geneid | 9145 |
---|---|
ensemblid | ENSG00000100321.15 |
hgncid | 11498 |
symbol | SYNGR1 |
name | synaptogyrin 1 |
refseq_nuc | NM_004711.5 |
refseq_prot | NP_004702.2 |
ensembl_nuc | ENST00000328933.10 |
ensembl_prot | ENSP00000332287.5 |
mane_status | MANE Select |
chr | chr22 |
start | 39349991 |
end | 39385575 |
strand | + |
ver | v1.2 |
region | chr22:39349991-39385575 |
region5000 | chr22:39344991-39390575 |
regionname0 | SYNGR1_chr22_39349991_39385575 |
regionname5000 | SYNGR1_chr22_39344991_39390575 |
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 | 0/1 | 234 | 261 | 86 | 51 | 78 | 11 | 34 | 44 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002 | 1/0 | 233 | 36 | 10 | 15 | 0 | 1 | 9 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0003 | 0/0 | 233 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0004 | 0/0 | 234 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
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 | 705 | 248 | 82 | 50 | 77 | 10 | 28 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0002 | 1/0 | 702 | 35 | 9 | 15 | 0 | 1 | 9 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0003 | 0/0 | 705 | 5 | 0 | 0 | 0 | 0 | 5 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0004 | 0/0 | 705 | 3 | 2 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0005 | 0/0 | 702 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0006 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0007 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0008 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0009 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0010 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0011 | 0/0 | 702 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
c0012 | 0/0 | 705 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3682 | 172 | 26 | 44 | 69 | 10 | 22 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0002 | 1/0 | 3682 | 28 | 6 | 12 | 0 | 0 | 9 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0003 | 0/0 | 3682 | 15 | 14 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0004 | 0/0 | 3682 | 15 | 14 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0005 | 0/0 | 3680 | 13 | 13 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0006 | 0/0 | 3682 | 5 | 4 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0007 | 0/0 | 3682 | 5 | 5 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0008 | 0/0 | 3682 | 4 | 1 | 2 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0009 | 0/0 | 3682 | 4 | 0 | 0 | 4 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0010 | 0/0 | 3682 | 4 | 0 | 0 | 0 | 0 | 4 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0011 | 0/0 | 3682 | 3 | 3 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0012 | 0/0 | 3682 | 3 | 0 | 0 | 0 | 0 | 3 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0013 | 0/0 | 3682 | 3 | 3 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0014 | 0/0 | 3682 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0015 | 0/0 | 3682 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0016 | 0/0 | 3682 | 2 | 0 | 0 | 0 | 0 | 2 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0017 | 0/0 | 3682 | 2 | 1 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0018 | 0/0 | 3682 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0019 | 0/0 | 3682 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0020 | 0/0 | 3682 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0021 | 0/0 | 3682 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0022 | 0/0 | 3682 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0023 | 0/0 | 3682 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0024 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0025 | 0/0 | 3682 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0026 | 0/0 | 3682 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0027 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0028 | 0/0 | 3682 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0029 | 0/0 | 3682 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0030 | 0/0 | 3682 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0031 | 0/0 | 3682 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
t0032 | 0/0 | 3682 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
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 | 4 | 0 | 0 | 2 | 0 | 2 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0004 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0255 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
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 | 705 | 248 | 82 | 50 | 77 | 10 | 28 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0003 | 0/0 | 705 | 5 | 0 | 0 | 0 | 0 | 5 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0004 | 0/0 | 705 | 3 | 2 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0007 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0008 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0009 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0010 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0012 | 0/0 | 705 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0002 | 1/0 | 702 | 35 | 9 | 15 | 0 | 1 | 9 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0011 | 0/0 | 702 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0003c0005 | 0/0 | 702 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0004c0006 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4386 | 166 | 25 | 44 | 68 | 9 | 19 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0003 | 0/0 | 4386 | 15 | 14 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0004 | 0/0 | 4386 | 15 | 14 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0005 | 0/0 | 4384 | 13 | 13 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0006 | 0/0 | 4386 | 5 | 4 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0007 | 0/0 | 4386 | 5 | 5 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0009 | 0/0 | 4386 | 4 | 0 | 0 | 4 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0010 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0012 | 0/0 | 4386 | 3 | 0 | 0 | 0 | 0 | 3 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0013 | 0/0 | 4386 | 3 | 3 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0015 | 0/0 | 4386 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0016 | 0/0 | 4386 | 2 | 0 | 0 | 0 | 0 | 2 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0017 | 0/0 | 4386 | 2 | 1 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0018 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0019 | 0/0 | 4386 | 2 | 0 | 0 | 2 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0021 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0023 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0024 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0025 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0026 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0027 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0029 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0030 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0001t0031 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0003t0001 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0003t0010 | 0/0 | 4386 | 3 | 0 | 0 | 0 | 0 | 3 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0003t0028 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0004t0001 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0004t0020 | 0/0 | 4386 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0007t0018 | 0/0 | 4386 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0008t0001 | 0/0 | 4386 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0009t0032 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0010t0001 | 0/0 | 4386 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0001c0012t0001 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0002t0002 | 1/0 | 4383 | 28 | 6 | 12 | 0 | 0 | 9 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0002t0008 | 0/0 | 4383 | 3 | 0 | 2 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0002t0011 | 0/0 | 4383 | 3 | 3 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0002t0022 | 0/0 | 4383 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0002c0011t0008 | 0/0 | 4383 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0003c0005t0014 | 0/0 | 4383 | 2 | 0 | 0 | 0 | 2 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
a0004c0006t0001 | 0/0 | 4386 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | copy fasta | chr22 | 39344991 | 39390575 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0007g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0007g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0010g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0012g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0013g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0015g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0016g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0016g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0017g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0018g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0019g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0019g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0021g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0023g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0024g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0025g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0026g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0027g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0029g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0030g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0001t0031g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0003t0010g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0003t0010g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0003t0010g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0003t0028g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0004t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0004t0020g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0004t0020g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0007t0018g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0008t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0009t0032g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0010t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0001c0012t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0255 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0002t0022g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0002c0011t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0003c0005t0014g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0003c0005t0014g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
a0004c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00099 | hp2 | a0001 | c0001 | t0026 | g0115 | EUR | GBR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00140 | hp1 | a0002 | c0002 | t0008 | g0138 | EUR | GBR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | FIN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00639 | hp1 | a0002 | c0002 | t0008 | g0142 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0245 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0258 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0159 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0256 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01099 | hp1 | a0001 | c0007 | t0018 | g0076 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0267 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01106 | hp2 | a0002 | c0002 | t0022 | g0268 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0101 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0257 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01168 | hp1 | a0001 | c0001 | t0015 | g0013 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01169 | hp1 | a0001 | c0001 | t0015 | g0013 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0221 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01243 | hp2 | a0001 | c0001 | t0017 | g0270 | AMR | PUR | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0246 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0254 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0252 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01433 | hp2 | a0002 | c0002 | t0008 | g0143 | AMR | CLM | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01516 | hp2 | a0003 | c0005 | t0014 | g0247 | EUR | IBS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01517 | hp1 | a0003 | c0005 | t0014 | g0259 | EUR | IBS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01884 | hp1 | a0002 | c0002 | t0011 | g0122 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0223 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0211 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02056 | hp1 | a0001 | c0001 | t0019 | g0135 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02083 | hp1 | a0001 | c0001 | t0027 | g0060 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02129 | hp1 | a0001 | c0001 | t0024 | g0098 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02129 | hp2 | a0001 | c0001 | t0009 | g0227 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CDX | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02257 | hp1 | a0002 | c0011 | t0008 | g0136 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02257 | hp2 | a0001 | c0010 | t0001 | g0275 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02258 | hp1 | a0001 | c0001 | t0023 | g0116 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02451 | hp1 | a0002 | c0002 | t0002 | g0269 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02630 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0253 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0186 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0172 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02735 | hp1 | a0001 | c0001 | t0025 | g0146 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0266 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02886 | hp1 | a0001 | c0001 | t0013 | g0273 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0264 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02970 | hp1 | a0001 | c0001 | t0013 | g0272 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03017 | hp1 | a0001 | c0001 | t0030 | g0158 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03017 | hp2 | a0001 | c0003 | t0028 | g0212 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0202 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0154 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03195 | hp1 | a0001 | c0009 | t0032 | g0193 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03239 | hp1 | a0001 | c0001 | t0012 | g0058 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0201 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0018 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03490 | hp1 | a0001 | c0001 | t0016 | g0153 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0160 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03492 | hp1 | a0001 | c0001 | t0016 | g0137 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03516 | hp2 | a0001 | c0004 | t0020 | g0219 | AFR | ESN | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03654 | hp1 | a0001 | c0001 | t0012 | g0001 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03669 | hp1 | a0001 | c0003 | t0010 | g0179 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0214 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0017 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0190 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03834 | hp2 | a0004 | c0006 | t0001 | g0165 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04115 | hp1 | a0001 | c0003 | t0010 | g0215 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04199 | hp2 | a0001 | c0001 | t0012 | g0048 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04204 | hp2 | a0001 | c0003 | t0010 | g0213 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0049 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18906 | hp2 | a0002 | c0002 | t0011 | g0112 | AFR | YRI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18939 | hp1 | a0001 | c0001 | t0018 | g0007 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18945 | hp2 | a0001 | c0001 | t0009 | g0056 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18968 | hp1 | a0001 | c0008 | t0001 | g0038 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18979 | hp2 | a0001 | c0001 | t0009 | g0228 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | LWK | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19043 | hp1 | a0001 | c0001 | t0031 | g0229 | AFR | LWK | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0200 | AFR | LWK | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19064 | hp2 | a0001 | c0001 | t0019 | g0127 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA19240 | hp2 | a0001 | c0004 | t0020 | g0218 | AFR | YRI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | ASW | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20129 | hp2 | a0002 | c0002 | t0011 | g0123 | AFR | ASW | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20805 | hp1 | a0001 | c0012 | t0001 | g0025 | EUR | TSI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | TSI | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20905 | hp1 | a0001 | c0001 | t0029 | g0004 | SAS | GIH | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | GIH | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG02559 | hp2 | a0001 | c0001 | t0017 | g0026 | AFR | ACB | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0014 | AFR | USA | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | USA | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | USA | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | LWK | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0255 | REF | REF | SYNGR1_chr22_39344991_39390575 | SYNGR1 | chr22 | 39344991 | 39390575 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39381810
|
G | A | 1 | a0004 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.598G>A | p.Val200Met | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 618/4383 | 598/702 | 200/233 | chr22 | 39381810 | ||
chr22:39381817
|
C | CCAA | 2 | a0001a0004 | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
disruptive_inframe_insertion | MODERATE | c.607_608insACA | p.Pro202_Thr203insAs others(1): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 628/4383 | 608/702 | 203/233 | INFO_REALIGN_3_PRIME | chr22 | 39381817 | |
chr22:39381834
|
G | A | 1 | a0003 | 2 | HG01516.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.622G>A | p.Ala208Thr | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 642/4383 | 622/702 | 208/233 | chr22 | 39381834 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39374375
|
C | T | 1 | a0001c0012 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.159C>T | p.Ser53Ser | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/4 | 179/4383 | 159/702 | 53/233 | chr22 | 39374375 | ||
chr22:39374414
|
C | T | 1 | a0002c0011 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.198C>T | p.Asn66Asn | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/4 | 218/4383 | 198/702 | 66/233 | chr22 | 39374414 | ||
chr22:39374495
|
G | A | 1 | a0001c0004 | 3 | HG03516.hp2 HG04228.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.279G>A | p.Pro93Pro | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/4 | 299/4383 | 279/702 | 93/233 | chr22 | 39374495 | ||
chr22:39374507
|
C | T | 1 | a0001c0003 | 5 | HG03017.hp2 HG03669.hp1 HG03688.hp1 others(2): Show |
synonymous_variant | LOW | c.291C>T | p.Ser97Ser | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/4 | 311/4383 | 291/702 | 97/233 | chr22 | 39374507 | ||
chr22:39376089
|
C | T | 1 | a0001c0010 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.375C>T | p.Tyr125Tyr | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/4 | 395/4383 | 375/702 | 125/233 | chr22 | 39376089 | ||
chr22:39376176
|
C | G | 1 | a0001c0009 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.462C>G | p.Ser154Ser | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/4 | 482/4383 | 462/702 | 154/233 | chr22 | 39376176 | ||
chr22:39381833
|
C | A | 1 | a0001c0007 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.621C>A | p.Pro207Pro | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 641/4383 | 621/702 | 207/233 | chr22 | 39381833 | ||
chr22:39381875
|
C | T | 1 | a0001c0008 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.663C>T | p.Phe221Phe | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 683/4383 | 663/702 | 221/233 | chr22 | 39381875 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39382003
|
C | T | 1 | a0001c0001t0004 | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*89C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 89 | chr22 | 39382003 | |||||
chr22:39382029
|
A | T | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(4): Show | 42 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*115A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 115 | chr22 | 39382029 | |||||
chr22:39382055
|
G | A | 2 | a0001c0001t0003a0001c0001t0007 | 20 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 141 | chr22 | 39382055 | |||||
chr22:39382162
|
A | G | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(31): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*248A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 248 | chr22 | 39382162 | |||||
chr22:39382322
|
T | C | 34 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(31): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*408T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 408 | chr22 | 39382322 | |||||
chr22:39382414
|
T | C | 28 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(25): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*500T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 500 | chr22 | 39382414 | |||||
chr22:39382481
|
G | A | 1 | a0001c0001t0023 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 567 | chr22 | 39382481 | |||||
chr22:39382604
|
G | C | 1 | a0001c0001t0009 | 4 | HG02129.hp2 NA18945.hp2 NA18979.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*690G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 690 | chr22 | 39382604 | |||||
chr22:39382742
|
C | T | 1 | a0001c0001t0030 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 828 | chr22 | 39382742 | |||||
chr22:39382743
|
G | A | 1 | a0001c0001t0015 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*829G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 829 | chr22 | 39382743 | |||||
chr22:39382910
|
C | T | 1 | a0001c0001t0007 | 5 | HG01884.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*996C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 996 | chr22 | 39382910 | |||||
chr22:39382983
|
C | T | 1 | a0002c0002t0022 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1069C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1069 | chr22 | 39382983 | |||||
chr22:39383108
|
CTA | C | 1 | a0001c0001t0005 | 13 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1196_*1197delAT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1196 | INFO_REALIGN_3_PRIME | chr22 | 39383108 | ||||
chr22:39383168
|
G | A | 1 | a0001c0001t0013 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1254G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1254 | chr22 | 39383168 | |||||
chr22:39383287
|
C | T | 1 | a0001c0001t0009 | 4 | HG02129.hp2 NA18945.hp2 NA18979.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1373C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1373 | chr22 | 39383287 | |||||
chr22:39383295
|
G | A | 25 | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(22): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*1381G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1381 | chr22 | 39383295 | |||||
chr22:39383361
|
G | T | 3 | a0001c0001t0003a0001c0001t0007a0001c0004t0020 | 22 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1447G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1447 | chr22 | 39383361 | |||||
chr22:39383452
|
C | T | 1 | a0001c0001t0029 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1538C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1538 | chr22 | 39383452 | |||||
chr22:39383532
|
G | C | 1 | a0001c0001t0024 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1618G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1618 | chr22 | 39383532 | |||||
chr22:39383581
|
G | A | 1 | a0001c0001t0004 | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1667G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1667 | chr22 | 39383581 | |||||
chr22:39383674
|
C | G | 1 | a0001c0001t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1760C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1760 | chr22 | 39383674 | |||||
chr22:39383737
|
G | A | 1 | a0001c0001t0025 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1823G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1823 | chr22 | 39383737 | |||||
chr22:39383866
|
C | G | 1 | a0001c0001t0012 | 3 | HG03239.hp1 HG03654.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1952C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 1952 | chr22 | 39383866 | |||||
chr22:39384012
|
G | T | 3 | a0001c0001t0010a0001c0003t0010a0001c0003t0028 | 5 | HG03017.hp2 HG03669.hp1 HG03831.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2098G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2098 | chr22 | 39384012 | |||||
chr22:39384038
|
G | A | 1 | a0001c0001t0026 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2124G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2124 | chr22 | 39384038 | |||||
chr22:39384092
|
C | T | 1 | a0003c0005t0014 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2178C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2178 | chr22 | 39384092 | |||||
chr22:39384382
|
G | T | 1 | a0001c0004t0020 | 2 | HG03516.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2468G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2468 | chr22 | 39384382 | |||||
chr22:39384402
|
A | C | 2 | a0001c0001t0018a0001c0007t0018 | 2 | HG01099.hp1 NA18939.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2488A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2488 | chr22 | 39384402 | |||||
chr22:39384511
|
G | A | 1 | a0001c0001t0016 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2597G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2597 | chr22 | 39384511 | |||||
chr22:39384802
|
G | A | 1 | a0001c0001t0004 | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2888G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2888 | chr22 | 39384802 | |||||
chr22:39384806
|
C | T | 2 | a0001c0001t0013a0001c0001t0031 | 4 | HG02886.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2892C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2892 | chr22 | 39384806 | |||||
chr22:39384838
|
G | A | 2 | a0001c0001t0013a0001c0001t0031 | 4 | HG02886.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2924G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 2924 | chr22 | 39384838 | |||||
chr22:39384956
|
C | T | 2 | a0002c0002t0008a0002c0011t0008 | 4 | HG00140.hp1 HG00639.hp1 HG01433.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3042C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3042 | chr22 | 39384956 | |||||
chr22:39385008
|
G | A | 1 | a0001c0001t0019 | 2 | HG02056.hp1 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3094G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3094 | chr22 | 39385008 | |||||
chr22:39385115
|
C | T | 2 | a0001c0001t0013a0001c0001t0031 | 4 | HG02886.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3201C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3201 | chr22 | 39385115 | |||||
chr22:39385228
|
C | T | 1 | a0001c0001t0027 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3314C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3314 | chr22 | 39385228 | |||||
chr22:39385266
|
C | T | 1 | a0001c0003t0028 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3352C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3352 | chr22 | 39385266 | |||||
chr22:39385349
|
A | T | 1 | a0001c0003t0028 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3435A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3435 | chr22 | 39385349 | |||||
chr22:39385424
|
C | T | 26 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(23): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*3510C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 4/4 | 3510 | chr22 | 39385424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39350163
|
C | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(90): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.99+54C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350163 | ||||||
chr22:39350181
|
ACCGACC | A | 126 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(123): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.99+87_99+92delGACC others(2): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39350181 | |||||
chr22:39350208
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99+99C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350208 | ||||||
chr22:39350213
|
G | GGCGGCGG others(1): Show |
5 | a0001c0001t0001g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+114_99+121dupCG others(6): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39350213 | |||||
chr22:39350419
|
C | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(124): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+310C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350419 | ||||||
chr22:39350462
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0003g0226 | 3 | HG02109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+353G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350462 | ||||||
chr22:39350502
|
G | A | 1 | a0001c0001t0006g0101 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.99+393G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350502 | ||||||
chr22:39350798
|
C | A | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(124): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+689C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350798 | ||||||
chr22:39350816
|
C | T | 54 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0181others(51): Show | 57 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+707C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350816 | ||||||
chr22:39350884
|
G | C | 2 | a0001c0001t0003g0166a0001c0001t0004g0167 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.99+775G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39350884 | ||||||
chr22:39351045
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+936G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351045 | ||||||
chr22:39351082
|
C | A | 54 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0181others(51): Show | 57 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+973C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351082 | ||||||
chr22:39351197
|
G | T | 4 | a0001c0003t0001g0214a0001c0003t0010g0213a0001c0003t0010g0215others(1): Show | 4 | HG03017.hp2 HG03688.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+1088G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351197 | ||||||
chr22:39351314
|
G | A | 13 | a0001c0001t0001g0169a0001c0001t0003g0166a0001c0001t0003g0168others(10): Show | 13 | HG01175.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1205G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351314 | ||||||
chr22:39351342
|
C | T | 2 | a0001c0001t0001g0164a0004c0006t0001g0165 | 2 | HG03834.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.99+1233C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351342 | ||||||
chr22:39351413
|
G | A | 54 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0181others(51): Show | 57 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+1304G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351413 | ||||||
chr22:39351414
|
C | A | 54 | a0001c0001t0001g0169a0001c0001t0001g0180a0001c0001t0001g0181others(51): Show | 57 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.99+1305C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351414 | ||||||
chr22:39351477
|
T | C | 1 | a0002c0002t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.99+1368T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351477 | ||||||
chr22:39351666
|
T | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(145): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.99+1557T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351666 | ||||||
chr22:39351775
|
G | A | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(143): Show | 158 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.99+1666G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351775 | ||||||
chr22:39351909
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+1800G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351909 | ||||||
chr22:39351922
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0006g0101a0001c0001t0006g0103 | 3 | HG00639.hp2 HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+1813T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351922 | ||||||
chr22:39351943
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.99+1834G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39351943 | ||||||
chr22:39352175
|
G | T | 12 | a0001c0001t0001g0104a0001c0001t0001g0220a0001c0001t0001g0276others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+2066G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352175 | ||||||
chr22:39352366
|
C | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0156a0001c0001t0001g0157others(13): Show | 18 | HG00140.hp2 HG01070.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+2257C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352366 | ||||||
chr22:39352767
|
G | T | 5 | a0001c0001t0001g0274a0001c0001t0007g0271a0001c0001t0013g0272others(2): Show | 5 | HG01243.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2658G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352767 | ||||||
chr22:39352849
|
A | G | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.99+2740A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352849 | ||||||
chr22:39352907
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+2798G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352907 | ||||||
chr22:39352947
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.99+2838C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352947 | ||||||
chr22:39352948
|
G | A | 5 | a0001c0003t0001g0214a0001c0003t0010g0179a0001c0003t0010g0213others(2): Show | 5 | HG03017.hp2 HG03669.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2839G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39352948 | ||||||
chr22:39353016
|
C | A | 1 | a0001c0001t0017g0270 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+2907C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353016 | ||||||
chr22:39353067
|
A | G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(227): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.99+2958A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353067 | ||||||
chr22:39353081
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+2972C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353081 | ||||||
chr22:39353087
|
C | A | 2 | a0001c0001t0006g0101a0001c0001t0006g0103 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+2978C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353087 | ||||||
chr22:39353152
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+3043G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353152 | ||||||
chr22:39353158
|
G | A | 1 | a0002c0002t0002g0155 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.99+3049G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353158 | ||||||
chr22:39353777
|
T | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.99+3668T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353777 | ||||||
chr22:39353976
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+3867G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353976 | ||||||
chr22:39353978
|
C | T | 5 | a0001c0003t0001g0214a0001c0003t0010g0179a0001c0003t0010g0213others(2): Show | 5 | HG03017.hp2 HG03669.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+3869C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353978 | ||||||
chr22:39353979
|
T | G | 65 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0169others(62): Show | 68 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.99+3870T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39353979 | ||||||
chr22:39354137
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0024g0098 | 2 | HG02129.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.99+4028C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354137 | ||||||
chr22:39354141
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+4032T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354141 | ||||||
chr22:39354153
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+4044T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354153 | ||||||
chr22:39354236
|
A | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(156): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.99+4127A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354236 | ||||||
chr22:39354288
|
T | C | 1 | a0001c0001t0001g0019 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.99+4179T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354288 | ||||||
chr22:39354342
|
C | T | 2 | a0001c0001t0006g0101a0001c0001t0006g0103 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+4233C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354342 | ||||||
chr22:39354351
|
G | A | 26 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(23): Show | 26 | HG00423.hp2 HG01243.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+4242G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354351 | ||||||
chr22:39354452
|
C | T | 53 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0180others(50): Show | 56 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+4343C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354452 | ||||||
chr22:39354577
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG00280.hp2 HG01943.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.99+4468C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354577 | ||||||
chr22:39354753
|
C | T | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.99+4644C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354753 | ||||||
chr22:39354843
|
T | TAA | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.99+4747_99+4748dup others(2): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39354843 | |||||
chr22:39354860
|
T | G | 2 | a0001c0001t0006g0101a0001c0001t0006g0103 | 2 | HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+4751T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39354860 | ||||||
chr22:39355129
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.99+5020G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355129 | ||||||
chr22:39355198
|
A | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0217a0001c0001t0015g0013 | 4 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+5089A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355198 | ||||||
chr22:39355201
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.99+5092C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355201 | ||||||
chr22:39355246
|
G | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+5137G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355246 | ||||||
chr22:39355346
|
G | A | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.99+5237G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355346 | ||||||
chr22:39355389
|
T | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.99+5280T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355389 | ||||||
chr22:39355395
|
T | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+5286T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355395 | ||||||
chr22:39355396
|
T | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+5287T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355396 | ||||||
chr22:39355460
|
C | T | 5 | a0001c0003t0001g0214a0001c0003t0010g0179a0001c0003t0010g0213others(2): Show | 5 | HG03017.hp2 HG03669.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5351C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355460 | ||||||
chr22:39355624
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+5515C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355624 | ||||||
chr22:39355706
|
G | A | 77 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0169others(74): Show | 80 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(77): Show |
intron_variant | MODIFIER | c.99+5597G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355706 | ||||||
chr22:39355711
|
G | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+5602G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355711 | ||||||
chr22:39355769
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+5660A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355769 | ||||||
chr22:39355892
|
G | A | 1 | a0002c0002t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.99+5783G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39355892 | ||||||
chr22:39356017
|
T | A | 1 | a0001c0001t0003g0168 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.99+5908T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356017 | ||||||
chr22:39356098
|
G | A | 76 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0169others(73): Show | 79 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(76): Show |
intron_variant | MODIFIER | c.99+5989G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356098 | ||||||
chr22:39356131
|
A | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.99+6022A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356131 | ||||||
chr22:39356198
|
A | ATGGGATT others(5): Show |
253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+6091_99+6092ins others(12): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39356198 | |||||
chr22:39356216
|
G | A | 7 | a0001c0001t0001g0220a0001c0001t0004g0221a0001c0001t0004g0222others(4): Show | 7 | HG01243.hp1 HG02129.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+6107G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356216 | ||||||
chr22:39356380
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.99+6271G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356380 | ||||||
chr22:39356463
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01358.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.99+6354C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356463 | ||||||
chr22:39356522
|
A | T | 77 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0169others(74): Show | 80 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(77): Show |
intron_variant | MODIFIER | c.99+6413A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356522 | ||||||
chr22:39356543
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.99+6434C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356543 | ||||||
chr22:39356544
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0003g0170a0001c0001t0003g0171 | 3 | HG02965.hp1 HG03579.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.99+6435G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356544 | ||||||
chr22:39356689
|
A | C | 3 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0005g0277 | 3 | HG02055.hp2 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.99+6580A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356689 | ||||||
chr22:39356823
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.99+6714G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356823 | ||||||
chr22:39356986
|
G | A | 53 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0180others(50): Show | 56 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+6877G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356986 | ||||||
chr22:39356998
|
T | C | 77 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0169others(74): Show | 80 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(77): Show |
intron_variant | MODIFIER | c.99+6889T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39356998 | ||||||
chr22:39357037
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+6928C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357037 | ||||||
chr22:39357261
|
T | C | 66 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0169others(63): Show | 69 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.99+7152T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357261 | ||||||
chr22:39357390
|
C | G | 1 | a0002c0002t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.99+7281C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357390 | ||||||
chr22:39357417
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.99+7308C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357417 | ||||||
chr22:39357435
|
G | A | 1 | a0001c0001t0021g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.99+7326G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357435 | ||||||
chr22:39357511
|
C | T | 5 | a0001c0001t0001g0220a0001c0001t0004g0221a0001c0001t0004g0222others(2): Show | 5 | HG01243.hp1 HG02258.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7402C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357511 | ||||||
chr22:39357558
|
G | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG02109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.99+7449G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357558 | ||||||
chr22:39357573
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+7464G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357573 | ||||||
chr22:39357599
|
TGGGCGTG others(55): Show |
T | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.99+7549_99+7610del others(62): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39357599 | |||||
chr22:39357677
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | HG03927.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.99+7568G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357677 | ||||||
chr22:39357717
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(172): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.99+7608C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357717 | ||||||
chr22:39357760
|
G | A | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.99+7651G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357760 | ||||||
chr22:39357774
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.99+7665T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357774 | ||||||
chr22:39357815
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0031g0229 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.99+7706T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357815 | ||||||
chr22:39357860
|
C | A | 1 | a0001c0001t0017g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.99+7751C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357860 | ||||||
chr22:39357945
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+7836C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357945 | ||||||
chr22:39357987
|
G | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+7878G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357987 | ||||||
chr22:39357996
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.99+7887G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39357996 | ||||||
chr22:39358080
|
T | G | 21 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(18): Show | 21 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+7971T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358080 | ||||||
chr22:39358303
|
T | G | 1 | a0001c0001t0007g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+8194T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358303 | ||||||
chr22:39358362
|
A | C | 1 | a0001c0001t0001g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+8253A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358362 | ||||||
chr22:39358411
|
G | A | 1 | a0001c0001t0005g0182 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+8302G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358411 | ||||||
chr22:39358419
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+8310C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358419 | ||||||
chr22:39358428
|
G | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.99+8319G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358428 | ||||||
chr22:39358536
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+8427C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358536 | ||||||
chr22:39358572
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+8463C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358572 | ||||||
chr22:39358689
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+8580G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358689 | ||||||
chr22:39358789
|
A | C | 8 | a0001c0001t0003g0243a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+8680A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358789 | ||||||
chr22:39358851
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+8742G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358851 | ||||||
chr22:39358859
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+8750G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358859 | ||||||
chr22:39358868
|
C | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+8759C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358868 | ||||||
chr22:39358898
|
T | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+8789T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358898 | ||||||
chr22:39358908
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+8799G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358908 | ||||||
chr22:39358986
|
A | C | 2 | a0001c0001t0001g0274a0001c0001t0031g0229 | 2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.99+8877A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39358986 | ||||||
chr22:39359049
|
C | T | 6 | a0001c0001t0031g0229a0001c0003t0001g0214a0001c0003t0010g0179others(3): Show | 6 | HG03017.hp2 HG03669.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+8940C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359049 | ||||||
chr22:39359143
|
T | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9034T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359143 | ||||||
chr22:39359170
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.99+9061A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359170 | ||||||
chr22:39359185
|
G | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.99+9076G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359185 | ||||||
chr22:39359274
|
G | A | 1 | a0002c0002t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.99+9165G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359274 | ||||||
chr22:39359347
|
C | T | 1 | a0001c0001t0017g0026 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.99+9238C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359347 | ||||||
chr22:39359350
|
G | A | 13 | a0001c0001t0001g0104a0001c0001t0001g0220a0001c0001t0001g0274others(10): Show | 13 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+9241G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359350 | ||||||
chr22:39359393
|
A | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9284A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359393 | ||||||
chr22:39359433
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9324G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359433 | ||||||
chr22:39359435
|
G | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9326G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359435 | ||||||
chr22:39359438
|
A | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9329A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359438 | ||||||
chr22:39359457
|
TA | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.99+9362delA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359457 | |||||
chr22:39359488
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99+9379G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359488 | ||||||
chr22:39359500
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.99+9391G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359500 | ||||||
chr22:39359501
|
G | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9392G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359501 | ||||||
chr22:39359523
|
C | T | 53 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0180others(50): Show | 56 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+9414C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359523 | ||||||
chr22:39359524
|
G | A | 1 | a0002c0002t0002g0245 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.99+9415G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359524 | ||||||
chr22:39359563
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0001g0183a0001c0001t0001g0187others(7): Show | 12 | HG01255.hp1 HG01346.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+9454G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359563 | ||||||
chr22:39359609
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.99+9500C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359609 | ||||||
chr22:39359616
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9507G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359616 | ||||||
chr22:39359630
|
C | CA | 11 | a0001c0001t0001g0251a0001c0001t0004g0248a0001c0001t0004g0249others(8): Show | 11 | HG00642.hp1 HG00642.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+9549dupA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAA | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0029others(21): Show | 24 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.99+9545_99+9549del others(5): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAA | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.99+9544_99+9549del others(6): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAAA | C | 16 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0104others(13): Show | 16 | HG00323.hp2 HG00639.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+9543_99+9549del others(7): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAAA others(1): Show |
C | 31 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0180others(28): Show | 33 | HG01175.hp1 HG01255.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.99+9542_99+9549del others(8): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAAA others(2): Show |
C | 22 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0197others(19): Show | 23 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+9541_99+9549del others(9): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAAA others(3): Show |
C | 17 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(14): Show | 17 | HG00423.hp2 HG02071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+9540_99+9549del others(10): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAAA others(5): Show |
C | 2 | a0002c0002t0002g0267a0002c0002t0022g0268 | 2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.99+9538_99+9549del others(12): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359630
|
CAAAAAAA others(6): Show |
C | 1 | a0002c0002t0002g0269 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+9537_99+9549del others(13): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39359630 | |||||
chr22:39359684
|
T | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.99+9575T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359684 | ||||||
chr22:39359698
|
G | A | 2 | a0001c0001t0001g0230a0002c0002t0002g0155 | 2 | HG03239.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.99+9589G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359698 | ||||||
chr22:39359720
|
T | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+9611T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359720 | ||||||
chr22:39359755
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0003g0226 | 3 | HG02109.hp1 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.99+9646G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359755 | ||||||
chr22:39359768
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+9659C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359768 | ||||||
chr22:39359782
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0039others(7): Show | 12 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+9673C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359782 | ||||||
chr22:39359797
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99+9688A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359797 | ||||||
chr22:39359948
|
T | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.99+9839T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359948 | ||||||
chr22:39359980
|
C | G | 1 | a0001c0001t0003g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+9871C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39359980 | ||||||
chr22:39360092
|
A | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.99+9983A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360092 | ||||||
chr22:39360211
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10102C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360211 | ||||||
chr22:39360265
|
A | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(173): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.99+10156A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360265 | ||||||
chr22:39360311
|
T | C | 8 | a0001c0001t0003g0243a0001c0001t0007g0209a0001c0001t0007g0210others(5): Show | 8 | HG01243.hp2 HG01891.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+10202T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360311 | ||||||
chr22:39360419
|
G | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10310G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360419 | ||||||
chr22:39360426
|
C | T | 17 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(14): Show | 17 | HG00423.hp2 HG02071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+10317C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360426 | ||||||
chr22:39360428
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.99+10319C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360428 | ||||||
chr22:39360506
|
C | T | 1 | a0001c0001t0010g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+10397C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360506 | ||||||
chr22:39360645
|
G | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(89): Show | 101 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.99+10536G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360645 | ||||||
chr22:39360782
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10673G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360782 | ||||||
chr22:39360849
|
G | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.99+10740G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360849 | ||||||
chr22:39360850
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0117 | 4 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+10741G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360850 | ||||||
chr22:39360891
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10782G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360891 | ||||||
chr22:39360968
|
A | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10859A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360968 | ||||||
chr22:39360980
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(250): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.99+10871C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39360980 | ||||||
chr22:39361090
|
A | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+10981A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361090 | ||||||
chr22:39361106
|
G | A | 1 | a0001c0001t0024g0098 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.99+10997G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361106 | ||||||
chr22:39361356
|
C | CT | 81 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0088others(78): Show | 86 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.99+11267dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39361356 | |||||
chr22:39361356
|
C | CTT | 16 | a0001c0001t0001g0169a0001c0001t0001g0225a0001c0001t0003g0168others(13): Show | 16 | HG01175.hp1 HG01358.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+11266_99+11267d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39361356 | |||||
chr22:39361356
|
CT | C | 16 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0104others(13): Show | 16 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+11267delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39361356 | |||||
chr22:39361421
|
C | T | 1 | a0001c0001t0013g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+11312C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361421 | ||||||
chr22:39361511
|
C | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+11402C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361511 | ||||||
chr22:39361528
|
T | C | 1 | a0002c0002t0002g0267 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.99+11419T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361528 | ||||||
chr22:39361618
|
C | G | 3 | a0002c0002t0002g0267a0002c0002t0002g0269a0002c0002t0022g0268 | 3 | HG01099.hp2 HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.99+11509C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361618 | ||||||
chr22:39361627
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+11518C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361627 | ||||||
chr22:39361651
|
C | T | 53 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0180others(50): Show | 56 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.99+11542C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361651 | ||||||
chr22:39361697
|
A | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+11588A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361697 | ||||||
chr22:39361790
|
A | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+11681A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361790 | ||||||
chr22:39361898
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+11789G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361898 | ||||||
chr22:39361907
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+11798G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361907 | ||||||
chr22:39361956
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.99+11847G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39361956 | ||||||
chr22:39362013
|
TC | T | 12 | a0001c0001t0001g0104a0001c0001t0001g0220a0001c0001t0001g0276others(9): Show | 12 | HG00639.hp2 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+11906delC | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39362013 | |||||
chr22:39362015
|
C | CT | 72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(69): Show | 78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.99+11919dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39362015 | |||||
chr22:39362015
|
C | CTT | 27 | a0001c0001t0001g0216a0001c0001t0001g0224a0001c0001t0001g0251others(24): Show | 28 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.99+11918_99+11919d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39362015 | |||||
chr22:39362015
|
C | CTTT | 49 | a0001c0001t0001g0106a0001c0001t0001g0169a0001c0001t0001g0180others(46): Show | 52 | HG01109.hp2 HG01175.hp1 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.99+11917_99+11919d others(5): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39362015 | |||||
chr22:39362212
|
A | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.99+12103A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362212 | ||||||
chr22:39362248
|
C | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(123): Show | 136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.100-12068C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362248 | ||||||
chr22:39362315
|
T | G | 12 | a0001c0001t0001g0220a0001c0001t0001g0274a0001c0001t0003g0243others(9): Show | 12 | HG01109.hp1 HG02258.hp2 HG03017.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-12001T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362315 | ||||||
chr22:39362324
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.100-11992C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362324 | ||||||
chr22:39362335
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG00544.hp1 NA18747.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-11981G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362335 | ||||||
chr22:39362343
|
G | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-11973G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362343 | ||||||
chr22:39362382
|
G | C | 13 | a0001c0001t0001g0169a0001c0001t0003g0166a0001c0001t0003g0168others(10): Show | 13 | HG01175.hp1 HG02145.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-11934G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362382 | ||||||
chr22:39362406
|
C | T | 7 | a0001c0001t0001g0207a0001c0001t0031g0229a0001c0003t0001g0214others(4): Show | 7 | HG03017.hp2 HG03669.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-11910C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362406 | ||||||
chr22:39362416
|
C | CA | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.100-11900_100-1189 others(5): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362416 | ||||||
chr22:39362434
|
T | C | 14 | a0001c0001t0001g0207a0001c0001t0006g0101a0001c0001t0006g0103others(11): Show | 14 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-11882T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362434 | ||||||
chr22:39362478
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0005g0277 | 2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.100-11838C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362478 | ||||||
chr22:39362504
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.100-11812A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362504 | ||||||
chr22:39362526
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-11790G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362526 | ||||||
chr22:39362536
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.100-11780A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362536 | ||||||
chr22:39362547
|
T | A | 5 | a0001c0001t0031g0229a0001c0010t0001g0275a0002c0002t0011g0112others(2): Show | 5 | HG01884.hp1 HG02257.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-11769T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362547 | ||||||
chr22:39362808
|
G | A | 1 | a0001c0001t0009g0227 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.100-11508G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362808 | ||||||
chr22:39362825
|
C | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.100-11491C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362825 | ||||||
chr22:39362839
|
C | G | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.100-11477C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362839 | ||||||
chr22:39362876
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.100-11440A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362876 | ||||||
chr22:39362880
|
C | A | 11 | a0001c0001t0001g0104a0001c0001t0001g0192a0001c0001t0001g0204others(8): Show | 12 | HG00639.hp2 HG01934.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-11436C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362880 | ||||||
chr22:39362928
|
A | G | 21 | a0001c0001t0001g0063a0001c0001t0001g0085a0001c0001t0001g0147others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-11388A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39362928 | ||||||
chr22:39363269
|
A | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.100-11047A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363269 | ||||||
chr22:39363301
|
C | A | 17 | a0001c0001t0001g0276a0001c0001t0004g0154a0001c0001t0004g0167others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-11015C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363301 | ||||||
chr22:39363335
|
A | G | 29 | a0001c0001t0001g0106a0001c0001t0001g0276a0001c0001t0004g0107others(26): Show | 29 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-10981A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363335 | ||||||
chr22:39363339
|
G | C | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-10977G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363339 | ||||||
chr22:39363529
|
G | A | 1 | a0001c0001t0004g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.100-10787G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363529 | ||||||
chr22:39363622
|
T | C | 27 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(24): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-10694T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363622 | ||||||
chr22:39363650
|
C | T | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.100-10666C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363650 | ||||||
chr22:39363651
|
G | A | 1 | a0001c0008t0001g0038 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.100-10665G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363651 | ||||||
chr22:39363791
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.100-10525G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363791 | ||||||
chr22:39363816
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-10500G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363816 | ||||||
chr22:39363843
|
C | T | 27 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(24): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-10473C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363843 | ||||||
chr22:39363850
|
C | T | 27 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(24): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-10466C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363850 | ||||||
chr22:39363987
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-10329C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39363987 | ||||||
chr22:39364068
|
TC | T | 27 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(24): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-10246delC | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39364068 | |||||
chr22:39364076
|
A | C | 27 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(24): Show | 27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.100-10240A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364076 | ||||||
chr22:39364167
|
G | A | 10 | a0001c0001t0001g0106a0001c0001t0004g0154a0001c0001t0004g0167others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-10149G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364167 | ||||||
chr22:39364256
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.100-10060A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364256 | ||||||
chr22:39364270
|
A | G | 2 | a0002c0002t0008g0142a0002c0002t0008g0143 | 2 | HG00639.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.100-10046A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364270 | ||||||
chr22:39364309
|
T | TTTAC | 28 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(25): Show | 28 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-10007_100-1000 others(8): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364309 | ||||||
chr22:39364384
|
A | G | 12 | a0001c0001t0001g0119a0001c0001t0001g0276a0001c0001t0001g0278others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-9932A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364384 | ||||||
chr22:39364639
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0236 | 2 | NA18945.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.100-9677C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364639 | ||||||
chr22:39364746
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-9570G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364746 | ||||||
chr22:39364878
|
C | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.100-9438C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364878 | ||||||
chr22:39364958
|
C | T | 16 | a0001c0001t0001g0106a0001c0001t0004g0107a0001c0001t0004g0154others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-9358C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39364958 | ||||||
chr22:39364960
|
GA | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-9349delA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39364960 | |||||
chr22:39365093
|
C | A | 12 | a0001c0001t0001g0119a0001c0001t0001g0276a0001c0001t0001g0278others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-9223C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365093 | ||||||
chr22:39365175
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-9141C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365175 | ||||||
chr22:39365222
|
A | G | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-9094A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365222 | ||||||
chr22:39365228
|
G | A | 16 | a0001c0001t0001g0106a0001c0001t0004g0107a0001c0001t0004g0154others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-9088G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365228 | ||||||
chr22:39365240
|
T | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 212 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.100-9076T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365240 | ||||||
chr22:39365250
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.100-9066G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365250 | ||||||
chr22:39365254
|
C | T | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-9062C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365254 | ||||||
chr22:39365264
|
C | T | 12 | a0001c0001t0001g0119a0001c0001t0001g0276a0001c0001t0001g0278others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-9052C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365264 | ||||||
chr22:39365403
|
C | T | 1 | a0002c0002t0002g0246 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.100-8913C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365403 | ||||||
chr22:39365451
|
G | C | 28 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(25): Show | 28 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-8865G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365451 | ||||||
chr22:39365499
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-8817C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365499 | ||||||
chr22:39365548
|
T | A | 12 | a0001c0001t0001g0119a0001c0001t0001g0276a0001c0001t0001g0278others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-8768T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365548 | ||||||
chr22:39365586
|
T | G | 29 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(26): Show | 29 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-8730T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365586 | ||||||
chr22:39365625
|
G | C | 28 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(25): Show | 28 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-8691G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365625 | ||||||
chr22:39365627
|
G | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-8689G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365627 | ||||||
chr22:39365644
|
AG | A | 28 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(25): Show | 28 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-8667delG | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365644 | |||||
chr22:39365679
|
A | G | 29 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0276others(26): Show | 29 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.100-8637A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365679 | ||||||
chr22:39365765
|
C | T | 12 | a0001c0001t0001g0119a0001c0001t0001g0276a0001c0001t0001g0278others(9): Show | 12 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-8551C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365765 | ||||||
chr22:39365840
|
T | C | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100-8476T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365840 | ||||||
chr22:39365923
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0085 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.100-8393A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365923 | ||||||
chr22:39365976
|
G | A | 2 | a0001c0001t0006g0263a0002c0002t0002g0264 | 2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-8340G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39365976 | ||||||
chr22:39365988
|
C | CT | 14 | a0001c0001t0001g0141a0001c0001t0001g0156a0001c0001t0001g0162others(11): Show | 14 | HG01175.hp1 HG01243.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-8301dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0265 | 3 | HG01167.hp1 HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.100-8310_100-8301d others(12): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0003 | 3 | HG01081.hp2 HG01169.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.100-8311_100-8301d others(13): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(5): Show |
12 | a0001c0001t0001g0066a0001c0001t0001g0132a0001c0001t0001g0151others(9): Show | 12 | HG01071.hp1 HG01358.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-8312_100-8301d others(14): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(6): Show |
34 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0027others(31): Show | 36 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.100-8313_100-8301d others(15): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(7): Show |
55 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 62 | HG00323.hp1 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.100-8314_100-8301d others(16): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(8): Show |
22 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0032others(19): Show | 22 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-8315_100-8301d others(17): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-8316_100-8301d others(18): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0027g0060 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100-8317_100-8301d others(19): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0061 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.100-8318_100-8301d others(20): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0001g0047 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.100-8320_100-8301d others(22): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0024 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.100-8321_100-8301d others(23): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
CT | C | 17 | a0001c0001t0001g0278a0001c0001t0003g0125a0001c0001t0003g0166others(14): Show | 17 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-8301delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39365988
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0017g0270others(2): Show | 5 | HG01243.hp2 HG02056.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-8310_100-8301d others(12): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39365988 | |||||
chr22:39366151
|
G | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-8165G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366151 | ||||||
chr22:39366196
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-8120C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366196 | ||||||
chr22:39366197
|
T | C | 1 | a0002c0002t0002g0252 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100-8119T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366197 | ||||||
chr22:39366197
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-8119T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366197 | ||||||
chr22:39366198
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-8118C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366198 | ||||||
chr22:39366199
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.100-8117A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366199 | ||||||
chr22:39366306
|
A | G | 20 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0187others(17): Show | 20 | HG01109.hp1 HG01109.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-8010A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366306 | ||||||
chr22:39366378
|
G | T | 1 | a0001c0001t0001g0106 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-7938G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366378 | ||||||
chr22:39366416
|
C | T | 1 | a0002c0002t0002g0245 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.100-7900C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366416 | ||||||
chr22:39366501
|
C | T | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7815C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366501 | ||||||
chr22:39366571
|
G | A | 6 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0006g0202others(3): Show | 6 | HG01243.hp2 HG02056.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-7745G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366571 | ||||||
chr22:39366578
|
G | A | 6 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(3): Show | 6 | HG02257.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-7738G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366578 | ||||||
chr22:39366651
|
T | A | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7665T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366651 | ||||||
chr22:39366707
|
C | A | 1 | a0001c0001t0004g0260 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100-7609C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366707 | ||||||
chr22:39366725
|
T | C | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7591T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366725 | ||||||
chr22:39366850
|
T | G | 1 | a0001c0001t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-7466T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366850 | ||||||
chr22:39366867
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.100-7449C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366867 | ||||||
chr22:39366945
|
G | A | 2 | a0001c0001t0001g0274a0001c0009t0032g0193 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.100-7371G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366945 | ||||||
chr22:39366966
|
A | G | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7350A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366966 | ||||||
chr22:39366982
|
C | T | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7334C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366982 | ||||||
chr22:39366985
|
A | C | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7331A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39366985 | ||||||
chr22:39367039
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-7277C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367039 | ||||||
chr22:39367059
|
A | G | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7257A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367059 | ||||||
chr22:39367093
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0087 | 2 | HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.100-7223C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367093 | ||||||
chr22:39367153
|
C | T | 16 | a0001c0001t0001g0106a0001c0001t0004g0107a0001c0001t0004g0154others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-7163C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367153 | ||||||
chr22:39367178
|
C | T | 14 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-7138C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367178 | ||||||
chr22:39367189
|
C | T | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-7127C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367189 | ||||||
chr22:39367252
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-7064C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367252 | ||||||
chr22:39367335
|
A | G | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-6981A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367335 | ||||||
chr22:39367438
|
G | A | 16 | a0001c0001t0001g0106a0001c0001t0004g0107a0001c0001t0004g0154others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-6878G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367438 | ||||||
chr22:39367542
|
A | G | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-6774A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367542 | ||||||
chr22:39367545
|
G | A | 21 | a0001c0001t0001g0106a0001c0001t0001g0119a0001c0001t0001g0278others(18): Show | 21 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.100-6771G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367545 | ||||||
chr22:39367598
|
A | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 211 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.100-6718A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367598 | ||||||
chr22:39367642
|
G | C | 10 | a0001c0001t0001g0106a0001c0001t0004g0154a0001c0001t0004g0167others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-6674G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367642 | ||||||
chr22:39367643
|
C | A | 10 | a0001c0001t0001g0106a0001c0001t0004g0154a0001c0001t0004g0167others(7): Show | 10 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-6673C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367643 | ||||||
chr22:39367759
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-6557G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367759 | ||||||
chr22:39367771
|
C | T | 1 | a0002c0002t0011g0123 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100-6545C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367771 | ||||||
chr22:39367822
|
C | CA | 44 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0064others(41): Show | 44 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.100-6474dupA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39367822 | |||||
chr22:39367822
|
CA | C | 9 | a0001c0001t0001g0072a0001c0001t0001g0104a0001c0001t0001g0119others(6): Show | 9 | HG00639.hp2 HG01070.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-6474delA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39367822 | |||||
chr22:39367842
|
A | C | 1 | a0001c0001t0001g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-6474A>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367842 | ||||||
chr22:39367908
|
G | A | 20 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0004g0107others(17): Show | 20 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-6408G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39367908 | ||||||
chr22:39368095
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.100-6221C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368095 | ||||||
chr22:39368099
|
G | C | 1 | a0002c0002t0002g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.100-6217G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368099 | ||||||
chr22:39368105
|
G | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-6211G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368105 | ||||||
chr22:39368136
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-6180T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368136 | ||||||
chr22:39368461
|
T | C | 22 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0004g0107others(19): Show | 22 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-5855T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368461 | ||||||
chr22:39368489
|
C | T | 1 | a0001c0001t0005g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-5827C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368489 | ||||||
chr22:39368495
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0087 | 2 | HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.100-5821G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368495 | ||||||
chr22:39368499
|
C | T | 3 | a0001c0001t0005g0128a0001c0001t0005g0140a0001c0001t0005g0145 | 3 | HG02896.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.100-5817C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368499 | ||||||
chr22:39368527
|
G | A | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-5789G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368527 | ||||||
chr22:39368549
|
C | T | 12 | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0230others(9): Show | 12 | HG02056.hp1 HG02647.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-5767C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368549 | ||||||
chr22:39368788
|
G | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0085a0001c0001t0001g0207others(1): Show | 4 | HG02258.hp2 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5528G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368788 | ||||||
chr22:39368819
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.100-5497T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39368819 | ||||||
chr22:39369072
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(5): Show | 8 | HG02056.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-5244C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369072 | ||||||
chr22:39369220
|
T | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-5096T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369220 | ||||||
chr22:39369288
|
G | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-5028G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369288 | ||||||
chr22:39369374
|
T | C | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-4942T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369374 | ||||||
chr22:39369436
|
G | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-4880G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369436 | ||||||
chr22:39369482
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0072 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.100-4834C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369482 | ||||||
chr22:39369549
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-4767C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369549 | ||||||
chr22:39369599
|
C | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.100-4717C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369599 | ||||||
chr22:39369702
|
C | G | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-4614C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369702 | ||||||
chr22:39369822
|
A | G | 4 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(1): Show | 4 | HG02071.hp1 NA18954.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-4494A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369822 | ||||||
chr22:39369941
|
C | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-4375C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39369941 | ||||||
chr22:39370124
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.100-4192T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370124 | ||||||
chr22:39370174
|
C | G | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-4142C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370174 | ||||||
chr22:39370200
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-4116G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370200 | ||||||
chr22:39370252
|
T | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(23): Show | 26 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.100-4064T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370252 | ||||||
chr22:39370324
|
G | T | 1 | a0001c0001t0007g0223 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100-3992G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370324 | ||||||
chr22:39370340
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-3976C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370340 | ||||||
chr22:39370435
|
C | G | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.100-3881C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370435 | ||||||
chr22:39370450
|
ATTTTTTG others(10): Show |
A | 1 | a0001c0001t0001g0238 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-3865_100-3849d others(19): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370450 | ||||||
chr22:39370463
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0001g0208 | 2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.100-3853A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370463 | ||||||
chr22:39370487
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.100-3829G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370487 | ||||||
chr22:39370564
|
G | A | 2 | a0001c0001t0006g0263a0002c0002t0002g0264 | 2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-3752G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370564 | ||||||
chr22:39370625
|
A | AT | 26 | a0001c0001t0001g0029a0001c0001t0001g0114a0001c0001t0001g0183others(23): Show | 26 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.100-3676dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39370625 | |||||
chr22:39370649
|
G | A | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.100-3667G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370649 | ||||||
chr22:39370653
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-3663C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370653 | ||||||
chr22:39370674
|
G | A | 4 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3642G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370674 | ||||||
chr22:39370681
|
A | G | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-3635A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370681 | ||||||
chr22:39370694
|
G | T | 26 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(23): Show | 26 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.100-3622G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370694 | ||||||
chr22:39370939
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0278a0001c0001t0005g0250others(1): Show | 4 | HG02647.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3377C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39370939 | ||||||
chr22:39371006
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(170): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.100-3310A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371006 | ||||||
chr22:39371075
|
T | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(5): Show | 8 | HG02056.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-3241T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371075 | ||||||
chr22:39371102
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100-3214A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371102 | ||||||
chr22:39371199
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0006g0202others(2): Show | 5 | HG02056.hp1 HG03041.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-3117G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371199 | ||||||
chr22:39371203
|
G | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0085 | 2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.100-3113G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371203 | ||||||
chr22:39371242
|
C | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.100-3074C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371242 | ||||||
chr22:39371278
|
A | G | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-3038A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371278 | ||||||
chr22:39371286
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.100-3030G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371286 | ||||||
chr22:39371302
|
C | T | 1 | a0001c0001t0023g0116 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100-3014C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371302 | ||||||
chr22:39371348
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.100-2968T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371348 | ||||||
chr22:39371372
|
A | G | 14 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-2944A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371372 | ||||||
chr22:39371385
|
A | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(20): Show | 23 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-2931A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371385 | ||||||
chr22:39371402
|
G | A | 3 | a0001c0001t0021g0172a0001c0004t0020g0218a0001c0004t0020g0219 | 3 | HG02723.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.100-2914G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371402 | ||||||
chr22:39371403
|
G | A | 2 | a0002c0002t0002g0254a0002c0002t0002g0258 | 2 | HG01069.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.100-2913G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371403 | ||||||
chr22:39371421
|
G | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-2895G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371421 | ||||||
chr22:39371451
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0072 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.100-2865G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371451 | ||||||
chr22:39371472
|
A | G | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-2844A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371472 | ||||||
chr22:39371476
|
CA | C | 199 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(196): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.100-2824delA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39371476 | |||||
chr22:39371512
|
G | A | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-2804G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371512 | ||||||
chr22:39371655
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0036others(7): Show | 11 | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-2661C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371655 | ||||||
chr22:39371656
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0189a0001c0001t0001g0192 | 3 | HG00639.hp2 HG01934.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.100-2660G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371656 | ||||||
chr22:39371664
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-2652C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371664 | ||||||
chr22:39371676
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-2640C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371676 | ||||||
chr22:39371677
|
G | A | 5 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0006g0202others(2): Show | 5 | HG02056.hp1 HG03041.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2639G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371677 | ||||||
chr22:39371725
|
T | G | 1 | a0001c0001t0001g0092 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.100-2591T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371725 | ||||||
chr22:39371782
|
G | A | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-2534G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371782 | ||||||
chr22:39371872
|
A | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.100-2444A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371872 | ||||||
chr22:39371874
|
AG | A | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-2441delG | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371874 | ||||||
chr22:39371889
|
G | A | 8 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(5): Show | 8 | HG02056.hp1 HG03041.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-2427G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371889 | ||||||
chr22:39371978
|
G | T | 3 | a0001c0001t0021g0172a0001c0004t0020g0218a0001c0004t0020g0219 | 3 | HG02723.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.100-2338G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371978 | ||||||
chr22:39371989
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0034others(30): Show | 36 | HG00280.hp1 HG00544.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-2327T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39371989 | ||||||
chr22:39372004
|
G | A | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.100-2312G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372004 | ||||||
chr22:39372051
|
C | T | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-2265C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372051 | ||||||
chr22:39372075
|
G | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0097a0001c0001t0001g0156others(8): Show | 12 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-2241G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372075 | ||||||
chr22:39372123
|
C | CT | 15 | a0001c0001t0003g0125a0001c0001t0003g0168a0001c0001t0003g0170others(12): Show | 15 | HG01069.hp2 HG01175.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-2168dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372123 | |||||
chr22:39372123
|
CT | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.100-2168delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372123 | |||||
chr22:39372123
|
CTT | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0051a0001c0001t0001g0097others(8): Show | 11 | HG00280.hp2 HG01074.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-2169_100-2168d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372123 | |||||
chr22:39372123
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0006g0202others(5): Show | 8 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-2175_100-2168d others(10): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372123 | |||||
chr22:39372153
|
C | T | 14 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-2163C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372153 | ||||||
chr22:39372192
|
GT | G | 11 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(8): Show | 11 | HG02056.hp1 HG02886.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-2122delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372192 | |||||
chr22:39372279
|
G | A | 4 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0019g0127others(1): Show | 4 | HG02056.hp1 HG03710.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2037G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372279 | ||||||
chr22:39372288
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.100-2028C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372288 | ||||||
chr22:39372429
|
C | T | 41 | a0001c0001t0001g0104a0001c0001t0001g0180a0001c0001t0001g0181others(38): Show | 41 | HG00639.hp2 HG01109.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.100-1887C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372429 | ||||||
chr22:39372430
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0032 | 3 | HG00621.hp2 HG03927.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.100-1886G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372430 | ||||||
chr22:39372438
|
C | CT | 59 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(56): Show | 64 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.100-1848dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372438 | |||||
chr22:39372438
|
C | CTT | 8 | a0001c0001t0001g0114a0001c0001t0001g0132a0001c0001t0003g0166others(5): Show | 8 | HG01175.hp1 HG02148.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-1849_100-1848d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372438 | |||||
chr22:39372438
|
CT | C | 18 | a0001c0001t0001g0023a0001c0001t0001g0097a0001c0001t0001g0104others(15): Show | 18 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.100-1848delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372438 | |||||
chr22:39372438
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0010t0001g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-1859_100-1848d others(14): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39372438 | |||||
chr22:39372474
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.100-1842G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372474 | ||||||
chr22:39372699
|
C | T | 2 | a0001c0004t0020g0218a0001c0004t0020g0219 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.100-1617C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372699 | ||||||
chr22:39372732
|
G | T | 1 | a0001c0001t0001g0108 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.100-1584G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372732 | ||||||
chr22:39372912
|
T | C | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1404T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39372912 | ||||||
chr22:39373039
|
G | C | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1277G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373039 | ||||||
chr22:39373070
|
A | T | 1 | a0002c0002t0008g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.100-1246A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373070 | ||||||
chr22:39373090
|
G | T | 1 | a0001c0001t0010g0190 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100-1226G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373090 | ||||||
chr22:39373134
|
T | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1182T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373134 | ||||||
chr22:39373138
|
T | TAC | 22 | a0001c0001t0001g0045a0001c0001t0001g0055a0001c0001t0001g0064others(19): Show | 22 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-1150_100-1149d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39373138 | |||||
chr22:39373138
|
T | TACAC | 3 | a0001c0001t0001g0220a0001c0003t0010g0179a0001c0003t0028g0212 | 3 | HG02258.hp2 HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.100-1152_100-1149d others(6): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39373138 | |||||
chr22:39373138
|
TAC | T | 64 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0063others(61): Show | 67 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.100-1150_100-1149d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39373138 | |||||
chr22:39373138
|
TACAC | T | 12 | a0001c0001t0001g0029a0001c0001t0001g0104a0001c0001t0001g0189others(9): Show | 12 | HG00639.hp2 HG01934.hp2 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.100-1152_100-1149d others(6): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr22 | 39373138 | |||||
chr22:39373140
|
C | G | 2 | a0002c0002t0011g0112a0002c0002t0011g0123 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100-1176C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373140 | ||||||
chr22:39373159
|
A | G | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1157A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373159 | ||||||
chr22:39373164
|
C | T | 14 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-1152C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373164 | ||||||
chr22:39373166
|
C | G | 14 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-1150C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373166 | ||||||
chr22:39373166
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1150C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373166 | ||||||
chr22:39373172
|
TAGA | T | 14 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(11): Show | 14 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-1143_100-1141d others(5): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373172 | ||||||
chr22:39373231
|
T | C | 26 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(23): Show | 26 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.100-1085T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373231 | ||||||
chr22:39373246
|
G | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-1070G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373246 | ||||||
chr22:39373325
|
T | C | 21 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0187others(18): Show | 21 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.100-991T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373325 | ||||||
chr22:39373404
|
G | C | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.100-912G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373404 | ||||||
chr22:39373515
|
C | G | 2 | a0001c0001t0006g0263a0002c0002t0002g0264 | 2 | HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.100-801C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373515 | ||||||
chr22:39373570
|
C | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-746C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373570 | ||||||
chr22:39373668
|
G | A | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-648G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373668 | ||||||
chr22:39373751
|
G | A | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.100-565G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373751 | ||||||
chr22:39373813
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(197): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.100-503T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373813 | ||||||
chr22:39373876
|
G | C | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-440G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39373876 | ||||||
chr22:39374113
|
A | G | 3 | a0002c0002t0002g0267a0002c0002t0002g0269a0002c0002t0022g0268 | 3 | HG01099.hp2 HG01106.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.100-203A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39374113 | ||||||
chr22:39374149
|
T | C | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100-167T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39374149 | ||||||
chr22:39374252
|
C | G | 23 | a0001c0001t0001g0029a0001c0001t0001g0230a0001c0001t0001g0274others(20): Show | 23 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-64C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 1/3 | chr22 | 39374252 | ||||||
chr22:39374592
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.337+39A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39374592 | ||||||
chr22:39374750
|
C | G | 2 | a0001c0004t0020g0218a0001c0004t0020g0219 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.337+197C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39374750 | ||||||
chr22:39374775
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.337+222G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39374775 | ||||||
chr22:39374930
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.337+377C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39374930 | ||||||
chr22:39375109
|
G | A | 1 | a0002c0002t0002g0102 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.337+556G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375109 | ||||||
chr22:39375173
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0013g0018a0001c0001t0013g0272others(1): Show | 4 | HG02074.hp2 HG02886.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+620G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375173 | ||||||
chr22:39375357
|
C | A | 1 | a0001c0001t0031g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.338-695C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375357 | ||||||
chr22:39375580
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.338-472G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375580 | ||||||
chr22:39375590
|
C | A | 2 | a0001c0001t0013g0272a0001c0001t0013g0273 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.338-462C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375590 | ||||||
chr22:39375664
|
C | T | 15 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0022others(12): Show | 15 | HG00423.hp2 HG01099.hp1 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.338-388C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375664 | ||||||
chr22:39375674
|
C | G | 1 | a0001c0001t0009g0228 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.338-378C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375674 | ||||||
chr22:39375682
|
C | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0077others(28): Show | 33 | HG00280.hp1 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.338-370C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375682 | ||||||
chr22:39375915
|
G | C | 27 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(24): Show | 29 | HG00140.hp1 HG00639.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.338-137G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39375915 | ||||||
chr22:39376024
|
T | C | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.338-28T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39376024 | ||||||
chr22:39376033
|
C | G | 1 | a0001c0001t0004g0154 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.338-19C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39376033 | ||||||
chr22:39376045
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG02083.hp2 | splice_region_variant&intron_variant | LOW | c.338-7C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 2/3 | chr22 | 39376045 | ||||||
chr22:39376215
|
G | C | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+18G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376215 | ||||||
chr22:39376396
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.483+199A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376396 | ||||||
chr22:39376453
|
G | A | 12 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(9): Show | 12 | HG01175.hp1 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.483+256G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376453 | ||||||
chr22:39376463
|
AC | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.483+276delC | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39376463 | |||||
chr22:39376463
|
ACC | A | 20 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(17): Show | 20 | HG01175.hp1 HG02129.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.483+275_483+276del others(2): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39376463 | |||||
chr22:39376632
|
A | G | 2 | a0001c0001t0009g0227a0001c0001t0009g0228 | 2 | HG02129.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.483+435A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376632 | ||||||
chr22:39376737
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.483+540C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376737 | ||||||
chr22:39376752
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0189a0001c0001t0001g0278 | 3 | HG02615.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.483+555G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376752 | ||||||
chr22:39376758
|
ATCCTAAG | A | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+569_483+575del others(7): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39376758 | |||||
chr22:39376787
|
C | T | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+590C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376787 | ||||||
chr22:39376910
|
T | C | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+713T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39376910 | ||||||
chr22:39376956
|
CCT | C | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+762_483+763del others(2): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39376956 | |||||
chr22:39377039
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.483+842T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377039 | ||||||
chr22:39377093
|
G | A | 1 | a0001c0001t0005g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.483+896G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377093 | ||||||
chr22:39377093
|
G | C | 18 | a0001c0001t0001g0220a0001c0001t0003g0125a0001c0001t0003g0166others(15): Show | 18 | HG01175.hp1 HG02145.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.483+896G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377093 | ||||||
chr22:39377182
|
GT | G | 6 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0001g0189others(3): Show | 6 | HG00639.hp2 HG01934.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+988delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39377182 | |||||
chr22:39377336
|
C | G | 3 | a0001c0001t0006g0101a0001c0001t0006g0103a0001c0001t0006g0188 | 3 | HG01109.hp1 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.483+1139C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377336 | ||||||
chr22:39377619
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.483+1422G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377619 | ||||||
chr22:39377735
|
C | T | 1 | a0001c0001t0005g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.483+1538C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377735 | ||||||
chr22:39377789
|
G | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0001g0189others(3): Show | 6 | HG00639.hp2 HG01934.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.483+1592G>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377789 | ||||||
chr22:39377856
|
C | T | 6 | a0001c0001t0004g0107a0001c0001t0004g0185a0001c0001t0004g0205others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.483+1659C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377856 | ||||||
chr22:39377857
|
G | A | 2 | a0001c0001t0003g0124a0001c0001t0003g0144 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.483+1660G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39377857 | ||||||
chr22:39378146
|
C | T | 3 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273 | 3 | HG02886.hp1 HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.483+1949C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378146 | ||||||
chr22:39378235
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.483+2038G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378235 | ||||||
chr22:39378283
|
A | G | 2 | a0001c0004t0020g0218a0001c0004t0020g0219 | 2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.483+2086A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378283 | ||||||
chr22:39378368
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.483+2171C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378368 | ||||||
chr22:39378373
|
G | GTTCA | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.483+2200_483+2203d others(6): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39378373 | |||||
chr22:39378373
|
G | GTTCATTC others(5): Show |
2 | a0001c0001t0001g0189a0001c0009t0032g0193 | 2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.483+2192_483+2203d others(14): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39378373 | |||||
chr22:39378373
|
G | GTTCATTC others(9): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0192 | 2 | HG00639.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.483+2188_483+2203d others(18): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39378373 | |||||
chr22:39378443
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.483+2246A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378443 | ||||||
chr22:39378520
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(201): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.483+2323A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378520 | ||||||
chr22:39378629
|
G | A | 1 | a0001c0001t0004g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.483+2432G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378629 | ||||||
chr22:39378815
|
C | T | 28 | a0001c0001t0003g0124a0001c0001t0003g0125a0001c0001t0003g0144others(25): Show | 28 | HG01109.hp1 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.483+2618C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378815 | ||||||
chr22:39378840
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.483+2643C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378840 | ||||||
chr22:39378844
|
T | C | 1 | a0001c0009t0032g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483+2647T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378844 | ||||||
chr22:39378919
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.483+2722T>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39378919 | ||||||
chr22:39379005
|
G | C | 19 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(16): Show | 19 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.484-2691G>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379005 | ||||||
chr22:39379042
|
C | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.484-2654C>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379042 | ||||||
chr22:39379150
|
G | A | 19 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(16): Show | 19 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.484-2546G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379150 | ||||||
chr22:39379151
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.484-2545G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379151 | ||||||
chr22:39379245
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.484-2451A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379245 | ||||||
chr22:39379263
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.484-2433T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379263 | ||||||
chr22:39379275
|
G | A | 1 | a0001c0010t0001g0275 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.484-2421G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379275 | ||||||
chr22:39379317
|
T | G | 19 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(16): Show | 19 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.484-2379T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379317 | ||||||
chr22:39379326
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.484-2370T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379326 | ||||||
chr22:39379362
|
G | A | 5 | a0001c0001t0001g0104a0001c0001t0001g0119a0001c0001t0001g0189others(2): Show | 5 | HG00639.hp2 HG01934.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.484-2334G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379362 | ||||||
chr22:39379395
|
A | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.484-2301A>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379395 | ||||||
chr22:39379479
|
C | G | 2 | a0001c0001t0001g0066a0001c0001t0001g0072 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.484-2217C>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379479 | ||||||
chr22:39379502
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.484-2194C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379502 | ||||||
chr22:39379578
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(184): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.484-2118G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379578 | ||||||
chr22:39379644
|
A | AAG | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.484-2052_484-2051i others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379644 | ||||||
chr22:39379645
|
G | A | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(205): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.484-2051G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379645 | ||||||
chr22:39379781
|
G | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.484-1915G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39379781 | ||||||
chr22:39380163
|
G | GA | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.484-1517dupA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39380163 | |||||
chr22:39380163
|
GA | G | 16 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(13): Show | 16 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.484-1517delA | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39380163 | |||||
chr22:39380164
|
A | G | 2 | a0001c0001t0013g0272a0001c0001t0013g0273 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.484-1532A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39380164 | ||||||
chr22:39380325
|
A | G | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-1371A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39380325 | ||||||
chr22:39380616
|
C | CT | 62 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0032others(59): Show | 62 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.484-1056dupT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39380616 | |||||
chr22:39380616
|
C | CTT | 8 | a0001c0001t0001g0187a0001c0001t0004g0184a0001c0001t0004g0260others(5): Show | 8 | HG02056.hp1 HG02129.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-1057_484-1056d others(4): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39380616 | |||||
chr22:39380616
|
C | CTTTTT | 15 | a0001c0001t0003g0125a0001c0001t0003g0166a0001c0001t0003g0168others(12): Show | 15 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-1060_484-1056d others(7): Show |
SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39380616 | |||||
chr22:39380616
|
CT | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0161a0001c0001t0001g0163others(7): Show | 12 | HG01109.hp1 HG01168.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.484-1056delT | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr22 | 39380616 | |||||
chr22:39380707
|
G | A | 4 | a0001c0001t0009g0056a0001c0001t0009g0075a0001c0001t0009g0227others(1): Show | 4 | HG02129.hp2 NA18945.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-989G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39380707 | ||||||
chr22:39380836
|
G | A | 19 | a0001c0001t0003g0124a0001c0001t0003g0125a0001c0001t0003g0144others(16): Show | 19 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.484-860G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39380836 | ||||||
chr22:39380898
|
A | G | 4 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02886.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-798A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39380898 | ||||||
chr22:39381054
|
A | G | 15 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(12): Show | 15 | HG01243.hp1 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.484-642A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381054 | ||||||
chr22:39381103
|
C | T | 2 | a0002c0002t0002g0196a0002c0002t0002g0199 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.484-593C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381103 | ||||||
chr22:39381139
|
A | G | 4 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02886.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-557A>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381139 | ||||||
chr22:39381174
|
T | C | 41 | a0001c0001t0003g0124a0001c0001t0003g0125a0001c0001t0003g0144others(38): Show | 41 | HG01175.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.484-522T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381174 | ||||||
chr22:39381249
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(195): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.484-447T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381249 | ||||||
chr22:39381451
|
G | A | 1 | a0002c0002t0002g0159 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.484-245G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381451 | ||||||
chr22:39381468
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.484-228G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381468 | ||||||
chr22:39381487
|
T | C | 17 | a0001c0001t0004g0107a0001c0001t0004g0154a0001c0001t0004g0167others(14): Show | 17 | HG01243.hp1 HG02056.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.484-209T>C | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381487 | ||||||
chr22:39381518
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(194): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.484-178G>A | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381518 | ||||||
chr22:39381560
|
T | G | 4 | a0001c0001t0013g0018a0001c0001t0013g0272a0001c0001t0013g0273others(1): Show | 4 | HG02886.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-136T>G | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381560 | ||||||
chr22:39381661
|
C | T | 1 | a0001c0009t0032g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.484-35C>T | SYNGR1 | ENSG00000100321.15 | transcript | ENST00000328933.10 | protein_coding | 3/3 | chr22 | 39381661 |