geneid | 2673 |
---|---|
ensemblid | ENSG00000198380.13 |
hgncid | 4241 |
symbol | GFPT1 |
name | glutamine--fructose-6-phosphate transaminase 1 |
refseq_nuc | NM_001244710.2 |
refseq_prot | NP_001231639.1 |
ensembl_nuc | ENST00000357308.9 |
ensembl_prot | ENSP00000349860.4 |
mane_status | MANE Select |
chr | chr2 |
start | 69319780 |
end | 69387227 |
strand | - |
ver | v1.2 |
region | chr2:69319780-69387227 |
region5000 | chr2:69314780-69392227 |
regionname0 | GFPT1_chr2_69319780_69387227 |
regionname5000 | GFPT1_chr2_69314780_69392227 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 699 | 365 | 90 | 58 | 169 | 10 | 36 | 127 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0002 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2100 | 318 | 88 | 57 | 129 | 10 | 32 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
c0002 | 0/0 | 2100 | 44 | 2 | 0 | 39 | 0 | 3 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
c0003 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
c0004 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
c0005 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
c0006 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 6566 | 97 | 4 | 23 | 59 | 1 | 9 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0002 | 0/0 | 6565 | 89 | 30 | 17 | 32 | 2 | 8 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0003 | 0/1 | 6565 | 37 | 14 | 7 | 6 | 4 | 5 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0004 | 0/0 | 6562 | 22 | 2 | 0 | 18 | 0 | 2 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0005 | 0/0 | 6566 | 19 | 2 | 0 | 14 | 0 | 3 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0006 | 0/0 | 6562 | 14 | 0 | 0 | 14 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0007 | 0/0 | 6565 | 7 | 7 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0008 | 0/0 | 6565 | 6 | 1 | 3 | 0 | 1 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0009 | 0/0 | 6565 | 5 | 5 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0010 | 0/0 | 6565 | 5 | 0 | 0 | 5 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0011 | 0/0 | 6566 | 4 | 4 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0012 | 0/0 | 6566 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0013 | 0/0 | 6564 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0014 | 0/0 | 6566 | 3 | 0 | 1 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0015 | 0/0 | 6565 | 3 | 2 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0016 | 0/0 | 6566 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0017 | 0/0 | 6562 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0018 | 0/0 | 6564 | 2 | 0 | 1 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0019 | 0/0 | 6568 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0020 | 0/0 | 6567 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0021 | 0/0 | 6565 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0022 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0023 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0024 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0025 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0026 | 0/0 | 6643 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0027 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0028 | 0/0 | 6566 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0029 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0030 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0031 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0032 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0033 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0034 | 0/0 | 6566 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0035 | 0/0 | 6566 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0036 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0037 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0038 | 0/0 | 6564 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0039 | 0/0 | 6564 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0040 | 0/0 | 6561 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0041 | 0/0 | 6563 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0042 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0043 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0044 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0045 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0046 | 0/0 | 6565 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0047 | 0/0 | 6562 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0048 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0049 | 0/0 | 6565 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0050 | 0/0 | 6566 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0051 | 0/0 | 6565 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0052 | 0/0 | 6564 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0053 | 0/0 | 6561 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0054 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0055 | 0/0 | 6562 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0056 | 0/0 | 6561 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0057 | 0/0 | 6566 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
t0058 | 0/0 | 6566 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
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 | 4 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0005 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2100 | 318 | 88 | 57 | 129 | 10 | 32 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002 | 0/0 | 2100 | 44 | 2 | 0 | 39 | 0 | 3 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0003 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0005 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0006 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0002c0004 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8665 | 94 | 4 | 23 | 57 | 1 | 8 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0002 | 0/0 | 8664 | 88 | 30 | 16 | 32 | 2 | 8 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0003 | 0/1 | 8664 | 37 | 14 | 7 | 6 | 4 | 5 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0005 | 0/0 | 8665 | 19 | 2 | 0 | 14 | 0 | 3 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0007 | 0/0 | 8664 | 7 | 7 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0008 | 0/0 | 8664 | 6 | 1 | 3 | 0 | 1 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0009 | 0/0 | 8664 | 5 | 5 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0010 | 0/0 | 8664 | 5 | 0 | 0 | 5 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0011 | 0/0 | 8665 | 4 | 4 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0012 | 0/0 | 8665 | 3 | 3 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0013 | 0/0 | 8663 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0014 | 0/0 | 8665 | 3 | 0 | 1 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0015 | 0/0 | 8664 | 3 | 2 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0016 | 0/0 | 8665 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0018 | 0/0 | 8663 | 2 | 0 | 1 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0019 | 0/0 | 8667 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0020 | 0/0 | 8666 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0021 | 0/0 | 8664 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0022 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0023 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0024 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0025 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0026 | 0/0 | 8742 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0027 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0028 | 0/0 | 8665 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0029 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0030 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0031 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0032 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0033 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0034 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0035 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0036 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0037 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0038 | 0/0 | 8663 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0039 | 0/0 | 8663 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0042 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0043 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0044 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0045 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0046 | 0/0 | 8664 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0048 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0049 | 0/0 | 8664 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0050 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0051 | 0/0 | 8664 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0052 | 0/0 | 8663 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0054 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0057 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0001t0058 | 0/0 | 8665 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0004 | 0/0 | 8661 | 22 | 2 | 0 | 18 | 0 | 2 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0006 | 0/0 | 8661 | 14 | 0 | 0 | 14 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0017 | 0/0 | 8661 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0040 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0041 | 0/0 | 8662 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0047 | 0/0 | 8661 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0053 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0055 | 0/0 | 8661 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0002t0056 | 0/0 | 8660 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0003t0002 | 0/0 | 8664 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0005t0001 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0001c0006t0001 | 0/0 | 8665 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
a0002c0004t0001 | 0/0 | 8665 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | copy fasta | chr2 | 69314780 | 69392227 |
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 | 4 | 0 | 4 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0005 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0008g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0010g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0010g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0010g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0011g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0012g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0013g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0013g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0013g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0014g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0014g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0014g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0015g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0016g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0016g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0018g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0018g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0019g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0019g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0020g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0021g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0021g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0022g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0023g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0024g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0025g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0026g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0027g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0028g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0029g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0030g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0031g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0032g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0033g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0034g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0035g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0036g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0037g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0038g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0039g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0042g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0043g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0044g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0045g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0046g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0048g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0049g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0050g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0051g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0052g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0054g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0057g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0001t0058g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0006g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0017g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0017g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0040g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0041g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0047g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0053g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0055g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0002t0056g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0005t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0001c0006t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
a0002c0004t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | GBR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00408 | hp1 | a0001 | c0001 | t0027 | g0278 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00544 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00597 | hp1 | a0001 | c0002 | t0004 | g0152 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00597 | hp2 | a0001 | c0001 | t0010 | g0198 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00609 | hp1 | a0001 | c0002 | t0006 | g0123 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00621 | hp1 | a0001 | c0002 | t0006 | g0243 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00673 | hp1 | a0001 | c0001 | t0010 | g0184 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00735 | hp2 | a0001 | c0001 | t0034 | g0247 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0011 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01069 | hp2 | a0001 | c0003 | t0002 | g0228 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01167 | hp1 | a0001 | c0001 | t0018 | g0172 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01167 | hp2 | a0001 | c0001 | t0039 | g0242 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01243 | hp1 | a0001 | c0001 | t0015 | g0034 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01243 | hp2 | a0001 | c0001 | t0058 | g0343 | AMR | PUR | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0168 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01433 | hp1 | a0001 | c0001 | t0050 | g0031 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01496 | hp1 | a0001 | c0001 | t0057 | g0264 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0214 | AMR | CLM | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01515 | hp2 | a0001 | c0001 | t0037 | g0213 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0066 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01516 | hp2 | a0001 | c0001 | t0008 | g0178 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01517 | hp1 | a0001 | c0001 | t0038 | g0179 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | IBS | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0028 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01978 | hp2 | a0001 | c0001 | t0014 | g0236 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02015 | hp1 | a0001 | c0002 | t0006 | g0149 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02027 | hp1 | a0001 | c0001 | t0046 | g0186 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0103 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0134 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02132 | hp1 | a0001 | c0002 | t0004 | g0136 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02145 | hp1 | a0001 | c0001 | t0030 | g0334 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CDX | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CDX | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0011 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0234 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02451 | hp2 | a0001 | c0001 | t0024 | g0045 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0107 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0043 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02717 | hp1 | a0001 | c0001 | t0025 | g0020 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02723 | hp1 | a0001 | c0001 | t0022 | g0017 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02735 | hp1 | a0001 | c0001 | t0052 | g0076 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02738 | hp1 | a0001 | c0002 | t0004 | g0137 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02886 | hp1 | a0001 | c0001 | t0048 | g0192 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02895 | hp2 | a0001 | c0001 | t0019 | g0055 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02897 | hp1 | a0001 | c0001 | t0019 | g0056 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02922 | hp1 | a0001 | c0001 | t0023 | g0018 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0121 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0036 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03041 | hp2 | a0001 | c0001 | t0020 | g0053 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03098 | hp1 | a0001 | c0001 | t0021 | g0189 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03139 | hp2 | a0001 | c0001 | t0035 | g0246 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03195 | hp2 | a0001 | c0001 | t0011 | g0119 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0222 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03239 | hp1 | a0001 | c0001 | t0032 | g0277 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03239 | hp2 | a0001 | c0001 | t0008 | g0199 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03486 | hp1 | a0001 | c0001 | t0009 | g0042 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0040 | AFR | ESN | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03540 | hp1 | a0001 | c0001 | t0021 | g0190 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03579 | hp1 | a0001 | c0001 | t0042 | g0108 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03654 | hp2 | a0001 | c0001 | t0043 | g0071 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03669 | hp2 | a0001 | c0001 | t0045 | g0058 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03710 | hp2 | a0001 | c0006 | t0001 | g0337 | SAS | PJL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03831 | hp1 | a0001 | c0001 | t0031 | g0330 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03834 | hp1 | a0001 | c0001 | t0028 | g0248 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0084 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0309 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04184 | hp2 | a0001 | c0002 | t0004 | g0154 | SAS | BEB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04199 | hp1 | a0001 | c0001 | t0005 | g0230 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04204 | hp2 | a0001 | c0001 | t0051 | g0113 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0118 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG04228 | hp2 | a0001 | c0002 | t0047 | g0046 | SAS | STU | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18612 | hp2 | a0001 | c0001 | t0054 | g0101 | EAS | CHB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0035 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18942 | hp1 | a0001 | c0001 | t0010 | g0180 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18942 | hp2 | a0001 | c0002 | t0056 | g0147 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18943 | hp1 | a0001 | c0002 | t0006 | g0150 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18946 | hp1 | a0001 | c0001 | t0018 | g0048 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18946 | hp2 | a0001 | c0002 | t0053 | g0127 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18952 | hp1 | a0001 | c0002 | t0017 | g0223 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18952 | hp2 | a0001 | c0001 | t0013 | g0298 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18954 | hp2 | a0001 | c0002 | t0004 | g0128 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0126 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18956 | hp2 | a0001 | c0001 | t0033 | g0270 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18963 | hp1 | a0001 | c0002 | t0004 | g0125 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0153 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18964 | hp2 | a0001 | c0001 | t0014 | g0232 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18966 | hp2 | a0002 | c0004 | t0001 | g0324 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18970 | hp1 | a0001 | c0001 | t0016 | g0312 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18972 | hp2 | a0001 | c0002 | t0006 | g0014 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18973 | hp1 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18973 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18980 | hp2 | a0001 | c0002 | t0006 | g0244 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18988 | hp2 | a0001 | c0002 | t0006 | g0129 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18992 | hp1 | a0001 | c0002 | t0006 | g0132 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19001 | hp2 | a0001 | c0002 | t0006 | g0245 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19002 | hp1 | a0001 | c0002 | t0006 | g0131 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19002 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19003 | hp2 | a0001 | c0002 | t0004 | g0151 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19005 | hp1 | a0001 | c0002 | t0004 | g0141 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19006 | hp1 | a0001 | c0001 | t0010 | g0211 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0193 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19010 | hp1 | a0001 | c0002 | t0006 | g0133 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19011 | hp2 | a0001 | c0002 | t0004 | g0124 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0025 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19030 | hp2 | a0001 | c0001 | t0012 | g0057 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19058 | hp1 | a0001 | c0001 | t0013 | g0301 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19060 | hp2 | a0001 | c0002 | t0004 | g0146 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19063 | hp1 | a0001 | c0002 | t0004 | g0138 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0006 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19065 | hp2 | a0001 | c0002 | t0017 | g0145 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19066 | hp2 | a0001 | c0002 | t0004 | g0140 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19067 | hp1 | a0001 | c0001 | t0014 | g0204 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19068 | hp1 | a0001 | c0002 | t0006 | g0224 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19070 | hp1 | a0001 | c0001 | t0029 | g0269 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19070 | hp2 | a0001 | c0002 | t0006 | g0014 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19074 | hp1 | a0001 | c0001 | t0044 | g0177 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19075 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19075 | hp2 | a0001 | c0001 | t0013 | g0303 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19077 | hp1 | a0001 | c0005 | t0001 | g0320 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19078 | hp1 | a0001 | c0002 | t0040 | g0148 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19079 | hp1 | a0001 | c0002 | t0055 | g0135 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19080 | hp2 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19081 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19084 | hp1 | a0001 | c0002 | t0041 | g0143 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19088 | hp2 | a0001 | c0002 | t0004 | g0139 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19089 | hp1 | a0001 | c0001 | t0016 | g0280 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19089 | hp2 | a0001 | c0001 | t0026 | g0165 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19090 | hp2 | a0001 | c0002 | t0006 | g0130 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA19240 | hp2 | a0001 | c0001 | t0036 | g0109 | AFR | YRI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0203 | AFR | ASW | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA20129 | hp2 | a0001 | c0001 | t0012 | g0088 | AFR | ASW | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0081 | EUR | TSI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | TSI | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0122 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0120 | AFR | ACB | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA20300 | hp2 | a0001 | c0002 | t0004 | g0142 | AFR | USA | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
NA21309 | hp2 | a0001 | c0001 | t0049 | g0037 | AFR | LWK | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0069 | REF | REF | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | GFPT1_chr2_69314780_69392227 | GFPT1 | chr2 | 69314780 | 69392227 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69363562
|
C | T | 1 | a0002 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.332G>A | p.Arg111His | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/20 | 488/8665 | 332/2100 | 111/699 | chr2 | 69363562 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69329393
|
G | A | 1 | a0001c0006 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.1629C>T | p.Asp543Asp | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/20 | 1785/8665 | 1629/2100 | 543/699 | chr2 | 69329393 | ||
chr2:69354499
|
G | A | 1 | a0001c0002 | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
synonymous_variant | LOW | c.675C>T | p.Leu225Leu | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 8/20 | 831/8665 | 675/2100 | 225/699 | chr2 | 69354499 | ||
chr2:69356525
|
A | C | 1 | a0001c0005 | 1 | NA19077.hp1 | synonymous_variant | LOW | c.576T>G | p.Val192Val | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/20 | 732/8665 | 576/2100 | 192/699 | chr2 | 69356525 | ||
chr2:69370077
|
A | G | 1 | a0001c0003 | 1 | HG01069.hp2 | synonymous_variant | LOW | c.147T>C | p.Asp49Asp | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/20 | 303/8665 | 147/2100 | 49/699 | chr2 | 69370077 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69319823
|
A | G | 1 | a0001c0001t0011 | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6366T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6366 | chr2 | 69319823 | |||||
chr2:69319884
|
A | G | 1 | a0001c0001t0029 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6305T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6305 | chr2 | 69319884 | |||||
chr2:69320095
|
G | A | 1 | a0001c0001t0007 | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6094C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6094 | chr2 | 69320095 | |||||
chr2:69320104
|
G | C | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(42): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*6085C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6085 | chr2 | 69320104 | |||||
chr2:69320186
|
C | A | 2 | a0001c0001t0035a0001c0001t0058 | 2 | HG01243.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6003G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 6003 | chr2 | 69320186 | |||||
chr2:69320409
|
T | C | 1 | a0001c0002t0047 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5780A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5780 | chr2 | 69320409 | |||||
chr2:69320413
|
C | G | 1 | a0001c0001t0045 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5776G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5776 | chr2 | 69320413 | |||||
chr2:69320516
|
G | A | 1 | a0001c0001t0044 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5673C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5673 | chr2 | 69320516 | |||||
chr2:69320725
|
T | C | 2 | a0001c0001t0037a0001c0001t0038 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5464A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5464 | chr2 | 69320725 | |||||
chr2:69320787
|
C | CA | 3 | a0001c0001t0005a0001c0001t0051a0001c0001t0054 | 21 | HG02074.hp1 HG02451.hp1 HG02602.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5401dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5401 | chr2 | 69320787 | |||||
chr2:69321188
|
C | T | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(43): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*5001G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 5001 | chr2 | 69321188 | |||||
chr2:69321363
|
T | G | 5 | a0001c0001t0003a0001c0001t0022a0001c0001t0043others(2): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*4826A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4826 | chr2 | 69321363 | |||||
chr2:69321459
|
C | T | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(39): Show | 245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*4730G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4730 | chr2 | 69321459 | |||||
chr2:69321509
|
A | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4680T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4680 | chr2 | 69321509 | |||||
chr2:69321574
|
C | T | 1 | a0001c0001t0058 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4615G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4615 | chr2 | 69321574 | |||||
chr2:69321786
|
C | A | 2 | a0001c0001t0012a0001c0001t0025 | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4403G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4403 | chr2 | 69321786 | |||||
chr2:69321845
|
ATG | A | 1 | a0001c0001t0013 | 3 | NA18952.hp2 NA19058.hp1 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4342_*4343delCA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4342 | chr2 | 69321845 | |||||
chr2:69321886
|
T | C | 1 | a0001c0001t0046 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4303A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4303 | chr2 | 69321886 | |||||
chr2:69321915
|
T | A | 1 | a0001c0001t0035 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4274A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4274 | chr2 | 69321915 | |||||
chr2:69322130
|
T | C | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*4059A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4059 | chr2 | 69322130 | |||||
chr2:69322136
|
A | T | 1 | a0001c0001t0043 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4053T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 4053 | chr2 | 69322136 | |||||
chr2:69322199
|
AAAT | A | 9 | a0001c0002t0004a0001c0002t0006a0001c0002t0017others(6): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*3987_*3989delATT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3987 | chr2 | 69322199 | |||||
chr2:69322408
|
C | A | 4 | a0001c0002t0006a0001c0002t0040a0001c0002t0055others(1): Show | 17 | HG00609.hp1 HG00621.hp1 HG02015.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3781G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3781 | chr2 | 69322408 | |||||
chr2:69322613
|
T | C | 1 | a0001c0002t0017 | 2 | NA18952.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3576A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3576 | chr2 | 69322613 | |||||
chr2:69322751
|
T | C | 1 | a0001c0001t0032 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3438A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3438 | chr2 | 69322751 | |||||
chr2:69322842
|
T | C | 1 | a0001c0001t0030 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3347 | chr2 | 69322842 | |||||
chr2:69322844
|
G | A | 1 | a0001c0001t0007 | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3345C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3345 | chr2 | 69322844 | |||||
chr2:69322904
|
T | C | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(43): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
3_prime_UTR_variant | MODIFIER | c.*3285A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3285 | chr2 | 69322904 | |||||
chr2:69322994
|
T | C | 1 | a0001c0001t0048 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3195A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3195 | chr2 | 69322994 | |||||
chr2:69323055
|
T | C | 1 | a0001c0001t0010 | 5 | HG00597.hp2 HG00673.hp1 NA18942.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3134A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3134 | chr2 | 69323055 | |||||
chr2:69323098
|
T | G | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*3091A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3091 | chr2 | 69323098 | |||||
chr2:69323124
|
C | T | 48 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(45): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*3065G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 3065 | chr2 | 69323124 | |||||
chr2:69323273
|
T | C | 1 | a0001c0001t0034 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2916A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2916 | chr2 | 69323273 | |||||
chr2:69323282
|
G | A | 2 | a0001c0001t0012a0001c0001t0025 | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2907C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2907 | chr2 | 69323282 | |||||
chr2:69323391
|
G | T | 1 | a0001c0001t0042 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2798C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2798 | chr2 | 69323391 | |||||
chr2:69323504
|
T | C | 2 | a0001c0001t0015a0001c0001t0049 | 4 | HG01243.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2685A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2685 | chr2 | 69323504 | |||||
chr2:69323520
|
G | A | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(39): Show | 245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2669C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2669 | chr2 | 69323520 | |||||
chr2:69323637
|
T | C | 1 | a0001c0001t0049 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2552A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2552 | chr2 | 69323637 | |||||
chr2:69323678
|
A | T | 2 | a0001c0001t0012a0001c0001t0025 | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2511T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2511 | chr2 | 69323678 | |||||
chr2:69323678
|
AT | A | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(28): Show | 230 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2510delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2510 | chr2 | 69323678 | |||||
chr2:69323678
|
ATT | A | 8 | a0001c0001t0018a0001c0001t0038a0001c0001t0039others(5): Show | 9 | HG01167.hp1 HG01167.hp2 HG01517.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2509_*2510delAA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2509 | chr2 | 69323678 | |||||
chr2:69323679
|
T | A | 2 | a0001c0001t0033a0001c0001t0050 | 2 | HG01433.hp1 NA18956.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2510A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2510 | chr2 | 69323679 | |||||
chr2:69323825
|
G | A | 1 | a0001c0001t0034 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2364 | chr2 | 69323825 | |||||
chr2:69323879
|
T | C | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(39): Show | 245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2310A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2310 | chr2 | 69323879 | |||||
chr2:69323920
|
T | C | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 246 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*2269A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2269 | chr2 | 69323920 | |||||
chr2:69323966
|
G | A | 1 | a0001c0001t0054 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2223C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2223 | chr2 | 69323966 | |||||
chr2:69323970
|
G | A | 2 | a0001c0001t0019a0001c0001t0020 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2219C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 2219 | chr2 | 69323970 | |||||
chr2:69324201
|
T | TTG | 2 | a0001c0001t0019a0001c0001t0020 | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1986_*1987dupCA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1987 | chr2 | 69324201 | |||||
chr2:69324369
|
C | T | 1 | a0001c0002t0040 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1820G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1820 | chr2 | 69324369 | |||||
chr2:69324402
|
A | ACAGATCT others(71): Show |
1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786_*1787insATAG others(74): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1786 | chr2 | 69324402 | |||||
chr2:69324451
|
G | T | 1 | a0001c0001t0016 | 2 | NA18970.hp1 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1738C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1738 | chr2 | 69324451 | |||||
chr2:69324547
|
A | T | 1 | a0001c0001t0028 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1642T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1642 | chr2 | 69324547 | |||||
chr2:69324548
|
A | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1641T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1641 | chr2 | 69324548 | |||||
chr2:69324549
|
G | A | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1640C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1640 | chr2 | 69324549 | |||||
chr2:69324667
|
G | C | 2 | a0001c0002t0055a0001c0002t0056 | 2 | NA18942.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1522C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1522 | chr2 | 69324667 | |||||
chr2:69324687
|
A | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1502 | chr2 | 69324687 | |||||
chr2:69324705
|
G | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1484 | chr2 | 69324705 | |||||
chr2:69324837
|
A | T | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1352T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1352 | chr2 | 69324837 | |||||
chr2:69324945
|
C | A | 1 | a0001c0001t0007 | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1244G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1244 | chr2 | 69324945 | |||||
chr2:69324995
|
G | T | 1 | a0001c0001t0027 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1194C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1194 | chr2 | 69324995 | |||||
chr2:69325104
|
T | C | 2 | a0001c0001t0021a0001c0001t0023 | 3 | HG02922.hp1 HG03098.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1085A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1085 | chr2 | 69325104 | |||||
chr2:69325136
|
C | T | 1 | a0001c0001t0039 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1053G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 1053 | chr2 | 69325136 | |||||
chr2:69325319
|
G | T | 3 | a0001c0001t0008a0001c0001t0037a0001c0001t0038 | 8 | HG00738.hp2 HG01361.hp2 HG01496.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*870C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 870 | chr2 | 69325319 | |||||
chr2:69325322
|
C | T | 1 | a0001c0001t0036 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 867 | chr2 | 69325322 | |||||
chr2:69325333
|
A | G | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*856T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 856 | chr2 | 69325333 | |||||
chr2:69325389
|
C | A | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(39): Show | 245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*800G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 800 | chr2 | 69325389 | |||||
chr2:69325407
|
A | C | 1 | a0001c0001t0026 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 782 | chr2 | 69325407 | |||||
chr2:69325427
|
C | G | 1 | a0001c0001t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 762 | chr2 | 69325427 | |||||
chr2:69325586
|
C | T | 2 | a0001c0001t0009a0001c0001t0024 | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*603G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 603 | chr2 | 69325586 | |||||
chr2:69325626
|
C | A | 1 | a0001c0001t0057 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*563G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 20/20 | 563 | chr2 | 69325626 | |||||
chr2:69387186
|
G | A | 1 | a0001c0001t0058 | 1 | HG01243.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-115C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/20 | chr2 | 69387186 | ||||||
chr2:69387217
|
C | T | 1 | a0001c0001t0023 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-146G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/20 | 146 | chr2 | 69387217 | |||||
chr2:69387224
|
C | T | 1 | a0001c0001t0022 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/20 | 153 | chr2 | 69387224 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:69326243
|
GA | G | 188 | a0001c0001t0001g0311a0001c0001t0002g0004a0001c0001t0002g0010others(185): Show | 198 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.2056-11delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326243 | ||||||
chr2:69326243
|
GAA | G | 49 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(46): Show | 52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2056-12_2056-11del others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326243 | ||||||
chr2:69326244
|
A | G | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2056-11T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326244 | ||||||
chr2:69326256
|
A | G | 2 | a0001c0001t0002g0050a0001c0001t0050g0031 | 2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2056-23T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326256 | ||||||
chr2:69326461
|
A | T | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2056-228T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326461 | ||||||
chr2:69326488
|
A | G | 6 | a0001c0001t0010g0180a0001c0001t0010g0184a0001c0001t0010g0193others(3): Show | 6 | HG00597.hp2 HG00673.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.2056-255T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326488 | ||||||
chr2:69326526
|
A | C | 52 | a0001c0001t0001g0251a0001c0001t0001g0256a0001c0001t0001g0313others(49): Show | 55 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.2056-293T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326526 | ||||||
chr2:69326729
|
T | TC | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2055+184dupG | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326729 | ||||||
chr2:69326800
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2055+114C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 19/19 | chr2 | 69326800 | ||||||
chr2:69327106
|
A | G | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1894-31T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327106 | ||||||
chr2:69327128
|
G | T | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-53C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327128 | ||||||
chr2:69327175
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1894-100T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327175 | ||||||
chr2:69327182
|
C | T | 3 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0044 | 3 | HG02559.hp1 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1894-107G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327182 | ||||||
chr2:69327229
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1894-154G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327229 | ||||||
chr2:69327238
|
G | A | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG01168.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1894-163C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327238 | ||||||
chr2:69327254
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1894-179A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327254 | ||||||
chr2:69327380
|
C | T | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1894-305G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327380 | ||||||
chr2:69327382
|
T | C | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1894-307A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327382 | ||||||
chr2:69327420
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1894-345T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327420 | ||||||
chr2:69327478
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1894-403C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327478 | ||||||
chr2:69327519
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1894-444A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327519 | ||||||
chr2:69327739
|
G | T | 5 | a0001c0001t0002g0047a0001c0001t0002g0158a0001c0001t0002g0159others(2): Show | 5 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1893+532C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327739 | ||||||
chr2:69327757
|
C | G | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1893+514G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327757 | ||||||
chr2:69327829
|
G | T | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1893+442C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69327829 | ||||||
chr2:69328094
|
C | CA | 14 | a0001c0001t0001g0262a0001c0001t0001g0267a0001c0001t0001g0279others(11): Show | 14 | HG01243.hp2 HG01261.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1893+176dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69328094 | ||||||
chr2:69328094
|
CA | C | 214 | a0001c0001t0001g0299a0001c0001t0002g0004a0001c0001t0002g0010others(211): Show | 227 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(224): Show |
intron_variant | MODIFIER | c.1893+176delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 18/19 | chr2 | 69328094 | ||||||
chr2:69328549
|
G | T | 1 | a0001c0001t0001g0315 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1726-111C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328549 | ||||||
chr2:69328700
|
C | CTTT | 3 | a0001c0001t0008g0011a0001c0001t0008g0214a0001c0003t0002g0228 | 4 | HG00738.hp2 HG01069.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-263_1726-262i others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328700 | ||||||
chr2:69328700
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1726-262G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328700 | ||||||
chr2:69328701
|
C | CT | 91 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(88): Show | 95 | HG00558.hp1 HG00642.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726-264dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | ||||||
chr2:69328701
|
C | CTT | 11 | a0001c0001t0002g0096a0001c0001t0003g0084a0001c0001t0005g0111others(8): Show | 11 | HG01516.hp2 HG02257.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1726-265_1726-264d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | ||||||
chr2:69328701
|
C | CTTT | 90 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(87): Show | 95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1726-266_1726-264d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | ||||||
chr2:69328701
|
C | T | 3 | a0001c0001t0008g0011a0001c0001t0008g0214a0001c0003t0002g0228 | 4 | HG00738.hp2 HG01069.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-263G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328701 | ||||||
chr2:69328726
|
A | G | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-288T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328726 | ||||||
chr2:69328770
|
G | A | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1726-332C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328770 | ||||||
chr2:69328843
|
G | C | 1 | a0001c0001t0001g0294 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1726-405C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328843 | ||||||
chr2:69328860
|
C | A | 1 | a0001c0001t0001g0338 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1726-422G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328860 | ||||||
chr2:69328915
|
C | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+382G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69328915 | ||||||
chr2:69329012
|
A | C | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1725+285T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69329012 | ||||||
chr2:69329113
|
T | C | 1 | a0001c0001t0001g0335 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1725+184A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69329113 | ||||||
chr2:69329169
|
C | A | 41 | a0001c0002t0004g0003a0001c0002t0004g0124a0001c0002t0004g0125others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1725+128G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 17/19 | chr2 | 69329169 | ||||||
chr2:69329559
|
C | T | 7 | a0001c0001t0002g0033a0001c0001t0002g0112a0001c0001t0002g0114others(4): Show | 7 | HG02572.hp1 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1597+125G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 16/19 | chr2 | 69329559 | ||||||
chr2:69329569
|
G | A | 1 | a0001c0001t0009g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1597+115C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 16/19 | chr2 | 69329569 | ||||||
chr2:69329931
|
G | A | 1 | a0001c0001t0008g0178 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1483-133C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69329931 | ||||||
chr2:69330016
|
G | A | 1 | a0001c0001t0012g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1483-218C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330016 | ||||||
chr2:69330018
|
G | A | 1 | a0001c0001t0002g0226 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1483-220C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330018 | ||||||
chr2:69330338
|
T | C | 1 | a0001c0001t0002g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1483-540A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330338 | ||||||
chr2:69330462
|
C | G | 1 | a0002c0004t0001g0324 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1483-664G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330462 | ||||||
chr2:69330495
|
A | AT | 49 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(46): Show | 52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1483-698dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330495 | ||||||
chr2:69330512
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1483-714G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330512 | ||||||
chr2:69330584
|
A | T | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-786T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330584 | ||||||
chr2:69330980
|
C | T | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1483-1182G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330980 | ||||||
chr2:69330996
|
T | A | 5 | a0001c0001t0001g0258a0001c0001t0001g0267a0001c0001t0001g0279others(2): Show | 5 | HG01261.hp2 HG01361.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483-1198A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69330996 | ||||||
chr2:69331107
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1483-1309C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331107 | ||||||
chr2:69331141
|
G | A | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1483-1343C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331141 | ||||||
chr2:69331434
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1483-1636G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331434 | ||||||
chr2:69331452
|
C | T | 4 | a0001c0001t0002g0170a0001c0001t0021g0189a0001c0001t0021g0190others(1): Show | 4 | HG02922.hp1 HG03098.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-1654G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331452 | ||||||
chr2:69331456
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1483-1658G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331456 | ||||||
chr2:69331591
|
A | G | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.1483-1793T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331591 | ||||||
chr2:69331620
|
C | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1483-1822G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331620 | ||||||
chr2:69331641
|
T | C | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-1843A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331641 | ||||||
chr2:69331709
|
A | C | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.1483-1911T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331709 | ||||||
chr2:69331746
|
TAGTA | T | 125 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(122): Show | 132 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1483-1952_1483-194 others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331746 | ||||||
chr2:69331774
|
A | T | 1 | a0001c0001t0002g0022 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1483-1976T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331774 | ||||||
chr2:69331810
|
T | C | 3 | a0001c0001t0015g0034a0001c0001t0015g0035a0001c0001t0049g0037 | 3 | HG01243.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1483-2012A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331810 | ||||||
chr2:69331838
|
A | G | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1483-2040T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331838 | ||||||
chr2:69331947
|
C | T | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2149G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69331947 | ||||||
chr2:69332078
|
T | C | 1 | a0001c0002t0004g0153 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1483-2280A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332078 | ||||||
chr2:69332088
|
A | G | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-2290T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332088 | ||||||
chr2:69332147
|
T | C | 1 | a0001c0001t0001g0314 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1483-2349A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332147 | ||||||
chr2:69332313
|
C | CT | 8 | a0001c0001t0002g0038a0001c0001t0003g0082a0001c0001t0015g0034others(5): Show | 8 | HG01243.hp1 HG02970.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483-2516dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332313 | ||||||
chr2:69332318
|
T | C | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2520A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332318 | ||||||
chr2:69332458
|
C | A | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1483-2660G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332458 | ||||||
chr2:69332458
|
C | T | 1 | a0001c0002t0006g0150 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1483-2660G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332458 | ||||||
chr2:69332488
|
G | A | 1 | a0001c0001t0045g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1483-2690C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332488 | ||||||
chr2:69332507
|
G | C | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1483-2709C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332507 | ||||||
chr2:69332767
|
G | C | 4 | a0001c0001t0015g0034a0001c0001t0015g0035a0001c0001t0015g0036others(1): Show | 4 | HG01243.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-2969C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332767 | ||||||
chr2:69332797
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1483-2999G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332797 | ||||||
chr2:69332867
|
G | C | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1483-3069C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332867 | ||||||
chr2:69332868
|
C | G | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1483-3070G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332868 | ||||||
chr2:69332877
|
G | GATA | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(339): Show | 363 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.1483-3080_1483-307 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332877 | ||||||
chr2:69332892
|
A | G | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1483-3094T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332892 | ||||||
chr2:69332941
|
A | G | 1 | a0001c0001t0022g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1483-3143T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69332941 | ||||||
chr2:69333012
|
T | G | 37 | a0001c0002t0004g0003a0001c0002t0004g0128a0001c0002t0004g0134others(34): Show | 40 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1483-3214A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333012 | ||||||
chr2:69333318
|
A | G | 1 | a0001c0001t0016g0280 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1483-3520T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333318 | ||||||
chr2:69333320
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1483-3522A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333320 | ||||||
chr2:69333385
|
T | A | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-3587A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333385 | ||||||
chr2:69333474
|
A | G | 1 | a0001c0001t0028g0248 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1483-3676T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333474 | ||||||
chr2:69333742
|
T | C | 49 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(46): Show | 52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1483-3944A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333742 | ||||||
chr2:69333806
|
G | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1483-4008C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333806 | ||||||
chr2:69333817
|
A | G | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1483-4019T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333817 | ||||||
chr2:69333908
|
A | T | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3990T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333908 | ||||||
chr2:69333909
|
G | C | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3989C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333909 | ||||||
chr2:69333910
|
C | A | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3988G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333910 | ||||||
chr2:69333911
|
A | G | 1 | a0001c0001t0026g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1482+3987T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333911 | ||||||
chr2:69333940
|
G | A | 1 | a0001c0001t0012g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1482+3958C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333940 | ||||||
chr2:69333941
|
T | A | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.1482+3957A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69333941 | ||||||
chr2:69334067
|
A | T | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+3831T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334067 | ||||||
chr2:69334081
|
G | A | 1 | a0001c0001t0030g0334 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1482+3817C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334081 | ||||||
chr2:69334153
|
T | A | 1 | a0001c0001t0002g0205 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1482+3745A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334153 | ||||||
chr2:69334292
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1482+3606A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334292 | ||||||
chr2:69334396
|
C | A | 11 | a0001c0001t0003g0008a0001c0001t0003g0072a0001c0001t0003g0074others(8): Show | 12 | HG01891.hp2 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1482+3502G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334396 | ||||||
chr2:69334525
|
A | T | 1 | a0001c0001t0002g0225 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1482+3373T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334525 | ||||||
chr2:69334641
|
C | T | 1 | a0001c0002t0004g0146 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1482+3257G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334641 | ||||||
chr2:69334676
|
A | T | 30 | a0001c0001t0002g0033a0001c0001t0002g0052a0001c0001t0002g0096others(27): Show | 31 | HG02074.hp1 HG02451.hp1 HG02572.hp1 others(28): Show |
intron_variant | MODIFIER | c.1482+3222T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334676 | ||||||
chr2:69334730
|
A | T | 3 | a0001c0001t0008g0178a0001c0001t0037g0213a0001c0001t0038g0179 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1482+3168T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334730 | ||||||
chr2:69334808
|
T | A | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+3090A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334808 | ||||||
chr2:69334836
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1482+3062C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334836 | ||||||
chr2:69334867
|
A | AT | 3 | a0001c0001t0015g0034a0001c0001t0015g0035a0001c0001t0049g0037 | 3 | HG01243.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1482+3030dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334867 | ||||||
chr2:69334995
|
T | C | 92 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(89): Show | 98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1482+2903A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69334995 | ||||||
chr2:69335153
|
C | T | 129 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(126): Show | 136 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1482+2745G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335153 | ||||||
chr2:69335169
|
G | A | 2 | a0001c0001t0015g0034a0001c0001t0049g0037 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1482+2729C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335169 | ||||||
chr2:69335186
|
T | G | 2 | a0001c0001t0002g0167a0001c0001t0002g0241 | 2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1482+2712A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335186 | ||||||
chr2:69335405
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1482+2493C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335405 | ||||||
chr2:69335424
|
T | C | 4 | a0001c0001t0001g0249a0001c0001t0001g0255a0001c0001t0001g0266others(1): Show | 4 | NA18963.hp2 NA18972.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+2474A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335424 | ||||||
chr2:69335447
|
ATTTTATG others(8): Show |
A | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1482+2436_1482+245 others(19): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335447 | ||||||
chr2:69335633
|
A | T | 1 | a0001c0002t0006g0129 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1482+2265T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335633 | ||||||
chr2:69335705
|
T | C | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+2193A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335705 | ||||||
chr2:69335717
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1482+2181G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335717 | ||||||
chr2:69335791
|
C | G | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+2107G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335791 | ||||||
chr2:69335801
|
G | A | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.1482+2097C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335801 | ||||||
chr2:69335813
|
G | A | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+2085C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69335813 | ||||||
chr2:69336048
|
G | A | 57 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(54): Show | 60 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1482+1850C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336048 | ||||||
chr2:69336050
|
T | G | 57 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(54): Show | 60 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1482+1848A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336050 | ||||||
chr2:69336050
|
TG | T | 186 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(183): Show | 196 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.1482+1847delC | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336050 | ||||||
chr2:69336051
|
G | T | 57 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(54): Show | 60 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1482+1847C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336051 | ||||||
chr2:69336339
|
C | CA | 170 | a0001c0001t0001g0249a0001c0001t0001g0266a0001c0001t0001g0283others(167): Show | 178 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.1482+1558dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336339 | ||||||
chr2:69336339
|
C | CAA | 65 | a0001c0001t0002g0004a0001c0001t0002g0030a0001c0001t0002g0038others(62): Show | 70 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1482+1557_1482+155 others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336339 | ||||||
chr2:69336339
|
C | CAAA | 6 | a0001c0001t0015g0034a0001c0001t0015g0035a0001c0001t0020g0054others(3): Show | 6 | HG01243.hp1 HG02257.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1482+1556_1482+155 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336339 | ||||||
chr2:69336353
|
A | AG | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1482+1544_1482+154 others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336353 | ||||||
chr2:69336353
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1482+1545T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336353 | ||||||
chr2:69336387
|
A | G | 13 | a0001c0001t0002g0038a0001c0001t0007g0024a0001c0001t0007g0025others(10): Show | 13 | HG01243.hp1 HG01433.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1482+1511T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336387 | ||||||
chr2:69336415
|
T | C | 16 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1482+1483A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336415 | ||||||
chr2:69336422
|
T | C | 1 | a0001c0001t0015g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1482+1476A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336422 | ||||||
chr2:69336602
|
T | G | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+1296A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336602 | ||||||
chr2:69336635
|
T | TA | 8 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(5): Show | 8 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+1262dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336635 | ||||||
chr2:69336635
|
TA | T | 93 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(90): Show | 99 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1482+1262delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336635 | ||||||
chr2:69336642
|
A | G | 1 | a0001c0001t0050g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1482+1256T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336642 | ||||||
chr2:69336663
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1482+1235G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336663 | ||||||
chr2:69336800
|
T | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1482+1098A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336800 | ||||||
chr2:69336955
|
A | C | 4 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0011g0121others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+943T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69336955 | ||||||
chr2:69337060
|
A | AT | 9 | a0001c0001t0001g0249a0001c0001t0001g0266a0001c0001t0001g0314others(6): Show | 9 | HG02074.hp2 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1482+837dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337060 | ||||||
chr2:69337060
|
AT | A | 185 | a0001c0001t0001g0271a0001c0001t0001g0276a0001c0001t0001g0294others(182): Show | 195 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.1482+837delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337060 | ||||||
chr2:69337060
|
ATT | A | 10 | a0001c0001t0002g0050a0001c0001t0002g0191a0001c0001t0007g0024others(7): Show | 10 | HG01516.hp2 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1482+836_1482+837d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337060 | ||||||
chr2:69337161
|
T | A | 95 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(92): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1482+737A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337161 | ||||||
chr2:69337163
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0050g0031 | 2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1482+735G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337163 | ||||||
chr2:69337183
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+715C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337183 | ||||||
chr2:69337191
|
G | C | 95 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(92): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1482+707C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337191 | ||||||
chr2:69337255
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1482+643C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337255 | ||||||
chr2:69337358
|
C | G | 1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1482+540G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337358 | ||||||
chr2:69337448
|
A | G | 24 | a0001c0001t0003g0007a0001c0001t0003g0009a0001c0001t0003g0032others(21): Show | 26 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1482+450T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 15/19 | chr2 | 69337448 | ||||||
chr2:69338059
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG00609.hp2 | splice_region_variant&intron_variant | LOW | c.1325-4A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338059 | ||||||
chr2:69338213
|
T | C | 92 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(89): Show | 98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1325-158A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338213 | ||||||
chr2:69338221
|
C | T | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1325-166G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338221 | ||||||
chr2:69338324
|
C | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0329 | 2 | HG01069.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1324+121G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338324 | ||||||
chr2:69338431
|
TA | T | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1324+13delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 14/19 | chr2 | 69338431 | ||||||
chr2:69338676
|
G | A | 2 | a0001c0001t0020g0053a0001c0001t0020g0054 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1204-111C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338676 | ||||||
chr2:69338710
|
TA | T | 244 | a0001c0001t0001g0329a0001c0001t0002g0004a0001c0001t0002g0010others(241): Show | 257 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.1204-146delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338710 | ||||||
chr2:69338712
|
A | T | 201 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(198): Show | 213 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(210): Show |
intron_variant | MODIFIER | c.1204-147T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338712 | ||||||
chr2:69338802
|
C | CTT | 26 | a0001c0001t0002g0022a0001c0001t0002g0030a0001c0001t0002g0096others(23): Show | 27 | HG01168.hp1 HG01975.hp1 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1204-239_1204-238d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338802 | ||||||
chr2:69338802
|
C | CTTT | 204 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(201): Show | 216 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.1204-240_1204-238d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338802 | ||||||
chr2:69338802
|
C | CTTTT | 13 | a0001c0001t0002g0051a0001c0001t0002g0175a0001c0001t0002g0197others(10): Show | 13 | HG00558.hp1 HG00735.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1204-241_1204-238d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338802 | ||||||
chr2:69338832
|
G | T | 1 | a0001c0001t0005g0098 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1204-267C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338832 | ||||||
chr2:69338881
|
C | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1204-316G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338881 | ||||||
chr2:69338885
|
C | T | 1 | a0001c0001t0002g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1204-320G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69338885 | ||||||
chr2:69339125
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1204-560C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339125 | ||||||
chr2:69339258
|
T | G | 1 | a0001c0001t0002g0182 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1204-693A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339258 | ||||||
chr2:69339364
|
GCTCA | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1204-803_1204-800d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339364 | ||||||
chr2:69339390
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0263a0001c0001t0001g0319others(1): Show | 5 | HG00408.hp1 HG02056.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-825A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339390 | ||||||
chr2:69339399
|
G | A | 4 | a0001c0001t0002g0169a0001c0001t0002g0194a0001c0001t0002g0195others(1): Show | 4 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-834C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339399 | ||||||
chr2:69339493
|
C | T | 1 | a0001c0001t0005g0107 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1204-928G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339493 | ||||||
chr2:69339707
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1204-1142T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339707 | ||||||
chr2:69339722
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1204-1157A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339722 | ||||||
chr2:69339814
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1204-1249G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339814 | ||||||
chr2:69339848
|
T | C | 4 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0011g0121others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-1283A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339848 | ||||||
chr2:69339965
|
T | G | 1 | a0001c0001t0002g0096 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1204-1400A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69339965 | ||||||
chr2:69340139
|
ACTTTT | A | 37 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(34): Show | 40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1204-1579_1204-157 others(9): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340139 | ||||||
chr2:69340140
|
C | CT | 9 | a0001c0001t0001g0262a0001c0001t0001g0283a0001c0001t0001g0285others(6): Show | 9 | HG01978.hp1 HG02027.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1204-1576dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340140 | ||||||
chr2:69340140
|
CTTT | C | 17 | a0001c0001t0002g0092a0001c0001t0002g0227a0001c0001t0002g0229others(14): Show | 17 | HG00735.hp2 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1204-1578_1204-157 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340140 | ||||||
chr2:69340140
|
CTTTT | C | 184 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(181): Show | 194 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.1204-1579_1204-157 others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340140 | ||||||
chr2:69340145
|
T | A | 37 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(34): Show | 40 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.1204-1580A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340145 | ||||||
chr2:69340146
|
T | A | 1 | a0001c0001t0003g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1204-1581A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340146 | ||||||
chr2:69340209
|
C | T | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.1204-1644G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340209 | ||||||
chr2:69340219
|
GAGGCATG others(1523): Show |
G | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+403_1204-1655 others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340219 | ||||||
chr2:69340287
|
G | A | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-1722C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340287 | ||||||
chr2:69340329
|
G | A | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(327): Show | 351 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(348): Show |
intron_variant | MODIFIER | c.1204-1764C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340329 | ||||||
chr2:69340544
|
G | T | 242 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(239): Show | 255 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(252): Show |
intron_variant | MODIFIER | c.1203+1608C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340544 | ||||||
chr2:69340645
|
T | TA | 8 | a0001c0001t0002g0112a0001c0001t0007g0024a0001c0001t0007g0025others(5): Show | 8 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1203+1506dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340645 | ||||||
chr2:69340788
|
C | T | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1203+1364G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340788 | ||||||
chr2:69340852
|
G | A | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(236): Show | 252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.1203+1300C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340852 | ||||||
chr2:69340897
|
C | T | 14 | a0001c0001t0002g0010a0001c0001t0002g0047a0001c0001t0002g0157others(11): Show | 15 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203+1255G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340897 | ||||||
chr2:69340981
|
A | G | 1 | a0001c0001t0025g0020 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1203+1171T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69340981 | ||||||
chr2:69341006
|
T | A | 1 | a0001c0001t0002g0174 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1203+1146A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341006 | ||||||
chr2:69341018
|
G | A | 42 | a0001c0001t0026g0165a0001c0002t0004g0003a0001c0002t0004g0124others(39): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1203+1134C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341018 | ||||||
chr2:69341051
|
T | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1203+1101A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341051 | ||||||
chr2:69341067
|
TCCTGCCT others(22): Show |
T | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1203+1056_1203+108 others(33): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341067 | ||||||
chr2:69341117
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1203+1035G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341117 | ||||||
chr2:69341125
|
A | AT | 7 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(4): Show | 7 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203+1026dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341125 | ||||||
chr2:69341125
|
AT | A | 6 | a0001c0001t0001g0249a0001c0001t0001g0255a0001c0001t0001g0266others(3): Show | 6 | NA18956.hp1 NA18963.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+1026delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341125 | ||||||
chr2:69341339
|
G | A | 1 | a0001c0002t0004g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1203+813C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341339 | ||||||
chr2:69341532
|
T | C | 3 | a0001c0001t0015g0034a0001c0001t0015g0035a0001c0001t0049g0037 | 3 | HG01243.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1203+620A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341532 | ||||||
chr2:69341550
|
A | G | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.1203+602T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341550 | ||||||
chr2:69341628
|
C | T | 2 | a0001c0001t0035g0246a0001c0001t0058g0343 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1203+524G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341628 | ||||||
chr2:69341642
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0305 | 3 | HG00741.hp1 HG02717.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1203+510A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341642 | ||||||
chr2:69341648
|
TAC | T | 53 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(50): Show | 56 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.1203+502_1203+503d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341648 | ||||||
chr2:69341705
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1203+447A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341705 | ||||||
chr2:69341751
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+401G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341751 | ||||||
chr2:69341753
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+399G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341753 | ||||||
chr2:69341754
|
A | T | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+398T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341754 | ||||||
chr2:69341755
|
A | C | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+397T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341755 | ||||||
chr2:69341759
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+393T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341759 | ||||||
chr2:69341760
|
A | T | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+392T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341760 | ||||||
chr2:69341762
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1203+390T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341762 | ||||||
chr2:69341955
|
C | G | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1203+197G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69341955 | ||||||
chr2:69342094
|
C | T | 1 | a0001c0001t0007g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1203+58G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 13/19 | chr2 | 69342094 | ||||||
chr2:69342316
|
G | T | 5 | a0001c0001t0005g0094a0001c0001t0005g0095a0001c0001t0005g0105others(2): Show | 5 | NA18961.hp2 NA18966.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1106-67C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342316 | ||||||
chr2:69342409
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1106-160A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342409 | ||||||
chr2:69342710
|
T | C | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-461A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342710 | ||||||
chr2:69342798
|
C | T | 183 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(180): Show | 193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1106-549G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342798 | ||||||
chr2:69342975
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1106-726C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69342975 | ||||||
chr2:69343123
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1106-874A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343123 | ||||||
chr2:69343225
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1106-976C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343225 | ||||||
chr2:69343229
|
A | C | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1106-980T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343229 | ||||||
chr2:69343313
|
TGAG | T | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1106-1067_1106-106 others(7): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343313 | ||||||
chr2:69343368
|
C | A | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1106-1119G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343368 | ||||||
chr2:69343414
|
C | CT | 6 | a0001c0001t0002g0187a0001c0001t0002g0226a0001c0001t0012g0019others(3): Show | 6 | HG00741.hp2 HG02109.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1106-1166dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343414 | ||||||
chr2:69343414
|
CT | C | 23 | a0001c0001t0002g0096a0001c0001t0002g0163a0001c0001t0002g0164others(20): Show | 24 | HG02074.hp1 HG02602.hp2 HG03540.hp2 others(21): Show |
intron_variant | MODIFIER | c.1106-1166delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343414 | ||||||
chr2:69343433
|
C | CA | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1106-1185dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343433 | ||||||
chr2:69343588
|
A | G | 3 | a0001c0002t0004g0124a0001c0002t0004g0125a0001c0002t0004g0126 | 3 | NA18956.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1106-1339T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343588 | ||||||
chr2:69343598
|
G | A | 1 | a0001c0002t0047g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1106-1349C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343598 | ||||||
chr2:69343654
|
C | T | 183 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(180): Show | 193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1106-1405G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343654 | ||||||
chr2:69343703
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1106-1454G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343703 | ||||||
chr2:69343992
|
T | C | 241 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(238): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.1106-1743A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69343992 | ||||||
chr2:69344186
|
C | CA | 17 | a0001c0001t0001g0255a0001c0001t0001g0260a0001c0001t0001g0266others(14): Show | 17 | HG00735.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1105+1717dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | ||||||
chr2:69344186
|
C | CAA | 5 | a0001c0001t0001g0016a0001c0001t0001g0263a0001c0001t0001g0319others(2): Show | 6 | HG00408.hp1 HG02056.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105+1716_1105+171 others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | ||||||
chr2:69344186
|
CA | C | 55 | a0001c0001t0001g0272a0001c0001t0002g0163a0001c0001t0002g0169others(52): Show | 58 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.1105+1717delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | ||||||
chr2:69344186
|
CAA | C | 174 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(171): Show | 184 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(181): Show |
intron_variant | MODIFIER | c.1105+1716_1105+171 others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344186 | ||||||
chr2:69344293
|
C | T | 4 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0011g0121others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+1611G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344293 | ||||||
chr2:69344544
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1105+1360A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344544 | ||||||
chr2:69344565
|
T | C | 1 | a0001c0001t0002g0164 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1105+1339A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344565 | ||||||
chr2:69344591
|
T | C | 41 | a0001c0002t0004g0003a0001c0002t0004g0124a0001c0002t0004g0125others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1105+1313A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344591 | ||||||
chr2:69344656
|
A | AT | 78 | a0001c0001t0001g0333a0001c0001t0003g0007a0001c0001t0003g0008others(75): Show | 84 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1105+1247dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344656 | ||||||
chr2:69344662
|
T | A | 1 | a0001c0001t0050g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1105+1242A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344662 | ||||||
chr2:69344663
|
T | A | 8 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0272others(5): Show | 8 | HG02071.hp1 HG02083.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1105+1241A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344663 | ||||||
chr2:69344685
|
C | T | 5 | a0001c0001t0001g0258a0001c0001t0001g0267a0001c0001t0001g0279others(2): Show | 5 | HG01261.hp2 HG01361.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+1219G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344685 | ||||||
chr2:69344700
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1105+1204C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344700 | ||||||
chr2:69344728
|
C | T | 130 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(127): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1105+1176G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344728 | ||||||
chr2:69344755
|
C | G | 1 | a0001c0001t0005g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1105+1149G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344755 | ||||||
chr2:69344804
|
C | T | 2 | a0001c0001t0035g0246a0001c0001t0058g0343 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1105+1100G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344804 | ||||||
chr2:69344816
|
T | A | 3 | a0001c0001t0002g0235a0001c0001t0003g0068a0001c0001t0003g0073 | 3 | HG02630.hp1 HG02818.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1105+1088A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344816 | ||||||
chr2:69344819
|
A | G | 1 | a0001c0001t0028g0248 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1105+1085T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344819 | ||||||
chr2:69344952
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1105+952C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69344952 | ||||||
chr2:69345159
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1105+745C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345159 | ||||||
chr2:69345697
|
C | G | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105+207G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345697 | ||||||
chr2:69345788
|
G | A | 1 | a0001c0002t0004g0144 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1105+116C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345788 | ||||||
chr2:69345897
|
T | C | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
splice_region_variant&intron_variant | LOW | c.1105+7A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 12/19 | chr2 | 69345897 | ||||||
chr2:69346141
|
T | C | 237 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(234): Show | 250 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(247): Show |
intron_variant | MODIFIER | c.1010-142A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346141 | ||||||
chr2:69346222
|
TACA | T | 41 | a0001c0002t0004g0003a0001c0002t0004g0124a0001c0002t0004g0125others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1010-226_1010-224d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346222 | ||||||
chr2:69346387
|
T | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0327a0001c0005t0001g0320 | 3 | HG02027.hp2 NA18983.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1010-388A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346387 | ||||||
chr2:69346396
|
G | A | 1 | a0001c0002t0004g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1010-397C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346396 | ||||||
chr2:69346459
|
C | T | 2 | a0001c0001t0003g0032a0001c0001t0003g0085 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1010-460G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346459 | ||||||
chr2:69346490
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1010-491C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346490 | ||||||
chr2:69346491
|
G | T | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-492C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346491 | ||||||
chr2:69346693
|
C | CAT | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1010-696_1010-695d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346693 | ||||||
chr2:69346705
|
T | G | 1 | a0001c0001t0001g0292 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1010-706A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346705 | ||||||
chr2:69346891
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1010-892C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346891 | ||||||
chr2:69346898
|
A | T | 1 | a0001c0001t0008g0178 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1010-899T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346898 | ||||||
chr2:69346898
|
AGTTTTGT others(3): Show |
A | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-909_1010-900d others(12): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346898 | ||||||
chr2:69346967
|
C | T | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1010-968G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69346967 | ||||||
chr2:69347060
|
C | T | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-1061G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347060 | ||||||
chr2:69347210
|
CT | C | 14 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(11): Show | 14 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1009+960delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347210 | ||||||
chr2:69347448
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1009+723G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347448 | ||||||
chr2:69347480
|
C | CT | 187 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(184): Show | 197 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(194): Show |
intron_variant | MODIFIER | c.1009+690dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347480 | ||||||
chr2:69347526
|
G | A | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1009+645C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347526 | ||||||
chr2:69347622
|
C | T | 183 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(180): Show | 193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.1009+549G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347622 | ||||||
chr2:69347680
|
G | A | 1 | a0001c0001t0005g0100 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1009+491C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347680 | ||||||
chr2:69347735
|
G | A | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009+436C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347735 | ||||||
chr2:69347936
|
TTAA | T | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1009+232_1009+234d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347936 | ||||||
chr2:69347971
|
CATTA | C | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG01168.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1009+196_1009+199d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69347971 | ||||||
chr2:69348041
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1009+130C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 11/19 | chr2 | 69348041 | ||||||
chr2:69348481
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.846-147G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348481 | ||||||
chr2:69348691
|
G | C | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.846-357C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348691 | ||||||
chr2:69348842
|
T | C | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.846-508A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348842 | ||||||
chr2:69348900
|
G | A | 3 | a0001c0001t0011g0120a0001c0001t0011g0121a0001c0001t0011g0122 | 3 | HG02486.hp2 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.846-566C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348900 | ||||||
chr2:69348930
|
C | A | 2 | a0001c0001t0003g0090a0001c0001t0003g0091 | 2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.846-596G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69348930 | ||||||
chr2:69349012
|
C | T | 48 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(45): Show | 51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.846-678G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349012 | ||||||
chr2:69349015
|
G | C | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.846-681C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349015 | ||||||
chr2:69349054
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.846-720A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349054 | ||||||
chr2:69349157
|
T | A | 1 | a0001c0001t0054g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.846-823A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349157 | ||||||
chr2:69349403
|
T | C | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.845+675A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349403 | ||||||
chr2:69349709
|
G | A | 1 | a0001c0001t0015g0035 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.845+369C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 10/19 | chr2 | 69349709 | ||||||
chr2:69350318
|
G | A | 1 | a0001c0001t0011g0122 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.740-135C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350318 | ||||||
chr2:69350435
|
A | T | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.740-252T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350435 | ||||||
chr2:69350463
|
C | T | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.740-280G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350463 | ||||||
chr2:69350579
|
C | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-396G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350579 | ||||||
chr2:69350612
|
C | T | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.740-429G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350612 | ||||||
chr2:69350763
|
C | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-580G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350763 | ||||||
chr2:69350852
|
G | A | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.740-669C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350852 | ||||||
chr2:69350861
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.740-678G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350861 | ||||||
chr2:69350916
|
A | G | 3 | a0001c0001t0008g0178a0001c0001t0037g0213a0001c0001t0038g0179 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.740-733T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350916 | ||||||
chr2:69350918
|
A | G | 4 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0011g0121others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-735T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69350918 | ||||||
chr2:69351078
|
G | T | 9 | a0001c0001t0002g0096a0001c0001t0005g0006a0001c0001t0005g0094others(6): Show | 10 | NA18961.hp2 NA18965.hp1 NA18966.hp1 others(7): Show |
intron_variant | MODIFIER | c.740-895C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351078 | ||||||
chr2:69351159
|
C | T | 14 | a0001c0001t0002g0010a0001c0001t0002g0047a0001c0001t0002g0157others(11): Show | 15 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.740-976G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351159 | ||||||
chr2:69351160
|
T | G | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.740-977A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351160 | ||||||
chr2:69351333
|
C | A | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.740-1150G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351333 | ||||||
chr2:69351524
|
G | A | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.740-1341C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351524 | ||||||
chr2:69351537
|
C | T | 1 | a0001c0001t0001g0314 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.740-1354G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351537 | ||||||
chr2:69351791
|
A | T | 1 | a0001c0001t0030g0334 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.740-1608T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69351791 | ||||||
chr2:69352008
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.740-1825A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352008 | ||||||
chr2:69352031
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.740-1848C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352031 | ||||||
chr2:69352068
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.740-1885G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352068 | ||||||
chr2:69352318
|
T | A | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(237): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.739+1941A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352318 | ||||||
chr2:69352332
|
C | T | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+1927G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352332 | ||||||
chr2:69352431
|
C | T | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+1828G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352431 | ||||||
chr2:69352471
|
G | C | 4 | a0001c0001t0007g0025a0001c0001t0007g0026a0001c0001t0007g0027others(1): Show | 4 | HG01884.hp2 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.739+1788C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352471 | ||||||
chr2:69352483
|
C | T | 2 | a0001c0001t0016g0280a0001c0001t0016g0312 | 2 | NA18970.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.739+1776G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352483 | ||||||
chr2:69352523
|
C | G | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.739+1736G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352523 | ||||||
chr2:69352562
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+1697C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352562 | ||||||
chr2:69352604
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.739+1655G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352604 | ||||||
chr2:69352612
|
C | CA | 118 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0253others(115): Show | 127 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.739+1646dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352612
|
C | CAA | 106 | a0001c0001t0001g0309a0001c0001t0002g0004a0001c0001t0002g0030others(103): Show | 111 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.739+1645_739+1646d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352612
|
C | CAAA | 34 | a0001c0001t0002g0226a0001c0001t0002g0233a0001c0001t0002g0238others(31): Show | 37 | HG00544.hp2 HG00621.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.739+1644_739+1646d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352612
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0012g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.739+1634_739+1646d others(15): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352612
|
C | CAAAAAAA others(7): Show |
2 | a0001c0001t0012g0057a0001c0001t0025g0020 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.739+1633_739+1646d others(16): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352612
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0012g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.739+1629_739+1646d others(20): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352612
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.739+1634_739+1646d others(15): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352612 | ||||||
chr2:69352777
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.739+1482C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352777 | ||||||
chr2:69352795
|
C | G | 1 | a0001c0001t0001g0250 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.739+1464G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352795 | ||||||
chr2:69352812
|
G | A | 3 | a0001c0001t0003g0080a0001c0001t0003g0081a0001c0001t0003g0082 | 3 | HG01168.hp1 HG03492.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.739+1447C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352812 | ||||||
chr2:69352837
|
G | A | 1 | a0001c0001t0005g0111 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.739+1422C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352837 | ||||||
chr2:69352891
|
C | T | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.739+1368G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352891 | ||||||
chr2:69352947
|
G | A | 2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | NA18984.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.739+1312C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69352947 | ||||||
chr2:69353012
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.739+1247G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353012 | ||||||
chr2:69353041
|
T | C | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.739+1218A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353041 | ||||||
chr2:69353218
|
A | C | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+1041T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353218 | ||||||
chr2:69353239
|
T | A | 1 | a0001c0001t0001g0307 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.739+1020A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353239 | ||||||
chr2:69353266
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.739+993C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353266 | ||||||
chr2:69353301
|
T | C | 3 | a0001c0002t0004g0124a0001c0002t0004g0125a0001c0002t0004g0126 | 3 | NA18956.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.739+958A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353301 | ||||||
chr2:69353329
|
G | T | 49 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(46): Show | 52 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.739+930C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353329 | ||||||
chr2:69353354
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.739+905A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353354 | ||||||
chr2:69353528
|
T | A | 1 | a0001c0001t0042g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.739+731A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353528 | ||||||
chr2:69353554
|
A | G | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.739+705T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353554 | ||||||
chr2:69353570
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.739+689C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353570 | ||||||
chr2:69353605
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.739+654T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353605 | ||||||
chr2:69353805
|
T | G | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+454A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353805 | ||||||
chr2:69353820
|
T | A | 1 | a0001c0001t0044g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.739+439A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353820 | ||||||
chr2:69353838
|
C | T | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.739+421G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353838 | ||||||
chr2:69353943
|
C | T | 41 | a0001c0002t0004g0003a0001c0002t0004g0124a0001c0002t0004g0125others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.739+316G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69353943 | ||||||
chr2:69354067
|
C | A | 1 | a0001c0001t0003g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.739+192G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 9/19 | chr2 | 69354067 | ||||||
chr2:69354346
|
T | C | 1 | a0001c0002t0004g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.686-34A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 8/19 | chr2 | 69354346 | ||||||
chr2:69354387
|
G | A | 1 | a0001c0001t0051g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.686-75C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 8/19 | chr2 | 69354387 | ||||||
chr2:69354628
|
T | A | 5 | a0001c0001t0005g0098a0001c0001t0005g0099a0001c0001t0005g0100others(2): Show | 5 | NA18612.hp2 NA18939.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-60A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354628 | ||||||
chr2:69354718
|
T | TA | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.606-151dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354718 | ||||||
chr2:69354758
|
C | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606-190G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354758 | ||||||
chr2:69354792
|
A | C | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.606-224T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354792 | ||||||
chr2:69354845
|
C | T | 4 | a0001c0002t0006g0224a0001c0002t0040g0148a0001c0002t0055g0135others(1): Show | 4 | NA18942.hp2 NA19068.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.606-277G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354845 | ||||||
chr2:69354875
|
G | A | 1 | a0001c0001t0002g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.606-307C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354875 | ||||||
chr2:69354896
|
C | T | 130 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(127): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.606-328G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354896 | ||||||
chr2:69354999
|
ATATCCAA others(9): Show |
A | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-447_606-432del others(16): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69354999 | ||||||
chr2:69355009
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.606-441A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355009 | ||||||
chr2:69355082
|
ATTTG | A | 3 | a0001c0001t0007g0024a0001c0001t0007g0029a0001c0001t0007g0039 | 3 | HG02258.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.606-518_606-515del others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355082 | ||||||
chr2:69355136
|
G | C | 1 | a0001c0001t0003g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.606-568C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355136 | ||||||
chr2:69355391
|
T | TG | 186 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(183): Show | 196 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(193): Show |
intron_variant | MODIFIER | c.606-824dupC | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355391 | ||||||
chr2:69355394
|
T | G | 55 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(52): Show | 58 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.606-826A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355394 | ||||||
chr2:69355408
|
T | TTTC | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(237): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.606-841_606-840ins others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355408 | ||||||
chr2:69355436
|
A | G | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.606-868T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355436 | ||||||
chr2:69355460
|
T | C | 1 | a0001c0001t0008g0214 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.606-892A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355460 | ||||||
chr2:69355575
|
G | A | 3 | a0001c0001t0002g0175a0001c0001t0002g0197a0001c0001t0003g0075 | 3 | HG03516.hp1 HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.605+921C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355575 | ||||||
chr2:69355680
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.605+816G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355680 | ||||||
chr2:69355763
|
C | T | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.605+733G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355763 | ||||||
chr2:69355817
|
T | A | 1 | a0001c0001t0031g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.605+679A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355817 | ||||||
chr2:69355870
|
A | G | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+626T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355870 | ||||||
chr2:69355932
|
T | C | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.605+564A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355932 | ||||||
chr2:69355983
|
C | CT | 9 | a0001c0001t0001g0249a0001c0001t0001g0262a0001c0001t0001g0266others(6): Show | 9 | HG01496.hp1 HG01928.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.605+512dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | ||||||
chr2:69355983
|
CT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(27): Show | 35 | HG00408.hp1 HG00642.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.605+512delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | ||||||
chr2:69355983
|
CTT | C | 93 | a0001c0001t0002g0013a0001c0001t0002g0033a0001c0001t0002g0052others(90): Show | 98 | HG00558.hp1 HG00642.hp2 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.605+511_605+512del others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | ||||||
chr2:69355983
|
CTTT | C | 127 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0038others(124): Show | 134 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.605+510_605+512del others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | ||||||
chr2:69355983
|
CTTTT | C | 11 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0160others(8): Show | 12 | HG01167.hp1 HG01168.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.605+509_605+512del others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69355983 | ||||||
chr2:69356152
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.605+344G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356152 | ||||||
chr2:69356166
|
C | G | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.605+330G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356166 | ||||||
chr2:69356238
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.605+258G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356238 | ||||||
chr2:69356269
|
C | G | 1 | a0001c0001t0003g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.605+227G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356269 | ||||||
chr2:69356290
|
G | A | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.605+206C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 7/19 | chr2 | 69356290 | ||||||
chr2:69356740
|
C | T | 47 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(44): Show | 50 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.544-183G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356740 | ||||||
chr2:69356741
|
AT | A | 232 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(229): Show | 245 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.544-185delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356741 | ||||||
chr2:69356743
|
T | A | 1 | a0001c0002t0004g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.544-186A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356743 | ||||||
chr2:69356764
|
A | G | 183 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(180): Show | 193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.544-207T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69356764 | ||||||
chr2:69357094
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.544-537A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357094 | ||||||
chr2:69357263
|
AG | A | 134 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(131): Show | 141 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.544-707delC | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357263 | ||||||
chr2:69357347
|
C | G | 2 | a0001c0001t0001g0281a0001c0001t0001g0335 | 2 | NA18961.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.544-790G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357347 | ||||||
chr2:69357413
|
G | A | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-856C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357413 | ||||||
chr2:69357467
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.543+862T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357467 | ||||||
chr2:69357484
|
C | A | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.543+845G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357484 | ||||||
chr2:69357553
|
G | C | 1 | a0001c0001t0001g0289 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.543+776C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357553 | ||||||
chr2:69357612
|
G | A | 4 | a0001c0001t0007g0025a0001c0001t0007g0026a0001c0001t0007g0027others(1): Show | 4 | HG01884.hp2 HG02818.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+717C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357612 | ||||||
chr2:69357691
|
G | C | 1 | a0001c0002t0004g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.543+638C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357691 | ||||||
chr2:69357790
|
C | T | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+539G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69357790 | ||||||
chr2:69358004
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.543+325G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358004 | ||||||
chr2:69358044
|
A | G | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.543+285T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358044 | ||||||
chr2:69358136
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+193C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358136 | ||||||
chr2:69358146
|
T | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+183A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358146 | ||||||
chr2:69358154
|
G | C | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+175C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358154 | ||||||
chr2:69358162
|
A | G | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.543+167T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358162 | ||||||
chr2:69358224
|
C | G | 1 | a0001c0001t0014g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.543+105G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358224 | ||||||
chr2:69358246
|
G | C | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.543+83C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 6/19 | chr2 | 69358246 | ||||||
chr2:69358778
|
C | A | 9 | a0001c0001t0002g0013a0001c0001t0002g0169a0001c0001t0002g0171others(6): Show | 10 | HG01109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-315G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69358778 | ||||||
chr2:69358909
|
C | T | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+359G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69358909 | ||||||
chr2:69359137
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.408+131G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359137 | ||||||
chr2:69359161
|
A | C | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.408+107T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359161 | ||||||
chr2:69359171
|
C | T | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+97G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359171 | ||||||
chr2:69359238
|
A | G | 69 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0047others(66): Show | 73 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.408+30T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359238 | ||||||
chr2:69359261
|
T | A | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.408+7A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 5/19 | chr2 | 69359261 | ||||||
chr2:69359432
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.350-106G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359432 | ||||||
chr2:69359447
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.350-121C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359447 | ||||||
chr2:69359656
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.350-330C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359656 | ||||||
chr2:69359756
|
A | C | 1 | a0001c0001t0044g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.350-430T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69359756 | ||||||
chr2:69360156
|
T | A | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.350-830A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360156 | ||||||
chr2:69360224
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.350-898C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360224 | ||||||
chr2:69360243
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.350-917G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360243 | ||||||
chr2:69360328
|
C | CA | 82 | a0001c0001t0001g0253a0001c0001t0001g0259a0001c0001t0001g0290others(79): Show | 87 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.350-1003dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360328 | ||||||
chr2:69360328
|
C | CAA | 18 | a0001c0001t0001g0279a0001c0001t0002g0231a0001c0001t0002g0237others(15): Show | 18 | HG00609.hp1 HG02148.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.350-1004_350-1003d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360328 | ||||||
chr2:69360328
|
CAAAAAAA others(2): Show |
C | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.350-1011_350-1003d others(11): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360328 | ||||||
chr2:69360440
|
A | ATT | 8 | a0001c0001t0005g0093a0001c0001t0005g0098a0001c0001t0009g0040others(5): Show | 8 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1115_350-1114i others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360440 | ||||||
chr2:69360442
|
A | AT | 89 | a0001c0001t0002g0030a0001c0001t0002g0038a0001c0001t0002g0203others(86): Show | 95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.350-1117dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | ||||||
chr2:69360442
|
A | ATT | 126 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(123): Show | 133 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.350-1118_350-1117d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | ||||||
chr2:69360442
|
A | ATTT | 9 | a0001c0001t0002g0226a0001c0001t0007g0024a0001c0001t0007g0025others(6): Show | 9 | HG00741.hp2 HG01433.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-1119_350-1117d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | ||||||
chr2:69360442
|
A | T | 11 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(8): Show | 11 | HG01109.hp2 HG01928.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.350-1116T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360442 | ||||||
chr2:69360444
|
T | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-1118A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360444 | ||||||
chr2:69360573
|
G | A | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.350-1247C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360573 | ||||||
chr2:69360746
|
C | G | 2 | a0001c0001t0019g0055a0001c0001t0019g0056 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-1420G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360746 | ||||||
chr2:69360923
|
C | T | 92 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(89): Show | 98 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.350-1597G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360923 | ||||||
chr2:69360963
|
A | G | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.350-1637T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69360963 | ||||||
chr2:69361031
|
G | A | 1 | a0001c0001t0011g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.350-1705C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361031 | ||||||
chr2:69361309
|
G | A | 2 | a0001c0001t0005g0105a0001c0001t0005g0106 | 2 | NA18984.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.350-1983C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361309 | ||||||
chr2:69361447
|
C | CA | 7 | a0001c0001t0001g0302a0001c0001t0001g0335a0001c0001t0002g0210others(4): Show | 7 | HG02559.hp2 HG02965.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+2097dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361447 | ||||||
chr2:69361447
|
CA | C | 224 | a0001c0001t0001g0258a0001c0001t0001g0265a0001c0001t0001g0281others(221): Show | 237 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.349+2097delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361447 | ||||||
chr2:69361447
|
CAA | C | 10 | a0001c0001t0002g0096a0001c0001t0002g0114a0001c0001t0002g0207others(7): Show | 10 | HG01168.hp1 HG01516.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.349+2096_349+2097d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361447 | ||||||
chr2:69361519
|
C | T | 15 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.349+2026G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361519 | ||||||
chr2:69361562
|
G | A | 2 | a0001c0001t0003g0077a0001c0001t0003g0079 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.349+1983C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361562 | ||||||
chr2:69361762
|
T | A | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.349+1783A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361762 | ||||||
chr2:69361948
|
C | G | 1 | a0001c0001t0042g0108 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.349+1597G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69361948 | ||||||
chr2:69362015
|
C | T | 5 | a0001c0001t0005g0098a0001c0001t0005g0099a0001c0001t0005g0100others(2): Show | 5 | NA18612.hp2 NA18939.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1530G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362015 | ||||||
chr2:69362066
|
A | T | 1 | a0001c0002t0004g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349+1479T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362066 | ||||||
chr2:69362205
|
C | T | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+1340G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362205 | ||||||
chr2:69362299
|
G | A | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1246C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362299 | ||||||
chr2:69362384
|
T | C | 1 | a0001c0001t0030g0334 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+1161A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362384 | ||||||
chr2:69362557
|
G | A | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+988C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362557 | ||||||
chr2:69362572
|
C | T | 3 | a0001c0002t0006g0129a0001c0002t0006g0130a0001c0002t0006g0131 | 3 | NA18988.hp2 NA19002.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.349+973G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362572 | ||||||
chr2:69362607
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349+938G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362607 | ||||||
chr2:69362747
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.349+798T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362747 | ||||||
chr2:69362751
|
C | T | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.349+794G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362751 | ||||||
chr2:69362816
|
A | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.349+729T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362816 | ||||||
chr2:69362824
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.349+721A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362824 | ||||||
chr2:69362908
|
A | C | 1 | a0001c0001t0002g0175 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.349+637T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69362908 | ||||||
chr2:69363011
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.349+534G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363011 | ||||||
chr2:69363017
|
G | A | 1 | a0001c0001t0023g0018 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+528C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363017 | ||||||
chr2:69363108
|
T | C | 31 | a0001c0001t0002g0033a0001c0001t0002g0052a0001c0001t0002g0096others(28): Show | 32 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(29): Show |
intron_variant | MODIFIER | c.349+437A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363108 | ||||||
chr2:69363207
|
G | A | 41 | a0001c0002t0004g0003a0001c0002t0004g0124a0001c0002t0004g0125others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.349+338C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 4/19 | chr2 | 69363207 | ||||||
chr2:69363682
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.224-12C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363682 | ||||||
chr2:69363725
|
C | T | 4 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(1): Show | 4 | HG01109.hp2 HG01928.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-55G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363725 | ||||||
chr2:69363801
|
C | T | 19 | a0001c0001t0002g0096a0001c0001t0005g0006a0001c0001t0005g0094others(16): Show | 20 | HG02074.hp1 HG02602.hp2 HG04199.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-131G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363801 | ||||||
chr2:69363809
|
A | C | 1 | a0001c0001t0001g0263 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.224-139T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363809 | ||||||
chr2:69363869
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.224-199G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363869 | ||||||
chr2:69363891
|
G | C | 1 | a0001c0001t0002g0021 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.224-221C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363891 | ||||||
chr2:69363965
|
A | C | 1 | a0001c0001t0002g0163 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.224-295T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363965 | ||||||
chr2:69363989
|
C | A | 1 | a0001c0001t0050g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.224-319G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69363989 | ||||||
chr2:69364032
|
C | T | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(339): Show | 363 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.224-362G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364032 | ||||||
chr2:69364070
|
A | G | 1 | a0001c0001t0002g0233 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.224-400T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364070 | ||||||
chr2:69364114
|
C | CA | 98 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(95): Show | 104 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.224-445dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364114 | ||||||
chr2:69364114
|
C | CAA | 7 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(4): Show | 7 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-446_224-445dup others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364114 | ||||||
chr2:69364188
|
C | T | 91 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(88): Show | 97 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.224-518G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364188 | ||||||
chr2:69364540
|
C | A | 3 | a0001c0002t0040g0148a0001c0002t0055g0135a0001c0002t0056g0147 | 3 | NA18942.hp2 NA19078.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.224-870G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364540 | ||||||
chr2:69364636
|
G | A | 3 | a0001c0001t0001g0339a0001c0001t0002g0030a0001c0001t0030g0334 | 3 | HG02145.hp1 HG02723.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.224-966C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364636 | ||||||
chr2:69364738
|
T | C | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.224-1068A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364738 | ||||||
chr2:69364744
|
C | G | 4 | a0001c0001t0002g0156a0001c0001t0002g0174a0001c0001t0002g0207others(1): Show | 4 | NA18953.hp1 NA18955.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-1074G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364744 | ||||||
chr2:69364784
|
C | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0157a0001c0001t0002g0217 | 4 | NA18969.hp2 NA18993.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-1114G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364784 | ||||||
chr2:69364811
|
A | G | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.224-1141T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364811 | ||||||
chr2:69364864
|
G | A | 1 | a0001c0001t0012g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224-1194C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364864 | ||||||
chr2:69364910
|
G | A | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.224-1240C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364910 | ||||||
chr2:69364982
|
G | A | 94 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(91): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.224-1312C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364982 | ||||||
chr2:69364994
|
C | CA | 148 | a0001c0001t0001g0002a0001c0001t0001g0257a0001c0001t0001g0262others(145): Show | 160 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.224-1325dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | ||||||
chr2:69364994
|
C | CAA | 78 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0306others(75): Show | 81 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.224-1326_224-1325d others(4): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | ||||||
chr2:69364994
|
C | CAAA | 20 | a0001c0001t0002g0023a0001c0001t0002g0033a0001c0001t0002g0038others(17): Show | 20 | HG01109.hp2 HG02015.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.224-1327_224-1325d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | ||||||
chr2:69364994
|
C | CAAAA | 12 | a0001c0001t0025g0020a0001c0002t0006g0014a0001c0002t0006g0123others(9): Show | 13 | HG00609.hp1 HG00621.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.224-1328_224-1325d others(6): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | ||||||
chr2:69364994
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0020g0053a0001c0001t0020g0054 | 2 | HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.224-1335_224-1325d others(13): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69364994 | ||||||
chr2:69365094
|
T | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.224-1424A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365094 | ||||||
chr2:69365111
|
C | T | 3 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0044 | 3 | HG02559.hp1 HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.224-1441G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365111 | ||||||
chr2:69365201
|
A | G | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(236): Show | 252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.224-1531T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365201 | ||||||
chr2:69365299
|
G | A | 41 | a0001c0001t0026g0165a0001c0002t0004g0003a0001c0002t0004g0124others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.224-1629C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365299 | ||||||
chr2:69365360
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224-1690A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365360 | ||||||
chr2:69365466
|
C | T | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.224-1796G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365466 | ||||||
chr2:69365529
|
A | T | 241 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(238): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.224-1859T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365529 | ||||||
chr2:69365678
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.224-2008A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365678 | ||||||
chr2:69365752
|
A | G | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.224-2082T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365752 | ||||||
chr2:69365808
|
C | T | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.224-2138G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365808 | ||||||
chr2:69365957
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224-2287G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365957 | ||||||
chr2:69365959
|
C | T | 1 | a0001c0002t0004g0134 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.224-2289G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365959 | ||||||
chr2:69365960
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG00558.hp2 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.224-2290C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69365960 | ||||||
chr2:69366142
|
A | AATTAAAG others(14): Show |
7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-2493_224-2473d others(23): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366142 | ||||||
chr2:69366182
|
C | T | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.224-2512G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366182 | ||||||
chr2:69366243
|
C | T | 11 | a0001c0002t0006g0014a0001c0002t0006g0129a0001c0002t0006g0130others(8): Show | 12 | HG00621.hp1 HG02015.hp1 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.224-2573G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366243 | ||||||
chr2:69366259
|
G | T | 182 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(179): Show | 192 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.224-2589C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366259 | ||||||
chr2:69366261
|
T | C | 244 | a0001c0001t0001g0295a0001c0001t0002g0004a0001c0001t0002g0010others(241): Show | 257 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.224-2591A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366261 | ||||||
chr2:69366638
|
A | G | 1 | a0001c0001t0001g0331 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.224-2968T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366638 | ||||||
chr2:69366672
|
C | T | 1 | a0001c0002t0004g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.224-3002G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69366672 | ||||||
chr2:69367152
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+2849C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367152 | ||||||
chr2:69367166
|
G | C | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.223+2835C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367166 | ||||||
chr2:69367208
|
T | C | 2 | a0001c0001t0035g0246a0001c0001t0058g0343 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.223+2793A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367208 | ||||||
chr2:69367215
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223+2786C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367215 | ||||||
chr2:69367344
|
T | TTTG | 127 | a0001c0001t0001g0296a0001c0001t0002g0004a0001c0001t0002g0010others(124): Show | 134 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.223+2654_223+2656d others(5): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | ||||||
chr2:69367344
|
T | TTTGTTG | 12 | a0001c0001t0002g0050a0001c0001t0009g0040a0001c0001t0009g0041others(9): Show | 12 | HG01433.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.223+2651_223+2656d others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | ||||||
chr2:69367344
|
T | TTTGTTGT others(2): Show |
42 | a0001c0001t0026g0165a0001c0002t0004g0003a0001c0002t0004g0124others(39): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.223+2648_223+2656d others(11): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | ||||||
chr2:69367344
|
T | TTTGTTGT others(11): Show |
1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.223+2639_223+2656d others(20): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367344 | ||||||
chr2:69367347
|
G | T | 48 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(45): Show | 51 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.223+2654C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367347 | ||||||
chr2:69367350
|
G | T | 1 | a0001c0001t0003g0065 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.223+2651C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367350 | ||||||
chr2:69367521
|
C | T | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+2480G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367521 | ||||||
chr2:69367522
|
G | A | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+2479C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367522 | ||||||
chr2:69367564
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223+2437A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367564 | ||||||
chr2:69367585
|
A | T | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.223+2416T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367585 | ||||||
chr2:69367657
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.223+2344C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367657 | ||||||
chr2:69367724
|
G | C | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+2277C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367724 | ||||||
chr2:69367842
|
T | C | 1 | a0001c0001t0009g0044 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+2159A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69367842 | ||||||
chr2:69368210
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.223+1791T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368210 | ||||||
chr2:69368256
|
G | A | 5 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(2): Show | 5 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1745C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368256 | ||||||
chr2:69368308
|
G | C | 1 | a0001c0001t0002g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.223+1693C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368308 | ||||||
chr2:69368470
|
G | A | 1 | a0001c0002t0040g0148 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.223+1531C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368470 | ||||||
chr2:69368545
|
T | C | 8 | a0001c0001t0001g0257a0001c0001t0001g0297a0001c0001t0001g0299others(5): Show | 8 | HG02165.hp2 NA18952.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+1456A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368545 | ||||||
chr2:69368556
|
C | T | 4 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0011g0121others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1445G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368556 | ||||||
chr2:69368590
|
T | G | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.223+1411A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368590 | ||||||
chr2:69368598
|
C | A | 1 | a0001c0001t0001g0304 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.223+1403G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368598 | ||||||
chr2:69368708
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.223+1293C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368708 | ||||||
chr2:69368715
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223+1286G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368715 | ||||||
chr2:69368716
|
G | A | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.223+1285C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368716 | ||||||
chr2:69368718
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.223+1283C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368718 | ||||||
chr2:69368784
|
T | C | 2 | a0001c0001t0002g0013a0001c0001t0002g0202 | 3 | HG02257.hp1 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.223+1217A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69368784 | ||||||
chr2:69369060
|
T | C | 239 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(236): Show | 252 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.223+941A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369060 | ||||||
chr2:69369247
|
A | G | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+754T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369247 | ||||||
chr2:69369369
|
A | T | 1 | a0001c0001t0018g0172 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.223+632T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369369 | ||||||
chr2:69369537
|
G | A | 1 | a0001c0002t0004g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.223+464C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369537 | ||||||
chr2:69369662
|
A | G | 1 | a0001c0001t0003g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.223+339T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369662 | ||||||
chr2:69369932
|
T | TA | 42 | a0001c0001t0026g0165a0001c0002t0004g0003a0001c0002t0004g0124others(39): Show | 45 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.223+68dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369932 | ||||||
chr2:69369996
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG04204.hp1 | splice_region_variant&intron_variant | LOW | c.223+5C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 3/19 | chr2 | 69369996 | ||||||
chr2:69370335
|
G | A | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.116-227C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370335 | ||||||
chr2:69370417
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.116-309C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370417 | ||||||
chr2:69370472
|
C | G | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.116-364G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370472 | ||||||
chr2:69370694
|
G | C | 183 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(180): Show | 193 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.116-586C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69370694 | ||||||
chr2:69371076
|
C | CT | 43 | a0001c0001t0001g0321a0001c0001t0002g0096a0001c0001t0002g0207others(40): Show | 47 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.116-969dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371076 | ||||||
chr2:69371076
|
CT | C | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0317others(5): Show | 8 | HG02015.hp1 HG02717.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-969delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371076 | ||||||
chr2:69371081
|
T | C | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-973A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371081 | ||||||
chr2:69371082
|
T | C | 1 | a0001c0001t0015g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.116-974A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371082 | ||||||
chr2:69371111
|
C | T | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.116-1003G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371111 | ||||||
chr2:69371130
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-1022C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371130 | ||||||
chr2:69371226
|
C | A | 1 | a0001c0001t0001g0307 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.116-1118G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371226 | ||||||
chr2:69371242
|
AT | A | 7 | a0001c0001t0001g0311a0001c0001t0001g0333a0001c0001t0002g0217others(4): Show | 7 | HG00558.hp1 HG01243.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.116-1135delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371242 | ||||||
chr2:69371371
|
G | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.116-1263C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371371 | ||||||
chr2:69371374
|
C | T | 1 | a0001c0001t0030g0334 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.116-1266G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371374 | ||||||
chr2:69371424
|
T | A | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.116-1316A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371424 | ||||||
chr2:69371483
|
A | G | 3 | a0001c0002t0004g0124a0001c0002t0004g0125a0001c0002t0004g0126 | 3 | NA18956.hp1 NA18963.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.116-1375T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371483 | ||||||
chr2:69371556
|
G | A | 235 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(232): Show | 248 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.116-1448C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371556 | ||||||
chr2:69371560
|
G | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0231a0001c0001t0002g0233others(7): Show | 12 | HG01258.hp1 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.116-1452C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371560 | ||||||
chr2:69371563
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.116-1455G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371563 | ||||||
chr2:69371691
|
G | T | 1 | a0001c0001t0002g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.116-1583C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371691 | ||||||
chr2:69371694
|
G | A | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.116-1586C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371694 | ||||||
chr2:69371762
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.116-1654C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371762 | ||||||
chr2:69371763
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.116-1655C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371763 | ||||||
chr2:69371766
|
G | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.116-1658C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371766 | ||||||
chr2:69371794
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-1686C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371794 | ||||||
chr2:69371892
|
A | C | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.116-1784T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69371892 | ||||||
chr2:69372082
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.115+1924G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372082 | ||||||
chr2:69372095
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.115+1911C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372095 | ||||||
chr2:69372198
|
C | CA | 19 | a0001c0001t0001g0308a0001c0001t0001g0309a0001c0001t0001g0310others(16): Show | 19 | HG00558.hp1 HG00741.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.115+1807dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372198 | ||||||
chr2:69372198
|
CA | C | 9 | a0001c0001t0002g0052a0001c0001t0002g0096a0001c0001t0007g0029others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.115+1807delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372198 | ||||||
chr2:69372216
|
A | G | 48 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(45): Show | 51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.115+1790T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372216 | ||||||
chr2:69372495
|
G | A | 12 | a0001c0001t0001g0251a0001c0001t0001g0256a0001c0001t0001g0313others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.115+1511C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372495 | ||||||
chr2:69372784
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.115+1222T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69372784 | ||||||
chr2:69373039
|
G | A | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+967C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373039 | ||||||
chr2:69373051
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115+955T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373051 | ||||||
chr2:69373093
|
C | T | 2 | a0001c0001t0019g0055a0001c0001t0019g0056 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.115+913G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373093 | ||||||
chr2:69373178
|
T | G | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.115+828A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373178 | ||||||
chr2:69373252
|
C | T | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+754G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373252 | ||||||
chr2:69373303
|
T | C | 35 | a0001c0001t0002g0033a0001c0001t0002g0052a0001c0001t0002g0096others(32): Show | 36 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(33): Show |
intron_variant | MODIFIER | c.115+703A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373303 | ||||||
chr2:69373334
|
T | A | 241 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(238): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.115+672A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373334 | ||||||
chr2:69373337
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0085 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.115+669C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373337 | ||||||
chr2:69373369
|
C | A | 8 | a0001c0001t0002g0033a0001c0001t0002g0112a0001c0001t0002g0114others(5): Show | 8 | HG02572.hp1 HG02922.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+637G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373369 | ||||||
chr2:69373434
|
T | C | 1 | a0001c0002t0004g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.115+572A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373434 | ||||||
chr2:69373522
|
C | T | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+484G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373522 | ||||||
chr2:69373551
|
C | T | 132 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(129): Show | 139 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.115+455G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373551 | ||||||
chr2:69373559
|
T | C | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.115+447A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373559 | ||||||
chr2:69373655
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.115+351C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373655 | ||||||
chr2:69373714
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.115+292T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373714 | ||||||
chr2:69373772
|
T | C | 2 | a0001c0001t0002g0050a0001c0001t0050g0031 | 2 | HG01433.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.115+234A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373772 | ||||||
chr2:69373956
|
G | A | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.115+50C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 2/19 | chr2 | 69373956 | ||||||
chr2:69374319
|
C | CT | 230 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(227): Show | 243 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(240): Show |
intron_variant | MODIFIER | c.8-207dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374319 | ||||||
chr2:69374370
|
G | A | 94 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(91): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.8-257C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374370 | ||||||
chr2:69374400
|
G | A | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-287C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374400 | ||||||
chr2:69374460
|
C | T | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-347G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374460 | ||||||
chr2:69374577
|
T | C | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-464A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374577 | ||||||
chr2:69374793
|
C | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-680G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374793 | ||||||
chr2:69374860
|
G | A | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8-747C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69374860 | ||||||
chr2:69375062
|
T | C | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.8-949A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375062 | ||||||
chr2:69375105
|
A | G | 1 | a0001c0001t0012g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8-992T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375105 | ||||||
chr2:69375137
|
T | C | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-1024A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375137 | ||||||
chr2:69375247
|
T | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.8-1134A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375247 | ||||||
chr2:69375252
|
TA | T | 94 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(91): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.8-1140delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375252 | ||||||
chr2:69375325
|
A | G | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-1212T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375325 | ||||||
chr2:69375343
|
T | C | 1 | a0001c0002t0006g0123 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.8-1230A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375343 | ||||||
chr2:69375355
|
C | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-1242G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375355 | ||||||
chr2:69375437
|
C | A | 3 | a0001c0001t0020g0053a0001c0001t0020g0054a0001c0001t0039g0242 | 3 | HG01167.hp2 HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.8-1324G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375437 | ||||||
chr2:69375501
|
T | C | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.8-1388A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375501 | ||||||
chr2:69375676
|
C | T | 1 | a0001c0001t0012g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8-1563G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375676 | ||||||
chr2:69375952
|
C | T | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(237): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.8-1839G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69375952 | ||||||
chr2:69376017
|
C | T | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.8-1904G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376017 | ||||||
chr2:69376043
|
T | C | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-1930A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376043 | ||||||
chr2:69376131
|
C | T | 130 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(127): Show | 137 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.8-2018G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376131 | ||||||
chr2:69376132
|
G | C | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.8-2019C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376132 | ||||||
chr2:69376324
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8-2211G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376324 | ||||||
chr2:69376340
|
G | A | 4 | a0001c0001t0011g0119a0001c0001t0011g0120a0001c0001t0011g0121others(1): Show | 4 | HG02486.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-2227C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376340 | ||||||
chr2:69376379
|
C | T | 1 | a0001c0001t0011g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.8-2266G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376379 | ||||||
chr2:69376429
|
T | C | 3 | a0001c0001t0001g0318a0001c0001t0001g0328a0001c0001t0001g0331 | 3 | HG00544.hp1 HG02080.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.8-2316A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376429 | ||||||
chr2:69376467
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-2354G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376467 | ||||||
chr2:69376470
|
G | A | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8-2357C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376470 | ||||||
chr2:69376491
|
C | G | 2 | a0001c0001t0012g0057a0001c0001t0012g0088 | 2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.8-2378G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376491 | ||||||
chr2:69376523
|
G | GA | 168 | a0001c0001t0001g0319a0001c0001t0002g0004a0001c0001t0002g0010others(165): Show | 178 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.8-2411dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376523 | ||||||
chr2:69376540
|
G | GA | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-2428dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376540 | ||||||
chr2:69376572
|
C | A | 1 | a0001c0001t0002g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8-2459G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376572 | ||||||
chr2:69376603
|
G | A | 15 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-2490C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376603 | ||||||
chr2:69376611
|
A | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-2498T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376611 | ||||||
chr2:69376645
|
G | A | 1 | a0001c0005t0001g0320 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.8-2532C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376645 | ||||||
chr2:69376651
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.8-2538A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376651 | ||||||
chr2:69376782
|
G | C | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-2669C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376782 | ||||||
chr2:69376948
|
G | A | 1 | a0002c0004t0001g0324 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.8-2835C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69376948 | ||||||
chr2:69377086
|
C | T | 241 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(238): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.8-2973G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377086 | ||||||
chr2:69377207
|
C | CA | 210 | a0001c0001t0001g0259a0001c0001t0001g0322a0001c0001t0001g0323others(207): Show | 222 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.8-3095dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377207 | ||||||
chr2:69377207
|
C | CAA | 16 | a0001c0001t0002g0112a0001c0001t0002g0221a0001c0001t0003g0064others(13): Show | 16 | HG00735.hp2 HG01884.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.8-3096_8-3095dupTT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377207 | ||||||
chr2:69377285
|
T | G | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-3172A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377285 | ||||||
chr2:69377313
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-3200T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377313 | ||||||
chr2:69377417
|
G | A | 1 | a0001c0001t0051g0113 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-3304C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377417 | ||||||
chr2:69377492
|
T | TAC | 14 | a0001c0001t0002g0205a0001c0001t0002g0215a0001c0001t0002g0216others(11): Show | 14 | HG01255.hp2 HG02109.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-3380_8-3379insGT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377492 | ||||||
chr2:69377493
|
A | AC | 215 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(212): Show | 228 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(225): Show |
intron_variant | MODIFIER | c.8-3381_8-3380insG | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377493 | ||||||
chr2:69377494
|
A | C | 11 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(8): Show | 11 | HG00558.hp1 HG02071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-3381T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377494 | ||||||
chr2:69377498
|
T | A | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.8-3385A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377498 | ||||||
chr2:69377503
|
A | T | 2 | a0001c0001t0035g0246a0001c0001t0058g0343 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.8-3390T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377503 | ||||||
chr2:69377538
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.8-3425A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377538 | ||||||
chr2:69377568
|
G | A | 3 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0002g0206 | 3 | HG00438.hp2 NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.8-3455C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377568 | ||||||
chr2:69377590
|
GC | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-3478delG | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377590 | ||||||
chr2:69377645
|
G | A | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-3532C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377645 | ||||||
chr2:69377765
|
C | A | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-3652G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377765 | ||||||
chr2:69377795
|
A | G | 15 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.8-3682T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377795 | ||||||
chr2:69377928
|
A | T | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-3815T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69377928 | ||||||
chr2:69378056
|
C | A | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | NA18953.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.8-3943G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378056 | ||||||
chr2:69378067
|
G | A | 3 | a0001c0001t0007g0024a0001c0001t0007g0029a0001c0001t0007g0039 | 3 | HG02258.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.8-3954C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378067 | ||||||
chr2:69378154
|
G | A | 1 | a0001c0001t0001g0327 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.8-4041C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378154 | ||||||
chr2:69378157
|
G | A | 1 | a0001c0001t0005g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.8-4044C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378157 | ||||||
chr2:69378174
|
T | C | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8-4061A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378174 | ||||||
chr2:69378416
|
T | C | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.8-4303A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378416 | ||||||
chr2:69378420
|
T | A | 236 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(233): Show | 249 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.8-4307A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378420 | ||||||
chr2:69378485
|
G | T | 2 | a0001c0001t0005g0094a0001c0001t0005g0095 | 2 | NA18966.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.8-4372C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378485 | ||||||
chr2:69378498
|
C | T | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.8-4385G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378498 | ||||||
chr2:69378692
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-4579G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378692 | ||||||
chr2:69378944
|
C | A | 4 | a0001c0001t0002g0114a0001c0001t0002g0115a0001c0001t0002g0116others(1): Show | 4 | HG02572.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-4831G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69378944 | ||||||
chr2:69379068
|
G | A | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4955C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379068 | ||||||
chr2:69379071
|
C | T | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.8-4958G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379071 | ||||||
chr2:69379204
|
C | T | 95 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(92): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.8-5091G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379204 | ||||||
chr2:69379388
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0003g0085 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.8-5275C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379388 | ||||||
chr2:69379515
|
T | A | 38 | a0001c0002t0004g0003a0001c0002t0004g0128a0001c0002t0004g0134others(35): Show | 41 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.8-5402A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379515 | ||||||
chr2:69379540
|
ATTTTC | A | 41 | a0001c0002t0004g0003a0001c0002t0004g0124a0001c0002t0004g0125others(38): Show | 44 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.8-5432_8-5428delGA others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379540 | ||||||
chr2:69379585
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.8-5472A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379585 | ||||||
chr2:69379686
|
T | C | 1 | a0001c0001t0003g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.8-5573A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379686 | ||||||
chr2:69379715
|
T | C | 4 | a0001c0001t0012g0019a0001c0001t0012g0057a0001c0001t0012g0088others(1): Show | 4 | HG02109.hp2 HG02717.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-5602A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379715 | ||||||
chr2:69379717
|
T | G | 1 | a0001c0001t0024g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8-5604A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379717 | ||||||
chr2:69379779
|
T | G | 1 | a0001c0001t0045g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.8-5666A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379779 | ||||||
chr2:69379971
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8-5858C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69379971 | ||||||
chr2:69380163
|
C | A | 1 | a0001c0001t0001g0328 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.8-6050G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380163 | ||||||
chr2:69380245
|
A | G | 241 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(238): Show | 254 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(251): Show |
intron_variant | MODIFIER | c.8-6132T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380245 | ||||||
chr2:69380260
|
C | T | 1 | a0001c0001t0005g0093 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.8-6147G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380260 | ||||||
chr2:69380268
|
T | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.8-6155A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380268 | ||||||
chr2:69380313
|
G | A | 6 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(3): Show | 6 | HG02451.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-6200C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380313 | ||||||
chr2:69380507
|
T | C | 2 | a0001c0001t0019g0055a0001c0001t0019g0056 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8-6394A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380507 | ||||||
chr2:69380514
|
T | C | 3 | a0001c0001t0007g0024a0001c0001t0007g0029a0001c0001t0007g0039 | 3 | HG02258.hp2 HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.8-6401A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380514 | ||||||
chr2:69380615
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+6450C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380615 | ||||||
chr2:69380768
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.7+6297G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380768 | ||||||
chr2:69380879
|
C | G | 1 | a0001c0002t0004g0152 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7+6186G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69380879 | ||||||
chr2:69381011
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+6054C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381011 | ||||||
chr2:69381041
|
G | A | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7+6024C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381041 | ||||||
chr2:69381098
|
G | A | 1 | a0001c0001t0002g0210 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+5967C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381098 | ||||||
chr2:69381246
|
G | C | 1 | a0001c0001t0010g0211 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.7+5819C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381246 | ||||||
chr2:69381262
|
C | T | 1 | a0001c0001t0002g0049 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.7+5803G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381262 | ||||||
chr2:69381344
|
C | G | 15 | a0001c0001t0002g0010a0001c0001t0002g0047a0001c0001t0002g0157others(12): Show | 16 | HG02056.hp2 HG02135.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+5721G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381344 | ||||||
chr2:69381408
|
T | C | 1 | a0001c0001t0002g0212 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+5657A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381408 | ||||||
chr2:69381539
|
C | T | 2 | a0001c0001t0035g0246a0001c0001t0058g0343 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7+5526G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381539 | ||||||
chr2:69381556
|
C | CT | 7 | a0001c0001t0009g0040a0001c0001t0009g0041a0001c0001t0009g0042others(4): Show | 7 | HG00609.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+5508dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381556 | ||||||
chr2:69381556
|
CT | C | 17 | a0001c0001t0001g0329a0001c0001t0001g0331a0001c0001t0002g0021others(14): Show | 17 | HG01069.hp1 HG01069.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.7+5508delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381556 | ||||||
chr2:69381720
|
A | AT | 233 | a0001c0001t0001g0249a0001c0001t0002g0004a0001c0001t0002g0010others(230): Show | 246 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.7+5344dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381720 | ||||||
chr2:69381839
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+5226G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381839 | ||||||
chr2:69381863
|
C | CT | 228 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(225): Show | 241 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(238): Show |
intron_variant | MODIFIER | c.7+5201dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381863 | ||||||
chr2:69381863
|
C | CTT | 6 | a0001c0001t0002g0156a0001c0001t0003g0059a0001c0001t0003g0060others(3): Show | 6 | HG01175.hp1 HG01515.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+5200_7+5201dupAA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381863 | ||||||
chr2:69381870
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7+5195A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69381870 | ||||||
chr2:69382061
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.7+5004C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382061 | ||||||
chr2:69382501
|
T | C | 31 | a0001c0001t0002g0033a0001c0001t0002g0052a0001c0001t0002g0096others(28): Show | 32 | HG02074.hp1 HG02280.hp1 HG02451.hp1 others(29): Show |
intron_variant | MODIFIER | c.7+4564A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382501 | ||||||
chr2:69382671
|
T | C | 1 | a0001c0002t0004g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7+4394A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382671 | ||||||
chr2:69382831
|
A | T | 342 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0015others(339): Show | 363 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.7+4234T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382831 | ||||||
chr2:69382849
|
C | T | 48 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(45): Show | 51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.7+4216G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382849 | ||||||
chr2:69382972
|
A | G | 95 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(92): Show | 101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.7+4093T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69382972 | ||||||
chr2:69383049
|
A | C | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+4016T>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383049 | ||||||
chr2:69383095
|
G | C | 1 | a0001c0001t0035g0246 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7+3970C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383095 | ||||||
chr2:69383371
|
A | T | 1 | a0001c0001t0002g0155 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7+3694T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383371 | ||||||
chr2:69383585
|
T | A | 4 | a0001c0001t0019g0055a0001c0001t0019g0056a0001c0001t0020g0053others(1): Show | 4 | HG02257.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+3480A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383585 | ||||||
chr2:69383601
|
C | CATTT | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+3460_7+3463dupAA others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383601 | ||||||
chr2:69383689
|
T | C | 1 | a0001c0001t0001g0333 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7+3376A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383689 | ||||||
chr2:69383733
|
C | T | 5 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0259others(2): Show | 9 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+3332G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383733 | ||||||
chr2:69383805
|
T | C | 1 | a0001c0001t0030g0334 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.7+3260A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383805 | ||||||
chr2:69383977
|
C | T | 1 | a0001c0001t0001g0335 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.7+3088G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69383977 | ||||||
chr2:69384138
|
CTTCTCTG others(18): Show |
C | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2902_7+2926delTA others(23): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384138 | ||||||
chr2:69384199
|
A | G | 1 | a0001c0001t0045g0058 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.7+2866T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384199 | ||||||
chr2:69384353
|
C | T | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(237): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.7+2712G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384353 | ||||||
chr2:69384540
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2525G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384540 | ||||||
chr2:69384541
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2524T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384541 | ||||||
chr2:69384556
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2509C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384556 | ||||||
chr2:69384557
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2508G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384557 | ||||||
chr2:69384572
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2493A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384572 | ||||||
chr2:69384580
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2485A>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384580 | ||||||
chr2:69384619
|
C | T | 1 | a0001c0001t0012g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.7+2446G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384619 | ||||||
chr2:69384620
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2445C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384620 | ||||||
chr2:69384650
|
T | C | 1 | a0001c0001t0001g0341 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7+2415A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384650 | ||||||
chr2:69384654
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2411C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384654 | ||||||
chr2:69384655
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2410G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384655 | ||||||
chr2:69384657
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2408C>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384657 | ||||||
chr2:69384658
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.7+2407G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384658 | ||||||
chr2:69384673
|
G | A | 1 | a0001c0002t0006g0224 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.7+2392C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384673 | ||||||
chr2:69384681
|
G | A | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2384C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384681 | ||||||
chr2:69384693
|
C | CA | 7 | a0001c0001t0001g0335a0001c0001t0001g0336a0001c0001t0001g0338others(4): Show | 7 | HG02074.hp2 HG02602.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+2371dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | ||||||
chr2:69384693
|
CA | C | 7 | a0001c0001t0001g0257a0001c0001t0011g0119a0001c0001t0011g0120others(4): Show | 7 | HG01243.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2371delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | ||||||
chr2:69384693
|
CAA | C | 6 | a0001c0001t0002g0220a0001c0001t0002g0221a0001c0001t0002g0240others(3): Show | 6 | HG02109.hp2 HG02717.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+2370_7+2371delTT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | ||||||
chr2:69384693
|
CAAA | C | 177 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(174): Show | 187 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.7+2369_7+2371delTT others(1): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | ||||||
chr2:69384693
|
CAAAAAAA others(3): Show |
C | 48 | a0001c0001t0002g0030a0001c0001t0009g0040a0001c0001t0009g0041others(45): Show | 51 | HG00544.hp2 HG00597.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.7+2362_7+2371delTT others(8): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384693 | ||||||
chr2:69384745
|
A | G | 7 | a0001c0001t0007g0024a0001c0001t0007g0025a0001c0001t0007g0026others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+2320T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384745 | ||||||
chr2:69384764
|
GAAGAAAG others(7): Show |
G | 1 | a0001c0001t0034g0247 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.7+2287_7+2300delTT others(12): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384764 | ||||||
chr2:69384777
|
A | AAAAG | 40 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(37): Show | 43 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.7+2284_7+2287dupCT others(2): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384777 | ||||||
chr2:69384791
|
AAG | A | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+2272_7+2273delCT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384791 | ||||||
chr2:69384875
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7+2190A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384875 | ||||||
chr2:69384987
|
A | G | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7+2078T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69384987 | ||||||
chr2:69385411
|
C | G | 243 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(240): Show | 256 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(253): Show |
intron_variant | MODIFIER | c.7+1654G>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385411 | ||||||
chr2:69385426
|
C | T | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(237): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.7+1639G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385426 | ||||||
chr2:69385523
|
C | T | 5 | a0001c0001t0002g0038a0001c0001t0015g0034a0001c0001t0015g0035others(2): Show | 5 | HG01243.hp1 HG02970.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+1542G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385523 | ||||||
chr2:69385539
|
TA | T | 6 | a0001c0001t0002g0038a0001c0001t0007g0024a0001c0001t0015g0034others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+1525delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385539 | ||||||
chr2:69385539
|
TATTTA | T | 38 | a0001c0001t0003g0007a0001c0001t0003g0008a0001c0001t0003g0009others(35): Show | 41 | HG00558.hp1 HG00642.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.7+1521_7+1525delTA others(3): Show |
GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385539 | ||||||
chr2:69385543
|
TA | T | 141 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0013others(138): Show | 149 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.7+1521delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385543 | ||||||
chr2:69385544
|
A | T | 12 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(9): Show | 12 | HG00609.hp2 HG00735.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+1521T>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385544 | ||||||
chr2:69385544
|
AT | A | 50 | a0001c0001t0002g0004a0001c0001t0002g0033a0001c0001t0002g0096others(47): Show | 52 | HG00741.hp2 HG01069.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.7+1520delA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385544 | ||||||
chr2:69385548
|
T | A | 1 | a0001c0001t0058g0343 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7+1517A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385548 | ||||||
chr2:69385549
|
T | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0231a0001c0001t0002g0233others(7): Show | 12 | HG01258.hp1 HG01928.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+1516A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385549 | ||||||
chr2:69385746
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | NA18948.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.7+1319T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385746 | ||||||
chr2:69385853
|
C | CT | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+1211dupA | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69385853 | ||||||
chr2:69386027
|
T | TA | 130 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(127): Show | 139 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.7+1037dupT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386027 | ||||||
chr2:69386027
|
TA | T | 13 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(10): Show | 13 | HG00558.hp2 HG01255.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.7+1037delT | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386027 | ||||||
chr2:69386215
|
T | A | 1 | a0001c0001t0002g0240 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.7+850A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386215 | ||||||
chr2:69386286
|
C | T | 238 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(235): Show | 251 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.7+779G>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386286 | ||||||
chr2:69386425
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0023 | 3 | HG01109.hp2 HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.7+640T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386425 | ||||||
chr2:69386629
|
T | A | 1 | a0001c0001t0002g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.7+436A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386629 | ||||||
chr2:69386633
|
T | A | 1 | a0001c0001t0039g0242 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.7+432A>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386633 | ||||||
chr2:69386676
|
G | T | 2 | a0001c0001t0035g0246a0001c0001t0058g0343 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.7+389C>A | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386676 | ||||||
chr2:69386794
|
T | C | 238 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(235): Show | 251 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(248): Show |
intron_variant | MODIFIER | c.7+271A>G | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386794 | ||||||
chr2:69386809
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.7+256C>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386809 | ||||||
chr2:69386826
|
A | G | 244 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(241): Show | 257 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.7+239T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69386826 | ||||||
chr2:69387025
|
C | A | 4 | a0001c0002t0006g0014a0001c0002t0006g0243a0001c0002t0006g0244others(1): Show | 5 | HG00621.hp1 NA18972.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+40G>T | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69387025 | ||||||
chr2:69387029
|
A | G | 240 | a0001c0001t0002g0004a0001c0001t0002g0010a0001c0001t0002g0012others(237): Show | 253 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(250): Show |
intron_variant | MODIFIER | c.7+36T>C | GFPT1 | ENSG00000198380.13 | transcript | ENST00000357308.9 | protein_coding | 1/19 | chr2 | 69387029 |