geneid | 115209 |
---|---|
ensemblid | ENSG00000162600.12 |
hgncid | 29661 |
symbol | OMA1 |
name | OMA1 zinc metallopeptidase |
refseq_nuc | NM_145243.5 |
refseq_prot | NP_660286.1 |
ensembl_nuc | ENST00000371226.8 |
ensembl_prot | ENSP00000360270.3 |
mane_status | MANE Select |
chr | chr1 |
start | 58480719 |
end | 58546726 |
strand | - |
ver | v1.2 |
region | chr1:58480719-58546726 |
region5000 | chr1:58475719-58551726 |
regionname0 | OMA1_chr1_58480719_58546726 |
regionname5000 | OMA1_chr1_58475719_58551726 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 524 | 294 | 57 | 61 | 126 | 15 | 33 | 91 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0002 | 0/0 | 524 | 31 | 0 | 2 | 27 | 0 | 2 | 24 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0003 | 0/0 | 524 | 29 | 18 | 5 | 0 | 1 | 5 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004 | 0/0 | 524 | 15 | 11 | 4 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0005 | 0/0 | 524 | 7 | 2 | 4 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0006 | 0/0 | 524 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0007 | 0/0 | 524 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0008 | 0/0 | 524 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0009 | 0/0 | 524 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0010 | 0/0 | 524 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1575 | 258 | 51 | 54 | 115 | 10 | 26 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0002 | 0/0 | 1575 | 35 | 6 | 6 | 11 | 5 | 7 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0003 | 0/0 | 1575 | 31 | 0 | 2 | 27 | 0 | 2 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0004 | 0/0 | 1575 | 29 | 18 | 5 | 0 | 1 | 5 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0005 | 0/0 | 1575 | 12 | 8 | 4 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0006 | 0/0 | 1575 | 7 | 2 | 4 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0007 | 0/0 | 1575 | 4 | 0 | 0 | 4 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0008 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0009 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0010 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0011 | 0/0 | 1575 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0012 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
c0013 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
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 | 0/1 | 287 | 306 | 57 | 63 | 140 | 11 | 34 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
t0002 | 0/0 | 288 | 51 | 17 | 9 | 12 | 5 | 8 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
t0003 | 1/0 | 287 | 15 | 12 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
t0004 | 0/0 | 287 | 6 | 0 | 0 | 6 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
t0005 | 0/0 | 287 | 4 | 3 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
t0006 | 0/0 | 287 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
t0007 | 0/0 | 287 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1575 | 258 | 51 | 54 | 115 | 10 | 26 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0002 | 0/0 | 1575 | 35 | 6 | 6 | 11 | 5 | 7 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0012 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0002c0003 | 0/0 | 1575 | 31 | 0 | 2 | 27 | 0 | 2 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0003c0004 | 0/0 | 1575 | 29 | 18 | 5 | 0 | 1 | 5 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004c0005 | 0/0 | 1575 | 12 | 8 | 4 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004c0008 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0005c0006 | 0/0 | 1575 | 7 | 2 | 4 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0006c0007 | 0/0 | 1575 | 4 | 0 | 0 | 4 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0007c0011 | 0/0 | 1575 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0008c0013 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0009c0010 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0010c0009 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1861 | 229 | 32 | 51 | 109 | 10 | 26 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0001t0002 | 0/0 | 1862 | 3 | 3 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0001t0003 | 1/0 | 1861 | 15 | 12 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0001t0004 | 0/0 | 1861 | 6 | 0 | 0 | 6 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0001t0005 | 0/0 | 1861 | 4 | 3 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0001t0007 | 0/0 | 1861 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0002t0002 | 0/0 | 1862 | 35 | 6 | 6 | 11 | 5 | 7 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0001c0012t0002 | 0/0 | 1862 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0002c0003t0001 | 0/0 | 1861 | 30 | 0 | 2 | 26 | 0 | 2 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0002c0003t0002 | 0/0 | 1862 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0003c0004t0001 | 0/0 | 1861 | 29 | 18 | 5 | 0 | 1 | 5 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004c0005t0001 | 0/0 | 1861 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004c0005t0002 | 0/0 | 1862 | 10 | 8 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004c0005t0006 | 0/0 | 1861 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0004c0008t0001 | 0/0 | 1861 | 3 | 3 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0005c0006t0001 | 0/0 | 1861 | 7 | 2 | 4 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0006c0007t0001 | 0/0 | 1861 | 4 | 0 | 0 | 4 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0007c0011t0002 | 0/0 | 1862 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0008c0013t0001 | 0/0 | 1861 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0009c0010t0001 | 0/0 | 1861 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
a0010c0009t0001 | 0/0 | 1861 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | copy fasta | chr1 | 58475719 | 58551726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0001t0007g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0001c0012t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0002c0003t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0003c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0005t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0008t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0008t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0004c0008t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0005c0006t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0005c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0005c0006t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0005c0006t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0005c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0005c0006t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0006c0007t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0006c0007t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0006c0007t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0006c0007t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0007c0011t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0008c0013t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0009c0010t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
a0010c0009t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0004 | t0001 | g0052 | EUR | GBR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0280 | EUR | GBR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0110 | EUR | GBR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | FIN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0358 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00544 | hp1 | a0006 | c0007 | t0001 | g0287 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0373 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00642 | hp1 | a0002 | c0003 | t0001 | g0369 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00642 | hp2 | a0003 | c0004 | t0001 | g0051 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00735 | hp2 | a0003 | c0004 | t0001 | g0055 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00738 | hp1 | a0001 | c0012 | t0002 | g0077 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01069 | hp2 | a0005 | c0006 | t0001 | g0005 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01071 | hp1 | a0005 | c0006 | t0001 | g0005 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01074 | hp2 | a0004 | c0005 | t0002 | g0012 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01081 | hp1 | a0004 | c0005 | t0002 | g0014 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01109 | hp2 | a0004 | c0005 | t0006 | g0013 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01175 | hp1 | a0002 | c0003 | t0001 | g0370 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01243 | hp1 | a0004 | c0005 | t0001 | g0023 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01256 | hp1 | a0005 | c0006 | t0001 | g0064 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01257 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01258 | hp1 | a0003 | c0004 | t0001 | g0003 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01258 | hp2 | a0005 | c0006 | t0001 | g0066 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01496 | hp1 | a0003 | c0004 | t0001 | g0058 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0112 | EUR | IBS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0079 | EUR | IBS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | IBS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | IBS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0111 | EUR | IBS | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01891 | hp1 | a0004 | c0005 | t0002 | g0024 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0113 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0062 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02129 | hp2 | a0001 | c0001 | t0004 | g0344 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02132 | hp1 | a0006 | c0007 | t0001 | g0265 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02145 | hp1 | a0010 | c0009 | t0001 | g0115 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02145 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CDX | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | CDX | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0068 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02258 | hp2 | a0004 | c0005 | t0002 | g0016 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0073 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02572 | hp2 | a0008 | c0013 | t0001 | g0054 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02615 | hp1 | a0003 | c0004 | t0001 | g0057 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02622 | hp1 | a0003 | c0004 | t0001 | g0065 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02647 | hp1 | a0003 | c0004 | t0001 | g0059 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02717 | hp1 | a0003 | c0004 | t0001 | g0071 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02723 | hp2 | a0005 | c0006 | t0001 | g0063 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02735 | hp1 | a0005 | c0006 | t0001 | g0069 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02809 | hp1 | a0003 | c0004 | t0001 | g0061 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02809 | hp2 | a0005 | c0006 | t0001 | g0074 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02818 | hp2 | a0003 | c0004 | t0001 | g0050 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02886 | hp1 | a0004 | c0008 | t0001 | g0022 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0107 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02896 | hp1 | a0004 | c0005 | t0002 | g0001 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02896 | hp2 | a0004 | c0008 | t0001 | g0017 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02897 | hp1 | a0004 | c0005 | t0002 | g0001 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02965 | hp2 | a0003 | c0004 | t0001 | g0049 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0376 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03041 | hp1 | a0003 | c0004 | t0001 | g0060 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03130 | hp1 | a0004 | c0005 | t0002 | g0018 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03195 | hp1 | a0003 | c0004 | t0001 | g0056 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0095 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03239 | hp1 | a0007 | c0011 | t0002 | g0048 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03239 | hp2 | a0003 | c0004 | t0001 | g0053 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0105 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03490 | hp1 | a0003 | c0004 | t0001 | g0004 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03492 | hp2 | a0003 | c0004 | t0001 | g0004 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03516 | hp2 | a0004 | c0008 | t0001 | g0021 | AFR | ESN | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03654 | hp2 | a0003 | c0004 | t0001 | g0076 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03834 | hp2 | a0003 | c0004 | t0001 | g0075 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0341 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0098 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0346 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0091 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0078 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18522 | hp1 | a0003 | c0004 | t0001 | g0067 | AFR | YRI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0361 | EAS | CHB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0070 | AFR | YRI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0356 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0364 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18948 | hp1 | a0006 | c0007 | t0001 | g0326 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0357 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0365 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18956 | hp2 | a0002 | c0003 | t0001 | g0375 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0371 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0363 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0368 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0374 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18970 | hp2 | a0002 | c0003 | t0001 | g0354 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18972 | hp1 | a0002 | c0003 | t0001 | g0362 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0355 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18975 | hp2 | a0002 | c0003 | t0002 | g0353 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18982 | hp2 | a0002 | c0003 | t0001 | g0347 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18983 | hp1 | a0002 | c0003 | t0001 | g0350 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18985 | hp2 | a0002 | c0003 | t0001 | g0366 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19004 | hp2 | a0006 | c0007 | t0001 | g0235 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19043 | hp2 | a0003 | c0004 | t0001 | g0106 | AFR | LWK | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19054 | hp2 | a0002 | c0003 | t0001 | g0352 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19056 | hp1 | a0002 | c0003 | t0001 | g0349 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0351 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19063 | hp1 | a0002 | c0003 | t0001 | g0348 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19075 | hp1 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19078 | hp1 | a0002 | c0003 | t0001 | g0372 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0367 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19086 | hp1 | a0009 | c0010 | t0001 | g0193 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19086 | hp2 | a0002 | c0003 | t0001 | g0360 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0359 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | YRI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ASW | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20129 | hp2 | a0004 | c0005 | t0002 | g0015 | AFR | ASW | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0096 | EUR | TSI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0288 | EUR | TSI | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0345 | SAS | GIH | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0104 | SAS | GIH | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02109 | hp2 | a0004 | c0005 | t0002 | g0020 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ACB | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | USA | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20300 | hp1 | a0004 | c0005 | t0002 | g0019 | AFR | USA | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
NA21309 | hp2 | a0003 | c0004 | t0001 | g0072 | AFR | LWK | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0123 | REF | REF | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0031 | REF | REF | OMA1_chr1_58475719_58551726 | OMA1 | chr1 | 58475719 | 58551726 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58480968
|
A | C | 1 | a0007 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.1572T>G | p.Ser524Arg | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 9/9 | 1612/1861 | 1572/1575 | 524/524 | chr1 | 58480968 | ||
chr1:58506076
|
T | A | 1 | a0008 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1349A>T | p.Asp450Val | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/9 | 1389/1861 | 1349/1575 | 450/524 | chr1 | 58506076 | ||
chr1:58533979
|
T | G | 3 | a0003a0005a0008 | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
missense_variant | MODERATE | c.985A>C | p.Ile329Leu | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/9 | 1025/1861 | 985/1575 | 329/524 | chr1 | 58533979 | ||
chr1:58534181
|
T | C | 1 | a0006 | 4 | HG00544.hp1 HG02132.hp1 NA18948.hp1 others(1): Show |
missense_variant | MODERATE | c.880A>G | p.Ile294Val | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 4/9 | 920/1861 | 880/1575 | 294/524 | chr1 | 58534181 | ||
chr1:58534277
|
C | T | 1 | a0009 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.784G>A | p.Ala262Thr | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 4/9 | 824/1861 | 784/1575 | 262/524 | chr1 | 58534277 | ||
chr1:58536610
|
A | C | 2 | a0002a0010 | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
missense_variant | MODERATE | c.632T>G | p.Phe211Cys | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/9 | 672/1861 | 632/1575 | 211/524 | chr1 | 58536610 | ||
chr1:58538930
|
A | C | 1 | a0010 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.365T>G | p.Leu122Trp | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/9 | 405/1861 | 365/1575 | 122/524 | chr1 | 58538930 | ||
chr1:58538945
|
G | A | 1 | a0002 | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
missense_variant | MODERATE | c.350C>T | p.Pro117Leu | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/9 | 390/1861 | 350/1575 | 117/524 | chr1 | 58538945 | ||
chr1:58539090
|
G | A | 1 | a0005 | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
missense_variant | MODERATE | c.205C>T | p.His69Tyr | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/9 | 245/1861 | 205/1575 | 69/524 | chr1 | 58539090 | ||
chr1:58539094
|
G | T | 1 | a0004 | 15 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
missense_variant | MODERATE | c.201C>A | p.Asn67Lys | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/9 | 241/1861 | 201/1575 | 67/524 | chr1 | 58539094 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58506080
|
A | G | 1 | a0010c0009 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1345T>C | p.Leu449Leu | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/9 | 1385/1861 | 1345/1575 | 449/524 | chr1 | 58506080 | ||
chr1:58506159
|
G | A | 7 | a0001c0002a0001c0012a0003c0004others(4): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
synonymous_variant | LOW | c.1266C>T | p.Phe422Phe | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/9 | 1306/1861 | 1266/1575 | 422/524 | chr1 | 58506159 | ||
chr1:58534040
|
G | A | 1 | a0001c0012 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.924C>T | p.Phe308Phe | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/9 | 964/1861 | 924/1575 | 308/524 | chr1 | 58534040 | ||
chr1:58536549
|
T | C | 5 | a0002c0003a0003c0004a0005c0006others(2): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
synonymous_variant | LOW | c.693A>G | p.Glu231Glu | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/9 | 733/1861 | 693/1575 | 231/524 | chr1 | 58536549 | ||
chr1:58536647
|
A | G | 1 | a0004c0005 | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
synonymous_variant | LOW | c.595T>C | p.Leu199Leu | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/9 | 635/1861 | 595/1575 | 199/524 | chr1 | 58536647 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58480760
|
T | C | 1 | a0001c0001t0005 | 4 | HG00738.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*205A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 9/9 | 205 | chr1 | 58480760 | |||||
chr1:58480771
|
T | C | 1 | a0004c0005t0006 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*194A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 9/9 | 194 | chr1 | 58480771 | |||||
chr1:58480830
|
T | A | 1 | a0001c0001t0004 | 6 | HG00621.hp2 HG02129.hp2 HG02165.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 9/9 | 135 | chr1 | 58480830 | |||||
chr1:58480867
|
C | CT | 6 | a0001c0001t0002a0001c0002t0002a0001c0012t0002others(3): Show | 51 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*97dupA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 9/9 | 97 | chr1 | 58480867 | |||||
chr1:58539307
|
C | T | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
5_prime_UTR_variant | MODIFIER | c.-13G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/9 | 13 | chr1 | 58539307 | |||||
chr1:58546724
|
G | A | 1 | a0001c0001t0007 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-38C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/9 | 7430 | chr1 | 58546724 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:58481189
|
T | G | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-15A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481189 | ||||||
chr1:58481275
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0040others(151): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1366-101A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481275 | ||||||
chr1:58481415
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1366-241C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481415 | ||||||
chr1:58481426
|
C | T | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-252G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481426 | ||||||
chr1:58481565
|
A | T | 1 | a0003c0004t0001g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1366-391T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481565 | ||||||
chr1:58481590
|
C | T | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1366-416G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481590 | ||||||
chr1:58481697
|
CAT | C | 64 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1366-525_1366-524d others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481697 | ||||||
chr1:58481740
|
G | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-566C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481740 | ||||||
chr1:58481819
|
T | C | 1 | a0001c0001t0004g0200 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1366-645A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481819 | ||||||
chr1:58481883
|
A | G | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1366-709T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481883 | ||||||
chr1:58481931
|
A | G | 1 | a0003c0004t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1366-757T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58481931 | ||||||
chr1:58482025
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1366-851G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482025 | ||||||
chr1:58482028
|
C | T | 4 | a0001c0001t0001g0245a0001c0001t0001g0264a0001c0001t0001g0266others(1): Show | 4 | HG02970.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-854G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482028 | ||||||
chr1:58482177
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-1003A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482177 | ||||||
chr1:58482289
|
T | C | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1366-1115A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482289 | ||||||
chr1:58482428
|
T | G | 1 | a0004c0008t0001g0017 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1366-1254A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482428 | ||||||
chr1:58482547
|
C | T | 1 | a0001c0001t0005g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1366-1373G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482547 | ||||||
chr1:58482573
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1366-1399A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482573 | ||||||
chr1:58482788
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1366-1614C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482788 | ||||||
chr1:58482945
|
G | T | 1 | a0001c0001t0001g0007 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1366-1771C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58482945 | ||||||
chr1:58483214
|
A | T | 154 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0040others(151): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1366-2040T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483214 | ||||||
chr1:58483270
|
G | C | 1 | a0001c0001t0007g0376 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1366-2096C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483270 | ||||||
chr1:58483299
|
T | C | 1 | a0001c0002t0002g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1366-2125A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483299 | ||||||
chr1:58483315
|
G | A | 1 | a0004c0008t0001g0017 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1366-2141C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483315 | ||||||
chr1:58483392
|
T | C | 2 | a0002c0003t0001g0345a0002c0003t0001g0346 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1366-2218A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483392 | ||||||
chr1:58483512
|
G | C | 1 | a0001c0002t0002g0078 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1366-2338C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483512 | ||||||
chr1:58483588
|
G | C | 114 | a0001c0001t0001g0205a0001c0002t0002g0011a0001c0002t0002g0078others(111): Show | 118 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1366-2414C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483588 | ||||||
chr1:58483752
|
C | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-2578G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483752 | ||||||
chr1:58483838
|
C | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-2664G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58483838 | ||||||
chr1:58484081
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1366-2907G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484081 | ||||||
chr1:58484082
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1366-2908C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484082 | ||||||
chr1:58484265
|
T | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-3091A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484265 | ||||||
chr1:58484315
|
T | C | 21 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(18): Show | 23 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1366-3141A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484315 | ||||||
chr1:58484483
|
C | G | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1366-3309G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484483 | ||||||
chr1:58484568
|
A | G | 10 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(7): Show | 12 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366-3394T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484568 | ||||||
chr1:58484595
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1366-3421C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484595 | ||||||
chr1:58484617
|
T | G | 7 | a0001c0002t0002g0094a0001c0002t0002g0095a0001c0002t0002g0096others(4): Show | 7 | HG02738.hp1 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-3443A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484617 | ||||||
chr1:58484681
|
G | T | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1366-3507C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484681 | ||||||
chr1:58484754
|
C | T | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(22): Show | 26 | HG00639.hp2 HG00738.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1366-3580G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484754 | ||||||
chr1:58484782
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1366-3608C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484782 | ||||||
chr1:58484901
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0241 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1366-3727C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58484901 | ||||||
chr1:58485029
|
A | G | 291 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0039others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1366-3855T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485029 | ||||||
chr1:58485044
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1366-3870A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485044 | ||||||
chr1:58485061
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1366-3887C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485061 | ||||||
chr1:58485069
|
A | G | 2 | a0001c0001t0004g0202a0001c0001t0004g0203 | 2 | HG00621.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1366-3895T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485069 | ||||||
chr1:58485071
|
G | C | 2 | a0001c0001t0001g0271a0001c0001t0001g0314 | 2 | HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1366-3897C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485071 | ||||||
chr1:58485225
|
T | C | 5 | a0001c0001t0001g0128a0001c0001t0001g0163a0001c0001t0001g0177others(2): Show | 5 | HG00544.hp2 NA18943.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1366-4051A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485225 | ||||||
chr1:58485227
|
C | CT | 12 | a0001c0001t0001g0172a0001c0002t0002g0112a0004c0005t0001g0023others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366-4054dupA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485227 | ||||||
chr1:58485228
|
T | TA | 96 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0039others(93): Show | 99 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1366-4055dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TAA | 15 | a0001c0001t0001g0046a0001c0001t0001g0161a0001c0001t0001g0186others(12): Show | 15 | HG00408.hp1 HG01074.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1366-4056_1366-405 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TAAAAAAA others(3): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0332a0001c0001t0001g0334others(2): Show | 6 | HG02109.hp1 HG02257.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366-4064_1366-405 others(14): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TAAAAAAA others(4): Show |
4 | a0001c0001t0001g0331a0001c0001t0001g0335a0001c0001t0001g0339others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-4065_1366-405 others(15): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TAAAAAAA others(8): Show |
1 | a0001c0001t0001g0342 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1366-4069_1366-405 others(19): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TAAAAAAA others(12): Show |
1 | a0001c0001t0001g0340 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1366-4073_1366-405 others(23): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TTA | 31 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(28): Show | 32 | HG00140.hp2 HG00673.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1366-4055_1366-405 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
T | TTAA | 6 | a0001c0002t0002g0082a0001c0002t0002g0089a0001c0002t0002g0090others(3): Show | 6 | HG00438.hp2 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1366-4055_1366-405 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485228
|
TA | T | 27 | a0001c0001t0001g0170a0001c0001t0001g0216a0001c0001t0001g0247others(24): Show | 29 | HG00099.hp1 HG00642.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1366-4055delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485228 | ||||||
chr1:58485257
|
G | A | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-4083C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485257 | ||||||
chr1:58485653
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1366-4479A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485653 | ||||||
chr1:58485758
|
C | T | 2 | a0001c0001t0005g0043a0001c0001t0005g0044 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1366-4584G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485758 | ||||||
chr1:58485944
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-4770A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485944 | ||||||
chr1:58485975
|
G | C | 1 | a0001c0001t0001g0181 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1366-4801C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58485975 | ||||||
chr1:58486087
|
T | C | 7 | a0001c0001t0001g0269a0001c0001t0001g0291a0001c0001t0001g0293others(4): Show | 7 | HG01168.hp1 HG01175.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-4913A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486087 | ||||||
chr1:58486487
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1366-5313A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486487 | ||||||
chr1:58486549
|
T | A | 328 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1366-5375A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486549 | ||||||
chr1:58486574
|
C | G | 112 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(109): Show | 116 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1366-5400G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486574 | ||||||
chr1:58486595
|
G | A | 1 | a0005c0006t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1366-5421C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486595 | ||||||
chr1:58486601
|
T | C | 3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1366-5427A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486601 | ||||||
chr1:58486742
|
A | G | 374 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(371): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.1366-5568T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486742 | ||||||
chr1:58486948
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-5774C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58486948 | ||||||
chr1:58487079
|
T | TTGAGGTG others(13): Show |
1 | a0003c0004t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1366-5925_1366-590 others(24): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487079 | ||||||
chr1:58487156
|
G | A | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-5982C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487156 | ||||||
chr1:58487272
|
A | G | 2 | a0002c0003t0001g0355a0002c0003t0001g0371 | 2 | NA18957.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1366-6098T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487272 | ||||||
chr1:58487366
|
A | T | 1 | a0001c0001t0001g0291 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1366-6192T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487366 | ||||||
chr1:58487412
|
G | C | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1366-6238C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487412 | ||||||
chr1:58487615
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-6441G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487615 | ||||||
chr1:58487672
|
C | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-6498G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487672 | ||||||
chr1:58487743
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1366-6569A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487743 | ||||||
chr1:58487835
|
TATTA | T | 8 | a0003c0004t0001g0003a0003c0004t0001g0051a0003c0004t0001g0052others(5): Show | 9 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366-6665_1366-666 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487835 | ||||||
chr1:58487861
|
A | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0219a0001c0001t0001g0251others(1): Show | 4 | NA18952.hp2 NA19011.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-6687T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487861 | ||||||
chr1:58487910
|
TCTC | T | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-6739_1366-673 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58487910 | ||||||
chr1:58488126
|
T | A | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1366-6952A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488126 | ||||||
chr1:58488127
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1366-6953T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488127 | ||||||
chr1:58488146
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0251 | 2 | NA18952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1366-6972T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488146 | ||||||
chr1:58488226
|
G | A | 62 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(59): Show | 62 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1366-7052C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488226 | ||||||
chr1:58488441
|
C | G | 1 | a0004c0005t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1366-7267G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488441 | ||||||
chr1:58488626
|
AT | A | 13 | a0001c0001t0003g0002a0001c0001t0003g0025a0001c0001t0003g0026others(10): Show | 14 | HG00639.hp2 HG01074.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1366-7453delA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488626 | ||||||
chr1:58488660
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1366-7486G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488660 | ||||||
chr1:58488709
|
A | G | 65 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1366-7535T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488709 | ||||||
chr1:58488730
|
G | A | 2 | a0001c0002t0002g0080a0001c0002t0002g0081 | 2 | NA18974.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1366-7556C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488730 | ||||||
chr1:58488742
|
G | A | 1 | a0003c0004t0001g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1366-7568C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488742 | ||||||
chr1:58488820
|
G | A | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1366-7646C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488820 | ||||||
chr1:58488935
|
G | C | 28 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(25): Show | 30 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1366-7761C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488935 | ||||||
chr1:58488981
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-7807A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58488981 | ||||||
chr1:58489017
|
G | A | 1 | a0004c0005t0002g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1366-7843C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489017 | ||||||
chr1:58489032
|
C | T | 3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1366-7858G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489032 | ||||||
chr1:58489106
|
G | A | 1 | a0005c0006t0001g0005 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1366-7932C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489106 | ||||||
chr1:58489130
|
G | A | 4 | a0001c0002t0002g0083a0001c0002t0002g0084a0001c0002t0002g0085others(1): Show | 4 | HG02083.hp2 NA18949.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-7956C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489130 | ||||||
chr1:58489142
|
G | A | 1 | a0001c0002t0002g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1366-7968C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489142 | ||||||
chr1:58489172
|
T | A | 64 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1366-7998A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489172 | ||||||
chr1:58489264
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | HG01255.hp1 HG01358.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-8090C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489264 | ||||||
chr1:58489276
|
C | T | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1366-8102G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489276 | ||||||
chr1:58489559
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1366-8385A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489559 | ||||||
chr1:58489609
|
T | C | 82 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(79): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1366-8435A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489609 | ||||||
chr1:58489685
|
C | T | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1366-8511G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489685 | ||||||
chr1:58489722
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0251 | 2 | NA18952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1366-8548G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489722 | ||||||
chr1:58489723
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0036 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1366-8549C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489723 | ||||||
chr1:58489779
|
T | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-8605A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489779 | ||||||
chr1:58489832
|
G | A | 29 | a0002c0003t0001g0347a0002c0003t0001g0348a0002c0003t0001g0349others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1366-8658C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489832 | ||||||
chr1:58489844
|
T | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-8670A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58489844 | ||||||
chr1:58490070
|
C | A | 2 | a0001c0001t0001g0336a0001c0001t0001g0338 | 2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1366-8896G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490070 | ||||||
chr1:58490088
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-8914G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490088 | ||||||
chr1:58490186
|
A | C | 11 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(8): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366-9012T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490186 | ||||||
chr1:58490312
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-9138G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490312 | ||||||
chr1:58490336
|
G | C | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-9162C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490336 | ||||||
chr1:58490426
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0216a0001c0001t0001g0217 | 3 | NA18953.hp1 NA19055.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1366-9252C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490426 | ||||||
chr1:58490442
|
T | G | 2 | a0003c0004t0001g0067a0003c0004t0001g0073 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1366-9268A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490442 | ||||||
chr1:58490448
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1366-9274C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490448 | ||||||
chr1:58490572
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1366-9398T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490572 | ||||||
chr1:58490610
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-9436G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490610 | ||||||
chr1:58490748
|
C | G | 1 | a0001c0001t0001g0325 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1366-9574G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490748 | ||||||
chr1:58490763
|
C | T | 4 | a0004c0005t0002g0012a0004c0005t0002g0014a0004c0005t0002g0015others(1): Show | 4 | HG01074.hp2 HG01081.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-9589G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490763 | ||||||
chr1:58490792
|
ATTCT | A | 11 | a0001c0001t0003g0002a0001c0001t0003g0025a0001c0001t0003g0026others(8): Show | 12 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1366-9622_1366-961 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490792 | ||||||
chr1:58490795
|
C | CT | 110 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(107): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1366-9622dupA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
C | CTT | 42 | a0001c0001t0001g0120a0001c0001t0001g0126a0001c0001t0001g0128others(39): Show | 42 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1366-9623_1366-962 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
C | CTTT | 8 | a0001c0001t0001g0116a0001c0001t0001g0163a0001c0001t0001g0173others(5): Show | 8 | HG01358.hp1 HG01358.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366-9624_1366-962 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
CT | C | 27 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(24): Show | 27 | HG00280.hp2 HG00408.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1366-9622delA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
CTT | C | 24 | a0001c0001t0001g0039a0001c0001t0001g0331a0001c0001t0001g0334others(21): Show | 25 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1366-9623_1366-962 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
CTTT | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0332a0001c0001t0001g0333others(70): Show | 76 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1366-9624_1366-962 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1366-9633_1366-962 others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490795
|
CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(1): Show | 4 | HG00738.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-9635_1366-962 others(18): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490795 | ||||||
chr1:58490812
|
T | C | 4 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(1): Show | 4 | HG00738.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-9638A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490812 | ||||||
chr1:58490845
|
G | A | 4 | a0001c0001t0001g0267a0001c0001t0005g0042a0002c0003t0001g0375others(1): Show | 4 | HG00738.hp2 NA18956.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-9671C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490845 | ||||||
chr1:58490882
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1366-9708T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490882 | ||||||
chr1:58490884
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1366-9710G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490884 | ||||||
chr1:58490998
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-9824C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58490998 | ||||||
chr1:58491061
|
C | T | 4 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(1): Show | 4 | HG00738.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1366-9887G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491061 | ||||||
chr1:58491086
|
C | T | 1 | a0001c0002t0002g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1366-9912G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491086 | ||||||
chr1:58491103
|
G | A | 8 | a0004c0005t0002g0001a0004c0005t0002g0012a0004c0005t0002g0014others(5): Show | 9 | HG01074.hp2 HG01081.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366-9929C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491103 | ||||||
chr1:58491194
|
C | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-10020G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491194 | ||||||
chr1:58491263
|
A | C | 2 | a0004c0005t0002g0012a0004c0005t0002g0014 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1366-10089T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491263 | ||||||
chr1:58491288
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1366-10114G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491288 | ||||||
chr1:58491394
|
G | C | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1366-10220C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491394 | ||||||
chr1:58491445
|
T | C | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-10271A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491445 | ||||||
chr1:58491446
|
T | C | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-10272A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491446 | ||||||
chr1:58491473
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0124 | 2 | HG00735.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1366-10299A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491473 | ||||||
chr1:58491546
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-10372A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491546 | ||||||
chr1:58491771
|
C | G | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1366-10597G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491771 | ||||||
chr1:58491787
|
G | A | 5 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0098others(2): Show | 5 | HG02738.hp1 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-10613C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491787 | ||||||
chr1:58491901
|
T | G | 13 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(10): Show | 15 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1366-10727A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58491901 | ||||||
chr1:58492022
|
A | T | 1 | a0001c0002t0002g0079 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1366-10848T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492022 | ||||||
chr1:58492039
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1366-10865T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492039 | ||||||
chr1:58492136
|
C | A | 291 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0039others(288): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1366-10962G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492136 | ||||||
chr1:58492148
|
A | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1366-10974T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492148 | ||||||
chr1:58492327
|
T | C | 2 | a0003c0004t0001g0068a0003c0004t0001g0070 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1366-11153A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492327 | ||||||
chr1:58492400
|
G | GAAAAT | 21 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(18): Show | 23 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1366-11231_1366-11 others(11): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492400 | ||||||
chr1:58492441
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1366-11267G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492441 | ||||||
chr1:58492478
|
T | C | 2 | a0002c0003t0001g0345a0002c0003t0001g0346 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1366-11304A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492478 | ||||||
chr1:58492591
|
C | T | 7 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0249others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.1366-11417G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492591 | ||||||
chr1:58492736
|
G | T | 1 | a0004c0005t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1366-11562C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492736 | ||||||
chr1:58492751
|
A | C | 349 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(346): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1366-11577T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492751 | ||||||
chr1:58492828
|
A | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-11654T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492828 | ||||||
chr1:58492882
|
C | T | 3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1366-11708G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492882 | ||||||
chr1:58492925
|
C | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-11751G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492925 | ||||||
chr1:58492959
|
A | AC | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-11786dupG | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492959 | ||||||
chr1:58492989
|
C | T | 3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1366-11815G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492989 | ||||||
chr1:58492993
|
T | C | 8 | a0004c0005t0002g0001a0004c0005t0002g0012a0004c0005t0002g0014others(5): Show | 9 | HG01074.hp2 HG01081.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1366-11819A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58492993 | ||||||
chr1:58493331
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1366-12157C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493331 | ||||||
chr1:58493395
|
T | C | 1 | a0003c0004t0001g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1366-12221A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493395 | ||||||
chr1:58493466
|
C | G | 154 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0040others(151): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1366-12292G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493466 | ||||||
chr1:58493492
|
T | C | 1 | a0003c0004t0001g0071 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1366-12318A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493492 | ||||||
chr1:58493522
|
C | T | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1366-12348G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493522 | ||||||
chr1:58493528
|
A | G | 2 | a0003c0004t0001g0052a0003c0004t0001g0055 | 2 | HG00099.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.1366-12354T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493528 | ||||||
chr1:58493590
|
T | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1366-12416A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493590 | ||||||
chr1:58493683
|
T | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1365+12377A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493683 | ||||||
chr1:58493702
|
A | C | 24 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(21): Show | 25 | HG00639.hp2 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.1365+12358T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493702 | ||||||
chr1:58493714
|
T | C | 4 | a0001c0001t0001g0006a0001c0001t0001g0141a0001c0001t0001g0184others(1): Show | 5 | HG00323.hp2 HG00733.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+12346A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493714 | ||||||
chr1:58493722
|
A | T | 1 | a0001c0001t0001g0252 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1365+12338T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493722 | ||||||
chr1:58493822
|
G | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0001g0269 | 3 | HG03669.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1365+12238C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493822 | ||||||
chr1:58493871
|
C | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(13): Show | 18 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1365+12189G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493871 | ||||||
chr1:58493886
|
A | G | 65 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1365+12174T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493886 | ||||||
chr1:58493925
|
T | C | 2 | a0001c0001t0001g0255a0001c0001t0001g0315 | 2 | NA18985.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1365+12135A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493925 | ||||||
chr1:58493934
|
T | A | 154 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0001t0001g0040others(151): Show | 161 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1365+12126A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493934 | ||||||
chr1:58493950
|
T | G | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+12110A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493950 | ||||||
chr1:58493960
|
G | A | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+12100C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493960 | ||||||
chr1:58493973
|
A | C | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+12087T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493973 | ||||||
chr1:58493979
|
A | C | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+12081T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58493979 | ||||||
chr1:58494002
|
A | AC | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+12057dupG | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494002 | ||||||
chr1:58494143
|
A | C | 1 | a0001c0001t0001g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1365+11917T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494143 | ||||||
chr1:58494177
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1365+11883G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494177 | ||||||
chr1:58494413
|
T | C | 1 | a0002c0003t0001g0369 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1365+11647A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494413 | ||||||
chr1:58494604
|
T | C | 3 | a0002c0003t0001g0347a0002c0003t0001g0350a0002c0003t0001g0359 | 3 | NA18982.hp2 NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1365+11456A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494604 | ||||||
chr1:58494644
|
T | C | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1365+11416A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494644 | ||||||
chr1:58494699
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1365+11361G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494699 | ||||||
chr1:58494727
|
T | A | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+11333A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494727 | ||||||
chr1:58494746
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1365+11314C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494746 | ||||||
chr1:58494768
|
T | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1365+11292A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494768 | ||||||
chr1:58494798
|
G | A | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+11262C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494798 | ||||||
chr1:58494831
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0045a0004c0008t0001g0017others(2): Show | 5 | HG01255.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+11229G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494831 | ||||||
chr1:58494840
|
A | C | 2 | a0004c0005t0002g0012a0004c0005t0002g0014 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1365+11220T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494840 | ||||||
chr1:58494847
|
G | T | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1365+11213C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494847 | ||||||
chr1:58494872
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0150a0001c0001t0001g0198others(1): Show | 4 | HG00597.hp2 HG03669.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+11188C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494872 | ||||||
chr1:58494883
|
T | G | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+11177A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494883 | ||||||
chr1:58494908
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1365+11152G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494908 | ||||||
chr1:58494970
|
G | A | 13 | a0001c0001t0003g0002a0001c0001t0003g0025a0001c0001t0003g0026others(10): Show | 14 | HG00639.hp2 HG01074.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1365+11090C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58494970 | ||||||
chr1:58495023
|
C | T | 2 | a0003c0004t0001g0053a0010c0009t0001g0115 | 2 | HG02145.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1365+11037G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495023 | ||||||
chr1:58495108
|
T | C | 1 | a0001c0002t0002g0100 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1365+10952A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495108 | ||||||
chr1:58495109
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1365+10951C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495109 | ||||||
chr1:58495185
|
T | C | 328 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(325): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1365+10875A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495185 | ||||||
chr1:58495238
|
G | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1365+10822C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495238 | ||||||
chr1:58495286
|
G | A | 1 | a0003c0004t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1365+10774C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495286 | ||||||
chr1:58495363
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0261a0001c0001t0001g0310 | 3 | NA18999.hp2 NA19010.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1365+10697A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495363 | ||||||
chr1:58495579
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1365+10481T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495579 | ||||||
chr1:58495580
|
CA | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0120others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1365+10479delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495580 | ||||||
chr1:58495616
|
T | C | 8 | a0003c0004t0001g0056a0003c0004t0001g0057a0003c0004t0001g0058others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+10444A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495616 | ||||||
chr1:58495701
|
T | TA | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1365+10358dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495701 | ||||||
chr1:58495701
|
TA | T | 67 | a0001c0001t0001g0227a0002c0003t0001g0345a0002c0003t0001g0346others(64): Show | 70 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1365+10358delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495701 | ||||||
chr1:58495884
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1365+10176G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58495884 | ||||||
chr1:58496014
|
C | G | 1 | a0001c0001t0005g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1365+10046G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496014 | ||||||
chr1:58496021
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1365+10039G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496021 | ||||||
chr1:58496059
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1365+10001A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496059 | ||||||
chr1:58496130
|
T | C | 3 | a0001c0001t0001g0245a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02970.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1365+9930A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496130 | ||||||
chr1:58496158
|
A | ATTTTTTC others(30): Show |
1 | a0001c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1365+9901_1365+990 others(41): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496158 | ||||||
chr1:58496158
|
A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1365+9901_1365+990 others(15): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496158 | ||||||
chr1:58496158
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0010 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1365+9901_1365+990 others(21): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496158 | ||||||
chr1:58496158
|
A | ATTTTTTT others(31): Show |
1 | a0001c0001t0001g0161 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1365+9901_1365+990 others(42): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496158 | ||||||
chr1:58496166
|
A | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | HG00408.hp1 HG00558.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+9894T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496166 | ||||||
chr1:58496167
|
G | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | HG00408.hp1 HG00558.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+9893C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496167 | ||||||
chr1:58496168
|
A | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | HG00408.hp1 HG00558.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+9892T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496168 | ||||||
chr1:58496169
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | HG00408.hp1 HG00558.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+9891G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496169 | ||||||
chr1:58496169
|
CTT | C | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+9889_1365+989 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496169 | ||||||
chr1:58496387
|
C | T | 4 | a0001c0001t0001g0178a0001c0001t0001g0247a0001c0001t0001g0261others(1): Show | 4 | NA18982.hp1 NA18999.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.1365+9673G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496387 | ||||||
chr1:58496396
|
C | G | 6 | a0001c0001t0001g0120a0001c0001t0001g0159a0001c0001t0001g0255others(3): Show | 6 | HG02129.hp1 NA18945.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+9664G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496396 | ||||||
chr1:58496602
|
G | A | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1365+9458C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496602 | ||||||
chr1:58496659
|
T | A | 1 | a0003c0004t0001g0050 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1365+9401A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496659 | ||||||
chr1:58496664
|
T | C | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+9396A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496664 | ||||||
chr1:58496936
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1365+9124T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58496936 | ||||||
chr1:58497038
|
C | A | 8 | a0003c0004t0001g0056a0003c0004t0001g0057a0003c0004t0001g0058others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+9022G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497038 | ||||||
chr1:58497098
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+8962A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497098 | ||||||
chr1:58497183
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1365+8877C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497183 | ||||||
chr1:58497256
|
A | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1365+8804T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497256 | ||||||
chr1:58497361
|
T | C | 1 | a0003c0004t0001g0003 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1365+8699A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497361 | ||||||
chr1:58497513
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1365+8547C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497513 | ||||||
chr1:58497614
|
GGAA | G | 83 | a0001c0001t0001g0281a0001c0002t0002g0011a0001c0002t0002g0078others(80): Show | 87 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1365+8443_1365+844 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497614 | ||||||
chr1:58497656
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1365+8404C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497656 | ||||||
chr1:58497659
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1365+8401C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497659 | ||||||
chr1:58497761
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1365+8299T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497761 | ||||||
chr1:58497775
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1365+8285G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497775 | ||||||
chr1:58497923
|
T | C | 1 | a0004c0008t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1365+8137A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58497923 | ||||||
chr1:58498049
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1365+8011T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498049 | ||||||
chr1:58498054
|
C | A | 1 | a0001c0001t0002g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1365+8006G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498054 | ||||||
chr1:58498054
|
C | G | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+8006G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498054 | ||||||
chr1:58498186
|
A | G | 7 | a0001c0002t0002g0094a0001c0002t0002g0095a0001c0002t0002g0096others(4): Show | 7 | HG02738.hp1 HG03209.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1365+7874T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498186 | ||||||
chr1:58498236
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1365+7824T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498236 | ||||||
chr1:58498241
|
TA | T | 23 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0348others(20): Show | 23 | HG00642.hp1 HG01175.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+7818delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498241 | ||||||
chr1:58498252
|
A | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+7808T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498252 | ||||||
chr1:58498253
|
AC | A | 11 | a0002c0003t0001g0347a0002c0003t0001g0349a0002c0003t0001g0350others(8): Show | 11 | HG00423.hp1 HG00621.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.1365+7806delG | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498253 | ||||||
chr1:58498516
|
T | C | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+7544A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498516 | ||||||
chr1:58498580
|
C | A | 2 | a0003c0004t0001g0067a0003c0004t0001g0073 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1365+7480G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498580 | ||||||
chr1:58498600
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1365+7460G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498600 | ||||||
chr1:58498621
|
ACT | A | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1365+7437_1365+743 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498621 | ||||||
chr1:58498714
|
T | C | 4 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(1): Show | 4 | HG00738.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+7346A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498714 | ||||||
chr1:58498797
|
TA | T | 13 | a0001c0001t0003g0002a0001c0001t0003g0025a0001c0001t0003g0026others(10): Show | 14 | HG00639.hp2 HG01074.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1365+7262delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498797 | ||||||
chr1:58498873
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0219a0001c0001t0001g0251others(1): Show | 4 | NA18952.hp2 NA19011.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+7187C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498873 | ||||||
chr1:58498905
|
T | A | 29 | a0002c0003t0001g0347a0002c0003t0001g0348a0002c0003t0001g0349others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1365+7155A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58498905 | ||||||
chr1:58499068
|
CCTACCAT others(6): Show |
C | 1 | a0001c0002t0002g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1365+6979_1365+699 others(17): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499068 | ||||||
chr1:58499156
|
T | C | 2 | a0005c0006t0001g0064a0005c0006t0001g0066 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1365+6904A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499156 | ||||||
chr1:58499189
|
C | CA | 11 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(8): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1365+6870dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499189 | ||||||
chr1:58499252
|
G | C | 2 | a0003c0004t0001g0067a0003c0004t0001g0073 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1365+6808C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499252 | ||||||
chr1:58499314
|
C | CA | 34 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0145others(31): Show | 35 | HG00738.hp2 HG01361.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1365+6745dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499314 | ||||||
chr1:58499314
|
CA | C | 13 | a0001c0002t0002g0099a0002c0003t0001g0363a0003c0004t0001g0049others(10): Show | 13 | HG01256.hp1 HG01258.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1365+6745delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499314 | ||||||
chr1:58499314
|
CAA | C | 56 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(53): Show | 59 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1365+6744_1365+674 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499314 | ||||||
chr1:58499314
|
CAAA | C | 13 | a0001c0002t0002g0086a0001c0002t0002g0111a0003c0004t0001g0105others(10): Show | 14 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1365+6743_1365+674 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499314 | ||||||
chr1:58499314
|
CAAAAAAA others(5): Show |
C | 1 | a0005c0006t0001g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1365+6734_1365+674 others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499314 | ||||||
chr1:58499477
|
T | TATAG | 7 | a0001c0001t0001g0010a0001c0001t0001g0138a0001c0001t0001g0185others(4): Show | 8 | HG00673.hp2 HG01257.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+6579_1365+658 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
T | TATAGATA others(1): Show |
15 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(12): Show | 16 | HG00735.hp1 HG01346.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.1365+6575_1365+658 others(12): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
T | TATAGATA others(5): Show |
67 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0040others(64): Show | 68 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.1365+6571_1365+658 others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
T | TATAGATA others(9): Show |
75 | a0001c0001t0001g0117a0001c0001t0001g0131a0001c0001t0001g0135others(72): Show | 76 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1365+6567_1365+658 others(20): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
T | TATAGATA others(13): Show |
38 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0001g0045others(35): Show | 38 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.1365+6563_1365+658 others(24): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
T | TATAGATA others(17): Show |
15 | a0001c0001t0001g0120a0001c0001t0001g0212a0001c0001t0001g0213others(12): Show | 15 | HG00558.hp2 HG01175.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1365+6559_1365+658 others(28): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
T | TATAGATA others(25): Show |
1 | a0001c0001t0001g0224 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1365+6582_1365+658 others(36): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499477
|
TATAG | T | 47 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(44): Show | 48 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1365+6579_1365+658 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499477 | ||||||
chr1:58499497
|
GATAGATA others(5): Show |
G | 1 | a0002c0003t0001g0346 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1365+6551_1365+656 others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499497 | ||||||
chr1:58499501
|
GATAGATA others(1): Show |
G | 5 | a0002c0003t0001g0345a0003c0004t0001g0004a0003c0004t0001g0065others(2): Show | 7 | HG01069.hp2 HG01071.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+6551_1365+655 others(12): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499501 | ||||||
chr1:58499505
|
GATAA | G | 18 | a0003c0004t0001g0049a0003c0004t0001g0050a0003c0004t0001g0052others(15): Show | 18 | HG00099.hp1 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1365+6551_1365+655 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499505 | ||||||
chr1:58499509
|
A | G | 14 | a0001c0001t0001g0228a0001c0001t0001g0281a0003c0004t0001g0003others(11): Show | 15 | HG00642.hp2 HG00735.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1365+6551T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499509 | ||||||
chr1:58499513
|
G | GATAGATA others(5): Show |
1 | a0001c0001t0001g0281 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1365+6546_1365+654 others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499513 | ||||||
chr1:58499635
|
G | A | 5 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(2): Show | 5 | HG00735.hp1 HG01346.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1365+6425C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499635 | ||||||
chr1:58499636
|
A | C | 1 | a0001c0001t0001g0251 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1365+6424T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499636 | ||||||
chr1:58499761
|
T | C | 2 | a0002c0003t0001g0345a0002c0003t0001g0346 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1365+6299A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499761 | ||||||
chr1:58499780
|
ATTAG | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1365+6276_1365+627 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499780 | ||||||
chr1:58499816
|
G | GA | 6 | a0001c0001t0001g0254a0001c0001t0001g0270a0001c0001t0001g0303others(3): Show | 6 | HG02027.hp2 HG02056.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1365+6243dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499816 | ||||||
chr1:58499921
|
A | G | 1 | a0002c0003t0001g0370 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1365+6139T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499921 | ||||||
chr1:58499991
|
C | T | 8 | a0003c0004t0001g0056a0003c0004t0001g0057a0003c0004t0001g0058others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+6069G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58499991 | ||||||
chr1:58500185
|
T | C | 8 | a0003c0004t0001g0056a0003c0004t0001g0057a0003c0004t0001g0058others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+5875A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58500185 | ||||||
chr1:58500191
|
T | A | 1 | a0001c0001t0001g0289 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1365+5869A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58500191 | ||||||
chr1:58500230
|
T | C | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1365+5830A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58500230 | ||||||
chr1:58500333
|
G | A | 2 | a0001c0002t0002g0087a0001c0002t0002g0093 | 2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1365+5727C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58500333 | ||||||
chr1:58500579
|
G | C | 2 | a0002c0003t0001g0349a0002c0003t0001g0356 | 2 | NA18941.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1365+5481C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58500579 | ||||||
chr1:58500643
|
C | T | 6 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0248others(3): Show | 6 | HG00408.hp2 HG01346.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1365+5417G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58500643 | ||||||
chr1:58501078
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1365+4982C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501078 | ||||||
chr1:58501174
|
T | G | 1 | a0001c0002t0002g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1365+4886A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501174 | ||||||
chr1:58501459
|
T | A | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+4601A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501459 | ||||||
chr1:58501669
|
C | T | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1365+4391G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501669 | ||||||
chr1:58501739
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294 | 3 | HG01358.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1365+4321G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501739 | ||||||
chr1:58501744
|
G | A | 13 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(10): Show | 15 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1365+4316C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501744 | ||||||
chr1:58501835
|
G | A | 1 | a0007c0011t0002g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1365+4225C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501835 | ||||||
chr1:58501933
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1365+4127G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58501933 | ||||||
chr1:58502162
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1365+3898T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502162 | ||||||
chr1:58502229
|
T | A | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1365+3831A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502229 | ||||||
chr1:58502270
|
T | C | 13 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(10): Show | 15 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1365+3790A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502270 | ||||||
chr1:58502293
|
G | A | 1 | a0002c0003t0001g0361 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1365+3767C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502293 | ||||||
chr1:58502845
|
A | C | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1365+3215T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502845 | ||||||
chr1:58502875
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1365+3185A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502875 | ||||||
chr1:58502895
|
T | G | 1 | a0002c0003t0001g0373 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1365+3165A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502895 | ||||||
chr1:58502959
|
C | G | 1 | a0003c0004t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1365+3101G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502959 | ||||||
chr1:58502967
|
T | C | 1 | a0002c0003t0001g0363 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1365+3093A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58502967 | ||||||
chr1:58503012
|
T | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1365+3048A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58503012 | ||||||
chr1:58503244
|
A | C | 2 | a0003c0004t0001g0067a0003c0004t0001g0073 | 2 | HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1365+2816T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58503244 | ||||||
chr1:58503278
|
G | A | 1 | a0001c0001t0005g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1365+2782C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58503278 | ||||||
chr1:58503302
|
C | A | 1 | a0001c0002t0002g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1365+2758G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58503302 | ||||||
chr1:58503461
|
C | T | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1365+2599G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58503461 | ||||||
chr1:58504071
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1365+1989C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504071 | ||||||
chr1:58504268
|
C | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1365+1792G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504268 | ||||||
chr1:58504325
|
C | T | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1365+1735G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504325 | ||||||
chr1:58504366
|
A | G | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1365+1694T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504366 | ||||||
chr1:58504420
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1365+1640G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504420 | ||||||
chr1:58504459
|
T | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0214 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1365+1601A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504459 | ||||||
chr1:58504557
|
T | C | 11 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(8): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1365+1503A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504557 | ||||||
chr1:58504691
|
C | T | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1365+1369G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504691 | ||||||
chr1:58504824
|
T | G | 362 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(359): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1365+1236A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504824 | ||||||
chr1:58504894
|
T | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(13): Show | 18 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.1365+1166A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504894 | ||||||
chr1:58504926
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1365+1134A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58504926 | ||||||
chr1:58505022
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1365+1038C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505022 | ||||||
chr1:58505036
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1365+1024A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505036 | ||||||
chr1:58505152
|
C | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1365+908G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505152 | ||||||
chr1:58505196
|
C | G | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1365+864G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505196 | ||||||
chr1:58505302
|
T | A | 1 | a0001c0001t0002g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1365+758A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505302 | ||||||
chr1:58505325
|
C | T | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1365+735G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505325 | ||||||
chr1:58505631
|
T | A | 1 | a0004c0005t0001g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1365+429A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505631 | ||||||
chr1:58505748
|
T | C | 4 | a0001c0002t0002g0091a0001c0002t0002g0100a0001c0002t0002g0101others(1): Show | 4 | HG01256.hp2 HG01257.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1365+312A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505748 | ||||||
chr1:58505760
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1365+300A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505760 | ||||||
chr1:58505830
|
C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0283 | 2 | HG01106.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1365+230G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505830 | ||||||
chr1:58505853
|
C | A | 8 | a0003c0004t0001g0056a0003c0004t0001g0057a0003c0004t0001g0058others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1365+207G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505853 | ||||||
chr1:58505870
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1365+190A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58505870 | ||||||
chr1:58506046
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1365+14G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 8/8 | chr1 | 58506046 | ||||||
chr1:58506268
|
C | A | 82 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(79): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1216-59G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506268 | ||||||
chr1:58506394
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1216-185C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506394 | ||||||
chr1:58506459
|
A | G | 9 | a0004c0005t0002g0001a0004c0005t0002g0012a0004c0005t0002g0014others(6): Show | 10 | HG01074.hp2 HG01081.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1216-250T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506459 | ||||||
chr1:58506558
|
T | C | 1 | a0001c0002t0002g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1216-349A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506558 | ||||||
chr1:58506602
|
C | A | 1 | a0001c0001t0001g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1216-393G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506602 | ||||||
chr1:58506697
|
A | C | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1216-488T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506697 | ||||||
chr1:58506974
|
C | T | 10 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-765G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58506974 | ||||||
chr1:58507000
|
A | G | 14 | a0002c0003t0001g0348a0002c0003t0001g0352a0002c0003t0001g0354others(11): Show | 14 | NA18956.hp2 NA18957.hp2 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.1216-791T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507000 | ||||||
chr1:58507064
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1216-855A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507064 | ||||||
chr1:58507070
|
G | A | 4 | a0003c0004t0001g0068a0003c0004t0001g0070a0003c0004t0001g0071others(1): Show | 4 | HG02258.hp1 HG02717.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-861C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507070 | ||||||
chr1:58507421
|
C | T | 10 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(7): Show | 10 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1216-1212G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507421 | ||||||
chr1:58507651
|
A | G | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1216-1442T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507651 | ||||||
chr1:58507716
|
T | C | 1 | a0001c0002t0002g0081 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1216-1507A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507716 | ||||||
chr1:58507792
|
A | T | 79 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(76): Show | 80 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1216-1583T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507792 | ||||||
chr1:58507795
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1216-1586A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507795 | ||||||
chr1:58507948
|
C | T | 13 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(10): Show | 15 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1216-1739G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507948 | ||||||
chr1:58507984
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 5 | HG02257.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-1775G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58507984 | ||||||
chr1:58508380
|
T | C | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1216-2171A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508380 | ||||||
chr1:58508384
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1216-2175G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508384 | ||||||
chr1:58508397
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1216-2188G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508397 | ||||||
chr1:58508468
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1216-2259C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508468 | ||||||
chr1:58508491
|
T | C | 156 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(153): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1216-2282A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508491 | ||||||
chr1:58508565
|
A | G | 1 | a0001c0002t0002g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1216-2356T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508565 | ||||||
chr1:58508705
|
C | T | 1 | a0001c0002t0002g0083 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1216-2496G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508705 | ||||||
chr1:58508899
|
C | CA | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1216-2691dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508899 | ||||||
chr1:58508915
|
G | A | 1 | a0001c0001t0001g0341 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1216-2706C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58508915 | ||||||
chr1:58509107
|
C | G | 24 | a0001c0002t0002g0078a0001c0002t0002g0079a0001c0002t0002g0080others(21): Show | 24 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.1216-2898G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509107 | ||||||
chr1:58509196
|
T | C | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1216-2987A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509196 | ||||||
chr1:58509271
|
T | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1216-3062A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509271 | ||||||
chr1:58509370
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1216-3161T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509370 | ||||||
chr1:58509422
|
C | A | 221 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1216-3213G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509422 | ||||||
chr1:58509536
|
T | TA | 39 | a0001c0001t0001g0225a0001c0002t0002g0011a0001c0002t0002g0078others(36): Show | 39 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1216-3328dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509536 | ||||||
chr1:58509600
|
G | GA | 87 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0118others(84): Show | 88 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1216-3392dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509600 | ||||||
chr1:58509738
|
C | T | 82 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(79): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1216-3529G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509738 | ||||||
chr1:58509772
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1216-3563A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509772 | ||||||
chr1:58509864
|
A | C | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1216-3655T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509864 | ||||||
chr1:58509913
|
A | G | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1216-3704T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509913 | ||||||
chr1:58509978
|
G | A | 1 | a0004c0005t0002g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1216-3769C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58509978 | ||||||
chr1:58510036
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1216-3827T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510036 | ||||||
chr1:58510039
|
G | A | 2 | a0002c0003t0001g0345a0002c0003t0001g0346 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1216-3830C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510039 | ||||||
chr1:58510144
|
GC | G | 82 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(79): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1216-3936delG | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510144 | ||||||
chr1:58510477
|
C | A | 1 | a0004c0005t0002g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1216-4268G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510477 | ||||||
chr1:58510543
|
T | G | 21 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(18): Show | 23 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-4334A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510543 | ||||||
chr1:58510582
|
C | T | 1 | a0001c0002t0002g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1216-4373G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510582 | ||||||
chr1:58510735
|
C | A | 1 | a0007c0011t0002g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1216-4526G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510735 | ||||||
chr1:58510737
|
A | C | 8 | a0003c0004t0001g0056a0003c0004t0001g0057a0003c0004t0001g0058others(5): Show | 8 | HG01496.hp1 HG02055.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-4528T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510737 | ||||||
chr1:58510744
|
A | T | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1216-4535T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510744 | ||||||
chr1:58510920
|
G | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1216-4711C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58510920 | ||||||
chr1:58511043
|
A | G | 1 | a0001c0002t0002g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1216-4834T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511043 | ||||||
chr1:58511083
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1216-4874A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511083 | ||||||
chr1:58511619
|
A | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1216-5410T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511619 | ||||||
chr1:58511656
|
C | T | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1216-5447G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511656 | ||||||
chr1:58511871
|
G | T | 65 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(62): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1216-5662C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511871 | ||||||
chr1:58511899
|
C | CA | 12 | a0001c0001t0001g0221a0001c0001t0001g0228a0001c0001t0001g0229others(9): Show | 12 | HG00741.hp1 HG01069.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1216-5691dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511899 | ||||||
chr1:58511968
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1216-5759T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58511968 | ||||||
chr1:58512066
|
C | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1216-5857G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512066 | ||||||
chr1:58512221
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0179 | 2 | HG02165.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1216-6012C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512221 | ||||||
chr1:58512287
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1216-6078A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512287 | ||||||
chr1:58512368
|
T | A | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1216-6159A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512368 | ||||||
chr1:58512560
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1216-6351A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512560 | ||||||
chr1:58512664
|
C | A | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1216-6455G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512664 | ||||||
chr1:58512725
|
T | C | 221 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1216-6516A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512725 | ||||||
chr1:58512751
|
G | C | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1216-6542C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512751 | ||||||
chr1:58512806
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1216-6597T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512806 | ||||||
chr1:58512929
|
A | G | 221 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1216-6720T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512929 | ||||||
chr1:58512934
|
C | T | 5 | a0001c0001t0001g0128a0001c0001t0001g0163a0001c0001t0001g0177others(2): Show | 5 | HG00544.hp2 NA18943.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-6725G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58512934 | ||||||
chr1:58513291
|
A | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1216-7082T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58513291 | ||||||
chr1:58513396
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1216-7187C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58513396 | ||||||
chr1:58513549
|
G | A | 1 | a0001c0002t0002g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1216-7340C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58513549 | ||||||
chr1:58513816
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1216-7607G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58513816 | ||||||
chr1:58513955
|
T | C | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1216-7746A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58513955 | ||||||
chr1:58514465
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1216-8256C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514465 | ||||||
chr1:58514530
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1216-8321G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514530 | ||||||
chr1:58514560
|
A | T | 64 | a0001c0001t0001g0117a0001c0001t0001g0178a0001c0001t0001g0216others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1216-8351T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514560 | ||||||
chr1:58514633
|
T | G | 4 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(1): Show | 4 | HG00738.hp2 HG01884.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-8424A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514633 | ||||||
chr1:58514694
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0045a0004c0008t0001g0017others(2): Show | 5 | HG01255.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1216-8485A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514694 | ||||||
chr1:58514817
|
A | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1216-8608T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514817 | ||||||
chr1:58514949
|
T | G | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1216-8740A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58514949 | ||||||
chr1:58515134
|
A | C | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0279others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-8925T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58515134 | ||||||
chr1:58515322
|
A | C | 3 | a0004c0005t0001g0023a0004c0005t0002g0018a0004c0005t0006g0013 | 3 | HG01109.hp2 HG01243.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1216-9113T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58515322 | ||||||
chr1:58515468
|
GTAAAGTT others(6): Show |
G | 1 | a0002c0003t0001g0366 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1216-9272_1216-926 others(17): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58515468 | ||||||
chr1:58515748
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0215 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1216-9539T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58515748 | ||||||
chr1:58515961
|
T | C | 1 | a0003c0004t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1216-9752A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58515961 | ||||||
chr1:58516013
|
T | TATCTCAG others(5): Show |
1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1216-9816_1216-980 others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516013 | ||||||
chr1:58516151
|
T | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1216-9942A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516151 | ||||||
chr1:58516286
|
C | A | 39 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(36): Show | 39 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1216-10077G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516286 | ||||||
chr1:58516333
|
A | G | 39 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(36): Show | 39 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1216-10124T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516333 | ||||||
chr1:58516449
|
A | G | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1216-10240T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516449 | ||||||
chr1:58516497
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1216-10288A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516497 | ||||||
chr1:58516520
|
A | T | 21 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(18): Show | 23 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-10311T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516520 | ||||||
chr1:58516580
|
A | G | 2 | a0001c0001t0005g0043a0001c0001t0005g0044 | 2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1216-10371T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516580 | ||||||
chr1:58516665
|
G | A | 11 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(8): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1216-10456C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516665 | ||||||
chr1:58516684
|
C | G | 2 | a0002c0003t0001g0349a0002c0003t0001g0356 | 2 | NA18941.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1216-10475G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516684 | ||||||
chr1:58516685
|
G | T | 2 | a0002c0003t0001g0349a0002c0003t0001g0356 | 2 | NA18941.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1216-10476C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516685 | ||||||
chr1:58516933
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0142 | 3 | HG00733.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1215+10328G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58516933 | ||||||
chr1:58517046
|
G | A | 1 | a0001c0002t0002g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1215+10215C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517046 | ||||||
chr1:58517115
|
G | T | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1215+10146C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517115 | ||||||
chr1:58517473
|
T | A | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1215+9788A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517473 | ||||||
chr1:58517544
|
C | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+9717G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517544 | ||||||
chr1:58517623
|
AAATT | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1215+9634_1215+963 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517623 | ||||||
chr1:58517758
|
G | A | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1215+9503C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517758 | ||||||
chr1:58517858
|
TCTGGTCA others(71): Show |
T | 1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1215+9325_1215+940 others(82): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517858 | ||||||
chr1:58517985
|
G | A | 2 | a0005c0006t0001g0005a0005c0006t0001g0069 | 3 | HG01069.hp2 HG01071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1215+9276C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58517985 | ||||||
chr1:58518143
|
G | A | 1 | a0001c0002t0002g0096 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1215+9118C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518143 | ||||||
chr1:58518162
|
G | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+9099C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518162 | ||||||
chr1:58518175
|
A | T | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+9086T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518175 | ||||||
chr1:58518196
|
A | AGGAGAGG | 4 | a0001c0001t0003g0027a0001c0001t0003g0030a0001c0001t0003g0034others(1): Show | 4 | HG01074.hp1 HG01891.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+9058_1215+906 others(11): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(7): Show |
3 | a0001c0001t0003g0002a0001c0001t0003g0026a0004c0008t0001g0021 | 4 | HG00639.hp2 HG02280.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+9051_1215+906 others(18): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(14): Show |
1 | a0001c0001t0001g0040 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1215+9044_1215+906 others(25): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(35): Show |
4 | a0001c0002t0002g0109a0001c0002t0002g0111a0001c0002t0002g0112others(1): Show | 4 | HG00741.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+9064_1215+906 others(46): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(42): Show |
4 | a0001c0002t0002g0094a0001c0002t0002g0098a0001c0002t0002g0101others(1): Show | 4 | HG01257.hp2 HG03927.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+9064_1215+906 others(53): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(63): Show |
1 | a0001c0002t0002g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1215+9064_1215+906 others(74): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(42): Show |
2 | a0001c0002t0002g0088a0001c0002t0002g0093 | 2 | HG00733.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1215+9064_1215+906 others(53): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(49): Show |
1 | a0001c0002t0002g0080 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1215+9064_1215+906 others(60): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(35): Show |
1 | a0001c0001t0001g0159 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1215+9023_1215+906 others(46): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(42): Show |
1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1215+9016_1215+906 others(53): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(49): Show |
1 | a0001c0001t0001g0160 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1215+9009_1215+906 others(60): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(63): Show |
2 | a0001c0001t0001g0178a0001c0001t0001g0311 | 2 | NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1215+8995_1215+906 others(74): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518196
|
A | AGGAGAGG others(84): Show |
1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1215+9064_1215+906 others(95): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518196 | ||||||
chr1:58518202
|
G | GGGGAGAG others(25): Show |
1 | a0001c0001t0001g0216 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1215+9058_1215+905 others(36): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518202 | ||||||
chr1:58518202
|
G | GGGGAGAG others(28): Show |
2 | a0001c0002t0002g0113a0001c0012t0002g0077 | 2 | HG00738.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1215+9058_1215+905 others(39): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518202 | ||||||
chr1:58518202
|
G | GGGGAGAG others(35): Show |
4 | a0001c0002t0002g0097a0001c0002t0002g0099a0001c0002t0002g0100others(1): Show | 4 | HG01256.hp2 HG02145.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+9058_1215+905 others(46): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518202 | ||||||
chr1:58518209
|
G | GGGGAGAG others(14): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0122a0001c0001t0001g0221 | 3 | HG01123.hp2 HG01993.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1215+9051_1215+905 others(25): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518209 | ||||||
chr1:58518209
|
G | GGGGAGAG others(35): Show |
1 | a0001c0001t0001g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1215+9051_1215+905 others(46): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518209 | ||||||
chr1:58518216
|
G | GGGGAGAG others(7): Show |
5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01081.hp2 HG01952.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+9044_1215+904 others(18): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518216 | ||||||
chr1:58518216
|
G | GGGGAGAG others(28): Show |
6 | a0001c0001t0001g0218a0001c0001t0001g0224a0001c0001t0001g0274others(3): Show | 6 | NA18939.hp2 NA18959.hp1 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+9044_1215+904 others(39): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518216 | ||||||
chr1:58518216
|
G | GGGGAGAG others(35): Show |
1 | a0001c0001t0001g0296 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1215+9044_1215+904 others(46): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518216 | ||||||
chr1:58518216
|
G | GGGGAGAG others(21): Show |
2 | a0001c0002t0002g0091a0001c0002t0002g0096 | 2 | HG04199.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1215+9044_1215+904 others(32): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518216 | ||||||
chr1:58518216
|
G | GGGGGAGA others(15): Show |
1 | a0001c0001t0001g0130 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1215+9044_1215+904 others(26): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518216 | ||||||
chr1:58518216
|
G | GGGGGAGA others(23): Show |
1 | a0001c0001t0001g0204 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1215+9044_1215+904 others(34): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518216 | ||||||
chr1:58518223
|
G | C | 1 | a0001c0001t0001g0264 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1215+9038C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518223 | ||||||
chr1:58518223
|
G | GGGGAGAC others(21): Show |
15 | a0001c0001t0001g0120a0001c0001t0001g0215a0001c0001t0001g0255others(12): Show | 15 | HG00140.hp1 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+9037_1215+903 others(32): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518223 | ||||||
chr1:58518223
|
G | GGGGAGAC others(21): Show |
1 | a0001c0001t0001g0253 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1215+9037_1215+903 others(32): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518223 | ||||||
chr1:58518230
|
G | C | 143 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0116others(140): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1215+9031C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518230 | ||||||
chr1:58518237
|
G | C | 88 | a0001c0001t0001g0119a0001c0001t0001g0127a0001c0001t0001g0128others(85): Show | 88 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1215+9024C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518237 | ||||||
chr1:58518244
|
G | C | 15 | a0001c0001t0001g0170a0001c0001t0001g0172a0004c0005t0001g0023others(12): Show | 16 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1215+9017C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518244 | ||||||
chr1:58518251
|
G | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0121others(49): Show | 53 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1215+9010C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518251 | ||||||
chr1:58518261
|
G | A | 1 | a0003c0004t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1215+9000C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518261 | ||||||
chr1:58518264
|
A | AGG | 26 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0143others(23): Show | 29 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1215+8995_1215+899 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518264 | ||||||
chr1:58518264
|
A | AGGGGAGA others(2): Show |
23 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0237others(20): Show | 24 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.1215+8996_1215+899 others(13): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518264 | ||||||
chr1:58518264
|
A | AGGGGAGA others(9): Show |
5 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0164others(2): Show | 5 | HG02155.hp1 HG03688.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+8996_1215+899 others(20): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518264 | ||||||
chr1:58518264
|
A | AGGGGAGA others(16): Show |
2 | a0001c0001t0001g0170a0001c0001t0005g0043 | 2 | HG01515.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1215+8996_1215+899 others(27): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518264 | ||||||
chr1:58518264
|
A | AGGGGAGA others(23): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0188 | 2 | HG00544.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1215+8996_1215+899 others(34): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518264 | ||||||
chr1:58518264
|
A | AGGGGAGA others(30): Show |
3 | a0001c0001t0001g0151a0001c0001t0001g0338a0003c0004t0001g0049 | 3 | HG02965.hp2 HG03579.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1215+8996_1215+899 others(41): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518264 | ||||||
chr1:58518266
|
G | A | 1 | a0003c0004t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1215+8995C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518266 | ||||||
chr1:58518266
|
G | GGGAGAGG others(31): Show |
6 | a0001c0001t0001g0291a0001c0001t0001g0293a0001c0001t0001g0294others(3): Show | 6 | HG01358.hp2 HG01516.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+8994_1215+899 others(42): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518266 | ||||||
chr1:58518266
|
G | GGGAGAGG others(36): Show |
1 | a0001c0001t0001g0317 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1215+8994_1215+899 others(47): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518266 | ||||||
chr1:58518266
|
G | GGGAGAGG others(45): Show |
1 | a0003c0004t0001g0072 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1215+8994_1215+899 others(56): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518266 | ||||||
chr1:58518266
|
G | GGGAGAGG others(32): Show |
1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1215+8994_1215+899 others(43): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518266 | ||||||
chr1:58518267
|
A | G | 253 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(250): Show | 255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1215+8994T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518267 | ||||||
chr1:58518271
|
A | G | 61 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0131others(58): Show | 65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1215+8990T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518271 | ||||||
chr1:58518272
|
G | A | 18 | a0001c0001t0001g0116a0001c0001t0001g0216a0001c0001t0001g0291others(15): Show | 19 | HG00741.hp2 HG01257.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1215+8989C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGA | 6 | a0001c0001t0001g0045a0001c0001t0001g0275a0001c0001t0003g0028others(3): Show | 6 | HG01255.hp2 HG02615.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+8987_1215+898 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGAGAA | 4 | a0001c0001t0001g0274a0001c0001t0001g0296a0001c0001t0001g0315others(1): Show | 4 | NA18939.hp2 NA18961.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(9): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGAGAAGA others(3): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0046 | 2 | HG01167.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(14): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGA | 37 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0001g0214others(34): Show | 37 | HG00639.hp1 HG00642.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(12): Show |
1 | a0004c0008t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(23): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(4): Show |
13 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(10): Show | 13 | HG00140.hp2 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(15): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(9): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0179 | 2 | HG00735.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(20): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(12): Show |
6 | a0001c0001t0001g0217a0001c0001t0001g0220a0001c0001t0001g0231others(3): Show | 6 | HG01106.hp2 HG01361.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(23): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(11): Show |
13 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0165others(10): Show | 13 | HG02056.hp2 HG02165.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(22): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(16): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0125others(12): Show | 15 | HG01070.hp2 HG01106.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(27): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(18): Show |
2 | a0001c0001t0001g0128a0001c0001t0001g0177 | 2 | NA19007.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(29): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(23): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0180 | 2 | HG03486.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(34): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(25): Show |
1 | a0001c0001t0001g0337 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(36): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(30): Show |
4 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0001g0183others(1): Show | 4 | HG00408.hp1 HG03942.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+8988_1215+898 others(41): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(32): Show |
1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(43): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(37): Show |
1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(48): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(44): Show |
1 | a0001c0001t0001g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(55): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(54): Show |
1 | a0001c0001t0001g0149 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(65): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(46): Show |
1 | a0001c0001t0001g0146 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(57): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(61): Show |
1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(72): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(58): Show |
1 | a0001c0001t0001g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(69): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
G | GGGGAGAG others(88): Show |
1 | a0001c0001t0001g0145 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1215+8988_1215+898 others(99): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518272
|
GGAGAGGA others(8): Show |
G | 1 | a0005c0006t0001g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1215+8974_1215+898 others(19): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518272 | ||||||
chr1:58518273
|
GAGA | G | 6 | a0001c0001t0001g0236a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG02004.hp1 HG02273.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+8985_1215+898 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518273 | ||||||
chr1:58518273
|
GAGAGGA | G | 9 | a0001c0001t0001g0226a0001c0001t0001g0249a0001c0001t0001g0261others(6): Show | 9 | HG00423.hp2 HG01346.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215+8982_1215+898 others(10): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518273 | ||||||
chr1:58518273
|
GAGAGGAG others(4): Show |
G | 6 | a0001c0001t0001g0246a0001c0001t0001g0263a0001c0001t0001g0284others(3): Show | 6 | HG00558.hp2 HG02976.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+8977_1215+898 others(15): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518273 | ||||||
chr1:58518274
|
A | G | 100 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0123others(97): Show | 102 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1215+8987T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518274 | ||||||
chr1:58518276
|
A | G | 68 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0135others(65): Show | 68 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1215+8985T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518276 | ||||||
chr1:58518276
|
AG | A | 11 | a0001c0001t0001g0152a0001c0001t0001g0225a0001c0001t0001g0238others(8): Show | 11 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.1215+8984delC | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518276 | ||||||
chr1:58518277
|
G | A | 66 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0046others(63): Show | 67 | HG00140.hp1 HG00741.hp2 HG01081.hp2 others(64): Show |
intron_variant | MODIFIER | c.1215+8984C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GA | 7 | a0001c0001t0001g0130a0001c0001t0001g0301a0001c0001t0001g0322others(4): Show | 7 | HG01168.hp1 HG02257.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(5): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAA | 7 | a0001c0002t0002g0088a0001c0002t0002g0093a0001c0002t0002g0095others(4): Show | 7 | HG00733.hp1 HG00738.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGA | 3 | a0001c0001t0001g0204a0001c0002t0002g0100a0001c0002t0002g0101 | 3 | HG01256.hp2 HG01257.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGA | 4 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0245others(1): Show | 4 | HG03834.hp1 HG06807.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(10): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(6): Show |
5 | a0001c0001t0001g0212a0001c0001t0001g0250a0001c0001t0001g0252others(2): Show | 5 | HG00280.hp1 HG01943.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(17): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(11): Show |
14 | a0001c0001t0001g0123a0001c0001t0001g0206a0001c0001t0001g0207others(11): Show | 14 | HG00099.hp2 HG00323.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(22): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(13): Show |
2 | a0001c0001t0001g0133a0001c0001t0001g0141 | 2 | HG00323.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(24): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(18): Show |
2 | a0001c0001t0001g0199a0001c0001t0004g0203 | 2 | NA18966.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(29): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(20): Show |
8 | a0001c0001t0001g0126a0001c0001t0001g0166a0001c0001t0001g0167others(5): Show | 8 | HG00597.hp2 HG00621.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(31): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(25): Show |
10 | a0001c0001t0001g0132a0001c0001t0001g0136a0001c0001t0001g0168others(7): Show | 11 | HG00438.hp1 HG01358.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(36): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(83): Show |
1 | a0003c0004t0001g0073 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(94): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(78): Show |
1 | a0003c0004t0001g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(89): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(27): Show |
4 | a0001c0001t0001g0172a0001c0001t0001g0198a0001c0002t0002g0084others(1): Show | 4 | HG01255.hp1 HG03239.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(38): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(32): Show |
2 | a0001c0002t0002g0078a0001c0002t0002g0090 | 2 | HG02622.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(43): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(55): Show |
3 | a0003c0004t0001g0068a0003c0004t0001g0070a0003c0004t0001g0071 | 3 | HG02258.hp1 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(66): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(37): Show |
1 | a0001c0002t0002g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(48): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(34): Show |
4 | a0001c0001t0001g0185a0001c0002t0002g0081a0001c0002t0002g0083others(1): Show | 4 | HG02083.hp2 HG03669.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(45): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(39): Show |
9 | a0001c0001t0001g0006a0001c0001t0001g0142a0001c0001t0001g0154others(6): Show | 10 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215+8983_1215+898 others(50): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(41): Show |
1 | a0001c0001t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(52): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(46): Show |
1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(57): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(53): Show |
1 | a0001c0001t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(64): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(62): Show |
1 | a0001c0002t0002g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(73): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(102): Show |
1 | a0001c0001t0001g0147 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(113): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GAGGGGAG others(137): Show |
1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(148): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
G | GGGAGAGG others(45): Show |
1 | a0001c0002t0002g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1215+8983_1215+898 others(56): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518277
|
GGAGAAGA others(12): Show |
G | 1 | a0004c0005t0006g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1215+8965_1215+898 others(23): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518277 | ||||||
chr1:58518279
|
A | AGAAGGGA others(33): Show |
1 | a0003c0004t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1215+8981_1215+898 others(44): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518279 | ||||||
chr1:58518279
|
A | G | 44 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0130others(41): Show | 46 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1215+8982T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518279 | ||||||
chr1:58518281
|
A | AG | 28 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0134others(25): Show | 30 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1215+8979_1215+898 others(5): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518281 | ||||||
chr1:58518281
|
A | AGAGGGGA others(20): Show |
2 | a0001c0001t0001g0143a0001c0002t0002g0011 | 2 | HG03471.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1215+8979_1215+898 others(31): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518281 | ||||||
chr1:58518281
|
A | AGAGGGGA others(27): Show |
2 | a0001c0001t0001g0131a0001c0001t0001g0189 | 2 | NA18943.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1215+8979_1215+898 others(38): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518281 | ||||||
chr1:58518281
|
A | AGAGGGGA others(48): Show |
1 | a0001c0001t0002g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1215+8979_1215+898 others(59): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518281 | ||||||
chr1:58518281
|
A | AGGGG | 34 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(31): Show | 34 | HG00140.hp2 HG01074.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1215+8979_1215+898 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518281 | ||||||
chr1:58518281
|
A | G | 55 | a0001c0001t0001g0039a0001c0001t0001g0126a0001c0001t0001g0130others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1215+8980T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518281 | ||||||
chr1:58518282
|
A | G | 92 | a0001c0001t0001g0006a0001c0001t0001g0123a0001c0001t0001g0128others(89): Show | 94 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1215+8979T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518282 | ||||||
chr1:58518284
|
A | AGAAGGGA others(23): Show |
1 | a0003c0004t0001g0003 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1215+8976_1215+897 others(34): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518284 | ||||||
chr1:58518284
|
A | G | 60 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0128others(57): Show | 62 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1215+8977T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518284 | ||||||
chr1:58518286
|
A | AG | 21 | a0001c0001t0001g0128a0001c0001t0001g0177a0001c0001t0001g0336others(18): Show | 21 | HG00642.hp1 HG01175.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1215+8974_1215+897 others(5): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518286 | ||||||
chr1:58518286
|
A | G | 90 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0127others(87): Show | 92 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1215+8975T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518286 | ||||||
chr1:58518287
|
A | AGGGAGGG others(28): Show |
1 | a0002c0003t0001g0346 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1215+8973_1215+897 others(39): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518287 | ||||||
chr1:58518287
|
A | AGGGAGGG others(33): Show |
1 | a0002c0003t0001g0345 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1215+8973_1215+897 others(44): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518287 | ||||||
chr1:58518287
|
A | G | 63 | a0001c0001t0001g0039a0001c0001t0001g0126a0001c0001t0001g0127others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.1215+8974T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518287 | ||||||
chr1:58518289
|
A | G | 32 | a0001c0001t0001g0128a0001c0001t0001g0177a0001c0001t0001g0336others(29): Show | 33 | HG00642.hp1 HG01175.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1215+8972T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518289 | ||||||
chr1:58518291
|
A | AGGGG | 7 | a0001c0001t0001g0127a0001c0001t0001g0137a0004c0005t0002g0012others(4): Show | 7 | HG01074.hp2 HG01081.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+8969_1215+897 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518291 | ||||||
chr1:58518291
|
A | AGGGGAG | 9 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(6): Show | 9 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+8969_1215+897 others(10): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518291 | ||||||
chr1:58518291
|
A | G | 59 | a0001c0001t0001g0007a0001c0001t0001g0119a0001c0001t0001g0128others(56): Show | 61 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1215+8970T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518291 | ||||||
chr1:58518292
|
A | G | 46 | a0001c0001t0001g0007a0001c0001t0001g0130a0001c0001t0001g0131others(43): Show | 48 | HG00423.hp2 HG00558.hp2 HG01346.hp2 others(45): Show |
intron_variant | MODIFIER | c.1215+8969T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518292 | ||||||
chr1:58518294
|
A | AGAAGGGA others(33): Show |
1 | a0003c0004t0001g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1215+8966_1215+896 others(44): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518294 | ||||||
chr1:58518294
|
A | AGAAGGGA others(38): Show |
1 | a0003c0004t0001g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1215+8966_1215+896 others(49): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518294 | ||||||
chr1:58518294
|
A | AGAAGGGA others(43): Show |
1 | a0003c0004t0001g0058 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1215+8966_1215+896 others(54): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518294 | ||||||
chr1:58518294
|
A | AGAAGGGA others(48): Show |
1 | a0003c0004t0001g0051 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1215+8966_1215+896 others(59): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518294 | ||||||
chr1:58518294
|
A | G | 20 | a0001c0001t0001g0331a0001c0001t0001g0334a0001c0001t0001g0335others(17): Show | 21 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1215+8967T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518294 | ||||||
chr1:58518296
|
A | AGGGG | 4 | a0001c0001t0001g0007a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 6 | HG02257.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+8964_1215+896 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518296 | ||||||
chr1:58518296
|
A | AGGGGAGA others(18): Show |
1 | a0001c0001t0001g0342 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1215+8964_1215+896 others(29): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518296 | ||||||
chr1:58518296
|
A | G | 38 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0137others(35): Show | 38 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1215+8965T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518296 | ||||||
chr1:58518297
|
A | G | 39 | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0163others(36): Show | 39 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.1215+8964T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518297 | ||||||
chr1:58518299
|
A | AGAAGGGA others(18): Show |
1 | a0008c0013t0001g0054 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1215+8961_1215+896 others(29): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(23): Show |
1 | a0003c0004t0001g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1215+8961_1215+896 others(34): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(28): Show |
5 | a0003c0004t0001g0004a0003c0004t0001g0049a0003c0004t0001g0050others(2): Show | 6 | HG02818.hp2 HG02965.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215+8961_1215+896 others(39): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(33): Show |
3 | a0003c0004t0001g0053a0003c0004t0001g0055a0003c0004t0001g0065 | 3 | HG00735.hp2 HG02622.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1215+8961_1215+896 others(44): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(38): Show |
1 | a0003c0004t0001g0060 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1215+8961_1215+896 others(49): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(43): Show |
1 | a0003c0004t0001g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1215+8961_1215+896 others(54): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(48): Show |
1 | a0003c0004t0001g0059 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1215+8961_1215+896 others(59): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | AGAAGGGA others(53): Show |
1 | a0003c0004t0001g0057 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1215+8961_1215+896 others(64): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518299
|
A | G | 18 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(15): Show | 19 | HG00642.hp2 HG01109.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1215+8962T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518299 | ||||||
chr1:58518301
|
A | AGGGG | 5 | a0004c0005t0002g0012a0004c0005t0002g0014a0004c0005t0002g0015others(2): Show | 5 | HG01074.hp2 HG01081.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+8959_1215+896 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518301 | ||||||
chr1:58518301
|
A | G | 16 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(13): Show | 18 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1215+8960T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518301 | ||||||
chr1:58518302
|
A | AGGGAGGG others(58): Show |
2 | a0002c0003t0001g0347a0002c0003t0001g0359 | 2 | NA18982.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1215+8958_1215+895 others(69): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518302 | ||||||
chr1:58518302
|
A | G | 26 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0137others(23): Show | 27 | HG00642.hp1 HG01099.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.1215+8959T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518302 | ||||||
chr1:58518304
|
A | AGAAGGGA others(33): Show |
2 | a0003c0004t0001g0105a0003c0004t0001g0107 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1215+8956_1215+895 others(44): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518304 | ||||||
chr1:58518304
|
A | G | 40 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(37): Show | 42 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1215+8957T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518304 | ||||||
chr1:58518306
|
A | G | 8 | a0004c0005t0001g0023a0004c0005t0002g0012a0004c0005t0002g0014others(5): Show | 8 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+8955T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518306 | ||||||
chr1:58518307
|
A | AGGGAGGG others(58): Show |
7 | a0002c0003t0001g0349a0002c0003t0001g0350a0002c0003t0001g0351others(4): Show | 7 | HG00423.hp1 HG00621.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+8953_1215+895 others(69): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518307 | ||||||
chr1:58518307
|
A | AGGGAGGG others(68): Show |
2 | a0002c0003t0001g0361a0002c0003t0001g0374 | 2 | NA18747.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1215+8953_1215+895 others(79): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518307 | ||||||
chr1:58518307
|
A | G | 15 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(12): Show | 16 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1215+8954T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518307 | ||||||
chr1:58518309
|
A | AAGGGAAG others(76): Show |
1 | a0002c0003t0001g0366 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1215+8951_1215+895 others(87): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518309 | ||||||
chr1:58518309
|
A | G | 58 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(55): Show | 60 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1215+8952T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518309 | ||||||
chr1:58518311
|
A | G | 2 | a0004c0005t0001g0023a0004c0005t0002g0001 | 3 | HG01243.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1215+8950T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518311 | ||||||
chr1:58518312
|
A | AGGGAGGG others(58): Show |
5 | a0002c0003t0001g0356a0002c0003t0001g0360a0002c0003t0001g0363others(2): Show | 5 | HG01175.hp1 NA18941.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+8948_1215+894 others(69): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518312 | ||||||
chr1:58518312
|
A | AGGGAGGG others(63): Show |
8 | a0002c0003t0001g0348a0002c0003t0001g0354a0002c0003t0001g0355others(5): Show | 8 | HG00642.hp1 NA18957.hp2 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+8948_1215+894 others(74): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518312 | ||||||
chr1:58518312
|
A | AGGGAGGG others(68): Show |
3 | a0002c0003t0001g0362a0002c0003t0001g0375a0002c0003t0002g0353 | 3 | NA18956.hp2 NA18972.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1215+8948_1215+894 others(79): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518312 | ||||||
chr1:58518312
|
A | AGGGAGGG others(88): Show |
1 | a0002c0003t0001g0352 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1215+8948_1215+894 others(99): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518312 | ||||||
chr1:58518312
|
A | G | 5 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0351others(2): Show | 5 | HG01243.hp1 HG04115.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+8949T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518312 | ||||||
chr1:58518314
|
A | G | 60 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(57): Show | 62 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1215+8947T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518314 | ||||||
chr1:58518316
|
A | G | 1 | a0004c0005t0006g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1215+8945T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518316 | ||||||
chr1:58518317
|
A | G | 4 | a0002c0003t0001g0346a0002c0003t0001g0365a0002c0003t0001g0370others(1): Show | 4 | HG01175.hp1 HG01243.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+8944T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518317 | ||||||
chr1:58518319
|
A | G | 60 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(57): Show | 62 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1215+8942T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518319 | ||||||
chr1:58518321
|
A | G | 1 | a0004c0005t0006g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1215+8940T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518321 | ||||||
chr1:58518322
|
A | G | 1 | a0004c0005t0006g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1215+8939T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518322 | ||||||
chr1:58518324
|
A | G | 59 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(56): Show | 61 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1215+8937T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518324 | ||||||
chr1:58518326
|
A | G | 1 | a0004c0005t0001g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1215+8935T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518326 | ||||||
chr1:58518329
|
A | G | 61 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(58): Show | 63 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1215+8932T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518329 | ||||||
chr1:58518331
|
A | G | 2 | a0004c0005t0001g0023a0004c0005t0006g0013 | 2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1215+8930T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518331 | ||||||
chr1:58518334
|
A | G | 59 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(56): Show | 61 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1215+8927T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518334 | ||||||
chr1:58518336
|
A | G | 2 | a0004c0005t0001g0023a0004c0005t0006g0013 | 2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1215+8925T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518336 | ||||||
chr1:58518339
|
A | G | 59 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(56): Show | 61 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1215+8922T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518339 | ||||||
chr1:58518339
|
AGAAGAGA others(8): Show |
A | 1 | a0001c0001t0001g0264 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1215+8907_1215+892 others(19): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518339 | ||||||
chr1:58518344
|
A | G | 59 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(56): Show | 61 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1215+8917T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518344 | ||||||
chr1:58518349
|
A | AGAAGG | 3 | a0005c0006t0001g0005a0005c0006t0001g0069a0005c0006t0001g0074 | 4 | HG01069.hp2 HG01071.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+8907_1215+891 others(9): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518349 | ||||||
chr1:58518349
|
A | AGAAGGGA others(8): Show |
3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1215+8911_1215+891 others(19): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518349 | ||||||
chr1:58518349
|
A | G | 60 | a0001c0002t0002g0011a0002c0003t0001g0345a0002c0003t0001g0346others(57): Show | 62 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1215+8912T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518349 | ||||||
chr1:58518349
|
AGAAGG | A | 30 | a0001c0001t0001g0007a0001c0001t0001g0116a0001c0001t0001g0217others(27): Show | 31 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1215+8907_1215+891 others(9): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518349 | ||||||
chr1:58518354
|
G | A | 202 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(199): Show | 204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1215+8907C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518354 | ||||||
chr1:58518359
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0272 | 2 | NA19078.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1215+8902C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518359 | ||||||
chr1:58518364
|
A | G | 37 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(34): Show | 37 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1215+8897T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518364 | ||||||
chr1:58518369
|
A | G | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+8892T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518369 | ||||||
chr1:58518389
|
A | G | 1 | a0001c0001t0001g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1215+8872T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518389 | ||||||
chr1:58518499
|
A | T | 1 | a0001c0001t0001g0330 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1215+8762T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518499 | ||||||
chr1:58518625
|
T | A | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1215+8636A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518625 | ||||||
chr1:58518627
|
TTTATCTA others(2): Show |
T | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1215+8625_1215+863 others(13): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518627 | ||||||
chr1:58518638
|
ACCCT | A | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1215+8619_1215+862 others(8): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518638 | ||||||
chr1:58518656
|
G | GT | 35 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0001g0150others(32): Show | 35 | HG00544.hp2 HG00673.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.1215+8604dupA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518656 | ||||||
chr1:58518662
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1215+8599A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518662 | ||||||
chr1:58518802
|
G | A | 1 | a0006c0007t0001g0287 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1215+8459C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518802 | ||||||
chr1:58518971
|
C | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215+8290G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58518971 | ||||||
chr1:58519007
|
G | A | 350 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(347): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1215+8254C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519007 | ||||||
chr1:58519150
|
G | T | 1 | a0001c0002t0002g0108 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1215+8111C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519150 | ||||||
chr1:58519277
|
G | T | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1215+7984C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519277 | ||||||
chr1:58519290
|
A | G | 1 | a0006c0007t0001g0326 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1215+7971T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519290 | ||||||
chr1:58519586
|
A | T | 157 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1215+7675T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519586 | ||||||
chr1:58519741
|
T | A | 1 | a0001c0001t0001g0308 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1215+7520A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519741 | ||||||
chr1:58519792
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1215+7469T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519792 | ||||||
chr1:58519793
|
T | C | 8 | a0001c0002t0002g0078a0001c0002t0002g0090a0001c0002t0002g0110others(5): Show | 8 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1215+7468A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519793 | ||||||
chr1:58519880
|
G | A | 1 | a0004c0005t0002g0020 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1215+7381C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519880 | ||||||
chr1:58519887
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 5 | HG02257.hp2 HG02572.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215+7374T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519887 | ||||||
chr1:58519899
|
C | T | 1 | a0002c0003t0001g0350 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1215+7362G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519899 | ||||||
chr1:58519966
|
C | CAT | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+7294_1215+729 others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58519966 | ||||||
chr1:58520006
|
C | T | 1 | a0001c0001t0005g0047 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1215+7255G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520006 | ||||||
chr1:58520031
|
G | T | 82 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(79): Show | 86 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.1215+7230C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520031 | ||||||
chr1:58520078
|
G | A | 71 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(68): Show | 74 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1215+7183C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520078 | ||||||
chr1:58520102
|
G | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+7159C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520102 | ||||||
chr1:58520124
|
T | A | 237 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(234): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1215+7137A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520124 | ||||||
chr1:58520158
|
C | T | 1 | a0007c0011t0002g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1215+7103G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520158 | ||||||
chr1:58520159
|
C | T | 5 | a0004c0005t0002g0012a0004c0005t0002g0014a0004c0005t0002g0015others(2): Show | 5 | HG01074.hp2 HG01081.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+7102G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520159 | ||||||
chr1:58520198
|
G | A | 2 | a0004c0005t0001g0023a0004c0005t0006g0013 | 2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.1215+7063C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520198 | ||||||
chr1:58520228
|
G | A | 362 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(359): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1215+7033C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520228 | ||||||
chr1:58520476
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1215+6785T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520476 | ||||||
chr1:58520808
|
C | T | 1 | a0003c0004t0001g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1215+6453G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520808 | ||||||
chr1:58520890
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1215+6371G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520890 | ||||||
chr1:58520997
|
C | T | 157 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1215+6264G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58520997 | ||||||
chr1:58521008
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+6253A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521008 | ||||||
chr1:58521012
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1215+6249G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521012 | ||||||
chr1:58521217
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215+6044G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521217 | ||||||
chr1:58521289
|
C | T | 29 | a0002c0003t0001g0347a0002c0003t0001g0348a0002c0003t0001g0349others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1215+5972G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521289 | ||||||
chr1:58521298
|
G | C | 237 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(234): Show | 240 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1215+5963C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521298 | ||||||
chr1:58521308
|
G | A | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+5953C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521308 | ||||||
chr1:58521328
|
G | GA | 157 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(154): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1215+5932dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521328 | ||||||
chr1:58521423
|
A | G | 11 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(8): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1215+5838T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521423 | ||||||
chr1:58521436
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1215+5825T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521436 | ||||||
chr1:58521444
|
T | C | 350 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(347): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1215+5817A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521444 | ||||||
chr1:58521602
|
C | G | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+5659G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521602 | ||||||
chr1:58521703
|
A | T | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1215+5558T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521703 | ||||||
chr1:58521840
|
A | G | 28 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(25): Show | 30 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1215+5421T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58521840 | ||||||
chr1:58522090
|
C | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+5171G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522090 | ||||||
chr1:58522107
|
G | T | 1 | a0001c0001t0001g0237 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1215+5154C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522107 | ||||||
chr1:58522156
|
A | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+5105T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522156 | ||||||
chr1:58522429
|
A | C | 28 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(25): Show | 30 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1215+4832T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522429 | ||||||
chr1:58522619
|
AC | A | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1215+4641delG | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522619 | ||||||
chr1:58522676
|
A | G | 11 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(8): Show | 12 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1215+4585T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522676 | ||||||
chr1:58522871
|
A | G | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1215+4390T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522871 | ||||||
chr1:58522878
|
C | T | 7 | a0003c0004t0001g0049a0003c0004t0001g0067a0003c0004t0001g0068others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+4383G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58522878 | ||||||
chr1:58523005
|
T | C | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1215+4256A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523005 | ||||||
chr1:58523291
|
C | G | 1 | a0001c0001t0005g0042 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1215+3970G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523291 | ||||||
chr1:58523553
|
G | T | 3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1215+3708C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523553 | ||||||
chr1:58523557
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1215+3704A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523557 | ||||||
chr1:58523622
|
G | A | 1 | a0001c0002t0002g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1215+3639C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523622 | ||||||
chr1:58523628
|
A | G | 2 | a0001c0001t0003g0025a0001c0001t0003g0036 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1215+3633T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523628 | ||||||
chr1:58523638
|
A | G | 68 | a0001c0001t0002g0008a0001c0001t0003g0025a0001c0001t0003g0036others(65): Show | 72 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.1215+3623T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523638 | ||||||
chr1:58523663
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+3598C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523663 | ||||||
chr1:58523681
|
C | T | 1 | a0003c0004t0001g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1215+3580G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523681 | ||||||
chr1:58523727
|
A | G | 2 | a0001c0001t0001g0178a0001c0001t0001g0311 | 2 | NA19067.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1215+3534T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523727 | ||||||
chr1:58523760
|
A | G | 363 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(360): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.1215+3501T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523760 | ||||||
chr1:58523886
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+3375C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523886 | ||||||
chr1:58523886
|
G | T | 1 | a0004c0005t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1215+3375C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58523886 | ||||||
chr1:58524009
|
C | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0255a0001c0001t0001g0256others(3): Show | 6 | HG02129.hp1 NA18945.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1215+3252G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524009 | ||||||
chr1:58524023
|
A | T | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1215+3238T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524023 | ||||||
chr1:58524104
|
C | G | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1215+3157G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524104 | ||||||
chr1:58524130
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+3131T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524130 | ||||||
chr1:58524144
|
A | T | 1 | a0001c0001t0001g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1215+3117T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524144 | ||||||
chr1:58524161
|
T | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+3100A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524161 | ||||||
chr1:58524189
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+3072T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524189 | ||||||
chr1:58524245
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1215+3016G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524245 | ||||||
chr1:58524245
|
C | T | 2 | a0003c0004t0001g0068a0003c0004t0001g0070 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1215+3016G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524245 | ||||||
chr1:58524369
|
T | C | 7 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0249others(4): Show | 7 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.1215+2892A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524369 | ||||||
chr1:58524383
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1215+2878C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524383 | ||||||
chr1:58524490
|
T | C | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1215+2771A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524490 | ||||||
chr1:58524583
|
A | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0194 | 2 | NA18939.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1215+2678T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524583 | ||||||
chr1:58524716
|
T | A | 1 | a0007c0011t0002g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1215+2545A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524716 | ||||||
chr1:58524840
|
G | T | 6 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(3): Show | 7 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+2421C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524840 | ||||||
chr1:58524881
|
C | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0264a0001c0001t0001g0266 | 3 | HG02970.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1215+2380G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524881 | ||||||
chr1:58524957
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1215+2304G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524957 | ||||||
chr1:58524995
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1215+2266C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58524995 | ||||||
chr1:58525150
|
T | C | 1 | a0001c0002t0002g0103 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1215+2111A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525150 | ||||||
chr1:58525165
|
A | G | 221 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1215+2096T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525165 | ||||||
chr1:58525282
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+1979T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525282 | ||||||
chr1:58525328
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1215+1933C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525328 | ||||||
chr1:58525357
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215+1904G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525357 | ||||||
chr1:58525568
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1215+1693A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525568 | ||||||
chr1:58525637
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+1624C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525637 | ||||||
chr1:58525770
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+1491A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525770 | ||||||
chr1:58525798
|
C | T | 35 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(32): Show | 35 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1215+1463G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525798 | ||||||
chr1:58525866
|
A | T | 1 | a0001c0001t0001g0301 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1215+1395T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525866 | ||||||
chr1:58525905
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1215+1356T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525905 | ||||||
chr1:58525926
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0170 | 2 | HG01099.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1215+1335T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58525926 | ||||||
chr1:58526067
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1215+1194A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526067 | ||||||
chr1:58526109
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1215+1152G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526109 | ||||||
chr1:58526154
|
T | A | 4 | a0001c0001t0001g0206a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | HG02486.hp1 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+1107A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526154 | ||||||
chr1:58526216
|
C | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+1045G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526216 | ||||||
chr1:58526239
|
A | G | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+1022T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526239 | ||||||
chr1:58526293
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1215+968T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526293 | ||||||
chr1:58526399
|
T | A | 113 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(110): Show | 117 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1215+862A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526399 | ||||||
chr1:58526475
|
A | G | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1215+786T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526475 | ||||||
chr1:58526601
|
C | CAAA | 19 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(16): Show | 21 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1215+657_1215+659d others(5): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526601 | ||||||
chr1:58526601
|
C | CAAAA | 15 | a0003c0004t0001g0049a0003c0004t0001g0056a0003c0004t0001g0057others(12): Show | 16 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1215+656_1215+659d others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526601 | ||||||
chr1:58526601
|
CA | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0117others(160): Show | 164 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1215+659delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526601 | ||||||
chr1:58526601
|
CAA | C | 59 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0120others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.1215+658_1215+659d others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526601 | ||||||
chr1:58526631
|
A | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1215+630T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526631 | ||||||
chr1:58526658
|
T | C | 221 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(218): Show | 222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.1215+603A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526658 | ||||||
chr1:58526665
|
T | G | 1 | a0001c0002t0002g0102 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1215+596A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526665 | ||||||
chr1:58526819
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1215+442G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526819 | ||||||
chr1:58526838
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1215+423A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526838 | ||||||
chr1:58526919
|
A | C | 1 | a0001c0001t0002g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1215+342T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526919 | ||||||
chr1:58526940
|
G | A | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1215+321C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526940 | ||||||
chr1:58526954
|
T | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0120others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1215+307A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58526954 | ||||||
chr1:58527005
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1215+256G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58527005 | ||||||
chr1:58527101
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1215+160C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 7/8 | chr1 | 58527101 | ||||||
chr1:58527620
|
C | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1141-285G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58527620 | ||||||
chr1:58527767
|
T | TA | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1141-433dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58527767 | ||||||
chr1:58527921
|
T | C | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1141-586A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58527921 | ||||||
chr1:58528003
|
C | T | 1 | a0002c0003t0001g0363 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1141-668G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528003 | ||||||
chr1:58528030
|
T | A | 1 | a0001c0001t0001g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1141-695A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528030 | ||||||
chr1:58528175
|
A | G | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1141-840T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528175 | ||||||
chr1:58528425
|
T | C | 21 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(18): Show | 23 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1141-1090A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528425 | ||||||
chr1:58528440
|
G | T | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1141-1105C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528440 | ||||||
chr1:58528508
|
C | T | 65 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(62): Show | 68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1141-1173G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528508 | ||||||
chr1:58528614
|
T | A | 4 | a0003c0004t0001g0068a0003c0004t0001g0070a0003c0004t0001g0071others(1): Show | 4 | HG02258.hp1 HG02717.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-1279A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528614 | ||||||
chr1:58528614
|
T | C | 1 | a0002c0003t0001g0361 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1141-1279A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528614 | ||||||
chr1:58528656
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1141-1321C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528656 | ||||||
chr1:58528763
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0251 | 2 | NA18952.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1141-1428T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58528763 | ||||||
chr1:58529041
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1140+1560T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529041 | ||||||
chr1:58529069
|
A | T | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1140+1532T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529069 | ||||||
chr1:58529132
|
C | G | 1 | a0003c0004t0001g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1140+1469G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529132 | ||||||
chr1:58529279
|
A | T | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1140+1322T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529279 | ||||||
chr1:58529504
|
A | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1140+1097T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529504 | ||||||
chr1:58529674
|
A | G | 13 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0050others(10): Show | 15 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1140+927T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529674 | ||||||
chr1:58529727
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1140+874A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529727 | ||||||
chr1:58529730
|
G | A | 2 | a0002c0003t0001g0345a0002c0003t0001g0346 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1140+871C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529730 | ||||||
chr1:58529776
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1140+825T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529776 | ||||||
chr1:58529819
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1140+782C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529819 | ||||||
chr1:58529837
|
T | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0001g0233others(2): Show | 5 | HG00741.hp1 HG01081.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+764A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529837 | ||||||
chr1:58529847
|
T | C | 220 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1140+754A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529847 | ||||||
chr1:58529913
|
C | A | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1140+688G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529913 | ||||||
chr1:58529980
|
A | T | 1 | a0001c0001t0001g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1140+621T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529980 | ||||||
chr1:58529981
|
C | T | 11 | a0001c0001t0001g0140a0001c0001t0001g0143a0001c0001t0001g0144others(8): Show | 11 | HG00609.hp1 NA18945.hp1 NA18975.hp1 others(8): Show |
intron_variant | MODIFIER | c.1140+620G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58529981 | ||||||
chr1:58530132
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1140+469A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58530132 | ||||||
chr1:58530135
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1140+466G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58530135 | ||||||
chr1:58530311
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1140+290C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58530311 | ||||||
chr1:58530531
|
T | C | 64 | a0001c0001t0001g0117a0001c0001t0001g0216a0001c0001t0001g0217others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1140+70A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 6/8 | chr1 | 58530531 | ||||||
chr1:58530755
|
C | T | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1012-26G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530755 | ||||||
chr1:58530778
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1012-49A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530778 | ||||||
chr1:58530857
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1012-128A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530857 | ||||||
chr1:58530877
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0214 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1012-148C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530877 | ||||||
chr1:58530915
|
A | G | 2 | a0002c0003t0001g0345a0002c0003t0001g0346 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1012-186T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530915 | ||||||
chr1:58530960
|
A | T | 29 | a0002c0003t0001g0347a0002c0003t0001g0348a0002c0003t0001g0349others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.1012-231T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530960 | ||||||
chr1:58530993
|
T | C | 62 | a0001c0001t0001g0117a0001c0001t0001g0216a0001c0001t0001g0217others(59): Show | 62 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1012-264A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58530993 | ||||||
chr1:58531019
|
A | G | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1012-290T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531019 | ||||||
chr1:58531146
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1012-417A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531146 | ||||||
chr1:58531348
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1012-619C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531348 | ||||||
chr1:58531372
|
G | A | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1012-643C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531372 | ||||||
chr1:58531405
|
T | C | 28 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(25): Show | 30 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1012-676A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531405 | ||||||
chr1:58531415
|
C | A | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1012-686G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531415 | ||||||
chr1:58531468
|
T | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0045a0004c0008t0001g0017others(2): Show | 5 | HG01255.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012-739A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531468 | ||||||
chr1:58531565
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1012-836A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531565 | ||||||
chr1:58531589
|
C | G | 3 | a0005c0006t0001g0063a0005c0006t0001g0064a0005c0006t0001g0066 | 3 | HG01256.hp1 HG01258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1012-860G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531589 | ||||||
chr1:58531613
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-884G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531613 | ||||||
chr1:58531628
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-899G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531628 | ||||||
chr1:58531716
|
CT | C | 316 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(313): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1012-988delA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531716 | ||||||
chr1:58531718
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-989A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531718 | ||||||
chr1:58531725
|
T | C | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1012-996A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531725 | ||||||
chr1:58531727
|
TG | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-999delC | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531727 | ||||||
chr1:58531800
|
C | T | 1 | a0001c0001t0001g0328 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1012-1071G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531800 | ||||||
chr1:58531826
|
A | G | 1 | a0002c0003t0001g0346 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1012-1097T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531826 | ||||||
chr1:58531833
|
C | T | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1012-1104G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531833 | ||||||
chr1:58531866
|
G | A | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1012-1137C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531866 | ||||||
chr1:58531916
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-1187G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531916 | ||||||
chr1:58531920
|
G | T | 1 | a0001c0001t0003g0027 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1012-1191C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531920 | ||||||
chr1:58531944
|
T | C | 1 | a0001c0002t0002g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1012-1215A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531944 | ||||||
chr1:58531954
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-1225T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58531954 | ||||||
chr1:58532015
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1012-1286T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58532015 | ||||||
chr1:58532063
|
T | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1012-1334A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58532063 | ||||||
chr1:58532456
|
ATAT | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1011+1494_1011+149 others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58532456 | ||||||
chr1:58532588
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1011+1365A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58532588 | ||||||
chr1:58532655
|
A | G | 35 | a0001c0001t0001g0322a0003c0004t0001g0003a0003c0004t0001g0004others(32): Show | 38 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1011+1298T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58532655 | ||||||
chr1:58532806
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1011+1147T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58532806 | ||||||
chr1:58533161
|
C | A | 3 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044 | 3 | HG00738.hp2 HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1011+792G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533161 | ||||||
chr1:58533173
|
C | T | 48 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(45): Show | 49 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1011+780G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533173 | ||||||
chr1:58533189
|
G | A | 1 | a0001c0002t0002g0114 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1011+764C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533189 | ||||||
chr1:58533239
|
C | A | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1011+714G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533239 | ||||||
chr1:58533255
|
G | T | 7 | a0003c0004t0001g0049a0003c0004t0001g0067a0003c0004t0001g0068others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1011+698C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533255 | ||||||
chr1:58533426
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0141a0001c0001t0001g0142 | 4 | HG00323.hp2 HG00733.hp2 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1011+527T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533426 | ||||||
chr1:58533471
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1011+482C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533471 | ||||||
chr1:58533484
|
AT | A | 236 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.1011+468delA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533484 | ||||||
chr1:58533629
|
G | C | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1011+324C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533629 | ||||||
chr1:58533701
|
C | T | 220 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.1011+252G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533701 | ||||||
chr1:58533731
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1011+222A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533731 | ||||||
chr1:58533952
|
C | G | 1 | a0008c0013t0001g0054 | 1 | HG02572.hp2 | splice_donor_variant&intron_variant | HIGH | c.1011+1G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 5/8 | chr1 | 58533952 | ||||||
chr1:58534384
|
C | T | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.730-53G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534384 | ||||||
chr1:58534419
|
T | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.730-88A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534419 | ||||||
chr1:58534442
|
T | C | 1 | a0009c0010t0001g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.730-111A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534442 | ||||||
chr1:58534523
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.730-192C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534523 | ||||||
chr1:58534759
|
A | ACC | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(4): Show | 7 | HG01167.hp1 HG01255.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.730-430_730-429dup others(2): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534759 | ||||||
chr1:58534764
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.730-433C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534764 | ||||||
chr1:58534796
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.730-465G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534796 | ||||||
chr1:58534885
|
G | A | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.730-554C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534885 | ||||||
chr1:58534917
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.730-586C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534917 | ||||||
chr1:58534997
|
C | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.730-666G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58534997 | ||||||
chr1:58535045
|
C | G | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.730-714G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535045 | ||||||
chr1:58535066
|
C | T | 2 | a0005c0006t0001g0005a0005c0006t0001g0069 | 3 | HG01069.hp2 HG01071.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.730-735G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535066 | ||||||
chr1:58535129
|
T | A | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.730-798A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535129 | ||||||
chr1:58535322
|
G | A | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.730-991C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535322 | ||||||
chr1:58535443
|
A | C | 236 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.729+1070T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535443 | ||||||
chr1:58535595
|
C | CA | 38 | a0001c0001t0001g0311a0001c0001t0003g0035a0001c0002t0002g0089others(35): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.729+917dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535595 | ||||||
chr1:58535595
|
CA | C | 241 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(238): Show | 244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.729+917delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535595 | ||||||
chr1:58535595
|
CAA | C | 32 | a0001c0001t0001g0128a0001c0001t0001g0205a0002c0003t0001g0345others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.729+916_729+917del others(2): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535595 | ||||||
chr1:58535628
|
C | A | 220 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(217): Show | 221 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.729+885G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535628 | ||||||
chr1:58535740
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.729+773A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535740 | ||||||
chr1:58535741
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.729+772T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535741 | ||||||
chr1:58535969
|
TGTTA | T | 7 | a0003c0004t0001g0049a0003c0004t0001g0067a0003c0004t0001g0068others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.729+540_729+543del others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58535969 | ||||||
chr1:58536024
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.729+489A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58536024 | ||||||
chr1:58536161
|
C | T | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.729+352G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58536161 | ||||||
chr1:58536162
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.729+351C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58536162 | ||||||
chr1:58536349
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.729+164A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58536349 | ||||||
chr1:58536425
|
A | C | 1 | a0001c0001t0003g0026 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.729+88T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 3/8 | chr1 | 58536425 | ||||||
chr1:58536788
|
A | T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.501-47T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58536788 | ||||||
chr1:58536810
|
T | A | 8 | a0001c0001t0001g0218a0001c0001t0001g0224a0001c0001t0001g0274others(5): Show | 8 | NA18939.hp2 NA18952.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.501-69A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58536810 | ||||||
chr1:58536853
|
G | A | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.501-112C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58536853 | ||||||
chr1:58536924
|
T | C | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.501-183A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58536924 | ||||||
chr1:58536949
|
A | G | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.501-208T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58536949 | ||||||
chr1:58537023
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501-282G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537023 | ||||||
chr1:58537062
|
T | TTC | 71 | a0001c0001t0001g0117a0001c0001t0001g0127a0001c0001t0001g0216others(68): Show | 72 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.501-323_501-322dup others(2): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537062 | ||||||
chr1:58537062
|
T | TTCTCTCT others(3): Show |
29 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.501-331_501-322dup others(10): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537062 | ||||||
chr1:58537062
|
T | TTCTCTCT others(5): Show |
2 | a0002c0003t0001g0360a0002c0003t0001g0361 | 2 | NA18747.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.501-333_501-322dup others(12): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537062 | ||||||
chr1:58537177
|
T | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.501-436A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537177 | ||||||
chr1:58537294
|
T | C | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.501-553A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537294 | ||||||
chr1:58537368
|
G | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.501-627C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537368 | ||||||
chr1:58537429
|
T | C | 1 | a0001c0002t0002g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.501-688A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537429 | ||||||
chr1:58537440
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.501-699T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537440 | ||||||
chr1:58537456
|
A | C | 2 | a0001c0001t0003g0002a0001c0001t0003g0026 | 3 | HG00639.hp2 HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.501-715T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537456 | ||||||
chr1:58537547
|
G | GC | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.501-807dupG | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537547 | ||||||
chr1:58537553
|
T | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.501-812A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537553 | ||||||
chr1:58537662
|
A | C | 1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.501-921T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537662 | ||||||
chr1:58537931
|
T | C | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.500+864A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537931 | ||||||
chr1:58537934
|
C | T | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.500+861G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537934 | ||||||
chr1:58537947
|
G | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+848C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537947 | ||||||
chr1:58537955
|
G | C | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.500+840C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537955 | ||||||
chr1:58537992
|
T | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.500+803A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58537992 | ||||||
chr1:58538029
|
A | T | 1 | a0001c0012t0002g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.500+766T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538029 | ||||||
chr1:58538200
|
C | T | 362 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(359): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.500+595G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538200 | ||||||
chr1:58538241
|
T | A | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.500+554A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538241 | ||||||
chr1:58538283
|
G | T | 1 | a0004c0005t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.500+512C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538283 | ||||||
chr1:58538308
|
T | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.500+487A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538308 | ||||||
chr1:58538328
|
T | A | 1 | a0002c0003t0001g0374 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.500+467A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538328 | ||||||
chr1:58538344
|
C | A | 1 | a0001c0002t0002g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.500+451G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538344 | ||||||
chr1:58538373
|
G | C | 1 | a0005c0006t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.500+422C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538373 | ||||||
chr1:58538459
|
C | T | 1 | a0001c0012t0002g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.500+336G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538459 | ||||||
chr1:58538494
|
ATT | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+299_500+300del others(2): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538494 | ||||||
chr1:58538607
|
T | C | 5 | a0003c0004t0001g0049a0003c0004t0001g0068a0003c0004t0001g0070others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.500+188A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538607 | ||||||
chr1:58538657
|
G | A | 2 | a0004c0005t0001g0023a0004c0005t0006g0013 | 2 | HG01109.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.500+138C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538657 | ||||||
chr1:58538731
|
G | A | 1 | a0002c0003t0001g0374 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.500+64C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538731 | ||||||
chr1:58538746
|
T | G | 1 | a0001c0001t0001g0010 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.500+49A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538746 | ||||||
chr1:58538766
|
A | G | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+29T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538766 | ||||||
chr1:58538772
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.500+23A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538772 | ||||||
chr1:58538779
|
T | G | 1 | a0001c0001t0001g0278 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.500+16A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 2/8 | chr1 | 58538779 | ||||||
chr1:58539421
|
C | T | 4 | a0003c0004t0001g0068a0003c0004t0001g0070a0003c0004t0001g0071others(1): Show | 4 | HG02258.hp1 HG02717.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-111G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539421 | ||||||
chr1:58539515
|
G | A | 51 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(48): Show | 52 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.-16-205C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539515 | ||||||
chr1:58539534
|
AT | A | 51 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(48): Show | 52 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.-16-225delA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539534 | ||||||
chr1:58539566
|
G | C | 5 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0279others(2): Show | 5 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16-256C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539566 | ||||||
chr1:58539719
|
C | G | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-409G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539719 | ||||||
chr1:58539744
|
C | G | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-434G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539744 | ||||||
chr1:58539879
|
G | A | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-569C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539879 | ||||||
chr1:58539888
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-16-578C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539888 | ||||||
chr1:58539932
|
T | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-622A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539932 | ||||||
chr1:58539953
|
A | G | 1 | a0001c0002t0002g0079 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-16-643T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539953 | ||||||
chr1:58539992
|
C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0312 | 2 | HG01109.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-16-682G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58539992 | ||||||
chr1:58540003
|
T | C | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-693A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540003 | ||||||
chr1:58540037
|
G | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0120others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-16-727C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540037 | ||||||
chr1:58540070
|
G | A | 1 | a0003c0004t0001g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-16-760C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540070 | ||||||
chr1:58540120
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-16-810C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540120 | ||||||
chr1:58540198
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0038 | 3 | HG03130.hp2 HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-16-888C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540198 | ||||||
chr1:58540233
|
A | T | 1 | a0001c0001t0007g0376 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-16-923T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540233 | ||||||
chr1:58540279
|
C | G | 5 | a0005c0006t0001g0005a0005c0006t0001g0063a0005c0006t0001g0064others(2): Show | 6 | HG01069.hp2 HG01071.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-969G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540279 | ||||||
chr1:58540282
|
G | GA | 67 | a0001c0001t0001g0039a0001c0001t0001g0186a0002c0003t0001g0345others(64): Show | 70 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-16-973dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540282 | ||||||
chr1:58540282
|
GA | G | 61 | a0001c0001t0001g0117a0001c0001t0001g0216a0001c0001t0001g0217others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-16-973delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540282 | ||||||
chr1:58540301
|
C | T | 1 | a0004c0005t0006g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-16-991G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540301 | ||||||
chr1:58540327
|
A | G | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-1017T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540327 | ||||||
chr1:58540446
|
C | G | 2 | a0001c0001t0001g0040a0001c0001t0001g0045 | 2 | HG01255.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16-1136G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540446 | ||||||
chr1:58540650
|
T | C | 1 | a0004c0005t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-16-1340A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540650 | ||||||
chr1:58540667
|
T | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-16-1357A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540667 | ||||||
chr1:58540711
|
A | G | 1 | a0001c0002t0002g0090 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-16-1401T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540711 | ||||||
chr1:58540715
|
T | TA | 61 | a0001c0001t0001g0117a0001c0001t0001g0216a0001c0001t0001g0217others(58): Show | 61 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-16-1406dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540715 | ||||||
chr1:58540815
|
G | GA | 52 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(49): Show | 53 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-16-1506dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540815 | ||||||
chr1:58540853
|
C | G | 1 | a0002c0003t0001g0369 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-16-1543G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540853 | ||||||
chr1:58540926
|
A | T | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-1616T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58540926 | ||||||
chr1:58541112
|
C | CCAGCCTG others(9): Show |
361 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(358): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.-16-1803_-16-1802i others(18): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541112 | ||||||
chr1:58541149
|
G | C | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-1839C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541149 | ||||||
chr1:58541219
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0003g0035 | 2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-16-1909C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541219 | ||||||
chr1:58541277
|
G | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0116a0001c0001t0001g0120others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.-16-1967C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541277 | ||||||
chr1:58541293
|
C | CAAAAA | 9 | a0001c0001t0001g0127a0001c0001t0001g0133a0001c0001t0001g0134others(6): Show | 9 | HG00544.hp2 HG02015.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-1988_-16-1984d others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0190others(4): Show | 7 | HG01515.hp1 HG01928.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16-1992_-16-1984d others(11): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG01255.hp1 HG01952.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-1993_-16-1984d others(12): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0137a0001c0001t0001g0175a0001c0001t0001g0197 | 3 | HG01099.hp2 HG01358.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-16-1994_-16-1984d others(13): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CA | C | 21 | a0001c0001t0001g0125a0001c0001t0001g0215a0001c0001t0001g0217others(18): Show | 21 | HG00140.hp1 HG00544.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16-1984delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAA | C | 54 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0120others(51): Show | 54 | HG00099.hp2 HG01070.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.-16-1985_-16-1984d others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAA | C | 42 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0122others(39): Show | 42 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.-16-1986_-16-1984d others(5): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(1): Show |
C | 10 | a0001c0001t0001g0162a0001c0001t0001g0163a0003c0004t0001g0004others(7): Show | 11 | HG00735.hp2 HG01258.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-1991_-16-1984d others(10): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(2): Show |
C | 35 | a0001c0001t0001g0118a0001c0001t0001g0138a0001c0001t0001g0157others(32): Show | 36 | HG00099.hp1 HG00408.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-16-1992_-16-1984d others(11): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(3): Show |
C | 29 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0126others(26): Show | 31 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.-16-1993_-16-1984d others(12): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(4): Show |
C | 33 | a0001c0002t0002g0090a0001c0002t0002g0091a0001c0002t0002g0092others(30): Show | 33 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.-16-1994_-16-1984d others(13): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(5): Show |
C | 53 | a0001c0001t0001g0119a0001c0001t0001g0221a0001c0001t0001g0230others(50): Show | 54 | HG00140.hp2 HG00423.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.-16-1995_-16-1984d others(14): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0298others(3): Show | 6 | HG01069.hp1 HG01074.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16-1996_-16-1984d others(15): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0178a0001c0001t0001g0297 | 2 | HG01243.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-16-1997_-16-1984d others(16): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-16-1998_-16-1984d others(17): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0177 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-16-2000_-16-1984d others(19): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(11): Show |
C | 2 | a0001c0001t0001g0039a0001c0001t0001g0139 | 2 | HG02056.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-16-2001_-16-1984d others(20): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(12): Show |
C | 7 | a0001c0001t0001g0041a0001c0001t0001g0046a0001c0001t0001g0130others(4): Show | 7 | HG01167.hp1 HG02155.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16-2002_-16-1984d others(21): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0001g0040a0001c0001t0001g0045 | 2 | HG01255.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-16-2003_-16-1984d others(22): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(15): Show |
C | 1 | a0003c0004t0001g0049 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-16-2005_-16-1984d others(24): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541293
|
CAAAAAAA others(21): Show |
C | 14 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(11): Show | 15 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-16-2011_-16-1984d others(30): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541293 | ||||||
chr1:58541326
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-16-2016T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541326 | ||||||
chr1:58541329
|
A | C | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-16-2019T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541329 | ||||||
chr1:58541371
|
C | G | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-2061G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541371 | ||||||
chr1:58541488
|
T | G | 1 | a0001c0002t0002g0095 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-16-2178A>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541488 | ||||||
chr1:58541514
|
G | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-2204C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541514 | ||||||
chr1:58541590
|
G | C | 362 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(359): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-16-2280C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541590 | ||||||
chr1:58541614
|
C | CA | 161 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(158): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-16-2305dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541614 | ||||||
chr1:58541614
|
C | CAA | 80 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0116others(77): Show | 80 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.-16-2306_-16-2305d others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541614 | ||||||
chr1:58541614
|
C | CAAA | 15 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0213others(12): Show | 15 | HG01192.hp2 HG01496.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16-2307_-16-2305d others(5): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541614 | ||||||
chr1:58541614
|
C | CAAAA | 9 | a0002c0003t0001g0345a0002c0003t0001g0346a0003c0004t0001g0065others(6): Show | 9 | HG01256.hp1 HG01258.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-2308_-16-2305d others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541614 | ||||||
chr1:58541614
|
C | CAAAAA | 7 | a0003c0004t0001g0068a0003c0004t0001g0070a0003c0004t0001g0071others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16-2309_-16-2305d others(7): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541614 | ||||||
chr1:58541614
|
CAAAAAAA others(5): Show |
C | 51 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(48): Show | 52 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.-16-2316_-16-2305d others(14): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541614 | ||||||
chr1:58541650
|
A | C | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-2340T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541650 | ||||||
chr1:58541656
|
C | CA | 6 | a0001c0001t0004g0203a0001c0002t0002g0096a0001c0002t0002g0097others(3): Show | 6 | HG02738.hp1 HG03704.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16-2347dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541656 | ||||||
chr1:58541656
|
CA | C | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-2347delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541656 | ||||||
chr1:58541746
|
TTATCTGA others(1): Show |
T | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-16-2444_-16-2437d others(10): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541746 | ||||||
chr1:58541749
|
TCTGA | T | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-2443_-16-2440d others(6): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541749 | ||||||
chr1:58541789
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-16-2479A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541789 | ||||||
chr1:58541793
|
T | C | 1 | a0001c0001t0001g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-16-2483A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541793 | ||||||
chr1:58541952
|
G | A | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-2642C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541952 | ||||||
chr1:58541964
|
T | C | 14 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(11): Show | 15 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-16-2654A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58541964 | ||||||
chr1:58542051
|
C | T | 66 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(63): Show | 69 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-16-2741G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542051 | ||||||
chr1:58542245
|
T | A | 7 | a0001c0001t0001g0119a0001c0001t0004g0129a0001c0001t0004g0200others(4): Show | 7 | HG00621.hp2 HG02129.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16-2935A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542245 | ||||||
chr1:58542306
|
T | A | 2 | a0001c0001t0004g0202a0001c0001t0004g0203 | 2 | HG00621.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-16-2996A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542306 | ||||||
chr1:58542575
|
C | CA | 54 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(51): Show | 55 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-16-3266dupT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542575 | ||||||
chr1:58542575
|
C | CAA | 32 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(29): Show | 32 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-16-3267_-16-3266d others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542575 | ||||||
chr1:58542580
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-16-3270T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542580 | ||||||
chr1:58542613
|
G | A | 1 | a0005c0006t0001g0074 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-16-3303C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542613 | ||||||
chr1:58542615
|
T | A | 362 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(359): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-16-3305A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542615 | ||||||
chr1:58542800
|
G | A | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-16-3490C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542800 | ||||||
chr1:58542863
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-16-3553A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542863 | ||||||
chr1:58542886
|
T | A | 34 | a0003c0004t0001g0003a0003c0004t0001g0004a0003c0004t0001g0049others(31): Show | 37 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-16-3576A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542886 | ||||||
chr1:58542984
|
C | CT | 277 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(274): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-16-3675dupA | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542984 | ||||||
chr1:58542990
|
T | A | 3 | a0001c0002t0002g0100a0001c0002t0002g0101a0001c0002t0002g0102 | 3 | HG01256.hp2 HG01257.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-16-3680A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542990 | ||||||
chr1:58542990
|
T | TTA | 13 | a0001c0001t0001g0007a0001c0001t0001g0332a0001c0001t0001g0333others(10): Show | 14 | HG01167.hp2 HG01261.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16-3681_-16-3680i others(4): Show |
OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542990 | ||||||
chr1:58542991
|
A | T | 11 | a0001c0001t0001g0117a0001c0001t0001g0128a0001c0001t0001g0205others(8): Show | 11 | HG01884.hp2 HG02698.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16-3681T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58542991 | ||||||
chr1:58543023
|
A | G | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-17+3680T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543023 | ||||||
chr1:58543028
|
C | T | 2 | a0001c0002t0002g0078a0001c0012t0002g0077 | 2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-17+3675G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543028 | ||||||
chr1:58543282
|
T | C | 1 | a0001c0002t0002g0103 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-17+3421A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543282 | ||||||
chr1:58543324
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-17+3379G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543324 | ||||||
chr1:58543372
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-17+3331C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543372 | ||||||
chr1:58543388
|
T | C | 1 | a0001c0002t0002g0104 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-17+3315A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543388 | ||||||
chr1:58543427
|
T | C | 37 | a0001c0002t0002g0011a0001c0002t0002g0078a0001c0002t0002g0079others(34): Show | 37 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.-17+3276A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543427 | ||||||
chr1:58543430
|
A | C | 1 | a0007c0011t0002g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-17+3273T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543430 | ||||||
chr1:58543504
|
A | G | 11 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-17+3199T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543504 | ||||||
chr1:58543607
|
T | C | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-17+3096A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543607 | ||||||
chr1:58543651
|
T | C | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17+3052A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543651 | ||||||
chr1:58543663
|
G | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+3040C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543663 | ||||||
chr1:58543810
|
G | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+2893C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543810 | ||||||
chr1:58543891
|
C | G | 84 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0118others(81): Show | 85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-17+2812G>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543891 | ||||||
chr1:58543989
|
G | A | 3 | a0003c0004t0001g0105a0003c0004t0001g0106a0003c0004t0001g0107 | 3 | HG02886.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-17+2714C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58543989 | ||||||
chr1:58544002
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0331a0001c0001t0001g0332others(12): Show | 16 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.-17+2701A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544002 | ||||||
chr1:58544003
|
T | A | 1 | a0001c0002t0002g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-17+2700A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544003 | ||||||
chr1:58544107
|
C | T | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17+2596G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544107 | ||||||
chr1:58544219
|
C | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+2484G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544219 | ||||||
chr1:58544283
|
G | A | 1 | a0001c0001t0004g0344 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-17+2420C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544283 | ||||||
chr1:58544309
|
G | C | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+2394C>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544309 | ||||||
chr1:58544325
|
C | A | 5 | a0001c0002t0002g0110a0001c0002t0002g0111a0001c0002t0002g0112others(2): Show | 5 | HG00140.hp2 HG00741.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-17+2378G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544325 | ||||||
chr1:58544356
|
T | A | 346 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(343): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-17+2347A>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544356 | ||||||
chr1:58544380
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-17+2323T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544380 | ||||||
chr1:58544468
|
G | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+2235C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544468 | ||||||
chr1:58544502
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-17+2201G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544502 | ||||||
chr1:58544534
|
G | A | 362 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(359): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.-17+2169C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544534 | ||||||
chr1:58544646
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-17+2057C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544646 | ||||||
chr1:58544711
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-17+1992T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544711 | ||||||
chr1:58544750
|
C | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+1953G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544750 | ||||||
chr1:58544783
|
G | A | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(262): Show | 267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-17+1920C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544783 | ||||||
chr1:58544854
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-17+1849T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58544854 | ||||||
chr1:58545037
|
T | C | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-17+1666A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545037 | ||||||
chr1:58545066
|
C | A | 31 | a0002c0003t0001g0345a0002c0003t0001g0346a0002c0003t0001g0347others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-17+1637G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545066 | ||||||
chr1:58545110
|
C | T | 14 | a0004c0005t0001g0023a0004c0005t0002g0001a0004c0005t0002g0012others(11): Show | 15 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-17+1593G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545110 | ||||||
chr1:58545177
|
A | G | 1 | a0001c0002t0002g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-17+1526T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545177 | ||||||
chr1:58545232
|
A | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+1471T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545232 | ||||||
chr1:58545276
|
A | C | 235 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(232): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-17+1427T>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545276 | ||||||
chr1:58545331
|
G | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+1372C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545331 | ||||||
chr1:58545337
|
A | T | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+1366T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545337 | ||||||
chr1:58545465
|
C | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+1238G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545465 | ||||||
chr1:58545506
|
T | C | 235 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(232): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-17+1197A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545506 | ||||||
chr1:58545509
|
GA | G | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+1193delT | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545509 | ||||||
chr1:58545850
|
T | C | 29 | a0002c0003t0001g0347a0002c0003t0001g0348a0002c0003t0001g0349others(26): Show | 29 | HG00423.hp1 HG00621.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-17+853A>G | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545850 | ||||||
chr1:58545901
|
C | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+802G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58545901 | ||||||
chr1:58546252
|
A | G | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+451T>C | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546252 | ||||||
chr1:58546309
|
G | T | 1 | a0010c0009t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-17+394C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546309 | ||||||
chr1:58546313
|
C | T | 235 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(232): Show | 237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-17+390G>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546313 | ||||||
chr1:58546315
|
C | A | 266 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(263): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.-17+388G>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546315 | ||||||
chr1:58546452
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-17+251C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546452 | ||||||
chr1:58546505
|
G | T | 1 | a0001c0001t0001g0010 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-17+198C>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546505 | ||||||
chr1:58546586
|
G | A | 1 | a0001c0001t0002g0008 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-17+117C>T | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546586 | ||||||
chr1:58546662
|
A | T | 1 | a0001c0001t0001g0009 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-17+41T>A | OMA1 | ENSG00000162600.12 | transcript | ENST00000371226.8 | protein_coding | 1/8 | chr1 | 58546662 |