geneid | 4967 |
---|---|
ensemblid | ENSG00000105953.16 |
hgncid | 8124 |
symbol | OGDH |
name | oxoglutarate dehydrogenase |
refseq_nuc | NM_002541.4 |
refseq_prot | NP_002532.2 |
ensembl_nuc | ENST00000222673.6 |
ensembl_prot | ENSP00000222673.5 |
mane_status | MANE Select |
chr | chr7 |
start | 44606627 |
end | 44709066 |
strand | + |
ver | v1.2 |
region | chr7:44606627-44709066 |
region5000 | chr7:44601627-44714066 |
regionname0 | OGDH_chr7_44606627_44709066 |
regionname5000 | OGDH_chr7_44601627_44714066 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1023 | 273 | 89 | 37 | 115 | 14 | 17 | 84 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0002 | 0/1 | 1023 | 29 | 1 | 2 | 18 | 2 | 5 | 12 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0003 | 0/0 | 1023 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0004 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0005 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0006 | 0/0 | 1023 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 3072 | 155 | 35 | 30 | 66 | 11 | 12 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0002 | 0/0 | 3072 | 97 | 42 | 5 | 45 | 0 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0003 | 0/1 | 3072 | 28 | 0 | 2 | 18 | 2 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0004 | 0/0 | 3072 | 8 | 5 | 1 | 0 | 2 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0005 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0006 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0007 | 0/0 | 3072 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0008 | 0/0 | 3072 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0009 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0010 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0011 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0012 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0013 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0014 | 0/0 | 3072 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0015 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0016 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0017 | 0/0 | 3072 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
c0018 | 0/0 | 3072 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
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 | 1123 | 129 | 46 | 10 | 60 | 2 | 10 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0002 | 0/0 | 1122 | 121 | 23 | 22 | 64 | 7 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0003 | 0/0 | 1122 | 16 | 14 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0004 | 1/0 | 1122 | 8 | 0 | 4 | 0 | 1 | 2 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0005 | 0/0 | 1121 | 8 | 0 | 1 | 3 | 1 | 3 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0006 | 0/0 | 1123 | 5 | 1 | 0 | 4 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0007 | 0/0 | 1122 | 5 | 0 | 0 | 0 | 4 | 1 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0008 | 0/0 | 1121 | 4 | 0 | 2 | 0 | 1 | 1 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0009 | 0/0 | 1123 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0010 | 0/0 | 1123 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0011 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0012 | 0/0 | 1123 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0013 | 0/0 | 1122 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0014 | 0/0 | 1123 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0015 | 0/0 | 1122 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
t0016 | 0/0 | 1122 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0259 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3072 | 155 | 35 | 30 | 66 | 11 | 12 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0002 | 0/0 | 3072 | 97 | 42 | 5 | 45 | 0 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0004 | 0/0 | 3072 | 8 | 5 | 1 | 0 | 2 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0005 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0006 | 0/0 | 3072 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0007 | 0/0 | 3072 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0008 | 0/0 | 3072 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0009 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0010 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0014 | 0/0 | 3072 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0016 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0017 | 0/0 | 3072 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0002c0003 | 0/1 | 3072 | 28 | 0 | 2 | 18 | 2 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0002c0013 | 0/0 | 3072 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0003c0018 | 0/0 | 3072 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0004c0015 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0005c0012 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0006c0011 | 0/0 | 3072 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4194 | 13 | 11 | 2 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0002 | 0/0 | 4193 | 106 | 18 | 20 | 58 | 5 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0003 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0004 | 1/0 | 4193 | 8 | 0 | 4 | 0 | 1 | 2 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0005 | 0/0 | 4192 | 7 | 0 | 1 | 3 | 0 | 3 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0006 | 0/0 | 4194 | 5 | 1 | 0 | 4 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0007 | 0/0 | 4193 | 5 | 0 | 0 | 0 | 4 | 1 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0008 | 0/0 | 4192 | 4 | 0 | 2 | 0 | 1 | 1 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0009 | 0/0 | 4194 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0011 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0012 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0015 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0001t0016 | 0/0 | 4193 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0002t0001 | 0/0 | 4194 | 79 | 27 | 5 | 42 | 0 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0002t0003 | 0/0 | 4193 | 14 | 13 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0002t0010 | 0/0 | 4194 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0002t0013 | 0/0 | 4193 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0002t0014 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0004t0002 | 0/0 | 4193 | 8 | 5 | 1 | 0 | 2 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0005t0001 | 0/0 | 4194 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0006t0001 | 0/0 | 4194 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0007t0002 | 0/0 | 4193 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0008t0002 | 0/0 | 4193 | 2 | 0 | 0 | 2 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0009t0001 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0010t0001 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0014t0002 | 0/0 | 4193 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0016t0001 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0001c0017t0005 | 0/0 | 4192 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0002c0003t0001 | 0/1 | 4194 | 27 | 0 | 2 | 17 | 2 | 5 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0002c0003t0003 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0002c0013t0001 | 0/0 | 4194 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0003c0018t0001 | 0/0 | 4194 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0004c0015t0002 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0005c0012t0001 | 0/0 | 4194 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
a0006c0011t0002 | 0/0 | 4193 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | copy fasta | chr7 | 44601627 | 44714066 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0004g0259 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0007g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0007g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0007g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0007g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0008g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0009g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0012g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0001t0016g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0010g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0002t0014g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0004t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0005t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0005t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0006t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0007t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0007t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0008t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0008t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0009t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0010t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0014t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0016t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0001c0017t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0002c0013t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0003c0018t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0004c0015t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0005c0012t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
a0006c0011t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0017 | t0005 | g0240 | EUR | GBR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00099 | hp2 | a0001 | c0001 | t0008 | g0248 | EUR | GBR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00140 | hp1 | a0001 | c0001 | t0007 | g0296 | EUR | GBR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0208 | EUR | GBR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0288 | EUR | FIN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0021 | EUR | FIN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00408 | hp1 | a0002 | c0003 | t0001 | g0105 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00544 | hp1 | a0002 | c0003 | t0001 | g0104 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00609 | hp2 | a0002 | c0003 | t0003 | g0076 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00673 | hp2 | a0002 | c0003 | t0001 | g0077 | EAS | CHS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00733 | hp1 | a0001 | c0001 | t0008 | g0214 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00733 | hp2 | a0002 | c0003 | t0001 | g0114 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0211 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01106 | hp1 | a0001 | c0001 | t0016 | g0245 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01106 | hp2 | a0003 | c0018 | t0001 | g0151 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0111 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01496 | hp1 | a0001 | c0004 | t0002 | g0229 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01515 | hp1 | a0001 | c0004 | t0002 | g0237 | EUR | IBS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0297 | EUR | IBS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01516 | hp1 | a0001 | c0001 | t0007 | g0298 | EUR | IBS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0242 | EUR | IBS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01517 | hp1 | a0001 | c0001 | t0007 | g0299 | EUR | IBS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01517 | hp2 | a0001 | c0004 | t0002 | g0227 | EUR | IBS | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0251 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01891 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01928 | hp1 | a0001 | c0014 | t0002 | g0051 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0266 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0283 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0098 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0108 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02148 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02155 | hp1 | a0001 | c0002 | t0010 | g0043 | EAS | CDX | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02155 | hp2 | a0004 | c0015 | t0002 | g0175 | EAS | CDX | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0200 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02258 | hp1 | a0002 | c0013 | t0001 | g0073 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0274 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0231 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0253 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0186 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02630 | hp2 | a0001 | c0004 | t0002 | g0221 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0009 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0119 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02818 | hp2 | a0001 | c0002 | t0014 | g0087 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0141 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02896 | hp2 | a0001 | c0010 | t0001 | g0302 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02922 | hp1 | a0001 | c0004 | t0002 | g0002 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0223 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02970 | hp2 | a0001 | c0002 | t0013 | g0006 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02976 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0122 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03195 | hp2 | a0001 | c0009 | t0001 | g0193 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0250 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0252 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03486 | hp1 | a0001 | c0004 | t0002 | g0247 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0187 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0113 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03491 | hp2 | a0001 | c0001 | t0008 | g0210 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03492 | hp1 | a0001 | c0001 | t0005 | g0238 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0112 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | ESN | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0263 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0234 | AFR | GWD | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03579 | hp1 | a0001 | c0004 | t0002 | g0002 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03579 | hp2 | a0001 | c0006 | t0001 | g0129 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0213 | SAS | PJL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | BEB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0089 | SAS | BEB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | STU | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04199 | hp2 | a0002 | c0003 | t0001 | g0110 | SAS | STU | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | STU | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0290 | SAS | STU | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | STU | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0184 | SAS | STU | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | CHB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | CHB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | CHB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18906 | hp1 | a0001 | c0016 | t0001 | g0246 | AFR | YRI | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0007 | AFR | YRI | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0074 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18945 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18947 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18950 | hp2 | a0001 | c0007 | t0002 | g0052 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18951 | hp2 | a0001 | c0007 | t0002 | g0029 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18954 | hp1 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0101 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18964 | hp1 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18968 | hp1 | a0005 | c0012 | t0001 | g0149 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18968 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18969 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18971 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0069 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0107 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18979 | hp2 | a0002 | c0003 | t0001 | g0118 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18980 | hp1 | a0001 | c0008 | t0002 | g0049 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18982 | hp2 | a0001 | c0008 | t0002 | g0041 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18989 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19003 | hp2 | a0002 | c0003 | t0001 | g0094 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19004 | hp2 | a0001 | c0001 | t0015 | g0040 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0103 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | LWK | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | LWK | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0225 | AFR | LWK | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | LWK | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19063 | hp2 | a0001 | c0002 | t0010 | g0042 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19065 | hp2 | a0002 | c0003 | t0001 | g0116 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19070 | hp1 | a0006 | c0011 | t0002 | g0277 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19083 | hp1 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19089 | hp1 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0109 | EAS | JPT | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | ASW | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0291 | EUR | TSI | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0099 | EUR | TSI | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | TSI | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0212 | EUR | TSI | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02486 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02559 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | ACB | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0005 | AFR | MSL | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0249 | AFR | USA | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | USA | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0148 | AFR | USA | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | LWK | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
NA21309 | hp2 | a0001 | c0006 | t0001 | g0120 | AFR | LWK | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0117 | REF | REF | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0259 | REF | REF | OGDH_chr7_44601627_44714066 | OGDH | chr7 | 44601627 | 44714066 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44624507
|
C | T | 1 | a0003 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.164C>T | p.Ser55Leu | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/23 | 218/4193 | 164/3072 | 55/1023 | chr7 | 44624507 | ||
chr7:44666840
|
C | T | 1 | a0004 | 1 | HG02155.hp2 | missense_variant | MODERATE | c.622C>T | p.Arg208Cys | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/23 | 676/4193 | 622/3072 | 208/1023 | chr7 | 44666840 | ||
chr7:44700162
|
G | A | 1 | a0006 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.2452G>A | p.Asp818Asn | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/23 | 2506/4193 | 2452/3072 | 818/1023 | chr7 | 44700162 | ||
chr7:44707350
|
G | A | 1 | a0005 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.2758G>A | p.Asp920Asn | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 21/23 | 2812/4193 | 2758/3072 | 920/1023 | chr7 | 44707350 | ||
chr7:44707979
|
G | A | 1 | a0002 | 29 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(26): Show |
missense_variant | MODERATE | c.3052G>A | p.Val1018Ile | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 3106/4193 | 3052/3072 | 1018/1023 | chr7 | 44707979 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44645380
|
C | G | 1 | a0001c0017 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.276C>G | p.Ala92Ala | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/23 | 330/4193 | 276/3072 | 92/1023 | chr7 | 44645380 | ||
chr7:44645449
|
A | G | 2 | a0001c0004a0001c0016 | 9 | HG01496.hp1 HG01515.hp1 HG01517.hp2 others(6): Show |
synonymous_variant | LOW | c.345A>G | p.Glu115Glu | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/23 | 399/4193 | 345/3072 | 115/1023 | chr7 | 44645449 | ||
chr7:44645500
|
G | A | 1 | a0001c0017 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.396G>A | p.Ser132Ser | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/23 | 450/4193 | 396/3072 | 132/1023 | chr7 | 44645500 | ||
chr7:44647716
|
C | T | 1 | a0001c0008 | 2 | NA18980.hp1 NA18982.hp2 |
synonymous_variant | LOW | c.474C>T | p.Asp158Asp | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/23 | 528/4193 | 474/3072 | 158/1023 | chr7 | 44647716 | ||
chr7:44674471
|
C | T | 1 | a0001c0014 | 1 | HG01928.hp1 | synonymous_variant | LOW | c.849C>T | p.Cys283Cys | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 7/23 | 903/4193 | 849/3072 | 283/1023 | chr7 | 44674471 | ||
chr7:44676080
|
C | T | 1 | a0002c0013 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1137C>T | p.Ala379Ala | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/23 | 1191/4193 | 1137/3072 | 379/1023 | chr7 | 44676080 | ||
chr7:44676095
|
G | A | 1 | a0002c0013 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.1152G>A | p.Val384Val | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/23 | 1206/4193 | 1152/3072 | 384/1023 | chr7 | 44676095 | ||
chr7:44693911
|
C | T | 1 | a0001c0007 | 2 | NA18950.hp2 NA18951.hp2 |
synonymous_variant | LOW | c.1422C>T | p.His474His | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 11/23 | 1476/4193 | 1422/3072 | 474/1023 | chr7 | 44693911 | ||
chr7:44696514
|
T | C | 1 | a0001c0005 | 2 | HG02257.hp2 HG02280.hp1 |
synonymous_variant | LOW | c.1857T>C | p.Asn619Asn | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 14/23 | 1911/4193 | 1857/3072 | 619/1023 | chr7 | 44696514 | ||
chr7:44697463
|
G | A | 1 | a0001c0009 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.2145G>A | p.Val715Val | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 16/23 | 2199/4193 | 2145/3072 | 715/1023 | chr7 | 44697463 | ||
chr7:44698230
|
G | A | 1 | a0001c0010 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.2397G>A | p.Leu799Leu | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/23 | 2451/4193 | 2397/3072 | 799/1023 | chr7 | 44698230 | ||
chr7:44707376
|
A | G | 1 | a0001c0006 | 2 | HG03579.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.2784A>G | p.Thr928Thr | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 21/23 | 2838/4193 | 2784/3072 | 928/1023 | chr7 | 44707376 | ||
chr7:44707900
|
G | A | 4 | a0001c0002a0001c0016a0003c0018others(1): Show | 100 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(97): Show |
synonymous_variant | LOW | c.2973G>A | p.Ala991Ala | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 3027/4193 | 2973/3072 | 991/1023 | chr7 | 44707900 | ||
chr7:44707915
|
C | T | 1 | a0002c0003 | 28 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(25): Show |
synonymous_variant | LOW | c.2988C>T | p.Thr996Thr | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 3042/4193 | 2988/3072 | 996/1023 | chr7 | 44707915 | ||
chr7:44707990
|
C | T | 1 | a0002c0003 | 28 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(25): Show |
synonymous_variant | LOW | c.3063C>T | p.Asn1021Asn | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 3117/4193 | 3063/3072 | 1021/1023 | chr7 | 44707990 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44708083
|
C | T | 1 | a0001c0002t0010 | 2 | HG02155.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*84C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 84 | chr7 | 44708083 | |||||
chr7:44708099
|
G | A | 1 | a0001c0001t0011 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 100 | chr7 | 44708099 | |||||
chr7:44708304
|
T | C | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(16): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 305 | chr7 | 44708304 | |||||
chr7:44708489
|
G | A | 1 | a0001c0001t0015 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 490 | chr7 | 44708489 | |||||
chr7:44708599
|
C | G | 1 | a0001c0002t0014 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*600C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 600 | chr7 | 44708599 | |||||
chr7:44708731
|
A | G | 32 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | 293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*732A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 732 | chr7 | 44708731 | |||||
chr7:44708794
|
C | T | 1 | a0001c0001t0009 | 2 | HG02895.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*795C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 795 | chr7 | 44708794 | |||||
chr7:44708852
|
G | A | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(16): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*853G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 853 | chr7 | 44708852 | |||||
chr7:44708868
|
C | G | 1 | a0001c0001t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*869C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 869 | chr7 | 44708868 | |||||
chr7:44708878
|
C | T | 1 | a0001c0001t0007 | 5 | HG00140.hp1 HG01516.hp1 HG01517.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*879C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 879 | chr7 | 44708878 | |||||
chr7:44708994
|
T | TA | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(13): Show | 140 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
3_prime_UTR_variant | MODIFIER | c.*1009dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 1010 | INFO_REALIGN_3_PRIME | chr7 | 44708994 | ||||
chr7:44708994
|
TA | T | 3 | a0001c0001t0005a0001c0001t0008a0001c0017t0005 | 12 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1009delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 1009 | INFO_REALIGN_3_PRIME | chr7 | 44708994 | ||||
chr7:44709062
|
C | G | 1 | a0001c0001t0012 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1063C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 1063 | chr7 | 44709062 | |||||
chr7:44709063
|
C | T | 1 | a0001c0002t0013 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1064C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 23/23 | 1064 | chr7 | 44709063 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44606811
|
G | A | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-28+158G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44606811 | ||||||
chr7:44606873
|
C | T | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+220C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44606873 | ||||||
chr7:44607110
|
G | C | 13 | a0001c0001t0001g0011a0001c0002t0003g0004a0001c0002t0003g0005others(10): Show | 13 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-28+457G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607110 | ||||||
chr7:44607164
|
G | A | 244 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(241): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.-28+511G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607164 | ||||||
chr7:44607211
|
A | G | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28+558A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607211 | ||||||
chr7:44607262
|
T | C | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG00741.hp2 HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-28+609T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607262 | ||||||
chr7:44607686
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-28+1033C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607686 | ||||||
chr7:44607801
|
A | G | 91 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-28+1148A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607801 | ||||||
chr7:44607839
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+1186T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607839 | ||||||
chr7:44607850
|
C | A | 91 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(88): Show | 91 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-28+1197C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607850 | ||||||
chr7:44607855
|
T | C | 299 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-28+1202T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607855 | ||||||
chr7:44607905
|
T | G | 1 | a0001c0002t0001g0123 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-28+1252T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44607905 | ||||||
chr7:44607998
|
GC | G | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+1349delC | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44607998 | |||||
chr7:44608198
|
G | A | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-28+1545G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44608198 | ||||||
chr7:44608407
|
C | CA | 62 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.-28+1763dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44608407 | |||||
chr7:44608524
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28+1871C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44608524 | ||||||
chr7:44608563
|
G | T | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-28+1910G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44608563 | ||||||
chr7:44608637
|
C | T | 1 | a0001c0004t0002g0002 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-28+1984C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44608637 | ||||||
chr7:44608676
|
G | C | 1 | a0002c0003t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-28+2023G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44608676 | ||||||
chr7:44609171
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-28+2518A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609171 | ||||||
chr7:44609201
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-28+2548G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609201 | ||||||
chr7:44609217
|
A | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+2564A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609217 | ||||||
chr7:44609226
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-28+2573C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609226 | ||||||
chr7:44609339
|
C | CA | 18 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 18 | HG00741.hp1 HG01433.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28+2707dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44609339 | |||||
chr7:44609339
|
C | CAAA | 36 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0270others(33): Show | 36 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.-28+2705_-28+2707d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44609339 | |||||
chr7:44609339
|
C | CAAAA | 7 | a0001c0001t0002g0260a0001c0001t0002g0264a0001c0001t0002g0265others(4): Show | 7 | HG00621.hp1 HG01934.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+2704_-28+2707d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44609339 | |||||
chr7:44609339
|
CA | C | 46 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(43): Show | 46 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-28+2707delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44609339 | |||||
chr7:44609380
|
T | C | 68 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00423.hp2 HG00597.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.-28+2727T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609380 | ||||||
chr7:44609509
|
C | CA | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-28+2873dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44609509 | |||||
chr7:44609509
|
CA | C | 54 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(51): Show | 54 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-28+2873delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44609509 | |||||
chr7:44609554
|
G | A | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-28+2901G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609554 | ||||||
chr7:44609740
|
C | T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-28+3087C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609740 | ||||||
chr7:44609853
|
G | C | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG01943.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.-28+3200G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44609853 | ||||||
chr7:44610022
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-28+3369C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610022 | ||||||
chr7:44610229
|
A | G | 1 | a0001c0002t0001g0132 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-28+3576A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610229 | ||||||
chr7:44610254
|
C | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-28+3601C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610254 | ||||||
chr7:44610302
|
T | G | 2 | a0001c0001t0002g0224a0001c0002t0001g0135 | 2 | HG00558.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-28+3649T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610302 | ||||||
chr7:44610306
|
G | A | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-28+3653G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610306 | ||||||
chr7:44610306
|
G | T | 11 | a0001c0001t0002g0115a0002c0003t0001g0089a0002c0003t0001g0110others(8): Show | 11 | HG00438.hp1 HG00733.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28+3653G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610306 | ||||||
chr7:44610372
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+3719G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610372 | ||||||
chr7:44610504
|
G | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | NA18945.hp2 NA18947.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+3851G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610504 | ||||||
chr7:44610524
|
G | A | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | NA18964.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-28+3871G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610524 | ||||||
chr7:44610628
|
G | C | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-28+3975G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610628 | ||||||
chr7:44610753
|
C | T | 8 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28+4100C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610753 | ||||||
chr7:44610862
|
C | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+4209C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610862 | ||||||
chr7:44610900
|
G | A | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-28+4247G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44610900 | ||||||
chr7:44611072
|
A | AT | 54 | a0001c0001t0002g0001a0001c0001t0002g0023a0001c0001t0002g0026others(51): Show | 55 | HG00423.hp2 HG00597.hp1 HG01496.hp2 others(52): Show |
intron_variant | MODIFIER | c.-28+4438dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44611072 | |||||
chr7:44611072
|
AT | A | 170 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(167): Show | 170 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.-28+4438delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44611072 | |||||
chr7:44611099
|
C | T | 12 | a0001c0001t0002g0027a0001c0001t0002g0064a0001c0001t0002g0066others(9): Show | 12 | HG00423.hp2 HG00597.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-28+4446C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611099 | ||||||
chr7:44611272
|
G | T | 7 | a0001c0002t0001g0222a0001c0002t0001g0226a0001c0002t0001g0249others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+4619G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611272 | ||||||
chr7:44611300
|
G | A | 2 | a0001c0001t0002g0204a0001c0001t0004g0205 | 2 | HG02148.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-28+4647G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611300 | ||||||
chr7:44611337
|
C | T | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+4684C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611337 | ||||||
chr7:44611338
|
A | G | 68 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(65): Show | 69 | HG00423.hp2 HG00597.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.-28+4685A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611338 | ||||||
chr7:44611376
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0002t0001g0124 | 3 | HG02258.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+4723C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611376 | ||||||
chr7:44611394
|
G | T | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-28+4741G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611394 | ||||||
chr7:44611435
|
A | AT | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG00741.hp1 HG01175.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28+4794dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44611435 | |||||
chr7:44611522
|
C | G | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-28+4869C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611522 | ||||||
chr7:44611556
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-28+4903G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611556 | ||||||
chr7:44611730
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-28+5077A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611730 | ||||||
chr7:44611899
|
T | C | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-28+5246T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611899 | ||||||
chr7:44611951
|
G | A | 150 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-28+5298G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611951 | ||||||
chr7:44611987
|
T | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+5334T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44611987 | ||||||
chr7:44612028
|
G | A | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-28+5375G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612028 | ||||||
chr7:44612086
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-28+5433A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612086 | ||||||
chr7:44612139
|
C | T | 37 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-28+5486C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612139 | ||||||
chr7:44612345
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+5692C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612345 | ||||||
chr7:44612558
|
T | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+5905T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612558 | ||||||
chr7:44612629
|
C | T | 1 | a0001c0002t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-28+5976C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612629 | ||||||
chr7:44612630
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+5977G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612630 | ||||||
chr7:44612731
|
C | CT | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-28+6079dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44612731 | |||||
chr7:44612817
|
T | C | 1 | a0001c0004t0002g0002 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-28+6164T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612817 | ||||||
chr7:44612833
|
C | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28+6180C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612833 | ||||||
chr7:44612842
|
C | A | 3 | a0001c0001t0006g0033a0001c0002t0001g0031a0001c0002t0001g0032 | 3 | HG02717.hp1 HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-28+6189C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612842 | ||||||
chr7:44612842
|
C | T | 1 | a0001c0001t0002g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-28+6189C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612842 | ||||||
chr7:44612865
|
T | TTTTTC | 37 | a0001c0001t0002g0034a0001c0001t0002g0091a0001c0001t0002g0095others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-28+6237_-28+6241d others(7): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44612865 | |||||
chr7:44612865
|
TTTTTC | T | 14 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-28+6237_-28+6241d others(7): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44612865 | |||||
chr7:44612920
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+6267G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612920 | ||||||
chr7:44612943
|
C | T | 1 | a0002c0003t0001g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-28+6290C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44612943 | ||||||
chr7:44613028
|
G | A | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+6375G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613028 | ||||||
chr7:44613037
|
A | G | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28+6384A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613037 | ||||||
chr7:44613097
|
C | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0026others(41): Show | 45 | HG00423.hp2 HG00597.hp1 HG01496.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+6444C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613097 | ||||||
chr7:44613125
|
C | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-28+6472C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613125 | ||||||
chr7:44613155
|
C | T | 1 | a0002c0003t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-28+6502C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613155 | ||||||
chr7:44613273
|
T | G | 1 | a0001c0001t0015g0040 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-28+6620T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613273 | ||||||
chr7:44613318
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-28+6665G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613318 | ||||||
chr7:44613485
|
G | A | 5 | a0001c0001t0002g0204a0001c0001t0002g0207a0001c0001t0002g0208others(2): Show | 5 | HG00140.hp2 HG01943.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28+6832G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613485 | ||||||
chr7:44613560
|
C | T | 3 | a0001c0001t0002g0023a0001c0001t0002g0039a0001c0002t0003g0028 | 3 | HG02109.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-28+6907C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613560 | ||||||
chr7:44613573
|
A | G | 2 | a0001c0002t0001g0128a0001c0002t0001g0190 | 2 | NA18989.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-28+6920A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613573 | ||||||
chr7:44613576
|
G | A | 1 | a0001c0002t0001g0249 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-28+6923G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613576 | ||||||
chr7:44613602
|
A | G | 64 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(61): Show | 65 | HG00423.hp2 HG00597.hp1 HG01496.hp2 others(62): Show |
intron_variant | MODIFIER | c.-28+6949A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613602 | ||||||
chr7:44613604
|
C | T | 4 | a0001c0002t0003g0004a0001c0002t0003g0014a0001c0002t0003g0015others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+6951C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613604 | ||||||
chr7:44613605
|
C | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-28+6952C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613605 | ||||||
chr7:44613638
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0007g0296 | 3 | HG00140.hp1 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-28+6985C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613638 | ||||||
chr7:44613639
|
G | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28+6986G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613639 | ||||||
chr7:44613751
|
C | T | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-28+7098C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613751 | ||||||
chr7:44613756
|
A | G | 43 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(40): Show | 43 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.-28+7103A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613756 | ||||||
chr7:44613802
|
C | CT | 92 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-28+7169dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44613802 | |||||
chr7:44613802
|
C | CTT | 46 | a0001c0001t0001g0196a0001c0001t0001g0254a0001c0001t0002g0260others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-28+7168_-28+7169d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44613802 | |||||
chr7:44613846
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+7193G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613846 | ||||||
chr7:44613866
|
G | A | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+7213G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613866 | ||||||
chr7:44613965
|
C | T | 1 | a0001c0002t0003g0013 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-28+7312C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613965 | ||||||
chr7:44613994
|
C | T | 88 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(85): Show | 88 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-28+7341C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44613994 | ||||||
chr7:44614052
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28+7399C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614052 | ||||||
chr7:44614058
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28+7405G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614058 | ||||||
chr7:44614180
|
C | G | 1 | a0002c0003t0001g0191 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-28+7527C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614180 | ||||||
chr7:44614232
|
CT | C | 5 | a0001c0002t0001g0024a0001c0002t0001g0199a0001c0004t0002g0002others(2): Show | 6 | HG02280.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28+7594delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44614232 | |||||
chr7:44614300
|
TTTGTTTT others(5): Show |
T | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28+7650_-28+7661d others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44614300 | |||||
chr7:44614305
|
T | G | 1 | a0001c0002t0001g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-28+7652T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614305 | ||||||
chr7:44614311
|
TG | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+7659delG | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614311 | ||||||
chr7:44614312
|
G | T | 139 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(136): Show | 139 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-28+7659G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614312 | ||||||
chr7:44614379
|
G | A | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-28+7726G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614379 | ||||||
chr7:44614436
|
A | G | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-28+7783A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614436 | ||||||
chr7:44614453
|
T | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28+7800T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614453 | ||||||
chr7:44614498
|
T | C | 150 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-28+7845T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614498 | ||||||
chr7:44614588
|
G | A | 1 | a0001c0002t0003g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-28+7935G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614588 | ||||||
chr7:44614834
|
C | CT | 50 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.-28+8201dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44614834 | |||||
chr7:44614834
|
CT | C | 94 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(91): Show | 95 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.-28+8201delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44614834 | |||||
chr7:44614974
|
G | A | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+8321G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44614974 | ||||||
chr7:44615058
|
G | T | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+8405G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615058 | ||||||
chr7:44615159
|
G | T | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-28+8506G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615159 | ||||||
chr7:44615540
|
A | G | 150 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(147): Show | 150 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-27-8777A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615540 | ||||||
chr7:44615825
|
C | T | 87 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(84): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-27-8492C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615825 | ||||||
chr7:44615898
|
C | T | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-27-8419C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615898 | ||||||
chr7:44615974
|
A | G | 2 | a0001c0001t0008g0214a0001c0001t0008g0248 | 2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.-27-8343A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615974 | ||||||
chr7:44615989
|
A | T | 2 | a0001c0002t0003g0263a0001c0010t0001g0302 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-27-8328A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44615989 | ||||||
chr7:44616027
|
A | G | 37 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-27-8290A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616027 | ||||||
chr7:44616032
|
G | GA | 9 | a0001c0001t0004g0215a0001c0001t0005g0266a0001c0002t0001g0085others(6): Show | 9 | HG01175.hp1 HG01934.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27-8271dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616032 | |||||
chr7:44616074
|
G | A | 1 | a0001c0001t0002g0137 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-27-8243G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616074 | ||||||
chr7:44616477
|
A | T | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-27-7840A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616477 | ||||||
chr7:44616548
|
T | C | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-27-7769T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616548 | ||||||
chr7:44616566
|
G | A | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-27-7751G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616566 | ||||||
chr7:44616617
|
G | GTA | 124 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(121): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.-27-7689_-27-7688d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616617 | |||||
chr7:44616617
|
G | GTATA | 3 | a0001c0002t0001g0185a0001c0002t0001g0186a0001c0002t0003g0014 | 3 | HG02055.hp2 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-27-7691_-27-7688d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616617 | |||||
chr7:44616640
|
T | TGTATATA others(23): Show |
5 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0006g0065others(2): Show | 5 | HG03195.hp2 NA18945.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-7660_-27-7631d others(32): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616640 | |||||
chr7:44616728
|
CAT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-7583_-27-7582d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616728 | |||||
chr7:44616757
|
A | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-7560A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616757 | ||||||
chr7:44616764
|
T | C | 2 | a0001c0002t0010g0042a0001c0002t0010g0043 | 2 | HG02155.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-27-7553T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616764 | ||||||
chr7:44616769
|
G | GTATATGT others(43): Show |
6 | a0001c0004t0002g0002a0001c0004t0002g0221a0001c0004t0002g0223others(3): Show | 7 | HG01496.hp1 HG02630.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-27-7534_-27-7485d others(52): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616769 | |||||
chr7:44616787
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0006g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-27-7511_-27-7482d others(32): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616787 | |||||
chr7:44616793
|
A | G | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-27-7524A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616793 | ||||||
chr7:44616797
|
G | A | 47 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-27-7520G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616797 | ||||||
chr7:44616798
|
T | TATATATA others(3): Show |
2 | a0001c0002t0001g0185a0001c0002t0001g0186 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-27-7511_-27-7510i others(12): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616798 | |||||
chr7:44616804
|
T | C | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-27-7513T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616804 | ||||||
chr7:44616806
|
T | C | 88 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.-27-7511T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616806 | ||||||
chr7:44616807
|
G | A | 188 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(185): Show | 188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.-27-7510G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616807 | ||||||
chr7:44616808
|
C | CAT | 57 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(54): Show | 57 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-27-7503_-27-7502d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616808 | |||||
chr7:44616808
|
C | CATATATA others(5): Show |
83 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.-27-7502_-27-7501i others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616808 | |||||
chr7:44616808
|
C | CATATATA others(45): Show |
1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-27-7502_-27-7501i others(54): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616808 | |||||
chr7:44616808
|
C | CATATATA others(79): Show |
1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-27-7502_-27-7501i others(88): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616808 | |||||
chr7:44616808
|
C | CGTATATA others(5): Show |
1 | a0001c0002t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27-7509_-27-7508i others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616808 | ||||||
chr7:44616808
|
C | T | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27-7509C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616808 | ||||||
chr7:44616817
|
G | GTGTATA | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-7499_-27-7498i others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616817 | |||||
chr7:44616823
|
A | ATATATG | 7 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0148others(4): Show | 7 | HG01261.hp2 NA18941.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27-7493_-27-7492i others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616823 | |||||
chr7:44616823
|
A | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-7494A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616823 | ||||||
chr7:44616827
|
G | A | 8 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0147others(5): Show | 8 | HG01261.hp2 HG02293.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27-7490G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616827 | ||||||
chr7:44616839
|
A | G | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-7478A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616839 | ||||||
chr7:44616844
|
C | T | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-7473C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616844 | ||||||
chr7:44616856
|
T | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-7461T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616856 | ||||||
chr7:44616858
|
CACATAT | C | 11 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-27-7457_-27-7452d others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616858 | |||||
chr7:44616865
|
A | ACACT | 5 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0141others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-7452_-27-7451i others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616865 | ||||||
chr7:44616873
|
GTA | G | 186 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(183): Show | 186 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-27-7434_-27-7433d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616873 | |||||
chr7:44616875
|
A | ATATATAC others(37): Show |
3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0002t0001g0124 | 3 | HG02258.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-27-7436_-27-7435i others(46): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44616875 | |||||
chr7:44616884
|
T | C | 1 | a0002c0003t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-27-7433T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616884 | ||||||
chr7:44616922
|
T | G | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-27-7395T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616922 | ||||||
chr7:44616937
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-27-7380C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616937 | ||||||
chr7:44616950
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-27-7367G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616950 | ||||||
chr7:44616957
|
T | A | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-27-7360T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616957 | ||||||
chr7:44616966
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-27-7351A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616966 | ||||||
chr7:44616981
|
C | A | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-27-7336C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616981 | ||||||
chr7:44616995
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0071 | 2 | HG00597.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-27-7322C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44616995 | ||||||
chr7:44617167
|
A | G | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.-27-7150A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617167 | ||||||
chr7:44617226
|
C | T | 1 | a0001c0001t0002g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-27-7091C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617226 | ||||||
chr7:44617235
|
T | A | 1 | a0001c0001t0001g0017 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-27-7082T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617235 | ||||||
chr7:44617481
|
A | C | 1 | a0001c0002t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-27-6836A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617481 | ||||||
chr7:44617596
|
T | C | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-27-6721T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617596 | ||||||
chr7:44617681
|
A | G | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-27-6636A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617681 | ||||||
chr7:44617716
|
A | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-27-6601A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617716 | ||||||
chr7:44617824
|
C | T | 1 | a0002c0003t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-27-6493C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617824 | ||||||
chr7:44617847
|
C | T | 1 | a0001c0001t0016g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-27-6470C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617847 | ||||||
chr7:44617876
|
C | T | 190 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(187): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-27-6441C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617876 | ||||||
chr7:44617980
|
A | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-27-6337A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617980 | ||||||
chr7:44617998
|
G | A | 1 | a0001c0001t0002g0297 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-27-6319G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44617998 | ||||||
chr7:44618141
|
T | C | 149 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(146): Show | 149 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.-27-6176T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618141 | ||||||
chr7:44618246
|
A | G | 1 | a0002c0003t0001g0110 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-27-6071A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618246 | ||||||
chr7:44618377
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-5940C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618377 | ||||||
chr7:44618389
|
T | C | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27-5928T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618389 | ||||||
chr7:44618421
|
G | A | 1 | a0003c0018t0001g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-27-5896G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618421 | ||||||
chr7:44618455
|
C | G | 3 | a0001c0002t0001g0127a0001c0002t0001g0179a0001c0002t0001g0180 | 3 | HG02015.hp1 HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-27-5862C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618455 | ||||||
chr7:44618565
|
C | G | 45 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-27-5752C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618565 | ||||||
chr7:44618594
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-5723G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618594 | ||||||
chr7:44618953
|
A | G | 1 | a0001c0001t0003g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-27-5364A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618953 | ||||||
chr7:44618976
|
A | G | 90 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-27-5341A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44618976 | ||||||
chr7:44619079
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-5238G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619079 | ||||||
chr7:44619193
|
A | G | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-27-5124A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619193 | ||||||
chr7:44619206
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-5111G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619206 | ||||||
chr7:44619318
|
G | A | 2 | a0001c0001t0012g0122a0002c0013t0001g0073 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-27-4999G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619318 | ||||||
chr7:44619432
|
A | G | 5 | a0001c0001t0002g0126a0001c0001t0002g0176a0001c0001t0002g0177others(2): Show | 5 | HG00423.hp1 HG02155.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-4885A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619432 | ||||||
chr7:44619538
|
A | G | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-27-4779A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619538 | ||||||
chr7:44619711
|
G | A | 90 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.-27-4606G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619711 | ||||||
chr7:44619884
|
T | C | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27-4433T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619884 | ||||||
chr7:44619919
|
C | T | 1 | a0001c0002t0003g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-27-4398C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44619919 | ||||||
chr7:44620034
|
G | A | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | NA18964.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-27-4283G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620034 | ||||||
chr7:44620076
|
G | A | 5 | a0001c0001t0012g0122a0001c0004t0002g0221a0001c0004t0002g0229others(2): Show | 5 | HG01496.hp1 HG02630.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27-4241G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620076 | ||||||
chr7:44620170
|
A | G | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27-4147A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620170 | ||||||
chr7:44620211
|
G | A | 1 | a0001c0001t0002g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-27-4106G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620211 | ||||||
chr7:44620614
|
A | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-27-3703A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620614 | ||||||
chr7:44620692
|
CT | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-3622delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44620692 | |||||
chr7:44620754
|
AT | A | 177 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(174): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.-27-3550delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44620754 | |||||
chr7:44620754
|
ATT | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-3551_-27-3550d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44620754 | |||||
chr7:44620830
|
A | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-3487A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620830 | ||||||
chr7:44620874
|
C | A | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-27-3443C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620874 | ||||||
chr7:44620982
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-27-3335C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44620982 | ||||||
chr7:44621149
|
C | T | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-27-3168C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621149 | ||||||
chr7:44621280
|
C | T | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27-3037C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621280 | ||||||
chr7:44621655
|
T | C | 222 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(219): Show | 223 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.-27-2662T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621655 | ||||||
chr7:44621656
|
G | A | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-27-2661G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621656 | ||||||
chr7:44621662
|
A | G | 2 | a0001c0002t0003g0263a0001c0010t0001g0302 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-27-2655A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621662 | ||||||
chr7:44621790
|
T | A | 1 | a0001c0002t0001g0146 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-27-2527T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621790 | ||||||
chr7:44621864
|
C | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-27-2453C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621864 | ||||||
chr7:44621870
|
C | CA | 45 | a0001c0001t0002g0224a0001c0001t0002g0260a0001c0001t0002g0261others(42): Show | 45 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.-27-2435dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44621870 | |||||
chr7:44621945
|
C | T | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-2372C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44621945 | ||||||
chr7:44622224
|
A | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-2093A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622224 | ||||||
chr7:44622508
|
A | G | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-27-1809A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622508 | ||||||
chr7:44622546
|
A | T | 1 | a0001c0001t0002g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-27-1771A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622546 | ||||||
chr7:44622558
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-1759C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622558 | ||||||
chr7:44622632
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27-1685A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622632 | ||||||
chr7:44622669
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-27-1648C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622669 | ||||||
chr7:44622909
|
T | C | 2 | a0001c0001t0009g0003a0001c0009t0001g0193 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-27-1408T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622909 | ||||||
chr7:44622967
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-27-1350G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44622967 | ||||||
chr7:44623030
|
C | T | 86 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(83): Show | 86 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-27-1287C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623030 | ||||||
chr7:44623039
|
A | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-1278A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623039 | ||||||
chr7:44623087
|
A | G | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-27-1230A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623087 | ||||||
chr7:44623094
|
A | G | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-27-1223A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623094 | ||||||
chr7:44623150
|
G | T | 2 | a0001c0004t0002g0002a0001c0004t0002g0223 | 3 | HG02922.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-27-1167G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623150 | ||||||
chr7:44623239
|
G | A | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27-1078G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623239 | ||||||
chr7:44623274
|
C | G | 189 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(186): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-27-1043C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623274 | ||||||
chr7:44623486
|
T | C | 2 | a0001c0001t0007g0298a0001c0001t0007g0299 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-27-831T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623486 | ||||||
chr7:44623496
|
T | TTTTACTT others(106): Show |
44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27-816_-27-704dup others(113): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44623496 | |||||
chr7:44623605
|
G | A | 2 | a0001c0005t0001g0200a0001c0006t0001g0129 | 2 | HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-27-712G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623605 | ||||||
chr7:44623655
|
G | A | 10 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(7): Show | 10 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27-662G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623655 | ||||||
chr7:44623760
|
C | T | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-27-557C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623760 | ||||||
chr7:44623890
|
C | T | 4 | a0001c0001t0005g0228a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG00099.hp1 HG02698.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27-427C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623890 | ||||||
chr7:44623959
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27-358A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623959 | ||||||
chr7:44623984
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-27-333T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44623984 | ||||||
chr7:44624085
|
A | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-27-232A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44624085 | ||||||
chr7:44624109
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-27-208G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44624109 | ||||||
chr7:44624171
|
A | G | 144 | a0001c0001t0001g0011a0001c0001t0001g0079a0001c0001t0001g0080others(141): Show | 144 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.-27-146A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44624171 | ||||||
chr7:44624291
|
G | GT | 29 | a0001c0001t0002g0022a0001c0001t0002g0034a0001c0001t0002g0038others(26): Show | 29 | HG00140.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.-27-7dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44624291 | |||||
chr7:44624291
|
GT | G | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0195others(10): Show | 13 | HG00609.hp1 HG02258.hp1 HG02258.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.-27-7delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44624291 | |||||
chr7:44624291
|
GTT | G | 7 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.-27-8_-27-7delTT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44624291 | |||||
chr7:44624291
|
GTTT | G | 84 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(81): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
splice_region_variant&intron_variant | LOW | c.-27-9_-27-7delTTT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44624291 | |||||
chr7:44624291
|
GTTTTTTT others(4): Show |
G | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.-27-17_-27-7delTTT others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr7 | 44624291 | |||||
chr7:44624292
|
T | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-27-25T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 1/22 | chr7 | 44624292 | ||||||
chr7:44624697
|
G | A | 2 | a0001c0002t0001g0225a0001c0002t0001g0230 | 2 | HG01978.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.222+132G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44624697 | ||||||
chr7:44624751
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.222+186C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44624751 | ||||||
chr7:44624856
|
AAAG | A | 90 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+297_222+299del others(3): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44624856 | |||||
chr7:44624865
|
A | T | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.222+300A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44624865 | ||||||
chr7:44625083
|
T | C | 90 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+518T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625083 | ||||||
chr7:44625194
|
G | A | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.222+629G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625194 | ||||||
chr7:44625395
|
G | T | 1 | a0001c0002t0003g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.222+830G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625395 | ||||||
chr7:44625465
|
G | A | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+900G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625465 | ||||||
chr7:44625743
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+1178A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625743 | ||||||
chr7:44625803
|
T | C | 1 | a0001c0002t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.222+1238T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625803 | ||||||
chr7:44625809
|
AT | A | 38 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(35): Show | 38 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.222+1255delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44625809 | |||||
chr7:44625820
|
T | A | 6 | a0002c0003t0001g0089a0002c0003t0001g0111a0002c0003t0001g0112others(3): Show | 6 | HG01358.hp1 HG02738.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+1255T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625820 | ||||||
chr7:44625906
|
G | A | 2 | a0001c0001t0012g0122a0002c0013t0001g0073 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.222+1341G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625906 | ||||||
chr7:44625997
|
C | T | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.222+1432C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44625997 | ||||||
chr7:44626256
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.222+1691A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626256 | ||||||
chr7:44626299
|
A | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+1734A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626299 | ||||||
chr7:44626301
|
A | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+1736A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626301 | ||||||
chr7:44626301
|
A | G | 1 | a0001c0001t0004g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.222+1736A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626301 | ||||||
chr7:44626302
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+1737C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626302 | ||||||
chr7:44626303
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+1738C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626303 | ||||||
chr7:44626305
|
C | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+1740C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626305 | ||||||
chr7:44626306
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+1741T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626306 | ||||||
chr7:44626306
|
TAC | T | 85 | a0001c0001t0001g0011a0001c0001t0002g0106a0001c0001t0002g0126others(82): Show | 85 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.222+1766_222+1767d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44626306 | |||||
chr7:44626306
|
TACAC | T | 3 | a0001c0001t0002g0207a0001c0005t0001g0200a0001c0006t0001g0129 | 3 | HG01943.hp2 HG02257.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222+1764_222+1767d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44626306 | |||||
chr7:44626308
|
CACACACA others(21): Show |
C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.222+1776_222+1803d others(30): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44626308 | |||||
chr7:44626333
|
C | A | 51 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(48): Show | 51 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.222+1768C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626333 | ||||||
chr7:44626335
|
C | A | 7 | a0001c0001t0012g0122a0001c0002t0001g0085a0001c0002t0001g0086others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+1770C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626335 | ||||||
chr7:44626336
|
T | C | 51 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(48): Show | 51 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.222+1771T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626336 | ||||||
chr7:44626336
|
T | TAC | 3 | a0001c0001t0002g0056a0001c0001t0004g0215a0001c0002t0001g0024 | 3 | HG01175.hp1 HG02040.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.222+1794_222+1795d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44626336 | |||||
chr7:44626336
|
TAC | T | 130 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(127): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.222+1794_222+1795d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44626336 | |||||
chr7:44626336
|
TACAC | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(3): Show | 6 | HG02258.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+1792_222+1795d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44626336 | |||||
chr7:44626337
|
A | C | 45 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(42): Show | 45 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.222+1772A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626337 | ||||||
chr7:44626338
|
C | T | 40 | a0001c0001t0002g0261a0001c0001t0002g0262a0001c0001t0002g0264others(37): Show | 40 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.222+1773C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626338 | ||||||
chr7:44626339
|
A | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG00741.hp1 HG01433.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+1774A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626339 | ||||||
chr7:44626340
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG00741.hp1 HG01433.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+1775C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626340 | ||||||
chr7:44626341
|
A | C | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.222+1776A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626341 | ||||||
chr7:44626342
|
C | T | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.222+1777C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626342 | ||||||
chr7:44626426
|
A | T | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.222+1861A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626426 | ||||||
chr7:44626680
|
A | G | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222+2115A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626680 | ||||||
chr7:44626755
|
T | C | 84 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(81): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.222+2190T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626755 | ||||||
chr7:44626786
|
G | C | 10 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(7): Show | 10 | HG00438.hp2 HG02132.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+2221G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626786 | ||||||
chr7:44626972
|
G | A | 2 | a0001c0001t0012g0122a0002c0013t0001g0073 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.222+2407G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626972 | ||||||
chr7:44626982
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.222+2417T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44626982 | ||||||
chr7:44627089
|
G | A | 2 | a0001c0001t0012g0122a0002c0013t0001g0073 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.222+2524G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627089 | ||||||
chr7:44627089
|
G | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+2524G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627089 | ||||||
chr7:44627115
|
G | A | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+2550G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627115 | ||||||
chr7:44627136
|
A | T | 1 | a0001c0001t0001g0011 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.222+2571A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627136 | ||||||
chr7:44627157
|
C | T | 5 | a0001c0001t0009g0003a0001c0002t0001g0085a0001c0002t0001g0086others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+2592C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627157 | ||||||
chr7:44627177
|
A | G | 1 | a0001c0001t0002g0137 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.222+2612A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627177 | ||||||
chr7:44627299
|
G | A | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+2734G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627299 | ||||||
chr7:44627318
|
T | A | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.222+2753T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627318 | ||||||
chr7:44627619
|
C | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+3054C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627619 | ||||||
chr7:44627787
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.222+3222G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627787 | ||||||
chr7:44627825
|
C | T | 2 | a0001c0002t0001g0086a0001c0002t0001g0088 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.222+3260C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627825 | ||||||
chr7:44627837
|
T | C | 134 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.222+3272T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627837 | ||||||
chr7:44627866
|
G | A | 1 | a0001c0001t0007g0290 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.222+3301G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627866 | ||||||
chr7:44627967
|
G | T | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.222+3402G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44627967 | ||||||
chr7:44628071
|
C | T | 1 | a0001c0002t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.222+3506C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44628071 | ||||||
chr7:44628180
|
A | T | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222+3615A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44628180 | ||||||
chr7:44628464
|
CT | C | 133 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(130): Show | 133 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.222+3907delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44628464 | |||||
chr7:44628465
|
T | TTTTTTTT others(294): Show |
1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222+3907_222+3908i others(303): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44628465 | |||||
chr7:44628619
|
A | T | 1 | a0001c0002t0001g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.222+4054A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44628619 | ||||||
chr7:44628714
|
T | C | 1 | a0001c0002t0001g0147 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.222+4149T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44628714 | ||||||
chr7:44628807
|
G | A | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.222+4242G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44628807 | ||||||
chr7:44628927
|
C | T | 6 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0153others(3): Show | 6 | HG02015.hp2 HG02080.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+4362C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44628927 | ||||||
chr7:44629206
|
T | A | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG02257.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.222+4641T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629206 | ||||||
chr7:44629512
|
C | T | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222+4947C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629512 | ||||||
chr7:44629575
|
C | CT | 5 | a0001c0001t0002g0137a0001c0002t0001g0124a0001c0002t0001g0132others(2): Show | 5 | HG00597.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.222+5014dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44629575 | |||||
chr7:44629575
|
CTTTTCTT | C | 42 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.222+5015_222+5021d others(9): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44629575 | |||||
chr7:44629578
|
TTC | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(4): Show | 7 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+5015_222+5016d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44629578 | |||||
chr7:44629579
|
TC | T | 45 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0083others(42): Show | 45 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.222+5015delC | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629579 | ||||||
chr7:44629580
|
C | CT | 11 | a0001c0001t0001g0254a0001c0001t0002g0022a0001c0001t0002g0056others(8): Show | 11 | HG01496.hp2 HG01978.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+5033dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44629580 | |||||
chr7:44629580
|
C | T | 89 | a0001c0001t0001g0011a0001c0001t0001g0196a0001c0001t0002g0126others(86): Show | 89 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.222+5015C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629580 | ||||||
chr7:44629580
|
CT | C | 7 | a0001c0001t0002g0027a0001c0001t0002g0071a0001c0002t0001g0085others(4): Show | 7 | HG00597.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+5033delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44629580 | |||||
chr7:44629611
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+5046G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629611 | ||||||
chr7:44629690
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.222+5125G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629690 | ||||||
chr7:44629697
|
A | G | 134 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.222+5132A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629697 | ||||||
chr7:44629715
|
G | A | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+5150G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629715 | ||||||
chr7:44629736
|
C | T | 1 | a0001c0002t0001g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.222+5171C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629736 | ||||||
chr7:44629737
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+5172G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629737 | ||||||
chr7:44629822
|
C | T | 84 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(81): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.222+5257C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629822 | ||||||
chr7:44629823
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+5258G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629823 | ||||||
chr7:44629826
|
C | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+5261C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629826 | ||||||
chr7:44629832
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+5267G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629832 | ||||||
chr7:44629860
|
G | A | 41 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(38): Show | 41 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.222+5295G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629860 | ||||||
chr7:44629928
|
A | T | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+5363A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629928 | ||||||
chr7:44629932
|
C | T | 6 | a0001c0001t0002g0001a0001c0001t0002g0050a0001c0001t0002g0053others(3): Show | 7 | HG01928.hp1 HG02300.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+5367C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44629932 | ||||||
chr7:44630047
|
G | A | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.222+5482G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630047 | ||||||
chr7:44630065
|
G | A | 134 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.222+5500G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630065 | ||||||
chr7:44630099
|
G | A | 134 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(131): Show | 134 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.222+5534G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630099 | ||||||
chr7:44630110
|
G | A | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222+5545G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630110 | ||||||
chr7:44630327
|
A | G | 2 | a0001c0001t0009g0003a0001c0009t0001g0193 | 2 | HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222+5762A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630327 | ||||||
chr7:44630382
|
G | A | 1 | a0001c0016t0001g0246 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.222+5817G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630382 | ||||||
chr7:44630555
|
T | C | 189 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(186): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.222+5990T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630555 | ||||||
chr7:44630557
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.222+5992T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630557 | ||||||
chr7:44630820
|
T | C | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.222+6255T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630820 | ||||||
chr7:44630921
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222+6356A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630921 | ||||||
chr7:44630947
|
C | T | 8 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.222+6382C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44630947 | ||||||
chr7:44631066
|
C | T | 10 | a0002c0003t0001g0075a0002c0003t0001g0077a0002c0003t0001g0090others(7): Show | 10 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.222+6501C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631066 | ||||||
chr7:44631083
|
G | T | 1 | a0002c0003t0001g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.222+6518G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631083 | ||||||
chr7:44631124
|
A | T | 90 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+6559A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631124 | ||||||
chr7:44631130
|
A | T | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.222+6565A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631130 | ||||||
chr7:44631146
|
C | G | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+6581C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631146 | ||||||
chr7:44631180
|
G | A | 2 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.222+6615G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631180 | ||||||
chr7:44631222
|
C | T | 1 | a0001c0001t0006g0069 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.222+6657C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631222 | ||||||
chr7:44631255
|
G | A | 3 | a0001c0001t0002g0279a0001c0001t0002g0280a0001c0001t0002g0297 | 3 | HG01175.hp2 HG01515.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.222+6690G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631255 | ||||||
chr7:44631384
|
A | G | 1 | a0001c0001t0002g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.222+6819A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631384 | ||||||
chr7:44631417
|
C | T | 189 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(186): Show | 189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.222+6852C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631417 | ||||||
chr7:44631427
|
A | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+6862A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631427 | ||||||
chr7:44631545
|
G | A | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.222+6980G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631545 | ||||||
chr7:44631614
|
A | C | 1 | a0001c0001t0004g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.222+7049A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631614 | ||||||
chr7:44631722
|
G | A | 2 | a0001c0001t0002g0216a0001c0001t0002g0217 | 2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.222+7157G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631722 | ||||||
chr7:44631792
|
T | G | 42 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.222+7227T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631792 | ||||||
chr7:44631876
|
A | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+7311A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631876 | ||||||
chr7:44631901
|
A | G | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.222+7336A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631901 | ||||||
chr7:44631972
|
A | G | 87 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(84): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.222+7407A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631972 | ||||||
chr7:44631984
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG00741.hp1 HG01433.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+7419G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44631984 | ||||||
chr7:44632023
|
G | A | 15 | a0001c0002t0001g0222a0001c0002t0001g0225a0001c0002t0001g0226others(12): Show | 15 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+7458G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632023 | ||||||
chr7:44632401
|
C | T | 3 | a0001c0002t0001g0172a0001c0002t0001g0184a0001c0002t0001g0187 | 3 | HG03490.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.222+7836C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632401 | ||||||
chr7:44632442
|
A | G | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+7877A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632442 | ||||||
chr7:44632521
|
C | G | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.222+7956C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632521 | ||||||
chr7:44632613
|
G | T | 188 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(185): Show | 188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.222+8048G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632613 | ||||||
chr7:44632619
|
GTTGTTA | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 6 | HG00741.hp1 HG01433.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+8060_222+8065d others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44632619 | |||||
chr7:44632622
|
GTTA | G | 84 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(81): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.222+8060_222+8062d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44632622 | |||||
chr7:44632710
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.222+8145C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632710 | ||||||
chr7:44632918
|
T | A | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+8353T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632918 | ||||||
chr7:44632938
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+8373T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44632938 | ||||||
chr7:44633023
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.222+8458G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633023 | ||||||
chr7:44633031
|
A | G | 90 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(87): Show | 90 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+8466A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633031 | ||||||
chr7:44633058
|
C | T | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.222+8493C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633058 | ||||||
chr7:44633069
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+8504T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633069 | ||||||
chr7:44633252
|
C | CA | 33 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(30): Show | 33 | HG00140.hp2 HG00597.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.222+8709dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44633252 | |||||
chr7:44633252
|
C | CAA | 38 | a0001c0001t0001g0017a0001c0001t0002g0260a0001c0001t0002g0261others(35): Show | 38 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.222+8708_222+8709d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44633252 | |||||
chr7:44633252
|
C | CAAA | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(10): Show | 13 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.222+8707_222+8709d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44633252 | |||||
chr7:44633252
|
CA | C | 74 | a0001c0001t0001g0011a0001c0001t0002g0022a0001c0001t0002g0026others(71): Show | 74 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.222+8709delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44633252 | |||||
chr7:44633252
|
CAAA | C | 35 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(32): Show | 35 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.222+8707_222+8709d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44633252 | |||||
chr7:44633265
|
A | C | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.222+8700A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633265 | ||||||
chr7:44633418
|
C | G | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222+8853C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633418 | ||||||
chr7:44633463
|
G | A | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.222+8898G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633463 | ||||||
chr7:44633507
|
T | C | 2 | a0001c0002t0001g0185a0001c0002t0001g0186 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.222+8942T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633507 | ||||||
chr7:44633563
|
C | T | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.222+8998C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633563 | ||||||
chr7:44633587
|
T | C | 1 | a0002c0003t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.222+9022T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633587 | ||||||
chr7:44633616
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+9051A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633616 | ||||||
chr7:44633712
|
G | A | 44 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262others(41): Show | 44 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.222+9147G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633712 | ||||||
chr7:44633802
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.222+9237G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633802 | ||||||
chr7:44633898
|
C | T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.222+9333C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633898 | ||||||
chr7:44633992
|
T | G | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.222+9427T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44633992 | ||||||
chr7:44634076
|
A | C | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.222+9511A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44634076 | ||||||
chr7:44634086
|
C | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0002t0001g0124 | 3 | HG02258.hp2 HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.222+9521C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44634086 | ||||||
chr7:44634281
|
T | A | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.222+9716T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44634281 | ||||||
chr7:44634813
|
A | G | 1 | a0001c0008t0002g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.222+10248A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44634813 | ||||||
chr7:44634824
|
C | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+10259C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44634824 | ||||||
chr7:44634964
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.223-10363C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44634964 | ||||||
chr7:44635161
|
G | C | 2 | a0001c0002t0001g0086a0001c0002t0001g0088 | 2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.223-10166G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635161 | ||||||
chr7:44635341
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-9986T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635341 | ||||||
chr7:44635347
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.223-9980G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635347 | ||||||
chr7:44635444
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-9883C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635444 | ||||||
chr7:44635448
|
G | C | 111 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(108): Show | 111 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.223-9879G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635448 | ||||||
chr7:44635449
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-9878C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635449 | ||||||
chr7:44635531
|
G | A | 4 | a0001c0001t0005g0228a0001c0001t0005g0238a0001c0001t0005g0239others(1): Show | 4 | HG00099.hp1 HG02698.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-9796G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635531 | ||||||
chr7:44635707
|
AT | A | 13 | a0001c0001t0002g0058a0001c0001t0002g0144a0001c0001t0002g0145others(10): Show | 13 | HG01884.hp1 HG02015.hp2 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.223-9605delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44635707 | |||||
chr7:44635727
|
A | T | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.223-9600A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635727 | ||||||
chr7:44635790
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223-9537C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635790 | ||||||
chr7:44635954
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.223-9373C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635954 | ||||||
chr7:44635975
|
T | C | 3 | a0001c0002t0003g0263a0001c0005t0001g0274a0001c0010t0001g0302 | 3 | HG02280.hp1 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-9352T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635975 | ||||||
chr7:44635982
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223-9345C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44635982 | ||||||
chr7:44636055
|
C | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-9272C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636055 | ||||||
chr7:44636068
|
CT | C | 3 | a0001c0002t0003g0263a0001c0005t0001g0274a0001c0010t0001g0302 | 3 | HG02280.hp1 HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-9255delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44636068 | |||||
chr7:44636349
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.223-8978G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636349 | ||||||
chr7:44636408
|
G | A | 4 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(1): Show | 4 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-8919G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636408 | ||||||
chr7:44636546
|
A | G | 1 | a0001c0001t0002g0287 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.223-8781A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636546 | ||||||
chr7:44636683
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.223-8644A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636683 | ||||||
chr7:44636687
|
C | T | 84 | a0001c0001t0001g0011a0001c0001t0002g0126a0001c0001t0002g0136others(81): Show | 84 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.223-8640C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636687 | ||||||
chr7:44636772
|
G | T | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.223-8555G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636772 | ||||||
chr7:44636784
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.223-8543T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636784 | ||||||
chr7:44636934
|
G | T | 1 | a0001c0001t0004g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.223-8393G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44636934 | ||||||
chr7:44637128
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.223-8199A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637128 | ||||||
chr7:44637154
|
T | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(17): Show | 20 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.223-8173T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637154 | ||||||
chr7:44637282
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.223-8045T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637282 | ||||||
chr7:44637463
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-7864T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637463 | ||||||
chr7:44637499
|
C | T | 148 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(145): Show | 148 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.223-7828C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637499 | ||||||
chr7:44637543
|
C | T | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.223-7784C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637543 | ||||||
chr7:44637818
|
C | CA | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.223-7494dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44637818 | |||||
chr7:44637818
|
CA | C | 9 | a0001c0001t0002g0276a0001c0001t0009g0003a0001c0002t0001g0235others(6): Show | 9 | HG00099.hp1 HG00609.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-7494delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44637818 | |||||
chr7:44637975
|
C | T | 1 | a0001c0002t0003g0010 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.223-7352C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44637975 | ||||||
chr7:44638066
|
A | C | 1 | a0001c0001t0002g0066 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223-7261A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638066 | ||||||
chr7:44638079
|
C | T | 2 | a0001c0002t0003g0263a0001c0010t0001g0302 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-7248C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638079 | ||||||
chr7:44638082
|
C | A | 8 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG00741.hp1 HG01433.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.223-7245C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638082 | ||||||
chr7:44638174
|
G | A | 1 | a0001c0001t0008g0210 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.223-7153G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638174 | ||||||
chr7:44638244
|
T | A | 1 | a0001c0001t0002g0066 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223-7083T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638244 | ||||||
chr7:44638274
|
G | T | 1 | a0001c0001t0002g0066 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.223-7053G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638274 | ||||||
chr7:44638337
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-6990C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638337 | ||||||
chr7:44638492
|
G | A | 2 | a0001c0002t0003g0263a0001c0010t0001g0302 | 2 | HG02896.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-6835G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638492 | ||||||
chr7:44638510
|
C | T | 1 | a0001c0002t0001g0171 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.223-6817C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638510 | ||||||
chr7:44638555
|
C | T | 1 | a0001c0001t0002g0265 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.223-6772C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638555 | ||||||
chr7:44638684
|
A | G | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.223-6643A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638684 | ||||||
chr7:44638922
|
G | A | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.223-6405G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44638922 | ||||||
chr7:44639009
|
T | C | 3 | a0001c0002t0001g0152a0001c0002t0001g0181a0001c0002t0001g0199 | 3 | HG00408.hp2 NA19003.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.223-6318T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639009 | ||||||
chr7:44639193
|
G | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0039 | 2 | HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.223-6134G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639193 | ||||||
chr7:44639363
|
C | T | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.223-5964C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639363 | ||||||
chr7:44639535
|
T | G | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-5792T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639535 | ||||||
chr7:44639611
|
G | A | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223-5716G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639611 | ||||||
chr7:44639649
|
A | G | 36 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.223-5678A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639649 | ||||||
chr7:44639746
|
G | C | 4 | a0002c0003t0001g0074a0002c0003t0001g0093a0002c0003t0001g0094others(1): Show | 4 | NA18941.hp1 NA18954.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.223-5581G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639746 | ||||||
chr7:44639866
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.223-5461C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44639866 | ||||||
chr7:44640020
|
G | A | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-5307G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640020 | ||||||
chr7:44640082
|
G | A | 10 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(7): Show | 10 | HG00438.hp2 HG02132.hp2 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-5245G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640082 | ||||||
chr7:44640141
|
C | T | 2 | a0001c0002t0001g0172a0001c0002t0001g0187 | 2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.223-5186C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640141 | ||||||
chr7:44640253
|
C | T | 1 | a0001c0002t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.223-5074C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640253 | ||||||
chr7:44640288
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223-5039C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640288 | ||||||
chr7:44640325
|
C | T | 2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-5002C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640325 | ||||||
chr7:44640329
|
A | G | 3 | a0001c0002t0003g0008a0001c0002t0003g0009a0001c0002t0003g0010 | 3 | HG01891.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.223-4998A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640329 | ||||||
chr7:44640397
|
C | T | 23 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0003others(20): Show | 23 | HG01884.hp1 HG01978.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.223-4930C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640397 | ||||||
chr7:44640581
|
G | A | 2 | a0001c0001t0002g0126a0001c0001t0002g0178 | 2 | NA18961.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.223-4746G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640581 | ||||||
chr7:44640629
|
A | G | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.223-4698A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640629 | ||||||
chr7:44640696
|
A | G | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223-4631A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640696 | ||||||
chr7:44640813
|
C | T | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-4514C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640813 | ||||||
chr7:44640895
|
G | GT | 11 | a0001c0001t0001g0081a0001c0001t0001g0083a0001c0002t0001g0037others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.223-4419dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44640895 | |||||
chr7:44640899
|
T | C | 2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-4428T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44640899 | ||||||
chr7:44641048
|
C | G | 2 | a0001c0002t0001g0225a0001c0002t0001g0230 | 2 | HG01978.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.223-4279C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641048 | ||||||
chr7:44641064
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.223-4263T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641064 | ||||||
chr7:44641122
|
C | T | 2 | a0001c0002t0010g0042a0001c0002t0010g0043 | 2 | HG02155.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.223-4205C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641122 | ||||||
chr7:44641148
|
G | A | 1 | a0001c0001t0004g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.223-4179G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641148 | ||||||
chr7:44641209
|
C | CT | 16 | a0001c0001t0002g0053a0001c0001t0002g0115a0001c0001t0002g0272others(13): Show | 16 | HG00099.hp1 HG00438.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.223-4103dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641209 | |||||
chr7:44641209
|
CTTTT | C | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(8): Show | 11 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-4106_223-4103d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641209 | |||||
chr7:44641209
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-4102_223-4085d others(20): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641209 | |||||
chr7:44641221
|
TTTTC | T | 24 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0003others(21): Show | 24 | HG01884.hp1 HG01978.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.223-4102_223-4099d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641221 | |||||
chr7:44641222
|
TTTC | T | 88 | a0001c0001t0001g0011a0001c0001t0002g0091a0001c0001t0002g0145others(85): Show | 88 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.223-4102_223-4100d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641222 | |||||
chr7:44641223
|
TTC | T | 25 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(22): Show | 25 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-4102_223-4101d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641223 | |||||
chr7:44641225
|
C | CT | 11 | a0001c0001t0002g0023a0001c0001t0002g0136a0001c0001t0002g0137others(8): Show | 11 | HG01175.hp1 HG01175.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.223-4085dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641225 | |||||
chr7:44641225
|
CTTTTTTT others(4): Show |
C | 10 | a0001c0001t0002g0022a0001c0001t0002g0056a0001c0001t0002g0058others(7): Show | 10 | HG01496.hp2 HG01978.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-4095_223-4085d others(13): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44641225 | |||||
chr7:44641226
|
T | C | 112 | a0001c0001t0001g0011a0001c0001t0002g0095a0001c0001t0002g0096others(109): Show | 112 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.223-4101T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641226 | ||||||
chr7:44641227
|
T | C | 36 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG00741.hp1 HG01433.hp1 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.223-4100T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641227 | ||||||
chr7:44641288
|
C | G | 87 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(84): Show | 87 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.223-4039C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641288 | ||||||
chr7:44641344
|
G | C | 1 | a0001c0002t0001g0063 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.223-3983G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641344 | ||||||
chr7:44641430
|
T | C | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-3897T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641430 | ||||||
chr7:44641476
|
T | C | 3 | a0001c0001t0002g0054a0001c0001t0002g0204a0001c0001t0002g0270 | 3 | HG01934.hp2 HG02148.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.223-3851T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641476 | ||||||
chr7:44641608
|
C | T | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.223-3719C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641608 | ||||||
chr7:44641780
|
C | G | 6 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0003others(3): Show | 6 | HG02257.hp2 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.223-3547C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641780 | ||||||
chr7:44641937
|
A | G | 1 | a0001c0002t0003g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.223-3390A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641937 | ||||||
chr7:44641945
|
T | C | 1 | a0001c0001t0004g0244 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.223-3382T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641945 | ||||||
chr7:44641970
|
G | C | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.223-3357G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44641970 | ||||||
chr7:44642086
|
G | A | 17 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(14): Show | 17 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.223-3241G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642086 | ||||||
chr7:44642141
|
G | GC | 124 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(121): Show | 124 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.223-3186_223-3185i others(3): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642141 | ||||||
chr7:44642149
|
C | G | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.223-3178C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642149 | ||||||
chr7:44642158
|
A | T | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.223-3169A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642158 | ||||||
chr7:44642288
|
G | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(8): Show | 11 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-3039G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642288 | ||||||
chr7:44642349
|
C | T | 17 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(14): Show | 17 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.223-2978C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642349 | ||||||
chr7:44642407
|
G | C | 1 | a0002c0003t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.223-2920G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642407 | ||||||
chr7:44642632
|
A | G | 1 | a0002c0003t0001g0119 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.223-2695A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642632 | ||||||
chr7:44642655
|
G | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0070a0001c0001t0002g0078 | 3 | HG02135.hp2 NA18981.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.223-2672G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642655 | ||||||
chr7:44642669
|
A | G | 1 | a0001c0001t0002g0288 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.223-2658A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642669 | ||||||
chr7:44642769
|
A | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-2558A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642769 | ||||||
chr7:44642798
|
T | A | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223-2529T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642798 | ||||||
chr7:44642815
|
G | A | 8 | a0001c0004t0002g0002a0001c0004t0002g0221a0001c0004t0002g0223others(5): Show | 9 | HG01496.hp1 HG01515.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-2512G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642815 | ||||||
chr7:44642921
|
C | CA | 116 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.223-2392dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44642921 | |||||
chr7:44642934
|
A | T | 1 | a0001c0001t0005g0285 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.223-2393A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642934 | ||||||
chr7:44642935
|
A | T | 7 | a0001c0001t0002g0284a0001c0001t0005g0266a0001c0001t0005g0285others(4): Show | 7 | HG00558.hp1 HG01934.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2392A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642935 | ||||||
chr7:44642936
|
T | A | 146 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(143): Show | 146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.223-2391T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642936 | ||||||
chr7:44642937
|
T | C | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.223-2390T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642937 | ||||||
chr7:44642945
|
A | G | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.223-2382A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44642945 | ||||||
chr7:44643094
|
TA | T | 36 | a0001c0001t0001g0019a0001c0001t0002g0022a0001c0001t0002g0054others(33): Show | 36 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.223-2210delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44643094 | |||||
chr7:44643094
|
TAA | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0079others(6): Show | 9 | HG01433.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-2211_223-2210d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44643094 | |||||
chr7:44643094
|
TAAA | T | 36 | a0001c0001t0001g0017a0001c0001t0001g0195a0001c0001t0001g0196others(33): Show | 36 | HG01884.hp1 HG01978.hp1 HG02257.hp2 others(33): Show |
intron_variant | MODIFIER | c.223-2212_223-2210d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44643094 | |||||
chr7:44643094
|
TAAAA | T | 77 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(74): Show | 77 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.223-2213_223-2210d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44643094 | |||||
chr7:44643121
|
AT | A | 150 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(147): Show | 150 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.223-2200delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44643121 | |||||
chr7:44643339
|
G | A | 150 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(147): Show | 150 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.223-1988G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44643339 | ||||||
chr7:44643453
|
C | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-1874C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44643453 | ||||||
chr7:44643565
|
T | C | 42 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0026others(39): Show | 43 | HG00423.hp2 HG00597.hp1 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.223-1762T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44643565 | ||||||
chr7:44643944
|
C | T | 25 | a0001c0001t0002g0091a0001c0001t0002g0095a0001c0001t0002g0096others(22): Show | 25 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-1383C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44643944 | ||||||
chr7:44644130
|
G | A | 1 | a0002c0003t0001g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.223-1197G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644130 | ||||||
chr7:44644173
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.223-1154G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644173 | ||||||
chr7:44644234
|
GCTTTT | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.223-1082_223-1078d others(7): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr7 | 44644234 | |||||
chr7:44644243
|
T | C | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.223-1084T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644243 | ||||||
chr7:44644271
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.223-1056C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644271 | ||||||
chr7:44644290
|
T | C | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.223-1037T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644290 | ||||||
chr7:44644939
|
C | T | 1 | a0001c0007t0002g0052 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.223-388C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644939 | ||||||
chr7:44644999
|
G | A | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.223-328G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 2/22 | chr7 | 44644999 | ||||||
chr7:44645629
|
C | T | 1 | a0001c0002t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.414+111C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44645629 | ||||||
chr7:44645724
|
A | G | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.414+206A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44645724 | ||||||
chr7:44645736
|
G | A | 1 | a0001c0001t0002g0284 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.414+218G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44645736 | ||||||
chr7:44645832
|
A | C | 1 | a0001c0002t0001g0024 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.414+314A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44645832 | ||||||
chr7:44645915
|
C | T | 2 | a0001c0001t0002g0267a0001c0002t0001g0283 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.414+397C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44645915 | ||||||
chr7:44645924
|
A | T | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414+406A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44645924 | ||||||
chr7:44646001
|
C | T | 1 | a0001c0002t0003g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.414+483C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646001 | ||||||
chr7:44646068
|
A | C | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.414+550A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646068 | ||||||
chr7:44646458
|
G | T | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01109.hp1 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+940G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646458 | ||||||
chr7:44646588
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.415-1069C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646588 | ||||||
chr7:44646898
|
G | A | 124 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(121): Show | 124 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.415-759G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646898 | ||||||
chr7:44646931
|
C | T | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.415-726C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646931 | ||||||
chr7:44646940
|
A | G | 1 | a0001c0001t0016g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.415-717A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44646940 | ||||||
chr7:44647116
|
A | G | 2 | a0001c0002t0001g0225a0001c0002t0001g0230 | 2 | HG01978.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.415-541A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44647116 | ||||||
chr7:44647271
|
C | T | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.415-386C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | chr7 | 44647271 | ||||||
chr7:44647576
|
C | CT | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.415-72dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr7 | 44647576 | |||||
chr7:44647835
|
C | G | 4 | a0001c0002t0001g0222a0001c0002t0001g0226a0001c0002t0001g0250others(1): Show | 4 | HG03209.hp1 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.517+76C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44647835 | ||||||
chr7:44647839
|
G | A | 11 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(8): Show | 11 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+80G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44647839 | ||||||
chr7:44648102
|
G | T | 2 | a0001c0002t0001g0172a0001c0002t0001g0187 | 2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.517+343G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44648102 | ||||||
chr7:44648135
|
C | G | 1 | a0001c0002t0001g0024 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.517+376C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44648135 | ||||||
chr7:44648646
|
TACAG | T | 23 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0003others(20): Show | 23 | HG01884.hp1 HG01978.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.517+892_517+895del others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44648646 | |||||
chr7:44648800
|
G | A | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.517+1041G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44648800 | ||||||
chr7:44648982
|
A | G | 1 | a0001c0002t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.517+1223A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44648982 | ||||||
chr7:44649049
|
T | C | 86 | a0001c0001t0001g0011a0001c0001t0002g0145a0001c0001t0002g0153others(83): Show | 86 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.517+1290T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44649049 | ||||||
chr7:44649245
|
G | GT | 122 | a0001c0001t0001g0011a0001c0001t0001g0254a0001c0001t0002g0066others(119): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.517+1508dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44649245 | |||||
chr7:44649245
|
G | GTT | 12 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0006g0033others(9): Show | 12 | HG00408.hp1 HG02080.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.517+1507_517+1508d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44649245 | |||||
chr7:44649245
|
GT | G | 28 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(25): Show | 28 | HG00099.hp1 HG00741.hp1 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.517+1508delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44649245 | |||||
chr7:44649245
|
GTT | G | 7 | a0001c0004t0002g0002a0001c0004t0002g0221a0001c0004t0002g0223others(4): Show | 8 | HG01496.hp1 HG01515.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.517+1507_517+1508d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44649245 | |||||
chr7:44649248
|
T | G | 2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+1489T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44649248 | ||||||
chr7:44649502
|
G | A | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.517+1743G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44649502 | ||||||
chr7:44649521
|
A | G | 1 | a0001c0002t0003g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.517+1762A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44649521 | ||||||
chr7:44649633
|
G | A | 1 | a0001c0002t0003g0007 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.517+1874G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44649633 | ||||||
chr7:44649876
|
A | G | 1 | a0001c0002t0003g0008 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+2117A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44649876 | ||||||
chr7:44650067
|
CAGGGAGT others(5): Show |
C | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.517+2309_517+2320d others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650067 | ||||||
chr7:44650174
|
C | T | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG00741.hp2 HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.517+2415C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650174 | ||||||
chr7:44650274
|
AC | A | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.517+2517delC | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44650274 | |||||
chr7:44650308
|
G | A | 23 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0009g0003others(20): Show | 23 | HG01884.hp1 HG01978.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.517+2549G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650308 | ||||||
chr7:44650311
|
G | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(98): Show | 101 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.517+2552G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650311 | ||||||
chr7:44650342
|
T | C | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+2583T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650342 | ||||||
chr7:44650423
|
G | A | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+2664G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650423 | ||||||
chr7:44650537
|
C | A | 1 | a0001c0002t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.517+2778C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650537 | ||||||
chr7:44650543
|
A | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(9): Show | 12 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.517+2784A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650543 | ||||||
chr7:44650985
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.517+3226G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44650985 | ||||||
chr7:44651063
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+3304C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651063 | ||||||
chr7:44651148
|
G | C | 119 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(116): Show | 119 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.517+3389G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651148 | ||||||
chr7:44651378
|
T | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(8): Show | 11 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+3619T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651378 | ||||||
chr7:44651387
|
A | G | 1 | a0001c0017t0005g0240 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.517+3628A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651387 | ||||||
chr7:44651564
|
A | C | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.517+3805A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651564 | ||||||
chr7:44651631
|
G | A | 1 | a0001c0002t0001g0166 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.517+3872G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651631 | ||||||
chr7:44651674
|
G | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+3915G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651674 | ||||||
chr7:44651675
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+3916C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44651675 | ||||||
chr7:44651766
|
T | TG | 150 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(147): Show | 150 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.517+4008dupG | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44651766 | |||||
chr7:44652091
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+4332G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652091 | ||||||
chr7:44652113
|
G | GT | 88 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(85): Show | 88 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.517+4366dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44652113 | |||||
chr7:44652141
|
T | C | 1 | a0001c0001t0002g0138 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.517+4382T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652141 | ||||||
chr7:44652234
|
A | G | 1 | a0001c0001t0002g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.517+4475A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652234 | ||||||
chr7:44652260
|
C | G | 1 | a0001c0001t0002g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.517+4501C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652260 | ||||||
chr7:44652269
|
C | A | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.517+4510C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652269 | ||||||
chr7:44652371
|
A | G | 1 | a0001c0017t0005g0240 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.517+4612A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652371 | ||||||
chr7:44652588
|
A | G | 52 | a0001c0001t0005g0163a0001c0002t0001g0024a0001c0002t0001g0092others(49): Show | 52 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.517+4829A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652588 | ||||||
chr7:44652615
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.517+4856C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652615 | ||||||
chr7:44652661
|
A | C | 1 | a0001c0002t0003g0008 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.517+4902A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652661 | ||||||
chr7:44652693
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0006t0001g0129 | 3 | HG02258.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.517+4934G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652693 | ||||||
chr7:44652846
|
C | G | 12 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(9): Show | 12 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.517+5087C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652846 | ||||||
chr7:44652885
|
T | C | 1 | a0001c0004t0002g0223 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.517+5126T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652885 | ||||||
chr7:44652944
|
A | G | 1 | a0001c0001t0002g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.517+5185A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44652944 | ||||||
chr7:44653094
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0006t0001g0129 | 3 | HG02258.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.517+5335T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653094 | ||||||
chr7:44653133
|
G | A | 6 | a0001c0001t0002g0271a0001c0001t0002g0272a0001c0001t0002g0288others(3): Show | 6 | HG00280.hp1 HG01109.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.517+5374G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653133 | ||||||
chr7:44653184
|
C | G | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.517+5425C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653184 | ||||||
chr7:44653253
|
C | T | 1 | a0001c0001t0006g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+5494C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653253 | ||||||
chr7:44653372
|
G | A | 1 | a0002c0003t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.517+5613G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653372 | ||||||
chr7:44653508
|
A | T | 5 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(2): Show | 5 | HG02717.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+5749A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653508 | ||||||
chr7:44653539
|
T | C | 1 | a0002c0003t0001g0090 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.517+5780T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653539 | ||||||
chr7:44653743
|
C | G | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+5984C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653743 | ||||||
chr7:44653806
|
G | A | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.517+6047G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653806 | ||||||
chr7:44653837
|
G | GT | 103 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(100): Show | 103 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.517+6087dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44653837 | |||||
chr7:44653837
|
GT | G | 8 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.517+6087delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44653837 | |||||
chr7:44653863
|
A | T | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.517+6104A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653863 | ||||||
chr7:44653889
|
C | A | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517+6130C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44653889 | ||||||
chr7:44654091
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+6332G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654091 | ||||||
chr7:44654124
|
G | C | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.517+6365G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654124 | ||||||
chr7:44654174
|
A | G | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.517+6415A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654174 | ||||||
chr7:44654181
|
C | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(8): Show | 11 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+6422C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654181 | ||||||
chr7:44654254
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+6495C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654254 | ||||||
chr7:44654298
|
G | T | 140 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(137): Show | 140 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.517+6539G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654298 | ||||||
chr7:44654359
|
T | G | 2 | a0001c0001t0002g0267a0001c0002t0001g0283 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.517+6600T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654359 | ||||||
chr7:44654384
|
C | A | 1 | a0001c0001t0002g0100 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.517+6625C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654384 | ||||||
chr7:44654400
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+6641C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654400 | ||||||
chr7:44654454
|
C | T | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.517+6695C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654454 | ||||||
chr7:44654533
|
A | G | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517+6774A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654533 | ||||||
chr7:44654536
|
T | C | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.517+6777T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654536 | ||||||
chr7:44654542
|
A | C | 1 | a0001c0001t0002g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.517+6783A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654542 | ||||||
chr7:44654857
|
C | T | 5 | a0001c0001t0002g0268a0001c0001t0002g0275a0001c0001t0002g0286others(2): Show | 5 | HG00673.hp1 HG02056.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+7098C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654857 | ||||||
chr7:44654987
|
A | C | 299 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(296): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.517+7228A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44654987 | ||||||
chr7:44655120
|
A | T | 2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+7361A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44655120 | ||||||
chr7:44655149
|
T | C | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.517+7390T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44655149 | ||||||
chr7:44655580
|
C | A | 17 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(14): Show | 17 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+7821C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44655580 | ||||||
chr7:44655589
|
C | T | 1 | a0001c0001t0002g0138 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.517+7830C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44655589 | ||||||
chr7:44655631
|
G | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(46): Show | 50 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.517+7872G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44655631 | ||||||
chr7:44655707
|
A | C | 1 | a0002c0003t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.517+7948A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44655707 | ||||||
chr7:44656050
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.517+8291C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656050 | ||||||
chr7:44656126
|
T | C | 139 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(136): Show | 139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.517+8367T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656126 | ||||||
chr7:44656177
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517+8418T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656177 | ||||||
chr7:44656244
|
G | A | 1 | a0001c0001t0015g0040 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.517+8485G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656244 | ||||||
chr7:44656464
|
C | T | 2 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.517+8705C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656464 | ||||||
chr7:44656604
|
T | C | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517+8845T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656604 | ||||||
chr7:44656882
|
G | A | 3 | a0001c0001t0002g0267a0001c0001t0002g0273a0001c0002t0001g0283 | 3 | HG00621.hp1 HG02132.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.517+9123G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656882 | ||||||
chr7:44656943
|
C | T | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.517+9184C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44656943 | ||||||
chr7:44657005
|
A | C | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+9246A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44657005 | ||||||
chr7:44657300
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-9436C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44657300 | ||||||
chr7:44657783
|
C | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-8953C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44657783 | ||||||
chr7:44657944
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.518-8792T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44657944 | ||||||
chr7:44658020
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.518-8716C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658020 | ||||||
chr7:44658042
|
A | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-8694A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658042 | ||||||
chr7:44658184
|
C | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.518-8552C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658184 | ||||||
chr7:44658203
|
A | AT | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.518-8528dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44658203 | |||||
chr7:44658452
|
C | CT | 14 | a0001c0001t0002g0057a0001c0002t0001g0031a0001c0002t0001g0032others(11): Show | 14 | HG01928.hp1 HG02451.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.518-8269dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44658452 | |||||
chr7:44658602
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-8134C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658602 | ||||||
chr7:44658649
|
C | G | 1 | a0001c0001t0007g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.518-8087C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658649 | ||||||
chr7:44658869
|
T | A | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.518-7867T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658869 | ||||||
chr7:44658945
|
C | T | 1 | a0001c0002t0001g0197 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.518-7791C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44658945 | ||||||
chr7:44659009
|
C | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-7727C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44659009 | ||||||
chr7:44659039
|
T | C | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-7697T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44659039 | ||||||
chr7:44659156
|
T | C | 1 | a0001c0001t0004g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.518-7580T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44659156 | ||||||
chr7:44659160
|
T | C | 119 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(116): Show | 119 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.518-7576T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44659160 | ||||||
chr7:44659373
|
C | A | 1 | a0001c0001t0002g0241 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.518-7363C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44659373 | ||||||
chr7:44659713
|
A | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0002c0013t0001g0073 | 3 | HG02258.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-7023A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44659713 | ||||||
chr7:44660010
|
G | A | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.518-6726G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660010 | ||||||
chr7:44660152
|
T | G | 1 | a0001c0001t0011g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.518-6584T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660152 | ||||||
chr7:44660365
|
C | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-6371C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660365 | ||||||
chr7:44660525
|
T | A | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-6211T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660525 | ||||||
chr7:44660630
|
C | G | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.518-6106C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660630 | ||||||
chr7:44660797
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.518-5939G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660797 | ||||||
chr7:44660934
|
G | A | 1 | a0001c0004t0002g0221 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.518-5802G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44660934 | ||||||
chr7:44660942
|
G | GCA | 4 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(1): Show | 4 | NA18945.hp2 NA18947.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-5781_518-5780d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44660942 | |||||
chr7:44660969
|
TGTTA | T | 115 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(112): Show | 115 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.518-5762_518-5759d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44660969 | |||||
chr7:44661279
|
A | G | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.518-5457A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661279 | ||||||
chr7:44661468
|
G | T | 1 | a0001c0001t0002g0176 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.518-5268G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661468 | ||||||
chr7:44661562
|
C | T | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518-5174C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661562 | ||||||
chr7:44661599
|
G | T | 4 | a0001c0004t0002g0002a0001c0004t0002g0223a0001c0004t0002g0227others(1): Show | 5 | HG01515.hp1 HG01517.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-5137G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661599 | ||||||
chr7:44661630
|
C | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(85): Show | 88 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.518-5106C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661630 | ||||||
chr7:44661631
|
G | A | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-5105G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661631 | ||||||
chr7:44661685
|
C | T | 1 | a0001c0002t0003g0068 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.518-5051C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661685 | ||||||
chr7:44661722
|
C | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.518-5014C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661722 | ||||||
chr7:44661768
|
ATTT | A | 8 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-4963_518-4961d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44661768 | |||||
chr7:44661806
|
G | T | 105 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(102): Show | 105 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.518-4930G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661806 | ||||||
chr7:44661878
|
C | T | 2 | a0001c0001t0002g0126a0001c0001t0002g0178 | 2 | NA18961.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.518-4858C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44661878 | ||||||
chr7:44662055
|
C | A | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518-4681C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662055 | ||||||
chr7:44662064
|
T | C | 1 | a0001c0001t0006g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.518-4672T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662064 | ||||||
chr7:44662096
|
T | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.518-4640T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662096 | ||||||
chr7:44662112
|
A | G | 1 | a0001c0002t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.518-4624A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662112 | ||||||
chr7:44662165
|
G | T | 6 | a0002c0003t0001g0089a0002c0003t0001g0111a0002c0003t0001g0112others(3): Show | 6 | HG01358.hp1 HG02738.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.518-4571G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662165 | ||||||
chr7:44662412
|
A | T | 120 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(117): Show | 120 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.518-4324A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662412 | ||||||
chr7:44662464
|
CT | C | 114 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(111): Show | 114 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.518-4256delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44662464 | |||||
chr7:44662697
|
A | G | 4 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302others(1): Show | 4 | HG02258.hp1 HG02896.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-4039A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662697 | ||||||
chr7:44662740
|
G | A | 2 | a0001c0002t0001g0225a0001c0002t0001g0230 | 2 | HG01978.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.518-3996G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662740 | ||||||
chr7:44662742
|
G | A | 4 | a0002c0003t0001g0089a0002c0003t0001g0111a0002c0003t0001g0112others(1): Show | 4 | HG01358.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-3994G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662742 | ||||||
chr7:44662758
|
A | G | 3 | a0001c0001t0005g0228a0001c0001t0005g0238a0001c0001t0005g0239 | 3 | HG02698.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.518-3978A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662758 | ||||||
chr7:44662776
|
C | G | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.518-3960C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44662776 | ||||||
chr7:44662900
|
TATC | T | 88 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(85): Show | 88 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.518-3833_518-3831d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44662900 | |||||
chr7:44663228
|
G | C | 1 | a0003c0018t0001g0151 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.518-3508G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663228 | ||||||
chr7:44663316
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.518-3420T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663316 | ||||||
chr7:44663360
|
A | C | 1 | a0001c0001t0002g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.518-3376A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663360 | ||||||
chr7:44663376
|
G | A | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-3360G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663376 | ||||||
chr7:44663398
|
C | T | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.518-3338C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663398 | ||||||
chr7:44663508
|
C | G | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.518-3228C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663508 | ||||||
chr7:44663707
|
G | A | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.518-3029G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663707 | ||||||
chr7:44663755
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.518-2981C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663755 | ||||||
chr7:44663796
|
T | C | 1 | a0001c0002t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.518-2940T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663796 | ||||||
chr7:44663831
|
T | A | 1 | a0002c0003t0001g0101 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.518-2905T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44663831 | ||||||
chr7:44664057
|
G | A | 12 | a0001c0002t0001g0222a0001c0002t0001g0225a0001c0002t0001g0226others(9): Show | 12 | HG01884.hp1 HG01978.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.518-2679G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664057 | ||||||
chr7:44664284
|
C | CTGA | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.518-2449_518-2447d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44664284 | |||||
chr7:44664313
|
A | T | 1 | a0001c0001t0002g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.518-2423A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664313 | ||||||
chr7:44664396
|
G | A | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-2340G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664396 | ||||||
chr7:44664544
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.518-2192G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664544 | ||||||
chr7:44664607
|
C | G | 1 | a0002c0003t0001g0116 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.518-2129C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664607 | ||||||
chr7:44664686
|
G | T | 116 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.518-2050G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664686 | ||||||
chr7:44664796
|
A | G | 1 | a0001c0001t0002g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.518-1940A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664796 | ||||||
chr7:44664991
|
G | A | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.518-1745G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664991 | ||||||
chr7:44664995
|
T | C | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518-1741T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44664995 | ||||||
chr7:44665002
|
A | G | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518-1734A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44665002 | ||||||
chr7:44665102
|
G | T | 1 | a0001c0001t0002g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.518-1634G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44665102 | ||||||
chr7:44665285
|
T | TA | 34 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(31): Show | 34 | HG00423.hp2 HG00621.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.518-1431dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44665285 | |||||
chr7:44665285
|
T | TAA | 83 | a0001c0001t0001g0011a0001c0001t0002g0023a0001c0001t0005g0163others(80): Show | 83 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.518-1432_518-1431d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44665285 | |||||
chr7:44665285
|
TAAAA | T | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.518-1434_518-1431d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr7 | 44665285 | |||||
chr7:44665414
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.518-1322C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44665414 | ||||||
chr7:44665694
|
A | G | 120 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(117): Show | 120 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.518-1042A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44665694 | ||||||
chr7:44665856
|
G | A | 1 | a0001c0001t0002g0144 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.518-880G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44665856 | ||||||
chr7:44665977
|
T | A | 1 | a0001c0002t0003g0263 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.518-759T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44665977 | ||||||
chr7:44666005
|
G | A | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.518-731G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666005 | ||||||
chr7:44666014
|
C | T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.518-722C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666014 | ||||||
chr7:44666085
|
T | C | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.518-651T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666085 | ||||||
chr7:44666091
|
C | T | 71 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(68): Show | 71 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.518-645C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666091 | ||||||
chr7:44666122
|
T | C | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.518-614T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666122 | ||||||
chr7:44666156
|
G | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.518-580G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666156 | ||||||
chr7:44666381
|
C | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(57): Show | 61 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.518-355C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666381 | ||||||
chr7:44666612
|
A | G | 1 | a0001c0002t0001g0130 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.518-124A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666612 | ||||||
chr7:44666637
|
C | T | 2 | a0001c0001t0002g0267a0001c0002t0001g0283 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.518-99C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666637 | ||||||
chr7:44666681
|
A | G | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518-55A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 4/22 | chr7 | 44666681 | ||||||
chr7:44666946
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.633+95A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44666946 | ||||||
chr7:44667045
|
C | T | 1 | a0001c0002t0001g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.633+194C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667045 | ||||||
chr7:44667066
|
C | G | 3 | a0001c0002t0001g0024a0001c0002t0010g0042a0001c0002t0010g0043 | 3 | HG02155.hp1 NA18953.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.633+215C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667066 | ||||||
chr7:44667120
|
T | A | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633+269T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667120 | ||||||
chr7:44667121
|
A | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.633+270A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667121 | ||||||
chr7:44667202
|
C | T | 17 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(14): Show | 17 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.633+351C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667202 | ||||||
chr7:44667332
|
A | G | 2 | a0001c0001t0005g0266a0001c0001t0005g0303 | 2 | HG01934.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.633+481A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667332 | ||||||
chr7:44667398
|
C | T | 1 | a0001c0004t0002g0247 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.633+547C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667398 | ||||||
chr7:44667582
|
A | G | 2 | a0001c0001t0002g0091a0001c0001t0002g0097 | 2 | NA19002.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.633+731A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667582 | ||||||
chr7:44667670
|
G | A | 2 | a0001c0004t0002g0227a0001c0004t0002g0237 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.633+819G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667670 | ||||||
chr7:44667738
|
A | G | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.633+887A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667738 | ||||||
chr7:44667841
|
C | G | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633+990C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667841 | ||||||
chr7:44667889
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.633+1038G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44667889 | ||||||
chr7:44668077
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.633+1226G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668077 | ||||||
chr7:44668255
|
C | T | 116 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.633+1404C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668255 | ||||||
chr7:44668308
|
G | C | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.633+1457G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668308 | ||||||
chr7:44668340
|
C | T | 17 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(14): Show | 17 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.633+1489C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668340 | ||||||
chr7:44668350
|
T | C | 16 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(13): Show | 16 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.633+1499T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668350 | ||||||
chr7:44668445
|
C | CA | 82 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.633+1603dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44668445 | |||||
chr7:44668457
|
G | A | 3 | a0001c0001t0002g0265a0001c0001t0002g0276a0001c0001t0002g0281 | 3 | HG00609.hp1 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.633+1606G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668457 | ||||||
chr7:44668540
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.633+1689G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668540 | ||||||
chr7:44668634
|
A | AG | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.633+1789dupG | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44668634 | |||||
chr7:44668722
|
T | C | 152 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.633+1871T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668722 | ||||||
chr7:44668846
|
G | T | 1 | a0001c0002t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.633+1995G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44668846 | ||||||
chr7:44669097
|
C | G | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.633+2246C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669097 | ||||||
chr7:44669139
|
C | T | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.633+2288C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669139 | ||||||
chr7:44669145
|
C | CT | 18 | a0001c0001t0002g0022a0001c0001t0002g0045a0001c0001t0002g0097others(15): Show | 18 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.633+2319dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTT | 9 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0079others(6): Show | 9 | HG00423.hp2 HG00741.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.633+2318_633+2319d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0159 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.633+2310_633+2319d others(12): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(4): Show |
27 | a0001c0002t0001g0134a0001c0002t0001g0140a0001c0002t0001g0142others(24): Show | 27 | HG01943.hp1 HG02015.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.633+2309_633+2319d others(13): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(5): Show |
34 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(31): Show | 34 | HG00597.hp2 HG00621.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.633+2308_633+2319d others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(6): Show |
7 | a0001c0002t0001g0128a0001c0002t0001g0135a0001c0002t0001g0171others(4): Show | 7 | HG00408.hp2 HG00558.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.633+2307_633+2319d others(15): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(7): Show |
2 | a0001c0002t0003g0014a0001c0005t0001g0200 | 2 | HG02055.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.633+2306_633+2319d others(16): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0001g0196a0001c0002t0001g0088a0001c0002t0001g0186others(2): Show | 5 | HG02615.hp2 HG02818.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+2305_633+2319d others(17): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(9): Show |
13 | a0001c0001t0001g0195a0001c0002t0001g0035a0001c0002t0001g0085others(10): Show | 13 | HG00408.hp1 HG00609.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.633+2304_633+2319d others(18): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(10): Show |
14 | a0001c0002t0001g0031a0001c0002t0001g0036a0001c0002t0001g0037others(11): Show | 14 | HG00280.hp2 HG00544.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.633+2303_633+2319d others(19): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(11): Show |
12 | a0001c0001t0002g0102a0001c0002t0001g0124a0001c0002t0001g0226others(9): Show | 12 | HG00733.hp2 HG01978.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.633+2302_633+2319d others(20): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(12): Show |
8 | a0001c0001t0002g0100a0001c0002t0001g0222a0001c0002t0001g0249others(5): Show | 8 | HG01358.hp1 HG01884.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+2301_633+2319d others(21): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(13): Show |
2 | a0002c0003t0001g0112a0002c0003t0001g0113 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.633+2300_633+2319d others(22): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(14): Show |
1 | a0002c0003t0001g0101 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.633+2299_633+2319d others(23): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(15): Show |
2 | a0001c0002t0001g0032a0002c0003t0001g0099 | 2 | HG03130.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.633+2298_633+2319d others(24): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.633+2297_633+2319d others(25): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(17): Show |
1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.633+2296_633+2319d others(26): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(18): Show |
1 | a0001c0002t0001g0234 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.633+2295_633+2319d others(27): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
C | CTTTTTTT others(24): Show |
1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.633+2319_633+2320i others(33): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669145
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633+2310_633+2319d others(12): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44669145 | |||||
chr7:44669176
|
A | G | 1 | a0001c0002t0003g0068 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.633+2325A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669176 | ||||||
chr7:44669363
|
G | A | 1 | a0001c0002t0001g0180 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.633+2512G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669363 | ||||||
chr7:44669377
|
C | T | 1 | a0001c0002t0003g0010 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.633+2526C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669377 | ||||||
chr7:44669631
|
C | A | 3 | a0002c0003t0001g0074a0002c0003t0001g0093a0002c0003t0001g0094 | 3 | NA18941.hp1 NA18954.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.633+2780C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669631 | ||||||
chr7:44669649
|
G | C | 1 | a0001c0001t0002g0267 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.633+2798G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669649 | ||||||
chr7:44669685
|
C | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.633+2834C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669685 | ||||||
chr7:44669773
|
T | C | 272 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(269): Show | 274 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.633+2922T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669773 | ||||||
chr7:44669822
|
A | G | 116 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(113): Show | 116 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.633+2971A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669822 | ||||||
chr7:44669855
|
T | C | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.633+3004T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669855 | ||||||
chr7:44669908
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.633+3057T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44669908 | ||||||
chr7:44670036
|
A | G | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.633+3185A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670036 | ||||||
chr7:44670122
|
C | T | 1 | a0001c0001t0007g0291 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.633+3271C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670122 | ||||||
chr7:44670270
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0006t0001g0129 | 3 | HG02258.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.633+3419G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670270 | ||||||
chr7:44670629
|
G | A | 2 | a0001c0001t0002g0272a0001c0002t0001g0194 | 2 | HG02698.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.634-3158G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670629 | ||||||
chr7:44670652
|
C | G | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.634-3135C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670652 | ||||||
chr7:44670690
|
A | G | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.634-3097A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670690 | ||||||
chr7:44670732
|
T | C | 198 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(195): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.634-3055T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670732 | ||||||
chr7:44670748
|
A | C | 4 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0016g0245others(1): Show | 4 | HG01106.hp1 HG02258.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.634-3039A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670748 | ||||||
chr7:44670748
|
A | T | 1 | a0001c0001t0002g0136 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.634-3039A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670748 | ||||||
chr7:44670787
|
A | G | 3 | a0001c0001t0002g0038a0001c0005t0001g0200a0001c0005t0001g0274 | 3 | HG02257.hp2 HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.634-3000A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670787 | ||||||
chr7:44670792
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.634-2995C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670792 | ||||||
chr7:44670874
|
G | A | 1 | a0001c0004t0002g0002 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.634-2913G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670874 | ||||||
chr7:44670889
|
T | C | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.634-2898T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670889 | ||||||
chr7:44670935
|
C | T | 14 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0226others(11): Show | 14 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.634-2852C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44670935 | ||||||
chr7:44671010
|
C | CA | 37 | a0001c0001t0002g0078a0001c0001t0002g0100a0001c0001t0002g0102others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.634-2759dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44671010 | |||||
chr7:44671010
|
CA | C | 112 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(109): Show | 112 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.634-2759delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44671010 | |||||
chr7:44671029
|
G | A | 1 | a0002c0003t0001g0118 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.634-2758G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671029 | ||||||
chr7:44671042
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.634-2745A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671042 | ||||||
chr7:44671043
|
G | A | 1 | a0001c0001t0002g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.634-2744G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671043 | ||||||
chr7:44671511
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.634-2276T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671511 | ||||||
chr7:44671559
|
C | T | 1 | a0001c0001t0002g0301 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.634-2228C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671559 | ||||||
chr7:44671767
|
C | CA | 24 | a0001c0001t0001g0083a0001c0001t0002g0047a0001c0001t0002g0115others(21): Show | 24 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.634-2000dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44671767 | |||||
chr7:44671767
|
CA | C | 26 | a0001c0001t0002g0022a0001c0001t0002g0057a0001c0001t0002g0058others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.634-2000delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44671767 | |||||
chr7:44671798
|
G | A | 1 | a0001c0002t0003g0008 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.634-1989G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671798 | ||||||
chr7:44671808
|
G | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0276a0001c0001t0002g0281 | 3 | HG00609.hp1 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.634-1979G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44671808 | ||||||
chr7:44672013
|
G | C | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634-1774G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672013 | ||||||
chr7:44672079
|
A | T | 97 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(94): Show | 97 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.634-1708A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672079 | ||||||
chr7:44672083
|
T | A | 4 | a0001c0001t0002g0038a0001c0001t0002g0265a0001c0001t0002g0276others(1): Show | 4 | HG00609.hp1 HG02615.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-1704T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672083 | ||||||
chr7:44672096
|
A | T | 3 | a0001c0001t0006g0033a0001c0004t0002g0227a0001c0004t0002g0237 | 3 | HG01515.hp1 HG01517.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.634-1691A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672096 | ||||||
chr7:44672105
|
A | C | 1 | a0001c0001t0008g0211 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.634-1682A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672105 | ||||||
chr7:44672155
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.634-1632G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672155 | ||||||
chr7:44672273
|
C | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.634-1514C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672273 | ||||||
chr7:44672544
|
C | G | 11 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(8): Show | 11 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.634-1243C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672544 | ||||||
chr7:44672571
|
G | A | 1 | a0001c0002t0001g0134 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.634-1216G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672571 | ||||||
chr7:44672588
|
C | A | 1 | a0001c0002t0001g0188 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.634-1199C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672588 | ||||||
chr7:44672637
|
G | GT | 24 | a0001c0001t0001g0196a0001c0002t0001g0127a0001c0002t0001g0130others(21): Show | 24 | HG01106.hp2 HG01261.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.634-1144dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44672637 | |||||
chr7:44672644
|
G | T | 109 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0002g0280others(106): Show | 109 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.634-1143G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672644 | ||||||
chr7:44672644
|
GT | G | 32 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(29): Show | 32 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.634-1127delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr7 | 44672644 | |||||
chr7:44672681
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0006t0001g0129 | 3 | HG02258.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.634-1106C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672681 | ||||||
chr7:44672729
|
G | A | 2 | a0001c0001t0002g0267a0001c0002t0001g0283 | 2 | HG00621.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.634-1058G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672729 | ||||||
chr7:44672824
|
G | T | 1 | a0001c0002t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.634-963G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672824 | ||||||
chr7:44672826
|
A | G | 1 | a0001c0002t0010g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.634-961A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672826 | ||||||
chr7:44672835
|
G | A | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.634-952G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672835 | ||||||
chr7:44672847
|
T | C | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.634-940T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672847 | ||||||
chr7:44672932
|
C | T | 105 | a0001c0001t0001g0011a0001c0001t0001g0195a0001c0001t0001g0196others(102): Show | 105 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.634-855C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672932 | ||||||
chr7:44672977
|
G | A | 4 | a0001c0002t0001g0124a0001c0002t0001g0231a0001c0002t0001g0232others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.634-810G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44672977 | ||||||
chr7:44673243
|
A | C | 1 | a0001c0002t0001g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.634-544A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673243 | ||||||
chr7:44673293
|
C | T | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.634-494C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673293 | ||||||
chr7:44673321
|
T | A | 2 | a0001c0001t0002g0208a0001c0009t0001g0193 | 2 | HG00140.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.634-466T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673321 | ||||||
chr7:44673462
|
A | T | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.634-325A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673462 | ||||||
chr7:44673536
|
G | A | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.634-251G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673536 | ||||||
chr7:44673547
|
G | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.634-240G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673547 | ||||||
chr7:44673605
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.634-182C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673605 | ||||||
chr7:44673654
|
C | T | 1 | a0001c0001t0002g0301 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.634-133C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673654 | ||||||
chr7:44673665
|
A | G | 141 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(138): Show | 141 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.634-122A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 5/22 | chr7 | 44673665 | ||||||
chr7:44673999
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.788+58C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44673999 | ||||||
chr7:44674092
|
G | A | 99 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(96): Show | 99 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.788+151G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44674092 | ||||||
chr7:44674201
|
C | T | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.789-210C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44674201 | ||||||
chr7:44674225
|
A | C | 1 | a0002c0003t0001g0101 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.789-186A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44674225 | ||||||
chr7:44674245
|
G | A | 141 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(138): Show | 141 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.789-166G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44674245 | ||||||
chr7:44674264
|
C | T | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.789-147C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44674264 | ||||||
chr7:44674377
|
A | G | 6 | a0001c0002t0001g0092a0001c0002t0001g0127a0001c0002t0001g0161others(3): Show | 6 | HG02015.hp1 HG02056.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.789-34A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 6/22 | chr7 | 44674377 | ||||||
chr7:44674863
|
G | C | 1 | a0001c0001t0002g0066 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.935+306G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 7/22 | chr7 | 44674863 | ||||||
chr7:44674913
|
T | C | 46 | a0001c0001t0002g0048a0001c0001t0002g0057a0001c0001t0002g0126others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.936-265T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 7/22 | chr7 | 44674913 | ||||||
chr7:44674964
|
C | A | 1 | a0001c0001t0002g0275 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.936-214C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 7/22 | chr7 | 44674964 | ||||||
chr7:44675095
|
AG | A | 125 | a0001c0001t0001g0011a0001c0001t0002g0100a0001c0001t0002g0102others(122): Show | 125 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.936-76delG | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr7 | 44675095 | |||||
chr7:44675501
|
G | C | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026+233G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 8/22 | chr7 | 44675501 | ||||||
chr7:44675734
|
G | A | 106 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0001t0009g0141others(103): Show | 106 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1027-236G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 8/22 | chr7 | 44675734 | ||||||
chr7:44675854
|
G | A | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.1027-116G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 8/22 | chr7 | 44675854 | ||||||
chr7:44675873
|
A | G | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1027-97A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 8/22 | chr7 | 44675873 | ||||||
chr7:44675877
|
C | CA | 6 | a0001c0001t0002g0115a0001c0001t0002g0126a0001c0001t0002g0282others(3): Show | 6 | HG00438.hp1 HG01261.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1027-77dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr7 | 44675877 | |||||
chr7:44675877
|
CA | C | 7 | a0001c0001t0002g0044a0001c0001t0002g0241a0001c0001t0002g0242others(4): Show | 7 | HG00558.hp1 HG01106.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027-77delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr7 | 44675877 | |||||
chr7:44676520
|
A | G | 82 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1206+371A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676520 | ||||||
chr7:44676592
|
A | G | 4 | a0001c0001t0009g0141a0001c0005t0001g0200a0001c0005t0001g0274others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+443A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676592 | ||||||
chr7:44676600
|
A | G | 1 | a0002c0003t0001g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1206+451A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676600 | ||||||
chr7:44676600
|
ATGTG | A | 6 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(3): Show | 6 | HG02717.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206+463_1206+466d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676600 | |||||
chr7:44676610
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1206+461G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676610 | ||||||
chr7:44676610
|
GTGTGTA | G | 86 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0001t0009g0003others(83): Show | 86 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.1206+463_1206+468d others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676610 | |||||
chr7:44676610
|
GTGTGTAT others(1): Show |
G | 6 | a0001c0002t0001g0225a0001c0002t0001g0234a0001c0002t0001g0235others(3): Show | 6 | HG02257.hp2 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1206+463_1206+470d others(10): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676610 | |||||
chr7:44676610
|
GTGTGTAT others(3): Show |
G | 2 | a0001c0002t0003g0007a0001c0006t0001g0120 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1206+463_1206+472d others(12): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676610 | |||||
chr7:44676612
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1206+463G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676612 | ||||||
chr7:44676612
|
G | GTA | 13 | a0001c0001t0002g0100a0002c0003t0001g0074a0002c0003t0001g0077others(10): Show | 13 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1206+464_1206+465i others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676612 | |||||
chr7:44676612
|
G | GTATA | 6 | a0001c0001t0001g0080a0002c0003t0001g0075a0002c0003t0001g0090others(3): Show | 6 | HG00609.hp2 HG01884.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.1206+464_1206+465i others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676612 | |||||
chr7:44676612
|
G | GTATATA | 5 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(2): Show | 5 | HG02486.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+464_1206+465i others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676612 | |||||
chr7:44676612
|
G | GTATATAT others(3): Show |
1 | a0002c0003t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1206+464_1206+465i others(12): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676612 | |||||
chr7:44676612
|
G | T | 2 | a0001c0001t0002g0294a0001c0001t0002g0295 | 2 | HG01109.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1206+463G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676612 | ||||||
chr7:44676612
|
GTGTATA | G | 3 | a0001c0002t0001g0088a0001c0002t0001g0135a0001c0002t0001g0169 | 3 | HG00558.hp2 HG03041.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1206+465_1206+470d others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676612 | |||||
chr7:44676614
|
G | A | 28 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.1206+465G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676614 | ||||||
chr7:44676614
|
G | GTA | 4 | a0001c0001t0002g0126a0001c0001t0002g0176a0001c0001t0002g0260others(1): Show | 4 | HG00423.hp1 HG02004.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+491_1206+492d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676614 | |||||
chr7:44676614
|
GTA | G | 119 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(116): Show | 121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1206+491_1206+492d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676614 | |||||
chr7:44676614
|
GTATA | G | 4 | a0001c0001t0002g0060a0001c0001t0002g0067a0001c0004t0002g0223others(1): Show | 4 | HG02738.hp2 HG02965.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1206+489_1206+492d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44676614 | |||||
chr7:44676616
|
A | G | 1 | a0001c0001t0002g0044 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1206+467A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676616 | ||||||
chr7:44676618
|
A | G | 18 | a0001c0001t0002g0115a0001c0001t0002g0265a0001c0001t0002g0276others(15): Show | 18 | HG00099.hp1 HG00438.hp1 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.1206+469A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676618 | ||||||
chr7:44676620
|
A | G | 3 | a0001c0004t0002g0223a0002c0003t0001g0114a0002c0003t0001g0119 | 3 | HG00733.hp2 HG02738.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1206+471A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676620 | ||||||
chr7:44676693
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1206+544G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676693 | ||||||
chr7:44676849
|
T | C | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+700T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44676849 | ||||||
chr7:44677010
|
G | A | 1 | a0001c0002t0003g0005 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1206+861G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677010 | ||||||
chr7:44677017
|
G | T | 1 | a0001c0002t0001g0037 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1206+868G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677017 | ||||||
chr7:44677224
|
C | T | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1206+1075C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677224 | ||||||
chr7:44677323
|
G | A | 2 | a0001c0002t0003g0004a0001c0002t0003g0016 | 2 | HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1206+1174G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677323 | ||||||
chr7:44677526
|
GGCCGGCC others(10): Show |
G | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1206+1381_1206+139 others(21): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44677526 | |||||
chr7:44677686
|
C | T | 99 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(96): Show | 99 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1206+1537C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677686 | ||||||
chr7:44677747
|
G | A | 2 | a0001c0002t0001g0185a0001c0002t0001g0186 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1206+1598G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677747 | ||||||
chr7:44677878
|
GA | G | 6 | a0001c0001t0002g0136a0001c0001t0002g0217a0001c0001t0006g0065others(3): Show | 6 | HG02155.hp1 HG03041.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1206+1745delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44677878 | |||||
chr7:44677924
|
C | T | 129 | a0001c0001t0001g0011a0001c0001t0002g0100a0001c0001t0002g0102others(126): Show | 129 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1206+1775C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44677924 | ||||||
chr7:44678035
|
C | T | 71 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(68): Show | 71 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1206+1886C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44678035 | ||||||
chr7:44678039
|
C | A | 1 | a0001c0002t0001g0085 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1206+1890C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44678039 | ||||||
chr7:44678231
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1206+2082C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44678231 | ||||||
chr7:44678243
|
A | G | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG00741.hp2 HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1206+2094A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44678243 | ||||||
chr7:44678688
|
C | T | 1 | a0001c0001t0002g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1206+2539C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44678688 | ||||||
chr7:44678828
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1206+2679T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44678828 | ||||||
chr7:44679020
|
A | C | 2 | a0001c0004t0002g0227a0001c0004t0002g0237 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1207-2700A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679020 | ||||||
chr7:44679121
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1207-2599G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679121 | ||||||
chr7:44679251
|
C | G | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1207-2469C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679251 | ||||||
chr7:44679383
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-2337G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679383 | ||||||
chr7:44679443
|
A | C | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-2277A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679443 | ||||||
chr7:44679501
|
C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1207-2219C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679501 | ||||||
chr7:44679574
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1207-2146G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679574 | ||||||
chr7:44679916
|
A | G | 1 | a0001c0001t0011g0131 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1207-1804A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679916 | ||||||
chr7:44679965
|
C | T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1207-1755C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679965 | ||||||
chr7:44679975
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1207-1745C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44679975 | ||||||
chr7:44680120
|
G | A | 2 | a0001c0001t0002g0280a0001c0001t0002g0297 | 2 | HG01515.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1207-1600G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680120 | ||||||
chr7:44680167
|
G | A | 1 | a0001c0001t0016g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1207-1553G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680167 | ||||||
chr7:44680435
|
T | C | 1 | a0001c0001t0004g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1207-1285T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680435 | ||||||
chr7:44680454
|
A | G | 1 | a0006c0011t0002g0277 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1207-1266A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680454 | ||||||
chr7:44680495
|
A | C | 1 | a0001c0002t0001g0168 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1207-1225A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680495 | ||||||
chr7:44680539
|
T | TAC | 18 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0002g0026others(15): Show | 18 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.1207-1147_1207-114 others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
T | TACAC | 16 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG00609.hp1 HG00741.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-1149_1207-114 others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
T | TACACAC | 22 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(19): Show | 22 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-1151_1207-114 others(10): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
T | TACACACA others(3): Show |
5 | a0001c0001t0002g0219a0002c0003t0001g0074a0002c0003t0001g0093others(2): Show | 5 | HG02965.hp1 NA18941.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-1155_1207-114 others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
T | TACACACA others(5): Show |
2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1207-1157_1207-114 others(16): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
TAC | T | 9 | a0001c0001t0001g0079a0001c0001t0006g0033a0001c0001t0009g0141others(6): Show | 9 | HG02257.hp2 HG02280.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-1147_1207-114 others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
TACAC | T | 6 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0008g0248others(3): Show | 6 | HG00099.hp2 HG01884.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-1149_1207-114 others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
TACACAC | T | 89 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(86): Show | 89 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.1207-1151_1207-114 others(10): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
TACACACA others(5): Show |
T | 4 | a0001c0001t0002g0289a0001c0002t0003g0004a0001c0002t0003g0015others(1): Show | 4 | HG01433.hp2 HG02486.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-1157_1207-114 others(16): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680539
|
TACACACA others(9): Show |
T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1207-1161_1207-114 others(20): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr7 | 44680539 | |||||
chr7:44680746
|
C | A | 3 | a0001c0001t0009g0003a0001c0009t0001g0193a0002c0013t0001g0073 | 3 | HG02258.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1207-974C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680746 | ||||||
chr7:44680764
|
A | G | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | NA18964.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1207-956A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680764 | ||||||
chr7:44680772
|
A | C | 10 | a0002c0003t0001g0075a0002c0003t0001g0077a0002c0003t0001g0090others(7): Show | 10 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-948A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680772 | ||||||
chr7:44680807
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207-913G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680807 | ||||||
chr7:44680882
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1207-838A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44680882 | ||||||
chr7:44681040
|
A | G | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-680A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681040 | ||||||
chr7:44681043
|
C | T | 3 | a0001c0001t0002g0054a0001c0001t0002g0204a0001c0001t0002g0270 | 3 | HG01934.hp2 HG02148.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1207-677C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681043 | ||||||
chr7:44681058
|
C | T | 1 | a0001c0002t0001g0179 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1207-662C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681058 | ||||||
chr7:44681073
|
C | G | 2 | a0001c0001t0002g0126a0001c0001t0002g0178 | 2 | NA18961.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1207-647C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681073 | ||||||
chr7:44681094
|
A | T | 16 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(13): Show | 16 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1207-626A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681094 | ||||||
chr7:44681217
|
T | C | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1207-503T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681217 | ||||||
chr7:44681238
|
G | C | 1 | a0002c0003t0001g0104 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1207-482G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681238 | ||||||
chr7:44681264
|
C | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.1207-456C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681264 | ||||||
chr7:44681593
|
A | G | 1 | a0001c0002t0001g0230 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1207-127A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 9/22 | chr7 | 44681593 | ||||||
chr7:44681910
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+62G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44681910 | ||||||
chr7:44682165
|
C | CA | 4 | a0001c0002t0001g0128a0001c0002t0001g0155a0001c0002t0001g0171others(1): Show | 4 | NA18989.hp1 NA18999.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1335+318dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44682165 | |||||
chr7:44682205
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1335+357T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682205 | ||||||
chr7:44682262
|
G | A | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1335+414G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682262 | ||||||
chr7:44682362
|
A | G | 3 | a0001c0001t0009g0003a0001c0009t0001g0193a0002c0013t0001g0073 | 3 | HG02258.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1335+514A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682362 | ||||||
chr7:44682385
|
C | CA | 7 | a0001c0002t0001g0222a0001c0002t0001g0226a0001c0002t0001g0249others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1335+549dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44682385 | |||||
chr7:44682496
|
G | A | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1335+648G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682496 | ||||||
chr7:44682515
|
T | C | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1335+667T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682515 | ||||||
chr7:44682563
|
C | T | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1335+715C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682563 | ||||||
chr7:44682564
|
G | A | 1 | a0001c0004t0002g0002 | 2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1335+716G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682564 | ||||||
chr7:44682701
|
A | T | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1335+853A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682701 | ||||||
chr7:44682751
|
T | G | 4 | a0001c0001t0002g0022a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 4 | NA18942.hp2 NA18947.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+903T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682751 | ||||||
chr7:44682874
|
C | T | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1335+1026C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682874 | ||||||
chr7:44682920
|
A | G | 298 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(295): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1335+1072A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44682920 | ||||||
chr7:44683267
|
T | C | 2 | a0001c0001t0002g0039a0001c0001t0002g0304 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1335+1419T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44683267 | ||||||
chr7:44683333
|
A | T | 82 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1335+1485A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44683333 | ||||||
chr7:44683421
|
G | A | 1 | a0001c0008t0002g0049 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1335+1573G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44683421 | ||||||
chr7:44683932
|
G | A | 1 | a0001c0001t0002g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1335+2084G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44683932 | ||||||
chr7:44683971
|
G | C | 1 | a0001c0001t0002g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1335+2123G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44683971 | ||||||
chr7:44684134
|
G | A | 1 | a0002c0003t0001g0108 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1335+2286G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684134 | ||||||
chr7:44684158
|
A | G | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1335+2310A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684158 | ||||||
chr7:44684209
|
G | A | 6 | a0002c0003t0001g0089a0002c0003t0001g0111a0002c0003t0001g0112others(3): Show | 6 | HG01358.hp1 HG02738.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335+2361G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684209 | ||||||
chr7:44684227
|
A | G | 30 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(27): Show | 30 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1335+2379A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684227 | ||||||
chr7:44684257
|
C | T | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1335+2409C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684257 | ||||||
chr7:44684306
|
G | C | 1 | a0002c0003t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1335+2458G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684306 | ||||||
chr7:44684437
|
T | C | 1 | a0001c0002t0003g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1335+2589T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684437 | ||||||
chr7:44684520
|
C | A | 1 | a0001c0004t0002g0223 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1335+2672C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684520 | ||||||
chr7:44684584
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1335+2736A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684584 | ||||||
chr7:44684586
|
C | G | 3 | a0001c0001t0002g0053a0001c0007t0002g0029a0001c0007t0002g0052 | 3 | NA18950.hp2 NA18951.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1335+2738C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684586 | ||||||
chr7:44684756
|
T | TA | 8 | a0001c0002t0001g0085a0001c0002t0001g0086a0001c0002t0001g0088others(5): Show | 8 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1335+2916dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44684756 | |||||
chr7:44684796
|
A | AT | 9 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(6): Show | 9 | HG02258.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+2959dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44684796 | |||||
chr7:44684899
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1335+3051C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684899 | ||||||
chr7:44684942
|
C | T | 1 | a0001c0001t0016g0245 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1335+3094C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44684942 | ||||||
chr7:44685035
|
T | C | 152 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.1335+3187T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685035 | ||||||
chr7:44685091
|
T | G | 1 | a0001c0010t0001g0302 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1335+3243T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685091 | ||||||
chr7:44685284
|
C | G | 16 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(13): Show | 16 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1335+3436C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685284 | ||||||
chr7:44685323
|
A | G | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1335+3475A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685323 | ||||||
chr7:44685404
|
G | T | 1 | a0001c0001t0002g0282 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1335+3556G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685404 | ||||||
chr7:44685641
|
C | T | 3 | a0001c0001t0009g0141a0001c0005t0001g0200a0001c0005t0001g0274 | 3 | HG02257.hp2 HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1335+3793C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685641 | ||||||
chr7:44685784
|
A | AT | 6 | a0001c0001t0002g0268a0001c0001t0002g0275a0001c0001t0002g0279others(3): Show | 6 | HG00408.hp2 HG01175.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.1335+3946dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44685784 | |||||
chr7:44685795
|
C | T | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1335+3947C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685795 | ||||||
chr7:44685814
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1335+3966G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685814 | ||||||
chr7:44685939
|
G | A | 20 | a0001c0001t0002g0100a0001c0001t0002g0102a0002c0003t0001g0021others(17): Show | 20 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.1335+4091G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685939 | ||||||
chr7:44685968
|
G | A | 99 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(96): Show | 99 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1335+4120G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44685968 | ||||||
chr7:44686046
|
C | CTTTTTTT others(3): Show |
5 | a0001c0001t0002g0102a0002c0003t0001g0108a0002c0003t0001g0113others(2): Show | 5 | HG02135.hp1 HG02300.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335+4200_1335+420 others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44686046 | |||||
chr7:44686046
|
C | CTTTTTTT others(4): Show |
26 | a0001c0001t0002g0100a0001c0001t0002g0115a0002c0003t0001g0021others(23): Show | 26 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.1335+4199_1335+420 others(15): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44686046 | |||||
chr7:44686046
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1335+4209_1335+421 others(17): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44686046 | |||||
chr7:44686063
|
T | C | 1 | a0001c0001t0002g0072 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1335+4215T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686063 | ||||||
chr7:44686130
|
A | G | 11 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(8): Show | 11 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1335+4282A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686130 | ||||||
chr7:44686163
|
T | C | 1 | a0001c0002t0003g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1335+4315T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686163 | ||||||
chr7:44686179
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1335+4331C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686179 | ||||||
chr7:44686323
|
C | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0071 | 2 | HG00597.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1335+4475C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686323 | ||||||
chr7:44686436
|
A | C | 82 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1335+4588A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686436 | ||||||
chr7:44686470
|
T | C | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1335+4622T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686470 | ||||||
chr7:44686521
|
G | A | 1 | a0002c0003t0001g0089 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1335+4673G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686521 | ||||||
chr7:44686536
|
G | C | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1335+4688G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686536 | ||||||
chr7:44686636
|
A | AGACT | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1335+4789_1335+479 others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44686636 | |||||
chr7:44686689
|
C | CT | 85 | a0001c0001t0001g0011a0001c0001t0002g0023a0001c0001t0002g0039others(82): Show | 85 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.1335+4858dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44686689 | |||||
chr7:44686696
|
T | G | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1335+4848T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686696 | ||||||
chr7:44686736
|
C | A | 2 | a0001c0001t0012g0122a0001c0002t0003g0263 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1335+4888C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686736 | ||||||
chr7:44686737
|
G | A | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1335+4889G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686737 | ||||||
chr7:44686833
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1335+4985G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44686833 | ||||||
chr7:44687082
|
T | A | 33 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(30): Show | 33 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1335+5234T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687082 | ||||||
chr7:44687089
|
T | A | 1 | a0002c0003t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1335+5241T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687089 | ||||||
chr7:44687091
|
A | AT | 135 | a0001c0001t0001g0011a0001c0001t0001g0081a0001c0001t0002g0023others(132): Show | 135 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1335+5265dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44687091 | |||||
chr7:44687091
|
A | ATT | 18 | a0001c0002t0001g0024a0001c0002t0001g0128a0001c0002t0001g0130others(15): Show | 18 | HG00544.hp1 HG01358.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1335+5264_1335+526 others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44687091 | |||||
chr7:44687091
|
A | T | 1 | a0002c0003t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1335+5243A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687091 | ||||||
chr7:44687221
|
C | T | 99 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(96): Show | 99 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1335+5373C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687221 | ||||||
chr7:44687378
|
A | G | 1 | a0001c0001t0002g0137 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1335+5530A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687378 | ||||||
chr7:44687693
|
G | C | 1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1335+5845G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687693 | ||||||
chr7:44687702
|
G | C | 1 | a0001c0001t0002g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1335+5854G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687702 | ||||||
chr7:44687704
|
G | A | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1335+5856G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687704 | ||||||
chr7:44687982
|
A | G | 1 | a0001c0001t0006g0069 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1336-5843A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44687982 | ||||||
chr7:44688277
|
A | G | 5 | a0001c0001t0002g0268a0001c0001t0002g0275a0001c0001t0002g0286others(2): Show | 5 | HG00673.hp1 HG02056.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-5548A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44688277 | ||||||
chr7:44688328
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1336-5497G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44688328 | ||||||
chr7:44688431
|
C | CT | 256 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1336-5377dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44688431 | |||||
chr7:44688431
|
C | CTT | 38 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(35): Show | 38 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1336-5378_1336-537 others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44688431 | |||||
chr7:44688469
|
C | T | 2 | a0001c0001t0009g0003a0002c0013t0001g0073 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1336-5356C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44688469 | ||||||
chr7:44688619
|
A | T | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-5206A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44688619 | ||||||
chr7:44688721
|
C | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336-5104C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44688721 | ||||||
chr7:44688722
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1336-5103G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44688722 | ||||||
chr7:44689013
|
G | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1336-4812G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689013 | ||||||
chr7:44689089
|
G | C | 34 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(31): Show | 34 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.1336-4736G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689089 | ||||||
chr7:44689138
|
G | C | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1336-4687G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689138 | ||||||
chr7:44689180
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(3): Show | 6 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336-4645C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689180 | ||||||
chr7:44689205
|
T | A | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-4620T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689205 | ||||||
chr7:44689208
|
C | CT | 25 | a0001c0001t0001g0080a0001c0001t0002g0023a0001c0001t0002g0027others(22): Show | 25 | HG00597.hp1 HG01175.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.1336-4592dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44689208 | |||||
chr7:44689208
|
CT | C | 21 | a0001c0001t0002g0022a0001c0001t0002g0060a0001c0001t0002g0273others(18): Show | 21 | HG01261.hp2 HG02040.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1336-4592delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44689208 | |||||
chr7:44689208
|
CTTTTTTT others(7): Show |
C | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-4605_1336-459 others(18): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44689208 | |||||
chr7:44689242
|
G | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0276a0001c0001t0002g0281 | 3 | HG00609.hp1 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1336-4583G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689242 | ||||||
chr7:44689250
|
C | T | 1 | a0001c0001t0015g0040 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1336-4575C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689250 | ||||||
chr7:44689352
|
A | G | 5 | a0002c0003t0001g0074a0002c0003t0001g0093a0002c0003t0001g0094others(2): Show | 5 | HG02132.hp2 NA18941.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-4473A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689352 | ||||||
chr7:44689392
|
C | CT | 35 | a0001c0001t0001g0018a0001c0001t0002g0022a0001c0001t0002g0034others(32): Show | 35 | HG00558.hp1 HG00741.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1336-4407dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44689392 | |||||
chr7:44689392
|
CT | C | 65 | a0001c0001t0001g0011a0001c0001t0002g0048a0001c0001t0002g0058others(62): Show | 65 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.1336-4407delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44689392 | |||||
chr7:44689392
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0009g0003 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1336-4418_1336-440 others(16): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44689392 | |||||
chr7:44689393
|
T | C | 1 | a0001c0001t0004g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1336-4432T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689393 | ||||||
chr7:44689394
|
T | C | 1 | a0001c0002t0003g0068 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1336-4431T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689394 | ||||||
chr7:44689404
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1336-4421T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689404 | ||||||
chr7:44689517
|
A | G | 136 | a0001c0001t0001g0011a0001c0001t0002g0100a0001c0001t0002g0102others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1336-4308A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689517 | ||||||
chr7:44689542
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1336-4283G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689542 | ||||||
chr7:44689600
|
A | G | 1 | a0001c0001t0004g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1336-4225A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44689600 | ||||||
chr7:44690015
|
A | G | 1 | a0001c0001t0004g0215 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1336-3810A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44690015 | ||||||
chr7:44690536
|
G | A | 99 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(96): Show | 99 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1336-3289G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44690536 | ||||||
chr7:44690624
|
G | A | 1 | a0001c0001t0002g0115 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1336-3201G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44690624 | ||||||
chr7:44690685
|
C | T | 106 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0001t0009g0141others(103): Show | 106 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1336-3140C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44690685 | ||||||
chr7:44690895
|
G | A | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1336-2930G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44690895 | ||||||
chr7:44690942
|
T | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336-2883T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44690942 | ||||||
chr7:44691020
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1336-2805C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691020 | ||||||
chr7:44691045
|
A | G | 1 | a0001c0001t0002g0273 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1336-2780A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691045 | ||||||
chr7:44691531
|
C | CA | 13 | a0001c0001t0002g0054a0001c0001t0002g0057a0001c0001t0002g0078others(10): Show | 13 | HG00544.hp2 HG01175.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1336-2276dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691531 | |||||
chr7:44691531
|
CA | C | 71 | a0001c0001t0001g0011a0001c0001t0002g0023a0001c0001t0002g0264others(68): Show | 71 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.1336-2276delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691531 | |||||
chr7:44691684
|
A | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(7): Show | 10 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1336-2141A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691684 | ||||||
chr7:44691700
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1336-2125G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691700 | ||||||
chr7:44691715
|
C | T | 3 | a0001c0001t0012g0122a0001c0002t0003g0263a0001c0010t0001g0302 | 3 | HG02896.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1336-2110C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691715 | ||||||
chr7:44691908
|
G | A | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-1917G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691908 | ||||||
chr7:44691915
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1336-1910G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691915 | ||||||
chr7:44691981
|
T | TAAA | 13 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1336-1822_1336-182 others(7): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691981
|
T | TAAAAAAA | 55 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(52): Show | 55 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1336-1826_1336-182 others(11): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691981
|
T | TAAAAAAA others(1): Show |
24 | a0001c0002t0001g0037a0001c0002t0001g0086a0001c0002t0001g0092others(21): Show | 24 | HG00597.hp2 HG01106.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1336-1827_1336-182 others(12): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691981
|
T | TAAAAAAA others(3): Show |
1 | a0001c0009t0001g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1336-1829_1336-182 others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691981
|
T | TTAAAAAA others(5): Show |
1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1336-1844_1336-184 others(16): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691981 | ||||||
chr7:44691981
|
TA | T | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0081others(22): Show | 25 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.1336-1820delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691981
|
TAA | T | 123 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(120): Show | 125 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1336-1821_1336-182 others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691981
|
TAAAAAAA others(3): Show |
T | 30 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(27): Show | 30 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.1336-1829_1336-182 others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44691981 | |||||
chr7:44691989
|
A | T | 1 | a0001c0005t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1336-1836A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44691989 | ||||||
chr7:44692130
|
C | T | 1 | a0001c0001t0002g0286 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1336-1695C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44692130 | ||||||
chr7:44692143
|
C | T | 1 | a0001c0001t0002g0057 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1336-1682C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44692143 | ||||||
chr7:44692547
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1336-1278A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44692547 | ||||||
chr7:44692558
|
T | C | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1336-1267T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44692558 | ||||||
chr7:44692948
|
G | A | 1 | a0001c0002t0003g0012 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1336-877G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44692948 | ||||||
chr7:44693006
|
T | TA | 8 | a0001c0001t0002g0198a0001c0001t0002g0201a0001c0001t0002g0202others(5): Show | 8 | HG02280.hp2 HG02559.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336-803dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44693006 | |||||
chr7:44693006
|
TA | T | 141 | a0001c0001t0001g0011a0001c0001t0002g0100a0001c0001t0002g0102others(138): Show | 141 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1336-803delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44693006 | |||||
chr7:44693059
|
A | C | 1 | a0001c0002t0001g0173 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1336-766A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44693059 | ||||||
chr7:44693135
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1336-690C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44693135 | ||||||
chr7:44693165
|
A | G | 4 | a0002c0003t0001g0074a0002c0003t0001g0093a0002c0003t0001g0094others(1): Show | 4 | NA18941.hp1 NA18954.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-660A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44693165 | ||||||
chr7:44693223
|
G | A | 82 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0002t0001g0024others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1336-602G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44693223 | ||||||
chr7:44693306
|
C | CA | 11 | a0001c0001t0001g0254a0001c0001t0002g0279a0001c0001t0008g0210others(8): Show | 11 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1336-504dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr7 | 44693306 | |||||
chr7:44693364
|
C | T | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1336-461C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44693364 | ||||||
chr7:44693371
|
C | G | 1 | a0001c0001t0002g0137 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1336-454C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 10/22 | chr7 | 44693371 | ||||||
chr7:44694028
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1515+24G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 11/22 | chr7 | 44694028 | ||||||
chr7:44694244
|
G | T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1516-180G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 11/22 | chr7 | 44694244 | ||||||
chr7:44694326
|
G | A | 1 | a0001c0001t0002g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1516-98G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 11/22 | chr7 | 44694326 | ||||||
chr7:44694365
|
A | G | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1516-59A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 11/22 | chr7 | 44694365 | ||||||
chr7:44694664
|
G | C | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1668+88G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44694664 | ||||||
chr7:44694666
|
C | A | 1 | a0001c0001t0009g0141 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1668+90C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44694666 | ||||||
chr7:44694724
|
C | G | 106 | a0001c0001t0001g0011a0001c0001t0005g0163a0001c0001t0009g0141others(103): Show | 106 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1668+148C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44694724 | ||||||
chr7:44695072
|
A | C | 4 | a0001c0002t0001g0092a0001c0002t0001g0127a0001c0002t0001g0179others(1): Show | 4 | HG02015.hp1 HG02056.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1668+496A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695072 | ||||||
chr7:44695119
|
G | A | 5 | a0001c0001t0002g0201a0001c0001t0002g0216a0001c0001t0002g0217others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1668+543G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695119 | ||||||
chr7:44695137
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1668+561C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695137 | ||||||
chr7:44695178
|
C | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(45): Show | 49 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1668+602C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695178 | ||||||
chr7:44695295
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1668+719C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695295 | ||||||
chr7:44695307
|
G | A | 1 | a0001c0001t0005g0163 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1669-718G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695307 | ||||||
chr7:44695339
|
G | T | 1 | a0001c0006t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1669-686G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695339 | ||||||
chr7:44695574
|
G | A | 31 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0002g0115others(28): Show | 31 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.1669-451G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695574 | ||||||
chr7:44695584
|
T | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1669-441T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695584 | ||||||
chr7:44695657
|
C | G | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1669-368C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695657 | ||||||
chr7:44695659
|
C | T | 2 | a0002c0003t0001g0105a0002c0003t0001g0108 | 2 | HG00408.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1669-366C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | chr7 | 44695659 | ||||||
chr7:44695701
|
CA | C | 35 | a0001c0001t0002g0056a0001c0001t0002g0100a0001c0001t0002g0102others(32): Show | 35 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1669-307delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr7 | 44695701 | |||||
chr7:44696241
|
T | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0196 | 2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1771+114T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 13/22 | chr7 | 44696241 | ||||||
chr7:44696307
|
G | A | 1 | a0001c0001t0002g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1772-122G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 13/22 | chr7 | 44696307 | ||||||
chr7:44696637
|
CCCCA | C | 37 | a0001c0001t0002g0100a0001c0001t0002g0102a0001c0001t0009g0003others(34): Show | 37 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.1900+85_1900+88del others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr7 | 44696637 | |||||
chr7:44696642
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1900+85C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 14/22 | chr7 | 44696642 | ||||||
chr7:44696717
|
C | T | 1 | a0001c0002t0001g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1900+160C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 14/22 | chr7 | 44696717 | ||||||
chr7:44696833
|
C | T | 1 | a0001c0002t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1901-81C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 14/22 | chr7 | 44696833 | ||||||
chr7:44697147
|
C | T | 3 | a0001c0001t0002g0265a0001c0001t0002g0276a0001c0001t0002g0281 | 3 | HG00609.hp1 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2051+83C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 15/22 | chr7 | 44697147 | ||||||
chr7:44697543
|
C | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0071 | 2 | HG00597.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2179+46C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 16/22 | chr7 | 44697543 | ||||||
chr7:44697574
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2180-30A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 16/22 | chr7 | 44697574 | ||||||
chr7:44697972
|
A | C | 15 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2358+190A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 17/22 | chr7 | 44697972 | ||||||
chr7:44698079
|
C | T | 2 | a0001c0002t0001g0166a0001c0002t0001g0167 | 2 | HG02080.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2359-113C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 17/22 | chr7 | 44698079 | ||||||
chr7:44698080
|
A | G | 136 | a0001c0001t0001g0254a0001c0001t0009g0141a0001c0001t0012g0122others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2359-112A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 17/22 | chr7 | 44698080 | ||||||
chr7:44698117
|
T | TAAG | 152 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2359-75_2359-74ins others(3): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 17/22 | chr7 | 44698117 | ||||||
chr7:44698323
|
G | A | 151 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(148): Show | 151 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.2430+60G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44698323 | ||||||
chr7:44698521
|
G | A | 1 | a0001c0004t0002g0247 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2430+258G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44698521 | ||||||
chr7:44698577
|
G | T | 1 | a0001c0001t0002g0280 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2430+314G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44698577 | ||||||
chr7:44698840
|
T | TA | 15 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2430+594dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 44698840 | |||||
chr7:44699017
|
A | C | 1 | a0001c0002t0003g0068 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2430+754A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699017 | ||||||
chr7:44699020
|
T | C | 2 | a0001c0001t0007g0298a0001c0001t0007g0299 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2430+757T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699020 | ||||||
chr7:44699097
|
T | C | 1 | a0001c0001t0002g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2430+834T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699097 | ||||||
chr7:44699287
|
G | A | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2431-854G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699287 | ||||||
chr7:44699319
|
A | C | 1 | a0001c0001t0002g0268 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2431-822A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699319 | ||||||
chr7:44699381
|
C | T | 84 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0032others(81): Show | 84 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.2431-760C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699381 | ||||||
chr7:44699425
|
C | CA | 19 | a0001c0001t0002g0026a0001c0001t0002g0044a0001c0001t0002g0045others(16): Show | 19 | HG01175.hp2 HG01358.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2431-692dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 44699425 | |||||
chr7:44699425
|
CA | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(14): Show | 17 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2431-692delA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 44699425 | |||||
chr7:44699425
|
CAA | C | 9 | a0001c0001t0001g0254a0001c0001t0012g0122a0001c0002t0001g0085others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.2431-693_2431-692d others(4): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 44699425 | |||||
chr7:44699425
|
CAAA | C | 114 | a0001c0001t0009g0003a0001c0001t0009g0141a0001c0002t0001g0024others(111): Show | 114 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2431-694_2431-692d others(5): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 44699425 | |||||
chr7:44699425
|
CAAAA | C | 15 | a0001c0002t0001g0160a0001c0002t0001g0161a0001c0002t0001g0222others(12): Show | 15 | HG01884.hp1 HG01978.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2431-695_2431-692d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr7 | 44699425 | |||||
chr7:44699595
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | HG01358.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2431-546G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699595 | ||||||
chr7:44699623
|
G | A | 11 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(8): Show | 11 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2431-518G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699623 | ||||||
chr7:44699656
|
G | T | 10 | a0002c0003t0001g0075a0002c0003t0001g0077a0002c0003t0001g0090others(7): Show | 10 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.2431-485G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699656 | ||||||
chr7:44699787
|
C | T | 2 | a0001c0001t0008g0210a0001c0001t0008g0211 | 2 | HG01081.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2431-354C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699787 | ||||||
chr7:44699795
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0078 | 2 | NA18981.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2431-346G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699795 | ||||||
chr7:44699856
|
C | T | 1 | a0001c0001t0008g0248 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2431-285C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699856 | ||||||
chr7:44699922
|
G | A | 2 | a0001c0006t0001g0120a0001c0006t0001g0129 | 2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2431-219G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 18/22 | chr7 | 44699922 | ||||||
chr7:44700543
|
G | A | 3 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG00741.hp2 HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2559+274G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700543 | ||||||
chr7:44700701
|
G | A | 1 | a0001c0001t0004g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2559+432G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700701 | ||||||
chr7:44700722
|
A | G | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2559+453A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700722 | ||||||
chr7:44700735
|
G | A | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2559+466G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700735 | ||||||
chr7:44700751
|
G | A | 3 | a0001c0002t0001g0172a0001c0002t0001g0184a0001c0002t0001g0187 | 3 | HG03490.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2559+482G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700751 | ||||||
chr7:44700853
|
A | C | 2 | a0001c0001t0009g0003a0001c0001t0009g0141 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2559+584A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700853 | ||||||
chr7:44700873
|
G | A | 2 | a0001c0001t0002g0241a0001c0001t0002g0288 | 2 | HG00280.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2559+604G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700873 | ||||||
chr7:44700905
|
A | G | 1 | a0001c0001t0002g0224 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2559+636A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700905 | ||||||
chr7:44700926
|
G | A | 1 | a0001c0001t0002g0198 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2560-617G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700926 | ||||||
chr7:44700949
|
G | A | 16 | a0001c0002t0001g0124a0001c0002t0001g0222a0001c0002t0001g0225others(13): Show | 16 | HG01884.hp1 HG01978.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2560-594G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44700949 | ||||||
chr7:44701011
|
G | A | 9 | a0001c0002t0001g0222a0001c0002t0001g0225a0001c0002t0001g0226others(6): Show | 9 | HG01884.hp1 HG01978.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2560-532G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44701011 | ||||||
chr7:44701130
|
G | A | 1 | a0002c0003t0001g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2560-413G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44701130 | ||||||
chr7:44701273
|
G | C | 2 | a0001c0007t0002g0029a0001c0007t0002g0052 | 2 | NA18950.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2560-270G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44701273 | ||||||
chr7:44701311
|
G | T | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2560-232G>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44701311 | ||||||
chr7:44701432
|
G | A | 1 | a0001c0002t0001g0128 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2560-111G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 19/22 | chr7 | 44701432 | ||||||
chr7:44701657
|
G | A | 1 | a0005c0012t0001g0149 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2632+42G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44701657 | ||||||
chr7:44701752
|
G | A | 2 | a0001c0001t0009g0003a0001c0001t0009g0141 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2632+137G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44701752 | ||||||
chr7:44701851
|
C | G | 28 | a0002c0003t0001g0021a0002c0003t0001g0074a0002c0003t0001g0075others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.2632+236C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44701851 | ||||||
chr7:44702041
|
A | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2632+426A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702041 | ||||||
chr7:44702066
|
C | T | 4 | a0001c0001t0012g0122a0001c0005t0001g0200a0001c0005t0001g0274others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2632+451C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702066 | ||||||
chr7:44702071
|
C | CA | 17 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0019others(14): Show | 17 | HG00741.hp1 HG01884.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.2632+472dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44702071 | |||||
chr7:44702073
|
A | C | 1 | a0001c0002t0003g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2632+458A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702073 | ||||||
chr7:44702220
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2632+605G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702220 | ||||||
chr7:44702464
|
AG | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2632+853delG | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44702464 | |||||
chr7:44702547
|
T | G | 11 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0035others(8): Show | 11 | HG02451.hp2 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2632+932T>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702547 | ||||||
chr7:44702581
|
T | TTTTA | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2632+990_2632+993d others(6): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44702581 | |||||
chr7:44702623
|
C | T | 2 | a0002c0003t0001g0116a0002c0003t0001g0118 | 2 | NA18979.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2632+1008C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702623 | ||||||
chr7:44702632
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2632+1017G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702632 | ||||||
chr7:44702686
|
G | A | 1 | a0001c0002t0001g0182 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2632+1071G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702686 | ||||||
chr7:44702738
|
G | A | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2632+1123G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702738 | ||||||
chr7:44702740
|
C | T | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2632+1125C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702740 | ||||||
chr7:44702821
|
C | A | 29 | a0002c0003t0001g0021a0002c0003t0001g0074a0002c0003t0001g0075others(26): Show | 29 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.2632+1206C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44702821 | ||||||
chr7:44703059
|
A | G | 14 | a0001c0002t0003g0004a0001c0002t0003g0005a0001c0002t0003g0007others(11): Show | 14 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2632+1444A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703059 | ||||||
chr7:44703232
|
A | C | 1 | a0001c0002t0001g0192 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2632+1617A>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703232 | ||||||
chr7:44703271
|
C | T | 1 | a0001c0002t0003g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2632+1656C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703271 | ||||||
chr7:44703422
|
C | A | 107 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(104): Show | 107 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.2632+1807C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703422 | ||||||
chr7:44703589
|
G | A | 2 | a0002c0003t0001g0112a0002c0003t0001g0113 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2632+1974G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703589 | ||||||
chr7:44703597
|
G | A | 3 | a0001c0001t0006g0065a0001c0001t0006g0069a0001c0001t0006g0125 | 3 | NA18945.hp1 NA18947.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2632+1982G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703597 | ||||||
chr7:44703732
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2632+2117T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703732 | ||||||
chr7:44703745
|
G | A | 152 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2632+2130G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703745 | ||||||
chr7:44703755
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2632+2140C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44703755 | ||||||
chr7:44703885
|
C | CA | 6 | a0001c0001t0002g0270a0001c0002t0001g0124a0001c0002t0001g0231others(3): Show | 6 | HG01934.hp2 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2632+2283dupA | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44703885 | |||||
chr7:44704071
|
C | A | 5 | a0001c0001t0002g0268a0001c0001t0002g0275a0001c0001t0002g0286others(2): Show | 5 | HG00673.hp1 HG02056.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.2632+2456C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704071 | ||||||
chr7:44704075
|
G | C | 83 | a0001c0002t0001g0024a0001c0002t0001g0031a0001c0002t0001g0032others(80): Show | 83 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.2632+2460G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704075 | ||||||
chr7:44704387
|
T | A | 14 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2632+2772T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704387 | ||||||
chr7:44704507
|
C | T | 105 | a0001c0001t0012g0122a0001c0002t0001g0024a0001c0002t0001g0031others(102): Show | 105 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.2633-2718C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704507 | ||||||
chr7:44704566
|
T | A | 1 | a0001c0001t0012g0122 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2633-2659T>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704566 | ||||||
chr7:44704637
|
G | A | 5 | a0001c0001t0005g0228a0001c0001t0005g0238a0001c0001t0005g0239others(2): Show | 5 | HG00099.hp1 HG02698.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2633-2588G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704637 | ||||||
chr7:44704695
|
G | C | 28 | a0002c0003t0001g0021a0002c0003t0001g0074a0002c0003t0001g0075others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.2633-2530G>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704695 | ||||||
chr7:44704703
|
T | C | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG00140.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2633-2522T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704703 | ||||||
chr7:44704791
|
A | G | 28 | a0002c0003t0001g0021a0002c0003t0001g0074a0002c0003t0001g0075others(25): Show | 28 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.2633-2434A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704791 | ||||||
chr7:44704838
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2633-2387G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704838 | ||||||
chr7:44704859
|
C | T | 2 | a0001c0007t0002g0029a0001c0007t0002g0052 | 2 | NA18950.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2633-2366C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704859 | ||||||
chr7:44704901
|
G | A | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2633-2324G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44704901 | ||||||
chr7:44705000
|
T | C | 152 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2633-2225T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705000 | ||||||
chr7:44705051
|
C | CT | 9 | a0001c0001t0002g0054a0001c0001t0002g0064a0001c0001t0002g0203others(6): Show | 9 | HG00099.hp1 HG01928.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.2633-2155dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(3): Show |
3 | a0002c0003t0001g0113a0002c0003t0001g0114a0002c0003t0001g0119 | 3 | HG00733.hp2 HG02738.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.2633-2164_2633-215 others(14): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(4): Show |
27 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0020others(24): Show | 27 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2633-2165_2633-215 others(15): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(5): Show |
16 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0079others(13): Show | 16 | HG00544.hp1 HG00741.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.2633-2166_2633-215 others(16): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0081 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2633-2167_2633-215 others(17): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(7): Show |
7 | a0001c0002t0001g0226a0001c0002t0001g0235a0001c0002t0001g0236others(4): Show | 7 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2633-2168_2633-215 others(18): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(8): Show |
5 | a0001c0001t0009g0141a0001c0002t0001g0222a0001c0002t0001g0225others(2): Show | 5 | HG02895.hp2 HG03209.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2633-2169_2633-215 others(19): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(9): Show |
2 | a0001c0002t0001g0230a0001c0002t0001g0231 | 2 | HG01978.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.2633-2170_2633-215 others(20): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(10): Show |
2 | a0001c0002t0001g0085a0001c0016t0001g0246 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2633-2171_2633-215 others(21): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(11): Show |
6 | a0001c0002t0001g0032a0001c0002t0001g0124a0001c0002t0003g0005others(3): Show | 6 | HG01891.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2633-2172_2633-215 others(22): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(12): Show |
29 | a0001c0002t0001g0031a0001c0002t0001g0035a0001c0002t0001g0036others(26): Show | 29 | HG00558.hp2 HG02040.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.2633-2173_2633-215 others(23): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(13): Show |
29 | a0001c0002t0001g0024a0001c0002t0001g0063a0001c0002t0001g0086others(26): Show | 29 | HG00597.hp2 HG01943.hp1 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.2633-2155_2633-215 others(24): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(14): Show |
13 | a0001c0002t0001g0092a0001c0002t0001g0127a0001c0002t0001g0142others(10): Show | 13 | HG00408.hp2 HG01106.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.2633-2155_2633-215 others(25): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(15): Show |
4 | a0001c0002t0001g0133a0001c0002t0001g0143a0001c0002t0001g0150others(1): Show | 4 | HG01261.hp2 HG02004.hp2 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.2633-2155_2633-215 others(26): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(16): Show |
2 | a0001c0002t0001g0186a0001c0002t0010g0042 | 2 | HG02615.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2633-2155_2633-215 others(27): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(17): Show |
1 | a0001c0002t0001g0156 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2633-2155_2633-215 others(28): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705051
|
C | CTTTTTTT others(18): Show |
1 | a0001c0002t0001g0157 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2633-2155_2633-215 others(29): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44705051 | |||||
chr7:44705121
|
C | T | 4 | a0001c0001t0002g0115a0001c0001t0002g0260a0001c0001t0002g0261others(1): Show | 4 | HG00438.hp1 HG00741.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2633-2104C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705121 | ||||||
chr7:44705122
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2633-2103G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705122 | ||||||
chr7:44705138
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2633-2087C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705138 | ||||||
chr7:44705139
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2633-2086A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705139 | ||||||
chr7:44705184
|
C | G | 2 | a0001c0006t0001g0120a0001c0006t0001g0129 | 2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2633-2041C>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705184 | ||||||
chr7:44705207
|
T | C | 136 | a0001c0001t0012g0122a0001c0002t0001g0024a0001c0002t0001g0031others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2633-2018T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705207 | ||||||
chr7:44705209
|
C | T | 136 | a0001c0001t0012g0122a0001c0002t0001g0024a0001c0002t0001g0031others(133): Show | 136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2633-2016C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705209 | ||||||
chr7:44705214
|
A | G | 292 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2633-2011A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705214 | ||||||
chr7:44705242
|
C | T | 1 | a0002c0003t0001g0077 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2633-1983C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705242 | ||||||
chr7:44705294
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2633-1931C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705294 | ||||||
chr7:44705299
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2633-1926G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705299 | ||||||
chr7:44705332
|
G | A | 59 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0023others(56): Show | 60 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.2633-1893G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705332 | ||||||
chr7:44705348
|
G | A | 1 | a0002c0013t0001g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2633-1877G>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705348 | ||||||
chr7:44705417
|
C | T | 1 | a0001c0006t0001g0129 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2633-1808C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705417 | ||||||
chr7:44705654
|
T | C | 292 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(289): Show | 294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.2633-1571T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705654 | ||||||
chr7:44705717
|
T | C | 1 | a0001c0002t0001g0226 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2633-1508T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705717 | ||||||
chr7:44705721
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2633-1504A>G | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44705721 | ||||||
chr7:44706050
|
C | A | 1 | a0001c0002t0013g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2633-1175C>A | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44706050 | ||||||
chr7:44706123
|
T | C | 15 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | HG00741.hp1 HG01433.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2633-1102T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44706123 | ||||||
chr7:44706323
|
AT | A | 152 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0018others(149): Show | 152 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2633-887delT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44706323 | |||||
chr7:44706414
|
C | T | 2 | a0001c0005t0001g0200a0001c0005t0001g0274 | 2 | HG02257.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2633-811C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44706414 | ||||||
chr7:44706624
|
A | AT | 50 | a0001c0001t0002g0001a0001c0001t0002g0022a0001c0001t0002g0026others(47): Show | 51 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2633-586dupT | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44706624 | |||||
chr7:44706624
|
A | ATTTTTT | 133 | a0001c0001t0001g0011a0001c0001t0001g0079a0001c0001t0001g0080others(130): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.2633-591_2633-586d others(8): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44706624 | |||||
chr7:44706624
|
A | ATTTTTTT | 13 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG00621.hp2 HG00741.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.2633-592_2633-586d others(9): Show |
OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr7 | 44706624 | |||||
chr7:44706624
|
A | T | 1 | a0001c0005t0001g0274 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2633-601A>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44706624 | ||||||
chr7:44706765
|
C | T | 2 | a0001c0001t0009g0003a0001c0001t0009g0141 | 2 | HG02895.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2633-460C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44706765 | ||||||
chr7:44706820
|
C | T | 3 | a0001c0002t0001g0225a0001c0002t0001g0230a0002c0013t0001g0073 | 3 | HG01978.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2633-405C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44706820 | ||||||
chr7:44707041
|
C | T | 2 | a0001c0006t0001g0120a0001c0006t0001g0129 | 2 | HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2633-184C>T | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 20/22 | chr7 | 44707041 | ||||||
chr7:44707765
|
T | C | 4 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(1): Show | 4 | HG00741.hp1 HG01433.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2951+29T>C | OGDH | ENSG00000105953.16 | transcript | ENST00000222673.6 | protein_coding | 22/22 | chr7 | 44707765 |