geneid | 113174 |
---|---|
ensemblid | ENSG00000166788.10 |
hgncid | 25158 |
symbol | SAAL1 |
name | serum amyloid A like 1 |
refseq_nuc | NM_138421.3 |
refseq_prot | NP_612430.2 |
ensembl_nuc | ENST00000524803.6 |
ensembl_prot | ENSP00000432487.1 |
mane_status | MANE Select |
chr | chr11 |
start | 18080292 |
end | 18106082 |
strand | - |
ver | v1.2 |
region | chr11:18080292-18106082 |
region5000 | chr11:18075292-18111082 |
regionname0 | SAAL1_chr11_18080292_18106082 |
regionname5000 | SAAL1_chr11_18075292_18111082 |
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 | 474 | 161 | 52 | 28 | 57 | 5 | 18 | 37 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0002 | 0/1 | 475 | 48 | 1 | 9 | 25 | 3 | 9 | 19 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0003 | 0/0 | 474 | 29 | 16 | 5 | 2 | 2 | 4 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0004 | 0/0 | 474 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0005 | 0/0 | 476 | 10 | 0 | 0 | 10 | 0 | 0 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0006 | 0/0 | 474 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0007 | 0/0 | 474 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0008 | 0/0 | 474 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0009 | 0/0 | 474 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0010 | 0/0 | 474 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0011 | 0/0 | 474 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0012 | 0/0 | 474 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0013 | 0/0 | 474 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0014 | 0/0 | 474 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0015 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
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 | 1425 | 151 | 43 | 28 | 57 | 5 | 17 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0002 | 0/0 | 1428 | 46 | 1 | 9 | 24 | 3 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0003 | 0/0 | 1425 | 29 | 16 | 5 | 2 | 2 | 4 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0004 | 0/0 | 1425 | 13 | 13 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0005 | 0/0 | 1431 | 10 | 0 | 0 | 10 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0006 | 0/0 | 1425 | 10 | 9 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0007 | 0/0 | 1425 | 8 | 8 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0008 | 0/1 | 1428 | 2 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0009 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0010 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0011 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0012 | 0/0 | 1425 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0013 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0014 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0015 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0016 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0017 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0018 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
c0019 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
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 | 149 | 283 | 96 | 44 | 98 | 12 | 31 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
t0002 | 0/0 | 149 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
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 | 1/0 | 46 | 7 | 13 | 17 | 2 | 6 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0002 | 0/0 | 16 | 1 | 5 | 7 | 1 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0004 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0005 | 0/0 | 9 | 2 | 4 | 2 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0007 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0009 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0012 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0020 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
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 | 1425 | 151 | 43 | 28 | 57 | 5 | 17 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0007 | 0/0 | 1425 | 8 | 8 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0016 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0018 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0002c0002 | 0/0 | 1428 | 46 | 1 | 9 | 24 | 3 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0002c0008 | 0/1 | 1428 | 2 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0003c0003 | 0/0 | 1425 | 29 | 16 | 5 | 2 | 2 | 4 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0004c0004 | 0/0 | 1425 | 13 | 13 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0005c0005 | 0/0 | 1431 | 10 | 0 | 0 | 10 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0006c0006 | 0/0 | 1425 | 10 | 9 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0007c0010 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0008c0011 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0009c0009 | 0/0 | 1425 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0010c0012 | 0/0 | 1425 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0011c0019 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0012c0014 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0013c0015 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0014c0017 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0015c0013 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1573 | 150 | 43 | 28 | 57 | 5 | 16 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0001t0002 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0007t0001 | 0/0 | 1573 | 8 | 8 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0016t0001 | 0/0 | 1573 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0001c0018t0001 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0002c0002t0001 | 0/0 | 1576 | 46 | 1 | 9 | 24 | 3 | 9 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0002c0008t0001 | 0/1 | 1576 | 2 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0003c0003t0001 | 0/0 | 1573 | 29 | 16 | 5 | 2 | 2 | 4 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0004c0004t0001 | 0/0 | 1573 | 13 | 13 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0005c0005t0001 | 0/0 | 1579 | 10 | 0 | 0 | 10 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0006c0006t0001 | 0/0 | 1573 | 10 | 9 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0007c0010t0001 | 0/0 | 1573 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0008c0011t0001 | 0/0 | 1573 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0009c0009t0001 | 0/0 | 1573 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0010c0012t0001 | 0/0 | 1573 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0011c0019t0001 | 0/0 | 1573 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0012c0014t0001 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0013c0015t0001 | 0/0 | 1573 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0014c0017t0001 | 0/0 | 1573 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
a0015c0013t0001 | 0/0 | 1576 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | copy fasta | chr11 | 18075292 | 18111082 |
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 | 1/0 | 46 | 7 | 13 | 17 | 2 | 6 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0005 | 0/0 | 9 | 2 | 4 | 2 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0007 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0007t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0016t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0001c0018t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0002 | 0/0 | 16 | 1 | 5 | 7 | 1 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0004 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0008t0001g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0002c0008t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0009 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0012 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0004c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0005c0005t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0005c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0005c0005t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0006c0006t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0006c0006t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0006c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0006c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0006c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0006c0006t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0007c0010t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0008c0011t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0009c0009t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0010c0012t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0011c0019t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0012c0014t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0013c0015t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0014c0017t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
a0015c0013t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0012 | EUR | GBR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00280 | hp1 | a0012 | c0014 | t0001 | g0060 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0024 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0012 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00438 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | CHS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00733 | hp2 | a0003 | c0003 | t0001 | g0012 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01081 | hp1 | a0006 | c0006 | t0001 | g0014 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01358 | hp1 | a0003 | c0003 | t0001 | g0009 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01433 | hp2 | a0010 | c0012 | t0001 | g0038 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | IBS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01884 | hp2 | a0006 | c0006 | t0001 | g0065 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0069 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02055 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02145 | hp1 | a0006 | c0006 | t0001 | g0063 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02257 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02258 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02280 | hp1 | a0001 | c0007 | t0001 | g0071 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02280 | hp2 | a0011 | c0019 | t0001 | g0121 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02451 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02572 | hp1 | a0001 | c0016 | t0001 | g0119 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02615 | hp1 | a0004 | c0004 | t0001 | g0067 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02615 | hp2 | a0009 | c0009 | t0001 | g0028 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02647 | hp2 | a0007 | c0010 | t0001 | g0032 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0022 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02717 | hp1 | a0004 | c0004 | t0001 | g0068 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0116 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02723 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0009 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02809 | hp2 | a0001 | c0007 | t0001 | g0072 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02886 | hp1 | a0006 | c0006 | t0001 | g0014 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02886 | hp2 | a0003 | c0003 | t0001 | g0111 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02895 | hp1 | a0006 | c0006 | t0001 | g0026 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02922 | hp1 | a0006 | c0006 | t0001 | g0026 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02922 | hp2 | a0006 | c0006 | t0001 | g0062 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02965 | hp1 | a0004 | c0004 | t0001 | g0066 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02970 | hp2 | a0001 | c0007 | t0001 | g0008 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02976 | hp1 | a0004 | c0004 | t0001 | g0017 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0115 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03195 | hp2 | a0006 | c0006 | t0001 | g0014 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03209 | hp1 | a0003 | c0003 | t0001 | g0114 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03225 | hp1 | a0003 | c0003 | t0001 | g0110 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0037 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0118 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0041 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03486 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03491 | hp2 | a0001 | c0018 | t0001 | g0084 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03516 | hp1 | a0001 | c0007 | t0001 | g0008 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03516 | hp2 | a0004 | c0004 | t0001 | g0070 | AFR | ESN | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03540 | hp1 | a0009 | c0009 | t0001 | g0028 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03540 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | GWD | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03579 | hp2 | a0004 | c0004 | t0001 | g0027 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03688 | hp1 | a0010 | c0012 | t0001 | g0038 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0009 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | STU | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18522 | hp1 | a0006 | c0006 | t0001 | g0014 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18906 | hp2 | a0004 | c0004 | t0001 | g0017 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18945 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18948 | hp1 | a0008 | c0011 | t0001 | g0025 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18968 | hp1 | a0013 | c0015 | t0001 | g0096 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0112 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18986 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18994 | hp2 | a0008 | c0011 | t0001 | g0025 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19001 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19001 | hp2 | a0005 | c0005 | t0001 | g0059 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19043 | hp2 | a0004 | c0004 | t0001 | g0027 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19060 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19074 | hp1 | a0005 | c0005 | t0001 | g0058 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19076 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19079 | hp1 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19079 | hp2 | a0015 | c0013 | t0001 | g0051 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19091 | hp1 | a0002 | c0008 | t0001 | g0047 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19091 | hp2 | a0005 | c0005 | t0001 | g0006 | EAS | JPT | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0013 | AFR | YRI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20129 | hp1 | a0007 | c0010 | t0001 | g0032 | AFR | ASW | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20752 | hp2 | a0014 | c0017 | t0001 | g0076 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0022 | SAS | GIH | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0002 | SAS | GIH | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02109 | hp2 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02486 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0113 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03471 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG06807 | hp1 | a0004 | c0004 | t0001 | g0017 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA20300 | hp2 | a0006 | c0006 | t0001 | g0064 | AFR | USA | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
homoSapiens_chm13v2 | hp1 | a0002 | c0008 | t0001 | g0040 | REF | REF | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | SAAL1_chr11_18075292_18111082 | SAAL1 | chr11 | 18075292 | 18111082 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:18080426
|
G | T | 1 | a0009 | 2 | HG02615.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.1398C>A | p.Asn466Lys | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 12/12 | 1439/1573 | 1398/1425 | 466/474 | chr11 | 18080426 | ||
chr11:18080467
|
G | A | 1 | a0010 | 2 | HG01433.hp2 HG03688.hp1 |
missense_variant | MODERATE | c.1357C>T | p.Arg453Cys | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 12/12 | 1398/1573 | 1357/1425 | 453/474 | chr11 | 18080467 | ||
chr11:18081467
|
T | C | 2 | a0004a0011 | 14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
missense_variant | MODERATE | c.1276A>G | p.Ser426Gly | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/12 | 1317/1573 | 1276/1425 | 426/474 | chr11 | 18081467 | ||
chr11:18083666
|
G | T | 1 | a0013 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1108C>A | p.Pro370Thr | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/12 | 1149/1573 | 1108/1425 | 370/474 | chr11 | 18083666 | ||
chr11:18086957
|
T | G | 1 | a0006 | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
missense_variant | MODERATE | c.951A>C | p.Gln317His | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 992/1573 | 951/1425 | 317/474 | chr11 | 18086957 | ||
chr11:18086965
|
T | C | 2 | a0003a0010 | 31 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
missense_variant | MODERATE | c.943A>G | p.Ile315Val | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 984/1573 | 943/1425 | 315/474 | chr11 | 18086965 | ||
chr11:18086985
|
T | C | 1 | a0014 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.923A>G | p.Gln308Arg | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 964/1573 | 923/1425 | 308/474 | chr11 | 18086985 | ||
chr11:18087019
|
A | T | 1 | a0008 | 2 | NA18948.hp1 NA18994.hp2 |
missense_variant | MODERATE | c.889T>A | p.Leu297Ile | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 930/1573 | 889/1425 | 297/474 | chr11 | 18087019 | ||
chr11:18089375
|
A | G | 1 | a0015 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.725T>C | p.Val242Ala | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/12 | 766/1573 | 725/1425 | 242/474 | chr11 | 18089375 | ||
chr11:18090237
|
C | T | 1 | a0007 | 2 | HG02647.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.527G>A | p.Arg176Lys | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/12 | 568/1573 | 527/1425 | 176/474 | chr11 | 18090237 | ||
chr11:18105917
|
C | T | 1 | a0012 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.125G>A | p.Gly42Glu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 166/1573 | 125/1425 | 42/474 | chr11 | 18105917 | ||
chr11:18105921
|
T | G | 1 | a0011 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.121A>C | p.Ser41Arg | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 162/1573 | 121/1425 | 41/474 | chr11 | 18105921 | ||
chr11:18105983
|
A | ACCTCCT | 1 | a0005 | 10 | HG00438.hp2 NA18945.hp2 NA18986.hp2 others(7): Show |
conservative_inframe_insertion | MODERATE | c.53_58dupAGGAGG | p.Glu18_Glu19dup | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 99/1573 | 58/1425 | 20/474 | chr11 | 18105983 | ||
chr11:18106011
|
C | CCGG | 2 | a0002a0015 | 49 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(46): Show |
conservative_inframe_insertion | MODERATE | c.28_30dupCCG | p.Pro10dup | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/12 | 71/1573 | 30/1425 | 10/474 | chr11 | 18106011 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:18081470
|
A | G | 1 | a0008c0011 | 2 | NA18948.hp1 NA18994.hp2 |
synonymous_variant | LOW | c.1273T>C | p.Leu425Leu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/12 | 1314/1573 | 1273/1425 | 425/474 | chr11 | 18081470 | ||
chr11:18083637
|
C | T | 1 | a0001c0016 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1137G>A | p.Glu379Glu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/12 | 1178/1573 | 1137/1425 | 379/474 | chr11 | 18083637 | ||
chr11:18086945
|
T | C | 2 | a0002c0002a0015c0013 | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
synonymous_variant | LOW | c.963A>G | p.Thr321Thr | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/12 | 1004/1573 | 963/1425 | 321/474 | chr11 | 18086945 | ||
chr11:18089491
|
C | A | 2 | a0001c0018a0011c0019 | 2 | HG02280.hp2 HG03491.hp2 |
synonymous_variant | LOW | c.609G>T | p.Val203Val | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/12 | 650/1573 | 609/1425 | 203/474 | chr11 | 18089491 | ||
chr11:18103290
|
C | T | 2 | a0001c0007a0009c0009 | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
synonymous_variant | LOW | c.192G>A | p.Glu64Glu | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/12 | 233/1573 | 192/1425 | 64/474 | chr11 | 18103290 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:18080396
|
G | A | 1 | a0001c0001t0002 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 12/12 | 3 | chr11 | 18080396 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:18080564
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1333-73G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18080564 | ||||||
chr11:18080685
|
C | T | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1333-194G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18080685 | ||||||
chr11:18080717
|
G | A | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1333-226C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18080717 | ||||||
chr11:18081164
|
G | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1332+247C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18081164 | ||||||
chr11:18081182
|
C | T | 71 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(68): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1332+229G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 11/11 | chr11 | 18081182 | ||||||
chr11:18081521
|
T | C | 9 | a0002c0002t0001g0004a0002c0002t0001g0022a0002c0002t0001g0023others(6): Show | 19 | HG02015.hp1 HG02129.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.1240-18A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081521 | ||||||
chr11:18081546
|
T | G | 1 | a0002c0002t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1240-43A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081546 | ||||||
chr11:18081675
|
C | T | 9 | a0003c0003t0001g0009a0003c0003t0001g0012a0003c0003t0001g0037others(6): Show | 21 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1240-172G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081675 | ||||||
chr11:18081702
|
C | T | 1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1240-199G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081702 | ||||||
chr11:18081734
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-231A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081734 | ||||||
chr11:18081783
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-280C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081783 | ||||||
chr11:18081953
|
T | C | 1 | a0002c0002t0001g0057 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1240-450A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18081953 | ||||||
chr11:18082155
|
A | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1240-652T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082155 | ||||||
chr11:18082229
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-726C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082229 | ||||||
chr11:18082444
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-941T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082444 | ||||||
chr11:18082476
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1240-973A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082476 | ||||||
chr11:18082518
|
T | TTAAATTA others(29): Show |
1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+1016_1240-101 others(40): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082518 | ||||||
chr11:18082544
|
A | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+991T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082544 | ||||||
chr11:18082547
|
A | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+988T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082547 | ||||||
chr11:18082589
|
G | A | 9 | a0004c0004t0001g0017a0004c0004t0001g0018a0004c0004t0001g0027others(6): Show | 14 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1239+946C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082589 | ||||||
chr11:18082781
|
G | A | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1239+754C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082781 | ||||||
chr11:18082876
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+659G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082876 | ||||||
chr11:18082907
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1239+628T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18082907 | ||||||
chr11:18083084
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1239+451T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083084 | ||||||
chr11:18083124
|
G | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(68): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1239+411C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083124 | ||||||
chr11:18083178
|
G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+357C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083178 | ||||||
chr11:18083197
|
TA | T | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1239+337delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083197 | ||||||
chr11:18083353
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+182C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083353 | ||||||
chr11:18083396
|
A | G | 1 | a0006c0006t0001g0062 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1239+139T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083396 | ||||||
chr11:18083439
|
A | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1239+96T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083439 | ||||||
chr11:18083480
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1239+55C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 10/11 | chr11 | 18083480 | ||||||
chr11:18083755
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1043-24A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18083755 | ||||||
chr11:18083793
|
T | C | 4 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0081others(1): Show | 8 | HG00423.hp1 HG02129.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1043-62A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18083793 | ||||||
chr11:18084101
|
C | A | 1 | a0003c0003t0001g0039 | 2 | HG02055.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1043-370G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084101 | ||||||
chr11:18084179
|
G | T | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1043-448C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084179 | ||||||
chr11:18084324
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1043-593G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084324 | ||||||
chr11:18084350
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0075 | 5 | HG02083.hp2 NA18983.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.1043-619T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084350 | ||||||
chr11:18084357
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(23): Show | 54 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.1043-626G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084357 | ||||||
chr11:18084493
|
T | C | 1 | a0003c0003t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1043-762A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084493 | ||||||
chr11:18084522
|
C | T | 16 | a0001c0016t0001g0119a0002c0002t0001g0002a0002c0002t0001g0024others(13): Show | 35 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.1043-791G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084522 | ||||||
chr11:18084544
|
A | C | 1 | a0002c0002t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1043-813T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084544 | ||||||
chr11:18084608
|
C | T | 1 | a0003c0003t0001g0012 | 5 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.1043-877G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084608 | ||||||
chr11:18084638
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0036others(5): Show | 21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1043-907T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084638 | ||||||
chr11:18084669
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-938G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084669 | ||||||
chr11:18084780
|
G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1049C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084780 | ||||||
chr11:18084815
|
G | C | 21 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0078others(18): Show | 41 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1043-1084C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084815 | ||||||
chr11:18084864
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1043-1133G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084864 | ||||||
chr11:18084955
|
A | G | 1 | a0005c0005t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1043-1224T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18084955 | ||||||
chr11:18085013
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1282C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085013 | ||||||
chr11:18085050
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1043-1319C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085050 | ||||||
chr11:18085141
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1410C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085141 | ||||||
chr11:18085184
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1043-1453G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085184 | ||||||
chr11:18085187
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1043-1456A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085187 | ||||||
chr11:18085202
|
G | C | 1 | a0002c0002t0001g0043 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1043-1471C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085202 | ||||||
chr11:18085383
|
T | C | 72 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(69): Show | 154 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1042+1483A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085383 | ||||||
chr11:18085437
|
AT | A | 66 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(63): Show | 144 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.1042+1428delA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085437 | ||||||
chr11:18085476
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+1390G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085476 | ||||||
chr11:18085560
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+1306C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085560 | ||||||
chr11:18085657
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+1209C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085657 | ||||||
chr11:18085718
|
T | C | 2 | a0004c0004t0001g0068a0004c0004t0001g0069 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1042+1148A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085718 | ||||||
chr11:18085725
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1042+1141T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085725 | ||||||
chr11:18085940
|
T | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+926A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085940 | ||||||
chr11:18085967
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+899G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18085967 | ||||||
chr11:18086031
|
T | C | 1 | a0001c0001t0001g0035 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1042+835A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086031 | ||||||
chr11:18086215
|
C | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+651G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086215 | ||||||
chr11:18086381
|
A | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1042+485T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086381 | ||||||
chr11:18086415
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+451G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086415 | ||||||
chr11:18086516
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+350G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086516 | ||||||
chr11:18086524
|
A | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1042+342T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086524 | ||||||
chr11:18086527
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+339G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086527 | ||||||
chr11:18086608
|
C | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1042+258G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086608 | ||||||
chr11:18086653
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+213T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086653 | ||||||
chr11:18086676
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0078a0001c0001t0001g0079others(9): Show | 21 | HG01255.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1042+190C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086676 | ||||||
chr11:18086677
|
T | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+189A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086677 | ||||||
chr11:18086777
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+89C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086777 | ||||||
chr11:18086798
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1042+68T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 9/11 | chr11 | 18086798 | ||||||
chr11:18087138
|
C | A | 1 | a0003c0003t0001g0113 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.853+5G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 8/11 | chr11 | 18087138 | ||||||
chr11:18087317
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.771-92G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087317 | ||||||
chr11:18087468
|
A | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-243T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087468 | ||||||
chr11:18087510
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-285T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087510 | ||||||
chr11:18087512
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.771-287G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087512 | ||||||
chr11:18087524
|
T | G | 1 | a0003c0003t0001g0012 | 5 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(2): Show |
intron_variant | MODIFIER | c.771-299A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087524 | ||||||
chr11:18087606
|
G | A | 1 | a0011c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.771-381C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087606 | ||||||
chr11:18087606
|
G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-381C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087606 | ||||||
chr11:18087761
|
A | G | 4 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(1): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.771-536T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087761 | ||||||
chr11:18087796
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0036others(5): Show | 21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.771-571C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087796 | ||||||
chr11:18087888
|
A | G | 1 | a0006c0006t0001g0065 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.771-663T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087888 | ||||||
chr11:18087893
|
C | G | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.771-668G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087893 | ||||||
chr11:18087928
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-703C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18087928 | ||||||
chr11:18088084
|
A | G | 1 | a0002c0002t0001g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.771-859T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088084 | ||||||
chr11:18088136
|
C | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771-911G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088136 | ||||||
chr11:18088136
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.771-911G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088136 | ||||||
chr11:18088148
|
A | G | 1 | a0008c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.771-923T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088148 | ||||||
chr11:18088436
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+894A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088436 | ||||||
chr11:18088459
|
T | C | 1 | a0002c0002t0001g0022 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.770+871A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088459 | ||||||
chr11:18088562
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0108 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.770+768G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088562 | ||||||
chr11:18088592
|
T | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(68): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.770+738A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088592 | ||||||
chr11:18088720
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+610C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088720 | ||||||
chr11:18088797
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+533C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088797 | ||||||
chr11:18088887
|
A | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0036others(5): Show | 21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.770+443T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088887 | ||||||
chr11:18088906
|
T | C | 1 | a0008c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.770+424A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088906 | ||||||
chr11:18088934
|
C | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0108others(1): Show | 9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+396G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088934 | ||||||
chr11:18088956
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+374T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18088956 | ||||||
chr11:18089095
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.770+235C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089095 | ||||||
chr11:18089216
|
G | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+114C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089216 | ||||||
chr11:18089241
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.770+89A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089241 | ||||||
chr11:18089289
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.770+41A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 7/11 | chr11 | 18089289 | ||||||
chr11:18089531
|
A | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.590-21T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089531 | ||||||
chr11:18089592
|
T | G | 6 | a0006c0006t0001g0014a0006c0006t0001g0026a0006c0006t0001g0062others(3): Show | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.590-82A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089592 | ||||||
chr11:18089670
|
C | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.590-160G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089670 | ||||||
chr11:18089699
|
C | T | 1 | a0006c0006t0001g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.590-189G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089699 | ||||||
chr11:18089794
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.590-284G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089794 | ||||||
chr11:18089841
|
C | T | 1 | a0001c0001t0001g0031 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.590-331G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089841 | ||||||
chr11:18089927
|
A | G | 4 | a0002c0002t0001g0024a0002c0002t0001g0055a0002c0002t0001g0056others(1): Show | 5 | HG00280.hp2 HG01081.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.589+248T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089927 | ||||||
chr11:18089970
|
A | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.589+205T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089970 | ||||||
chr11:18089971
|
T | C | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.589+204A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18089971 | ||||||
chr11:18090084
|
T | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.589+91A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18090084 | ||||||
chr11:18090145
|
A | AT | 64 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 135 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.589+29dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18090145 | ||||||
chr11:18090145
|
A | ATT | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.589+28_589+29dupAA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 6/11 | chr11 | 18090145 | ||||||
chr11:18090325
|
C | CA | 4 | a0001c0001t0001g0010a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 8 | HG01255.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.474-36dupT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090325 | ||||||
chr11:18090325
|
CA | C | 5 | a0001c0001t0001g0020a0002c0002t0001g0044a0002c0002t0001g0045others(2): Show | 7 | HG01099.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-36delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090325 | ||||||
chr11:18090326
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.474-36T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090326 | ||||||
chr11:18090417
|
T | TAAAAGGA others(23): Show |
1 | a0011c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.460_473+16dupCTGGA others(25): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 5/11 | chr11 | 18090417 | ||||||
chr11:18090515
|
C | T | 6 | a0006c0006t0001g0014a0006c0006t0001g0026a0006c0006t0001g0062others(3): Show | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.414-22G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090515 | ||||||
chr11:18090650
|
C | T | 9 | a0003c0003t0001g0009a0003c0003t0001g0012a0003c0003t0001g0037others(6): Show | 21 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.414-157G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090650 | ||||||
chr11:18090659
|
G | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.414-166C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090659 | ||||||
chr11:18090779
|
T | C | 1 | a0003c0003t0001g0114 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414-286A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18090779 | ||||||
chr11:18091137
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.414-644G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091137 | ||||||
chr11:18091137
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-644G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091137 | ||||||
chr11:18091226
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0044a0002c0002t0001g0045 | 4 | NA18981.hp1 NA19009.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-733A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091226 | ||||||
chr11:18091235
|
G | C | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.414-742C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091235 | ||||||
chr11:18091253
|
A | ACTATT | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.414-761_414-760ins others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091253 | ||||||
chr11:18091318
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-825G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091318 | ||||||
chr11:18091329
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-836G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091329 | ||||||
chr11:18091781
|
T | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.413+464A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091781 | ||||||
chr11:18091802
|
G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413+443C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091802 | ||||||
chr11:18091908
|
G | A | 3 | a0004c0004t0001g0017a0004c0004t0001g0066a0004c0004t0001g0067 | 5 | HG02615.hp1 HG02965.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+337C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18091908 | ||||||
chr11:18092071
|
G | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413+174C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18092071 | ||||||
chr11:18092114
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.413+131T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18092114 | ||||||
chr11:18092116
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+129A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 4/11 | chr11 | 18092116 | ||||||
chr11:18092406
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-82C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092406 | ||||||
chr11:18092653
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-329C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092653 | ||||||
chr11:18092891
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-567C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092891 | ||||||
chr11:18092960
|
T | TAAAAGTA others(303): Show |
1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-637_334-636ins others(310): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092960 | ||||||
chr11:18092991
|
A | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-667T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092991 | ||||||
chr11:18092992
|
A | C | 1 | a0011c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.334-668T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18092992 | ||||||
chr11:18093000
|
T | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.334-676A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093000 | ||||||
chr11:18093032
|
G | A | 34 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(31): Show | 71 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.334-708C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093032 | ||||||
chr11:18093087
|
T | A | 4 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(1): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.334-763A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093087 | ||||||
chr11:18093099
|
G | A | 71 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(68): Show | 153 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.334-775C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093099 | ||||||
chr11:18093147
|
G | A | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-823C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093147 | ||||||
chr11:18093153
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0078others(17): Show | 40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.334-829G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093153 | ||||||
chr11:18093154
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-830C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093154 | ||||||
chr11:18093157
|
A | G | 60 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.334-833T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093157 | ||||||
chr11:18093170
|
C | T | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-846G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093170 | ||||||
chr11:18093250
|
A | T | 1 | a0001c0001t0001g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.334-926T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093250 | ||||||
chr11:18093329
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-1005A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093329 | ||||||
chr11:18093463
|
C | A | 1 | a0011c0019t0001g0121 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.334-1139G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093463 | ||||||
chr11:18093574
|
G | T | 60 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.334-1250C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093574 | ||||||
chr11:18093619
|
T | C | 4 | a0001c0001t0001g0007a0004c0004t0001g0017a0004c0004t0001g0066others(1): Show | 13 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.334-1295A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093619 | ||||||
chr11:18093669
|
G | A | 1 | a0002c0002t0001g0054 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.334-1345C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093669 | ||||||
chr11:18093720
|
C | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-1396G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18093720 | ||||||
chr11:18094073
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0073others(4): Show | 19 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.334-1749A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094073 | ||||||
chr11:18094106
|
TTTCCAGG others(13): Show |
T | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.334-1802_334-1783d others(22): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094106 | ||||||
chr11:18094210
|
A | G | 1 | a0008c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.334-1886T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094210 | ||||||
chr11:18094278
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0108others(1): Show | 9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-1954A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094278 | ||||||
chr11:18094464
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-2140C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094464 | ||||||
chr11:18094526
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.334-2202C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094526 | ||||||
chr11:18094567
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+2204T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094567 | ||||||
chr11:18094603
|
T | C | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+2168A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094603 | ||||||
chr11:18094631
|
T | C | 1 | a0005c0005t0001g0059 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.333+2140A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094631 | ||||||
chr11:18094689
|
A | C | 1 | a0002c0002t0001g0050 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.333+2082T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094689 | ||||||
chr11:18094725
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.333+2046G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094725 | ||||||
chr11:18094749
|
G | A | 6 | a0006c0006t0001g0014a0006c0006t0001g0026a0006c0006t0001g0062others(3): Show | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.333+2022C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094749 | ||||||
chr11:18094913
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1858C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094913 | ||||||
chr11:18094913
|
G | C | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.333+1858C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094913 | ||||||
chr11:18094955
|
C | T | 1 | a0004c0004t0001g0018 | 3 | HG02109.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.333+1816G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094955 | ||||||
chr11:18094956
|
T | C | 1 | a0001c0001t0001g0021 | 3 | HG00735.hp1 HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.333+1815A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18094956 | ||||||
chr11:18095106
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1665C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095106 | ||||||
chr11:18095159
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1612G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095159 | ||||||
chr11:18095168
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1603A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095168 | ||||||
chr11:18095210
|
G | A | 1 | a0001c0007t0001g0071 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.333+1561C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095210 | ||||||
chr11:18095220
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1551C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095220 | ||||||
chr11:18095331
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+1440A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095331 | ||||||
chr11:18095333
|
A | C | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.333+1438T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095333 | ||||||
chr11:18095347
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.333+1424T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095347 | ||||||
chr11:18095386
|
G | A | 13 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(10): Show | 24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.333+1385C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095386 | ||||||
chr11:18095463
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.333+1308G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095463 | ||||||
chr11:18095530
|
A | G | 1 | a0008c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.333+1241T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095530 | ||||||
chr11:18095622
|
C | T | 1 | a0006c0006t0001g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.333+1149G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095622 | ||||||
chr11:18095701
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0073a0001c0001t0001g0074others(1): Show | 12 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.333+1070A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095701 | ||||||
chr11:18095815
|
A | G | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+956T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095815 | ||||||
chr11:18095855
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+916C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095855 | ||||||
chr11:18095947
|
G | A | 1 | a0006c0006t0001g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.333+824C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095947 | ||||||
chr11:18095969
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0078others(17): Show | 40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.333+802G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095969 | ||||||
chr11:18095998
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+773T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18095998 | ||||||
chr11:18096011
|
G | A | 9 | a0003c0003t0001g0009a0003c0003t0001g0012a0003c0003t0001g0037others(6): Show | 21 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.333+760C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096011 | ||||||
chr11:18096077
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+694A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096077 | ||||||
chr11:18096096
|
A | AGGGGGGG others(18): Show |
1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+674_333+675ins others(25): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096096 | ||||||
chr11:18096098
|
A | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+673T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096098 | ||||||
chr11:18096101
|
A | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+670T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096101 | ||||||
chr11:18096102
|
A | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+669T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096102 | ||||||
chr11:18096103
|
T | G | 1 | a0003c0003t0001g0115 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.333+668A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096103 | ||||||
chr11:18096224
|
C | T | 1 | a0002c0002t0001g0055 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.333+547G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096224 | ||||||
chr11:18096250
|
T | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+521A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096250 | ||||||
chr11:18096274
|
A | G | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.333+497T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096274 | ||||||
chr11:18096281
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.333+490T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096281 | ||||||
chr11:18096318
|
G | A | 2 | a0001c0001t0001g0061a0001c0016t0001g0119 | 2 | HG02572.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.333+453C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096318 | ||||||
chr11:18096329
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0090 | 6 | NA18963.hp1 NA19011.hp2 NA19057.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+442G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096329 | ||||||
chr11:18096334
|
C | A | 1 | a0003c0003t0001g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.333+437G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096334 | ||||||
chr11:18096353
|
G | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+418C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096353 | ||||||
chr11:18096463
|
C | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.333+308G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096463 | ||||||
chr11:18096532
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0078others(17): Show | 40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.333+239C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096532 | ||||||
chr11:18096575
|
C | A | 1 | a0001c0018t0001g0084 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.333+196G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096575 | ||||||
chr11:18096599
|
T | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.333+172A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096599 | ||||||
chr11:18096615
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.333+156T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 3/11 | chr11 | 18096615 | ||||||
chr11:18096906
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.250-52G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096906 | ||||||
chr11:18096915
|
C | T | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250-61G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096915 | ||||||
chr11:18096953
|
A | G | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.250-99T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096953 | ||||||
chr11:18096954
|
C | T | 5 | a0002c0002t0001g0024a0002c0002t0001g0049a0002c0002t0001g0055others(2): Show | 6 | HG00280.hp2 HG01081.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.250-100G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096954 | ||||||
chr11:18096961
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0073others(4): Show | 19 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-107G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096961 | ||||||
chr11:18096991
|
A | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.250-137T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18096991 | ||||||
chr11:18097092
|
C | A | 7 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0073others(4): Show | 19 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.250-238G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097092 | ||||||
chr11:18097094
|
G | A | 4 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(1): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-240C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097094 | ||||||
chr11:18097132
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(38): Show | 85 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.250-278C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097132 | ||||||
chr11:18097177
|
C | T | 15 | a0003c0003t0001g0009a0003c0003t0001g0012a0003c0003t0001g0013others(12): Show | 31 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.250-323G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097177 | ||||||
chr11:18097266
|
A | G | 5 | a0001c0001t0001g0010a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 9 | HG01255.hp1 HG02451.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.250-412T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097266 | ||||||
chr11:18097343
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0036others(5): Show | 21 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.250-489A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097343 | ||||||
chr11:18097684
|
C | T | 1 | a0003c0003t0001g0112 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.250-830G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097684 | ||||||
chr11:18097773
|
A | G | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.250-919T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097773 | ||||||
chr11:18097826
|
C | G | 2 | a0001c0001t0001g0007a0001c0016t0001g0119 | 9 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-972G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097826 | ||||||
chr11:18097838
|
GA | G | 59 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 122 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(119): Show |
intron_variant | MODIFIER | c.250-985delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097838 | ||||||
chr11:18097838
|
GAA | G | 10 | a0001c0001t0001g0108a0003c0003t0001g0009a0003c0003t0001g0012others(7): Show | 22 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-986_250-985del others(2): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097838 | ||||||
chr11:18097851
|
A | C | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.250-997T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097851 | ||||||
chr11:18097872
|
AGGT | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.250-1021_250-1019d others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097872 | ||||||
chr11:18097894
|
T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-1040A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097894 | ||||||
chr11:18097963
|
T | C | 13 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(10): Show | 24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.250-1109A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097963 | ||||||
chr11:18097983
|
A | C | 6 | a0006c0006t0001g0014a0006c0006t0001g0026a0006c0006t0001g0062others(3): Show | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.250-1129T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18097983 | ||||||
chr11:18098199
|
G | C | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.250-1345C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098199 | ||||||
chr11:18098202
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.250-1348T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098202 | ||||||
chr11:18098337
|
C | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(25): Show | 61 | HG00099.hp2 HG00323.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.250-1483G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098337 | ||||||
chr11:18098341
|
A | G | 1 | a0003c0003t0001g0111 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.250-1487T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098341 | ||||||
chr11:18098348
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.250-1494C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098348 | ||||||
chr11:18098447
|
C | A | 1 | a0002c0002t0001g0046 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.250-1593G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098447 | ||||||
chr11:18098605
|
G | A | 1 | a0004c0004t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.250-1751C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098605 | ||||||
chr11:18098661
|
G | A | 1 | a0001c0001t0001g0034 | 2 | HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.250-1807C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098661 | ||||||
chr11:18098789
|
C | A | 1 | a0001c0001t0001g0036 | 2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.250-1935G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098789 | ||||||
chr11:18098969
|
T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-2115A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18098969 | ||||||
chr11:18099079
|
C | CAT | 65 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0010others(62): Show | 143 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.250-2227_250-2226d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099079 | ||||||
chr11:18099100
|
T | C | 22 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(19): Show | 48 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.250-2246A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099100 | ||||||
chr11:18099278
|
C | A | 2 | a0004c0004t0001g0017a0004c0004t0001g0066 | 4 | HG02965.hp1 HG02976.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-2424G>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099278 | ||||||
chr11:18099325
|
T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-2471A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099325 | ||||||
chr11:18099371
|
T | C | 4 | a0002c0002t0001g0024a0002c0002t0001g0055a0002c0002t0001g0056others(1): Show | 5 | HG00280.hp2 HG01081.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.250-2517A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099371 | ||||||
chr11:18099537
|
C | T | 1 | a0001c0001t0001g0015 | 4 | HG02132.hp2 NA18963.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-2683G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099537 | ||||||
chr11:18099547
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.250-2693A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099547 | ||||||
chr11:18099601
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.250-2747C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099601 | ||||||
chr11:18099721
|
GACATTGA others(1): Show |
G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.250-2875_250-2868d others(10): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099721 | ||||||
chr11:18099745
|
A | G | 1 | a0004c0004t0001g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-2891T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099745 | ||||||
chr11:18099943
|
G | A | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.250-3089C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099943 | ||||||
chr11:18099992
|
G | A | 12 | a0002c0002t0001g0002a0002c0002t0001g0024a0002c0002t0001g0048others(9): Show | 28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.250-3138C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18099992 | ||||||
chr11:18100006
|
A | G | 1 | a0002c0002t0001g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.250-3152T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100006 | ||||||
chr11:18100047
|
G | A | 1 | a0001c0007t0001g0072 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+3186C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100047 | ||||||
chr11:18100402
|
A | G | 1 | a0002c0002t0001g0022 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.249+2831T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100402 | ||||||
chr11:18100452
|
G | A | 1 | a0004c0004t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.249+2781C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100452 | ||||||
chr11:18100888
|
A | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+2345T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100888 | ||||||
chr11:18100958
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.249+2275T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18100958 | ||||||
chr11:18101000
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.249+2233G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101000 | ||||||
chr11:18101252
|
C | CGT | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+1979_249+1980d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101252 | ||||||
chr11:18101253
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+1980C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101253 | ||||||
chr11:18101351
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.249+1882C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101351 | ||||||
chr11:18101379
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+1854G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101379 | ||||||
chr11:18101384
|
G | A | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.249+1849C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101384 | ||||||
chr11:18101450
|
G | A | 12 | a0002c0002t0001g0002a0002c0002t0001g0024a0002c0002t0001g0048others(9): Show | 28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.249+1783C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101450 | ||||||
chr11:18101467
|
C | T | 12 | a0002c0002t0001g0002a0002c0002t0001g0024a0002c0002t0001g0048others(9): Show | 28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.249+1766G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101467 | ||||||
chr11:18101506
|
C | T | 8 | a0004c0004t0001g0017a0004c0004t0001g0018a0004c0004t0001g0027others(5): Show | 13 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+1727G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101506 | ||||||
chr11:18101530
|
T | C | 4 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(1): Show | 10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+1703A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101530 | ||||||
chr11:18101579
|
A | G | 1 | a0004c0004t0001g0027 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.249+1654T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101579 | ||||||
chr11:18101820
|
TAA | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0036others(56): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.249+1411_249+1412d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101820 | ||||||
chr11:18101820
|
TAAA | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 9 | HG02257.hp2 HG02258.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.249+1410_249+1412d others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101820 | ||||||
chr11:18101857
|
GGAT | G | 21 | a0002c0002t0001g0002a0002c0002t0001g0004a0002c0002t0001g0022others(18): Show | 47 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.249+1373_249+1375d others(5): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18101857 | ||||||
chr11:18102005
|
G | A | 1 | a0003c0003t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+1228C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102005 | ||||||
chr11:18102045
|
C | T | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+1188G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102045 | ||||||
chr11:18102083
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0061a0001c0001t0001g0085others(1): Show | 14 | HG00408.hp2 HG00438.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.249+1150T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102083 | ||||||
chr11:18102127
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.249+1106A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102127 | ||||||
chr11:18102167
|
C | T | 1 | a0005c0005t0001g0058 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.249+1066G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102167 | ||||||
chr11:18102171
|
GA | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0083a0001c0018t0001g0084 | 4 | HG01257.hp1 HG01258.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.249+1061delT | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102171 | ||||||
chr11:18102179
|
A | C | 6 | a0006c0006t0001g0014a0006c0006t0001g0026a0006c0006t0001g0062others(3): Show | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+1054T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102179 | ||||||
chr11:18102212
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.249+1021C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102212 | ||||||
chr11:18102239
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+994A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102239 | ||||||
chr11:18102261
|
G | A | 1 | a0008c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.249+972C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102261 | ||||||
chr11:18102271
|
T | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+962A>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102271 | ||||||
chr11:18102299
|
C | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(60): Show | 133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.249+934G>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102299 | ||||||
chr11:18102313
|
A | C | 1 | a0003c0003t0001g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.249+920T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102313 | ||||||
chr11:18102333
|
C | T | 1 | a0008c0011t0001g0025 | 2 | NA18948.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.249+900G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102333 | ||||||
chr11:18102356
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0073others(39): Show | 91 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.249+877G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102356 | ||||||
chr11:18102446
|
G | GT | 21 | a0001c0001t0001g0010a0001c0001t0001g0036a0001c0001t0001g0077others(18): Show | 42 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.249+786dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102446 | ||||||
chr11:18102562
|
A | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+671T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102562 | ||||||
chr11:18102572
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.249+661C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102572 | ||||||
chr11:18102575
|
T | TG | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.249+657dupC | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102575 | ||||||
chr11:18102940
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.249+293G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18102940 | ||||||
chr11:18103002
|
T | A | 1 | a0004c0004t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.249+231A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18103002 | ||||||
chr11:18103177
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.249+56A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 2/11 | chr11 | 18103177 | ||||||
chr11:18103441
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.136-95C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103441 | ||||||
chr11:18103497
|
T | C | 1 | a0001c0001t0001g0035 | 2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.136-151A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103497 | ||||||
chr11:18103571
|
A | C | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.136-225T>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103571 | ||||||
chr11:18103585
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.136-239C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103585 | ||||||
chr11:18103696
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.136-350G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103696 | ||||||
chr11:18103905
|
A | T | 1 | a0002c0002t0001g0041 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.136-559T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18103905 | ||||||
chr11:18104126
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.136-780A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104126 | ||||||
chr11:18104347
|
A | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0108others(1): Show | 9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1001T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104347 | ||||||
chr11:18104390
|
A | T | 1 | a0012c0014t0001g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.136-1044T>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104390 | ||||||
chr11:18104401
|
T | C | 12 | a0002c0002t0001g0002a0002c0002t0001g0024a0002c0002t0001g0048others(9): Show | 28 | HG00280.hp2 HG00738.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-1055A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104401 | ||||||
chr11:18104440
|
C | CT | 56 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(53): Show | 122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.136-1095dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104440 | ||||||
chr11:18104440
|
C | CTT | 4 | a0004c0004t0001g0018a0004c0004t0001g0068a0004c0004t0001g0069others(1): Show | 6 | HG01891.hp1 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-1096_136-1095d others(4): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104440 | ||||||
chr11:18104550
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0108others(1): Show | 9 | HG02258.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-1204T>C | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104550 | ||||||
chr11:18104744
|
T | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0036others(55): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.135+1163A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104744 | ||||||
chr11:18104753
|
G | A | 1 | a0003c0003t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.135+1154C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104753 | ||||||
chr11:18104944
|
G | A | 60 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(57): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.135+963C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104944 | ||||||
chr11:18104947
|
G | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0011others(57): Show | 134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.135+960C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18104947 | ||||||
chr11:18105222
|
T | C | 1 | a0003c0003t0001g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.135+685A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105222 | ||||||
chr11:18105332
|
C | CT | 9 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0073others(6): Show | 21 | HG00733.hp1 HG01106.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+574dupA | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105332 | ||||||
chr11:18105332
|
CTT | C | 5 | a0001c0001t0001g0007a0006c0006t0001g0014a0006c0006t0001g0064others(2): Show | 16 | HG00639.hp1 HG01081.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.135+573_135+574del others(2): Show |
SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105332 | ||||||
chr11:18105359
|
G | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0108others(16): Show | 40 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.135+548C>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105359 | ||||||
chr11:18105385
|
G | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.135+522C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105385 | ||||||
chr11:18105454
|
TG | T | 12 | a0001c0007t0001g0008a0001c0007t0001g0071a0001c0007t0001g0072others(9): Show | 23 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.135+452delC | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105454 | ||||||
chr11:18105671
|
T | C | 1 | a0001c0001t0001g0007 | 8 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+236A>G | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105671 | ||||||
chr11:18105705
|
T | A | 1 | a0001c0016t0001g0119 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.135+202A>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105705 | ||||||
chr11:18105723
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.135+184C>T | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105723 | ||||||
chr11:18105724
|
G | T | 6 | a0006c0006t0001g0014a0006c0006t0001g0026a0006c0006t0001g0062others(3): Show | 10 | HG01081.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+183C>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105724 | ||||||
chr11:18105762
|
C | T | 2 | a0001c0001t0001g0007a0008c0011t0001g0025 | 10 | HG00639.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+145G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105762 | ||||||
chr11:18105885
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.135+22G>A | SAAL1 | ENSG00000166788.10 | transcript | ENST00000524803.6 | protein_coding | 1/11 | chr11 | 18105885 |