geneid | 3267 |
---|---|
ensemblid | ENSG00000173744.18 |
hgncid | 5175 |
symbol | AGFG1 |
name | ArfGAP with FG repeats 1 |
refseq_nuc | NM_004504.5 |
refseq_prot | NP_004495.2 |
ensembl_nuc | ENST00000310078.13 |
ensembl_prot | ENSP00000312059.7 |
mane_status | MANE Select |
chr | chr2 |
start | 227472156 |
end | 227561217 |
strand | + |
ver | v1.2 |
region | chr2:227472156-227561217 |
region5000 | chr2:227467156-227566217 |
regionname0 | AGFG1_chr2_227472156_227561217 |
regionname5000 | AGFG1_chr2_227467156_227566217 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 562 | 325 | 91 | 44 | 138 | 10 | 40 | 100 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0002 | 0/0 | 562 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0003 | 0/0 | 562 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
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 | 0/1 | 1689 | 196 | 63 | 28 | 75 | 7 | 22 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0002 | 1/0 | 1689 | 78 | 14 | 8 | 43 | 2 | 10 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0003 | 0/0 | 1689 | 28 | 0 | 7 | 15 | 1 | 5 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0004 | 0/0 | 1689 | 21 | 12 | 1 | 5 | 0 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0005 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0006 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0007 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
c0008 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
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 | 0/0 | 6989 | 122 | 25 | 15 | 67 | 2 | 13 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0002 | 0/0 | 6990 | 64 | 7 | 5 | 42 | 2 | 8 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0003 | 0/0 | 6992 | 25 | 0 | 7 | 13 | 1 | 4 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0004 | 0/1 | 6989 | 16 | 1 | 6 | 2 | 3 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0005 | 0/0 | 6989 | 15 | 10 | 3 | 0 | 2 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0006 | 0/0 | 6993 | 14 | 6 | 1 | 4 | 0 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0007 | 0/0 | 6989 | 7 | 5 | 2 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0008 | 0/0 | 6985 | 7 | 1 | 2 | 0 | 0 | 4 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0009 | 0/0 | 6993 | 6 | 6 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0010 | 0/0 | 6989 | 4 | 3 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0011 | 0/0 | 6989 | 3 | 2 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0012 | 0/0 | 6989 | 3 | 3 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0013 | 0/0 | 6993 | 3 | 0 | 0 | 3 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0014 | 0/0 | 6989 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0015 | 0/0 | 6989 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0016 | 0/0 | 6989 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0017 | 0/0 | 6989 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0018 | 0/0 | 6989 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0019 | 0/0 | 6989 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0020 | 0/0 | 6989 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0021 | 0/0 | 6993 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0022 | 1/0 | 6989 | 2 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0023 | 0/0 | 6985 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0024 | 0/0 | 6990 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0025 | 0/0 | 6989 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0026 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0027 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0028 | 0/0 | 6990 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0029 | 0/0 | 6990 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0030 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0031 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0032 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0033 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0034 | 0/0 | 6990 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0035 | 0/0 | 6989 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0036 | 0/0 | 6990 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0037 | 0/0 | 6989 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0038 | 0/0 | 6989 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0039 | 0/0 | 6992 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0040 | 0/0 | 6989 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0041 | 0/0 | 6993 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
t0042 | 0/0 | 6993 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
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 | 0/1 | 1689 | 196 | 63 | 28 | 75 | 7 | 22 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002 | 1/0 | 1689 | 78 | 14 | 8 | 43 | 2 | 10 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0003 | 0/0 | 1689 | 28 | 0 | 7 | 15 | 1 | 5 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0004 | 0/0 | 1689 | 21 | 12 | 1 | 5 | 0 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0005 | 0/0 | 1689 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0002c0006 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0002c0007 | 0/0 | 1689 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0003c0008 | 0/0 | 1689 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8677 | 122 | 25 | 15 | 67 | 2 | 13 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0004 | 0/1 | 8677 | 16 | 1 | 6 | 2 | 3 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0005 | 0/0 | 8677 | 15 | 10 | 3 | 0 | 2 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0008 | 0/0 | 8673 | 7 | 1 | 2 | 0 | 0 | 4 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0010 | 0/0 | 8677 | 4 | 3 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0011 | 0/0 | 8677 | 3 | 2 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0012 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0015 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0016 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0017 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0018 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0019 | 0/0 | 8677 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0020 | 0/0 | 8677 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0021 | 0/0 | 8681 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0023 | 0/0 | 8673 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0025 | 0/0 | 8677 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0026 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0027 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0030 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0031 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0032 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0033 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0037 | 0/0 | 8677 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0038 | 0/0 | 8677 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0040 | 0/0 | 8677 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0001t0041 | 0/0 | 8681 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0002 | 0/0 | 8678 | 63 | 7 | 5 | 41 | 2 | 8 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0007 | 0/0 | 8677 | 7 | 5 | 2 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0022 | 1/0 | 8677 | 2 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0024 | 0/0 | 8678 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0028 | 0/0 | 8678 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0029 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0034 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0035 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0002t0036 | 0/0 | 8678 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0003t0003 | 0/0 | 8680 | 25 | 0 | 7 | 13 | 1 | 4 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0003t0013 | 0/0 | 8681 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0003t0039 | 0/0 | 8680 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0004t0006 | 0/0 | 8681 | 14 | 6 | 1 | 4 | 0 | 3 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0004t0009 | 0/0 | 8681 | 6 | 6 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0004t0042 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0001c0005t0014 | 0/0 | 8677 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0002c0006t0002 | 0/0 | 8678 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0002c0007t0012 | 0/0 | 8677 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
a0003c0008t0013 | 0/0 | 8681 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | copy fasta | chr2 | 227467156 | 227566217 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0010g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0010g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0010g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0011g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0011g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0012g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0015g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0016g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0016g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0017g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0017g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0019g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0019g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0020g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0020g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0021g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0021g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0023g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0023g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0025g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0026g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0027g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0030g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0031g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0032g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0033g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0037g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0038g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0040g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0001t0041g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0022g0051 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0024g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0028g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0029g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0034g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0035g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0002t0036g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0013g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0013g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0003t0039g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0006g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0004t0042g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0005t0014g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0001c0005t0014g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0002c0006t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0002c0007t0012g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
a0003c0008t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0003 | g0069 | EUR | GBR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0191 | EUR | GBR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00423 | hp1 | a0001 | c0003 | t0003 | g0071 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0305 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00609 | hp2 | a0001 | c0003 | t0003 | g0070 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00639 | hp1 | a0001 | c0001 | t0008 | g0019 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00639 | hp2 | a0001 | c0001 | t0011 | g0091 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0317 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00738 | hp2 | a0001 | c0004 | t0006 | g0044 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0318 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG00741 | hp2 | a0001 | c0001 | t0037 | g0116 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0316 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0286 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0020 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0291 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0290 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01243 | hp1 | a0001 | c0002 | t0007 | g0088 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01243 | hp2 | a0001 | c0002 | t0024 | g0279 | AMR | PUR | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01255 | hp1 | a0001 | c0002 | t0007 | g0086 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0255 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0314 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0197 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0257 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0315 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | IBS | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01884 | hp1 | a0001 | c0002 | t0007 | g0085 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01934 | hp2 | a0001 | c0003 | t0003 | g0059 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01952 | hp2 | a0001 | c0003 | t0003 | g0054 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01993 | hp2 | a0001 | c0003 | t0003 | g0052 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02004 | hp2 | a0001 | c0003 | t0003 | g0078 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02015 | hp1 | a0001 | c0001 | t0020 | g0146 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0301 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02074 | hp1 | a0001 | c0003 | t0003 | g0060 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0274 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02129 | hp1 | a0001 | c0004 | t0042 | g0032 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02135 | hp1 | a0001 | c0004 | t0006 | g0049 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02145 | hp1 | a0001 | c0002 | t0035 | g0083 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0283 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02273 | hp1 | a0001 | c0003 | t0003 | g0053 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02293 | hp2 | a0001 | c0003 | t0003 | g0064 | AMR | PEL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02451 | hp1 | a0001 | c0004 | t0006 | g0033 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02523 | hp1 | a0001 | c0003 | t0003 | g0062 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | KHV | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0284 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0272 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02615 | hp2 | a0001 | c0004 | t0009 | g0040 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0320 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02630 | hp2 | a0001 | c0001 | t0032 | g0093 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02647 | hp1 | a0001 | c0001 | t0033 | g0183 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02647 | hp2 | a0001 | c0001 | t0026 | g0231 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0321 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02723 | hp1 | a0001 | c0004 | t0009 | g0039 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02723 | hp2 | a0001 | c0001 | t0041 | g0081 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02735 | hp1 | a0001 | c0003 | t0003 | g0050 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0245 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0082 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0309 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02886 | hp1 | a0001 | c0002 | t0007 | g0087 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02895 | hp2 | a0001 | c0001 | t0023 | g0021 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02896 | hp2 | a0001 | c0004 | t0009 | g0041 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02897 | hp1 | a0001 | c0001 | t0023 | g0017 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0027 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02922 | hp1 | a0001 | c0002 | t0022 | g0056 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0310 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02965 | hp1 | a0001 | c0004 | t0006 | g0001 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0312 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02976 | hp1 | a0001 | c0004 | t0009 | g0036 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03017 | hp1 | a0001 | c0003 | t0039 | g0074 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03041 | hp1 | a0002 | c0007 | t0012 | g0195 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0292 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0237 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03098 | hp2 | a0001 | c0002 | t0007 | g0084 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03130 | hp1 | a0001 | c0004 | t0006 | g0001 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03195 | hp2 | a0001 | c0001 | t0021 | g0238 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0235 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03225 | hp1 | a0001 | c0001 | t0031 | g0193 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03225 | hp2 | a0001 | c0001 | t0027 | g0242 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0215 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03239 | hp2 | a0001 | c0003 | t0003 | g0055 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0307 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03453 | hp2 | a0001 | c0005 | t0014 | g0022 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03490 | hp2 | a0001 | c0001 | t0008 | g0014 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03491 | hp1 | a0001 | c0004 | t0006 | g0043 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0092 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03492 | hp1 | a0001 | c0004 | t0006 | g0042 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0015 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0319 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0313 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0306 | AFR | GWD | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03579 | hp1 | a0001 | c0004 | t0006 | g0035 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03654 | hp1 | a0001 | c0002 | t0036 | g0281 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0030 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0270 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0287 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03834 | hp2 | a0001 | c0002 | t0028 | g0303 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03942 | hp2 | a0001 | c0003 | t0003 | g0068 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0289 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04115 | hp2 | a0001 | c0001 | t0010 | g0029 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | BEB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04199 | hp1 | a0001 | c0003 | t0003 | g0073 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0253 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04204 | hp2 | a0001 | c0004 | t0006 | g0047 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04228 | hp1 | a0001 | c0001 | t0038 | g0113 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0232 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18522 | hp2 | a0001 | c0004 | t0009 | g0038 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | CHB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0240 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18906 | hp2 | a0001 | c0001 | t0030 | g0243 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18940 | hp1 | a0002 | c0006 | t0002 | g0260 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18943 | hp1 | a0001 | c0003 | t0013 | g0077 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18944 | hp1 | a0001 | c0003 | t0013 | g0067 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18946 | hp1 | a0003 | c0008 | t0013 | g0075 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18947 | hp2 | a0001 | c0003 | t0003 | g0066 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18949 | hp1 | a0001 | c0003 | t0003 | g0061 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18950 | hp1 | a0001 | c0001 | t0025 | g0224 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18957 | hp2 | a0001 | c0003 | t0003 | g0058 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18960 | hp1 | a0001 | c0004 | t0006 | g0031 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18962 | hp1 | a0001 | c0003 | t0003 | g0076 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18966 | hp2 | a0001 | c0004 | t0006 | g0045 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18969 | hp2 | a0001 | c0002 | t0029 | g0275 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18975 | hp1 | a0001 | c0002 | t0034 | g0261 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18985 | hp2 | a0001 | c0001 | t0020 | g0164 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18986 | hp2 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18989 | hp1 | a0001 | c0001 | t0019 | g0167 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0249 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19001 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19007 | hp2 | a0001 | c0001 | t0040 | g0140 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19009 | hp1 | a0001 | c0003 | t0003 | g0072 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19030 | hp2 | a0001 | c0005 | t0014 | g0023 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0028 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19043 | hp2 | a0001 | c0001 | t0016 | g0308 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19057 | hp2 | a0001 | c0003 | t0003 | g0079 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19065 | hp2 | a0001 | c0004 | t0006 | g0048 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19083 | hp1 | a0001 | c0003 | t0003 | g0080 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0063 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19090 | hp1 | a0001 | c0001 | t0019 | g0203 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19240 | hp1 | a0001 | c0002 | t0007 | g0090 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA19240 | hp2 | a0001 | c0001 | t0017 | g0233 | AFR | YRI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0256 | EUR | TSI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0133 | EUR | TSI | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA20905 | hp1 | a0001 | c0001 | t0008 | g0018 | SAS | GIH | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | GIH | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG01123 | hp2 | a0001 | c0003 | t0003 | g0065 | AMR | CLM | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02109 | hp2 | a0001 | c0004 | t0006 | g0034 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0089 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0194 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0025 | AFR | ACB | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0239 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG03471 | hp2 | a0001 | c0004 | t0009 | g0037 | AFR | MSL | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
HG06807 | hp2 | a0001 | c0004 | t0006 | g0046 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA20300 | hp1 | a0001 | c0001 | t0012 | g0192 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0311 | AFR | USA | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0230 | AFR | LWK | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0115 | REF | REF | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0022 | g0051 | REF | REF | AGFG1_chr2_227467156_227566217 | AGFG1 | chr2 | 227467156 | 227566217 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227533711
|
A | G | 1 | a0003 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.977A>G | p.Lys326Arg | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/13 | 1243/8677 | 977/1689 | 326/562 | chr2 | 227533711 | ||
chr2:227533738
|
A | G | 1 | a0002 | 2 | HG03041.hp1 NA18940.hp1 |
missense_variant | MODERATE | c.1004A>G | p.Asn335Ser | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/13 | 1270/8677 | 1004/1689 | 335/562 | chr2 | 227533738 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227520019
|
A | G | 1 | a0001c0004 | 21 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
synonymous_variant | LOW | c.333A>G | p.Gln111Gln | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/13 | 599/8677 | 333/1689 | 111/562 | chr2 | 227520019 | ||
chr2:227533706
|
A | G | 2 | a0001c0003a0003c0008 | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
synonymous_variant | LOW | c.972A>G | p.Ala324Ala | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/13 | 1238/8677 | 972/1689 | 324/562 | chr2 | 227533706 | ||
chr2:227536953
|
T | G | 1 | a0001c0005 | 2 | HG03453.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1338T>G | p.Ser446Ser | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/13 | 1604/8677 | 1338/1689 | 446/562 | chr2 | 227536953 | ||
chr2:227551996
|
A | G | 4 | a0001c0001a0001c0004a0001c0005others(1): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
synonymous_variant | LOW | c.1416A>G | p.Thr472Thr | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/13 | 1682/8677 | 1416/1689 | 472/562 | chr2 | 227551996 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227472184
|
G | A | 1 | a0001c0002t0024 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 238 | chr2 | 227472184 | |||||
chr2:227472195
|
G | A | 1 | a0001c0001t0025 | 1 | NA18950.hp1 | 5_prime_UTR_variant | MODIFIER | c.-227G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 227 | chr2 | 227472195 | |||||
chr2:227472225
|
C | T | 1 | a0001c0004t0042 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-197C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 197 | chr2 | 227472225 | |||||
chr2:227472263
|
G | A | 2 | a0001c0001t0011a0001c0001t0026 | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-159G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 159 | chr2 | 227472263 | |||||
chr2:227472334
|
G | A | 1 | a0001c0005t0014 | 2 | HG03453.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-88G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/13 | 88 | chr2 | 227472334 | |||||
chr2:227554657
|
C | T | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*162C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 162 | chr2 | 227554657 | |||||
chr2:227554686
|
T | C | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*191T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 191 | chr2 | 227554686 | |||||
chr2:227555019
|
A | G | 1 | a0001c0001t0040 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*524A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 524 | chr2 | 227555019 | |||||
chr2:227555048
|
A | T | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*553A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 553 | chr2 | 227555048 | |||||
chr2:227555347
|
T | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*852T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 852 | chr2 | 227555347 | |||||
chr2:227555348
|
C | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*853C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 853 | chr2 | 227555348 | |||||
chr2:227555349
|
T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*854T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 854 | chr2 | 227555349 | |||||
chr2:227555350
|
T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*855T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 855 | chr2 | 227555350 | |||||
chr2:227555352
|
G | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*857G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 857 | chr2 | 227555352 | |||||
chr2:227555353
|
C | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*858C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 858 | chr2 | 227555353 | |||||
chr2:227555355
|
G | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*860G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 860 | chr2 | 227555355 | |||||
chr2:227555358
|
T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*863T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 863 | chr2 | 227555358 | |||||
chr2:227555375
|
T | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 880 | chr2 | 227555375 | |||||
chr2:227555377
|
G | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*882G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 882 | chr2 | 227555377 | |||||
chr2:227555380
|
T | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 885 | chr2 | 227555380 | |||||
chr2:227555381
|
A | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*886A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 886 | chr2 | 227555381 | |||||
chr2:227555382
|
T | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*887T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 887 | chr2 | 227555382 | |||||
chr2:227555383
|
A | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*888A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 888 | chr2 | 227555383 | |||||
chr2:227555404
|
G | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 909 | chr2 | 227555404 | |||||
chr2:227555405
|
T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*910T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 910 | chr2 | 227555405 | |||||
chr2:227555413
|
A | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 918 | chr2 | 227555413 | |||||
chr2:227555415
|
T | G | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*920T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 920 | chr2 | 227555415 | |||||
chr2:227555427
|
T | A | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*932T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 932 | chr2 | 227555427 | |||||
chr2:227555446
|
A | C | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*951A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 951 | chr2 | 227555446 | |||||
chr2:227555448
|
A | T | 1 | a0001c0001t0027 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 953 | chr2 | 227555448 | |||||
chr2:227555468
|
A | AT | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*981dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 982 | INFO_REALIGN_3_PRIME | chr2 | 227555468 | ||||
chr2:227555477
|
A | T | 7 | a0001c0001t0004a0001c0001t0037a0001c0001t0038others(4): Show | 47 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*982A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 982 | chr2 | 227555477 | |||||
chr2:227555587
|
T | C | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1092T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1092 | chr2 | 227555587 | |||||
chr2:227555678
|
T | C | 2 | a0001c0001t0005a0001c0001t0016 | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1183T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1183 | chr2 | 227555678 | |||||
chr2:227555935
|
A | G | 1 | a0001c0002t0036 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1440 | chr2 | 227555935 | |||||
chr2:227556025
|
G | A | 1 | a0001c0002t0028 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1530 | chr2 | 227556025 | |||||
chr2:227556174
|
A | T | 1 | a0001c0001t0023 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1679A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1679 | chr2 | 227556174 | |||||
chr2:227556230
|
G | C | 1 | a0001c0002t0029 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1735G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1735 | chr2 | 227556230 | |||||
chr2:227556491
|
A | G | 2 | a0001c0001t0008a0001c0001t0023 | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1996A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 1996 | chr2 | 227556491 | |||||
chr2:227556495
|
C | T | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2000C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2000 | chr2 | 227556495 | |||||
chr2:227556510
|
T | C | 1 | a0001c0001t0017 | 2 | HG03209.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2015T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2015 | chr2 | 227556510 | |||||
chr2:227556554
|
G | A | 1 | a0001c0001t0017 | 2 | HG03209.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2059G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2059 | chr2 | 227556554 | |||||
chr2:227556745
|
G | C | 5 | a0001c0001t0008a0001c0001t0010a0001c0001t0018others(2): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2250G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2250 | chr2 | 227556745 | |||||
chr2:227556747
|
G | A | 1 | a0001c0001t0019 | 2 | NA18989.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2252G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2252 | chr2 | 227556747 | |||||
chr2:227556758
|
A | G | 2 | a0001c0002t0007a0001c0002t0035 | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2263A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2263 | chr2 | 227556758 | |||||
chr2:227556856
|
C | G | 2 | a0001c0001t0005a0001c0001t0016 | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2361 | chr2 | 227556856 | |||||
chr2:227557045
|
C | CT | 7 | a0001c0002t0002a0001c0002t0024a0001c0002t0028others(4): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2551dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2552 | INFO_REALIGN_3_PRIME | chr2 | 227557045 | ||||
chr2:227557073
|
G | A | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2578G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2578 | chr2 | 227557073 | |||||
chr2:227557176
|
A | G | 1 | a0001c0003t0039 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2681A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2681 | chr2 | 227557176 | |||||
chr2:227557388
|
C | T | 1 | a0001c0001t0038 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2893C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 2893 | chr2 | 227557388 | |||||
chr2:227557535
|
C | G | 4 | a0001c0003t0003a0001c0003t0013a0001c0003t0039others(1): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3040C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3040 | chr2 | 227557535 | |||||
chr2:227557592
|
GTTTA | G | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(18): Show | 171 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*3106_*3109delTTTA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3106 | INFO_REALIGN_3_PRIME | chr2 | 227557592 | ||||
chr2:227557857
|
A | T | 1 | a0001c0005t0014 | 2 | HG03453.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3362A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3362 | chr2 | 227557857 | |||||
chr2:227557905
|
G | A | 2 | a0001c0001t0030a0001c0001t0031 | 2 | HG03225.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3410G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3410 | chr2 | 227557905 | |||||
chr2:227557935
|
T | C | 1 | a0001c0001t0026 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3440T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3440 | chr2 | 227557935 | |||||
chr2:227558386
|
T | C | 6 | a0001c0001t0008a0001c0001t0010a0001c0001t0018others(3): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3891T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3891 | chr2 | 227558386 | |||||
chr2:227558394
|
G | T | 3 | a0001c0001t0011a0001c0001t0026a0001c0001t0033 | 5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3899G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3899 | chr2 | 227558394 | |||||
chr2:227558394
|
GT | G | 6 | a0001c0001t0041a0001c0003t0003a0001c0003t0039others(3): Show | 48 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3910delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3910 | INFO_REALIGN_3_PRIME | chr2 | 227558394 | ||||
chr2:227558426
|
A | G | 3 | a0001c0001t0012a0001c0001t0027a0002c0007t0012 | 4 | HG02559.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3931A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3931 | chr2 | 227558426 | |||||
chr2:227558445
|
G | C | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3950G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 3950 | chr2 | 227558445 | |||||
chr2:227558572
|
G | C | 4 | a0001c0001t0041a0001c0004t0006a0001c0004t0009others(1): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4077G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4077 | chr2 | 227558572 | |||||
chr2:227558586
|
G | A | 1 | a0001c0002t0035 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4091G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4091 | chr2 | 227558586 | |||||
chr2:227558677
|
A | G | 2 | a0001c0001t0005a0001c0001t0016 | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4182A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4182 | chr2 | 227558677 | |||||
chr2:227558973
|
G | A | 19 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(16): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*4478G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4478 | chr2 | 227558973 | |||||
chr2:227559055
|
C | G | 19 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(16): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*4560C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4560 | chr2 | 227559055 | |||||
chr2:227559062
|
G | T | 1 | a0001c0001t0018 | 2 | HG02559.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4567G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4567 | chr2 | 227559062 | |||||
chr2:227559410
|
G | A | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4915G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 4915 | chr2 | 227559410 | |||||
chr2:227559499
|
A | C | 1 | a0001c0001t0018 | 2 | HG02559.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5004A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5004 | chr2 | 227559499 | |||||
chr2:227559593
|
C | T | 2 | a0001c0002t0007a0001c0002t0035 | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5098C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5098 | chr2 | 227559593 | |||||
chr2:227559692
|
C | T | 1 | a0001c0001t0005 | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5197C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5197 | chr2 | 227559692 | |||||
chr2:227559763
|
C | G | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5268C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5268 | chr2 | 227559763 | |||||
chr2:227559894
|
A | G | 1 | a0001c0001t0026 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5399A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5399 | chr2 | 227559894 | |||||
chr2:227559978
|
G | A | 1 | a0001c0001t0015 | 2 | HG03471.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5483G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5483 | chr2 | 227559978 | |||||
chr2:227560008
|
C | T | 1 | a0001c0001t0037 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5513C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5513 | chr2 | 227560008 | |||||
chr2:227560014
|
C | T | 35 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(32): Show | 249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*5519C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5519 | chr2 | 227560014 | |||||
chr2:227560238
|
T | G | 1 | a0001c0002t0034 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5743T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5743 | chr2 | 227560238 | |||||
chr2:227560436
|
C | CTAAT | 28 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(25): Show | 215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5942_*5943insAATT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5943 | INFO_REALIGN_3_PRIME | chr2 | 227560436 | ||||
chr2:227560453
|
T | C | 1 | a0001c0004t0009 | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5958T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 5958 | chr2 | 227560453 | |||||
chr2:227560613
|
A | T | 1 | a0001c0001t0032 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6118A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6118 | chr2 | 227560613 | |||||
chr2:227560711
|
C | G | 4 | a0001c0003t0003a0001c0003t0013a0001c0003t0039others(1): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6216C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6216 | chr2 | 227560711 | |||||
chr2:227560723
|
A | T | 4 | a0001c0003t0003a0001c0003t0013a0001c0003t0039others(1): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6228A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6228 | chr2 | 227560723 | |||||
chr2:227560741
|
A | G | 4 | a0001c0003t0003a0001c0003t0013a0001c0003t0039others(1): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*6246A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6246 | chr2 | 227560741 | |||||
chr2:227560746
|
T | C | 1 | a0001c0001t0020 | 2 | HG02015.hp1 NA18985.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6251T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6251 | chr2 | 227560746 | |||||
chr2:227560817
|
C | T | 2 | a0001c0001t0008a0001c0001t0023 | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6322C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6322 | chr2 | 227560817 | |||||
chr2:227561074
|
T | C | 1 | a0001c0001t0041 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6579T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6579 | chr2 | 227561074 | |||||
chr2:227561123
|
T | C | 1 | a0001c0001t0030 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6628T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 13/13 | 6628 | chr2 | 227561123 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:227472605
|
C | T | 16 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0005g0311others(13): Show | 16 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.167+17C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472605 | ||||||
chr2:227472634
|
T | C | 2 | a0001c0002t0002g0007a0001c0002t0002g0008 | 2 | HG02071.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.167+46T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472634 | ||||||
chr2:227472763
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG00423.hp2 HG02071.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+175G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472763 | ||||||
chr2:227472817
|
T | C | 1 | a0001c0002t0002g0013 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.167+229T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472817 | ||||||
chr2:227472872
|
G | C | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+284G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472872 | ||||||
chr2:227472903
|
C | T | 67 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(64): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.167+315C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472903 | ||||||
chr2:227472942
|
C | A | 20 | a0001c0004t0006g0001a0001c0004t0006g0031a0001c0004t0006g0033others(17): Show | 21 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.167+354C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472942 | ||||||
chr2:227472947
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.167+359C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472947 | ||||||
chr2:227472958
|
G | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.167+370G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472958 | ||||||
chr2:227472988
|
G | A | 1 | a0001c0001t0011g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.167+400G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227472988 | ||||||
chr2:227473028
|
A | G | 1 | a0001c0002t0002g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.167+440A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473028 | ||||||
chr2:227473042
|
C | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.167+454C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473042 | ||||||
chr2:227473083
|
G | A | 1 | a0001c0002t0002g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.167+495G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473083 | ||||||
chr2:227473243
|
G | T | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+655G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473243 | ||||||
chr2:227473262
|
G | C | 1 | a0001c0003t0003g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.167+674G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473262 | ||||||
chr2:227473273
|
A | T | 1 | a0001c0002t0002g0305 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.167+685A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473273 | ||||||
chr2:227473415
|
C | T | 15 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.167+827C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473415 | ||||||
chr2:227473425
|
C | T | 1 | a0001c0002t0002g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.167+837C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473425 | ||||||
chr2:227473491
|
A | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.167+903A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473491 | ||||||
chr2:227473648
|
C | T | 2 | a0001c0001t0027g0242a0001c0001t0030g0243 | 2 | HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.167+1060C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473648 | ||||||
chr2:227473768
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.167+1180A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473768 | ||||||
chr2:227473792
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+1204A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473792 | ||||||
chr2:227473937
|
G | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.167+1349G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473937 | ||||||
chr2:227473937
|
G | T | 1 | a0001c0001t0005g0082 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.167+1349G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473937 | ||||||
chr2:227473944
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.167+1356C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227473944 | ||||||
chr2:227474020
|
A | G | 1 | a0001c0001t0017g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.167+1432A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474020 | ||||||
chr2:227474026
|
C | T | 1 | a0001c0001t0008g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.167+1438C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474026 | ||||||
chr2:227474188
|
T | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+1600T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474188 | ||||||
chr2:227474309
|
C | G | 1 | a0001c0001t0005g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.167+1721C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474309 | ||||||
chr2:227474535
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.167+1947C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474535 | ||||||
chr2:227474792
|
T | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+2204T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474792 | ||||||
chr2:227474921
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.167+2333A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474921 | ||||||
chr2:227474925
|
T | C | 1 | a0001c0001t0004g0092 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.167+2337T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227474925 | ||||||
chr2:227475051
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.167+2463A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475051 | ||||||
chr2:227475165
|
G | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.167+2577G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475165 | ||||||
chr2:227475174
|
T | C | 2 | a0001c0002t0002g0246a0001c0002t0002g0247 | 2 | HG00408.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.167+2586T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475174 | ||||||
chr2:227475322
|
G | A | 1 | a0001c0004t0006g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.167+2734G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475322 | ||||||
chr2:227475346
|
T | C | 1 | a0001c0001t0032g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.167+2758T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475346 | ||||||
chr2:227475806
|
T | C | 1 | a0001c0001t0004g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.167+3218T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475806 | ||||||
chr2:227475878
|
T | C | 1 | a0001c0002t0002g0248 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.167+3290T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475878 | ||||||
chr2:227475932
|
A | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+3344A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475932 | ||||||
chr2:227475998
|
T | C | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.167+3410T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227475998 | ||||||
chr2:227476029
|
G | T | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.167+3441G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476029 | ||||||
chr2:227476067
|
C | A | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.167+3479C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476067 | ||||||
chr2:227476182
|
G | A | 2 | a0001c0001t0008g0014a0001c0001t0008g0015 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.167+3594G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476182 | ||||||
chr2:227476227
|
C | T | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+3639C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476227 | ||||||
chr2:227476362
|
A | G | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+3774A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476362 | ||||||
chr2:227476544
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.167+3956C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476544 | ||||||
chr2:227476750
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+4162C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476750 | ||||||
chr2:227476903
|
CT | C | 316 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(313): Show | 321 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.167+4331delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227476903 | |||||
chr2:227476996
|
G | A | 1 | a0001c0001t0008g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.167+4408G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227476996 | ||||||
chr2:227477046
|
C | T | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.167+4458C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477046 | ||||||
chr2:227477099
|
G | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.167+4511G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477099 | ||||||
chr2:227477751
|
A | G | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.167+5163A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477751 | ||||||
chr2:227477793
|
A | G | 1 | a0001c0001t0025g0224 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.167+5205A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477793 | ||||||
chr2:227477962
|
T | C | 4 | a0001c0003t0003g0052a0001c0003t0003g0053a0001c0003t0003g0054others(1): Show | 4 | HG01952.hp2 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+5374T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227477962 | ||||||
chr2:227478046
|
A | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.167+5458A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478046 | ||||||
chr2:227478119
|
T | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.167+5531T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478119 | ||||||
chr2:227478125
|
G | T | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219others(2): Show | 5 | HG00621.hp2 NA18940.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.167+5537G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478125 | ||||||
chr2:227478134
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0226 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.167+5546G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478134 | ||||||
chr2:227478139
|
A | AT | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.167+5557dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478139 | |||||
chr2:227478239
|
T | TA | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(153): Show | 158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.167+5664dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478239 | |||||
chr2:227478239
|
T | TAA | 14 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(11): Show | 14 | HG00738.hp2 HG02055.hp1 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.167+5663_167+5664d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478239 | |||||
chr2:227478239
|
T | TAAA | 12 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0033others(9): Show | 13 | HG02109.hp2 HG02129.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.167+5662_167+5664d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478239 | |||||
chr2:227478251
|
AATAC | A | 28 | a0001c0003t0003g0052a0001c0003t0003g0053a0001c0003t0003g0054others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.167+5670_167+5673d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227478251 | |||||
chr2:227478327
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.167+5739G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478327 | ||||||
chr2:227478352
|
T | C | 1 | a0001c0003t0003g0050 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.167+5764T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478352 | ||||||
chr2:227478409
|
C | T | 1 | a0001c0002t0002g0304 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.167+5821C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478409 | ||||||
chr2:227478632
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.167+6044C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478632 | ||||||
chr2:227478864
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.167+6276A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478864 | ||||||
chr2:227478894
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.167+6306G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478894 | ||||||
chr2:227478940
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.167+6352T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227478940 | ||||||
chr2:227479085
|
A | G | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.167+6497A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479085 | ||||||
chr2:227479326
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.167+6738T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479326 | ||||||
chr2:227479444
|
T | G | 68 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(65): Show | 70 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.167+6856T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479444 | ||||||
chr2:227479510
|
T | C | 1 | a0001c0001t0038g0113 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.167+6922T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479510 | ||||||
chr2:227479525
|
AG | A | 4 | a0001c0001t0004g0114a0001c0001t0004g0115a0001c0001t0004g0117others(1): Show | 4 | HG00738.hp1 HG00741.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.167+6938delG | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479525 | ||||||
chr2:227479629
|
C | T | 28 | a0001c0003t0003g0052a0001c0003t0003g0053a0001c0003t0003g0054others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.167+7041C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479629 | ||||||
chr2:227479841
|
A | T | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.167+7253A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479841 | ||||||
chr2:227479904
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.167+7316T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479904 | ||||||
chr2:227479952
|
A | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.167+7364A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227479952 | ||||||
chr2:227480008
|
A | G | 1 | a0001c0004t0006g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.167+7420A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480008 | ||||||
chr2:227480084
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.167+7496G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480084 | ||||||
chr2:227480237
|
A | G | 1 | a0001c0002t0028g0303 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.167+7649A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480237 | ||||||
chr2:227480386
|
C | T | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.167+7798C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480386 | ||||||
chr2:227480394
|
CTTATT | C | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+7824_167+7828d others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227480394 | |||||
chr2:227480591
|
CT | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.167+8018delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227480591 | |||||
chr2:227480599
|
T | C | 10 | a0001c0004t0006g0031a0001c0004t0006g0042a0001c0004t0006g0043others(7): Show | 10 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+8011T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480599 | ||||||
chr2:227480692
|
C | G | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.167+8104C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480692 | ||||||
chr2:227480770
|
G | A | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.167+8182G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480770 | ||||||
chr2:227480867
|
A | G | 10 | a0001c0002t0002g0006a0001c0002t0002g0246a0001c0002t0002g0247others(7): Show | 11 | HG00408.hp2 HG00438.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.167+8279A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227480867 | ||||||
chr2:227481043
|
G | T | 1 | a0001c0004t0009g0041 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.167+8455G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481043 | ||||||
chr2:227481099
|
CT | C | 75 | a0001c0001t0011g0091a0001c0001t0011g0232a0001c0001t0015g0239others(72): Show | 77 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.167+8535delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | |||||
chr2:227481099
|
CTT | C | 26 | a0001c0001t0001g0225a0001c0001t0011g0230a0001c0001t0017g0233others(23): Show | 26 | HG00738.hp2 HG01952.hp2 HG02129.hp1 others(23): Show |
intron_variant | MODIFIER | c.167+8534_167+8535d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | |||||
chr2:227481099
|
CTTT | C | 18 | a0001c0001t0001g0106a0001c0001t0004g0092a0001c0001t0004g0215others(15): Show | 19 | HG02109.hp2 HG02273.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.167+8533_167+8535d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | |||||
chr2:227481099
|
CTTTT | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(149): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.167+8532_167+8535d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | |||||
chr2:227481099
|
CTTTTT | C | 15 | a0001c0001t0001g0098a0001c0001t0001g0118a0001c0001t0001g0119others(12): Show | 15 | HG00558.hp1 HG00558.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.167+8531_167+8535d others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | |||||
chr2:227481099
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0094 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.167+8526_167+8535d others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481099 | |||||
chr2:227481120
|
TTTTG | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0210a0001c0001t0001g0211others(3): Show | 7 | HG02074.hp2 NA18944.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.167+8533_167+8536d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481120 | ||||||
chr2:227481259
|
T | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.167+8671T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481259 | ||||||
chr2:227481326
|
T | C | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.167+8738T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481326 | ||||||
chr2:227481806
|
T | C | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.167+9218T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481806 | ||||||
chr2:227481863
|
C | CT | 33 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0124others(30): Show | 33 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.167+9297dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481863 | |||||
chr2:227481863
|
CT | C | 24 | a0001c0001t0001g0004a0001c0001t0001g0210a0001c0001t0001g0211others(21): Show | 25 | HG00639.hp1 HG01069.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.167+9297delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227481863 | |||||
chr2:227481899
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.167+9311G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481899 | ||||||
chr2:227481959
|
G | A | 10 | a0001c0004t0006g0031a0001c0004t0006g0042a0001c0004t0006g0043others(7): Show | 10 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.167+9371G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481959 | ||||||
chr2:227481959
|
G | T | 1 | a0001c0002t0002g0277 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.167+9371G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481959 | ||||||
chr2:227481966
|
C | T | 1 | a0001c0001t0016g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.167+9378C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481966 | ||||||
chr2:227481985
|
C | A | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.167+9397C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227481985 | ||||||
chr2:227482009
|
G | A | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.167+9421G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482009 | ||||||
chr2:227482011
|
G | A | 2 | a0001c0002t0002g0250a0001c0002t0002g0297 | 2 | NA18971.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.167+9423G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482011 | ||||||
chr2:227482055
|
C | T | 12 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0005g0311others(9): Show | 12 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.167+9467C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482055 | ||||||
chr2:227482071
|
C | T | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.168-9476C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482071 | ||||||
chr2:227482101
|
G | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.168-9446G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482101 | ||||||
chr2:227482232
|
A | C | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | NA18960.hp2 NA18975.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-9315A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482232 | ||||||
chr2:227482293
|
C | T | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-9254C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482293 | ||||||
chr2:227482370
|
A | T | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-9177A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482370 | ||||||
chr2:227482407
|
T | A | 2 | a0001c0001t0008g0014a0001c0001t0008g0015 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.168-9140T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482407 | ||||||
chr2:227482480
|
T | C | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-9067T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482480 | ||||||
chr2:227482498
|
A | G | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-9049A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482498 | ||||||
chr2:227482534
|
C | T | 6 | a0001c0004t0009g0036a0001c0004t0009g0037a0001c0004t0009g0038others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-9013C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482534 | ||||||
chr2:227482577
|
C | T | 3 | a0001c0002t0002g0291a0001c0002t0002g0292a0001c0002t0002g0293 | 3 | HG01106.hp1 HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.168-8970C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482577 | ||||||
chr2:227482609
|
G | A | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-8938G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227482609 | ||||||
chr2:227482979
|
CT | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.168-8550delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227482979 | |||||
chr2:227482979
|
CTT | C | 9 | a0001c0001t0001g0127a0001c0002t0007g0084a0001c0002t0007g0085others(6): Show | 9 | HG01243.hp1 HG01255.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.168-8551_168-8550d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227482979 | |||||
chr2:227483178
|
C | G | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-8369C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483178 | ||||||
chr2:227483337
|
C | T | 59 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(56): Show | 61 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.168-8210C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483337 | ||||||
chr2:227483569
|
T | C | 1 | a0001c0001t0001g0009 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.168-7978T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483569 | ||||||
chr2:227483593
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.168-7954C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483593 | ||||||
chr2:227483596
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.168-7951T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483596 | ||||||
chr2:227483655
|
A | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-7892A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483655 | ||||||
chr2:227483766
|
T | A | 3 | a0001c0004t0006g0042a0001c0004t0006g0043a0001c0004t0006g0044 | 3 | HG00738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.168-7781T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483766 | ||||||
chr2:227483789
|
C | T | 4 | a0001c0004t0006g0001a0001c0004t0006g0033a0001c0004t0006g0034others(1): Show | 5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-7758C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483789 | ||||||
chr2:227483957
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168-7590T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227483957 | ||||||
chr2:227484257
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.168-7290C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484257 | ||||||
chr2:227484406
|
C | T | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.168-7141C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484406 | ||||||
chr2:227484570
|
A | G | 1 | a0001c0002t0002g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.168-6977A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484570 | ||||||
chr2:227484677
|
GTTTTTTT others(7): Show |
G | 6 | a0001c0001t0008g0020a0001c0001t0008g0030a0001c0001t0018g0024others(3): Show | 6 | HG01081.hp2 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-6859_168-6846d others(16): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484677
|
GTTTTTTT others(8): Show |
G | 11 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(8): Show | 11 | HG00639.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-6859_168-6845d others(17): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484677
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-6859_168-6843d others(19): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484677
|
GTTTTTTT others(17): Show |
G | 1 | a0001c0003t0003g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.168-6859_168-6836d others(26): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484677
|
GTTTTTTT others(18): Show |
G | 35 | a0001c0001t0004g0202a0001c0001t0017g0233a0001c0003t0003g0050others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.168-6859_168-6835d others(27): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484677
|
GTTTTTTT others(19): Show |
G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.168-6859_168-6834d others(28): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484677
|
GTTTTTTT others(20): Show |
G | 2 | a0001c0001t0001g0129a0001c0001t0001g0241 | 2 | HG01884.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.168-6859_168-6833d others(29): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484677 | |||||
chr2:227484686
|
T | G | 1 | a0001c0002t0002g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.168-6861T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484686 | ||||||
chr2:227484688
|
GT | G | 9 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0271others(6): Show | 10 | HG02027.hp1 HG02602.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-6826delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | |||||
chr2:227484688
|
GTT | G | 23 | a0001c0002t0002g0006a0001c0002t0002g0248a0001c0002t0002g0249others(20): Show | 24 | HG00438.hp2 HG00609.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.168-6827_168-6826d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | |||||
chr2:227484688
|
GTTT | G | 28 | a0001c0002t0002g0007a0001c0002t0002g0008a0001c0002t0002g0245others(25): Show | 28 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.168-6828_168-6826d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | |||||
chr2:227484688
|
GTTTTT | G | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6830_168-6826d others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227484688 | |||||
chr2:227484689
|
T | G | 1 | a0001c0002t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.168-6858T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484689 | ||||||
chr2:227484692
|
T | G | 1 | a0001c0002t0002g0278 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.168-6855T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484692 | ||||||
chr2:227484700
|
T | G | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-6847T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484700 | ||||||
chr2:227484702
|
T | G | 1 | a0001c0002t0002g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.168-6845T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484702 | ||||||
chr2:227484704
|
T | G | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6843T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484704 | ||||||
chr2:227484705
|
T | G | 5 | a0001c0002t0002g0282a0001c0002t0002g0283a0001c0002t0002g0291others(2): Show | 5 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-6842T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484705 | ||||||
chr2:227484715
|
T | G | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6832T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227484715 | ||||||
chr2:227485023
|
T | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.168-6524T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485023 | ||||||
chr2:227485053
|
T | C | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-6494T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485053 | ||||||
chr2:227485061
|
T | G | 1 | a0001c0004t0006g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.168-6486T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485061 | ||||||
chr2:227485182
|
A | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0201 | 2 | HG01081.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.168-6365A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485182 | ||||||
chr2:227485243
|
CT | C | 29 | a0001c0002t0002g0280a0001c0003t0003g0050a0001c0003t0003g0052others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-6285delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485243 | |||||
chr2:227485243
|
CTT | C | 29 | a0001c0001t0001g0012a0001c0001t0004g0196a0001c0001t0005g0082others(26): Show | 29 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.168-6286_168-6285d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485243 | |||||
chr2:227485243
|
CTTT | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 196 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.168-6287_168-6285d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485243 | |||||
chr2:227485271
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168-6276G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485271 | ||||||
chr2:227485279
|
C | T | 3 | a0001c0004t0009g0039a0001c0004t0009g0040a0001c0004t0009g0041 | 3 | HG02615.hp2 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.168-6268C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485279 | ||||||
chr2:227485297
|
C | T | 6 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0012g0192others(3): Show | 6 | HG01081.hp1 HG01993.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-6250C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485297 | ||||||
chr2:227485334
|
T | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-6213T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485334 | ||||||
chr2:227485403
|
A | AT | 15 | a0001c0002t0002g0249a0001c0002t0002g0252a0001c0002t0002g0269others(12): Show | 15 | HG00609.hp1 HG01243.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-6125dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485403 | |||||
chr2:227485403
|
AT | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 176 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.168-6125delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485403 | |||||
chr2:227485403
|
ATT | A | 6 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(3): Show | 6 | HG02257.hp2 HG02976.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-6126_168-6125d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485403 | |||||
chr2:227485428
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.168-6119A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485428 | ||||||
chr2:227485643
|
A | G | 5 | a0001c0001t0005g0314a0001c0001t0005g0315a0001c0001t0005g0316others(2): Show | 5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-5904A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485643 | ||||||
chr2:227485680
|
C | CTT | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.168-5866_168-5865i others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227485680 | |||||
chr2:227485745
|
T | C | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.168-5802T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485745 | ||||||
chr2:227485852
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-5695C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227485852 | ||||||
chr2:227486067
|
A | G | 9 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(6): Show | 9 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-5480A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486067 | ||||||
chr2:227486116
|
TAA | T | 15 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-5430_168-5429d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486116 | ||||||
chr2:227486150
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.168-5397C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486150 | ||||||
chr2:227486256
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.168-5291T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486256 | ||||||
chr2:227486291
|
T | C | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-5256T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486291 | ||||||
chr2:227486486
|
G | A | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.168-5061G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486486 | ||||||
chr2:227486520
|
A | G | 15 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-5027A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486520 | ||||||
chr2:227486545
|
T | C | 5 | a0001c0001t0004g0133a0001c0001t0004g0197a0001c0001t0004g0202others(2): Show | 5 | HG01071.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-5002T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486545 | ||||||
chr2:227486588
|
ATATT | A | 12 | a0001c0001t0005g0309a0001c0001t0005g0310a0001c0001t0005g0311others(9): Show | 12 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-4958_168-4955d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486588 | ||||||
chr2:227486696
|
T | C | 1 | a0001c0002t0002g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.168-4851T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486696 | ||||||
chr2:227486717
|
A | G | 1 | a0001c0001t0008g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.168-4830A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486717 | ||||||
chr2:227486746
|
G | T | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.168-4801G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227486746 | ||||||
chr2:227487048
|
G | A | 1 | a0001c0002t0036g0281 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.168-4499G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487048 | ||||||
chr2:227487058
|
A | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-4489A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487058 | ||||||
chr2:227487295
|
G | A | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.168-4252G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487295 | ||||||
chr2:227487536
|
C | G | 13 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(10): Show | 13 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.168-4011C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487536 | ||||||
chr2:227487730
|
C | T | 20 | a0001c0004t0006g0001a0001c0004t0006g0031a0001c0004t0006g0033others(17): Show | 21 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.168-3817C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487730 | ||||||
chr2:227487752
|
G | T | 1 | a0001c0001t0001g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.168-3795G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227487752 | ||||||
chr2:227488024
|
T | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG00423.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.168-3523T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488024 | ||||||
chr2:227488099
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0229 | 3 | HG03017.hp2 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.168-3448T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488099 | ||||||
chr2:227488268
|
G | A | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-3279G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488268 | ||||||
chr2:227488355
|
G | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(67): Show | 71 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.168-3192G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488355 | ||||||
chr2:227488405
|
G | A | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168-3142G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488405 | ||||||
chr2:227488454
|
G | A | 1 | a0001c0002t0002g0271 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.168-3093G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488454 | ||||||
chr2:227488495
|
T | C | 1 | a0001c0002t0002g0285 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.168-3052T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488495 | ||||||
chr2:227488595
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.168-2952G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488595 | ||||||
chr2:227488599
|
G | A | 2 | a0001c0004t0006g0042a0001c0004t0006g0043 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.168-2948G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488599 | ||||||
chr2:227488948
|
G | A | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-2599G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227488948 | ||||||
chr2:227489084
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-2463G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489084 | ||||||
chr2:227489110
|
C | T | 6 | a0001c0004t0009g0036a0001c0004t0009g0037a0001c0004t0009g0038others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2437C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489110 | ||||||
chr2:227489215
|
T | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.168-2332T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489215 | ||||||
chr2:227489223
|
G | GT | 28 | a0001c0001t0008g0016a0001c0002t0002g0006a0001c0002t0002g0246others(25): Show | 29 | HG00408.hp2 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.168-2299dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | |||||
chr2:227489223
|
G | GTT | 9 | a0001c0001t0018g0024a0001c0001t0018g0025a0001c0002t0002g0268others(6): Show | 10 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-2300_168-2299d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | |||||
chr2:227489223
|
GT | G | 48 | a0001c0001t0001g0097a0001c0001t0001g0104a0001c0001t0001g0111others(45): Show | 48 | HG00642.hp2 HG00741.hp2 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.168-2299delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | |||||
chr2:227489223
|
GTT | G | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(145): Show | 150 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.168-2300_168-2299d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489223 | |||||
chr2:227489291
|
C | T | 8 | a0001c0001t0001g0225a0001c0001t0032g0093a0001c0004t0009g0036others(5): Show | 8 | HG02615.hp2 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2256C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489291 | ||||||
chr2:227489437
|
G | T | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-2110G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489437 | ||||||
chr2:227489560
|
T | G | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1987T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489560 | ||||||
chr2:227489708
|
C | T | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.168-1839C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489708 | ||||||
chr2:227489726
|
C | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-1821C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489726 | ||||||
chr2:227489756
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.168-1791G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489756 | ||||||
chr2:227489819
|
C | CT | 42 | a0001c0001t0001g0244a0001c0001t0004g0196a0001c0001t0018g0025others(39): Show | 42 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.168-1714dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227489819 | |||||
chr2:227489865
|
G | T | 1 | a0001c0004t0006g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.168-1682G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489865 | ||||||
chr2:227489878
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.168-1669C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489878 | ||||||
chr2:227489917
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.168-1630G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489917 | ||||||
chr2:227489971
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.168-1576A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227489971 | ||||||
chr2:227490112
|
A | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.168-1435A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490112 | ||||||
chr2:227490178
|
A | C | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.168-1369A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490178 | ||||||
chr2:227490360
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.168-1187C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490360 | ||||||
chr2:227490495
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-1052G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490495 | ||||||
chr2:227490577
|
C | CA | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 155 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.168-953dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227490577 | |||||
chr2:227490577
|
CA | C | 25 | a0001c0003t0003g0052a0001c0003t0003g0053a0001c0003t0003g0054others(22): Show | 25 | HG00423.hp1 HG00609.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.168-953delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227490577 | |||||
chr2:227490702
|
C | T | 5 | a0001c0001t0004g0133a0001c0001t0004g0197a0001c0001t0004g0202others(2): Show | 5 | HG01071.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-845C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490702 | ||||||
chr2:227490816
|
G | A | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.168-731G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490816 | ||||||
chr2:227490830
|
A | T | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-717A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490830 | ||||||
chr2:227490899
|
A | T | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.168-648A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490899 | ||||||
chr2:227490934
|
C | T | 1 | a0001c0001t0004g0215 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.168-613C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490934 | ||||||
chr2:227490935
|
G | A | 3 | a0001c0001t0001g0225a0001c0001t0017g0233a0001c0001t0017g0235 | 3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.168-612G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227490935 | ||||||
chr2:227491055
|
T | A | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.168-492T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491055 | ||||||
chr2:227491161
|
A | G | 2 | a0001c0001t0010g0026a0001c0001t0010g0027 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.168-386A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491161 | ||||||
chr2:227491432
|
A | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-115A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491432 | ||||||
chr2:227491442
|
T | C | 1 | a0001c0003t0003g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.168-105T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491442 | ||||||
chr2:227491466
|
GAAATATT others(1): Show |
G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-80_168-73delAA others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491466 | ||||||
chr2:227491498
|
A | T | 1 | a0001c0003t0003g0053 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.168-49A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 1/12 | chr2 | 227491498 | ||||||
chr2:227491648
|
G | GT | 6 | a0001c0002t0002g0247a0001c0002t0002g0266a0001c0002t0002g0302others(3): Show | 6 | HG00408.hp2 HG01243.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+23dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227491648 | |||||
chr2:227491648
|
GT | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(225): Show | 231 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.261+23delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227491648 | |||||
chr2:227491898
|
C | T | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+258C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227491898 | ||||||
chr2:227492361
|
G | A | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+721G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492361 | ||||||
chr2:227492399
|
C | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.261+759C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492399 | ||||||
chr2:227492534
|
A | T | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.261+894A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492534 | ||||||
chr2:227492663
|
G | C | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.261+1023G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492663 | ||||||
chr2:227492666
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+1026A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492666 | ||||||
chr2:227492986
|
A | C | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.261+1346A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227492986 | ||||||
chr2:227493255
|
G | C | 1 | a0002c0006t0002g0260 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.261+1615G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493255 | ||||||
chr2:227493327
|
T | G | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+1687T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493327 | ||||||
chr2:227493725
|
A | G | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+2085A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493725 | ||||||
chr2:227493943
|
C | G | 7 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0265others(4): Show | 7 | HG02083.hp1 HG02132.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+2303C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227493943 | ||||||
chr2:227494001
|
A | G | 1 | a0001c0002t0002g0246 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.261+2361A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494001 | ||||||
chr2:227494037
|
G | GTAAA | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+2399_261+2402d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227494037 | |||||
chr2:227494184
|
A | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+2544A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494184 | ||||||
chr2:227494193
|
C | T | 11 | a0001c0002t0022g0056a0001c0004t0006g0031a0001c0004t0006g0042others(8): Show | 11 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.261+2553C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494193 | ||||||
chr2:227494194
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+2554G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494194 | ||||||
chr2:227494245
|
C | CGTGCAAG others(1): Show |
6 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0018others(3): Show | 6 | HG00639.hp1 HG01081.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+2608_261+2615d others(10): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227494245 | |||||
chr2:227494365
|
G | A | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+2725G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494365 | ||||||
chr2:227494479
|
C | A | 2 | a0001c0001t0019g0167a0001c0001t0019g0203 | 2 | NA18989.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.261+2839C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494479 | ||||||
chr2:227494574
|
G | T | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+2934G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494574 | ||||||
chr2:227494594
|
A | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+2954A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494594 | ||||||
chr2:227494699
|
T | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02257.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.261+3059T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227494699 | ||||||
chr2:227495507
|
C | T | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+3867C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495507 | ||||||
chr2:227495533
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02132.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.261+3893G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495533 | ||||||
chr2:227495545
|
C | CA | 37 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0171others(34): Show | 37 | HG00639.hp2 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.261+3924dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227495545 | |||||
chr2:227495545
|
CA | C | 24 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(21): Show | 24 | HG00609.hp1 HG00639.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.261+3924delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227495545 | |||||
chr2:227495812
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0017g0233a0001c0001t0017g0235 | 3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.261+4172A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495812 | ||||||
chr2:227495857
|
G | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 203 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.261+4217G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495857 | ||||||
chr2:227495873
|
C | G | 1 | a0001c0001t0032g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.261+4233C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495873 | ||||||
chr2:227495881
|
T | A | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+4241T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495881 | ||||||
chr2:227495913
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.261+4273G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227495913 | ||||||
chr2:227496033
|
G | A | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+4393G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496033 | ||||||
chr2:227496085
|
C | T | 2 | a0001c0003t0003g0058a0001c0003t0003g0066 | 2 | NA18947.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.261+4445C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496085 | ||||||
chr2:227496093
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.261+4453A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496093 | ||||||
chr2:227496121
|
A | AAAAG | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 203 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.261+4485_261+4488d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227496121 | |||||
chr2:227496129
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.261+4489A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496129 | ||||||
chr2:227496145
|
T | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.261+4505T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496145 | ||||||
chr2:227496436
|
C | T | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+4796C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496436 | ||||||
chr2:227496441
|
C | CA | 251 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.261+4813dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227496441 | |||||
chr2:227496453
|
A | T | 3 | a0001c0002t0002g0251a0001c0002t0002g0277a0001c0002t0002g0304 | 3 | NA18986.hp1 NA18999.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.261+4813A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496453 | ||||||
chr2:227496454
|
T | A | 292 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(289): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.261+4814T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496454 | ||||||
chr2:227496675
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+5035A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496675 | ||||||
chr2:227496703
|
T | G | 1 | a0001c0002t0028g0303 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.261+5063T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496703 | ||||||
chr2:227496712
|
C | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18943.hp2 NA19054.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.261+5072C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496712 | ||||||
chr2:227496984
|
A | T | 1 | a0001c0002t0002g0251 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.261+5344A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496984 | ||||||
chr2:227496991
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+5351C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227496991 | ||||||
chr2:227497080
|
G | T | 1 | a0001c0001t0001g0168 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.261+5440G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497080 | ||||||
chr2:227497165
|
T | TC | 41 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0155others(38): Show | 41 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.261+5533dupC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497165 | |||||
chr2:227497171
|
C | A | 1 | a0001c0004t0006g0045 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.261+5531C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497171 | ||||||
chr2:227497179
|
A | C | 9 | a0001c0001t0001g0138a0001c0002t0007g0084a0001c0002t0007g0085others(6): Show | 9 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+5539A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497179 | ||||||
chr2:227497540
|
A | T | 2 | a0001c0002t0002g0270a0001c0002t0002g0272 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.261+5900A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497540 | ||||||
chr2:227497574
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.261+5934A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497574 | ||||||
chr2:227497601
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.261+5961T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497601 | ||||||
chr2:227497613
|
G | A | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.261+5973G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497613 | ||||||
chr2:227497717
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0236 | 2 | HG02818.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.261+6077G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497717 | ||||||
chr2:227497719
|
GTTTC | G | 4 | a0001c0001t0008g0014a0001c0001t0008g0016a0001c0001t0023g0017others(1): Show | 4 | HG02895.hp2 HG02897.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+6086_261+6089d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497719 | |||||
chr2:227497724
|
TTTC | T | 3 | a0001c0001t0008g0015a0001c0001t0008g0018a0001c0001t0008g0020 | 3 | HG01081.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.261+6087_261+6089d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497724 | |||||
chr2:227497727
|
C | CTTGTTT | 5 | a0001c0001t0005g0311a0001c0001t0005g0312a0001c0001t0005g0313others(2): Show | 5 | HG02717.hp1 HG02970.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+6089_261+6094d others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497727 | |||||
chr2:227497727
|
C | G | 1 | a0001c0001t0008g0019 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.261+6087C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497727 | ||||||
chr2:227497728
|
T | G | 1 | a0001c0001t0008g0030 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.261+6088T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497728 | ||||||
chr2:227497729
|
T | G | 3 | a0001c0001t0008g0015a0001c0001t0008g0018a0001c0001t0008g0020 | 3 | HG01081.hp2 HG03492.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.261+6089T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497729 | ||||||
chr2:227497730
|
G | GTTTTTTT others(12): Show |
1 | a0001c0002t0002g0293 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.261+6094_261+6095i others(21): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | |||||
chr2:227497730
|
G | T | 5 | a0001c0001t0008g0015a0001c0001t0008g0018a0001c0001t0008g0019others(2): Show | 5 | HG00639.hp1 HG01081.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.261+6090G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497730 | ||||||
chr2:227497730
|
GTTTTGTT others(4): Show |
G | 1 | a0001c0001t0021g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.261+6095_261+6105d others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | |||||
chr2:227497730
|
GTTTTGTT others(6): Show |
G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+6095_261+6107d others(15): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | |||||
chr2:227497730
|
GTTTTGTT others(7): Show |
G | 2 | a0001c0004t0006g0033a0001c0004t0042g0032 | 2 | HG02129.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.261+6095_261+6108d others(16): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497730 | |||||
chr2:227497731
|
T | TTTTTG | 6 | a0001c0001t0005g0310a0001c0001t0005g0314a0001c0001t0005g0315others(3): Show | 6 | HG00733.hp2 HG01069.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+6094_261+6095i others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497731 | |||||
chr2:227497731
|
TTTTG | T | 29 | a0001c0002t0002g0006a0001c0002t0002g0008a0001c0002t0002g0245others(26): Show | 30 | HG00408.hp2 HG00609.hp1 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.261+6095_261+6098d others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497731 | |||||
chr2:227497732
|
T | TTTTG | 4 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0320others(1): Show | 4 | HG02622.hp2 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+6094_261+6095i others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497732 | |||||
chr2:227497732
|
TTTG | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(131): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.261+6095_261+6097d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497732 | |||||
chr2:227497733
|
TTG | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0097a0001c0001t0001g0103others(52): Show | 55 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.261+6095_261+6096d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227497733 | |||||
chr2:227497734
|
TG | T | 11 | a0001c0001t0010g0029a0001c0001t0011g0091a0001c0001t0011g0232others(8): Show | 11 | HG00639.hp2 HG01243.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.261+6095delG | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497734 | ||||||
chr2:227497735
|
G | T | 67 | a0001c0001t0001g0108a0001c0001t0005g0082a0001c0001t0005g0309others(64): Show | 67 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.261+6095G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497735 | ||||||
chr2:227497736
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.261+6096T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497736 | ||||||
chr2:227497737
|
T | G | 5 | a0001c0001t0011g0091a0001c0001t0011g0232a0001c0001t0017g0233others(2): Show | 5 | HG00639.hp2 HG03209.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+6097T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497737 | ||||||
chr2:227497738
|
T | G | 44 | a0001c0001t0001g0003a0001c0001t0001g0097a0001c0001t0001g0103others(41): Show | 44 | HG00597.hp1 HG00621.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.261+6098T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497738 | ||||||
chr2:227497739
|
T | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.261+6099T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497739 | ||||||
chr2:227497761
|
T | TTTTTG | 9 | a0001c0003t0003g0053a0001c0003t0003g0057a0001c0003t0003g0059others(6): Show | 9 | HG00423.hp1 HG00609.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+6121_261+6122i others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | ||||||
chr2:227497761
|
T | TTTTTTG | 13 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0061others(10): Show | 13 | HG00099.hp1 HG01123.hp2 HG01993.hp2 others(10): Show |
intron_variant | MODIFIER | c.261+6121_261+6122i others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | ||||||
chr2:227497761
|
T | TTTTTTTT others(3): Show |
2 | a0001c0003t0013g0077a0003c0008t0013g0075 | 2 | NA18943.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.261+6121_261+6122i others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | ||||||
chr2:227497761
|
T | TTTTTTTT others(4): Show |
1 | a0001c0003t0013g0067 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.261+6121_261+6122i others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497761 | ||||||
chr2:227497935
|
G | A | 1 | a0001c0004t0042g0032 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.261+6295G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227497935 | ||||||
chr2:227498041
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.261+6401C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498041 | ||||||
chr2:227498089
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.261+6449A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498089 | ||||||
chr2:227498273
|
T | C | 1 | a0001c0004t0009g0037 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.261+6633T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498273 | ||||||
chr2:227498548
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.261+6908A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498548 | ||||||
chr2:227498576
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.261+6936A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498576 | ||||||
chr2:227498598
|
T | C | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.261+6958T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498598 | ||||||
chr2:227498716
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.261+7076C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227498716 | ||||||
chr2:227499024
|
GTAACAAA others(3): Show |
G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+7385_261+7394d others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499024 | ||||||
chr2:227499461
|
AAAACCCC others(9): Show |
A | 6 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(3): Show | 6 | HG00639.hp2 HG02647.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+7825_261+7840d others(18): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227499461 | |||||
chr2:227499468
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+7828C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499468 | ||||||
chr2:227499501
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0171a0001c0001t0001g0172others(1): Show | 4 | HG01106.hp2 HG01123.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.261+7861G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499501 | ||||||
chr2:227499639
|
C | CA | 35 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(32): Show | 35 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.261+8013dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227499639 | |||||
chr2:227499639
|
CA | C | 6 | a0001c0001t0016g0307a0001c0001t0016g0308a0001c0001t0018g0024others(3): Show | 6 | HG02559.hp2 HG02622.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+8013delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227499639 | |||||
chr2:227499697
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+8057C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499697 | ||||||
chr2:227499743
|
A | G | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+8103A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499743 | ||||||
chr2:227499769
|
G | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+8129G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227499769 | ||||||
chr2:227500091
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | NA18949.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.261+8451G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500091 | ||||||
chr2:227500124
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.261+8484C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500124 | ||||||
chr2:227500133
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.261+8493C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500133 | ||||||
chr2:227500134
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.261+8494A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500134 | ||||||
chr2:227500408
|
G | T | 1 | a0001c0003t0003g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.261+8768G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500408 | ||||||
chr2:227500490
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.261+8850T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500490 | ||||||
chr2:227500790
|
A | T | 20 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(17): Show | 20 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.261+9150A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500790 | ||||||
chr2:227500799
|
AT | A | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0018others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+9169delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227500799 | |||||
chr2:227500800
|
T | A | 54 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(51): Show | 54 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.261+9160T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500800 | ||||||
chr2:227500915
|
C | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0147 | 2 | NA18999.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.261+9275C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500915 | ||||||
chr2:227500927
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0188 | 2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.261+9287G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500927 | ||||||
chr2:227500950
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.261+9310G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500950 | ||||||
chr2:227500953
|
C | T | 15 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.261+9313C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227500953 | ||||||
chr2:227501074
|
G | A | 2 | a0001c0001t0001g0011a0001c0003t0003g0070 | 2 | HG00609.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.261+9434G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501074 | ||||||
chr2:227501083
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.261+9443C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501083 | ||||||
chr2:227501107
|
CAG | C | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.261+9470_261+9471d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227501107 | |||||
chr2:227501131
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+9491G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501131 | ||||||
chr2:227501273
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.261+9633G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501273 | ||||||
chr2:227501414
|
C | T | 4 | a0001c0004t0006g0001a0001c0004t0006g0033a0001c0004t0006g0034others(1): Show | 5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+9774C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501414 | ||||||
chr2:227501652
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01256.hp2 HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.261+10012C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501652 | ||||||
chr2:227501741
|
G | A | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.261+10101G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501741 | ||||||
chr2:227501770
|
G | A | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.261+10130G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501770 | ||||||
chr2:227501792
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+10152C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501792 | ||||||
chr2:227501885
|
T | G | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.261+10245T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227501885 | ||||||
chr2:227501893
|
CTG | C | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.261+10255_261+1025 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227501893 | |||||
chr2:227502006
|
G | A | 1 | a0001c0004t0006g0044 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.261+10366G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502006 | ||||||
chr2:227502012
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0221 | 3 | NA18940.hp2 NA19012.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.261+10372C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502012 | ||||||
chr2:227502025
|
A | G | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.261+10385A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502025 | ||||||
chr2:227502069
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.261+10429A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502069 | ||||||
chr2:227502514
|
A | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.261+10874A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502514 | ||||||
chr2:227502655
|
C | T | 19 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(16): Show | 19 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.261+11015C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502655 | ||||||
chr2:227502865
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+11225A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502865 | ||||||
chr2:227502870
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+11230A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502870 | ||||||
chr2:227502872
|
A | G | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.261+11232A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502872 | ||||||
chr2:227502931
|
T | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+11291T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502931 | ||||||
chr2:227502985
|
C | T | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+11345C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227502985 | ||||||
chr2:227503174
|
T | A | 2 | a0001c0001t0021g0237a0001c0001t0021g0238 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.261+11534T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503174 | ||||||
chr2:227503201
|
A | C | 1 | a0001c0002t0002g0008 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.261+11561A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503201 | ||||||
chr2:227503239
|
TA | T | 41 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(38): Show | 41 | HG00639.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.261+11615delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227503239 | |||||
chr2:227503501
|
A | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.261+11861A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503501 | ||||||
chr2:227503604
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.261+11964G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503604 | ||||||
chr2:227503606
|
G | A | 1 | a0001c0003t0003g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.261+11966G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503606 | ||||||
chr2:227503650
|
A | G | 1 | a0001c0001t0025g0224 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.261+12010A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503650 | ||||||
chr2:227503687
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.261+12047G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503687 | ||||||
chr2:227503806
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.261+12166A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503806 | ||||||
chr2:227503873
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.261+12233A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227503873 | ||||||
chr2:227504188
|
A | AT | 25 | a0001c0001t0001g0098a0001c0001t0001g0161a0001c0001t0005g0082others(22): Show | 25 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.261+12566dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227504188 | |||||
chr2:227504188
|
A | G | 6 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0012g0192others(3): Show | 6 | HG01081.hp1 HG01993.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+12548A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504188 | ||||||
chr2:227504188
|
AT | A | 6 | a0001c0001t0001g0118a0001c0001t0001g0156a0001c0001t0001g0172others(3): Show | 6 | HG00558.hp2 HG00733.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.261+12566delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227504188 | |||||
chr2:227504300
|
C | G | 5 | a0001c0003t0003g0058a0001c0003t0003g0066a0001c0003t0013g0067others(2): Show | 5 | NA18943.hp1 NA18944.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+12660C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504300 | ||||||
chr2:227504359
|
A | T | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.261+12719A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504359 | ||||||
chr2:227504475
|
G | A | 5 | a0001c0001t0005g0314a0001c0001t0005g0315a0001c0001t0005g0316others(2): Show | 5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.261+12835G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504475 | ||||||
chr2:227504494
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.261+12854A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504494 | ||||||
chr2:227504620
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+12980C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504620 | ||||||
chr2:227504621
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.261+12981A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504621 | ||||||
chr2:227504652
|
A | G | 1 | a0001c0002t0002g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.261+13012A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504652 | ||||||
chr2:227504747
|
C | G | 1 | a0001c0002t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.261+13107C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504747 | ||||||
chr2:227504889
|
G | A | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.261+13249G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504889 | ||||||
chr2:227504955
|
T | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+13315T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227504955 | ||||||
chr2:227505207
|
T | TTATCTC | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(110): Show | 114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.261+13567_261+1356 others(10): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505207 | ||||||
chr2:227505460
|
GGCATTTT others(11): Show |
G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.261+13824_261+1384 others(22): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227505460 | |||||
chr2:227505490
|
A | G | 1 | a0001c0001t0001g0110 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.261+13850A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505490 | ||||||
chr2:227505708
|
T | C | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.261+14068T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505708 | ||||||
chr2:227505711
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.261+14071G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505711 | ||||||
chr2:227505782
|
A | G | 3 | a0001c0001t0011g0230a0001c0001t0026g0231a0001c0001t0033g0183 | 3 | HG02647.hp1 HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261+14142A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505782 | ||||||
chr2:227505886
|
C | T | 1 | a0001c0001t0008g0018 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.262-14062C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505886 | ||||||
chr2:227505887
|
G | A | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.262-14061G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227505887 | ||||||
chr2:227506058
|
A | T | 2 | a0001c0002t0002g0284a0001c0002t0002g0294 | 2 | HG02572.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.262-13890A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506058 | ||||||
chr2:227506084
|
T | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.262-13864T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506084 | ||||||
chr2:227506183
|
T | C | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-13765T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506183 | ||||||
chr2:227506249
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.262-13699T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506249 | ||||||
chr2:227506333
|
A | T | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-13615A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506333 | ||||||
chr2:227506378
|
G | A | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.262-13570G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506378 | ||||||
chr2:227506466
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.262-13482C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506466 | ||||||
chr2:227506477
|
C | G | 1 | a0001c0003t0003g0065 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.262-13471C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506477 | ||||||
chr2:227506482
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.262-13466A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506482 | ||||||
chr2:227506536
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.262-13412A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506536 | ||||||
chr2:227506558
|
T | TA | 32 | a0001c0001t0005g0319a0001c0001t0016g0307a0001c0001t0016g0308others(29): Show | 33 | HG00738.hp2 HG01106.hp1 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.262-13369dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | |||||
chr2:227506558
|
T | TAA | 8 | a0001c0001t0001g0173a0001c0001t0001g0210a0001c0001t0017g0233others(5): Show | 8 | HG00438.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.262-13370_262-1336 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | |||||
chr2:227506558
|
T | TAAA | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 111 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.262-13371_262-1336 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | |||||
chr2:227506558
|
T | TAAAA | 43 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0119others(40): Show | 43 | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.262-13372_262-1336 others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | |||||
chr2:227506558
|
TA | T | 12 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(9): Show | 12 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.262-13369delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227506558 | |||||
chr2:227506630
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-13318G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506630 | ||||||
chr2:227506639
|
G | A | 1 | a0001c0002t0002g0301 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.262-13309G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506639 | ||||||
chr2:227506984
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.262-12964G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227506984 | ||||||
chr2:227507001
|
A | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(110): Show | 114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.262-12947A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507001 | ||||||
chr2:227507059
|
A | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-12889A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507059 | ||||||
chr2:227507076
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.262-12872A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507076 | ||||||
chr2:227507183
|
T | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0160 | 2 | HG01256.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.262-12765T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507183 | ||||||
chr2:227507323
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.262-12625A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507323 | ||||||
chr2:227507462
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.262-12486G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507462 | ||||||
chr2:227507463
|
C | T | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.262-12485C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507463 | ||||||
chr2:227507560
|
G | A | 1 | a0001c0002t0002g0252 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.262-12388G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507560 | ||||||
chr2:227507589
|
C | T | 1 | a0001c0004t0006g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.262-12359C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507589 | ||||||
chr2:227507590
|
G | A | 11 | a0001c0001t0005g0310a0001c0001t0005g0311a0001c0001t0005g0312others(8): Show | 11 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.262-12358G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507590 | ||||||
chr2:227507602
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.262-12322dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507602
|
C | CAA | 51 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(48): Show | 51 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.262-12323_262-1232 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507602
|
C | CAAA | 9 | a0001c0001t0001g0010a0001c0001t0001g0109a0001c0001t0001g0175others(6): Show | 9 | HG00423.hp2 HG00639.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.262-12324_262-1232 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507602
|
C | CAAAAAA | 21 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(18): Show | 21 | HG00099.hp1 HG01123.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.262-12327_262-1232 others(10): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507602
|
C | CAAAAAAA | 7 | a0001c0003t0003g0058a0001c0003t0003g0059a0001c0003t0003g0061others(4): Show | 7 | HG00423.hp1 HG00609.hp2 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.262-12328_262-1232 others(11): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507602
|
CA | C | 14 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0099others(11): Show | 14 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.262-12322delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507602
|
CAAAAAAA others(1): Show |
C | 19 | a0001c0004t0006g0001a0001c0004t0006g0031a0001c0004t0006g0033others(16): Show | 20 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.262-12329_262-1232 others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507602 | |||||
chr2:227507657
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.262-12291A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507657 | ||||||
chr2:227507760
|
G | GC | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-12187dupC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227507760 | |||||
chr2:227507870
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.262-12078A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227507870 | ||||||
chr2:227508002
|
CT | C | 47 | a0001c0001t0001g0112a0001c0002t0002g0005a0001c0002t0002g0013others(44): Show | 48 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.262-11933delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227508002 | |||||
chr2:227508175
|
A | G | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262-11773A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508175 | ||||||
chr2:227508192
|
C | G | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.262-11756C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508192 | ||||||
chr2:227508240
|
T | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-11708T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508240 | ||||||
chr2:227508339
|
T | A | 2 | a0001c0001t0023g0017a0001c0001t0023g0021 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.262-11609T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508339 | ||||||
chr2:227508353
|
A | T | 3 | a0001c0004t0006g0042a0001c0004t0006g0043a0001c0004t0006g0044 | 3 | HG00738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.262-11595A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508353 | ||||||
chr2:227508551
|
G | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.262-11397G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508551 | ||||||
chr2:227508688
|
A | AT | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(144): Show | 149 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.262-11247dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227508688 | |||||
chr2:227508899
|
C | T | 67 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(64): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.262-11049C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508899 | ||||||
chr2:227508967
|
G | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.262-10981G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227508967 | ||||||
chr2:227509254
|
T | G | 17 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(14): Show | 17 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-10694T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509254 | ||||||
chr2:227509528
|
A | C | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-10420A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509528 | ||||||
chr2:227509530
|
G | T | 1 | a0001c0002t0002g0272 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.262-10418G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509530 | ||||||
chr2:227509619
|
A | G | 4 | a0001c0002t0002g0013a0001c0002t0002g0264a0001c0002t0002g0266others(1): Show | 4 | NA18975.hp1 NA18980.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-10329A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509619 | ||||||
chr2:227509812
|
A | C | 10 | a0001c0004t0006g0031a0001c0004t0006g0042a0001c0004t0006g0043others(7): Show | 10 | HG00738.hp2 HG02129.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-10136A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509812 | ||||||
chr2:227509973
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-9975C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227509973 | ||||||
chr2:227510051
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.262-9897T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510051 | ||||||
chr2:227510071
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.262-9877A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510071 | ||||||
chr2:227510269
|
C | T | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.262-9679C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510269 | ||||||
chr2:227510311
|
C | T | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-9637C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510311 | ||||||
chr2:227510366
|
G | T | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-9582G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510366 | ||||||
chr2:227510532
|
GGAGGGGT | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-9412_262-9406d others(9): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227510532 | |||||
chr2:227510791
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.262-9157G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510791 | ||||||
chr2:227510892
|
A | T | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.262-9056A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510892 | ||||||
chr2:227510923
|
TC | T | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0104 | 3 | HG02572.hp1 HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.262-9024delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227510923 | ||||||
chr2:227511067
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.262-8881A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511067 | ||||||
chr2:227511261
|
A | G | 1 | a0001c0001t0001g0137 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.262-8687A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511261 | ||||||
chr2:227511322
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.262-8626T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511322 | ||||||
chr2:227511496
|
C | T | 1 | a0001c0002t0002g0285 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.262-8452C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511496 | ||||||
chr2:227511640
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.262-8308A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511640 | ||||||
chr2:227511865
|
A | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-8083A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227511865 | ||||||
chr2:227512028
|
T | C | 1 | a0001c0001t0008g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.262-7920T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512028 | ||||||
chr2:227512166
|
A | G | 1 | a0001c0003t0003g0068 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.262-7782A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512166 | ||||||
chr2:227512239
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.262-7709C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512239 | ||||||
chr2:227512382
|
A | G | 5 | a0001c0001t0005g0314a0001c0001t0005g0315a0001c0001t0005g0316others(2): Show | 5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.262-7566A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512382 | ||||||
chr2:227512403
|
C | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.262-7545C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512403 | ||||||
chr2:227512573
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-7375C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512573 | ||||||
chr2:227512578
|
A | G | 5 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 5 | NA18960.hp2 NA18975.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.262-7370A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512578 | ||||||
chr2:227512615
|
T | C | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-7333T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512615 | ||||||
chr2:227512632
|
G | T | 2 | a0001c0002t0002g0252a0001c0002t0002g0269 | 2 | NA18948.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.262-7316G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227512632 | ||||||
chr2:227513004
|
C | T | 3 | a0001c0004t0006g0042a0001c0004t0006g0043a0001c0004t0006g0044 | 3 | HG00738.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.262-6944C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513004 | ||||||
chr2:227513034
|
T | C | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.262-6914T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513034 | ||||||
chr2:227513197
|
G | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.262-6751G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513197 | ||||||
chr2:227513236
|
A | G | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(1): Show | 4 | HG00733.hp1 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.262-6712A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513236 | ||||||
chr2:227513357
|
G | A | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-6591G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513357 | ||||||
chr2:227513521
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.262-6427C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513521 | ||||||
chr2:227513556
|
A | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-6392A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513556 | ||||||
chr2:227513651
|
T | A | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-6297T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513651 | ||||||
chr2:227513829
|
T | C | 17 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(14): Show | 17 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-6119T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513829 | ||||||
chr2:227513986
|
G | A | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.262-5962G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227513986 | ||||||
chr2:227514142
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.262-5806T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514142 | ||||||
chr2:227514145
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(129): Show | 134 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.262-5803C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514145 | ||||||
chr2:227514304
|
C | T | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.262-5644C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514304 | ||||||
chr2:227514426
|
C | T | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-5522C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514426 | ||||||
chr2:227514506
|
T | G | 1 | a0001c0001t0019g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.262-5442T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514506 | ||||||
chr2:227514578
|
T | C | 2 | a0001c0001t0005g0082a0001c0001t0005g0309 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.262-5370T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514578 | ||||||
chr2:227514683
|
C | G | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-5265C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514683 | ||||||
chr2:227514784
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.262-5164A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227514784 | ||||||
chr2:227515005
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.262-4943C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515005 | ||||||
chr2:227515021
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-4927C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515021 | ||||||
chr2:227515160
|
A | G | 1 | a0001c0002t0002g0265 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.262-4788A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515160 | ||||||
chr2:227515178
|
C | T | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.262-4770C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515178 | ||||||
chr2:227515341
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.262-4607A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515341 | ||||||
chr2:227515489
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.262-4459A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515489 | ||||||
chr2:227515585
|
T | G | 1 | a0001c0002t0028g0303 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.262-4363T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515585 | ||||||
chr2:227515732
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.262-4216T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515732 | ||||||
chr2:227515966
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.262-3982C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227515966 | ||||||
chr2:227516087
|
T | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-3861T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516087 | ||||||
chr2:227516304
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.262-3644A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516304 | ||||||
chr2:227516317
|
T | C | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.262-3631T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516317 | ||||||
chr2:227516378
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0017g0233a0001c0001t0017g0235 | 3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.262-3570A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516378 | ||||||
chr2:227516392
|
T | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.262-3556T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516392 | ||||||
chr2:227516727
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.262-3221C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516727 | ||||||
chr2:227516860
|
G | C | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-3088G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227516860 | ||||||
chr2:227517134
|
C | G | 2 | a0001c0002t0002g0270a0001c0002t0002g0272 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.262-2814C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517134 | ||||||
chr2:227517147
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.262-2801A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517147 | ||||||
chr2:227517306
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 185 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(182): Show |
intron_variant | MODIFIER | c.262-2642A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517306 | ||||||
chr2:227517453
|
G | A | 1 | a0001c0001t0019g0167 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.262-2495G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517453 | ||||||
chr2:227517482
|
T | A | 1 | a0001c0002t0002g0288 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.262-2466T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517482 | ||||||
chr2:227517491
|
C | T | 1 | a0001c0001t0033g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.262-2457C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517491 | ||||||
chr2:227517512
|
C | T | 1 | a0001c0001t0010g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.262-2436C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517512 | ||||||
chr2:227517550
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.262-2398G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517550 | ||||||
chr2:227517574
|
A | G | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.262-2374A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517574 | ||||||
chr2:227517632
|
C | T | 1 | a0001c0001t0018g0024 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.262-2316C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517632 | ||||||
chr2:227517637
|
A | G | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186 | 3 | NA18943.hp2 NA19054.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.262-2311A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517637 | ||||||
chr2:227517696
|
C | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-2252C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517696 | ||||||
chr2:227517768
|
C | T | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.262-2180C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227517768 | ||||||
chr2:227518064
|
G | A | 2 | a0001c0001t0005g0313a0001c0001t0005g0322 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.262-1884G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518064 | ||||||
chr2:227518207
|
A | G | 1 | a0001c0002t0007g0084 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.262-1741A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518207 | ||||||
chr2:227518255
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.262-1693C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518255 | ||||||
chr2:227518287
|
G | A | 2 | a0001c0001t0004g0092a0001c0001t0038g0113 | 2 | HG03491.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.262-1661G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518287 | ||||||
chr2:227518306
|
A | G | 1 | a0001c0001t0008g0019 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.262-1642A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518306 | ||||||
chr2:227518413
|
GAATTCCG others(602): Show |
G | 1 | a0001c0001t0001g0138 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.262-1530_262-922de others(1): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518413 | |||||
chr2:227518469
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.262-1479G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518469 | ||||||
chr2:227518482
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.262-1466G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518482 | ||||||
chr2:227518516
|
C | CT | 25 | a0001c0001t0001g0003a0001c0001t0001g0107a0001c0001t0001g0111others(22): Show | 25 | HG00558.hp2 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.262-1409dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518516 | |||||
chr2:227518516
|
C | CTT | 10 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0018others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.262-1410_262-1409d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518516 | |||||
chr2:227518516
|
CT | C | 33 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0104others(30): Show | 34 | HG00423.hp1 HG00597.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.262-1409delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227518516 | |||||
chr2:227518528
|
T | C | 1 | a0001c0001t0038g0113 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.262-1420T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518528 | ||||||
chr2:227518540
|
A | C | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-1408A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518540 | ||||||
chr2:227518544
|
A | G | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.262-1404A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518544 | ||||||
chr2:227518604
|
A | G | 1 | a0001c0001t0004g0215 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.262-1344A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518604 | ||||||
chr2:227518609
|
C | T | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.262-1339C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518609 | ||||||
chr2:227518642
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.262-1306G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518642 | ||||||
chr2:227518681
|
G | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0111a0001c0001t0001g0126others(22): Show | 26 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.262-1267G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518681 | ||||||
chr2:227518746
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.262-1202G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518746 | ||||||
chr2:227518782
|
C | T | 67 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(64): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.262-1166C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518782 | ||||||
chr2:227518843
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.262-1105T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518843 | ||||||
chr2:227518874
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.262-1074C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518874 | ||||||
chr2:227518875
|
G | A | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.262-1073G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227518875 | ||||||
chr2:227519172
|
A | G | 2 | a0001c0002t0002g0282a0001c0002t0002g0283 | 2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.262-776A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519172 | ||||||
chr2:227519189
|
T | G | 10 | a0001c0002t0002g0255a0001c0002t0002g0256a0001c0002t0002g0257others(7): Show | 10 | HG01069.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.262-759T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519189 | ||||||
chr2:227519239
|
T | C | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.262-709T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519239 | ||||||
chr2:227519317
|
T | C | 2 | a0001c0003t0003g0060a0001c0003t0003g0071 | 2 | HG00423.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.262-631T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519317 | ||||||
chr2:227519598
|
T | C | 1 | a0001c0003t0013g0067 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.262-350T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | chr2 | 227519598 | ||||||
chr2:227519684
|
GCCAAGAC others(10): Show |
G | 2 | a0001c0001t0005g0082a0001c0001t0005g0309 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.262-260_262-244del others(17): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227519684 | |||||
chr2:227520207
|
T | C | 1 | a0001c0002t0002g0306 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.377+144T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520207 | ||||||
chr2:227520288
|
AC | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.377+227delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227520288 | |||||
chr2:227520366
|
G | A | 1 | a0001c0004t0006g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.377+303G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520366 | ||||||
chr2:227520678
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.377+615A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520678 | ||||||
chr2:227520801
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377+738T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520801 | ||||||
chr2:227520915
|
A | G | 1 | a0001c0002t0002g0257 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.377+852A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520915 | ||||||
chr2:227520917
|
G | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.377+854G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227520917 | ||||||
chr2:227521071
|
CT | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.377+1018delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227521071 | |||||
chr2:227521129
|
G | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.377+1066G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521129 | ||||||
chr2:227521188
|
C | G | 25 | a0001c0001t0001g0004a0001c0001t0001g0111a0001c0001t0001g0126others(22): Show | 26 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.377+1125C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521188 | ||||||
chr2:227521340
|
T | A | 1 | a0001c0001t0001g0162 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.377+1277T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521340 | ||||||
chr2:227521512
|
A | G | 1 | a0001c0002t0002g0290 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.377+1449A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521512 | ||||||
chr2:227521587
|
C | G | 1 | a0001c0001t0017g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.377+1524C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521587 | ||||||
chr2:227521769
|
T | C | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.377+1706T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521769 | ||||||
chr2:227521825
|
CA | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.377+1765delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227521825 | |||||
chr2:227521908
|
T | C | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.377+1845T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521908 | ||||||
chr2:227521926
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.378-1837G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227521926 | ||||||
chr2:227522109
|
T | C | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.378-1654T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522109 | ||||||
chr2:227522224
|
A | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.378-1539A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522224 | ||||||
chr2:227522473
|
A | T | 1 | a0001c0001t0004g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.378-1290A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522473 | ||||||
chr2:227522482
|
G | A | 11 | a0001c0001t0005g0310a0001c0001t0005g0311a0001c0001t0005g0312others(8): Show | 11 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.378-1281G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522482 | ||||||
chr2:227522649
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.378-1114A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227522649 | ||||||
chr2:227523074
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.378-689C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523074 | ||||||
chr2:227523075
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.378-688A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523075 | ||||||
chr2:227523083
|
A | G | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.378-680A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523083 | ||||||
chr2:227523601
|
C | T | 1 | a0001c0001t0040g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.378-162C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523601 | ||||||
chr2:227523678
|
G | C | 1 | a0001c0001t0012g0194 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.378-85G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523678 | ||||||
chr2:227523742
|
A | G | 1 | a0001c0001t0004g0133 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.378-21A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 3/12 | chr2 | 227523742 | ||||||
chr2:227524079
|
G | T | 11 | a0001c0001t0005g0310a0001c0001t0005g0311a0001c0001t0005g0312others(8): Show | 11 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.540+154G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524079 | ||||||
chr2:227524105
|
T | C | 2 | a0001c0001t0021g0237a0001c0001t0021g0238 | 2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.540+180T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524105 | ||||||
chr2:227524155
|
GGTGAGTT | G | 6 | a0001c0004t0009g0036a0001c0004t0009g0037a0001c0004t0009g0038others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+231_540+237del others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524155 | ||||||
chr2:227524163
|
A | C | 6 | a0001c0004t0009g0036a0001c0004t0009g0037a0001c0004t0009g0038others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+238A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524163 | ||||||
chr2:227524164
|
T | A | 6 | a0001c0004t0009g0036a0001c0004t0009g0037a0001c0004t0009g0038others(3): Show | 6 | HG02615.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+239T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524164 | ||||||
chr2:227524292
|
AC | A | 23 | a0001c0001t0041g0081a0001c0003t0003g0060a0001c0003t0003g0071others(20): Show | 24 | HG00423.hp1 HG00738.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.540+368delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524292 | ||||||
chr2:227524388
|
A | C | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.541-374A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 4/12 | chr2 | 227524388 | ||||||
chr2:227524963
|
C | G | 1 | a0001c0001t0016g0308 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.694+48C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227524963 | ||||||
chr2:227524988
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.694+73A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227524988 | ||||||
chr2:227525095
|
A | ATTATATT others(2106): Show |
2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.694+347_694+348ins others(2113): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227525095 | |||||
chr2:227525263
|
G | C | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(216): Show | 222 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.694+348G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525263 | ||||||
chr2:227525370
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 186 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.694+455T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525370 | ||||||
chr2:227525470
|
A | G | 1 | a0001c0001t0026g0231 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.694+555A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525470 | ||||||
chr2:227525474
|
G | A | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.694+559G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525474 | ||||||
chr2:227525544
|
G | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.694+629G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525544 | ||||||
chr2:227525800
|
C | G | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+885C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525800 | ||||||
chr2:227525969
|
T | G | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+1054T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525969 | ||||||
chr2:227525987
|
T | C | 23 | a0001c0001t0041g0081a0001c0003t0003g0060a0001c0003t0003g0071others(20): Show | 24 | HG00423.hp1 HG00738.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.694+1072T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227525987 | ||||||
chr2:227526286
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 188 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.694+1371T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526286 | ||||||
chr2:227526360
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.694+1445T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526360 | ||||||
chr2:227526406
|
T | TTTTTTAT others(318): Show |
12 | a0001c0003t0003g0060a0001c0003t0003g0071a0001c0004t0006g0031others(9): Show | 12 | HG00423.hp1 HG00738.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.694+1501_694+1502i others(327): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | |||||
chr2:227526406
|
T | TTTTTTAT others(321): Show |
2 | a0001c0004t0009g0037a0001c0004t0009g0041 | 2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694+1501_694+1502i others(330): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | |||||
chr2:227526406
|
T | TTTTTTAT others(319): Show |
1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.694+1501_694+1502i others(328): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | |||||
chr2:227526406
|
T | TTTTTTAT others(318): Show |
3 | a0001c0004t0006g0001a0001c0004t0006g0033a0001c0004t0006g0034 | 4 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+1501_694+1502i others(327): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | |||||
chr2:227526406
|
T | TTTTTTAT others(319): Show |
1 | a0001c0004t0006g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.694+1501_694+1502i others(328): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | |||||
chr2:227526406
|
T | TTTTTTAT others(321): Show |
4 | a0001c0004t0009g0036a0001c0004t0009g0038a0001c0004t0009g0039others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.694+1501_694+1502i others(330): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526406 | |||||
chr2:227526485
|
A | G | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694+1570A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526485 | ||||||
chr2:227526518
|
A | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.694+1603A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526518 | ||||||
chr2:227526539
|
C | CT | 48 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0107others(45): Show | 50 | HG00438.hp1 HG00597.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.694+1645dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526539 | |||||
chr2:227526539
|
C | CTT | 16 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(13): Show | 16 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.694+1644_694+1645d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526539 | |||||
chr2:227526539
|
CT | C | 66 | a0001c0001t0001g0142a0001c0001t0004g0197a0001c0002t0002g0005others(63): Show | 68 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.694+1645delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227526539 | |||||
chr2:227526736
|
G | A | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.694+1821G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526736 | ||||||
chr2:227526763
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.694+1848C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227526763 | ||||||
chr2:227527036
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.694+2121T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527036 | ||||||
chr2:227527054
|
A | G | 7 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(4): Show | 7 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.694+2139A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527054 | ||||||
chr2:227527370
|
C | T | 5 | a0001c0003t0003g0058a0001c0003t0003g0066a0001c0003t0013g0067others(2): Show | 5 | NA18943.hp1 NA18944.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+2455C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527370 | ||||||
chr2:227527382
|
T | C | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.694+2467T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527382 | ||||||
chr2:227527482
|
A | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.694+2567A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527482 | ||||||
chr2:227527498
|
C | T | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.694+2583C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527498 | ||||||
chr2:227527776
|
G | A | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.694+2861G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527776 | ||||||
chr2:227527806
|
T | C | 5 | a0001c0001t0005g0314a0001c0001t0005g0315a0001c0001t0005g0316others(2): Show | 5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.694+2891T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527806 | ||||||
chr2:227527914
|
C | G | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.694+2999C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227527914 | ||||||
chr2:227528115
|
C | G | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.695-2976C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528115 | ||||||
chr2:227528125
|
A | G | 2 | a0001c0001t0023g0017a0001c0001t0023g0021 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.695-2966A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528125 | ||||||
chr2:227528369
|
C | T | 1 | a0001c0002t0002g0251 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.695-2722C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528369 | ||||||
chr2:227528406
|
A | T | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.695-2685A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528406 | ||||||
chr2:227528452
|
C | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 153 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.695-2639C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528452 | ||||||
chr2:227528567
|
T | C | 1 | a0001c0001t0011g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.695-2524T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528567 | ||||||
chr2:227528674
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.695-2417T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528674 | ||||||
chr2:227528772
|
T | C | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.695-2319T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528772 | ||||||
chr2:227528821
|
T | C | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.695-2270T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227528821 | ||||||
chr2:227529107
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.695-1984C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529107 | ||||||
chr2:227529208
|
T | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 203 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(200): Show |
intron_variant | MODIFIER | c.695-1883T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529208 | ||||||
chr2:227529270
|
T | A | 1 | a0001c0001t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.695-1821T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529270 | ||||||
chr2:227529289
|
C | A | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.695-1802C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529289 | ||||||
chr2:227529341
|
T | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.695-1750T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529341 | ||||||
chr2:227529342
|
A | T | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.695-1749A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529342 | ||||||
chr2:227529351
|
T | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.695-1740T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529351 | ||||||
chr2:227529425
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.695-1666A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529425 | ||||||
chr2:227529444
|
G | A | 1 | a0001c0001t0033g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695-1647G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227529444 | ||||||
chr2:227530009
|
G | A | 1 | a0001c0003t0003g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.695-1082G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530009 | ||||||
chr2:227530290
|
G | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.695-801G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530290 | ||||||
chr2:227530392
|
A | G | 3 | a0001c0001t0001g0225a0001c0001t0017g0233a0001c0001t0017g0235 | 3 | HG03209.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.695-699A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530392 | ||||||
chr2:227530636
|
AT | A | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.695-453delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227530636 | |||||
chr2:227530663
|
AAGTATTT others(18): Show |
A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.695-426_695-402del others(25): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227530663 | |||||
chr2:227530856
|
G | A | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.695-235G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530856 | ||||||
chr2:227530932
|
C | A | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.695-159C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 5/12 | chr2 | 227530932 | ||||||
chr2:227531312
|
C | A | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.814+102C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531312 | ||||||
chr2:227531495
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.814+285A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531495 | ||||||
chr2:227531521
|
G | GTC | 4 | a0001c0004t0006g0001a0001c0004t0006g0033a0001c0004t0006g0034others(1): Show | 5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.814+315_814+316dup others(2): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531521 | |||||
chr2:227531525
|
C | CT | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.814+330dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531525 | |||||
chr2:227531525
|
C | CTT | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(32): Show | 35 | HG00558.hp2 HG00642.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.814+329_814+330dup others(2): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531525 | |||||
chr2:227531526
|
T | TC | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0229 | 3 | HG03017.hp2 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.814+316_814+317ins others(1): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531526 | ||||||
chr2:227531596
|
A | AT | 11 | a0001c0001t0005g0314a0001c0004t0006g0031a0001c0004t0006g0042others(8): Show | 11 | HG00738.hp2 HG01515.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.814+402dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531596 | |||||
chr2:227531596
|
AT | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 159 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.814+402delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227531596 | |||||
chr2:227531620
|
G | T | 1 | a0001c0001t0018g0025 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.814+410G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531620 | ||||||
chr2:227531795
|
A | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.814+585A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531795 | ||||||
chr2:227531933
|
G | C | 1 | a0001c0001t0001g0165 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.814+723G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227531933 | ||||||
chr2:227532050
|
C | G | 2 | a0001c0001t0005g0082a0001c0001t0005g0309 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.814+840C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532050 | ||||||
chr2:227532168
|
T | C | 1 | a0001c0001t0032g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.814+958T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532168 | ||||||
chr2:227532287
|
G | A | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.814+1077G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532287 | ||||||
chr2:227532383
|
A | G | 1 | a0001c0004t0009g0041 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.815-1166A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532383 | ||||||
chr2:227532585
|
A | G | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.815-964A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532585 | ||||||
chr2:227532610
|
C | G | 1 | a0001c0001t0021g0237 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.815-939C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532610 | ||||||
chr2:227532850
|
T | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(110): Show | 114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.815-699T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532850 | ||||||
chr2:227532878
|
A | G | 1 | a0001c0002t0002g0013 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.815-671A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532878 | ||||||
chr2:227532914
|
AATGT | A | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.815-632_815-629del others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227532914 | |||||
chr2:227532925
|
T | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(67): Show | 71 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.815-624T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227532925 | ||||||
chr2:227533285
|
A | AC | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 188 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.815-260dupC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 227533285 | |||||
chr2:227533355
|
C | T | 1 | a0001c0001t0004g0115 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.815-194C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227533355 | ||||||
chr2:227533386
|
T | C | 1 | a0001c0002t0002g0247 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.815-163T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227533386 | ||||||
chr2:227533510
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.815-39A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 6/12 | chr2 | 227533510 | ||||||
chr2:227533864
|
A | G | 1 | a0001c0001t0025g0224 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1024+106A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227533864 | ||||||
chr2:227534039
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1024+281T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534039 | ||||||
chr2:227534112
|
G | A | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1024+354G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534112 | ||||||
chr2:227534152
|
T | A | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1024+394T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534152 | ||||||
chr2:227534385
|
A | G | 1 | a0001c0001t0040g0140 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1025-460A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534385 | ||||||
chr2:227534696
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1025-149G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534696 | ||||||
chr2:227534764
|
T | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1025-81T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534764 | ||||||
chr2:227534827
|
G | A | 2 | a0001c0001t0001g0178a0001c0001t0001g0204 | 2 | NA19085.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1025-18G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 7/12 | chr2 | 227534827 | ||||||
chr2:227535369
|
T | C | 2 | a0001c0001t0005g0313a0001c0001t0005g0322 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1205+344T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535369 | ||||||
chr2:227535461
|
C | A | 1 | a0001c0002t0002g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1205+436C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535461 | ||||||
chr2:227535737
|
G | A | 63 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(60): Show | 64 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1205+712G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535737 | ||||||
chr2:227535861
|
C | T | 13 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1206-764C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227535861 | ||||||
chr2:227536051
|
G | A | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206-574G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536051 | ||||||
chr2:227536062
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-563C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536062 | ||||||
chr2:227536169
|
A | AC | 5 | a0001c0004t0006g0001a0001c0004t0006g0033a0001c0004t0006g0047others(2): Show | 6 | HG02451.hp1 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1206-456_1206-455i others(3): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536169 | ||||||
chr2:227536170
|
G | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-455G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536170 | ||||||
chr2:227536322
|
T | C | 1 | a0001c0001t0033g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1206-303T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536322 | ||||||
chr2:227536377
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-248A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536377 | ||||||
chr2:227536579
|
T | C | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1206-46T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | chr2 | 227536579 | ||||||
chr2:227536590
|
GA | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206-27delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 227536590 | |||||
chr2:227537494
|
A | G | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1378+501A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537494 | ||||||
chr2:227537546
|
T | C | 5 | a0001c0001t0001g0119a0001c0001t0001g0142a0001c0001t0001g0148others(2): Show | 5 | HG00558.hp1 HG02135.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+553T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537546 | ||||||
chr2:227537569
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378+576C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537569 | ||||||
chr2:227537673
|
T | C | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1378+680T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537673 | ||||||
chr2:227537725
|
A | G | 2 | a0001c0001t0020g0146a0001c0001t0020g0164 | 2 | HG02015.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1378+732A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537725 | ||||||
chr2:227537910
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+917A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537910 | ||||||
chr2:227537979
|
G | C | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1378+986G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227537979 | ||||||
chr2:227538099
|
A | G | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+1106A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538099 | ||||||
chr2:227538121
|
G | A | 20 | a0001c0003t0003g0057a0001c0003t0003g0058a0001c0003t0003g0059others(17): Show | 20 | HG00423.hp1 HG00609.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1378+1128G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538121 | ||||||
chr2:227538457
|
G | T | 1 | a0001c0004t0006g0045 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1378+1464G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538457 | ||||||
chr2:227538469
|
T | C | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1378+1476T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538469 | ||||||
chr2:227538535
|
C | A | 1 | a0001c0001t0001g0009 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1378+1542C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538535 | ||||||
chr2:227538622
|
G | A | 3 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028 | 3 | HG02896.hp1 HG02897.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1378+1629G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538622 | ||||||
chr2:227538839
|
A | G | 1 | a0001c0002t0002g0297 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1378+1846A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538839 | ||||||
chr2:227538863
|
C | G | 2 | a0001c0001t0030g0243a0001c0001t0031g0193 | 2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1378+1870C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227538863 | ||||||
chr2:227539087
|
A | G | 67 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(64): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1378+2094A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539087 | ||||||
chr2:227539226
|
T | A | 1 | a0001c0003t0003g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1378+2233T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539226 | ||||||
chr2:227539289
|
A | T | 1 | a0001c0001t0001g0186 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1378+2296A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539289 | ||||||
chr2:227539442
|
C | CAAAAAAA | 19 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(16): Show | 20 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.1378+2451_1378+245 others(11): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539442 | |||||
chr2:227539451
|
C | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1378+2458C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539451 | ||||||
chr2:227539457
|
A | AAAAAAAA others(3): Show |
3 | a0001c0001t0001g0221a0001c0001t0011g0232a0001c0001t0015g0239 | 3 | HG03471.hp1 NA18522.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1378+2464_1378+246 others(14): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539457 | ||||||
chr2:227539457
|
A | AAAAAAAA others(2): Show |
36 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0100others(33): Show | 36 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.1378+2464_1378+246 others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539457 | ||||||
chr2:227539457
|
A | AAAAAAAA others(1): Show |
122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 124 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1378+2464_1378+246 others(12): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539457 | ||||||
chr2:227539521
|
G | A | 20 | a0001c0003t0003g0057a0001c0003t0003g0058a0001c0003t0003g0059others(17): Show | 20 | HG00423.hp1 HG00609.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1378+2528G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539521 | ||||||
chr2:227539665
|
A | T | 5 | a0001c0003t0003g0059a0001c0003t0003g0062a0001c0003t0003g0064others(2): Show | 5 | HG01123.hp2 HG01934.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+2672A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539665 | ||||||
chr2:227539746
|
C | CA | 57 | a0001c0001t0001g0009a0001c0001t0001g0122a0001c0001t0001g0128others(54): Show | 57 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.1378+2775dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | |||||
chr2:227539746
|
CA | C | 35 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(32): Show | 35 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1378+2775delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | |||||
chr2:227539746
|
CAA | C | 9 | a0001c0004t0006g0031a0001c0004t0006g0042a0001c0004t0006g0043others(6): Show | 9 | HG02129.hp1 HG02615.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.1378+2774_1378+277 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | |||||
chr2:227539746
|
CAAA | C | 11 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0033others(8): Show | 12 | HG02109.hp2 HG02135.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+2773_1378+277 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227539746 | |||||
chr2:227539747
|
A | C | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1378+2754A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539747 | ||||||
chr2:227539851
|
T | C | 8 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0018others(5): Show | 8 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+2858T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539851 | ||||||
chr2:227539913
|
G | A | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+2920G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227539913 | ||||||
chr2:227540113
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1378+3120G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540113 | ||||||
chr2:227540197
|
G | GT | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1378+3218dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227540197 | |||||
chr2:227540260
|
T | G | 1 | a0001c0003t0003g0053 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1378+3267T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540260 | ||||||
chr2:227540288
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1378+3295C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540288 | ||||||
chr2:227540341
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1378+3348C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540341 | ||||||
chr2:227540369
|
C | T | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1378+3376C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540369 | ||||||
chr2:227540392
|
G | C | 1 | a0001c0001t0001g0153 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1378+3399G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540392 | ||||||
chr2:227540454
|
T | C | 4 | a0001c0004t0006g0001a0001c0004t0006g0033a0001c0004t0006g0034others(1): Show | 5 | HG02109.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+3461T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540454 | ||||||
chr2:227540465
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1378+3472G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540465 | ||||||
chr2:227540641
|
T | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3648T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540641 | ||||||
chr2:227540654
|
G | A | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3661G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540654 | ||||||
chr2:227540670
|
C | G | 8 | a0001c0002t0002g0282a0001c0002t0002g0283a0001c0002t0002g0284others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1378+3677C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540670 | ||||||
chr2:227540701
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0189 | 2 | HG00642.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+3708G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540701 | ||||||
chr2:227540774
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1378+3781G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540774 | ||||||
chr2:227540991
|
T | C | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3998T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540991 | ||||||
chr2:227540992
|
G | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+3999G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227540992 | ||||||
chr2:227541022
|
C | T | 1 | a0001c0004t0006g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1378+4029C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541022 | ||||||
chr2:227541042
|
T | G | 1 | a0001c0001t0017g0233 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1378+4049T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541042 | ||||||
chr2:227541084
|
C | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+4091C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541084 | ||||||
chr2:227541248
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1378+4255T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541248 | ||||||
chr2:227541285
|
A | G | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1378+4292A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541285 | ||||||
chr2:227541491
|
T | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(214): Show | 220 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.1378+4498T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541491 | ||||||
chr2:227541516
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG02132.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1378+4523A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541516 | ||||||
chr2:227541619
|
T | A | 2 | a0001c0003t0003g0058a0001c0003t0003g0066 | 2 | NA18947.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1378+4626T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541619 | ||||||
chr2:227541668
|
T | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1378+4675T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541668 | ||||||
chr2:227541677
|
A | T | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1378+4684A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541677 | ||||||
chr2:227541694
|
C | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1378+4701C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541694 | ||||||
chr2:227541820
|
A | G | 1 | a0001c0001t0011g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1378+4827A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541820 | ||||||
chr2:227541885
|
G | T | 15 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1378+4892G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541885 | ||||||
chr2:227541987
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1378+4994G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541987 | ||||||
chr2:227541990
|
C | G | 5 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+4997C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227541990 | ||||||
chr2:227542248
|
A | T | 1 | a0001c0003t0003g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1378+5255A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542248 | ||||||
chr2:227542298
|
C | T | 2 | a0001c0001t0011g0230a0001c0001t0026g0231 | 2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1378+5305C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542298 | ||||||
chr2:227542314
|
T | A | 1 | a0001c0002t0002g0291 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1378+5321T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542314 | ||||||
chr2:227542389
|
A | T | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1378+5396A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542389 | ||||||
chr2:227542404
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1378+5411A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542404 | ||||||
chr2:227542439
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0105 | 3 | HG01109.hp2 HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1378+5446C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542439 | ||||||
chr2:227542528
|
A | G | 59 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(56): Show | 61 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1378+5535A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542528 | ||||||
chr2:227542886
|
GTGT | G | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.1378+5897_1378+589 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227542886 | |||||
chr2:227542948
|
G | A | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1378+5955G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542948 | ||||||
chr2:227542984
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 184 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.1378+5991C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227542984 | ||||||
chr2:227543077
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1378+6084G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543077 | ||||||
chr2:227543089
|
G | A | 1 | a0001c0002t0002g0266 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1378+6096G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543089 | ||||||
chr2:227543222
|
T | C | 5 | a0001c0002t0002g0006a0001c0002t0002g0246a0001c0002t0002g0247others(2): Show | 6 | HG00408.hp2 NA18950.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+6229T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543222 | ||||||
chr2:227543228
|
A | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.1378+6235A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543228 | ||||||
chr2:227543421
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1378+6428T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543421 | ||||||
chr2:227543529
|
A | C | 5 | a0001c0001t0005g0314a0001c0001t0005g0315a0001c0001t0005g0316others(2): Show | 5 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1378+6536A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543529 | ||||||
chr2:227543622
|
G | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0118a0001c0001t0001g0122others(20): Show | 24 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1378+6629G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543622 | ||||||
chr2:227543664
|
A | G | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+6671A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543664 | ||||||
chr2:227543776
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1378+6783T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543776 | ||||||
chr2:227543839
|
C | CTGT | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 161 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1378+6847_1378+684 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227543839 | |||||
chr2:227543851
|
C | CAT | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1378+6865_1378+686 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227543851 | |||||
chr2:227543935
|
T | G | 1 | a0001c0002t0002g0300 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1378+6942T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543935 | ||||||
chr2:227543964
|
T | G | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1378+6971T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543964 | ||||||
chr2:227543987
|
A | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1378+6994A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543987 | ||||||
chr2:227543997
|
C | A | 1 | a0001c0001t0041g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1378+7004C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227543997 | ||||||
chr2:227544146
|
C | CT | 6 | a0001c0002t0002g0008a0001c0002t0002g0249a0001c0002t0002g0272others(3): Show | 6 | HG01255.hp1 HG02071.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+7179dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | |||||
chr2:227544146
|
CT | C | 72 | a0001c0001t0005g0320a0001c0001t0005g0321a0001c0001t0008g0014others(69): Show | 73 | HG00423.hp1 HG00609.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1378+7179delT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | |||||
chr2:227544146
|
CTT | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0095a0001c0001t0001g0097others(15): Show | 18 | HG00099.hp1 HG00423.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1378+7178_1378+717 others(6): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | |||||
chr2:227544146
|
CTTT | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(138): Show | 143 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1378+7177_1378+717 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | |||||
chr2:227544146
|
CTTTT | C | 6 | a0001c0001t0001g0102a0001c0001t0001g0190a0001c0001t0001g0200others(3): Show | 6 | HG01081.hp1 HG01515.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1378+7176_1378+717 others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227544146 | |||||
chr2:227544178
|
G | A | 5 | a0001c0001t0001g0119a0001c0001t0001g0142a0001c0001t0001g0148others(2): Show | 5 | HG00558.hp1 HG02135.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+7185G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544178 | ||||||
chr2:227544216
|
G | A | 2 | a0001c0003t0003g0053a0001c0003t0003g0054 | 2 | HG01952.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1378+7223G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544216 | ||||||
chr2:227544290
|
G | C | 1 | a0001c0004t0006g0047 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1378+7297G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544290 | ||||||
chr2:227544368
|
A | T | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1378+7375A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544368 | ||||||
chr2:227544376
|
G | A | 5 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(2): Show | 5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1378+7383G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544376 | ||||||
chr2:227544384
|
G | A | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1378+7391G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544384 | ||||||
chr2:227544546
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-7413C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544546 | ||||||
chr2:227544559
|
G | A | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1379-7400G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544559 | ||||||
chr2:227544666
|
C | G | 1 | a0001c0002t0002g0297 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1379-7293C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544666 | ||||||
chr2:227544825
|
C | A | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1379-7134C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544825 | ||||||
chr2:227544863
|
C | T | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-7096C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544863 | ||||||
chr2:227544941
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1379-7018G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227544941 | ||||||
chr2:227545077
|
C | T | 2 | a0001c0003t0003g0060a0001c0003t0003g0071 | 2 | HG00423.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1379-6882C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545077 | ||||||
chr2:227545078
|
G | A | 15 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(12): Show | 15 | HG00642.hp1 HG01109.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1379-6881G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545078 | ||||||
chr2:227545091
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1379-6868A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545091 | ||||||
chr2:227545253
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-6706C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545253 | ||||||
chr2:227545286
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1379-6673T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545286 | ||||||
chr2:227545328
|
C | T | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-6631C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545328 | ||||||
chr2:227545742
|
G | A | 2 | a0001c0001t0005g0320a0001c0001t0005g0321 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1379-6217G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545742 | ||||||
chr2:227545781
|
A | G | 5 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(2): Show | 5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-6178A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545781 | ||||||
chr2:227545933
|
C | T | 5 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(2): Show | 5 | HG00639.hp2 HG02647.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1379-6026C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545933 | ||||||
chr2:227545940
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-6019C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227545940 | ||||||
chr2:227546098
|
C | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.1379-5861C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546098 | ||||||
chr2:227546128
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1379-5831C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546128 | ||||||
chr2:227546198
|
G | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0118a0001c0001t0001g0122others(19): Show | 23 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1379-5761G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546198 | ||||||
chr2:227546201
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1379-5758C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546201 | ||||||
chr2:227546220
|
C | T | 32 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(29): Show | 32 | HG00639.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1379-5739C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546220 | ||||||
chr2:227546289
|
G | A | 1 | a0001c0001t0019g0203 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1379-5670G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546289 | ||||||
chr2:227546297
|
C | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-5662C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546297 | ||||||
chr2:227546320
|
C | T | 1 | a0001c0002t0002g0297 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1379-5639C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546320 | ||||||
chr2:227546327
|
T | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1379-5632T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546327 | ||||||
chr2:227546441
|
G | A | 2 | a0001c0002t0002g0253a0001c0002t0002g0254 | 2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1379-5518G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546441 | ||||||
chr2:227546471
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1379-5488T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546471 | ||||||
chr2:227546480
|
G | A | 1 | a0001c0001t0001g0137 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1379-5479G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546480 | ||||||
chr2:227546595
|
C | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 152 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.1379-5364C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546595 | ||||||
chr2:227546596
|
G | A | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1379-5363G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546596 | ||||||
chr2:227546640
|
T | G | 2 | a0001c0002t0002g0270a0001c0002t0002g0272 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1379-5319T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546640 | ||||||
chr2:227546943
|
C | T | 67 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(64): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1379-5016C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546943 | ||||||
chr2:227546958
|
T | G | 1 | a0001c0002t0002g0257 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1379-5001T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227546958 | ||||||
chr2:227547016
|
A | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1379-4943A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547016 | ||||||
chr2:227547019
|
C | T | 1 | a0001c0004t0006g0035 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1379-4940C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547019 | ||||||
chr2:227547038
|
A | G | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02055.hp1 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1379-4921A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547038 | ||||||
chr2:227547067
|
A | T | 1 | a0001c0001t0005g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1379-4892A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547067 | ||||||
chr2:227547346
|
TC | T | 8 | a0001c0002t0007g0084a0001c0002t0007g0085a0001c0002t0007g0086others(5): Show | 8 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1379-4610delC | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227547346 | |||||
chr2:227547397
|
A | G | 1 | a0001c0001t0032g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-4562A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547397 | ||||||
chr2:227547552
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-4407G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547552 | ||||||
chr2:227547574
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1379-4385A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547574 | ||||||
chr2:227547582
|
C | T | 19 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(16): Show | 19 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1379-4377C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547582 | ||||||
chr2:227547668
|
G | A | 2 | a0001c0005t0014g0022a0001c0005t0014g0023 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1379-4291G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547668 | ||||||
chr2:227547869
|
G | C | 4 | a0001c0001t0011g0091a0001c0001t0011g0230a0001c0001t0011g0232others(1): Show | 4 | HG00639.hp2 HG02647.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1379-4090G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547869 | ||||||
chr2:227547916
|
T | C | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1379-4043T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227547916 | ||||||
chr2:227548081
|
G | A | 17 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(14): Show | 17 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1379-3878G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548081 | ||||||
chr2:227548106
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1379-3853T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548106 | ||||||
chr2:227548111
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1379-3848A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548111 | ||||||
chr2:227548195
|
TG | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1379-3761delG | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227548195 | |||||
chr2:227548217
|
A | G | 2 | a0001c0001t0001g0139a0001c0001t0001g0141 | 2 | HG02015.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1379-3742A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548217 | ||||||
chr2:227548237
|
G | A | 1 | a0001c0001t0008g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1379-3722G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548237 | ||||||
chr2:227548241
|
A | G | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-3718A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548241 | ||||||
chr2:227548280
|
C | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1379-3679C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548280 | ||||||
chr2:227548426
|
G | A | 17 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(14): Show | 17 | HG00639.hp1 HG01081.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1379-3533G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548426 | ||||||
chr2:227548660
|
G | A | 1 | a0001c0004t0006g0049 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1379-3299G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548660 | ||||||
chr2:227548669
|
G | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(159): Show | 164 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1379-3290G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548669 | ||||||
chr2:227548686
|
C | T | 1 | a0001c0001t0033g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1379-3273C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548686 | ||||||
chr2:227548713
|
G | A | 1 | a0001c0001t0032g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-3246G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548713 | ||||||
chr2:227548764
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1379-3195C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548764 | ||||||
chr2:227548765
|
G | A | 1 | a0001c0001t0004g0196 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1379-3194G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548765 | ||||||
chr2:227548773
|
T | C | 1 | a0001c0004t0006g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1379-3186T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548773 | ||||||
chr2:227548853
|
C | T | 1 | a0001c0002t0002g0245 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1379-3106C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548853 | ||||||
chr2:227548932
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1379-3027G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227548932 | ||||||
chr2:227549011
|
C | CT | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 163 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1379-2937dupT | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227549011 | |||||
chr2:227549127
|
C | T | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1379-2832C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549127 | ||||||
chr2:227549238
|
C | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02257.hp2 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1379-2721C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549238 | ||||||
chr2:227549315
|
A | G | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1379-2644A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549315 | ||||||
chr2:227549629
|
A | G | 1 | a0001c0002t0007g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1379-2330A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549629 | ||||||
chr2:227549643
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1379-2316A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549643 | ||||||
chr2:227549667
|
T | G | 1 | a0001c0001t0001g0221 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1379-2292T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549667 | ||||||
chr2:227549773
|
G | A | 13 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(10): Show | 13 | HG01109.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1379-2186G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549773 | ||||||
chr2:227549803
|
T | A | 3 | a0001c0003t0003g0050a0001c0003t0003g0068a0001c0003t0003g0069 | 3 | HG00099.hp1 HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1379-2156T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549803 | ||||||
chr2:227549901
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1379-2058T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549901 | ||||||
chr2:227549989
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1379-1970G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227549989 | ||||||
chr2:227550071
|
C | G | 1 | a0001c0001t0001g0205 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1379-1888C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550071 | ||||||
chr2:227550258
|
A | G | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1379-1701A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550258 | ||||||
chr2:227550498
|
C | T | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1379-1461C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550498 | ||||||
chr2:227550532
|
TGTC | T | 9 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(6): Show | 9 | HG00099.hp1 HG01952.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.1379-1423_1379-142 others(7): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227550532 | |||||
chr2:227550764
|
A | G | 1 | a0001c0001t0017g0233 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1379-1195A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550764 | ||||||
chr2:227550810
|
C | T | 1 | a0001c0001t0019g0167 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1379-1149C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550810 | ||||||
chr2:227550887
|
G | T | 2 | a0001c0002t0002g0270a0001c0002t0002g0272 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1379-1072G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227550887 | ||||||
chr2:227551044
|
A | G | 1 | a0001c0001t0031g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1379-915A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551044 | ||||||
chr2:227551093
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1379-866C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551093 | ||||||
chr2:227551279
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1379-680C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551279 | ||||||
chr2:227551459
|
A | G | 1 | a0001c0002t0002g0301 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1379-500A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551459 | ||||||
chr2:227551468
|
A | G | 1 | a0001c0002t0022g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1379-491A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551468 | ||||||
chr2:227551512
|
A | T | 21 | a0001c0001t0041g0081a0001c0004t0006g0001a0001c0004t0006g0031others(18): Show | 22 | HG00738.hp2 HG02109.hp2 HG02129.hp1 others(19): Show |
intron_variant | MODIFIER | c.1379-447A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551512 | ||||||
chr2:227551558
|
G | T | 1 | a0001c0001t0032g0093 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1379-401G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551558 | ||||||
chr2:227551782
|
C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(178): Show | 184 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.1379-177C>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 10/12 | chr2 | 227551782 | ||||||
chr2:227552145
|
A | C | 2 | a0001c0001t0016g0307a0001c0001t0016g0308 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1537+28A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552145 | ||||||
chr2:227552295
|
A | T | 15 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(12): Show | 15 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1537+178A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552295 | ||||||
chr2:227552466
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1537+349T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552466 | ||||||
chr2:227552557
|
T | G | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1537+440T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552557 | ||||||
chr2:227552740
|
G | T | 1 | a0001c0002t0002g0284 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1537+623G>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552740 | ||||||
chr2:227552827
|
C | A | 22 | a0001c0001t0001g0002a0001c0001t0001g0118a0001c0001t0001g0122others(19): Show | 23 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1537+710C>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552827 | ||||||
chr2:227552853
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1537+736T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552853 | ||||||
chr2:227552862
|
G | A | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1537+745G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552862 | ||||||
chr2:227552957
|
G | A | 2 | a0001c0001t0015g0239a0001c0001t0015g0240 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1538-747G>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552957 | ||||||
chr2:227552987
|
T | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.1538-717T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227552987 | ||||||
chr2:227553000
|
C | CA | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1538-683dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | |||||
chr2:227553000
|
C | CAA | 28 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0171others(25): Show | 29 | HG00621.hp1 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1538-684_1538-683d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | |||||
chr2:227553000
|
C | CAAA | 16 | a0001c0001t0005g0082a0001c0001t0005g0309a0001c0001t0005g0310others(13): Show | 16 | HG00733.hp2 HG00741.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1538-685_1538-683d others(5): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | |||||
chr2:227553000
|
CA | C | 30 | a0001c0001t0001g0121a0001c0002t0002g0245a0001c0002t0007g0086others(27): Show | 30 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1538-683delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553000 | |||||
chr2:227553329
|
C | G | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1538-375C>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553329 | ||||||
chr2:227553436
|
CAGTGAGC others(4): Show |
C | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-266_1538-256d others(13): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553436 | |||||
chr2:227553448
|
A | T | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-256A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553448 | ||||||
chr2:227553449
|
T | C | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-255T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553449 | ||||||
chr2:227553458
|
T | A | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-246T>A | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553458 | ||||||
chr2:227553459
|
GGACTCTG others(49): Show |
G | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-244_1538-189d others(58): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553459 | ||||||
chr2:227553495
|
C | CA | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1538-192dupA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553495 | |||||
chr2:227553495
|
C | CAA | 6 | a0001c0001t0001g0166a0001c0001t0001g0199a0001c0001t0001g0200others(3): Show | 6 | HG00597.hp2 HG01081.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1538-193_1538-192d others(4): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553495 | |||||
chr2:227553495
|
CA | C | 9 | a0001c0002t0002g0245a0001c0002t0007g0084a0001c0002t0007g0085others(6): Show | 9 | HG01243.hp1 HG01255.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1538-192delA | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227553495 | |||||
chr2:227553518
|
T | G | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-186T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553518 | ||||||
chr2:227553519
|
T | C | 2 | a0001c0001t0018g0024a0001c0001t0018g0025 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1538-185T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553519 | ||||||
chr2:227553527
|
A | G | 2 | a0001c0001t0032g0093a0001c0001t0041g0081 | 2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1538-177A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553527 | ||||||
chr2:227553544
|
T | G | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1538-160T>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553544 | ||||||
chr2:227553547
|
T | C | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1538-157T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553547 | ||||||
chr2:227553577
|
A | G | 4 | a0001c0001t0010g0026a0001c0001t0010g0027a0001c0001t0010g0028others(1): Show | 4 | HG02896.hp1 HG02897.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-127A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 11/12 | chr2 | 227553577 | ||||||
chr2:227553894
|
TATATTG | T | 29 | a0001c0003t0003g0050a0001c0003t0003g0052a0001c0003t0003g0053others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1629+104_1629+109d others(8): Show |
AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 227553894 | |||||
chr2:227553915
|
A | G | 2 | a0001c0001t0017g0233a0001c0001t0017g0235 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1629+120A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227553915 | ||||||
chr2:227553953
|
A | T | 1 | a0001c0001t0001g0150 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1629+158A>T | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227553953 | ||||||
chr2:227554013
|
A | C | 9 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(6): Show | 9 | HG00639.hp1 HG01081.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1629+218A>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554013 | ||||||
chr2:227554028
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1629+233A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554028 | ||||||
chr2:227554141
|
G | C | 67 | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0007others(64): Show | 69 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1630-295G>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554141 | ||||||
chr2:227554241
|
A | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 137 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.1630-195A>G | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554241 | ||||||
chr2:227554265
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1630-171T>C | AGFG1 | ENSG00000173744.18 | transcript | ENST00000310078.13 | protein_coding | 12/12 | chr2 | 227554265 |