geneid | 4522 |
---|---|
ensemblid | ENSG00000100714.18 |
hgncid | 7432 |
symbol | MTHFD1 |
name | methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1 |
refseq_nuc | NM_005956.4 |
refseq_prot | NP_005947.3 |
ensembl_nuc | ENST00000652337.1 |
ensembl_prot | ENSP00000498336.1 |
mane_status | MANE Select |
chr | chr14 |
start | 64388353 |
end | 64460025 |
strand | + |
ver | v1.2 |
region | chr14:64388353-64460025 |
region5000 | chr14:64383353-64465025 |
regionname0 | MTHFD1_chr14_64388353_64460025 |
regionname5000 | MTHFD1_chr14_64383353_64465025 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 935 | 170 | 44 | 25 | 76 | 5 | 19 | 65 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0002 | 0/0 | 935 | 88 | 13 | 25 | 29 | 6 | 15 | 21 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0003 | 1/0 | 935 | 55 | 5 | 3 | 43 | 1 | 2 | 26 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0004 | 0/0 | 935 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0005 | 0/0 | 935 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0006 | 0/0 | 935 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0007 | 0/0 | 935 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0008 | 0/0 | 935 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0009 | 0/0 | 935 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0010 | 0/0 | 935 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0011 | 0/0 | 935 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2808 | 168 | 43 | 24 | 76 | 5 | 19 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0002 | 0/0 | 2808 | 88 | 13 | 25 | 29 | 6 | 15 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0003 | 1/0 | 2808 | 54 | 5 | 3 | 42 | 1 | 2 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0004 | 0/0 | 2808 | 11 | 10 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0005 | 0/0 | 2808 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0006 | 0/0 | 2808 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0007 | 0/0 | 2808 | 2 | 1 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0008 | 0/0 | 2808 | 2 | 0 | 0 | 0 | 0 | 2 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0009 | 0/0 | 2808 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0010 | 0/0 | 2808 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0011 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0012 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0013 | 0/0 | 2808 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
c0014 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
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 | 1/1 | 347 | 330 | 75 | 53 | 150 | 12 | 38 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
t0002 | 0/0 | 347 | 12 | 11 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2808 | 168 | 43 | 24 | 76 | 5 | 19 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0001c0011 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0001c0014 | 0/0 | 2808 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0002c0002 | 0/0 | 2808 | 88 | 13 | 25 | 29 | 6 | 15 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0003c0003 | 1/0 | 2808 | 54 | 5 | 3 | 42 | 1 | 2 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0003c0010 | 0/0 | 2808 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0004c0004 | 0/0 | 2808 | 11 | 10 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0005c0005 | 0/0 | 2808 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0006c0006 | 0/0 | 2808 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0007c0007 | 0/0 | 2808 | 2 | 1 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0008c0008 | 0/0 | 2808 | 2 | 0 | 0 | 0 | 0 | 2 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0009c0009 | 0/0 | 2808 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0010c0012 | 0/0 | 2808 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0011c0013 | 0/0 | 2808 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3154 | 159 | 35 | 23 | 76 | 5 | 19 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0001c0001t0002 | 0/0 | 3154 | 9 | 8 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0001c0011t0001 | 0/0 | 3154 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0001c0014t0001 | 0/0 | 3154 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0002c0002t0001 | 0/0 | 3154 | 88 | 13 | 25 | 29 | 6 | 15 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0003c0003t0001 | 1/0 | 3154 | 51 | 2 | 3 | 42 | 1 | 2 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0003c0003t0002 | 0/0 | 3154 | 3 | 3 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0003c0010t0001 | 0/0 | 3154 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0004c0004t0001 | 0/0 | 3154 | 11 | 10 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0005c0005t0001 | 0/0 | 3154 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0006c0006t0001 | 0/0 | 3154 | 5 | 5 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0007c0007t0001 | 0/0 | 3154 | 2 | 1 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0008c0008t0001 | 0/0 | 3154 | 2 | 0 | 0 | 0 | 0 | 2 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0009c0009t0001 | 0/0 | 3154 | 2 | 2 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0010c0012t0001 | 0/0 | 3154 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
a0011c0013t0001 | 0/0 | 3154 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | copy fasta | chr14 | 64383353 | 64465025 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0011t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0001c0014t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0003t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0003c0010t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0004c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0005c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0005c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0005c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0005c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0005c0005t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0006c0006t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0006c0006t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0006c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0006c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0006c0006t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0007c0007t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0007c0007t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0008c0008t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0008c0008t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0009c0009t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0009c0009t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0010c0012t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
a0011c0013t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0079 | EUR | GBR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0018 | EUR | GBR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0306 | EUR | GBR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0056 | EUR | GBR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | FIN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0319 | EUR | FIN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0089 | EUR | FIN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00408 | hp1 | a0003 | c0003 | t0001 | g0285 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00423 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0264 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0279 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00673 | hp1 | a0003 | c0003 | t0001 | g0167 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00673 | hp2 | a0003 | c0010 | t0001 | g0176 | EAS | CHS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01099 | hp1 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0132 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01175 | hp1 | a0001 | c0014 | t0001 | g0009 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0117 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01243 | hp2 | a0004 | c0004 | t0001 | g0098 | AMR | PUR | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0307 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0239 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0178 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0262 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0293 | AMR | CLM | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0045 | EUR | IBS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01884 | hp2 | a0006 | c0006 | t0001 | g0126 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0257 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01891 | hp2 | a0010 | c0012 | t0001 | g0003 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0260 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0017 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02055 | hp1 | a0004 | c0004 | t0001 | g0110 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02083 | hp1 | a0003 | c0003 | t0001 | g0321 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02129 | hp2 | a0003 | c0003 | t0001 | g0135 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02132 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0136 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02135 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0273 | EAS | CDX | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | CDX | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | CDX | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0157 | EAS | CDX | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02257 | hp1 | a0004 | c0004 | t0001 | g0106 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02258 | hp2 | a0005 | c0005 | t0001 | g0029 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0300 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02280 | hp1 | a0009 | c0009 | t0001 | g0083 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0329 | AMR | PEL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02451 | hp2 | a0007 | c0007 | t0001 | g0219 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0082 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02622 | hp2 | a0004 | c0004 | t0001 | g0062 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02647 | hp1 | a0003 | c0003 | t0002 | g0100 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02647 | hp2 | a0004 | c0004 | t0001 | g0049 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0287 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0322 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0124 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02922 | hp1 | a0006 | c0006 | t0001 | g0229 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02922 | hp2 | a0004 | c0004 | t0001 | g0096 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02965 | hp2 | a0006 | c0006 | t0001 | g0002 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0207 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03041 | hp2 | a0005 | c0005 | t0001 | g0048 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0005 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0105 | AFR | ESN | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0258 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03209 | hp2 | a0003 | c0003 | t0002 | g0190 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03239 | hp1 | a0008 | c0008 | t0001 | g0338 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0179 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03453 | hp2 | a0001 | c0011 | t0001 | g0097 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0268 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0274 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03579 | hp2 | a0009 | c0009 | t0001 | g0113 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0266 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0276 | SAS | PJL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03927 | hp1 | a0008 | c0008 | t0001 | g0139 | SAS | BEB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | BEB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0335 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0331 | SAS | BEB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0323 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0101 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0088 | SAS | STU | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18522 | hp2 | a0003 | c0003 | t0001 | g0061 | AFR | YRI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | CHB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | CHB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | YRI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18906 | hp2 | a0004 | c0004 | t0001 | g0109 | AFR | YRI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0180 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18941 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18943 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0182 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18953 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18961 | hp1 | a0003 | c0003 | t0001 | g0220 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18970 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18971 | hp1 | a0003 | c0003 | t0001 | g0311 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18974 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18979 | hp1 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18985 | hp1 | a0003 | c0003 | t0001 | g0297 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18989 | hp2 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18990 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18999 | hp1 | a0011 | c0013 | t0001 | g0209 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA18999 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19005 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | LWK | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19043 | hp1 | a0006 | c0006 | t0001 | g0116 | AFR | LWK | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19063 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19065 | hp1 | a0003 | c0003 | t0001 | g0204 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19077 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19086 | hp1 | a0003 | c0003 | t0001 | g0312 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19090 | hp1 | a0007 | c0007 | t0001 | g0289 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | YRI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA19240 | hp2 | a0004 | c0004 | t0001 | g0095 | AFR | YRI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20129 | hp1 | a0005 | c0005 | t0001 | g0023 | AFR | ASW | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0305 | AFR | ASW | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0304 | EUR | TSI | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | GIH | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | GIH | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02109 | hp2 | a0004 | c0004 | t0001 | g0256 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0277 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02486 | hp2 | a0005 | c0005 | t0001 | g0063 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG02559 | hp2 | a0005 | c0005 | t0001 | g0022 | AFR | ACB | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | USA | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20300 | hp1 | a0006 | c0006 | t0001 | g0140 | AFR | USA | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0288 | AFR | USA | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | LWK | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0339 | AFR | LWK | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0282 | REF | REF | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0159 | REF | REF | MTHFD1_chr14_64383353_64465025 | MTHFD1 | chr14 | 64383353 | 64465025 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:64415662
|
A | G | 8 | a0001a0002a0004others(5): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
missense_variant | MODERATE | c.401A>G | p.Lys134Arg | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/28 | 476/3154 | 401/2808 | 134/935 | chr14 | 64415662 | ||
chr14:64442127
|
G | A | 4 | a0002a0007a0008others(1): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
missense_variant | MODERATE | c.1958G>A | p.Arg653Gln | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 20/28 | 2033/3154 | 1958/2808 | 653/935 | chr14 | 64442127 | ||
chr14:64449447
|
C | T | 3 | a0005a0008a0009 | 9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.2282C>T | p.Thr761Met | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/28 | 2357/3154 | 2282/2808 | 761/935 | chr14 | 64449447 | ||
chr14:64449470
|
C | T | 1 | a0004 | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
missense_variant | MODERATE | c.2305C>T | p.Leu769Phe | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/28 | 2380/3154 | 2305/2808 | 769/935 | chr14 | 64449470 | ||
chr14:64449480
|
G | A | 2 | a0006a0010 | 6 | HG01884.hp2 HG01891.hp2 HG02922.hp1 others(3): Show |
missense_variant | MODERATE | c.2315G>A | p.Arg772His | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/28 | 2390/3154 | 2315/2808 | 772/935 | chr14 | 64449480 | ||
chr14:64454724
|
G | A | 1 | a0011 | 1 | NA18999.hp1 | missense_variant&splice_region_variant | MODERATE | c.2567G>A | p.Gly856Asp | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/28 | 2642/3154 | 2567/2808 | 856/935 | chr14 | 64454724 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:64417901
|
C | T | 1 | a0003c0010 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.492C>T | p.Ala164Ala | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/28 | 567/3154 | 492/2808 | 164/935 | chr14 | 64417901 | ||
chr14:64419900
|
C | T | 1 | a0001c0014 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.702C>T | p.Ile234Ile | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/28 | 777/3154 | 702/2808 | 234/935 | chr14 | 64419900 | ||
chr14:64435635
|
T | C | 1 | a0001c0011 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1561T>C | p.Leu521Leu | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/28 | 1636/3154 | 1561/2808 | 521/935 | chr14 | 64435635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:64459902
|
A | C | 2 | a0001c0001t0002a0003c0003t0002 | 12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*148A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 28/28 | 1599 | chr14 | 64459902 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:64388622
|
C | T | 1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.41+154C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64388622 | ||||||
chr14:64388707
|
A | G | 87 | a0001c0001t0001g0255a0001c0001t0001g0261a0001c0001t0001g0267others(84): Show | 87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.41+239A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64388707 | ||||||
chr14:64388743
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+275C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64388743 | ||||||
chr14:64388931
|
T | A | 1 | a0006c0006t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.41+463T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64388931 | ||||||
chr14:64388962
|
T | C | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41+494T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64388962 | ||||||
chr14:64389003
|
A | G | 18 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0240others(15): Show | 19 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.41+535A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64389003 | ||||||
chr14:64389076
|
A | T | 6 | a0001c0001t0001g0230a0001c0001t0001g0233a0001c0001t0001g0234others(3): Show | 6 | HG02165.hp1 HG02698.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+608A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64389076 | ||||||
chr14:64389564
|
C | T | 1 | a0002c0002t0001g0340 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.41+1096C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64389564 | ||||||
chr14:64389664
|
C | T | 2 | a0001c0001t0001g0228a0006c0006t0001g0229 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.41+1196C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64389664 | ||||||
chr14:64389703
|
C | T | 1 | a0002c0002t0001g0339 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41+1235C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64389703 | ||||||
chr14:64389920
|
A | G | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+1452A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64389920 | ||||||
chr14:64390009
|
T | C | 2 | a0001c0001t0001g0255a0002c0002t0001g0254 | 2 | HG00733.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.41+1541T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390009 | ||||||
chr14:64390193
|
A | G | 1 | a0002c0002t0001g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.41+1725A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390193 | ||||||
chr14:64390308
|
C | G | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+1840C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390308 | ||||||
chr14:64390314
|
C | CT | 84 | a0001c0001t0001g0221a0001c0001t0001g0255a0001c0001t0001g0261others(81): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.41+1859dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64390314 | |||||
chr14:64390354
|
AT | A | 165 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.41+1897delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64390354 | |||||
chr14:64390378
|
T | G | 165 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(162): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.41+1910T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390378 | ||||||
chr14:64390389
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.41+1921A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390389 | ||||||
chr14:64390523
|
G | T | 1 | a0007c0007t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.41+2055G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390523 | ||||||
chr14:64390545
|
G | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.41+2077G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390545 | ||||||
chr14:64390609
|
A | G | 1 | a0008c0008t0001g0338 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.41+2141A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390609 | ||||||
chr14:64390629
|
G | A | 1 | a0002c0002t0001g0260 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.41+2161G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390629 | ||||||
chr14:64390645
|
A | G | 2 | a0002c0002t0001g0131a0002c0002t0001g0132 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.41+2177A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390645 | ||||||
chr14:64390665
|
T | C | 33 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(30): Show | 33 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.41+2197T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390665 | ||||||
chr14:64390701
|
T | G | 1 | a0001c0001t0001g0261 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.41+2233T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390701 | ||||||
chr14:64390735
|
A | G | 188 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(185): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.41+2267A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390735 | ||||||
chr14:64390943
|
C | T | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41+2475C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64390943 | ||||||
chr14:64391468
|
C | T | 24 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0236others(21): Show | 25 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.41+3000C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64391468 | ||||||
chr14:64391812
|
T | G | 1 | a0001c0001t0002g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.41+3344T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64391812 | ||||||
chr14:64391827
|
C | T | 1 | a0005c0005t0001g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.41+3359C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64391827 | ||||||
chr14:64391862
|
C | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0125a0003c0003t0002g0124 | 3 | HG02897.hp2 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.41+3394C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64391862 | ||||||
chr14:64391961
|
T | C | 26 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(23): Show | 26 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.41+3493T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64391961 | ||||||
chr14:64391962
|
T | C | 1 | a0003c0003t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.41+3494T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64391962 | ||||||
chr14:64392075
|
A | T | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41+3607A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392075 | ||||||
chr14:64392076
|
C | G | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | NA18968.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.41+3608C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392076 | ||||||
chr14:64392080
|
C | T | 1 | a0002c0002t0001g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.41+3612C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392080 | ||||||
chr14:64392099
|
G | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+3631G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392099 | ||||||
chr14:64392320
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | HG02615.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+3852G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392320 | ||||||
chr14:64392462
|
A | G | 2 | a0003c0003t0001g0061a0004c0004t0001g0062 | 2 | HG02622.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.41+3994A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392462 | ||||||
chr14:64392473
|
C | T | 143 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.41+4005C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392473 | ||||||
chr14:64392575
|
C | G | 106 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0001g0237others(103): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.41+4107C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392575 | ||||||
chr14:64392907
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18953.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.41+4439T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64392907 | ||||||
chr14:64393019
|
C | G | 64 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.41+4551C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393019 | ||||||
chr14:64393136
|
A | T | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.41+4668A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393136 | ||||||
chr14:64393166
|
C | G | 254 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.41+4698C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393166 | ||||||
chr14:64393198
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.41+4730G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393198 | ||||||
chr14:64393291
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18953.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.41+4823C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393291 | ||||||
chr14:64393413
|
G | GA | 15 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(12): Show | 15 | HG00099.hp2 HG01167.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.41+4959dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64393413 | |||||
chr14:64393522
|
G | A | 3 | a0003c0003t0001g0134a0003c0003t0001g0135a0003c0003t0001g0136 | 3 | HG02129.hp2 HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.41+5054G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393522 | ||||||
chr14:64393612
|
A | C | 1 | a0003c0003t0001g0191 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.41+5144A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393612 | ||||||
chr14:64393647
|
T | C | 2 | a0002c0002t0001g0192a0002c0002t0001g0193 | 2 | NA18939.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.41+5179T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393647 | ||||||
chr14:64393867
|
T | C | 2 | a0001c0001t0001g0195a0002c0002t0001g0194 | 2 | NA18963.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.41+5399T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64393867 | ||||||
chr14:64394291
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0253others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+5823C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394291 | ||||||
chr14:64394292
|
G | C | 37 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0069others(34): Show | 37 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.41+5824G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394292 | ||||||
chr14:64394320
|
C | G | 1 | a0002c0002t0001g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.41+5852C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394320 | ||||||
chr14:64394538
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.41+6070G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394538 | ||||||
chr14:64394622
|
AG | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(11): Show | 14 | HG00099.hp2 HG01167.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.41+6156delG | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64394622 | |||||
chr14:64394669
|
G | A | 62 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.42-6124G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394669 | ||||||
chr14:64394697
|
CTT | C | 3 | a0001c0001t0001g0127a0001c0001t0001g0128a0006c0006t0001g0126 | 3 | HG01109.hp1 HG01884.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.42-6095_42-6094del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394697 | ||||||
chr14:64394721
|
G | A | 1 | a0002c0002t0001g0238 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.42-6072G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394721 | ||||||
chr14:64394752
|
G | A | 26 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0221others(23): Show | 27 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.42-6041G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394752 | ||||||
chr14:64394909
|
C | T | 1 | a0002c0002t0001g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.42-5884C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394909 | ||||||
chr14:64394997
|
A | G | 1 | a0004c0004t0001g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.42-5796A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64394997 | ||||||
chr14:64395098
|
A | G | 1 | a0002c0002t0001g0059 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.42-5695A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64395098 | ||||||
chr14:64395241
|
C | T | 2 | a0003c0003t0002g0190a0007c0007t0001g0219 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.42-5552C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64395241 | ||||||
chr14:64395726
|
C | A | 25 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0236others(22): Show | 26 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.42-5067C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64395726 | ||||||
chr14:64395785
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.42-5008A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64395785 | ||||||
chr14:64395837
|
A | G | 278 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.42-4956A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64395837 | ||||||
chr14:64395869
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.42-4924G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64395869 | ||||||
chr14:64396174
|
G | A | 111 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.42-4619G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396174 | ||||||
chr14:64396386
|
A | G | 2 | a0001c0001t0001g0333a0001c0001t0001g0334 | 2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.42-4407A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396386 | ||||||
chr14:64396389
|
G | GT | 8 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0188others(5): Show | 8 | HG00544.hp2 HG02135.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-4385dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64396389 | |||||
chr14:64396389
|
GT | G | 248 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(245): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.42-4385delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64396389 | |||||
chr14:64396463
|
C | T | 259 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.42-4330C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396463 | ||||||
chr14:64396493
|
G | A | 34 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0065others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.42-4300G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396493 | ||||||
chr14:64396558
|
A | AT | 115 | a0001c0001t0001g0019a0001c0001t0001g0051a0001c0001t0001g0052others(112): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.42-4217dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64396558 | |||||
chr14:64396558
|
A | ATT | 9 | a0001c0001t0001g0215a0001c0001t0001g0320a0001c0001t0001g0324others(6): Show | 9 | HG00558.hp1 HG02083.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.42-4218_42-4217dup others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64396558 | |||||
chr14:64396558
|
AT | A | 13 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(10): Show | 13 | HG01891.hp1 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-4217delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64396558 | |||||
chr14:64396622
|
C | A | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.42-4171C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396622 | ||||||
chr14:64396636
|
T | G | 32 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0065others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.42-4157T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396636 | ||||||
chr14:64396997
|
T | C | 1 | a0002c0002t0001g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.42-3796T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64396997 | ||||||
chr14:64397013
|
G | C | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.42-3780G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397013 | ||||||
chr14:64397068
|
G | A | 2 | a0002c0002t0001g0339a0003c0003t0001g0259 | 2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.42-3725G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397068 | ||||||
chr14:64397099
|
CGT | C | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3693_42-3692del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397099 | ||||||
chr14:64397103
|
T | C | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3690T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397103 | ||||||
chr14:64397104
|
CAAAAAAA others(13): Show |
C | 1 | a0001c0001t0001g0325 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.42-3673_42-3654del others(20): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397104 | |||||
chr14:64397105
|
AAAAAAAA others(54): Show |
A | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3686_42-3626del others(61): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397105 | |||||
chr14:64397118
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0324 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.42-3673_42-3650del others(24): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397118 | |||||
chr14:64397120
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0319 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.42-3671_42-3648del others(24): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397120 | |||||
chr14:64397122
|
AAAAAAAA others(51): Show |
A | 2 | a0003c0003t0001g0017a0003c0003t0001g0018 | 2 | HG00099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.42-3669_42-3612del others(58): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397122 | |||||
chr14:64397123
|
AAAAAAAA others(34): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.42-3668_42-3628del others(41): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397123 | |||||
chr14:64397124
|
AAAAAAAA others(15): Show |
A | 1 | a0004c0004t0001g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.42-3667_42-3646del others(22): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397124 | |||||
chr14:64397125
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42-3666_42-3648del others(19): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397125 | |||||
chr14:64397126
|
AAAAAAAA others(7): Show |
A | 1 | a0002c0002t0001g0260 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.42-3665_42-3652del others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397126 | |||||
chr14:64397128
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.42-3663_42-3644del others(20): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397128 | |||||
chr14:64397128
|
AAAAAAAA others(21): Show |
A | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.42-3663_42-3636del others(28): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397128 | |||||
chr14:64397130
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0001g0019a0001c0001t0001g0214 | 2 | HG01993.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.42-3661_42-3646del others(16): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397130 | |||||
chr14:64397131
|
AAAAAAAA others(4): Show |
A | 1 | a0003c0003t0001g0182 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.42-3660_42-3650del others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397131 | |||||
chr14:64397131
|
AAAAAAAA others(6): Show |
A | 2 | a0003c0003t0001g0181a0007c0007t0001g0219 | 2 | HG02451.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.42-3660_42-3648del others(13): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397131 | |||||
chr14:64397131
|
AAAAAAAA others(14): Show |
A | 1 | a0005c0005t0001g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.42-3660_42-3640del others(21): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397131 | |||||
chr14:64397131
|
AAAAAAAA others(22): Show |
A | 1 | a0003c0003t0001g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.42-3660_42-3632del others(29): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397131 | |||||
chr14:64397132
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42-3659_42-3650del others(10): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397132 | |||||
chr14:64397132
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.42-3659_42-3646del others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397132 | |||||
chr14:64397132
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.42-3659_42-3636del others(24): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397132 | |||||
chr14:64397132
|
AAAAAAAA others(31): Show |
A | 1 | a0001c0001t0001g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.42-3659_42-3622del others(38): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397132 | |||||
chr14:64397132
|
AAAAAAAA others(37): Show |
A | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.42-3659_42-3616del others(44): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397132 | |||||
chr14:64397133
|
AAAAAAAT others(4): Show |
A | 3 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0318 | 3 | HG00280.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.42-3658_42-3648del others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(6): Show |
A | 1 | a0001c0001t0001g0317 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.42-3658_42-3646del others(13): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(8): Show |
A | 1 | a0006c0006t0001g0229 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-3658_42-3644del others(15): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(10): Show |
A | 1 | a0002c0002t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.42-3658_42-3642del others(17): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(12): Show |
A | 1 | a0002c0002t0001g0252 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.42-3658_42-3640del others(19): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(14): Show |
A | 3 | a0001c0001t0001g0092a0001c0001t0001g0237a0001c0001t0002g0068 | 3 | HG00738.hp1 HG02622.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.42-3658_42-3638del others(21): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(16): Show |
A | 4 | a0001c0001t0001g0091a0001c0001t0001g0236a0002c0002t0001g0131others(1): Show | 4 | HG01074.hp1 HG01099.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-3658_42-3636del others(23): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397133
|
AAAAAAAT others(18): Show |
A | 2 | a0001c0001t0001g0090a0001c0001t0001g0213 | 2 | HG00733.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.42-3658_42-3634del others(25): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397133 | |||||
chr14:64397134
|
AAAAAATA others(3): Show |
A | 4 | a0001c0001t0001g0246a0001c0001t0001g0314a0001c0001t0001g0315others(1): Show | 4 | HG04204.hp2 NA18961.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3657_42-3648del others(10): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(5): Show |
A | 2 | a0001c0001t0001g0313a0003c0003t0001g0180 | 2 | NA18939.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.42-3657_42-3646del others(12): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0002g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42-3657_42-3644del others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(11): Show |
A | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.42-3657_42-3640del others(18): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(13): Show |
A | 2 | a0001c0001t0001g0245a0002c0002t0001g0089 | 2 | HG00323.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.42-3657_42-3638del others(20): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(15): Show |
A | 3 | a0002c0002t0001g0001a0002c0002t0001g0243a0002c0002t0001g0244 | 4 | HG01070.hp2 HG01071.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-3657_42-3636del others(22): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(17): Show |
A | 1 | a0001c0001t0002g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.42-3657_42-3634del others(24): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397134
|
AAAAAATA others(33): Show |
A | 1 | a0003c0003t0001g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.42-3657_42-3618del others(40): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397134 | |||||
chr14:64397135
|
AAAAAT | A | 6 | a0001c0001t0001g0008a0002c0002t0001g0212a0002c0002t0001g0222others(3): Show | 6 | HG01071.hp2 HG01361.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-3656_42-3652del others(5): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(2): Show |
A | 6 | a0001c0001t0001g0052a0001c0001t0001g0177a0001c0001t0001g0308others(3): Show | 6 | HG00741.hp2 NA18954.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3656_42-3648del others(9): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(4): Show |
A | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0211others(2): Show | 5 | HG00673.hp2 HG04228.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3656_42-3646del others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(6): Show |
A | 3 | a0001c0001t0001g0087a0001c0001t0001g0119a0002c0002t0001g0210 | 3 | HG03471.hp2 HG04115.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.42-3656_42-3644del others(13): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(8): Show |
A | 2 | a0001c0001t0001g0175a0002c0002t0001g0307 | 2 | HG01255.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.42-3656_42-3642del others(15): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(12): Show |
A | 3 | a0002c0002t0001g0242a0002c0002t0001g0305a0002c0002t0001g0306 | 3 | HG00140.hp1 HG01993.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.42-3656_42-3638del others(19): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(14): Show |
A | 2 | a0001c0001t0001g0086a0002c0002t0001g0241 | 2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.42-3656_42-3636del others(21): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(16): Show |
A | 2 | a0001c0001t0001g0085a0002c0002t0001g0094 | 2 | HG01255.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.42-3656_42-3634del others(23): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(18): Show |
A | 1 | a0002c0002t0001g0304 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.42-3656_42-3632del others(25): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(22): Show |
A | 1 | a0011c0013t0001g0209 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.42-3656_42-3628del others(29): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(24): Show |
A | 1 | a0001c0001t0001g0334 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.42-3656_42-3626del others(31): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397135
|
AAAAATAT others(32): Show |
A | 1 | a0002c0002t0001g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.42-3656_42-3618del others(39): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397135 | |||||
chr14:64397136
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.42-3657A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397136 | ||||||
chr14:64397136
|
AAAATATA others(1): Show |
A | 11 | a0001c0001t0001g0189a0001c0001t0001g0208a0001c0001t0001g0234others(8): Show | 11 | HG00438.hp2 HG01516.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.42-3655_42-3648del others(8): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(3): Show |
A | 9 | a0001c0001t0001g0043a0001c0001t0001g0172a0001c0001t0001g0188others(6): Show | 9 | HG01361.hp2 HG02273.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-3655_42-3646del others(10): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(5): Show |
A | 4 | a0001c0001t0001g0042a0001c0001t0001g0169a0001c0001t0001g0170others(1): Show | 4 | HG02165.hp1 HG02717.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3655_42-3644del others(12): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(7): Show |
A | 2 | a0001c0001t0001g0084a0001c0001t0001g0218 | 2 | HG02683.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.42-3655_42-3642del others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(11): Show |
A | 1 | a0001c0001t0002g0004 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.42-3655_42-3638del others(18): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(13): Show |
A | 6 | a0001c0001t0001g0021a0001c0001t0001g0078a0001c0001t0001g0081others(3): Show | 6 | HG00280.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3655_42-3636del others(20): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(15): Show |
A | 2 | a0002c0002t0001g0079a0002c0002t0001g0080 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.42-3655_42-3634del others(22): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(23): Show |
A | 1 | a0001c0001t0002g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.42-3655_42-3626del others(30): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(25): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42-3655_42-3624del others(32): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397136
|
AAAATATA others(27): Show |
A | 2 | a0002c0002t0001g0192a0002c0002t0001g0193 | 2 | NA18939.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.42-3655_42-3622del others(34): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397136 | |||||
chr14:64397137
|
AAATATAT others(2): Show |
A | 6 | a0001c0001t0001g0168a0001c0001t0001g0336a0001c0001t0001g0337others(3): Show | 6 | HG01175.hp2 HG01346.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3654_42-3646del others(9): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(4): Show |
A | 11 | a0001c0001t0001g0041a0001c0001t0001g0166a0001c0001t0001g0217others(8): Show | 11 | HG00597.hp1 HG00673.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.42-3654_42-3644del others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(8): Show |
A | 1 | a0001c0001t0001g0206 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.42-3654_42-3640del others(15): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(10): Show |
A | 2 | a0001c0001t0001g0076a0003c0003t0001g0165 | 2 | HG01516.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.42-3654_42-3638del others(17): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(12): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.42-3654_42-3636del others(19): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(14): Show |
A | 2 | a0001c0001t0001g0074a0003c0003t0001g0186 | 2 | HG00544.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.42-3654_42-3634del others(21): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(16): Show |
A | 1 | a0003c0003t0001g0191 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.42-3654_42-3632del others(23): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(20): Show |
A | 1 | a0001c0001t0001g0228 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.42-3654_42-3628del others(27): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(22): Show |
A | 2 | a0001c0001t0001g0205a0001c0001t0001g0333 | 2 | HG03710.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.42-3654_42-3626del others(29): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397137
|
AAATATAT others(26): Show |
A | 1 | a0003c0003t0001g0204 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.42-3654_42-3622del others(33): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397137 | |||||
chr14:64397138
|
A | T | 11 | a0001c0001t0001g0044a0001c0001t0001g0125a0001c0001t0001g0133others(8): Show | 11 | HG00558.hp2 HG02257.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.42-3655A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397138 | ||||||
chr14:64397138
|
AATATATA others(3): Show |
A | 5 | a0001c0001t0001g0142a0001c0001t0001g0149a0001c0001t0001g0150others(2): Show | 5 | HG02523.hp2 NA18964.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3611_42-3602del others(10): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397138 | |||||
chr14:64397138
|
AATATATA others(5): Show |
A | 1 | a0003c0003t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.42-3613_42-3602del others(12): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397138 | |||||
chr14:64397138
|
AATATATA others(11): Show |
A | 1 | a0006c0006t0001g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.42-3619_42-3602del others(18): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397138 | |||||
chr14:64397138
|
AATATATA others(13): Show |
A | 1 | a0003c0003t0001g0148 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.42-3621_42-3602del others(20): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397138 | |||||
chr14:64397139
|
AT | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0112others(4): Show | 7 | HG00639.hp2 HG02155.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-3653delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATAT | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0033a0001c0001t0001g0272others(5): Show | 8 | HG01109.hp2 HG01175.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-3653_42-3651del others(3): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATAT | A | 7 | a0001c0001t0001g0055a0001c0001t0001g0320a0001c0001t0001g0327others(4): Show | 7 | HG01928.hp2 HG02055.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-3653_42-3649del others(5): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATATAT | A | 4 | a0001c0001t0001g0230a0001c0001t0001g0253a0001c0011t0001g0097others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-3653_42-3647del others(7): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATATAT others(2): Show |
A | 6 | a0001c0001t0001g0137a0001c0001t0001g0271a0002c0002t0001g0138others(3): Show | 6 | HG01070.hp1 HG02132.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3653_42-3645del others(9): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATATAT others(4): Show |
A | 7 | a0001c0001t0001g0031a0001c0001t0001g0199a0001c0001t0001g0221others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-3653_42-3643del others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATATAT others(6): Show |
A | 4 | a0001c0001t0001g0198a0001c0001t0001g0216a0001c0001t0001g0270others(1): Show | 4 | HG02080.hp1 HG02080.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3653_42-3641del others(13): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATATAT others(8): Show |
A | 3 | a0001c0001t0001g0071a0001c0001t0001g0196a0003c0003t0001g0259 | 3 | HG01099.hp1 HG02258.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.42-3653_42-3639del others(15): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397139
|
ATATATAT others(10): Show |
A | 3 | a0001c0001t0001g0069a0001c0001t0001g0269a0001c0001t0001g0341 | 3 | HG01934.hp2 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-3653_42-3637del others(17): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397139 | ||||||
chr14:64397140
|
T | A | 32 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(29): Show | 32 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.42-3653T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397140 | ||||||
chr14:64397142
|
T | A | 15 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG00621.hp1 HG01167.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.42-3651T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397142 | ||||||
chr14:64397144
|
T | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 13 | HG00621.hp1 HG01167.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-3649T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397144 | ||||||
chr14:64397146
|
T | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(7): Show | 10 | HG00621.hp1 HG01167.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-3647T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397146 | ||||||
chr14:64397148
|
T | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0184a0001c0011t0001g0097others(3): Show | 6 | HG01175.hp1 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3645T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397148 | ||||||
chr14:64397150
|
T | A | 8 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0184others(5): Show | 8 | HG01070.hp1 HG01175.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-3643T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397150 | ||||||
chr14:64397150
|
TATATATA others(34): Show |
T | 4 | a0002c0002t0001g0102a0002c0002t0001g0104a0002c0002t0001g0105others(1): Show | 4 | HG01074.hp2 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3641_42-3601del others(41): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397150 | |||||
chr14:64397152
|
T | A | 3 | a0001c0001t0001g0137a0001c0014t0001g0009a0002c0002t0001g0138 | 3 | HG01070.hp1 HG01175.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.42-3641T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397152 | ||||||
chr14:64397154
|
T | A | 1 | a0002c0002t0001g0024 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.42-3639T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397154 | ||||||
chr14:64397156
|
T | A | 2 | a0001c0001t0001g0196a0002c0002t0001g0024 | 2 | HG02080.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.42-3637T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397156 | ||||||
chr14:64397158
|
T | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0341a0002c0002t0001g0024others(1): Show | 4 | HG02080.hp1 HG03540.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3635T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397158 | ||||||
chr14:64397158
|
TATATATA others(27): Show |
T | 1 | a0001c0001t0001g0261 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.42-3633_42-3600del others(34): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397158 | |||||
chr14:64397164
|
TATATATA others(21): Show |
T | 1 | a0003c0003t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.42-3627_42-3600del others(28): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397164 | |||||
chr14:64397169
|
A | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3624A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397169 | ||||||
chr14:64397172
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.42-3621T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397172 | ||||||
chr14:64397172
|
T | TCCCCTGC others(4): Show |
5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3621_42-3620ins others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397172 | ||||||
chr14:64397172
|
TATATATA others(13): Show |
T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01167.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.42-3619_42-3600del others(20): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397172 | |||||
chr14:64397172
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0002g0066 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.42-3619_42-3598del others(22): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397172 | |||||
chr14:64397174
|
TATATATA others(11): Show |
T | 1 | a0002c0002t0001g0275 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42-3617_42-3600del others(18): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397174 | |||||
chr14:64397176
|
T | G | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3617T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397176 | ||||||
chr14:64397176
|
TATATATA others(9): Show |
T | 4 | a0001c0001t0001g0070a0002c0002t0001g0239a0002c0002t0001g0276others(1): Show | 4 | HG01257.hp2 HG03710.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-3615_42-3600del others(16): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397176 | |||||
chr14:64397178
|
T | G | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.42-3615T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397178 | ||||||
chr14:64397178
|
TA | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3614delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397178 | ||||||
chr14:64397178
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0215 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.42-3613_42-3600del others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397178 | |||||
chr14:64397180
|
TATATATA others(5): Show |
T | 7 | a0001c0001t0001g0014a0001c0001t0001g0197a0002c0002t0001g0129others(4): Show | 7 | HG00597.hp2 HG01192.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-3611_42-3600del others(12): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397180 | |||||
chr14:64397182
|
T | C | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3611T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397182 | ||||||
chr14:64397182
|
TATATATA others(3): Show |
T | 8 | a0001c0001t0001g0183a0001c0001t0001g0195a0001c0001t0001g0326others(5): Show | 8 | HG02129.hp1 HG02486.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-3609_42-3600del others(10): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397182 | |||||
chr14:64397182
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.42-3609_42-3598del others(12): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397182 | |||||
chr14:64397183
|
A | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3610A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397183 | ||||||
chr14:64397184
|
T | G | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3609T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397184 | ||||||
chr14:64397184
|
TATATATA others(1): Show |
T | 6 | a0001c0001t0001g0006a0001c0001t0001g0202a0001c0001t0001g0267others(3): Show | 6 | HG00639.hp1 HG02109.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3607_42-3600del others(8): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397184 | |||||
chr14:64397185
|
A | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3608A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397185 | ||||||
chr14:64397186
|
TATATAA | T | 7 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0203others(4): Show | 7 | HG00544.hp1 HG00621.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-3605_42-3600del others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397186 | |||||
chr14:64397187
|
A | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3606A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397187 | ||||||
chr14:64397188
|
TATAA | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0015a0002c0002t0001g0028others(3): Show | 6 | HG00140.hp2 HG00738.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-3603_42-3600del others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397188 | |||||
chr14:64397189
|
A | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-3604A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397189 | ||||||
chr14:64397189
|
AT | A | 3 | a0001c0001t0001g0250a0001c0011t0001g0097a0004c0004t0001g0098 | 3 | HG01243.hp2 HG03453.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.42-3603delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397189 | ||||||
chr14:64397190
|
TA | T | 12 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(9): Show | 12 | HG00735.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.42-3597delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397190 | |||||
chr14:64397192
|
A | T | 197 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.42-3601A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397192 | ||||||
chr14:64397193
|
A | G | 1 | a0002c0002t0001g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.42-3600A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397193 | ||||||
chr14:64397193
|
A | T | 1 | a0009c0009t0001g0113 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.42-3600A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397193 | ||||||
chr14:64397194
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.42-3599A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397194 | ||||||
chr14:64397247
|
C | CT | 237 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(234): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.42-3534dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397247 | |||||
chr14:64397347
|
C | T | 1 | a0002c0002t0001g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.42-3446C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397347 | ||||||
chr14:64397369
|
T | C | 278 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.42-3424T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397369 | ||||||
chr14:64397378
|
T | C | 277 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.42-3415T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397378 | ||||||
chr14:64397455
|
G | A | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.42-3338G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397455 | ||||||
chr14:64397738
|
G | T | 281 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.42-3055G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397738 | ||||||
chr14:64397809
|
ATATTT | A | 6 | a0001c0001t0001g0216a0001c0001t0001g0223a0001c0001t0001g0225others(3): Show | 6 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-2973_42-2969del others(5): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64397809 | |||||
chr14:64397994
|
A | G | 26 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(23): Show | 26 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.42-2799A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64397994 | ||||||
chr14:64398034
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.42-2759C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398034 | ||||||
chr14:64398163
|
TA | T | 252 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.42-2619delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64398163 | |||||
chr14:64398264
|
A | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.42-2529A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398264 | ||||||
chr14:64398313
|
A | G | 2 | a0002c0002t0001g0339a0003c0003t0001g0259 | 2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.42-2480A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398313 | ||||||
chr14:64398455
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.42-2338G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398455 | ||||||
chr14:64398461
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0214 | 2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.42-2332G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398461 | ||||||
chr14:64398493
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.42-2300G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398493 | ||||||
chr14:64398538
|
C | G | 1 | a0001c0001t0001g0064 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42-2255C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398538 | ||||||
chr14:64398836
|
C | T | 1 | a0002c0002t0001g0193 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.42-1957C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64398836 | ||||||
chr14:64399014
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01975.hp2 NA18956.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-1779T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399014 | ||||||
chr14:64399015
|
T | C | 6 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(3): Show | 6 | HG01975.hp2 NA18956.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-1778T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399015 | ||||||
chr14:64399015
|
T | G | 5 | a0001c0001t0001g0137a0001c0001t0001g0142a0001c0001t0001g0189others(2): Show | 5 | HG01070.hp1 NA18945.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-1778T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399015 | ||||||
chr14:64399490
|
C | G | 1 | a0002c0002t0001g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.42-1303C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399490 | ||||||
chr14:64399530
|
G | A | 2 | a0001c0001t0001g0006a0001c0001t0002g0007 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.42-1263G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399530 | ||||||
chr14:64399589
|
G | T | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.42-1204G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399589 | ||||||
chr14:64399612
|
T | C | 2 | a0002c0002t0001g0339a0003c0003t0001g0259 | 2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.42-1181T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399612 | ||||||
chr14:64399656
|
CA | C | 67 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075others(64): Show | 68 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.42-1117delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64399656 | |||||
chr14:64399656
|
CAA | C | 210 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.42-1118_42-1117del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr14 | 64399656 | |||||
chr14:64399668
|
A | G | 1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.42-1125A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399668 | ||||||
chr14:64399672
|
A | G | 83 | a0001c0001t0001g0255a0001c0001t0001g0261a0001c0001t0001g0267others(80): Show | 83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.42-1121A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399672 | ||||||
chr14:64399721
|
T | C | 26 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(23): Show | 26 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.42-1072T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399721 | ||||||
chr14:64399815
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0075 | 3 | HG01243.hp1 HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.42-978G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399815 | ||||||
chr14:64399816
|
T | C | 2 | a0003c0003t0002g0190a0007c0007t0001g0219 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.42-977T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399816 | ||||||
chr14:64399891
|
G | A | 1 | a0002c0002t0001g0056 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.42-902G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64399891 | ||||||
chr14:64400259
|
A | G | 2 | a0003c0003t0002g0190a0007c0007t0001g0219 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.42-534A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64400259 | ||||||
chr14:64400427
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.42-366C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64400427 | ||||||
chr14:64400450
|
G | A | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.42-343G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64400450 | ||||||
chr14:64400537
|
T | C | 5 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0014t0001g0009others(2): Show | 5 | HG01175.hp1 HG02622.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-256T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64400537 | ||||||
chr14:64400661
|
C | T | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-132C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 1/27 | chr14 | 64400661 | ||||||
chr14:64401016
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.126+139C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401016 | ||||||
chr14:64401063
|
T | C | 1 | a0001c0001t0001g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.126+186T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401063 | ||||||
chr14:64401301
|
T | C | 114 | a0001c0001t0001g0076a0001c0001t0001g0195a0001c0001t0001g0196others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.126+424T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401301 | ||||||
chr14:64401444
|
C | T | 2 | a0002c0002t0001g0294a0002c0002t0001g0295 | 2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.126+567C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401444 | ||||||
chr14:64401576
|
G | C | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+699G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401576 | ||||||
chr14:64401700
|
C | CA | 262 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.126+837dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64401700 | |||||
chr14:64401713
|
A | G | 1 | a0001c0001t0001g0330 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.126+836A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401713 | ||||||
chr14:64401827
|
G | A | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126+950G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401827 | ||||||
chr14:64401953
|
T | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(64): Show | 67 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.126+1076T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401953 | ||||||
chr14:64401997
|
A | G | 1 | a0002c0002t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.126+1120A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64401997 | ||||||
chr14:64402336
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.126+1459C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402336 | ||||||
chr14:64402424
|
C | T | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.126+1547C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402424 | ||||||
chr14:64402436
|
G | A | 277 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.126+1559G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402436 | ||||||
chr14:64402790
|
C | CAG | 277 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(274): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.126+1914_126+1915d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64402790 | |||||
chr14:64402806
|
C | CA | 273 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.126+1938dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64402806 | |||||
chr14:64402816
|
T | A | 1 | a0002c0002t0001g0060 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.126+1939T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402816 | ||||||
chr14:64402878
|
T | C | 3 | a0002c0002t0001g0117a0006c0006t0001g0116a0006c0006t0001g0229 | 3 | HG01192.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.126+2001T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402878 | ||||||
chr14:64402899
|
G | A | 1 | a0004c0004t0001g0106 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.126+2022G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402899 | ||||||
chr14:64402938
|
G | T | 1 | a0002c0002t0001g0266 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.126+2061G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402938 | ||||||
chr14:64402972
|
A | T | 3 | a0001c0001t0001g0076a0003c0003t0002g0190a0007c0007t0001g0219 | 3 | HG01516.hp2 HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.126+2095A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64402972 | ||||||
chr14:64403280
|
A | AT | 275 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.126+2415dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64403280 | |||||
chr14:64403487
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.126+2610C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64403487 | ||||||
chr14:64403559
|
C | T | 27 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0001t0001g0108others(24): Show | 27 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+2682C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64403559 | ||||||
chr14:64403593
|
G | GT | 203 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0064others(200): Show | 204 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.126+2725dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64403593 | |||||
chr14:64403734
|
C | T | 13 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0035others(10): Show | 13 | HG00597.hp1 HG00621.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.126+2857C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64403734 | ||||||
chr14:64403742
|
T | C | 6 | a0001c0001t0001g0341a0003c0003t0002g0190a0004c0004t0001g0256others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+2865T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64403742 | ||||||
chr14:64403941
|
T | A | 1 | a0002c0002t0001g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.126+3064T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64403941 | ||||||
chr14:64404292
|
C | T | 82 | a0001c0001t0001g0255a0001c0001t0001g0261a0001c0001t0001g0267others(79): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.126+3415C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64404292 | ||||||
chr14:64404492
|
C | T | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.126+3615C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64404492 | ||||||
chr14:64404507
|
A | G | 1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.126+3630A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64404507 | ||||||
chr14:64404510
|
A | C | 1 | a0002c0002t0001g0145 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.126+3633A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64404510 | ||||||
chr14:64404581
|
C | T | 2 | a0003c0003t0001g0173a0003c0003t0001g0174 | 2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.126+3704C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64404581 | ||||||
chr14:64404837
|
G | A | 5 | a0001c0001t0001g0223a0001c0001t0001g0225a0001c0001t0001g0226others(2): Show | 5 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+3960G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64404837 | ||||||
chr14:64405353
|
T | C | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.126+4476T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64405353 | ||||||
chr14:64405373
|
A | G | 28 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0001t0001g0108others(25): Show | 28 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.126+4496A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64405373 | ||||||
chr14:64405512
|
G | C | 281 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(278): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.126+4635G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64405512 | ||||||
chr14:64405566
|
T | C | 1 | a0002c0002t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.126+4689T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64405566 | ||||||
chr14:64405962
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.126+5085T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64405962 | ||||||
chr14:64405991
|
T | TTA | 3 | a0002c0002t0001g0117a0006c0006t0001g0116a0006c0006t0001g0229 | 3 | HG01192.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-5091_127-5090d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64405991 | |||||
chr14:64406001
|
G | A | 280 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(277): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.127-5089G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406001 | ||||||
chr14:64406011
|
G | A | 3 | a0002c0002t0001g0117a0006c0006t0001g0116a0006c0006t0001g0229 | 3 | HG01192.hp2 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.127-5079G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406011 | ||||||
chr14:64406031
|
A | T | 1 | a0003c0003t0001g0182 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.127-5059A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406031 | ||||||
chr14:64406034
|
T | A | 21 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 22 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-5056T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406034 | ||||||
chr14:64406037
|
T | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0253others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-5053T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406037 | ||||||
chr14:64406044
|
A | AT | 29 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0065others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-5044dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64406044 | |||||
chr14:64406044
|
A | T | 2 | a0002c0002t0001g0254a0003c0003t0001g0204 | 2 | HG00733.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.127-5046A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406044 | ||||||
chr14:64406047
|
A | AT | 5 | a0001c0001t0001g0074a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG00099.hp1 HG00741.hp1 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-5035dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64406047 | |||||
chr14:64406047
|
A | T | 269 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(266): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.127-5043A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406047 | ||||||
chr14:64406108
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.127-4982G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406108 | ||||||
chr14:64406186
|
G | C | 1 | a0005c0005t0001g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-4904G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406186 | ||||||
chr14:64406231
|
A | G | 23 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0001g0237others(20): Show | 24 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.127-4859A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406231 | ||||||
chr14:64406490
|
G | GT | 55 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0112others(52): Show | 56 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.127-4580dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64406490 | |||||
chr14:64406490
|
G | GTT | 7 | a0001c0001t0001g0221a0001c0001t0001g0341a0002c0002t0001g0117others(4): Show | 7 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-4581_127-4580d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64406490 | |||||
chr14:64406490
|
G | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0081 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-4600G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406490 | ||||||
chr14:64406490
|
GT | G | 7 | a0001c0001t0001g0047a0001c0001t0001g0076a0001c0001t0001g0199others(4): Show | 7 | HG01516.hp2 HG02723.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-4580delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64406490 | |||||
chr14:64406499
|
T | G | 2 | a0001c0001t0001g0006a0001c0001t0002g0007 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.127-4591T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406499 | ||||||
chr14:64406532
|
G | T | 1 | a0001c0001t0001g0206 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.127-4558G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406532 | ||||||
chr14:64406634
|
A | G | 2 | a0002c0002t0001g0268a0002c0002t0001g0274 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.127-4456A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406634 | ||||||
chr14:64406676
|
T | A | 1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.127-4414T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406676 | ||||||
chr14:64406709
|
T | C | 53 | a0001c0001t0001g0008a0001c0001t0001g0107a0001c0001t0001g0108others(50): Show | 54 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.127-4381T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406709 | ||||||
chr14:64406881
|
A | C | 34 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0065others(31): Show | 34 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-4209A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406881 | ||||||
chr14:64406924
|
G | T | 19 | a0001c0001t0001g0221a0001c0001t0001g0236a0001c0001t0001g0237others(16): Show | 20 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-4166G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64406924 | ||||||
chr14:64407018
|
C | T | 4 | a0001c0001t0001g0341a0004c0004t0001g0256a0004c0004t0001g0257others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-4072C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407018 | ||||||
chr14:64407092
|
T | C | 26 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0221others(23): Show | 27 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-3998T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407092 | ||||||
chr14:64407278
|
A | C | 276 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(273): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.127-3812A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407278 | ||||||
chr14:64407328
|
G | A | 1 | a0002c0002t0001g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.127-3762G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407328 | ||||||
chr14:64407464
|
C | CA | 34 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(31): Show | 34 | HG00735.hp2 HG01074.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.127-3612dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64407464 | |||||
chr14:64407478
|
AG | A | 3 | a0005c0005t0001g0022a0005c0005t0001g0023a0005c0005t0001g0029 | 3 | HG02258.hp2 HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.127-3611delG | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407478 | ||||||
chr14:64407537
|
ACT | A | 23 | a0001c0001t0001g0076a0001c0001t0001g0221a0001c0001t0001g0236others(20): Show | 24 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.127-3544_127-3543d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64407537 | |||||
chr14:64407544
|
C | CT | 4 | a0001c0001t0001g0230a0001c0001t0001g0233a0003c0003t0001g0005others(1): Show | 4 | HG02647.hp2 HG03098.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-3545dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64407544 | |||||
chr14:64407545
|
TC | T | 189 | a0001c0001t0001g0021a0001c0001t0001g0064a0001c0001t0001g0065others(186): Show | 189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.127-3544delC | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407545 | ||||||
chr14:64407546
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(68): Show | 71 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.127-3544C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407546 | ||||||
chr14:64407611
|
C | A | 2 | a0003c0003t0002g0190a0007c0007t0001g0219 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.127-3479C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407611 | ||||||
chr14:64407720
|
G | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0253others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-3370G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407720 | ||||||
chr14:64407744
|
C | T | 1 | a0002c0002t0001g0038 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.127-3346C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64407744 | ||||||
chr14:64408006
|
GTAGACCA others(14): Show |
G | 66 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.127-3082_127-3062d others(23): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64408006 | |||||
chr14:64408198
|
A | G | 2 | a0003c0003t0002g0190a0007c0007t0001g0219 | 2 | HG02451.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.127-2892A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408198 | ||||||
chr14:64408240
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.127-2850T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408240 | ||||||
chr14:64408284
|
T | TC | 34 | a0001c0001t0001g0040a0001c0001t0001g0118a0001c0001t0001g0119others(31): Show | 35 | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-2805dupC | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64408284 | |||||
chr14:64408285
|
C | CCT | 107 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(104): Show | 107 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.127-2805_127-2804i others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408285 | ||||||
chr14:64408285
|
C | CCTT | 4 | a0001c0001t0001g0282a0001c0001t0001g0320a0002c0002t0001g0322others(1): Show | 4 | HG02698.hp2 NA18990.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2805_127-2804i others(5): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408285 | ||||||
chr14:64408285
|
C | CT | 7 | a0001c0001t0001g0149a0001c0001t0001g0223a0001c0001t0001g0225others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-2785dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64408285 | |||||
chr14:64408285
|
CT | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0137a0001c0001t0001g0341others(4): Show | 7 | HG00323.hp2 HG01070.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-2785delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64408285 | |||||
chr14:64408286
|
T | C | 122 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.127-2804T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408286 | ||||||
chr14:64408287
|
T | C | 5 | a0001c0001t0001g0030a0002c0002t0001g0027a0002c0002t0001g0045others(2): Show | 5 | HG00323.hp2 HG01099.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-2803T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408287 | ||||||
chr14:64408371
|
T | C | 4 | a0001c0001t0001g0341a0004c0004t0001g0256a0004c0004t0001g0257others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2719T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408371 | ||||||
chr14:64408461
|
G | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-2629G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408461 | ||||||
chr14:64408536
|
G | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0253others(1): Show | 4 | HG01884.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2554G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408536 | ||||||
chr14:64408589
|
A | G | 2 | a0003c0003t0001g0025a0003c0003t0001g0057 | 2 | HG00408.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.127-2501A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408589 | ||||||
chr14:64408654
|
C | T | 2 | a0002c0002t0001g0339a0003c0003t0001g0259 | 2 | HG01099.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.127-2436C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408654 | ||||||
chr14:64408669
|
T | C | 66 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(63): Show | 66 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.127-2421T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408669 | ||||||
chr14:64408818
|
G | A | 1 | a0002c0002t0001g0088 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.127-2272G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408818 | ||||||
chr14:64408928
|
G | A | 4 | a0001c0001t0001g0341a0004c0004t0001g0256a0004c0004t0001g0257others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2162G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64408928 | ||||||
chr14:64409125
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.127-1965C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409125 | ||||||
chr14:64409161
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.127-1929G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409161 | ||||||
chr14:64409340
|
T | TA | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.127-1749dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64409340 | |||||
chr14:64409354
|
T | C | 4 | a0001c0001t0001g0341a0004c0004t0001g0256a0004c0004t0001g0257others(1): Show | 4 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-1736T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409354 | ||||||
chr14:64409617
|
GACCAAAG others(5): Show |
G | 112 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.127-1470_127-1459d others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64409617 | |||||
chr14:64409665
|
C | T | 1 | a0002c0002t0001g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-1425C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409665 | ||||||
chr14:64409724
|
C | T | 4 | a0005c0005t0001g0022a0005c0005t0001g0023a0005c0005t0001g0029others(1): Show | 4 | HG02258.hp2 HG02559.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1366C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409724 | ||||||
chr14:64409827
|
G | T | 105 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(102): Show | 105 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.127-1263G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409827 | ||||||
chr14:64409996
|
C | T | 65 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(62): Show | 65 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.127-1094C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64409996 | ||||||
chr14:64410180
|
A | C | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.127-910A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410180 | ||||||
chr14:64410185
|
T | C | 1 | a0002c0002t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.127-905T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410185 | ||||||
chr14:64410407
|
TG | T | 110 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0012others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.127-672delG | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64410407 | |||||
chr14:64410407
|
TGG | T | 141 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0127others(138): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.127-673_127-672del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr14 | 64410407 | |||||
chr14:64410409
|
G | A | 3 | a0004c0004t0001g0256a0004c0004t0001g0257a0004c0004t0001g0258 | 3 | HG01891.hp1 HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.127-681G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410409 | ||||||
chr14:64410410
|
G | C | 1 | a0003c0003t0001g0180 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.127-680G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410410 | ||||||
chr14:64410412
|
G | C | 1 | a0003c0003t0001g0050 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.127-678G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410412 | ||||||
chr14:64410417
|
G | T | 111 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0195others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.127-673G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410417 | ||||||
chr14:64410522
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0214 | 2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.127-568G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410522 | ||||||
chr14:64410661
|
C | T | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-429C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410661 | ||||||
chr14:64410666
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-424G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410666 | ||||||
chr14:64410709
|
T | G | 1 | a0005c0005t0001g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-381T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 2/27 | chr14 | 64410709 | ||||||
chr14:64411151
|
T | TA | 6 | a0002c0002t0001g0155a0003c0003t0001g0143a0003c0003t0001g0148others(3): Show | 6 | NA18941.hp1 NA18970.hp1 NA18974.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.186+4dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr14 | 64411151 | |||||
chr14:64411484
|
T | A | 1 | a0001c0001t0001g0324 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.186+335T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411484 | ||||||
chr14:64411547
|
G | A | 113 | a0001c0001t0001g0030a0001c0001t0001g0073a0001c0001t0001g0111others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.186+398G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411547 | ||||||
chr14:64411572
|
C | T | 72 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(69): Show | 72 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.186+423C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411572 | ||||||
chr14:64411575
|
C | T | 1 | a0002c0002t0001g0265 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.186+426C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411575 | ||||||
chr14:64411608
|
G | A | 1 | a0002c0002t0001g0200 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.186+459G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411608 | ||||||
chr14:64411611
|
G | T | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(2): Show | 5 | HG02280.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+462G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411611 | ||||||
chr14:64411625
|
C | T | 1 | a0002c0002t0001g0027 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.186+476C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411625 | ||||||
chr14:64411689
|
C | T | 2 | a0001c0001t0001g0255a0001c0001t0001g0318 | 2 | HG00280.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.186+540C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411689 | ||||||
chr14:64411757
|
T | C | 290 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(287): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.186+608T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411757 | ||||||
chr14:64411769
|
C | T | 10 | a0002c0002t0001g0155a0003c0003t0001g0143a0003c0003t0001g0146others(7): Show | 10 | HG02155.hp2 NA18941.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.186+620C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411769 | ||||||
chr14:64411793
|
C | G | 3 | a0003c0003t0002g0100a0003c0003t0002g0190a0007c0007t0001g0219 | 3 | HG02451.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.186+644C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411793 | ||||||
chr14:64411825
|
T | A | 1 | a0001c0001t0001g0327 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.187-647T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411825 | ||||||
chr14:64411916
|
G | A | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0121others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-556G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411916 | ||||||
chr14:64411934
|
A | G | 1 | a0002c0002t0001g0323 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.187-538A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64411934 | ||||||
chr14:64412043
|
T | C | 208 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(205): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.187-429T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64412043 | ||||||
chr14:64412086
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG01192.hp1 HG01978.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-386G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64412086 | ||||||
chr14:64412294
|
GT | G | 13 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0065others(10): Show | 13 | HG00423.hp2 HG00621.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.187-177delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64412294 | ||||||
chr14:64412329
|
G | A | 1 | a0002c0002t0001g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.187-143G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64412329 | ||||||
chr14:64412411
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.187-61G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 3/27 | chr14 | 64412411 | ||||||
chr14:64412596
|
G | C | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.240+71G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412596 | ||||||
chr14:64412634
|
A | AT | 201 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(198): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.240+129dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64412634 | |||||
chr14:64412634
|
A | ATT | 77 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0032others(74): Show | 77 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.240+128_240+129dup others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64412634 | |||||
chr14:64412712
|
T | C | 281 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(278): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.240+187T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412712 | ||||||
chr14:64412724
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0280 | 2 | NA18972.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.240+199G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412724 | ||||||
chr14:64412782
|
C | T | 3 | a0003c0003t0001g0285a0003c0003t0001g0297a0003c0003t0001g0303 | 3 | HG00408.hp1 NA18979.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.240+257C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412782 | ||||||
chr14:64412840
|
G | A | 1 | a0003c0003t0001g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.240+315G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412840 | ||||||
chr14:64412917
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.240+392C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412917 | ||||||
chr14:64412939
|
C | T | 7 | a0001c0001t0002g0007a0004c0004t0001g0106a0004c0004t0001g0109others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.240+414C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64412939 | ||||||
chr14:64413216
|
G | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0077 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.240+691G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413216 | ||||||
chr14:64413276
|
C | T | 8 | a0001c0001t0001g0341a0001c0001t0002g0007a0004c0004t0001g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+751C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413276 | ||||||
chr14:64413306
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.240+781C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413306 | ||||||
chr14:64413430
|
G | T | 8 | a0001c0001t0001g0341a0001c0001t0002g0007a0004c0004t0001g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.240+905G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413430 | ||||||
chr14:64413639
|
T | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0084 | 2 | HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.240+1114T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413639 | ||||||
chr14:64413900
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0002g0120 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.240+1375G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413900 | ||||||
chr14:64413946
|
T | C | 279 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(276): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.241-1412T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64413946 | ||||||
chr14:64414018
|
G | C | 1 | a0003c0003t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.241-1340G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414018 | ||||||
chr14:64414061
|
A | G | 1 | a0003c0003t0001g0158 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.241-1297A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414061 | ||||||
chr14:64414068
|
C | T | 279 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(276): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.241-1290C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414068 | ||||||
chr14:64414176
|
A | G | 279 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(276): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.241-1182A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414176 | ||||||
chr14:64414286
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.241-1063_241-1048d others(18): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414286 | |||||
chr14:64414286
|
CT | C | 27 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0050others(24): Show | 27 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(24): Show |
intron_variant | MODIFIER | c.241-1048delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414286 | |||||
chr14:64414286
|
CTT | C | 8 | a0003c0003t0001g0173a0003c0003t0001g0178a0003c0003t0001g0285others(5): Show | 8 | HG00408.hp1 HG01361.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.241-1049_241-1048d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414286 | |||||
chr14:64414286
|
CTTTT | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0149a0001c0001t0001g0203others(11): Show | 14 | HG01109.hp2 HG02080.hp1 HG03130.hp1 others(11): Show |
intron_variant | MODIFIER | c.241-1051_241-1048d others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414286 | |||||
chr14:64414286
|
CTTTTT | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(261): Show | 265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.241-1052_241-1048d others(7): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414286 | |||||
chr14:64414315
|
CAG | C | 10 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0050others(7): Show | 10 | HG00099.hp2 HG01099.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.241-1040_241-1039d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414315 | |||||
chr14:64414377
|
C | T | 279 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(276): Show | 280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.241-981C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414377 | ||||||
chr14:64414401
|
C | T | 2 | a0001c0001t0002g0224a0006c0006t0001g0126 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.241-957C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414401 | ||||||
chr14:64414618
|
G | A | 3 | a0002c0002t0001g0307a0002c0002t0001g0322a0002c0002t0001g0339 | 3 | HG01255.hp1 HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.241-740G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414618 | ||||||
chr14:64414644
|
C | T | 4 | a0002c0002t0001g0020a0004c0004t0001g0095a0004c0004t0001g0096others(1): Show | 4 | HG01243.hp2 HG02922.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-714C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414644 | ||||||
chr14:64414656
|
A | AT | 13 | a0001c0001t0001g0085a0001c0001t0001g0114a0001c0001t0001g0235others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.241-684dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414656 | |||||
chr14:64414689
|
C | T | 2 | a0003c0003t0001g0181a0003c0003t0001g0292 | 2 | NA18951.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.241-669C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414689 | ||||||
chr14:64414692
|
T | C | 4 | a0003c0003t0002g0100a0003c0003t0002g0124a0003c0003t0002g0190others(1): Show | 4 | HG02451.hp2 HG02647.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-666T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414692 | ||||||
chr14:64414734
|
T | C | 283 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(280): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.241-624T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414734 | ||||||
chr14:64414763
|
G | C | 280 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(277): Show | 281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.241-595G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414763 | ||||||
chr14:64414932
|
A | G | 1 | a0001c0001t0001g0282 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.241-426A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414932 | ||||||
chr14:64414963
|
ACAGTCGT others(4): Show |
A | 4 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0130others(1): Show | 4 | HG01496.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-392_241-382del others(11): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr14 | 64414963 | |||||
chr14:64414970
|
T | C | 4 | a0003c0003t0001g0264a0003c0003t0001g0285a0003c0003t0001g0297others(1): Show | 4 | HG00408.hp1 HG00597.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-388T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64414970 | ||||||
chr14:64415049
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.241-309G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 4/27 | chr14 | 64415049 | ||||||
chr14:64415807
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.478+68A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64415807 | ||||||
chr14:64415971
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.478+232C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64415971 | ||||||
chr14:64416012
|
G | A | 3 | a0001c0001t0001g0142a0002c0002t0001g0138a0002c0002t0001g0141 | 3 | NA18945.hp1 NA18977.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.478+273G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416012 | ||||||
chr14:64416111
|
G | T | 2 | a0001c0001t0001g0302a0001c0001t0001g0328 | 2 | NA18977.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.478+372G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416111 | ||||||
chr14:64416152
|
G | A | 8 | a0001c0001t0001g0341a0001c0001t0002g0007a0004c0004t0001g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.478+413G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416152 | ||||||
chr14:64416209
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478+470C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416209 | ||||||
chr14:64416236
|
C | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0118a0001c0001t0001g0119others(3): Show | 6 | HG02717.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+497C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416236 | ||||||
chr14:64416246
|
A | AAAAC | 17 | a0001c0001t0001g0044a0001c0001t0001g0072a0001c0001t0001g0074others(14): Show | 17 | HG00280.hp1 HG00733.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.478+510_478+511ins others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr14 | 64416246 | |||||
chr14:64416246
|
AAAAT | A | 4 | a0001c0001t0001g0085a0001c0001t0001g0107a0002c0002t0001g0210others(1): Show | 4 | HG02572.hp1 HG03834.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.478+511_478+514del others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr14 | 64416246 | |||||
chr14:64416250
|
T | C | 275 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(272): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.478+511T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416250 | ||||||
chr14:64416304
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.478+565G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416304 | ||||||
chr14:64416373
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.478+634A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64416373 | ||||||
chr14:64416974
|
G | GA | 18 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0041others(15): Show | 18 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.479-906dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | INFO_REALIGN_3_PRIME | chr14 | 64416974 | |||||
chr14:64417121
|
G | A | 4 | a0003c0003t0001g0264a0003c0003t0001g0285a0003c0003t0001g0297others(1): Show | 4 | HG00408.hp1 HG00597.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-767G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417121 | ||||||
chr14:64417259
|
G | A | 2 | a0001c0001t0001g0313a0002c0002t0001g0309 | 2 | NA18954.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.479-629G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417259 | ||||||
chr14:64417358
|
C | T | 51 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(48): Show | 51 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.479-530C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417358 | ||||||
chr14:64417388
|
T | C | 8 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(5): Show | 8 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.479-500T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417388 | ||||||
chr14:64417583
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02976.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.479-305G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417583 | ||||||
chr14:64417633
|
C | G | 9 | a0003c0003t0001g0017a0003c0003t0001g0018a0003c0003t0001g0050others(6): Show | 9 | HG00099.hp2 HG01099.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.479-255C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417633 | ||||||
chr14:64417718
|
T | C | 1 | a0008c0008t0001g0338 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.479-170T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417718 | ||||||
chr14:64417866
|
T | C | 1 | a0002c0002t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.479-22T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 6/27 | chr14 | 64417866 | ||||||
chr14:64418101
|
C | T | 1 | a0004c0004t0001g0062 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.615+77C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64418101 | ||||||
chr14:64418158
|
A | G | 4 | a0002c0002t0001g0102a0002c0002t0001g0104a0002c0002t0001g0105others(1): Show | 4 | HG01074.hp2 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+134A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64418158 | ||||||
chr14:64418352
|
G | A | 1 | a0003c0003t0001g0061 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.615+328G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64418352 | ||||||
chr14:64418401
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.615+377C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64418401 | ||||||
chr14:64418450
|
C | CA | 16 | a0001c0001t0001g0128a0001c0001t0001g0341a0001c0001t0002g0007others(13): Show | 16 | HG01109.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.615+441dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr14 | 64418450 | |||||
chr14:64418450
|
C | CAA | 64 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0030others(61): Show | 64 | HG00280.hp1 HG00423.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.615+440_615+441dup others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr14 | 64418450 | |||||
chr14:64418450
|
C | CAAA | 189 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.615+439_615+441dup others(3): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr14 | 64418450 | |||||
chr14:64418450
|
C | CAAAA | 10 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0228others(7): Show | 10 | HG02080.hp2 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.615+438_615+441dup others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr14 | 64418450 | |||||
chr14:64418480
|
A | G | 8 | a0001c0001t0001g0341a0001c0001t0002g0007a0004c0004t0001g0106others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.615+456A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64418480 | ||||||
chr14:64418831
|
C | T | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.615+807C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64418831 | ||||||
chr14:64419054
|
C | T | 261 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(258): Show | 261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.616-760C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64419054 | ||||||
chr14:64419372
|
GCA | G | 260 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(257): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.616-430_616-429del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr14 | 64419372 | |||||
chr14:64419672
|
G | A | 1 | a0003c0003t0001g0061 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.616-142G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64419672 | ||||||
chr14:64419703
|
T | C | 21 | a0001c0001t0001g0042a0001c0001t0001g0112a0001c0001t0001g0175others(18): Show | 21 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.616-111T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64419703 | ||||||
chr14:64419708
|
C | G | 281 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.616-106C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64419708 | ||||||
chr14:64419747
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02976.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.616-67T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 7/27 | chr14 | 64419747 | ||||||
chr14:64420405
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.727+480C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64420405 | ||||||
chr14:64420483
|
C | T | 7 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0267others(4): Show | 7 | HG00408.hp1 HG00597.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.727+558C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64420483 | ||||||
chr14:64420798
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.727+873G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64420798 | ||||||
chr14:64420992
|
C | T | 1 | a0006c0006t0001g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.727+1067C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64420992 | ||||||
chr14:64420993
|
G | A | 19 | a0001c0001t0001g0021a0001c0001t0001g0044a0001c0001t0001g0074others(16): Show | 19 | HG00280.hp1 HG00733.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.727+1068G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64420993 | ||||||
chr14:64421078
|
C | T | 3 | a0006c0006t0001g0002a0006c0006t0001g0116a0006c0006t0001g0229 | 3 | HG02922.hp1 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.727+1153C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421078 | ||||||
chr14:64421090
|
C | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | NA18953.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.727+1165C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421090 | ||||||
chr14:64421139
|
C | A | 1 | a0001c0014t0001g0009 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.727+1214C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421139 | ||||||
chr14:64421282
|
C | T | 18 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(15): Show | 18 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.727+1357C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421282 | ||||||
chr14:64421337
|
C | T | 287 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(284): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.727+1412C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421337 | ||||||
chr14:64421363
|
T | C | 1 | a0006c0006t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.727+1438T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421363 | ||||||
chr14:64421486
|
A | G | 24 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0065others(21): Show | 24 | HG00741.hp1 HG02129.hp1 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.727+1561A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421486 | ||||||
chr14:64421624
|
AT | A | 157 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(154): Show | 157 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.727+1713delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr14 | 64421624 | |||||
chr14:64421646
|
C | T | 33 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0033others(30): Show | 33 | HG00280.hp2 HG00621.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.727+1721C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421646 | ||||||
chr14:64421693
|
G | A | 3 | a0002c0002t0001g0307a0002c0002t0001g0322a0002c0002t0001g0339 | 3 | HG01255.hp1 HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.727+1768G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421693 | ||||||
chr14:64421697
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.727+1772C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421697 | ||||||
chr14:64421724
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.727+1799T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421724 | ||||||
chr14:64421777
|
C | T | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.727+1852C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421777 | ||||||
chr14:64421815
|
C | T | 339 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(336): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.727+1890C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421815 | ||||||
chr14:64421816
|
G | T | 1 | a0001c0001t0001g0326 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.727+1891G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421816 | ||||||
chr14:64421827
|
A | G | 20 | a0001c0001t0001g0016a0001c0001t0001g0031a0001c0001t0001g0055others(17): Show | 20 | HG01109.hp1 HG01175.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.727+1902A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421827 | ||||||
chr14:64421855
|
G | A | 1 | a0002c0002t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727+1930G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421855 | ||||||
chr14:64421875
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.727+1950T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421875 | ||||||
chr14:64421917
|
A | G | 2 | a0004c0004t0001g0049a0004c0004t0001g0062 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.727+1992A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421917 | ||||||
chr14:64421921
|
A | G | 12 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0160others(9): Show | 12 | NA18944.hp1 NA18963.hp1 NA18964.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+1996A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421921 | ||||||
chr14:64421958
|
A | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0093 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.727+2033A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64421958 | ||||||
chr14:64421978
|
A | AT | 12 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(9): Show | 12 | HG02451.hp2 HG02717.hp2 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.727+2063dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr14 | 64421978 | |||||
chr14:64422041
|
T | C | 1 | a0001c0001t0001g0282 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.727+2116T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64422041 | ||||||
chr14:64422086
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0130 | 3 | HG01496.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.727+2161C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64422086 | ||||||
chr14:64422318
|
A | C | 12 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0004others(9): Show | 12 | HG01496.hp1 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.727+2393A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64422318 | ||||||
chr14:64422507
|
C | T | 2 | a0003c0003t0001g0187a0003c0010t0001g0176 | 2 | HG00673.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.728-2297C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64422507 | ||||||
chr14:64422682
|
A | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0004others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-2122A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64422682 | ||||||
chr14:64422991
|
C | T | 1 | a0002c0002t0001g0305 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.728-1813C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64422991 | ||||||
chr14:64423022
|
G | C | 13 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0004others(10): Show | 13 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.728-1782G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423022 | ||||||
chr14:64423060
|
C | T | 1 | a0002c0002t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.728-1744C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423060 | ||||||
chr14:64423069
|
C | G | 2 | a0003c0003t0002g0100a0003c0003t0002g0124 | 2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.728-1735C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423069 | ||||||
chr14:64423091
|
A | G | 14 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0223others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.728-1713A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423091 | ||||||
chr14:64423116
|
A | T | 1 | a0002c0002t0001g0323 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.728-1688A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423116 | ||||||
chr14:64423123
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0214a0001c0001t0001g0223others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.728-1681T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423123 | ||||||
chr14:64423209
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.728-1595C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423209 | ||||||
chr14:64423326
|
T | C | 1 | a0002c0002t0001g0082 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.728-1478T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423326 | ||||||
chr14:64423451
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.728-1353G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423451 | ||||||
chr14:64423495
|
A | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.728-1309A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423495 | ||||||
chr14:64423509
|
C | T | 139 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.728-1295C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423509 | ||||||
chr14:64423522
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0043 | 3 | NA18956.hp2 NA18979.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.728-1282C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423522 | ||||||
chr14:64423678
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.728-1126G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423678 | ||||||
chr14:64423734
|
C | CT | 8 | a0001c0001t0001g0087a0002c0002t0001g0088a0002c0002t0001g0262others(5): Show | 8 | HG00140.hp1 HG01361.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.728-1062dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr14 | 64423734 | |||||
chr14:64423743
|
C | T | 340 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.728-1061C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423743 | ||||||
chr14:64423758
|
G | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-1046G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423758 | ||||||
chr14:64423927
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(49): Show | 52 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.728-877C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64423927 | ||||||
chr14:64424134
|
C | T | 2 | a0002c0002t0001g0200a0002c0002t0001g0340 | 2 | NA18971.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.728-670C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64424134 | ||||||
chr14:64424160
|
C | A | 1 | a0003c0003t0002g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.728-644C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64424160 | ||||||
chr14:64424636
|
T | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0069others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.728-168T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64424636 | ||||||
chr14:64424685
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.728-119G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 8/27 | chr14 | 64424685 | ||||||
chr14:64425035
|
A | G | 20 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(17): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.855+104A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425035 | ||||||
chr14:64425105
|
T | G | 4 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0128others(1): Show | 4 | HG01109.hp1 HG01175.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+174T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425105 | ||||||
chr14:64425210
|
CT | C | 37 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0071others(34): Show | 37 | HG01070.hp1 HG01243.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.855+298delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr14 | 64425210 | |||||
chr14:64425214
|
T | C | 6 | a0005c0005t0001g0022a0005c0005t0001g0023a0005c0005t0001g0029others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.855+283T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425214 | ||||||
chr14:64425412
|
C | T | 1 | a0002c0002t0001g0300 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.856-318C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425412 | ||||||
chr14:64425454
|
G | A | 3 | a0002c0002t0001g0089a0002c0002t0001g0283a0002c0002t0001g0298 | 3 | HG00323.hp2 HG00738.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.856-276G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425454 | ||||||
chr14:64425459
|
C | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-271C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425459 | ||||||
chr14:64425575
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.856-155G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425575 | ||||||
chr14:64425618
|
G | A | 13 | a0001c0001t0001g0214a0001c0001t0001g0223a0004c0004t0001g0049others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.856-112G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425618 | ||||||
chr14:64425701
|
C | G | 1 | a0001c0001t0001g0261 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.856-29C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 9/27 | chr14 | 64425701 | ||||||
chr14:64425921
|
C | A | 3 | a0001c0001t0001g0037a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG00741.hp1 HG02257.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.953+94C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 10/27 | chr14 | 64425921 | ||||||
chr14:64426211
|
T | C | 2 | a0003c0003t0002g0100a0003c0003t0002g0124 | 2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1127+19T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426211 | ||||||
chr14:64426511
|
C | G | 41 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0108others(38): Show | 41 | HG01243.hp2 HG01496.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1127+319C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426511 | ||||||
chr14:64426534
|
G | A | 20 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(17): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1127+342G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426534 | ||||||
chr14:64426535
|
A | G | 20 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(17): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1127+343A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426535 | ||||||
chr14:64426591
|
C | A | 20 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(17): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1127+399C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426591 | ||||||
chr14:64426595
|
C | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0211a0002c0002t0001g0268others(1): Show | 4 | HG03490.hp2 HG03492.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+403C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426595 | ||||||
chr14:64426659
|
G | C | 73 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0090others(70): Show | 73 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1127+467G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426659 | ||||||
chr14:64426702
|
C | CACA | 71 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0090others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1127+510_1127+511i others(5): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426702 | ||||||
chr14:64426850
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0014t0001g0009 | 3 | HG01175.hp1 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1128-487T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64426850 | ||||||
chr14:64427071
|
T | A | 1 | a0002c0002t0001g0299 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1128-266T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64427071 | ||||||
chr14:64427104
|
G | A | 1 | a0004c0004t0001g0258 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1128-233G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64427104 | ||||||
chr14:64427141
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-196G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64427141 | ||||||
chr14:64427152
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1128-185C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 11/27 | chr14 | 64427152 | ||||||
chr14:64427641
|
G | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0253a0001c0001t0002g0077others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+168G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64427641 | ||||||
chr14:64427644
|
C | T | 29 | a0001c0001t0001g0090a0001c0001t0001g0247a0001c0001t0001g0282others(26): Show | 29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.1264+171C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64427644 | ||||||
chr14:64427746
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1264+273T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64427746 | ||||||
chr14:64427816
|
A | G | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264+343A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64427816 | ||||||
chr14:64427912
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1264+439C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64427912 | ||||||
chr14:64427960
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1264+487A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64427960 | ||||||
chr14:64428004
|
T | A | 20 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(17): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1264+531T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428004 | ||||||
chr14:64428102
|
G | GT | 45 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0031others(42): Show | 45 | HG00408.hp1 HG00735.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.1264+654dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64428102 | |||||
chr14:64428102
|
GT | G | 117 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0087others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1264+654delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64428102 | |||||
chr14:64428102
|
GTT | G | 17 | a0001c0001t0001g0042a0001c0001t0001g0118a0001c0001t0001g0119others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1264+653_1264+654d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64428102 | |||||
chr14:64428106
|
T | G | 2 | a0004c0004t0001g0110a0004c0004t0001g0256 | 2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1264+633T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428106 | ||||||
chr14:64428107
|
T | G | 11 | a0001c0001t0001g0214a0001c0001t0001g0223a0004c0004t0001g0049others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1264+634T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428107 | ||||||
chr14:64428111
|
T | TG | 4 | a0006c0006t0001g0002a0006c0006t0001g0116a0006c0006t0001g0126others(1): Show | 4 | HG01884.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264+638_1264+639i others(3): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428111 | ||||||
chr14:64428115
|
T | G | 1 | a0002c0002t0001g0293 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1264+642T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428115 | ||||||
chr14:64428123
|
T | C | 28 | a0001c0001t0001g0090a0001c0001t0001g0247a0001c0001t0001g0282others(25): Show | 28 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.1264+650T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428123 | ||||||
chr14:64428136
|
G | T | 1 | a0001c0001t0001g0218 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1264+663G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428136 | ||||||
chr14:64428189
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1264+716T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428189 | ||||||
chr14:64428304
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1264+831C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428304 | ||||||
chr14:64428324
|
C | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0253a0001c0001t0002g0077others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264+851C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428324 | ||||||
chr14:64428379
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1264+906C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428379 | ||||||
chr14:64428436
|
G | T | 304 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(301): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1264+963G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428436 | ||||||
chr14:64428555
|
CT | C | 251 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0030others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1264+1097delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64428555 | |||||
chr14:64428555
|
CTT | C | 17 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0001g0223others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1264+1096_1264+109 others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64428555 | |||||
chr14:64428676
|
C | T | 4 | a0001c0001t0002g0007a0003c0003t0002g0100a0003c0003t0002g0124others(1): Show | 4 | HG02647.hp1 HG02886.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264+1203C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428676 | ||||||
chr14:64428700
|
C | T | 53 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(50): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1264+1227C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428700 | ||||||
chr14:64428756
|
A | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(8): Show | 11 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1264+1283A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428756 | ||||||
chr14:64428834
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1265-1350G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428834 | ||||||
chr14:64428842
|
G | A | 13 | a0001c0001t0001g0214a0001c0001t0001g0223a0004c0004t0001g0049others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1265-1342G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428842 | ||||||
chr14:64428969
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1265-1215C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64428969 | ||||||
chr14:64429093
|
G | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0128others(1): Show | 4 | HG01109.hp1 HG01175.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-1091G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429093 | ||||||
chr14:64429117
|
C | T | 1 | a0002c0002t0001g0306 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1265-1067C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429117 | ||||||
chr14:64429155
|
C | T | 1 | a0003c0003t0001g0180 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1265-1029C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429155 | ||||||
chr14:64429261
|
A | AACATATA others(1): Show |
11 | a0004c0004t0001g0049a0004c0004t0001g0062a0004c0004t0001g0095others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(10): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(19): Show |
1 | a0001c0001t0001g0111 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1265-922_1265-921i others(28): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(5): Show |
1 | a0001c0001t0001g0198 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1265-922_1265-921i others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(9): Show |
12 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0002g0007others(9): Show | 12 | HG02615.hp2 HG02647.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(18): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(15): Show |
33 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(30): Show | 33 | HG00741.hp1 HG01070.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(24): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(17): Show |
10 | a0001c0001t0001g0031a0001c0001t0001g0065a0001c0001t0001g0084others(7): Show | 10 | HG00140.hp1 HG00558.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(26): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(19): Show |
21 | a0001c0001t0001g0041a0001c0001t0001g0047a0001c0001t0001g0051others(18): Show | 21 | HG00597.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(28): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(21): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0033others(15): Show | 18 | HG00280.hp2 HG01109.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(30): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(23): Show |
6 | a0001c0001t0001g0053a0001c0001t0001g0070a0001c0001t0001g0128others(3): Show | 6 | HG00621.hp1 HG01109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(32): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(25): Show |
4 | a0001c0001t0001g0032a0001c0001t0001g0042a0001c0001t0001g0052others(1): Show | 4 | HG00639.hp2 HG00741.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(34): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(27): Show |
7 | a0001c0001t0002g0224a0005c0005t0001g0022a0005c0005t0001g0023others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(36): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(29): Show |
4 | a0001c0001t0001g0127a0001c0001t0001g0341a0003c0003t0001g0180others(1): Show | 4 | HG02486.hp2 NA18939.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(38): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(31): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0030others(5): Show | 8 | HG01099.hp1 HG01496.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(40): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(33): Show |
4 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0327others(1): Show | 4 | HG01257.hp1 HG01516.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(42): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(35): Show |
18 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0168others(15): Show | 18 | HG00408.hp2 HG00438.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(44): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(37): Show |
31 | a0001c0001t0001g0034a0001c0001t0001g0044a0001c0001t0001g0064others(28): Show | 31 | HG00099.hp2 HG00733.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(46): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(39): Show |
27 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0040others(24): Show | 27 | HG00673.hp2 HG01975.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(48): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(41): Show |
6 | a0002c0002t0001g0322a0003c0003t0001g0147a0003c0003t0001g0156others(3): Show | 6 | HG00423.hp1 HG00673.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.1265-922_1265-921i others(50): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(45): Show |
1 | a0003c0003t0001g0204 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1265-922_1265-921i others(54): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(47): Show |
1 | a0001c0001t0001g0218 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1265-922_1265-921i others(56): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(37): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0255 | 2 | HG01106.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1265-922_1265-921i others(46): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(39): Show |
1 | a0002c0002t0001g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1265-922_1265-921i others(48): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429261
|
A | AACATATA others(43): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0092 | 2 | HG00280.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.1265-922_1265-921i others(52): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429261 | |||||
chr14:64429262
|
A | ACATATAT others(41): Show |
1 | a0003c0003t0001g0186 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1265-922_1265-921i others(50): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429262 | ||||||
chr14:64429266
|
A | C | 1 | a0003c0003t0001g0186 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1265-918A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429266 | ||||||
chr14:64429332
|
T | TTG | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1265-851_1265-850i others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429332 | |||||
chr14:64429334
|
T | G | 1 | a0002c0002t0001g0105 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1265-850T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429334 | ||||||
chr14:64429412
|
C | A | 17 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0004others(14): Show | 17 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1265-772C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429412 | ||||||
chr14:64429433
|
C | T | 4 | a0001c0001t0002g0007a0003c0003t0002g0100a0003c0003t0002g0124others(1): Show | 4 | HG02647.hp1 HG02886.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1265-751C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429433 | ||||||
chr14:64429665
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1265-519A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429665 | ||||||
chr14:64429740
|
A | C | 13 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0013others(10): Show | 13 | HG01070.hp1 HG01167.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1265-444A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64429740 | ||||||
chr14:64429762
|
GCTTT | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1265-419_1265-416d others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr14 | 64429762 | |||||
chr14:64430065
|
C | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1265-119C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64430065 | ||||||
chr14:64430102
|
A | G | 1 | a0003c0003t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1265-82A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 12/27 | chr14 | 64430102 | ||||||
chr14:64430238
|
A | G | 2 | a0003c0003t0001g0057a0003c0003t0001g0273 | 2 | HG00408.hp2 HG02155.hp1 |
splice_region_variant&intron_variant | LOW | c.1311+8A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430238 | ||||||
chr14:64430277
|
CG | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1311+54delG | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr14 | 64430277 | |||||
chr14:64430300
|
C | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1311+70C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430300 | ||||||
chr14:64430434
|
G | GATTACAG others(30): Show |
4 | a0001c0001t0002g0007a0003c0003t0002g0100a0003c0003t0002g0124others(1): Show | 4 | HG02647.hp1 HG02886.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+208_1311+244d others(39): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr14 | 64430434 | |||||
chr14:64430514
|
T | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0043 | 3 | NA18956.hp2 NA18979.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1311+284T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430514 | ||||||
chr14:64430574
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0128others(1): Show | 4 | HG01109.hp1 HG01175.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+344G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430574 | ||||||
chr14:64430585
|
C | T | 68 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(65): Show | 68 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1311+355C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430585 | ||||||
chr14:64430650
|
C | T | 2 | a0003c0003t0001g0182a0003c0003t0001g0186 | 2 | HG00544.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1311+420C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430650 | ||||||
chr14:64430860
|
T | C | 2 | a0002c0002t0001g0200a0002c0002t0001g0340 | 2 | NA18971.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1311+630T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430860 | ||||||
chr14:64430904
|
G | A | 18 | a0001c0001t0001g0090a0001c0001t0001g0247a0001c0001t0001g0282others(15): Show | 18 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.1312-628G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64430904 | ||||||
chr14:64431003
|
T | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-529T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431003 | ||||||
chr14:64431005
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-527C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431005 | ||||||
chr14:64431035
|
A | G | 25 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0112others(22): Show | 25 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1312-497A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431035 | ||||||
chr14:64431076
|
CTTTT | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-443_1312-440d others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | INFO_REALIGN_3_PRIME | chr14 | 64431076 | |||||
chr14:64431213
|
G | A | 29 | a0001c0001t0001g0090a0001c0001t0001g0247a0001c0001t0001g0282others(26): Show | 29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.1312-319G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431213 | ||||||
chr14:64431215
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-317A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431215 | ||||||
chr14:64431309
|
G | A | 1 | a0002c0002t0001g0298 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1312-223G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431309 | ||||||
chr14:64431358
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1312-174A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431358 | ||||||
chr14:64431411
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1312-121C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431411 | ||||||
chr14:64431467
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1312-65A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 13/27 | chr14 | 64431467 | ||||||
chr14:64431741
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1420-46A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 14/27 | chr14 | 64431741 | ||||||
chr14:64431745
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1420-42G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 14/27 | chr14 | 64431745 | ||||||
chr14:64431928
|
A | C | 1 | a0001c0001t0001g0261 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1494+67A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64431928 | ||||||
chr14:64431969
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1494+108A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64431969 | ||||||
chr14:64431974
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+113T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64431974 | ||||||
chr14:64432053
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1494+192G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432053 | ||||||
chr14:64432057
|
C | T | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1494+196C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432057 | ||||||
chr14:64432337
|
A | C | 28 | a0001c0001t0001g0016a0001c0001t0001g0042a0001c0001t0001g0055others(25): Show | 28 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1494+476A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432337 | ||||||
chr14:64432517
|
C | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0130 | 3 | HG01496.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1494+656C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432517 | ||||||
chr14:64432545
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1494+684A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432545 | ||||||
chr14:64432639
|
G | A | 14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0040others(11): Show | 14 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1494+778G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432639 | ||||||
chr14:64432690
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+829T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432690 | ||||||
chr14:64432786
|
C | T | 2 | a0002c0002t0001g0138a0002c0002t0001g0141 | 2 | NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1494+925C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432786 | ||||||
chr14:64432798
|
C | T | 60 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 60 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1494+937C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432798 | ||||||
chr14:64432900
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+1039A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64432900 | ||||||
chr14:64433053
|
C | T | 1 | a0002c0002t0001g0067 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1494+1192C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433053 | ||||||
chr14:64433121
|
G | T | 28 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0108others(25): Show | 28 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1494+1260G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433121 | ||||||
chr14:64433125
|
T | G | 29 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0032others(26): Show | 29 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.1494+1264T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433125 | ||||||
chr14:64433146
|
G | A | 1 | a0003c0003t0001g0025 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1494+1285G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433146 | ||||||
chr14:64433223
|
G | A | 1 | a0002c0002t0001g0288 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1494+1362G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433223 | ||||||
chr14:64433315
|
C | T | 2 | a0002c0002t0001g0001a0002c0002t0001g0241 | 3 | HG00735.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1494+1454C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433315 | ||||||
chr14:64433370
|
T | C | 1 | a0002c0002t0001g0266 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1494+1509T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433370 | ||||||
chr14:64433491
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+1630T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433491 | ||||||
chr14:64433501
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1494+1640T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433501 | ||||||
chr14:64433503
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+1642A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433503 | ||||||
chr14:64433504
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0001t0001g0128others(1): Show | 4 | HG01109.hp1 HG01175.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1494+1643A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433504 | ||||||
chr14:64433605
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+1744G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433605 | ||||||
chr14:64433653
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1494+1792A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433653 | ||||||
chr14:64433713
|
C | CT | 9 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0108others(6): Show | 9 | HG00741.hp2 HG02109.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1494+1852_1494+185 others(5): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433713 | ||||||
chr14:64433713
|
C | CTTT | 14 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0001g0223others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1494+1852_1494+185 others(7): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433713 | ||||||
chr14:64433713
|
C | CTTTT | 3 | a0001c0001t0001g0310a0001c0001t0001g0315a0004c0004t0001g0110 | 3 | HG02055.hp1 NA18994.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1494+1852_1494+185 others(8): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433713 | ||||||
chr14:64433714
|
A | AT | 68 | a0001c0001t0001g0030a0001c0001t0001g0034a0001c0001t0001g0046others(65): Show | 68 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1495-1833dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64433714 | |||||
chr14:64433714
|
A | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(88): Show | 91 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1494+1853A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433714 | ||||||
chr14:64433714
|
AT | A | 18 | a0001c0001t0001g0036a0001c0001t0001g0125a0001c0001t0001g0317others(15): Show | 18 | HG00140.hp1 HG01074.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.1495-1833delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64433714 | |||||
chr14:64433786
|
G | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-1783G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433786 | ||||||
chr14:64433819
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1495-1750T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433819 | ||||||
chr14:64433891
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-1678A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433891 | ||||||
chr14:64433947
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1495-1622T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433947 | ||||||
chr14:64433954
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-1615T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64433954 | ||||||
chr14:64434031
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-1538A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434031 | ||||||
chr14:64434136
|
A | G | 17 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0001g0223others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1495-1433A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434136 | ||||||
chr14:64434233
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-1336A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434233 | ||||||
chr14:64434262
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0002g0120 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1495-1307G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434262 | ||||||
chr14:64434429
|
G | A | 11 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(8): Show | 11 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495-1140G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434429 | ||||||
chr14:64434457
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1495-1112A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434457 | ||||||
chr14:64434542
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495-1027T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434542 | ||||||
chr14:64434810
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-759C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434810 | ||||||
chr14:64434821
|
G | GT | 47 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0043others(44): Show | 47 | HG00140.hp1 HG00544.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.1495-732dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64434821 | |||||
chr14:64434845
|
G | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-724G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434845 | ||||||
chr14:64434872
|
T | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0047others(11): Show | 14 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1495-697T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434872 | ||||||
chr14:64434949
|
C | CT | 151 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0030others(148): Show | 151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1495-594dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64434949 | |||||
chr14:64434949
|
C | CTT | 21 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0073others(18): Show | 21 | HG00408.hp1 HG00597.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.1495-595_1495-594d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64434949 | |||||
chr14:64434949
|
CT | C | 9 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(6): Show | 9 | HG00323.hp2 HG01255.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1495-594delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64434949 | |||||
chr14:64434949
|
CTT | C | 17 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0001g0223others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1495-595_1495-594d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64434949 | |||||
chr14:64434949
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0099a0002c0002t0001g0103 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1495-604_1495-594d others(13): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr14 | 64434949 | |||||
chr14:64434955
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495-614T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434955 | ||||||
chr14:64434956
|
T | C | 17 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0001g0223others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1495-613T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434956 | ||||||
chr14:64434960
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495-609T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434960 | ||||||
chr14:64434961
|
T | C | 17 | a0001c0001t0001g0189a0001c0001t0001g0214a0001c0001t0001g0223others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1495-608T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434961 | ||||||
chr14:64434964
|
T | C | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495-605T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64434964 | ||||||
chr14:64435010
|
C | T | 116 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0034others(113): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1495-559C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435010 | ||||||
chr14:64435038
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1495-531C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435038 | ||||||
chr14:64435043
|
G | C | 11 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(8): Show | 11 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1495-526G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435043 | ||||||
chr14:64435076
|
A | C | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-493A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435076 | ||||||
chr14:64435150
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-419C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435150 | ||||||
chr14:64435198
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1495-371A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435198 | ||||||
chr14:64435294
|
T | G | 1 | a0003c0003t0002g0190 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1495-275T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435294 | ||||||
chr14:64435308
|
A | G | 1 | a0002c0002t0001g0248 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1495-261A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435308 | ||||||
chr14:64435314
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-255G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435314 | ||||||
chr14:64435333
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1495-236T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435333 | ||||||
chr14:64435367
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-202C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435367 | ||||||
chr14:64435398
|
T | C | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-171T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435398 | ||||||
chr14:64435412
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1495-157G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 15/27 | chr14 | 64435412 | ||||||
chr14:64435775
|
T | C | 85 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1597+104T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64435775 | ||||||
chr14:64435879
|
A | G | 3 | a0001c0001t0001g0310a0001c0001t0001g0314a0001c0001t0001g0315 | 3 | NA18961.hp2 NA18994.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1597+208A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64435879 | ||||||
chr14:64435896
|
C | T | 1 | a0003c0003t0001g0187 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1597+225C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64435896 | ||||||
chr14:64436099
|
A | G | 2 | a0002c0002t0001g0200a0002c0002t0001g0340 | 2 | NA18971.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1597+428A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436099 | ||||||
chr14:64436151
|
G | A | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597+480G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436151 | ||||||
chr14:64436225
|
A | G | 85 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1597+554A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436225 | ||||||
chr14:64436241
|
C | T | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597+570C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436241 | ||||||
chr14:64436255
|
C | T | 1 | a0003c0003t0001g0180 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1597+584C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436255 | ||||||
chr14:64436304
|
T | C | 1 | a0001c0001t0002g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1597+633T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436304 | ||||||
chr14:64436316
|
A | G | 24 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(21): Show | 24 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1597+645A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436316 | ||||||
chr14:64436730
|
T | C | 139 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(136): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1597+1059T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436730 | ||||||
chr14:64436744
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0318 | 2 | HG00280.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1597+1073C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436744 | ||||||
chr14:64436870
|
C | G | 1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1597+1199C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64436870 | ||||||
chr14:64436997
|
GGT | G | 11 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(8): Show | 11 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(8): Show |
intron_variant | MODIFIER | c.1597+1335_1597+133 others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr14 | 64436997 | |||||
chr14:64437101
|
TCTC | T | 70 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(67): Show | 70 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1597+1436_1597+143 others(7): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr14 | 64437101 | |||||
chr14:64437217
|
A | C | 2 | a0001c0001t0002g0066a0001c0001t0002g0120 | 2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1597+1546A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437217 | ||||||
chr14:64437547
|
A | G | 1 | a0002c0002t0001g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1598-1549A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437547 | ||||||
chr14:64437570
|
C | G | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1598-1526C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437570 | ||||||
chr14:64437622
|
C | T | 85 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1598-1474C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437622 | ||||||
chr14:64437628
|
G | C | 1 | a0003c0003t0001g0162 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1598-1468G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437628 | ||||||
chr14:64437746
|
C | T | 140 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(137): Show | 140 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1598-1350C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437746 | ||||||
chr14:64437806
|
G | A | 7 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0118others(4): Show | 7 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1598-1290G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437806 | ||||||
chr14:64437806
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0253 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1598-1290G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437806 | ||||||
chr14:64437889
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0081a0001c0011t0001g0097 | 3 | HG02809.hp2 HG03453.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1598-1207T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437889 | ||||||
chr14:64437916
|
T | C | 143 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(140): Show | 143 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.1598-1180T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437916 | ||||||
chr14:64437931
|
T | C | 141 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(138): Show | 141 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.1598-1165T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64437931 | ||||||
chr14:64438705
|
T | C | 1 | a0002c0002t0001g0238 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1598-391T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64438705 | ||||||
chr14:64438754
|
A | C | 1 | a0002c0002t0001g0080 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1598-342A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 16/27 | chr14 | 64438754 | ||||||
chr14:64439258
|
C | T | 85 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1674+86C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439258 | ||||||
chr14:64439411
|
A | G | 1 | a0003c0003t0001g0321 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1674+239A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439411 | ||||||
chr14:64439547
|
G | A | 13 | a0001c0001t0001g0214a0001c0001t0001g0223a0004c0004t0001g0049others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1674+375G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439547 | ||||||
chr14:64439655
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1675-471C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439655 | ||||||
chr14:64439766
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(66): Show | 69 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.1675-360C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439766 | ||||||
chr14:64439812
|
T | G | 110 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1675-314T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439812 | ||||||
chr14:64439828
|
A | G | 1 | a0003c0003t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1675-298A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439828 | ||||||
chr14:64439872
|
C | T | 9 | a0004c0004t0001g0095a0004c0004t0001g0096a0004c0004t0001g0098others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1675-254C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439872 | ||||||
chr14:64439873
|
A | G | 159 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(156): Show | 159 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1675-253A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439873 | ||||||
chr14:64439881
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1675-245G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439881 | ||||||
chr14:64439894
|
C | CA | 51 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0016others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1675-208dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439894 | |||||
chr14:64439894
|
C | CAA | 8 | a0001c0001t0001g0031a0001c0001t0001g0112a0001c0001t0001g0127others(5): Show | 8 | HG01109.hp1 HG02559.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1675-209_1675-208d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439894 | |||||
chr14:64439894
|
CA | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0036others(9): Show | 12 | HG01975.hp2 HG02109.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1675-208delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439894 | |||||
chr14:64439894
|
CAAAAAAA others(4): Show |
C | 2 | a0002c0002t0001g0088a0002c0002t0001g0288 | 2 | HG04228.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1675-218_1675-208d others(13): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439894 | |||||
chr14:64439894
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1675-219_1675-208d others(14): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439894 | |||||
chr14:64439896
|
A | G | 10 | a0004c0004t0001g0049a0004c0004t0001g0062a0004c0004t0001g0095others(7): Show | 10 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1675-230A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439896 | ||||||
chr14:64439897
|
A | G | 1 | a0004c0004t0001g0258 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1675-229A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439897 | ||||||
chr14:64439918
|
A | AT | 14 | a0001c0001t0001g0078a0001c0001t0001g0172a0001c0001t0001g0188others(11): Show | 14 | HG00280.hp1 HG01928.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.1675-207dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439918 | |||||
chr14:64439918
|
A | T | 96 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(93): Show | 96 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1675-208A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439918 | ||||||
chr14:64439920
|
G | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0253 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1675-206G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439920 | ||||||
chr14:64439953
|
TA | T | 100 | a0001c0001t0001g0046a0001c0001t0001g0151a0001c0001t0001g0161others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1675-172delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439953 | ||||||
chr14:64439954
|
AT | A | 110 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(107): Show | 110 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1675-165delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr14 | 64439954 | |||||
chr14:64439962
|
G | A | 1 | a0002c0002t0001g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1675-164G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439962 | ||||||
chr14:64439964
|
T | C | 1 | a0002c0002t0001g0254 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1675-162T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 17/27 | chr14 | 64439964 | ||||||
chr14:64440294
|
C | T | 1 | a0002c0002t0001g0222 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1815+28C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440294 | ||||||
chr14:64440515
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1815+249G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440515 | ||||||
chr14:64440583
|
C | G | 16 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0002g0004others(13): Show | 16 | HG01496.hp1 HG01884.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.1815+317C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440583 | ||||||
chr14:64440765
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1815+499C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440765 | ||||||
chr14:64440810
|
T | A | 2 | a0002c0002t0001g0131a0002c0002t0001g0132 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1815+544T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440810 | ||||||
chr14:64440865
|
C | T | 29 | a0001c0001t0001g0090a0001c0001t0001g0215a0001c0001t0001g0247others(26): Show | 29 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.1816-520C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440865 | ||||||
chr14:64440949
|
T | C | 1 | a0003c0003t0001g0061 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1816-436T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64440949 | ||||||
chr14:64441048
|
C | T | 71 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(68): Show | 71 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.1816-337C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64441048 | ||||||
chr14:64441097
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1816-288C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64441097 | ||||||
chr14:64441174
|
A | G | 42 | a0001c0001t0001g0064a0001c0001t0001g0090a0001c0001t0001g0198others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1816-211A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64441174 | ||||||
chr14:64441204
|
A | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0014t0001g0009 | 3 | HG01175.hp1 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1816-181A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64441204 | ||||||
chr14:64441276
|
A | G | 33 | a0001c0001t0001g0090a0001c0001t0001g0215a0001c0001t0001g0247others(30): Show | 33 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1816-109A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 18/27 | chr14 | 64441276 | ||||||
chr14:64441542
|
C | G | 1 | a0001c0001t0001g0247 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1884+89C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441542 | ||||||
chr14:64441577
|
T | A | 2 | a0002c0002t0001g0099a0002c0002t0001g0103 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1884+124T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441577 | ||||||
chr14:64441581
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0123others(34): Show | 37 | HG00544.hp2 HG00673.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.1884+128C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441581 | ||||||
chr14:64441582
|
A | G | 39 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0123others(36): Show | 39 | HG00544.hp2 HG00673.hp2 HG01928.hp2 others(36): Show |
intron_variant | MODIFIER | c.1884+129A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441582 | ||||||
chr14:64441589
|
A | G | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1884+136A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441589 | ||||||
chr14:64441602
|
C | T | 1 | a0002c0002t0001g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1884+149C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441602 | ||||||
chr14:64441622
|
T | C | 3 | a0001c0001t0001g0037a0002c0002t0001g0335a0003c0003t0001g0204 | 3 | HG02257.hp2 HG04115.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1884+169T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441622 | ||||||
chr14:64441623
|
G | A | 1 | a0002c0002t0001g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1884+170G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441623 | ||||||
chr14:64441624
|
G | A | 1 | a0002c0002t0001g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1884+171G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441624 | ||||||
chr14:64441633
|
C | T | 1 | a0002c0002t0001g0335 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1884+180C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441633 | ||||||
chr14:64441634
|
G | A | 1 | a0002c0002t0001g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1884+181G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441634 | ||||||
chr14:64441759
|
C | T | 7 | a0002c0002t0001g0088a0002c0002t0001g0262a0002c0002t0001g0268others(4): Show | 7 | HG00140.hp1 HG01361.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885-295C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441759 | ||||||
chr14:64441790
|
G | A | 7 | a0001c0001t0002g0077a0005c0005t0001g0022a0005c0005t0001g0023others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885-264G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441790 | ||||||
chr14:64441802
|
C | CA | 6 | a0001c0001t0001g0087a0001c0001t0001g0189a0001c0001t0001g0261others(3): Show | 6 | HG01928.hp2 HG04115.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885-234dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr14 | 64441802 | |||||
chr14:64441802
|
CA | C | 97 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0137others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1885-234delA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | INFO_REALIGN_3_PRIME | chr14 | 64441802 | |||||
chr14:64441933
|
A | G | 42 | a0001c0001t0001g0064a0001c0001t0001g0090a0001c0001t0001g0198others(39): Show | 42 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1885-121A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441933 | ||||||
chr14:64441954
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1885-100T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64441954 | ||||||
chr14:64442034
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1885-20C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 19/27 | chr14 | 64442034 | ||||||
chr14:64442224
|
A | G | 5 | a0006c0006t0001g0002a0006c0006t0001g0116a0006c0006t0001g0126others(2): Show | 5 | HG01884.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1997-39A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 20/27 | chr14 | 64442224 | ||||||
chr14:64442432
|
C | T | 1 | a0001c0001t0002g0093 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2136+30C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64442432 | ||||||
chr14:64442433
|
G | A | 80 | a0001c0001t0001g0046a0001c0001t0001g0151a0001c0001t0001g0161others(77): Show | 81 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.2136+31G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64442433 | ||||||
chr14:64442727
|
T | C | 7 | a0002c0002t0001g0088a0002c0002t0001g0262a0002c0002t0001g0268others(4): Show | 7 | HG00140.hp1 HG01361.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2136+325T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64442727 | ||||||
chr14:64442759
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2136+357G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64442759 | ||||||
chr14:64443189
|
G | A | 2 | a0003c0003t0001g0134a0003c0003t0001g0136 | 2 | HG02132.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.2136+787G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64443189 | ||||||
chr14:64443660
|
C | A | 1 | a0003c0003t0001g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2137-1033C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64443660 | ||||||
chr14:64443730
|
C | T | 4 | a0001c0001t0001g0072a0003c0003t0001g0017a0003c0003t0001g0018others(1): Show | 4 | HG00099.hp2 HG01099.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.2137-963C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64443730 | ||||||
chr14:64444076
|
G | A | 203 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(200): Show | 203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.2137-617G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444076 | ||||||
chr14:64444095
|
T | C | 2 | a0002c0002t0001g0099a0002c0002t0001g0103 | 2 | HG02723.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2137-598T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444095 | ||||||
chr14:64444303
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2137-390A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444303 | ||||||
chr14:64444418
|
G | A | 2 | a0002c0002t0001g0039a0003c0003t0001g0297 | 2 | NA18747.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2137-275G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444418 | ||||||
chr14:64444452
|
C | T | 1 | a0006c0006t0001g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2137-241C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444452 | ||||||
chr14:64444511
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0070 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2137-182C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444511 | ||||||
chr14:64444545
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2137-148C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444545 | ||||||
chr14:64444548
|
T | C | 1 | a0001c0001t0001g0282 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2137-145T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444548 | ||||||
chr14:64444596
|
G | A | 2 | a0002c0002t0001g0026a0002c0002t0001g0027 | 2 | NA18993.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.2137-97G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | chr14 | 64444596 | ||||||
chr14:64444674
|
CTG | C | 4 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0291others(1): Show | 4 | NA18951.hp1 NA18970.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2137-17_2137-16del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr14 | 64444674 | |||||
chr14:64444759
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2178+25G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64444759 | ||||||
chr14:64444844
|
T | C | 34 | a0001c0001t0001g0090a0001c0001t0001g0160a0001c0001t0001g0164others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.2178+110T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64444844 | ||||||
chr14:64444909
|
T | C | 297 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(294): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.2178+175T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64444909 | ||||||
chr14:64444910
|
A | G | 1 | a0003c0003t0002g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2178+176A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64444910 | ||||||
chr14:64445007
|
T | G | 10 | a0003c0003t0001g0143a0003c0003t0001g0144a0003c0003t0001g0146others(7): Show | 10 | HG02135.hp2 NA18941.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.2178+273T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64445007 | ||||||
chr14:64445231
|
C | A | 1 | a0001c0001t0001g0149 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2178+497C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64445231 | ||||||
chr14:64445263
|
A | T | 1 | a0004c0004t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2178+529A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64445263 | ||||||
chr14:64445310
|
C | T | 16 | a0001c0001t0001g0037a0001c0001t0001g0065a0001c0001t0001g0084others(13): Show | 16 | HG00741.hp1 HG02257.hp2 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.2178+576C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64445310 | ||||||
chr14:64445514
|
C | T | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2178+780C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64445514 | ||||||
chr14:64445863
|
A | T | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2178+1129A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64445863 | ||||||
chr14:64446047
|
C | T | 6 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0119others(3): Show | 6 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2178+1313C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446047 | ||||||
chr14:64446216
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2178+1482C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446216 | ||||||
chr14:64446315
|
C | G | 1 | a0002c0002t0001g0295 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2178+1581C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446315 | ||||||
chr14:64446393
|
G | A | 60 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2178+1659G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446393 | ||||||
chr14:64446411
|
A | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0253a0006c0006t0001g0002others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2178+1677A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446411 | ||||||
chr14:64446450
|
T | C | 1 | a0010c0012t0001g0003 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2178+1716T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446450 | ||||||
chr14:64446594
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2179-1623T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446594 | ||||||
chr14:64446610
|
C | T | 34 | a0001c0001t0001g0090a0001c0001t0001g0160a0001c0001t0001g0164others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.2179-1607C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446610 | ||||||
chr14:64446623
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2179-1594G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446623 | ||||||
chr14:64446691
|
A | G | 61 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2179-1526A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446691 | ||||||
chr14:64446711
|
T | C | 1 | a0006c0006t0001g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2179-1506T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446711 | ||||||
chr14:64446727
|
T | A | 61 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(58): Show | 61 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.2179-1490T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446727 | ||||||
chr14:64446793
|
C | G | 2 | a0002c0002t0001g0131a0002c0002t0001g0132 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.2179-1424C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446793 | ||||||
chr14:64446827
|
C | T | 1 | a0003c0003t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2179-1390C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446827 | ||||||
chr14:64446852
|
G | GT | 6 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0149others(3): Show | 6 | HG00741.hp2 HG01167.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.2179-1357dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64446852 | |||||
chr14:64446951
|
C | T | 218 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(215): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.2179-1266C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64446951 | ||||||
chr14:64447102
|
G | A | 1 | a0001c0001t0001g0282 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2179-1115G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447102 | ||||||
chr14:64447149
|
C | CT | 56 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0033others(53): Show | 56 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.2179-1043dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64447149 | |||||
chr14:64447149
|
C | CTT | 14 | a0001c0001t0001g0073a0001c0001t0001g0090a0001c0001t0001g0175others(11): Show | 14 | HG00423.hp1 HG00673.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.2179-1044_2179-104 others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64447149 | |||||
chr14:64447149
|
CT | C | 190 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0012others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2179-1043delT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64447149 | |||||
chr14:64447149
|
CTT | C | 7 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0137others(4): Show | 7 | HG01070.hp1 HG02451.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2179-1044_2179-104 others(6): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64447149 | |||||
chr14:64447222
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2179-995T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447222 | ||||||
chr14:64447265
|
C | G | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2179-952C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447265 | ||||||
chr14:64447274
|
G | C | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2179-943G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447274 | ||||||
chr14:64447319
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2179-898T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447319 | ||||||
chr14:64447321
|
A | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0119others(3): Show | 6 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2179-896A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447321 | ||||||
chr14:64447344
|
C | T | 2 | a0001c0001t0001g0087a0006c0006t0001g0002 | 2 | HG02965.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.2179-873C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447344 | ||||||
chr14:64447394
|
T | G | 1 | a0006c0006t0001g0140 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2179-823T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447394 | ||||||
chr14:64447408
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2179-809C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447408 | ||||||
chr14:64447434
|
A | G | 45 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.2179-783A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447434 | ||||||
chr14:64447454
|
C | CT | 34 | a0001c0001t0001g0016a0001c0001t0001g0030a0001c0001t0001g0042others(31): Show | 34 | HG00558.hp1 HG00673.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.2179-744dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64447454 | |||||
chr14:64447454
|
C | CTT | 45 | a0001c0001t0001g0090a0001c0001t0001g0160a0001c0001t0001g0164others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.2179-745_2179-744d others(4): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | INFO_REALIGN_3_PRIME | chr14 | 64447454 | |||||
chr14:64447594
|
G | A | 8 | a0001c0001t0001g0030a0001c0001t0001g0253a0006c0006t0001g0002others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2179-623G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447594 | ||||||
chr14:64447666
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2179-551G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447666 | ||||||
chr14:64447819
|
T | C | 60 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.2179-398T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447819 | ||||||
chr14:64447912
|
A | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2179-305A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447912 | ||||||
chr14:64447967
|
T | G | 1 | a0001c0001t0001g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2179-250T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 22/27 | chr14 | 64447967 | ||||||
chr14:64448464
|
A | G | 45 | a0001c0001t0001g0042a0001c0001t0001g0090a0001c0001t0001g0108others(42): Show | 45 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.2279+147A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64448464 | ||||||
chr14:64448802
|
C | CT | 200 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(197): Show | 201 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.2279+498dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr14 | 64448802 | |||||
chr14:64448815
|
T | TG | 6 | a0001c0001t0001g0127a0006c0006t0001g0002a0006c0006t0001g0116others(3): Show | 6 | HG01884.hp2 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2279+503dupG | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | INFO_REALIGN_3_PRIME | chr14 | 64448815 | |||||
chr14:64448944
|
T | C | 9 | a0004c0004t0001g0095a0004c0004t0001g0096a0004c0004t0001g0098others(6): Show | 9 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.2280-501T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64448944 | ||||||
chr14:64448956
|
T | C | 1 | a0002c0002t0001g0276 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2280-489T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64448956 | ||||||
chr14:64448961
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0278 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2280-484A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64448961 | ||||||
chr14:64449000
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2280-445C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64449000 | ||||||
chr14:64449051
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280-394G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64449051 | ||||||
chr14:64449095
|
A | G | 1 | a0003c0003t0001g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2280-350A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64449095 | ||||||
chr14:64449227
|
G | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2280-218G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 23/27 | chr14 | 64449227 | ||||||
chr14:64449716
|
C | T | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | NA18968.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2457+94C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449716 | ||||||
chr14:64449729
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2457+107G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449729 | ||||||
chr14:64449730
|
C | A | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2457+108C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449730 | ||||||
chr14:64449787
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2457+165A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449787 | ||||||
chr14:64449811
|
C | T | 1 | a0003c0003t0001g0005 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2457+189C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449811 | ||||||
chr14:64449905
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0014t0001g0009 | 3 | HG01175.hp1 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2457+283C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449905 | ||||||
chr14:64449914
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2457+292A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449914 | ||||||
chr14:64449980
|
T | C | 254 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(251): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.2457+358T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64449980 | ||||||
chr14:64450183
|
C | G | 11 | a0004c0004t0001g0049a0004c0004t0001g0062a0004c0004t0001g0095others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2457+561C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450183 | ||||||
chr14:64450192
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2457+570G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450192 | ||||||
chr14:64450476
|
C | T | 1 | a0001c0001t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2457+854C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450476 | ||||||
chr14:64450830
|
CCTGAG | C | 11 | a0004c0004t0001g0049a0004c0004t0001g0062a0004c0004t0001g0095others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2457+1209_2457+121 others(9): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450830 | ||||||
chr14:64450836
|
T | A | 11 | a0004c0004t0001g0049a0004c0004t0001g0062a0004c0004t0001g0095others(8): Show | 11 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2457+1214T>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450836 | ||||||
chr14:64450933
|
C | T | 1 | a0003c0003t0001g0061 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2457+1311C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450933 | ||||||
chr14:64450934
|
G | A | 26 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0149others(23): Show | 26 | HG00544.hp2 HG01928.hp2 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.2457+1312G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64450934 | ||||||
chr14:64451084
|
G | A | 3 | a0002c0002t0001g0275a0002c0002t0001g0307a0002c0002t0001g0322 | 3 | HG01255.hp1 HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2457+1462G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64451084 | ||||||
chr14:64451232
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2457+1610G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64451232 | ||||||
chr14:64451472
|
T | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0119others(3): Show | 6 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2457+1850T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64451472 | ||||||
chr14:64451658
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2457+2036A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64451658 | ||||||
chr14:64451694
|
A | G | 83 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(80): Show | 84 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.2458-2060A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64451694 | ||||||
chr14:64451855
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2458-1899T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64451855 | ||||||
chr14:64452375
|
T | C | 5 | a0006c0006t0001g0002a0006c0006t0001g0116a0006c0006t0001g0126others(2): Show | 5 | HG01884.hp2 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2458-1379T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64452375 | ||||||
chr14:64452522
|
C | T | 1 | a0006c0006t0001g0002 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2458-1232C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64452522 | ||||||
chr14:64452858
|
T | TCTACTTT others(325): Show |
1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2458-880_2458-879i others(334): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr14 | 64452858 | |||||
chr14:64452909
|
C | CA | 3 | a0001c0001t0001g0064a0001c0001t0001g0198a0001c0001t0001g0223 | 3 | HG02615.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2458-844dupA | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr14 | 64452909 | |||||
chr14:64453068
|
A | T | 1 | a0002c0002t0001g0306 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2458-686A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64453068 | ||||||
chr14:64453143
|
T | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18956.hp1 NA18961.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.2458-611T>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64453143 | ||||||
chr14:64453323
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2458-431G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64453323 | ||||||
chr14:64453428
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2458-326G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64453428 | ||||||
chr14:64453710
|
CAT | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0170a0004c0004t0001g0256 | 3 | HG02109.hp2 NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.2458-43_2458-42del others(2): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 24/27 | chr14 | 64453710 | ||||||
chr14:64453947
|
G | A | 64 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 64 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.2565+86G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64453947 | ||||||
chr14:64453953
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2565+92G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64453953 | ||||||
chr14:64454059
|
G | A | 1 | a0002c0002t0001g0024 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2565+198G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454059 | ||||||
chr14:64454149
|
A | T | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2565+288A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454149 | ||||||
chr14:64454158
|
G | T | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2565+297G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454158 | ||||||
chr14:64454247
|
C | G | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2565+386C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454247 | ||||||
chr14:64454247
|
C | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0070others(1): Show | 4 | HG02109.hp1 HG02258.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2565+386C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454247 | ||||||
chr14:64454513
|
G | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2566-210G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454513 | ||||||
chr14:64454546
|
C | CT | 15 | a0002c0002t0001g0275a0002c0002t0001g0307a0002c0002t0001g0322others(12): Show | 15 | HG01243.hp2 HG01255.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.2566-162dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr14 | 64454546 | |||||
chr14:64454563
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2566-160G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454563 | ||||||
chr14:64454588
|
C | A | 2 | a0004c0004t0001g0049a0004c0004t0001g0062 | 2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.2566-135C>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454588 | ||||||
chr14:64454667
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2566-56C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454667 | ||||||
chr14:64454701
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2566-22C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 25/27 | chr14 | 64454701 | ||||||
chr14:64454908
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2718+33A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64454908 | ||||||
chr14:64455270
|
G | A | 1 | a0002c0002t0001g0241 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2718+395G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64455270 | ||||||
chr14:64455364
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2718+489C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64455364 | ||||||
chr14:64455488
|
G | T | 2 | a0002c0002t0001g0082a0002c0002t0001g0117 | 2 | HG01192.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2718+613G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64455488 | ||||||
chr14:64455670
|
A | C | 1 | a0001c0001t0001g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2718+795A>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64455670 | ||||||
chr14:64455772
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2718+897C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64455772 | ||||||
chr14:64455778
|
C | T | 1 | a0002c0002t0001g0054 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2718+903C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64455778 | ||||||
chr14:64456077
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2718+1202G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456077 | ||||||
chr14:64456084
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0055a0001c0014t0001g0009 | 3 | HG01175.hp1 HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2718+1209G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456084 | ||||||
chr14:64456198
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0253 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2718+1323C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456198 | ||||||
chr14:64456206
|
GC | G | 51 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.2718+1333delC | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr14 | 64456206 | |||||
chr14:64456238
|
G | T | 7 | a0002c0002t0001g0088a0002c0002t0001g0262a0002c0002t0001g0268others(4): Show | 7 | HG00140.hp1 HG01361.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2718+1363G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456238 | ||||||
chr14:64456332
|
G | A | 1 | a0002c0002t0001g0059 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2718+1457G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456332 | ||||||
chr14:64456346
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2718+1471G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456346 | ||||||
chr14:64456425
|
T | C | 2 | a0001c0001t0001g0033a0001c0001t0001g0051 | 2 | HG01109.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.2718+1550T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456425 | ||||||
chr14:64456448
|
G | T | 106 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(103): Show | 106 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2718+1573G>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456448 | ||||||
chr14:64456664
|
C | G | 8 | a0001c0001t0001g0030a0001c0001t0001g0253a0006c0006t0001g0002others(5): Show | 8 | HG01884.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2719-1550C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456664 | ||||||
chr14:64456733
|
T | C | 10 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0119others(7): Show | 10 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2719-1481T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456733 | ||||||
chr14:64456920
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2719-1294T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456920 | ||||||
chr14:64456986
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2719-1228C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64456986 | ||||||
chr14:64457191
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2719-1023G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457191 | ||||||
chr14:64457259
|
G | A | 101 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.2719-955G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457259 | ||||||
chr14:64457279
|
T | C | 1 | a0002c0002t0001g0238 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2719-935T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457279 | ||||||
chr14:64457281
|
G | C | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2719-933G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457281 | ||||||
chr14:64457459
|
C | CT | 79 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 79 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.2719-741dupT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr14 | 64457459 | |||||
chr14:64457575
|
CCTCCCAA others(29): Show |
C | 1 | a0003c0003t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2719-638_2719-603d others(38): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457575 | ||||||
chr14:64457600
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2719-614C>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457600 | ||||||
chr14:64457604
|
C | T | 12 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0066others(9): Show | 12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.2719-610C>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457604 | ||||||
chr14:64457752
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2719-462G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457752 | ||||||
chr14:64457828
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0125 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2719-386T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457828 | ||||||
chr14:64457930
|
G | A | 1 | a0002c0002t0001g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2719-284G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64457930 | ||||||
chr14:64458088
|
AC | A | 7 | a0001c0001t0001g0189a0001c0001t0001g0310a0001c0001t0001g0314others(4): Show | 7 | NA18956.hp1 NA18961.hp2 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.2719-125delC | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 26/27 | chr14 | 64458088 | ||||||
chr14:64458367
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.*4+60T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64458367 | ||||||
chr14:64458536
|
A | AGGTTGAC others(29): Show |
1 | a0003c0003t0001g0163 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.*4+246_*4+247insGG others(34): Show |
MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr14 | 64458536 | |||||
chr14:64458837
|
A | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0119others(7): Show | 10 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.*4+530A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64458837 | ||||||
chr14:64459379
|
T | C | 82 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(79): Show | 83 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.*5-380T>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64459379 | ||||||
chr14:64459487
|
CTA | C | 51 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0035others(48): Show | 51 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.*5-270_*5-269delAT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr14 | 64459487 | |||||
chr14:64459574
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | HG02615.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.*5-185A>G | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64459574 | ||||||
chr14:64459599
|
A | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0278 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.*5-160A>T | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64459599 | ||||||
chr14:64459683
|
G | C | 12 | a0001c0001t0002g0004a0001c0001t0002g0007a0001c0001t0002g0066others(9): Show | 12 | HG01496.hp1 HG02280.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.*5-76G>C | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64459683 | ||||||
chr14:64459684
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.*5-75G>A | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | chr14 | 64459684 | ||||||
chr14:64459715
|
GTGCT | G | 340 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0010others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.*5-38_*5-35delGCTT | MTHFD1 | ENSG00000100714.18 | transcript | ENST00000652337.1 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr14 | 64459715 |