | 2 | a0001c0001t0001g0159a0005c0008t0001g0214 | 2 | NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1857-2143C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915158 | ||||||
chr20:32915193
|
C | T | 1 | a0008c0007t0003g0280 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1857-2108C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915193 | ||||||
chr20:32915307
|
T | C | 12 | a0002c0002t0003g0275a0002c0002t0003g0276a0002c0011t0001g0100others(9): Show | 12 | HG01167.hp1 HG01169.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1857-1994T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915307 | ||||||
chr20:32915559
|
C | T | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-1742C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915559 | ||||||
chr20:32915569
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1857-1732C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915569 | ||||||
chr20:32915637
|
C | T | 75 | a0002c0002t0001g0119a0002c0002t0001g0190a0002c0002t0002g0003others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1857-1664C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915637 | ||||||
chr20:32915672
|
C | CT | 23 | a0001c0001t0001g0160a0001c0001t0002g0052a0006c0005t0003g0064others(20): Show | 23 | HG00423.hp1 HG00423.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.1857-1612dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32915672 | |||||
chr20:32915672
|
CT | C | 17 | a0001c0001t0001g0104a0001c0001t0001g0166a0001c0001t0001g0212others(14): Show | 17 | HG00741.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1857-1612delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | INFO_REALIGN_3_PRIME | chr20 | 32915672 | |||||
chr20:32915676
|
T | C | 4 | a0001c0001t0001g0144a0001c0001t0001g0155a0001c0001t0001g0175others(1): Show | 4 | HG00323.hp2 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857-1625T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915676 | ||||||
chr20:32915760
|
G | A | 3 | a0022c0031t0002g0196a0022c0031t0002g0230a0025c0025t0001g0193 | 3 | HG01167.hp2 HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1857-1541G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915760 | ||||||
chr20:32915765
|
G | A | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-1536G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915765 | ||||||
chr20:32915879
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1857-1422G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915879 | ||||||
chr20:32915917
|
C | T | 4 | a0004c0004t0003g0253a0008c0007t0006g0013a0008c0007t0006g0016others(1): Show | 4 | HG00733.hp1 HG01168.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857-1384C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915917 | ||||||
chr20:32915965
|
C | T | 3 | a0002c0002t0001g0093a0002c0002t0004g0101a0002c0002t0004g0102 | 3 | HG02630.hp1 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1857-1336C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915965 | ||||||
chr20:32915999
|
C | T | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-1302C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32915999 | ||||||
chr20:32916490
|
C | T | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1857-811C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32916490 | ||||||
chr20:32916661
|
G | A | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1857-640G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32916661 | ||||||
chr20:32917013
|
C | G | 1 | a0002c0002t0002g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1857-288C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917013 | ||||||
chr20:32917014
|
C | G | 1 | a0003c0003t0001g0210 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1857-287C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917014 | ||||||
chr20:32917032
|
T | G | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1857-269T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917032 | ||||||
chr20:32917206
|
C | T | 41 | a0002c0002t0001g0119a0002c0002t0001g0190a0002c0002t0002g0003others(38): Show | 41 | HG01099.hp2 HG01258.hp1 HG01515.hp1 others(38): Show |
intron_variant | MODIFIER | c.1857-95C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917206 | ||||||
chr20:32917226
|
G | A | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1857-75G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 17/26 | chr20 | 32917226 | ||||||
chr20:32917548
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2061+43C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917548 | ||||||
chr20:32917718
|
C | T | 1 | a0004c0004t0001g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2061+213C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917718 | ||||||
chr20:32917942
|
G | A | 3 | a0001c0001t0001g0159a0005c0008t0001g0214a0018c0026t0001g0283 | 3 | HG01109.hp2 NA18944.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2062-420G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917942 | ||||||
chr20:32917969
|
C | G | 1 | a0001c0001t0001g0154 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2062-393C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32917969 | ||||||
chr20:32918234
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2062-128G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32918234 | ||||||
chr20:32918309
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2062-53A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 18/26 | chr20 | 32918309 | ||||||
chr20:32918623
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2274+49G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918623 | ||||||
chr20:32918626
|
G | A | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2274+52G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918626 | ||||||
chr20:32918858
|
C | G | 1 | a0006c0005t0003g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2274+284C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918858 | ||||||
chr20:32918883
|
A | G | 1 | a0002c0046t0003g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2274+309A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918883 | ||||||
chr20:32918916
|
G | T | 1 | a0002c0002t0001g0119 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2274+342G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32918916 | ||||||
chr20:32919056
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0052t0001g0185 | 3 | HG01071.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2274+482C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919056 | ||||||
chr20:32919087
|
G | A | 23 | a0002c0042t0001g0198a0010c0009t0001g0248a0010c0009t0004g0120others(20): Show | 23 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.2274+513G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919087 | ||||||
chr20:32919091
|
A | C | 4 | a0024c0024t0005g0041a0024c0024t0005g0111a0030c0063t0004g0081others(1): Show | 4 | HG01243.hp1 HG01346.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.2274+517A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919091 | ||||||
chr20:32919125
|
C | T | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2274+551C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919125 | ||||||
chr20:32919341
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-737A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919341 | ||||||
chr20:32919468
|
G | A | 1 | a0021c0061t0001g0238 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2275-610G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919468 | ||||||
chr20:32919566
|
C | T | 10 | a0010c0009t0004g0120a0010c0009t0004g0122a0010c0009t0004g0250others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2275-512C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919566 | ||||||
chr20:32919640
|
G | A | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-438G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919640 | ||||||
chr20:32919669
|
T | C | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2275-409T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919669 | ||||||
chr20:32919824
|
G | T | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-254G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919824 | ||||||
chr20:32919956
|
C | G | 164 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(161): Show | 164 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.2275-122C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919956 | ||||||
chr20:32919979
|
T | C | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-99T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32919979 | ||||||
chr20:32920025
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2275-53A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 19/26 | chr20 | 32920025 | ||||||
chr20:32920346
|
T | G | 19 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2412+131T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920346 | ||||||
chr20:32920403
|
G | T | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+188G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920403 | ||||||
chr20:32920419
|
G | A | 1 | a0002c0002t0002g0028 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2412+204G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920419 | ||||||
chr20:32920483
|
T | C | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+268T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920483 | ||||||
chr20:32920526
|
G | A | 1 | a0015c0019t0005g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2412+311G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920526 | ||||||
chr20:32920563
|
A | G | 1 | a0005c0008t0001g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2412+348A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920563 | ||||||
chr20:32920580
|
CGGAAACC others(3): Show |
C | 2 | a0001c0001t0001g0116a0001c0001t0001g0151 | 2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.2412+367_2412+376d others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32920580 | |||||
chr20:32920605
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+390A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920605 | ||||||
chr20:32920648
|
G | A | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+433G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920648 | ||||||
chr20:32920720
|
A | G | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2412+505A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920720 | ||||||
chr20:32920747
|
C | G | 2 | a0008c0007t0006g0013a0008c0007t0006g0044 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2412+532C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32920747 | ||||||
chr20:32921009
|
A | C | 19 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.2412+794A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921009 | ||||||
chr20:32921153
|
G | A | 1 | a0011c0010t0006g0030 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2412+938G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921153 | ||||||
chr20:32921196
|
CTCT | C | 14 | a0010c0009t0001g0248a0010c0009t0004g0120a0010c0009t0004g0122others(11): Show | 14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2412+982_2412+984d others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921196 | ||||||
chr20:32921201
|
C | CT | 262 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2412+995dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921201 | |||||
chr20:32921201
|
C | CTT | 6 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(3): Show | 6 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2412+994_2412+995d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921201 | |||||
chr20:32921201
|
C | T | 14 | a0010c0009t0001g0248a0010c0009t0004g0120a0010c0009t0004g0122others(11): Show | 14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2412+986C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921201 | ||||||
chr20:32921222
|
G | A | 14 | a0010c0009t0001g0248a0010c0009t0004g0120a0010c0009t0004g0122others(11): Show | 14 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2412+1007G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921222 | ||||||
chr20:32921230
|
G | A | 1 | a0041c0050t0002g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2412+1015G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921230 | ||||||
chr20:32921267
|
C | T | 42 | a0002c0002t0001g0093a0002c0002t0001g0128a0002c0002t0001g0129others(39): Show | 42 | HG00323.hp1 HG00741.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.2412+1052C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921267 | ||||||
chr20:32921295
|
G | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2412+1080G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921295 | ||||||
chr20:32921329
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2412+1114G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921329 | ||||||
chr20:32921342
|
T | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2412+1127T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921342 | ||||||
chr20:32921361
|
T | TTG | 39 | a0001c0001t0004g0048a0002c0002t0001g0128a0002c0002t0001g0129others(36): Show | 39 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.2412+1176_2412+117 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
T | TTGTG | 28 | a0002c0002t0003g0262a0002c0002t0003g0263a0002c0002t0003g0265others(25): Show | 28 | HG00733.hp1 HG00741.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+1174_2412+117 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
T | TTGTGTG | 26 | a0002c0002t0003g0275a0002c0002t0003g0276a0003c0003t0001g0130others(23): Show | 26 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.2412+1172_2412+117 others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
T | TTGTGTGT others(1): Show |
26 | a0004c0004t0001g0089a0004c0004t0003g0085a0004c0004t0003g0086others(23): Show | 26 | HG00280.hp1 HG00639.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2412+1170_2412+117 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
T | TTGTGTGT others(3): Show |
4 | a0004c0004t0003g0069a0008c0007t0003g0280a0008c0007t0003g0281others(1): Show | 4 | HG01516.hp1 HG01975.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.2412+1168_2412+117 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
T | TTGTGTGT others(5): Show |
5 | a0004c0004t0003g0058a0006c0005t0003g0076a0006c0005t0003g0078others(2): Show | 5 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2412+1166_2412+117 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
TTG | T | 5 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(2): Show | 5 | HG01433.hp1 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.2412+1176_2412+117 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921361
|
TTGTGTGT others(1): Show |
T | 40 | a0002c0002t0001g0119a0002c0002t0001g0190a0002c0002t0002g0003others(37): Show | 40 | HG01099.hp2 HG01258.hp1 HG01515.hp1 others(37): Show |
intron_variant | MODIFIER | c.2412+1170_2412+117 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921361 | |||||
chr20:32921391
|
G | T | 1 | a0003c0003t0002g0136 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2412+1176G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921391 | ||||||
chr20:32921393
|
T | G | 53 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0221others(50): Show | 53 | HG00323.hp1 HG00741.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.2412+1178T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921393 | ||||||
chr20:32921394
|
T | G | 1 | a0002c0002t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2412+1179T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921394 | ||||||
chr20:32921416
|
A | G | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+1201A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921416 | ||||||
chr20:32921431
|
G | T | 161 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(158): Show | 161 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.2412+1216G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921431 | ||||||
chr20:32921573
|
T | G | 3 | a0002c0002t0001g0221a0002c0002t0001g0234a0002c0002t0001g0235 | 3 | HG02451.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2412+1358T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921573 | ||||||
chr20:32921574
|
A | G | 1 | a0008c0007t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2412+1359A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921574 | ||||||
chr20:32921700
|
C | CTT | 163 | a0002c0002t0001g0093a0002c0002t0001g0119a0002c0002t0001g0128others(160): Show | 163 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.2412+1496_2412+149 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921700 | |||||
chr20:32921828
|
A | G | 1 | a0010c0009t0004g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2412+1613A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921828 | ||||||
chr20:32921831
|
C | CT | 129 | a0002c0002t0001g0119a0002c0002t0001g0128a0002c0002t0001g0129others(126): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.2412+1633dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921831 | |||||
chr20:32921831
|
CT | C | 7 | a0001c0001t0001g0118a0001c0001t0001g0140a0001c0001t0001g0212others(4): Show | 7 | HG01167.hp2 HG01261.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.2412+1633delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32921831 | |||||
chr20:32921832
|
T | C | 1 | a0044c0044t0002g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2412+1617T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921832 | ||||||
chr20:32921836
|
T | C | 1 | a0027c0029t0003g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2412+1621T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921836 | ||||||
chr20:32921853
|
C | T | 1 | a0021c0062t0001g0072 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2412+1638C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921853 | ||||||
chr20:32921882
|
G | A | 6 | a0005c0037t0004g0183a0011c0010t0003g0141a0011c0010t0006g0009others(3): Show | 6 | HG01261.hp1 HG01943.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.2412+1667G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921882 | ||||||
chr20:32921894
|
G | A | 1 | a0005c0033t0008g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2412+1679G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921894 | ||||||
chr20:32921983
|
C | A | 1 | a0013c0020t0003g0080 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2412+1768C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32921983 | ||||||
chr20:32922310
|
G | A | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+2095G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32922310 | ||||||
chr20:32922393
|
T | C | 2 | a0029c0059t0003g0071a0037c0057t0004g0249 | 2 | HG01975.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2412+2178T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32922393 | ||||||
chr20:32922444
|
C | T | 142 | a0001c0001t0001g0243a0002c0002t0001g0128a0002c0002t0001g0129others(139): Show | 142 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.2412+2229C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32922444 | ||||||
chr20:32922813
|
T | TTC | 26 | a0002c0002t0001g0225a0002c0002t0001g0261a0006c0005t0003g0064others(23): Show | 26 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2412+2612_2412+261 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32922813 | |||||
chr20:32923029
|
A | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+2814A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923029 | ||||||
chr20:32923150
|
C | T | 1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2412+2935C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923150 | ||||||
chr20:32923166
|
A | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+2951A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923166 | ||||||
chr20:32923303
|
C | T | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2412+3088C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923303 | ||||||
chr20:32923314
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2412+3099C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923314 | ||||||
chr20:32923763
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0242 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2412+3548G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923763 | ||||||
chr20:32923772
|
G | A | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2412+3557G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923772 | ||||||
chr20:32923896
|
A | C | 78 | a0002c0002t0001g0190a0002c0002t0002g0003a0002c0002t0002g0004others(75): Show | 78 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.2412+3681A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923896 | ||||||
chr20:32923974
|
C | G | 28 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(25): Show | 28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+3759C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32923974 | ||||||
chr20:32924106
|
T | C | 1 | a0008c0007t0006g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2412+3891T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924106 | ||||||
chr20:32924129
|
T | C | 34 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0128others(31): Show | 34 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(31): Show |
intron_variant | MODIFIER | c.2412+3914T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924129 | ||||||
chr20:32924366
|
A | C | 1 | a0027c0029t0003g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2412+4151A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924366 | ||||||
chr20:32924457
|
C | G | 28 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(25): Show | 28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+4242C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924457 | ||||||
chr20:32924479
|
G | A | 28 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(25): Show | 28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+4264G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924479 | ||||||
chr20:32924632
|
A | G | 28 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(25): Show | 28 | HG00323.hp1 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.2412+4417A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924632 | ||||||
chr20:32924698
|
C | T | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2412+4483C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924698 | ||||||
chr20:32924821
|
G | A | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2412+4606G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924821 | ||||||
chr20:32924923
|
T | G | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2412+4708T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32924923 | ||||||
chr20:32925572
|
C | T | 1 | a0002c0002t0002g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2413-4826C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925572 | ||||||
chr20:32925719
|
C | T | 1 | a0020c0032t0004g0277 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2413-4679C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925719 | ||||||
chr20:32925779
|
C | T | 82 | a0001c0001t0005g0220a0001c0001t0005g0255a0001c0001t0005g0256others(79): Show | 82 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.2413-4619C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925779 | ||||||
chr20:32925960
|
G | T | 1 | a0006c0005t0003g0237 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2413-4438G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32925960 | ||||||
chr20:32926045
|
C | T | 1 | a0002c0002t0002g0056 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2413-4353C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926045 | ||||||
chr20:32926073
|
C | T | 7 | a0001c0001t0005g0255a0001c0001t0005g0256a0001c0056t0001g0121others(4): Show | 7 | HG01891.hp2 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2413-4325C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926073 | ||||||
chr20:32926098
|
C | T | 72 | a0002c0002t0001g0190a0002c0002t0002g0003a0002c0002t0002g0004others(69): Show | 72 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.2413-4300C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926098 | ||||||
chr20:32926218
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2413-4180T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926218 | ||||||
chr20:32926236
|
T | G | 1 | a0009c0015t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2413-4162T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926236 | ||||||
chr20:32926446
|
T | C | 1 | a0033c0065t0001g0060 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2413-3952T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926446 | ||||||
chr20:32926489
|
A | C | 9 | a0005c0033t0008g0113a0017c0017t0007g0217a0017c0017t0007g0227others(6): Show | 9 | HG01261.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2413-3909A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926489 | ||||||
chr20:32926520
|
T | TA | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2413-3878_2413-387 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926520 | ||||||
chr20:32926520
|
T | TTA | 53 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0225others(50): Show | 53 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.2413-3877_2413-387 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32926520 | |||||
chr20:32926599
|
C | T | 15 | a0001c0001t0005g0255a0001c0001t0005g0256a0010c0009t0001g0248others(12): Show | 15 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2413-3799C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926599 | ||||||
chr20:32926654
|
TC | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-3738delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32926654 | |||||
chr20:32926660
|
C | G | 1 | a0002c0002t0002g0051 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2413-3738C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926660 | ||||||
chr20:32926666
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG01943.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413-3732C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926666 | ||||||
chr20:32926756
|
C | T | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-3642C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926756 | ||||||
chr20:32926758
|
G | A | 1 | a0002c0002t0002g0006 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2413-3640G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926758 | ||||||
chr20:32926907
|
T | C | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-3491T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926907 | ||||||
chr20:32926915
|
G | C | 7 | a0002c0002t0003g0223a0002c0002t0003g0262a0002c0002t0003g0263others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2413-3483G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926915 | ||||||
chr20:32926960
|
G | A | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-3438G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32926960 | ||||||
chr20:32927405
|
C | T | 3 | a0010c0009t0001g0248a0015c0019t0005g0231a0015c0019t0005g0232 | 3 | HG00741.hp1 HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2413-2993C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927405 | ||||||
chr20:32927489
|
T | C | 5 | a0005c0033t0008g0113a0017c0017t0007g0217a0017c0017t0007g0227others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2413-2909T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927489 | ||||||
chr20:32927591
|
C | T | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2413-2807C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927591 | ||||||
chr20:32927805
|
T | G | 1 | a0020c0032t0004g0062 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2413-2593T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32927805 | ||||||
chr20:32928240
|
A | AT | 31 | a0001c0001t0001g0208a0001c0001t0005g0220a0002c0002t0001g0093others(28): Show | 31 | HG00323.hp1 HG01123.hp2 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.2413-2145dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32928240 | |||||
chr20:32928246
|
T | A | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2413-2152T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928246 | ||||||
chr20:32928246
|
T | TA | 38 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0225others(35): Show | 38 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2413-2152_2413-215 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928246 | ||||||
chr20:32928298
|
C | T | 28 | a0004c0004t0003g0058a0004c0004t0003g0059a0004c0004t0003g0066others(25): Show | 28 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.2413-2100C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928298 | ||||||
chr20:32928396
|
T | C | 1 | a0026c0027t0003g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2413-2002T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928396 | ||||||
chr20:32928404
|
A | G | 46 | a0001c0001t0005g0255a0001c0001t0005g0256a0002c0002t0001g0225others(43): Show | 46 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.2413-1994A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928404 | ||||||
chr20:32928514
|
C | G | 29 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(26): Show | 29 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.2413-1884C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928514 | ||||||
chr20:32928540
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0167 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2413-1858G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928540 | ||||||
chr20:32928596
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2413-1802G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928596 | ||||||
chr20:32928597
|
C | G | 1 | a0001c0001t0001g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2413-1801C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928597 | ||||||
chr20:32928893
|
AT | A | 23 | a0001c0001t0001g0115a0001c0001t0001g0165a0001c0001t0004g0048others(20): Show | 23 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.2413-1493delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32928893 | |||||
chr20:32928935
|
T | C | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-1463T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928935 | ||||||
chr20:32928940
|
T | C | 38 | a0005c0033t0008g0113a0006c0005t0003g0064a0006c0005t0003g0065others(35): Show | 38 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.2413-1458T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32928940 | ||||||
chr20:32929019
|
A | G | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-1379A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929019 | ||||||
chr20:32929138
|
CT | C | 16 | a0001c0001t0001g0115a0001c0001t0005g0255a0001c0001t0005g0256others(13): Show | 16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2413-1249delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929138 | |||||
chr20:32929143
|
T | G | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-1255T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929143 | ||||||
chr20:32929321
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2413-1077A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929321 | ||||||
chr20:32929379
|
T | A | 2 | a0041c0050t0002g0218a0044c0044t0002g0202 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2413-1019T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929379 | ||||||
chr20:32929445
|
T | A | 1 | a0009c0041t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2413-953T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929445 | ||||||
chr20:32929454
|
T | TCCCTCCC others(3): Show |
8 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(5): Show | 8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413-940_2413-939i others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929454 | |||||
chr20:32929459
|
T | C | 8 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(5): Show | 8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2413-939T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929459 | ||||||
chr20:32929459
|
T | TCCCTCCC others(3): Show |
11 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0004g0101others(8): Show | 11 | HG00323.hp1 HG01123.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2413-922_2413-913d others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929459 | |||||
chr20:32929502
|
G | GT | 31 | a0002c0002t0003g0263a0005c0033t0008g0113a0006c0005t0003g0064others(28): Show | 31 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.2413-881dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | INFO_REALIGN_3_PRIME | chr20 | 32929502 | |||||
chr20:32929589
|
G | A | 1 | a0043c0045t0007g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2413-809G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929589 | ||||||
chr20:32929594
|
G | A | 19 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(16): Show | 19 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2413-804G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929594 | ||||||
chr20:32929768
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2413-630C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929768 | ||||||
chr20:32929786
|
T | G | 1 | a0008c0007t0003g0281 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2413-612T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929786 | ||||||
chr20:32929857
|
C | G | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2413-541C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929857 | ||||||
chr20:32929983
|
A | G | 3 | a0007c0006t0004g0142a0007c0030t0004g0127a0007c0030t0004g0266 | 3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2413-415A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32929983 | ||||||
chr20:32930008
|
C | T | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-390C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930008 | ||||||
chr20:32930035
|
C | T | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2413-363C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930035 | ||||||
chr20:32930143
|
C | T | 4 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0025others(1): Show | 4 | NA18946.hp2 NA18950.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.2413-255C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930143 | ||||||
chr20:32930154
|
G | T | 17 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(14): Show | 17 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2413-244G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930154 | ||||||
chr20:32930189
|
C | T | 1 | a0002c0002t0002g0003 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2413-209C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 20/26 | chr20 | 32930189 | ||||||
chr20:32930746
|
C | G | 167 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(164): Show | 167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2631+130C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930746 | ||||||
chr20:32930747
|
G | A | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2631+131G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930747 | ||||||
chr20:32930787
|
C | T | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2631+171C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930787 | ||||||
chr20:32930951
|
T | G | 30 | a0005c0033t0008g0113a0006c0005t0003g0064a0006c0005t0003g0065others(27): Show | 30 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.2632-227T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930951 | ||||||
chr20:32930978
|
C | T | 1 | a0008c0007t0006g0016 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2632-200C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 21/26 | chr20 | 32930978 | ||||||
chr20:32931484
|
C | T | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+148C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931484 | ||||||
chr20:32931633
|
T | C | 1 | a0040c0049t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2790+297T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931633 | ||||||
chr20:32931673
|
G | T | 13 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(10): Show | 13 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2790+337G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931673 | ||||||
chr20:32931761
|
AAAGAAAA others(6): Show |
A | 32 | a0004c0004t0003g0058a0004c0004t0003g0059a0004c0004t0003g0066others(29): Show | 32 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2790+427_2790+439d others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32931761 | |||||
chr20:32931972
|
T | C | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+636T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32931972 | ||||||
chr20:32932337
|
G | A | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2790+1001G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932337 | ||||||
chr20:32932376
|
C | CA | 171 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0001g0211others(168): Show | 171 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.2790+1051dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32932376 | |||||
chr20:32932481
|
C | T | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+1145C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932481 | ||||||
chr20:32932665
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2790+1329A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932665 | ||||||
chr20:32932914
|
A | G | 49 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(46): Show | 49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2790+1578A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32932914 | ||||||
chr20:32933057
|
T | C | 174 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0001g0211others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.2790+1721T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933057 | ||||||
chr20:32933071
|
TC | T | 5 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2790+1736delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933071 | ||||||
chr20:32933177
|
T | C | 1 | a0002c0002t0002g0054 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2790+1841T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933177 | ||||||
chr20:32933197
|
A | G | 2 | a0002c0002t0002g0006a0002c0002t0002g0017 | 2 | HG04204.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2790+1861A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933197 | ||||||
chr20:32933379
|
C | T | 173 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0001g0211others(170): Show | 173 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(170): Show |
intron_variant | MODIFIER | c.2790+2043C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933379 | ||||||
chr20:32933453
|
C | G | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2790+2117C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933453 | ||||||
chr20:32933587
|
A | AC | 13 | a0001c0001t0001g0106a0001c0001t0001g0155a0001c0001t0001g0167others(10): Show | 13 | HG01109.hp2 HG01175.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.2790+2255dupC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32933587 | |||||
chr20:32933608
|
C | T | 1 | a0004c0004t0003g0084 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2790+2272C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933608 | ||||||
chr20:32933633
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2790+2297C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933633 | ||||||
chr20:32933645
|
G | A | 5 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2790+2309G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933645 | ||||||
chr20:32933703
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2790+2367G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933703 | ||||||
chr20:32933750
|
G | T | 2 | a0020c0032t0004g0062a0020c0032t0004g0277 | 2 | HG01891.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2790+2414G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933750 | ||||||
chr20:32933849
|
G | A | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+2513G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933849 | ||||||
chr20:32933971
|
C | T | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+2635C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32933971 | ||||||
chr20:32934013
|
C | CT | 149 | a0001c0001t0001g0115a0001c0001t0001g0155a0001c0001t0001g0206others(146): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2790+2692dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934013 | |||||
chr20:32934013
|
C | CTT | 27 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(24): Show | 27 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.2790+2691_2790+269 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934013 | |||||
chr20:32934279
|
A | AT | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+2951dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934279 | |||||
chr20:32934287
|
T | TC | 40 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(37): Show | 40 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.2790+2952dupC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32934287 | |||||
chr20:32934298
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2790+2962G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934298 | ||||||
chr20:32934454
|
T | C | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2790+3118T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934454 | ||||||
chr20:32934547
|
G | A | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+3211G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934547 | ||||||
chr20:32934617
|
A | G | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2790+3281A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934617 | ||||||
chr20:32934642
|
G | A | 2 | a0002c0002t0001g0128a0002c0002t0001g0129 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2790+3306G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934642 | ||||||
chr20:32934656
|
G | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG01346.hp2 HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2790+3320G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934656 | ||||||
chr20:32934771
|
C | T | 24 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(21): Show | 24 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.2790+3435C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934771 | ||||||
chr20:32934945
|
T | C | 1 | a0015c0019t0005g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2790+3609T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934945 | ||||||
chr20:32934965
|
T | C | 31 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2790+3629T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32934965 | ||||||
chr20:32935098
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2790+3762C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935098 | ||||||
chr20:32935116
|
G | A | 28 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(25): Show | 28 | HG00323.hp1 HG01123.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.2790+3780G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935116 | ||||||
chr20:32935172
|
TTTTC | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+3856_2790+385 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935172 | |||||
chr20:32935185
|
T | TTTC | 6 | a0004c0004t0003g0058a0004c0004t0003g0069a0004c0004t0003g0085others(3): Show | 6 | HG00733.hp1 HG01123.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.2790+3852_2790+385 others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935185 | |||||
chr20:32935188
|
C | CT | 4 | a0002c0002t0002g0003a0002c0002t0002g0004a0002c0002t0002g0038others(1): Show | 4 | HG01515.hp1 NA18946.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.2790+3855dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTT | 24 | a0001c0001t0001g0115a0002c0002t0001g0190a0002c0002t0002g0006others(21): Show | 24 | HG01099.hp2 HG01169.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.2790+3854_2790+385 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTCT | 4 | a0004c0004t0003g0077a0004c0004t0003g0189a0027c0029t0003g0239others(1): Show | 4 | HG00280.hp2 HG00642.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2790+3854_2790+385 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTT | 19 | a0002c0002t0002g0025a0002c0002t0002g0033a0002c0002t0002g0039others(16): Show | 19 | HG01167.hp1 HG01168.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+3853_2790+385 others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTT | 12 | a0004c0004t0003g0084a0004c0004t0003g0086a0008c0007t0003g0194others(9): Show | 12 | HG00741.hp2 HG01261.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTT | 7 | a0002c0002t0003g0275a0002c0002t0003g0276a0004c0004t0001g0089others(4): Show | 7 | HG00280.hp1 HG01496.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(9): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(3): Show |
1 | a0017c0017t0007g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(4): Show |
3 | a0017c0017t0007g0217a0017c0017t0007g0228a0043c0045t0007g0133 | 3 | HG02145.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(5): Show |
1 | a0005c0033t0008g0113 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(6): Show |
2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(9): Show |
3 | a0002c0002t0003g0262a0002c0002t0003g0263a0048c0058t0002g0257 | 3 | HG01261.hp2 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(10): Show |
2 | a0002c0002t0003g0223a0002c0002t0003g0265 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2790+3855_2790+385 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0206 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(22): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0211 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(23): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
C | CTTTTTTT others(17): Show |
1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2790+3855_2790+385 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
CTTTCTTT | C | 19 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(16): Show | 19 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.2790+3856_2790+386 others(11): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
CTTTCTTT others(2): Show |
C | 7 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0246others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2790+3856_2790+386 others(13): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935188
|
CTTTCTTT others(3): Show |
C | 1 | a0002c0011t0001g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2790+3856_2790+386 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935188 | |||||
chr20:32935192
|
C | CT | 20 | a0001c0001t0001g0124a0001c0001t0001g0131a0001c0001t0001g0146others(17): Show | 20 | HG00099.hp2 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.2790+3881dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTT | 12 | a0006c0005t0003g0065a0006c0005t0003g0067a0006c0005t0003g0076others(9): Show | 12 | HG00639.hp2 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.2790+3878_2790+388 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTT | 6 | a0006c0005t0003g0064a0006c0005t0003g0074a0006c0005t0003g0075others(3): Show | 6 | HG01175.hp1 HG02148.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.2790+3877_2790+388 others(9): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(3): Show |
1 | a0002c0002t0001g0261 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2790+3872_2790+388 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0005g0256 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2790+3871_2790+388 others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0005g0255a0010c0009t0004g0250 | 2 | HG02630.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2790+3870_2790+388 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(6): Show |
1 | a0023c0028t0005g0258 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2790+3869_2790+388 others(17): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(8): Show |
1 | a0015c0019t0005g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2790+3867_2790+388 others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(9): Show |
2 | a0010c0009t0001g0248a0020c0032t0004g0062 | 2 | HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2790+3866_2790+388 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(10): Show |
4 | a0010c0009t0004g0120a0020c0032t0004g0277a0050c0068t0004g0216others(1): Show | 4 | HG01891.hp2 HG02922.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2790+3865_2790+388 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(11): Show |
1 | a0015c0019t0005g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2790+3864_2790+388 others(22): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(12): Show |
1 | a0010c0009t0005g0007 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2790+3863_2790+388 others(23): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | CTTTTTTT others(15): Show |
1 | a0015c0019t0005g0231 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2790+3860_2790+388 others(26): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935192
|
C | T | 96 | a0001c0001t0001g0115a0001c0001t0001g0206a0001c0001t0001g0211others(93): Show | 96 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.2790+3856C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935192 | ||||||
chr20:32935192
|
CT | C | 11 | a0001c0001t0001g0105a0001c0001t0001g0144a0001c0001t0001g0151others(8): Show | 11 | HG00323.hp2 HG00639.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.2790+3881delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32935192 | |||||
chr20:32935288
|
C | T | 1 | a0041c0050t0002g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2790+3952C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935288 | ||||||
chr20:32935314
|
C | A | 1 | a0008c0007t0003g0281 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2790+3978C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935314 | ||||||
chr20:32935327
|
A | T | 2 | a0002c0002t0002g0045a0002c0002t0002g0047 | 2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2790+3991A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935327 | ||||||
chr20:32935388
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2790+4052C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935388 | ||||||
chr20:32935446
|
C | T | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2790+4110C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935446 | ||||||
chr20:32935491
|
C | T | 1 | a0003c0003t0002g0005 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2790+4155C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935491 | ||||||
chr20:32935656
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2790+4320G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935656 | ||||||
chr20:32935742
|
G | A | 37 | a0001c0001t0001g0115a0002c0002t0001g0190a0002c0002t0002g0003others(34): Show | 37 | HG01099.hp2 HG01258.hp1 HG01515.hp1 others(34): Show |
intron_variant | MODIFIER | c.2790+4406G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935742 | ||||||
chr20:32935922
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+4586C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32935922 | ||||||
chr20:32936014
|
A | ATTTATT | 3 | a0002c0002t0001g0221a0002c0002t0001g0234a0002c0002t0001g0235 | 3 | HG02451.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2790+4700_2790+470 others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32936014 | |||||
chr20:32936020
|
T | A | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2790+4684T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936020 | ||||||
chr20:32936032
|
T | G | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2790+4696T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936032 | ||||||
chr20:32936192
|
C | T | 17 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(14): Show | 17 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.2790+4856C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936192 | ||||||
chr20:32936278
|
C | A | 8 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(5): Show | 8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2790+4942C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936278 | ||||||
chr20:32936625
|
G | A | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2790+5289G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32936625 | ||||||
chr20:32937152
|
G | C | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2790+5816G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937152 | ||||||
chr20:32937163
|
A | G | 1 | a0007c0006t0001g0236 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2790+5827A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937163 | ||||||
chr20:32937168
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2790+5832C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937168 | ||||||
chr20:32937223
|
G | T | 1 | a0030c0063t0004g0081 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2790+5887G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937223 | ||||||
chr20:32937344
|
C | A | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2790+6008C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937344 | ||||||
chr20:32937345
|
A | T | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2790+6009A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937345 | ||||||
chr20:32937624
|
CT | C | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-6003delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32937624 | |||||
chr20:32937640
|
A | G | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-5996A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937640 | ||||||
chr20:32937670
|
G | A | 1 | a0001c0001t0002g0027 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2791-5966G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937670 | ||||||
chr20:32937680
|
GTGATCTT others(3880): Show |
G | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-5955_2791-206 others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937680 | ||||||
chr20:32937762
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2791-5874G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937762 | ||||||
chr20:32937793
|
A | G | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2791-5843A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937793 | ||||||
chr20:32937979
|
C | T | 2 | a0022c0031t0002g0196a0022c0031t0002g0230 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2791-5657C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32937979 | ||||||
chr20:32938204
|
C | A | 1 | a0014c0014t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2791-5432C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938204 | ||||||
chr20:32938433
|
A | T | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-5203A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938433 | ||||||
chr20:32938511
|
A | G | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2791-5125A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938511 | ||||||
chr20:32938526
|
A | G | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2791-5110A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938526 | ||||||
chr20:32938753
|
A | G | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2791-4883A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32938753 | ||||||
chr20:32938983
|
CCCTT | C | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2791-4638_2791-463 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32938983 | |||||
chr20:32939014
|
TTCCC | T | 21 | a0001c0001t0001g0243a0001c0001t0005g0220a0002c0002t0001g0093others(18): Show | 21 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.2791-4606_2791-460 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939014 | |||||
chr20:32939051
|
C | CTCTT | 3 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0264 | 3 | HG02965.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2791-4573_2791-457 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939051 | |||||
chr20:32939051
|
CTCTT | C | 20 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(17): Show | 20 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.2791-4573_2791-457 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939051 | |||||
chr20:32939104
|
CCTTTCTT others(27): Show |
C | 1 | a0014c0014t0002g0040 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2791-4521_2791-448 others(38): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939104 | |||||
chr20:32939104
|
CCTTTCTT others(31): Show |
C | 1 | a0014c0014t0002g0014 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2791-4521_2791-448 others(42): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939104 | |||||
chr20:32939115
|
CTCTTTCT others(19): Show |
C | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2791-4509_2791-448 others(30): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939115 | |||||
chr20:32939116
|
T | C | 1 | a0003c0003t0001g0210 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2791-4520T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939116 | ||||||
chr20:32939119
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2791-4517T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939119 | ||||||
chr20:32939123
|
TTCTCTTT others(17): Show |
T | 1 | a0017c0017t0007g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2791-4511_2791-448 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939123 | |||||
chr20:32939125
|
C | CCCTT | 3 | a0002c0002t0002g0004a0002c0002t0002g0047a0027c0029t0003g0239 | 3 | HG03688.hp1 HG03688.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.2791-4511_2791-451 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
C | CCCTTTCT others(1): Show |
7 | a0002c0002t0002g0022a0002c0002t0002g0028a0002c0022t0002g0015others(4): Show | 7 | HG00741.hp2 HG01255.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791-4511_2791-451 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
C | CCCTTTCT others(5): Show |
1 | a0004c0004t0003g0059 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
C | CCCTTTCT others(9): Show |
1 | a0004c0004t0003g0068 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
C | CCCTTTCT others(13): Show |
1 | a0029c0059t0003g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
C | CCCTTTCT others(25): Show |
1 | a0004c0004t0003g0073 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2791-4511_2791-451 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
C | CTCTT | 14 | a0001c0001t0001g0157a0001c0001t0001g0165a0001c0001t0001g0168others(11): Show | 14 | HG00642.hp2 HG01071.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2791-4436_2791-443 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
C | CTCTTTCT others(1): Show |
8 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0001g0158others(5): Show | 8 | HG00423.hp1 HG00621.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-4440_2791-443 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
C | CTCTTTCT others(5): Show |
3 | a0001c0001t0001g0144a0003c0003t0001g0210a0003c0003t0002g0136 | 3 | HG00323.hp2 HG02071.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2791-4444_2791-443 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
C | CTCTTTCT others(9): Show |
2 | a0001c0001t0001g0061a0003c0003t0001g0173 | 2 | HG04204.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2791-4448_2791-443 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
C | CTCTTTCT others(13): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0213 | 2 | HG02071.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2791-4452_2791-443 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
C | CTCTTTCT others(17): Show |
2 | a0001c0001t0001g0154a0003c0003t0001g0145 | 2 | HG00621.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.2791-4456_2791-443 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
C | T | 2 | a0001c0001t0001g0166a0034c0040t0002g0259 | 2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2791-4511C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939125 | ||||||
chr20:32939125
|
CTCTT | C | 28 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0124others(25): Show | 28 | HG00733.hp1 HG01167.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.2791-4436_2791-443 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(1): Show |
C | 22 | a0001c0001t0001g0116a0001c0001t0001g0131a0001c0001t0001g0187others(19): Show | 22 | HG01109.hp1 HG01192.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2791-4440_2791-443 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(5): Show |
C | 29 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0150others(26): Show | 29 | HG00280.hp1 HG01099.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2791-4444_2791-443 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(9): Show |
C | 27 | a0001c0001t0001g0138a0001c0001t0001g0188a0001c0001t0001g0206others(24): Show | 27 | HG00639.hp2 HG01099.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-4448_2791-443 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(13): Show |
C | 19 | a0001c0001t0001g0161a0002c0002t0001g0221a0002c0002t0001g0235others(16): Show | 19 | HG00280.hp2 HG01081.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2791-4452_2791-443 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(17): Show |
C | 22 | a0001c0001t0001g0118a0001c0001t0001g0159a0002c0002t0001g0269others(19): Show | 22 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2791-4456_2791-443 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(21): Show |
C | 6 | a0001c0001t0001g0140a0002c0002t0001g0267a0002c0002t0001g0268others(3): Show | 6 | HG01361.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2791-4460_2791-443 others(32): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(25): Show |
C | 1 | a0001c0001t0005g0220 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2791-4464_2791-443 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(29): Show |
C | 1 | a0025c0025t0002g0019 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2791-4468_2791-443 others(40): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939125
|
CTCTTTCT others(33): Show |
C | 2 | a0005c0035t0001g0095a0025c0025t0001g0193 | 2 | HG01123.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2791-4472_2791-443 others(44): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939125 | |||||
chr20:32939126
|
T | C | 11 | a0002c0002t0002g0023a0002c0002t0002g0025a0002c0002t0002g0053others(8): Show | 11 | HG00642.hp1 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.2791-4510T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939126 | ||||||
chr20:32939127
|
CTTTCTTT others(10): Show |
C | 1 | a0031c0060t0001g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2791-4506_2791-449 others(21): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939127 | |||||
chr20:32939127
|
CTTTCTTT others(22): Show |
C | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2791-4506_2791-447 others(33): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939127 | |||||
chr20:32939130
|
T | C | 9 | a0002c0002t0002g0045a0002c0002t0002g0046a0002c0011t0001g0244others(6): Show | 9 | HG00733.hp1 HG02083.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2791-4506T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939130 | ||||||
chr20:32939134
|
T | C | 13 | a0001c0001t0001g0211a0001c0001t0001g0212a0002c0002t0001g0190others(10): Show | 13 | HG01109.hp1 HG01258.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2791-4502T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939134 | ||||||
chr20:32939138
|
T | C | 13 | a0001c0001t0001g0212a0002c0002t0002g0012a0002c0002t0002g0017others(10): Show | 13 | HG00280.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2791-4498T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939138 | ||||||
chr20:32939142
|
T | C | 15 | a0001c0001t0001g0206a0002c0002t0002g0003a0002c0002t0002g0051others(12): Show | 15 | HG01099.hp2 HG02135.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2791-4494T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939142 | ||||||
chr20:32939146
|
T | C | 7 | a0002c0002t0002g0033a0002c0002t0002g0034a0002c0002t0003g0223others(4): Show | 7 | HG00280.hp2 HG01943.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791-4490T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939146 | ||||||
chr20:32939149
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2791-4487T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939149 | ||||||
chr20:32939150
|
T | C | 4 | a0002c0002t0003g0276a0007c0030t0004g0127a0008c0007t0003g0280others(1): Show | 4 | HG02976.hp2 HG03098.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2791-4486T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939150 | ||||||
chr20:32939152
|
T | TTTCTTTC others(18): Show |
1 | a0002c0002t0002g0025 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2791-4463_2791-446 others(29): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939152 | |||||
chr20:32939154
|
T | C | 1 | a0002c0002t0003g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2791-4482T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939154 | ||||||
chr20:32939179
|
CTTTCTTT others(14): Show |
C | 1 | a0018c0026t0001g0283 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2791-4454_2791-443 others(25): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939179 | |||||
chr20:32939188
|
TTTCTTTC others(8): Show |
T | 2 | a0001c0001t0001g0160a0009c0015t0001g0098 | 2 | HG00423.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2791-4447_2791-443 others(19): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939188 | ||||||
chr20:32939200
|
T | TTTCTTTC others(4): Show |
1 | a0001c0001t0001g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(15): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939200 | |||||
chr20:32939201
|
T | TTCTTTCT others(7): Show |
1 | a0004c0004t0003g0085 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(18): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939201 | |||||
chr20:32939203
|
C | CCT | 9 | a0001c0001t0001g0144a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG00323.hp2 HG00621.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.2791-4410_2791-440 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939203 | |||||
chr20:32939203
|
C | CTTTCTTT others(3): Show |
1 | a0019c0016t0001g0178 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939203 | ||||||
chr20:32939203
|
C | CTTTCTTT others(7): Show |
1 | a0001c0001t0002g0027 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(18): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939203 | ||||||
chr20:32939203
|
C | CTTTCTTT others(16): Show |
1 | a0005c0034t0002g0031 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2791-4433_2791-443 others(27): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939203 | ||||||
chr20:32939203
|
CCTCT | C | 36 | a0002c0002t0001g0190a0002c0002t0002g0003a0002c0002t0002g0004others(33): Show | 36 | HG01099.hp2 HG01258.hp1 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.2791-4412_2791-440 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939203 | |||||
chr20:32939204
|
C | T | 1 | a0002c0022t0002g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2791-4432C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939204 | ||||||
chr20:32939207
|
T | C | 1 | a0002c0002t0002g0053 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2791-4429T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939207 | ||||||
chr20:32939242
|
G | C | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2791-4394G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939242 | ||||||
chr20:32939289
|
G | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0167 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2791-4347G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939289 | ||||||
chr20:32939290
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2791-4346T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939290 | ||||||
chr20:32939484
|
T | C | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2791-4152T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939484 | ||||||
chr20:32939518
|
T | C | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2791-4118T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939518 | ||||||
chr20:32939804
|
C | T | 7 | a0002c0002t0003g0223a0002c0002t0003g0262a0002c0002t0003g0263others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2791-3832C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939804 | ||||||
chr20:32939820
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2791-3816G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939820 | ||||||
chr20:32939928
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2791-3708C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939928 | ||||||
chr20:32939985
|
G | GTGCC | 3 | a0001c0001t0001g0140a0001c0001t0001g0212a0003c0003t0001g0145 | 3 | HG00621.hp1 NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2791-3633_2791-363 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939985 | |||||
chr20:32939999
|
G | C | 1 | a0002c0002t0002g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2791-3637G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32939999 | ||||||
chr20:32939999
|
G | GCCTCCCT others(1): Show |
16 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(13): Show | 16 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2791-3634_2791-363 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | |||||
chr20:32939999
|
G | GCCTCCCT others(5): Show |
3 | a0004c0004t0003g0085a0011c0010t0003g0141a0018c0026t0001g0283 | 3 | HG01109.hp2 HG01123.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2791-3634_2791-363 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | |||||
chr20:32939999
|
G | GCCTCCCT others(9): Show |
1 | a0026c0027t0003g0092 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2791-3634_2791-363 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | |||||
chr20:32939999
|
G | GCCTCCCT others(17): Show |
1 | a0018c0026t0003g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2791-3634_2791-363 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32939999 | |||||
chr20:32940003
|
G | C | 25 | a0002c0002t0002g0017a0004c0004t0003g0085a0006c0005t0003g0064others(22): Show | 25 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2791-3633G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940003 | ||||||
chr20:32940003
|
G | GCCTC | 25 | a0001c0001t0001g0116a0001c0001t0001g0144a0001c0001t0001g0152others(22): Show | 25 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.2791-3613_2791-361 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(1): Show |
20 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0206others(17): Show | 20 | HG01109.hp1 HG01943.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.2791-3617_2791-361 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(5): Show |
8 | a0002c0002t0002g0004a0002c0002t0002g0033a0002c0002t0002g0036others(5): Show | 8 | HG01516.hp1 HG01516.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2791-3621_2791-361 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(9): Show |
15 | a0002c0002t0002g0025a0002c0002t0002g0038a0002c0002t0002g0047others(12): Show | 15 | HG01261.hp1 HG02040.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.2791-3625_2791-361 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(13): Show |
14 | a0002c0002t0001g0190a0004c0004t0003g0066a0004c0004t0003g0073others(11): Show | 14 | HG00733.hp1 HG01099.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.2791-3629_2791-361 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(17): Show |
1 | a0002c0002t0002g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(21): Show |
4 | a0004c0004t0003g0058a0004c0004t0003g0059a0005c0033t0008g0113others(1): Show | 4 | HG00642.hp1 HG01496.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(32): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(25): Show |
6 | a0004c0004t0003g0068a0004c0004t0003g0084a0005c0013t0004g0097others(3): Show | 6 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(29): Show |
1 | a0017c0017t0007g0217 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(40): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940003
|
G | GCCTCCCT others(37): Show |
1 | a0004c0004t0003g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(48): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940003 | |||||
chr20:32940007
|
C | G | 3 | a0001c0001t0001g0186a0001c0001t0001g0203a0001c0001t0001g0209 | 3 | HG03491.hp1 HG03492.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.2791-3629C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940007 | ||||||
chr20:32940023
|
C | CCCTCCCT others(25): Show |
1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(36): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTCCCT others(21): Show |
2 | a0040c0049t0001g0197a0048c0058t0002g0257 | 2 | HG01261.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(32): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTCCCT others(9): Show |
1 | a0002c0046t0003g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2791-3610_2791-360 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTCCCT others(9): Show |
2 | a0001c0001t0002g0137a0031c0060t0001g0079 | 2 | HG00733.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2791-3610_2791-360 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTT | 19 | a0001c0001t0001g0131a0001c0001t0001g0151a0001c0001t0001g0155others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.2791-3556_2791-355 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTTCCT others(1): Show |
12 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0146others(9): Show | 12 | HG00423.hp1 HG01081.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.2791-3560_2791-355 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTTCCT others(5): Show |
3 | a0001c0001t0001g0105a0002c0002t0001g0128a0003c0003t0002g0005 | 3 | NA18946.hp1 NA19043.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2791-3564_2791-355 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTTCCT others(9): Show |
1 | a0001c0001t0001g0186 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2791-3568_2791-355 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | CCCTTCCT others(13): Show |
1 | a0001c0001t0001g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2791-3572_2791-355 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
C | T | 3 | a0001c0001t0001g0158a0002c0042t0001g0198a0003c0003t0001g0145 | 3 | HG00621.hp1 HG01255.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2791-3613C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940023 | ||||||
chr20:32940023
|
CCCTT | C | 27 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0153others(24): Show | 28 | HG00639.hp1 HG01123.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.2791-3556_2791-355 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
CCCTTCCT others(1): Show |
C | 7 | a0001c0001t0001g0242a0002c0002t0002g0034a0002c0002t0004g0102others(4): Show | 7 | HG00323.hp1 HG01167.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2791-3560_2791-355 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
CCCTTCCT others(5): Show |
C | 17 | a0001c0001t0001g0168a0001c0001t0001g0187a0001c0001t0005g0220others(14): Show | 17 | HG01071.hp2 HG01243.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.2791-3564_2791-355 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940023
|
CCCTTCCT others(9): Show |
C | 2 | a0003c0003t0001g0282a0007c0006t0001g0247 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2791-3568_2791-355 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32940023 | |||||
chr20:32940027
|
T | C | 118 | a0001c0001t0001g0061a0001c0001t0001g0104a0001c0001t0001g0115others(115): Show | 118 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.2791-3609T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940027 | ||||||
chr20:32940031
|
T | C | 90 | a0001c0001t0001g0206a0001c0001t0001g0211a0001c0001t0001g0213others(87): Show | 90 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.2791-3605T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940031 | ||||||
chr20:32940035
|
T | C | 81 | a0002c0002t0001g0190a0002c0002t0002g0003a0002c0002t0002g0004others(78): Show | 81 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.2791-3601T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940035 | ||||||
chr20:32940038
|
T | C | 1 | a0002c0002t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2791-3598T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940038 | ||||||
chr20:32940039
|
T | C | 72 | a0001c0001t0005g0220a0002c0002t0001g0190a0002c0002t0001g0267others(69): Show | 72 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(69): Show |
intron_variant | MODIFIER | c.2791-3597T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940039 | ||||||
chr20:32940043
|
T | C | 52 | a0001c0001t0005g0220a0002c0002t0001g0190a0002c0002t0001g0267others(49): Show | 52 | HG00323.hp1 HG01099.hp2 HG01258.hp1 others(49): Show |
intron_variant | MODIFIER | c.2791-3593T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940043 | ||||||
chr20:32940047
|
T | C | 8 | a0002c0002t0002g0012a0002c0002t0002g0028a0002c0002t0002g0034others(5): Show | 8 | HG02055.hp1 HG02083.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-3589T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940047 | ||||||
chr20:32940049
|
C | T | 19 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(16): Show | 19 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2791-3587C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940049 | ||||||
chr20:32940051
|
T | C | 4 | a0002c0002t0002g0034a0002c0002t0002g0039a0002c0002t0002g0056others(1): Show | 4 | NA18964.hp2 NA18998.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.2791-3585T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940051 | ||||||
chr20:32940243
|
A | G | 6 | a0005c0033t0008g0113a0017c0017t0007g0217a0017c0017t0007g0227others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2791-3393A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940243 | ||||||
chr20:32940270
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2791-3366C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940270 | ||||||
chr20:32940396
|
T | G | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2791-3240T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940396 | ||||||
chr20:32940505
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2791-3131T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940505 | ||||||
chr20:32940748
|
C | T | 1 | a0041c0050t0002g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2791-2888C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940748 | ||||||
chr20:32940751
|
G | A | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-2885G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32940751 | ||||||
chr20:32941054
|
C | A | 1 | a0002c0002t0002g0012 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2791-2582C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941054 | ||||||
chr20:32941144
|
C | T | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-2492C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941144 | ||||||
chr20:32941145
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0242 | 2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2791-2491G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941145 | ||||||
chr20:32941169
|
T | C | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2791-2467T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941169 | ||||||
chr20:32941423
|
A | G | 1 | a0002c0002t0001g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2791-2213A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941423 | ||||||
chr20:32941568
|
A | G | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2068A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941568 | ||||||
chr20:32941572
|
AT | A | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2063delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941572 | ||||||
chr20:32941575
|
A | T | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2061A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941575 | ||||||
chr20:32941577
|
CCTTGAA | C | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2791-2058_2791-205 others(10): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941577 | ||||||
chr20:32941722
|
G | T | 78 | a0001c0001t0001g0206a0001c0001t0001g0211a0002c0002t0001g0190others(75): Show | 78 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2791-1914G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941722 | ||||||
chr20:32941841
|
G | A | 29 | a0005c0033t0008g0113a0006c0005t0003g0064a0006c0005t0003g0065others(26): Show | 29 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2791-1795G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941841 | ||||||
chr20:32941989
|
A | T | 2 | a0002c0002t0001g0225a0002c0002t0001g0261 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2791-1647A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32941989 | ||||||
chr20:32942028
|
T | C | 29 | a0005c0033t0008g0113a0006c0005t0003g0064a0006c0005t0003g0065others(26): Show | 29 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2791-1608T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942028 | ||||||
chr20:32942157
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2791-1479C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942157 | ||||||
chr20:32942273
|
T | C | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2791-1363T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942273 | ||||||
chr20:32942533
|
C | A | 2 | a0002c0002t0001g0225a0002c0002t0001g0261 | 2 | HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2791-1103C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942533 | ||||||
chr20:32942630
|
G | C | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2791-1006G>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942630 | ||||||
chr20:32942893
|
C | G | 2 | a0016c0018t0004g0147a0016c0018t0004g0192 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2791-743C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942893 | ||||||
chr20:32942894
|
C | T | 5 | a0001c0001t0001g0148a0001c0001t0001g0163a0001c0001t0009g0114others(2): Show | 5 | HG01070.hp2 NA18951.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.2791-742C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32942894 | ||||||
chr20:32943344
|
TAGTCATA others(4): Show |
T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2791-271_2791-261d others(13): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | INFO_REALIGN_3_PRIME | chr20 | 32943344 | |||||
chr20:32943363
|
T | G | 31 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2791-273T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32943363 | ||||||
chr20:32943479
|
G | A | 3 | a0016c0018t0004g0147a0016c0018t0004g0192a0016c0018t0005g0229 | 3 | HG01167.hp1 HG01169.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2791-157G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 22/26 | chr20 | 32943479 | ||||||
chr20:32943889
|
A | G | 1 | a0011c0010t0006g0049 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2959+85A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32943889 | ||||||
chr20:32943985
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2959+181T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32943985 | ||||||
chr20:32944250
|
C | T | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2959+446C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944250 | ||||||
chr20:32944320
|
C | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG01071.hp2 HG01346.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2959+516C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944320 | ||||||
chr20:32944356
|
T | C | 1 | a0002c0046t0003g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2959+552T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944356 | ||||||
chr20:32944471
|
A | T | 11 | a0007c0006t0004g0142a0007c0030t0004g0127a0007c0030t0004g0266others(8): Show | 11 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2959+667A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944471 | ||||||
chr20:32944501
|
G | T | 1 | a0002c0002t0002g0036 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2959+697G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944501 | ||||||
chr20:32944518
|
A | G | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+714A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944518 | ||||||
chr20:32944521
|
G | A | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+717G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944521 | ||||||
chr20:32944847
|
T | C | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2959+1043T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944847 | ||||||
chr20:32944972
|
G | A | 4 | a0001c0001t0001g0153a0019c0016t0001g0143a0019c0016t0001g0177others(1): Show | 4 | HG00099.hp1 HG04184.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2959+1168G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944972 | ||||||
chr20:32944990
|
TAA | T | 6 | a0005c0033t0008g0113a0017c0017t0007g0217a0017c0017t0007g0227others(3): Show | 6 | HG01891.hp1 HG02145.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2959+1187_2959+118 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32944990 | ||||||
chr20:32945474
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2959+1670A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945474 | ||||||
chr20:32945551
|
G | A | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+1747G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945551 | ||||||
chr20:32945594
|
T | C | 4 | a0001c0001t0001g0106a0001c0001t0001g0146a0001c0001t0001g0158others(1): Show | 4 | HG01175.hp2 HG01255.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2959+1790T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945594 | ||||||
chr20:32945779
|
G | A | 6 | a0010c0009t0001g0248a0015c0019t0005g0219a0015c0019t0005g0231others(3): Show | 6 | HG00741.hp1 HG01884.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2959+1975G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945779 | ||||||
chr20:32945997
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2959+2193G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32945997 | ||||||
chr20:32946308
|
G | A | 1 | a0006c0005t0003g0065 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2959+2504G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946308 | ||||||
chr20:32946328
|
A | C | 19 | a0006c0005t0003g0064a0006c0005t0003g0065a0006c0005t0003g0067others(16): Show | 19 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.2959+2524A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946328 | ||||||
chr20:32946397
|
T | C | 10 | a0001c0001t0001g0206a0001c0001t0001g0211a0002c0002t0003g0223others(7): Show | 10 | HG01109.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2959+2593T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946397 | ||||||
chr20:32946505
|
G | A | 1 | a0015c0019t0005g0219 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2959+2701G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946505 | ||||||
chr20:32946766
|
A | C | 1 | a0044c0044t0002g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2959+2962A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946766 | ||||||
chr20:32946836
|
T | C | 3 | a0007c0006t0004g0142a0007c0030t0004g0127a0007c0030t0004g0266 | 3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2959+3032T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946836 | ||||||
chr20:32946844
|
A | G | 31 | a0004c0004t0001g0089a0004c0004t0003g0058a0004c0004t0003g0059others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.2959+3040A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946844 | ||||||
chr20:32946852
|
G | A | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+3048G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946852 | ||||||
chr20:32946895
|
G | A | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2959+3091G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946895 | ||||||
chr20:32946928
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2959+3124A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32946928 | ||||||
chr20:32947041
|
G | A | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+3237G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947041 | ||||||
chr20:32947085
|
G | A | 2 | a0047c0055t0001g0278a0048c0058t0002g0257 | 2 | HG01261.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2959+3281G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947085 | ||||||
chr20:32947175
|
A | G | 78 | a0001c0001t0001g0206a0001c0001t0001g0211a0002c0002t0001g0190others(75): Show | 78 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.2959+3371A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947175 | ||||||
chr20:32947379
|
A | C | 1 | a0037c0057t0004g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2959+3575A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947379 | ||||||
chr20:32947459
|
C | A | 167 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(164): Show | 167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2959+3655C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947459 | ||||||
chr20:32947668
|
TA | T | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+3866delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32947668 | |||||
chr20:32947764
|
T | A | 167 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(164): Show | 167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2959+3960T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32947764 | ||||||
chr20:32947903
|
T | TA | 9 | a0004c0004t0003g0077a0009c0015t0001g0096a0009c0015t0001g0098others(6): Show | 9 | HG00280.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2959+4114dupA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32947903 | |||||
chr20:32947903
|
TA | T | 15 | a0001c0001t0001g0115a0001c0001t0001g0151a0004c0004t0001g0089others(12): Show | 15 | HG00280.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2959+4114delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32947903 | |||||
chr20:32948065
|
T | C | 1 | a0009c0015t0001g0096 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2959+4261T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948065 | ||||||
chr20:32948315
|
G | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+4511G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948315 | ||||||
chr20:32948437
|
C | T | 49 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(46): Show | 49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2959+4633C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948437 | ||||||
chr20:32948524
|
A | AAAAG | 41 | a0001c0001t0001g0103a0001c0001t0001g0106a0001c0001t0001g0124others(38): Show | 41 | HG00280.hp2 HG00323.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.2959+4776_2959+477 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
A | AAAAGAAA others(1): Show |
15 | a0001c0001t0001g0061a0001c0001t0001g0208a0001c0001t0005g0220others(12): Show | 15 | HG00642.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2959+4772_2959+477 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
A | AAAAGAAA others(5): Show |
3 | a0001c0001t0001g0211a0030c0063t0004g0081a0041c0050t0002g0218 | 3 | HG01109.hp1 HG01243.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2959+4768_2959+477 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
AAAAG | A | 63 | a0001c0001t0001g0132a0001c0001t0001g0138a0001c0001t0001g0146others(60): Show | 63 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.2959+4776_2959+477 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
AAAAGAAA others(1): Show |
A | 48 | a0001c0001t0001g0088a0001c0001t0001g0171a0001c0001t0001g0207others(45): Show | 48 | HG00323.hp1 HG00733.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.2959+4772_2959+477 others(12): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
AAAAGAAA others(5): Show |
A | 16 | a0001c0001t0001g0187a0001c0001t0001g0188a0003c0003t0001g0274others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2959+4768_2959+477 others(16): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
AAAAGAAA others(9): Show |
A | 1 | a0028c0021t0002g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2959+4764_2959+477 others(20): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2959+4760_2959+477 others(24): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948524
|
AAAAGAAA others(17): Show |
A | 2 | a0026c0027t0003g0126a0048c0058t0002g0257 | 2 | HG01261.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.2959+4756_2959+477 others(28): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948524 | |||||
chr20:32948570
|
A | AAG | 3 | a0002c0011t0001g0245a0002c0011t0001g0246a0021c0061t0001g0238 | 3 | HG02486.hp2 HG02965.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2959+4768_2959+476 others(6): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948570 | |||||
chr20:32948570
|
A | AAGAAAGA others(3): Show |
2 | a0007c0006t0004g0142a0007c0030t0004g0266 | 2 | HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2959+4768_2959+477 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948570 | |||||
chr20:32948580
|
G | GAAAGAAA others(3): Show |
1 | a0025c0025t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2959+4779_2959+478 others(14): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32948580 | |||||
chr20:32948808
|
A | G | 8 | a0002c0002t0001g0267a0002c0002t0001g0268a0002c0002t0001g0269others(5): Show | 8 | HG01361.hp2 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2959+5004A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32948808 | ||||||
chr20:32949213
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2959+5409C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949213 | ||||||
chr20:32949641
|
A | G | 7 | a0002c0002t0003g0223a0002c0002t0003g0262a0002c0002t0003g0263others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2959+5837A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949641 | ||||||
chr20:32949705
|
C | G | 11 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(8): Show | 11 | HG01891.hp2 HG02630.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.2959+5901C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949705 | ||||||
chr20:32949721
|
A | G | 170 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2959+5917A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949721 | ||||||
chr20:32949931
|
C | T | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2959+6127C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949931 | ||||||
chr20:32949954
|
C | T | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+6150C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949954 | ||||||
chr20:32949995
|
G | A | 2 | a0017c0017t0007g0217a0017c0017t0007g0228 | 2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2959+6191G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32949995 | ||||||
chr20:32950001
|
A | AAAAC | 84 | a0002c0002t0001g0190a0002c0002t0002g0003a0002c0002t0002g0004others(81): Show | 84 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2959+6205_2959+620 others(8): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32950001 | |||||
chr20:32950012
|
A | AC | 76 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(73): Show | 76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6208_2959+620 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950012 | ||||||
chr20:32950014
|
C | A | 76 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(73): Show | 76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6210C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950014 | ||||||
chr20:32950019
|
AAAC | A | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2959+6233_2959+623 others(7): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32950019 | |||||
chr20:32950020
|
A | C | 76 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(73): Show | 76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6216A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950020 | ||||||
chr20:32950022
|
C | A | 76 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(73): Show | 76 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.2959+6218C>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950022 | ||||||
chr20:32950053
|
A | C | 2 | a0002c0011t0001g0245a0002c0011t0001g0246 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2959+6249A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950053 | ||||||
chr20:32950515
|
C | T | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2959+6711C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950515 | ||||||
chr20:32950650
|
G | A | 2 | a0001c0001t0001g0215a0002c0002t0002g0055 | 2 | NA18979.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2959+6846G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950650 | ||||||
chr20:32950664
|
C | T | 11 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(8): Show | 11 | HG01891.hp2 HG02630.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.2959+6860C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950664 | ||||||
chr20:32950918
|
G | A | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2959+7114G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950918 | ||||||
chr20:32950927
|
C | T | 1 | a0002c0011t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2959+7123C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950927 | ||||||
chr20:32950989
|
A | G | 1 | a0043c0045t0007g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2959+7185A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32950989 | ||||||
chr20:32951024
|
A | T | 1 | a0002c0011t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2959+7220A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951024 | ||||||
chr20:32951138
|
G | A | 29 | a0005c0033t0008g0113a0006c0005t0003g0064a0006c0005t0003g0065others(26): Show | 29 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.2960-7283G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951138 | ||||||
chr20:32951245
|
T | C | 1 | a0025c0025t0002g0019 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2960-7176T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951245 | ||||||
chr20:32951302
|
T | C | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2960-7119T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951302 | ||||||
chr20:32951414
|
G | A | 1 | a0005c0008t0001g0063 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2960-7007G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951414 | ||||||
chr20:32951547
|
TA | T | 3 | a0016c0018t0004g0147a0016c0018t0004g0192a0016c0018t0005g0229 | 3 | HG01167.hp1 HG01169.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2960-6873delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32951547 | ||||||
chr20:32952400
|
C | T | 3 | a0016c0018t0004g0147a0016c0018t0004g0192a0016c0018t0005g0229 | 3 | HG01167.hp1 HG01169.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2960-6021C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952400 | ||||||
chr20:32952449
|
A | T | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-5972A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952449 | ||||||
chr20:32952606
|
A | G | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-5815A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952606 | ||||||
chr20:32952659
|
C | T | 2 | a0019c0016t0001g0177a0019c0016t0001g0178 | 2 | HG00099.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2960-5762C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952659 | ||||||
chr20:32952715
|
A | G | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2960-5706A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32952715 | ||||||
chr20:32953027
|
C | T | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.2960-5394C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953027 | ||||||
chr20:32953118
|
A | C | 2 | a0003c0003t0001g0172a0003c0003t0001g0173 | 2 | NA18947.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2960-5303A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953118 | ||||||
chr20:32953501
|
T | C | 17 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(14): Show | 17 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2960-4920T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953501 | ||||||
chr20:32953613
|
A | G | 17 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(14): Show | 17 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2960-4808A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953613 | ||||||
chr20:32953913
|
C | T | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2960-4508C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953913 | ||||||
chr20:32953935
|
C | T | 1 | a0008c0007t0003g0194 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2960-4486C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953935 | ||||||
chr20:32953936
|
G | T | 1 | a0020c0032t0004g0062 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2960-4485G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953936 | ||||||
chr20:32953942
|
C | T | 2 | a0014c0014t0002g0014a0014c0014t0002g0040 | 2 | HG01515.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2960-4479C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32953942 | ||||||
chr20:32954054
|
C | T | 49 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(46): Show | 49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2960-4367C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954054 | ||||||
chr20:32954478
|
T | C | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-3943T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954478 | ||||||
chr20:32954509
|
C | T | 1 | a0005c0034t0002g0031 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2960-3912C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954509 | ||||||
chr20:32954684
|
T | G | 1 | a0003c0003t0001g0164 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2960-3737T>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954684 | ||||||
chr20:32954718
|
A | G | 167 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(164): Show | 167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2960-3703A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954718 | ||||||
chr20:32954772
|
C | G | 1 | a0020c0032t0004g0277 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2960-3649C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32954772 | ||||||
chr20:32955014
|
TC | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0088others(279): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.2960-3403delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32955014 | |||||
chr20:32955291
|
G | A | 3 | a0007c0006t0004g0142a0007c0030t0004g0127a0007c0030t0004g0266 | 3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2960-3130G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955291 | ||||||
chr20:32955358
|
T | C | 170 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(167): Show | 170 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.2960-3063T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955358 | ||||||
chr20:32955374
|
T | C | 2 | a0001c0001t0005g0255a0001c0001t0005g0256 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2960-3047T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955374 | ||||||
chr20:32955412
|
C | T | 3 | a0007c0006t0004g0142a0007c0030t0004g0127a0007c0030t0004g0266 | 3 | HG02922.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2960-3009C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955412 | ||||||
chr20:32955497
|
G | A | 1 | a0002c0011t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2960-2924G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955497 | ||||||
chr20:32955673
|
G | A | 1 | a0003c0003t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2960-2748G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955673 | ||||||
chr20:32955716
|
C | T | 2 | a0022c0031t0002g0196a0022c0031t0002g0230 | 2 | HG01167.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2960-2705C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955716 | ||||||
chr20:32955846
|
C | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0212 | 2 | NA19011.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2960-2575C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955846 | ||||||
chr20:32955984
|
A | AC | 8 | a0012c0012t0004g0094a0012c0012t0004g0108a0012c0012t0004g0109others(5): Show | 8 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-2437_2960-243 others(5): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32955984 | ||||||
chr20:32956089
|
A | T | 168 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(165): Show | 168 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.2960-2332A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956089 | ||||||
chr20:32956097
|
G | A | 4 | a0002c0011t0001g0244a0002c0011t0001g0245a0002c0011t0001g0246others(1): Show | 4 | HG02486.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2960-2324G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956097 | ||||||
chr20:32956125
|
G | A | 75 | a0002c0002t0001g0190a0002c0002t0002g0003a0002c0002t0002g0004others(72): Show | 75 | HG00280.hp2 HG00642.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.2960-2296G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956125 | ||||||
chr20:32956223
|
G | A | 2 | a0002c0002t0001g0093a0007c0006t0001g0247 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2960-2198G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956223 | ||||||
chr20:32956284
|
C | T | 167 | a0001c0001t0004g0048a0001c0001t0005g0220a0001c0001t0005g0255others(164): Show | 167 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.2960-2137C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956284 | ||||||
chr20:32956530
|
C | T | 27 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(24): Show | 27 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.2960-1891C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956530 | ||||||
chr20:32956943
|
C | CT | 8 | a0002c0011t0001g0100a0002c0011t0001g0244a0002c0011t0001g0245others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2960-1464dupT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32956943 | |||||
chr20:32956943
|
CT | C | 31 | a0001c0001t0001g0158a0002c0002t0001g0225a0002c0002t0001g0261others(28): Show | 31 | HG00639.hp2 HG01070.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.2960-1464delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32956943 | |||||
chr20:32956958
|
C | T | 16 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(13): Show | 16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-1463C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956958 | ||||||
chr20:32956959
|
A | C | 16 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(13): Show | 16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-1462A>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956959 | ||||||
chr20:32956959
|
AT | A | 11 | a0002c0002t0001g0225a0002c0002t0001g0261a0010c0009t0001g0248others(8): Show | 11 | HG01243.hp1 HG01346.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.2960-1454delT | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32956959 | |||||
chr20:32956960
|
T | A | 16 | a0001c0001t0004g0048a0001c0001t0005g0255a0001c0001t0005g0256others(13): Show | 16 | HG00741.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-1461T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32956960 | ||||||
chr20:32957099
|
A | T | 49 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(46): Show | 49 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(46): Show |
intron_variant | MODIFIER | c.2960-1322A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957099 | ||||||
chr20:32957287
|
C | T | 5 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2960-1134C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957287 | ||||||
chr20:32957318
|
TA | T | 20 | a0002c0002t0002g0039a0002c0002t0003g0275a0002c0002t0003g0276others(17): Show | 20 | HG01261.hp2 HG02109.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.2960-1091delA | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32957318 | |||||
chr20:32957319
|
A | T | 2 | a0002c0042t0001g0198a0009c0041t0001g0251 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2960-1102A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957319 | ||||||
chr20:32957330
|
AC | A | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2960-1088delC | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | INFO_REALIGN_3_PRIME | chr20 | 32957330 | |||||
chr20:32957494
|
G | T | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2960-927G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957494 | ||||||
chr20:32957542
|
C | T | 2 | a0031c0060t0001g0079a0033c0065t0001g0060 | 2 | HG00733.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2960-879C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957542 | ||||||
chr20:32957735
|
C | G | 1 | a0041c0050t0002g0218 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2960-686C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957735 | ||||||
chr20:32957757
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.2960-664C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957757 | ||||||
chr20:32957824
|
A | T | 2 | a0004c0004t0003g0069a0029c0059t0003g0071 | 2 | HG01516.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.2960-597A>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32957824 | ||||||
chr20:32958208
|
G | T | 2 | a0008c0007t0006g0013a0008c0007t0006g0044 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2960-213G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32958208 | ||||||
chr20:32958326
|
T | A | 1 | a0047c0055t0001g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2960-95T>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32958326 | ||||||
chr20:32958404
|
G | A | 4 | a0006c0005t0003g0075a0006c0005t0003g0082a0006c0005t0003g0091others(1): Show | 4 | HG01361.hp1 HG02602.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.2960-17G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 23/26 | chr20 | 32958404 | ||||||
chr20:32958678
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0181 | 2 | HG02735.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3089+128G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32958678 | ||||||
chr20:32958804
|
C | G | 1 | a0001c0001t0001g0165 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3089+254C>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32958804 | ||||||
chr20:32958833
|
G | T | 1 | a0025c0025t0001g0193 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3089+283G>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32958833 | ||||||
chr20:32959102
|
G | A | 1 | a0018c0026t0003g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3089+552G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959102 | ||||||
chr20:32959227
|
ATG | A | 5 | a0005c0033t0008g0113a0017c0017t0007g0217a0017c0017t0007g0227others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3090-548_3090-547d others(4): Show |
EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | INFO_REALIGN_3_PRIME | chr20 | 32959227 | |||||
chr20:32959312
|
G | A | 20 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(17): Show | 20 | HG00323.hp1 HG01123.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.3090-466G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959312 | ||||||
chr20:32959353
|
A | G | 1 | a0005c0036t0004g0180 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3090-425A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959353 | ||||||
chr20:32959482
|
T | C | 3 | a0002c0002t0001g0225a0002c0002t0001g0261a0002c0002t0002g0039 | 3 | HG01884.hp1 HG02809.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.3090-296T>C | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 24/26 | chr20 | 32959482 | ||||||
chr20:32960216
|
C | T | 8 | a0009c0015t0001g0096a0009c0015t0001g0098a0009c0015t0001g0112others(5): Show | 8 | HG01167.hp1 HG01169.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.3393+55C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960216 | ||||||
chr20:32960275
|
C | T | 1 | a0006c0005t0003g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3393+114C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960275 | ||||||
chr20:32960307
|
A | G | 1 | a0006c0005t0003g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3393+146A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960307 | ||||||
chr20:32960724
|
A | G | 57 | a0001c0001t0005g0220a0002c0002t0001g0093a0002c0002t0001g0267others(54): Show | 57 | HG00323.hp1 HG00639.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.3394-412A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960724 | ||||||
chr20:32960743
|
C | T | 1 | a0002c0002t0003g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3394-393C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960743 | ||||||
chr20:32960857
|
G | A | 1 | a0006c0005t0003g0091 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3394-279G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960857 | ||||||
chr20:32960974
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.3394-162C>T | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32960974 | ||||||
chr20:32961012
|
G | A | 1 | a0005c0013t0004g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3394-124G>A | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32961012 | ||||||
chr20:32961096
|
A | G | 1 | a0017c0017t0007g0228 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3394-40A>G | EFCAB8 | ENSG00000215529.13 | transcript | ENST00000400522.9 | protein_coding | 26/26 | chr20 | 32961096 |