geneid | 9054 |
---|---|
ensemblid | ENSG00000244005.13 |
hgncid | 15910 |
symbol | NFS1 |
name | NFS1 cysteine desulfurase |
refseq_nuc | NM_021100.5 |
refseq_prot | NP_066923.3 |
ensembl_nuc | ENST00000374092.9 |
ensembl_prot | ENSP00000363205.3 |
mane_status | MANE Select |
chr | chr20 |
start | 35668052 |
end | 35699352 |
strand | - |
ver | v1.2 |
region | chr20:35668052-35699352 |
region5000 | chr20:35663052-35704352 |
regionname0 | NFS1_chr20_35668052_35699352 |
regionname5000 | NFS1_chr20_35663052_35704352 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1374 | 263 | 82 | 44 | 91 | 14 | 30 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
c0002 | 0/0 | 1374 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
c0003 | 0/0 | 1374 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1635 | 186 | 59 | 32 | 69 | 10 | 14 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0002 | 0/0 | 1635 | 43 | 8 | 11 | 18 | 2 | 4 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0003 | 0/0 | 1635 | 31 | 10 | 1 | 6 | 2 | 12 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0004 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0005 | 0/0 | 1635 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0006 | 0/0 | 1635 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0007 | 0/0 | 1635 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0008 | 0/0 | 1635 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
t0009 | 0/0 | 1635 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 9 | 0 | 3 | 2 | 1 | 2 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0003 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0017 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1374 | 263 | 82 | 44 | 91 | 14 | 30 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0003 | 0/0 | 1374 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0002c0002 | 0/0 | 1374 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3008 | 184 | 57 | 32 | 69 | 10 | 14 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0002 | 0/0 | 3008 | 40 | 8 | 11 | 15 | 2 | 4 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0003 | 0/0 | 3008 | 31 | 10 | 1 | 6 | 2 | 12 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0004 | 0/0 | 3008 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0005 | 0/0 | 3008 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0006 | 0/0 | 3008 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0007 | 0/0 | 3008 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0008 | 0/0 | 3008 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0001t0009 | 0/0 | 3008 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0001c0003t0001 | 0/0 | 3008 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
a0002c0002t0002 | 0/0 | 3008 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | copy fasta | chr20 | 35663052 | 35704352 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 9 | 0 | 3 | 2 | 1 | 2 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0003 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0017 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0001c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | GBR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0191 | EUR | IBS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0192 | EUR | IBS | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0199 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03041 | hp1 | a0001 | c0001 | t0009 | g0183 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0193 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0194 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | YRI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | CHB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | LWK | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | LWK | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | YRI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0061 | EUR | TSI | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | GIH | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | GIH | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | ACB | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0055 | EAS | JPT | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | USA | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | NFS1_chr20_35663052_35704352 | NFS1 | chr20 | 35663052 | 35704352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:35669644
|
C | T | 1 | a0002 | 3 | NA18959.hp1 NA19011.hp2 NA19090.hp2 |
missense_variant | MODERATE | c.1352G>A | p.Ser451Asn | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 1416/3008 | 1352/1374 | 451/457 | chr20 | 35669644 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:35698522
|
G | A | 1 | a0001c0003 | 2 | HG03041.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.166C>T | p.Leu56Leu | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/13 | 230/3008 | 166/1374 | 56/457 | chr20 | 35698522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:35668332
|
C | A | 1 | a0001c0001t0007 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1290G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 1290 | chr20 | 35668332 | |||||
chr20:35668552
|
T | C | 1 | a0001c0001t0006 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1070A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 1070 | chr20 | 35668552 | |||||
chr20:35668718
|
A | C | 2 | a0001c0001t0003a0001c0001t0009 | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*904T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 904 | chr20 | 35668718 | |||||
chr20:35668939
|
C | G | 1 | a0001c0001t0004 | 2 | HG02280.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*683G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 683 | chr20 | 35668939 | |||||
chr20:35669040
|
T | C | 1 | a0001c0001t0009 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 582 | chr20 | 35669040 | |||||
chr20:35669315
|
T | C | 1 | a0001c0001t0008 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 307 | chr20 | 35669315 | |||||
chr20:35669362
|
G | T | 3 | a0001c0001t0002a0001c0001t0006a0002c0002t0002 | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*260C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 260 | chr20 | 35669362 | |||||
chr20:35669375
|
T | C | 1 | a0001c0001t0005 | 2 | HG02451.hp2 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*247A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 247 | chr20 | 35669375 | |||||
chr20:35669429
|
T | C | 2 | a0001c0001t0003a0001c0001t0009 | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*193A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 13/13 | 193 | chr20 | 35669429 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:35669741
|
A | C | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.1311-56T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35669741 | ||||||
chr20:35669873
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311-188C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35669873 | ||||||
chr20:35670007
|
A | G | 1 | a0001c0001t0002g0061 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1311-322T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35670007 | ||||||
chr20:35670563
|
A | T | 1 | a0001c0001t0003g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1311-878T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35670563 | ||||||
chr20:35670802
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1311-1117C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35670802 | ||||||
chr20:35670991
|
G | C | 1 | a0001c0001t0002g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1311-1306C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35670991 | ||||||
chr20:35671020
|
T | C | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1311-1335A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671020 | ||||||
chr20:35671120
|
T | C | 5 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0119others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311-1435A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671120 | ||||||
chr20:35671127
|
A | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0210others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.1311-1442T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671127 | ||||||
chr20:35671474
|
A | G | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1310+1281T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671474 | ||||||
chr20:35671589
|
T | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0042 | 2 | HG01168.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1310+1166A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671589 | ||||||
chr20:35671774
|
C | T | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.1310+981G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671774 | ||||||
chr20:35671890
|
C | CA | 14 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(11): Show | 14 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1310+864dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671890 | ||||||
chr20:35671937
|
T | C | 7 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 8 | HG01109.hp2 HG01261.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1310+818A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671937 | ||||||
chr20:35671948
|
GTTGTTT | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0099a0001c0001t0001g0104others(6): Show | 10 | HG01167.hp1 HG01891.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1310+801_1310+806d others(8): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35671948 | ||||||
chr20:35672028
|
G | A | 1 | a0001c0001t0003g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1310+727C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672028 | ||||||
chr20:35672076
|
A | AG | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1310+678_1310+679i others(3): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672076 | ||||||
chr20:35672086
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1310+669A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672086 | ||||||
chr20:35672114
|
C | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02698.hp2 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1310+641G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672114 | ||||||
chr20:35672261
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1310+494A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672261 | ||||||
chr20:35672327
|
G | A | 3 | a0001c0001t0001g0095a0001c0001t0001g0149a0001c0001t0001g0209 | 3 | HG00323.hp2 HG00639.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1310+428C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672327 | ||||||
chr20:35672498
|
G | A | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.1310+257C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672498 | ||||||
chr20:35672502
|
C | T | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.1310+253G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 12/12 | chr20 | 35672502 | ||||||
chr20:35672958
|
T | A | 3 | a0001c0001t0003g0010a0001c0001t0003g0185a0001c0001t0003g0186 | 5 | HG03195.hp1 HG03516.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1221-114A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35672958 | ||||||
chr20:35672999
|
A | G | 3 | a0001c0001t0001g0094a0001c0001t0001g0105a0001c0001t0001g0115 | 3 | HG01192.hp1 HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1221-155T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35672999 | ||||||
chr20:35673016
|
G | A | 1 | a0001c0001t0004g0081 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1221-172C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673016 | ||||||
chr20:35673058
|
T | C | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.1221-214A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673058 | ||||||
chr20:35673075
|
G | A | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1221-231C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673075 | ||||||
chr20:35673116
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1221-272G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673116 | ||||||
chr20:35673204
|
C | T | 39 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1221-360G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673204 | ||||||
chr20:35673289
|
G | GA | 78 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(75): Show | 86 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1220+311dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673289 | ||||||
chr20:35673309
|
A | G | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.1220+292T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673309 | ||||||
chr20:35673361
|
C | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1220+240G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673361 | ||||||
chr20:35673538
|
G | C | 5 | a0001c0001t0001g0098a0001c0001t0001g0109a0001c0001t0001g0119others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1220+63C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673538 | ||||||
chr20:35673564
|
G | C | 1 | a0001c0001t0001g0146 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1220+37C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 11/12 | chr20 | 35673564 | ||||||
chr20:35674089
|
A | C | 21 | a0001c0001t0003g0021a0001c0001t0003g0187a0001c0001t0003g0189others(18): Show | 22 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.1136+261T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 10/12 | chr20 | 35674089 | ||||||
chr20:35674095
|
A | AC | 114 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 125 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1136+254dupG | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 10/12 | chr20 | 35674095 | ||||||
chr20:35674339
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.1136+11C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 10/12 | chr20 | 35674339 | ||||||
chr20:35674863
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.948+182G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 8/12 | chr20 | 35674863 | ||||||
chr20:35675007
|
G | A | 1 | a0001c0001t0003g0197 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.948+38C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 8/12 | chr20 | 35675007 | ||||||
chr20:35675364
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0003g0181a0001c0001t0003g0182 | 3 | HG02258.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.791-162A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675364 | ||||||
chr20:35675479
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.791-277T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675479 | ||||||
chr20:35675481
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.791-279A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675481 | ||||||
chr20:35675483
|
A | T | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.791-281T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675483 | ||||||
chr20:35675594
|
G | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.791-392C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675594 | ||||||
chr20:35675660
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.791-458A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675660 | ||||||
chr20:35675872
|
C | CA | 31 | a0001c0001t0001g0033a0001c0001t0001g0124a0001c0001t0001g0150others(28): Show | 34 | HG01074.hp2 HG01261.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.791-671dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675872 | ||||||
chr20:35675872
|
CA | C | 57 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(54): Show | 63 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.791-671delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675872 | ||||||
chr20:35675890
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.791-688T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35675890 | ||||||
chr20:35676012
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0152 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.791-810C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676012 | ||||||
chr20:35676353
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0052 | 2 | NA18964.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.791-1151G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676353 | ||||||
chr20:35676414
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0134 | 3 | HG01361.hp1 HG01981.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.791-1212G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676414 | ||||||
chr20:35676474
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.791-1272A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676474 | ||||||
chr20:35676623
|
T | C | 1 | a0001c0001t0009g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.791-1421A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676623 | ||||||
chr20:35676643
|
T | A | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.791-1441A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676643 | ||||||
chr20:35676667
|
A | C | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.791-1465T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676667 | ||||||
chr20:35676749
|
A | G | 1 | a0001c0001t0009g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.791-1547T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676749 | ||||||
chr20:35676758
|
G | GA | 21 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0034others(18): Show | 24 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.791-1557dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676758 | ||||||
chr20:35676758
|
G | GAA | 5 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0001g0170others(2): Show | 7 | HG01928.hp2 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.791-1558_791-1557d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676758 | ||||||
chr20:35676758
|
G | GAAAAAAA | 13 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0003g0021others(10): Show | 14 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.791-1563_791-1557d others(9): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676758 | ||||||
chr20:35676758
|
G | GAAAAAAA others(1): Show |
9 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043others(6): Show | 9 | HG00099.hp2 HG02738.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.791-1564_791-1557d others(10): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676758 | ||||||
chr20:35676758
|
G | GAAAAAAA others(2): Show |
7 | a0001c0001t0001g0037a0001c0001t0001g0040a0001c0001t0001g0044others(4): Show | 7 | HG01168.hp2 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.791-1565_791-1557d others(11): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676758 | ||||||
chr20:35676758
|
G | GAAAAAAA others(4): Show |
1 | a0001c0001t0003g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.791-1567_791-1557d others(13): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676758 | ||||||
chr20:35676774
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0003g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.791-1584_791-1573d others(14): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676774 | ||||||
chr20:35676779
|
AAAAAAAC | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.791-1584_791-1578d others(9): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676779 | ||||||
chr20:35676781
|
AAAAAC | A | 33 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(30): Show | 38 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.791-1584_791-1580d others(7): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676781 | ||||||
chr20:35676784
|
AAC | A | 18 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(15): Show | 19 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.791-1584_791-1583d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676784 | ||||||
chr20:35676786
|
C | A | 40 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(37): Show | 43 | HG00099.hp2 HG00639.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.791-1584G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676786 | ||||||
chr20:35676873
|
C | G | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.791-1671G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676873 | ||||||
chr20:35676977
|
C | A | 1 | a0001c0001t0003g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.791-1775G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35676977 | ||||||
chr20:35677090
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.791-1888A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677090 | ||||||
chr20:35677112
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.791-1910C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677112 | ||||||
chr20:35677145
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791-1943C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677145 | ||||||
chr20:35677257
|
C | G | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.791-2055G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677257 | ||||||
chr20:35677368
|
C | CA | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.791-2167dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677368 | ||||||
chr20:35677386
|
C | T | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.791-2184G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677386 | ||||||
chr20:35677585
|
A | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.791-2383T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677585 | ||||||
chr20:35677589
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.791-2387C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677589 | ||||||
chr20:35677881
|
T | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0210a0001c0001t0001g0211others(4): Show | 8 | NA18961.hp2 NA18986.hp1 NA18992.hp2 others(5): Show |
intron_variant | MODIFIER | c.791-2679A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677881 | ||||||
chr20:35677951
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.791-2749C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677951 | ||||||
chr20:35677965
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.791-2763G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35677965 | ||||||
chr20:35678072
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.790+2665C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678072 | ||||||
chr20:35678176
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790+2561G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678176 | ||||||
chr20:35678192
|
C | CAAAA | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.790+2541_790+2544d others(6): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678192 | ||||||
chr20:35678418
|
C | T | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.790+2319G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678418 | ||||||
chr20:35678436
|
G | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0106others(7): Show | 15 | HG00408.hp1 HG00597.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.790+2301C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678436 | ||||||
chr20:35678442
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.790+2295G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678442 | ||||||
chr20:35678476
|
C | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.790+2261G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678476 | ||||||
chr20:35678528
|
C | CA | 10 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0085others(7): Show | 11 | HG01515.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.790+2208dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678528 | ||||||
chr20:35678528
|
C | CAA | 7 | a0001c0001t0001g0101a0001c0001t0003g0010a0001c0001t0003g0181others(4): Show | 9 | HG02559.hp2 HG02723.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.790+2207_790+2208d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678528 | ||||||
chr20:35678528
|
C | CAAA | 19 | a0001c0001t0003g0021a0001c0001t0003g0185a0001c0001t0003g0187others(16): Show | 20 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.790+2206_790+2208d others(5): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678528 | ||||||
chr20:35678528
|
CA | C | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(8): Show | 13 | HG00423.hp1 HG02723.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.790+2208delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678528 | ||||||
chr20:35678548
|
A | G | 10 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.790+2189T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678548 | ||||||
chr20:35678699
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.790+2038A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678699 | ||||||
chr20:35678720
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.790+2017C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678720 | ||||||
chr20:35678961
|
A | T | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.790+1776T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35678961 | ||||||
chr20:35679253
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.790+1484C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679253 | ||||||
chr20:35679270
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.790+1467C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679270 | ||||||
chr20:35679397
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.790+1340A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679397 | ||||||
chr20:35679464
|
A | G | 94 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(91): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.790+1273T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679464 | ||||||
chr20:35679496
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(16): Show | 20 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.790+1241T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679496 | ||||||
chr20:35679602
|
G | T | 21 | a0001c0001t0003g0021a0001c0001t0003g0187a0001c0001t0003g0189others(18): Show | 22 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(19): Show |
intron_variant | MODIFIER | c.790+1135C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679602 | ||||||
chr20:35679791
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.790+946C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679791 | ||||||
chr20:35679803
|
A | T | 1 | a0001c0001t0001g0123 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.790+934T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35679803 | ||||||
chr20:35680048
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.790+689A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35680048 | ||||||
chr20:35680198
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.790+539C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35680198 | ||||||
chr20:35680259
|
G | T | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.790+478C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35680259 | ||||||
chr20:35680292
|
G | A | 4 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG01081.hp1 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.790+445C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 7/12 | chr20 | 35680292 | ||||||
chr20:35680952
|
T | TCCA | 114 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(111): Show | 125 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.656-84_656-82dupTG others(1): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35680952 | ||||||
chr20:35681070
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.656-199C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681070 | ||||||
chr20:35681117
|
G | C | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.656-246C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681117 | ||||||
chr20:35681218
|
C | CA | 4 | a0001c0001t0002g0006a0001c0001t0002g0014a0001c0001t0002g0047others(1): Show | 7 | HG00408.hp2 HG02015.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-348dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681218 | ||||||
chr20:35681232
|
TAA | T | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.656-363_656-362del others(2): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681232 | ||||||
chr20:35681261
|
T | G | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.656-390A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681261 | ||||||
chr20:35681298
|
T | G | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-427A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681298 | ||||||
chr20:35681303
|
G | T | 52 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(49): Show | 57 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.656-432C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681303 | ||||||
chr20:35681370
|
G | C | 1 | a0001c0001t0003g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.656-499C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681370 | ||||||
chr20:35681469
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(215): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.655+419T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681469 | ||||||
chr20:35681472
|
C | T | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.655+416G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681472 | ||||||
chr20:35681625
|
A | G | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+263T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681625 | ||||||
chr20:35681655
|
A | G | 52 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(49): Show | 57 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.655+233T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681655 | ||||||
chr20:35681795
|
AACT | A | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+90_655+92delAG others(1): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 6/12 | chr20 | 35681795 | ||||||
chr20:35682229
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.562-248T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682229 | ||||||
chr20:35682344
|
C | T | 39 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.562-363G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682344 | ||||||
chr20:35682395
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.562-414G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682395 | ||||||
chr20:35682442
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.562-461G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682442 | ||||||
chr20:35682503
|
T | G | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-522A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682503 | ||||||
chr20:35682527
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG01109.hp2 HG01261.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.562-546C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682527 | ||||||
chr20:35682597
|
T | A | 1 | a0001c0001t0001g0146 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.562-616A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682597 | ||||||
chr20:35682606
|
A | C | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.562-625T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682606 | ||||||
chr20:35682801
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.562-820T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682801 | ||||||
chr20:35682826
|
C | A | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.562-845G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682826 | ||||||
chr20:35682842
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.562-861C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35682842 | ||||||
chr20:35683056
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.562-1075G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683056 | ||||||
chr20:35683059
|
C | A | 4 | a0001c0001t0003g0010a0001c0001t0003g0184a0001c0001t0003g0185others(1): Show | 6 | HG02723.hp1 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.562-1078G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683059 | ||||||
chr20:35683170
|
C | G | 65 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(62): Show | 72 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.562-1189G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683170 | ||||||
chr20:35683206
|
G | C | 1 | a0001c0001t0003g0184 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.562-1225C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683206 | ||||||
chr20:35683221
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.562-1240G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683221 | ||||||
chr20:35683249
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0145a0001c0001t0001g0153 | 6 | HG01934.hp2 HG01952.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.562-1268C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683249 | ||||||
chr20:35683339
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.562-1358C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683339 | ||||||
chr20:35683383
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.562-1402C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683383 | ||||||
chr20:35683406
|
C | T | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.562-1425G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683406 | ||||||
chr20:35683458
|
G | C | 4 | a0001c0001t0002g0013a0001c0001t0002g0058a0001c0001t0002g0067others(1): Show | 5 | HG00738.hp1 HG01192.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-1477C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683458 | ||||||
chr20:35683541
|
G | A | 5 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(2): Show | 5 | NA18747.hp1 NA18943.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-1560C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683541 | ||||||
chr20:35683585
|
C | T | 14 | a0001c0001t0003g0021a0001c0001t0003g0189a0001c0001t0003g0190others(11): Show | 15 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-1604G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683585 | ||||||
chr20:35683602
|
A | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.562-1621T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683602 | ||||||
chr20:35683652
|
C | T | 39 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.562-1671G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683652 | ||||||
chr20:35683697
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.562-1716C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683697 | ||||||
chr20:35683790
|
C | CA | 7 | a0001c0001t0001g0030a0001c0001t0001g0098a0001c0001t0001g0110others(4): Show | 7 | HG02486.hp2 HG02572.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-1810dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683790 | ||||||
chr20:35683790
|
CA | C | 68 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(65): Show | 75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.562-1810delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683790 | ||||||
chr20:35683827
|
G | GCTGGGTA others(13): Show |
2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.562-1866_562-1847d others(22): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683827 | ||||||
chr20:35683852
|
G | A | 39 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.562-1871C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683852 | ||||||
chr20:35683939
|
G | C | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.562-1958C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683939 | ||||||
chr20:35683969
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562-1988A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35683969 | ||||||
chr20:35684042
|
G | T | 1 | a0001c0001t0001g0128 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.562-2061C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684042 | ||||||
chr20:35684104
|
A | G | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.562-2123T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684104 | ||||||
chr20:35684245
|
A | G | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.562-2264T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684245 | ||||||
chr20:35684265
|
G | C | 1 | a0001c0001t0002g0072 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.562-2284C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684265 | ||||||
chr20:35684272
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.562-2291G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684272 | ||||||
chr20:35684284
|
G | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02698.hp2 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.562-2303C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684284 | ||||||
chr20:35684302
|
A | G | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.562-2321T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684302 | ||||||
chr20:35684356
|
AGAGATCG others(1443): Show |
A | 7 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 8 | HG01109.hp2 HG01261.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-3825_562-2376d others(2): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684356 | ||||||
chr20:35684411
|
T | TAAATA | 17 | a0001c0001t0001g0016a0001c0001t0001g0080a0001c0001t0001g0089others(14): Show | 18 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.562-2435_562-2431d others(7): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAA others(3): Show |
12 | a0001c0001t0001g0094a0001c0001t0001g0115a0001c0001t0001g0176others(9): Show | 13 | HG00597.hp1 HG01192.hp1 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.562-2440_562-2431d others(12): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAA others(8): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0178 | 2 | HG03130.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.562-2445_562-2431d others(17): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAC others(67): Show |
1 | a0001c0001t0001g0218 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.562-2431_562-2430i others(76): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAC others(62): Show |
1 | a0001c0001t0001g0215 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.562-2431_562-2430i others(71): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAC others(72): Show |
4 | a0001c0001t0001g0023a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 5 | NA18961.hp2 NA18992.hp2 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-2431_562-2430i others(81): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAC others(77): Show |
3 | a0001c0001t0001g0022a0001c0001t0001g0216a0001c0001t0001g0217 | 4 | HG00423.hp1 NA18962.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.562-2431_562-2430i others(86): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAC others(72): Show |
2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG00544.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.562-2431_562-2430i others(81): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
T | TAAATAAC others(82): Show |
1 | a0001c0001t0001g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.562-2431_562-2430i others(91): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
TAAATA | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(62): Show | 85 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.562-2435_562-2431d others(7): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
TAAATAAA others(3): Show |
T | 27 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0139others(24): Show | 30 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.562-2440_562-2431d others(12): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684411
|
TAAATAAA others(13): Show |
T | 3 | a0001c0001t0003g0193a0001c0001t0003g0194a0001c0001t0009g0183 | 3 | HG03041.hp1 HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.562-2450_562-2431d others(22): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684411 | ||||||
chr20:35684413
|
A | AATAACAT others(77): Show |
1 | a0001c0001t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.562-2433_562-2432i others(86): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684413 | ||||||
chr20:35684416
|
A | T | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.562-2435T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684416 | ||||||
chr20:35684418
|
A | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.562-2437T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684418 | ||||||
chr20:35684423
|
A | C | 1 | a0001c0001t0001g0219 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.562-2442T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684423 | ||||||
chr20:35684428
|
A | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.562-2447T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684428 | ||||||
chr20:35684748
|
C | T | 1 | a0001c0001t0005g0025 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.562-2767G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684748 | ||||||
chr20:35684773
|
A | G | 1 | a0001c0001t0003g0200 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.562-2792T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35684773 | ||||||
chr20:35685181
|
T | C | 39 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(36): Show | 42 | HG01074.hp2 HG01361.hp2 HG01515.hp1 others(39): Show |
intron_variant | MODIFIER | c.562-3200A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685181 | ||||||
chr20:35685458
|
A | G | 39 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(36): Show | 42 | HG01074.hp2 HG01361.hp2 HG01515.hp1 others(39): Show |
intron_variant | MODIFIER | c.562-3477T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685458 | ||||||
chr20:35685549
|
T | A | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.562-3568A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685549 | ||||||
chr20:35685558
|
T | TTA | 60 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(57): Show | 67 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.562-3579_562-3578d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685558 | ||||||
chr20:35685558
|
T | TTATA | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.562-3581_562-3578d others(6): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685558 | ||||||
chr20:35685576
|
C | A | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.562-3595G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685576 | ||||||
chr20:35685580
|
C | T | 29 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(26): Show | 32 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.562-3599G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685580 | ||||||
chr20:35685865
|
C | CA | 15 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(12): Show | 15 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.562-3885dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685865 | ||||||
chr20:35685865
|
C | CAA | 7 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 8 | HG01109.hp2 HG01261.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-3886_562-3885d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685865 | ||||||
chr20:35685925
|
ATTCT | A | 3 | a0001c0001t0001g0096a0001c0001t0005g0025a0001c0001t0005g0026 | 3 | HG01081.hp2 HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.562-3948_562-3945d others(6): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685925 | ||||||
chr20:35685936
|
A | C | 6 | a0001c0001t0001g0018a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 7 | HG02083.hp1 NA18943.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.562-3955T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685936 | ||||||
chr20:35685944
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0137a0001c0001t0001g0138 | 4 | HG00423.hp2 HG00621.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.562-3963A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685944 | ||||||
chr20:35685949
|
G | C | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-3968C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35685949 | ||||||
chr20:35686039
|
G | C | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.562-4058C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686039 | ||||||
chr20:35686180
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.562-4199G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686180 | ||||||
chr20:35686274
|
C | T | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(7): Show | 10 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.561+4139G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686274 | ||||||
chr20:35686281
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.561+4132G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686281 | ||||||
chr20:35686350
|
CA | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(122): Show | 144 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.561+4062delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686350 | ||||||
chr20:35686515
|
T | C | 46 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(43): Show | 50 | HG01074.hp2 HG01109.hp2 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.561+3898A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686515 | ||||||
chr20:35686660
|
AG | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.561+3752delC | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686660 | ||||||
chr20:35686838
|
T | C | 20 | a0001c0001t0003g0021a0001c0001t0003g0189a0001c0001t0003g0190others(17): Show | 21 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(18): Show |
intron_variant | MODIFIER | c.561+3575A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35686838 | ||||||
chr20:35687044
|
G | C | 1 | a0001c0001t0008g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.561+3369C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687044 | ||||||
chr20:35687052
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.561+3361C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687052 | ||||||
chr20:35687105
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.561+3308C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687105 | ||||||
chr20:35687110
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.561+3303A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687110 | ||||||
chr20:35687167
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0139a0001c0001t0001g0140others(3): Show | 7 | HG02083.hp1 HG02818.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.561+3246C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687167 | ||||||
chr20:35687263
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.561+3150C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687263 | ||||||
chr20:35687284
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.561+3129G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687284 | ||||||
chr20:35687415
|
C | CCT | 12 | a0001c0001t0001g0031a0001c0001t0001g0086a0001c0001t0001g0087others(9): Show | 12 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+2996_561+2997d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687415 | ||||||
chr20:35687511
|
A | G | 46 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(43): Show | 50 | HG01074.hp2 HG01109.hp2 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.561+2902T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687511 | ||||||
chr20:35687673
|
C | T | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.561+2740G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687673 | ||||||
chr20:35687710
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.561+2703C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35687710 | ||||||
chr20:35688105
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.561+2308C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688105 | ||||||
chr20:35688107
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.561+2306C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688107 | ||||||
chr20:35688173
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.561+2240G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688173 | ||||||
chr20:35688311
|
T | C | 4 | a0001c0001t0001g0038a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 4 | HG01081.hp1 HG02818.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2102A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688311 | ||||||
chr20:35688314
|
G | C | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.561+2099C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688314 | ||||||
chr20:35688316
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.561+2097C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688316 | ||||||
chr20:35688472
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.561+1941C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688472 | ||||||
chr20:35688739
|
GAGAGGGA others(9): Show |
G | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG02486.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.561+1658_561+1673d others(18): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688739 | ||||||
chr20:35688750
|
AGGAAAAG others(10): Show |
A | 40 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(37): Show | 45 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.561+1646_561+1662d others(19): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688750 | ||||||
chr20:35688812
|
G | C | 5 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0003g0202others(2): Show | 5 | NA18747.hp1 NA18943.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.561+1601C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688812 | ||||||
chr20:35688892
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.561+1521A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688892 | ||||||
chr20:35688989
|
G | A | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.561+1424C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35688989 | ||||||
chr20:35689017
|
C | A | 1 | a0001c0001t0002g0067 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.561+1396G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689017 | ||||||
chr20:35689674
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.561+739C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689674 | ||||||
chr20:35689756
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+657C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689756 | ||||||
chr20:35689768
|
T | A | 1 | a0001c0001t0002g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.561+645A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689768 | ||||||
chr20:35689768
|
TA | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0097a0001c0001t0001g0116others(6): Show | 9 | HG00323.hp2 HG01261.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+644delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689768 | ||||||
chr20:35689769
|
A | T | 1 | a0001c0001t0001g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.561+644T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689769 | ||||||
chr20:35689929
|
C | CA | 46 | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0102others(43): Show | 51 | HG00408.hp2 HG00597.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.561+483dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689929 | ||||||
chr20:35689929
|
C | CAA | 48 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0037others(45): Show | 53 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.561+482_561+483dup others(2): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689929 | ||||||
chr20:35689929
|
C | CAAA | 12 | a0001c0001t0001g0027a0001c0001t0001g0084a0001c0001t0001g0085others(9): Show | 12 | HG01361.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.561+481_561+483dup others(3): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689929 | ||||||
chr20:35689929
|
C | CAAAA | 6 | a0001c0001t0001g0011a0001c0001t0001g0028a0001c0001t0001g0029others(3): Show | 7 | HG01109.hp2 HG01261.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.561+480_561+483dup others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689929 | ||||||
chr20:35689996
|
G | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.561+417C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689996 | ||||||
chr20:35689998
|
G | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0105a0001c0001t0001g0115 | 3 | HG01192.hp1 HG03669.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.561+415C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35689998 | ||||||
chr20:35690043
|
G | A | 2 | a0001c0001t0002g0014a0001c0001t0002g0047 | 3 | HG00408.hp2 HG02040.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.561+370C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 5/12 | chr20 | 35690043 | ||||||
chr20:35690604
|
C | G | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | HG02280.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.409-39G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35690604 | ||||||
chr20:35690684
|
TA | T | 28 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(25): Show | 31 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.409-120delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35690684 | ||||||
chr20:35690832
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.409-267C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35690832 | ||||||
chr20:35690887
|
A | G | 1 | a0001c0001t0007g0151 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.409-322T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35690887 | ||||||
chr20:35690922
|
T | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0014a0001c0001t0002g0047others(1): Show | 7 | HG00408.hp2 HG02015.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-357A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35690922 | ||||||
chr20:35690968
|
T | C | 65 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(62): Show | 72 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.409-403A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35690968 | ||||||
chr20:35691237
|
A | G | 2 | a0001c0001t0003g0202a0001c0001t0003g0204 | 2 | NA18747.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.409-672T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691237 | ||||||
chr20:35691490
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.409-925C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691490 | ||||||
chr20:35691738
|
C | CA | 72 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(69): Show | 79 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.409-1174dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691738 | ||||||
chr20:35691738
|
C | CAA | 13 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0084others(10): Show | 13 | HG01081.hp1 HG01361.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.409-1175_409-1174d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691738 | ||||||
chr20:35691738
|
C | CAAA | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0039others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.409-1176_409-1174d others(5): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691738 | ||||||
chr20:35691738
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0008g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.409-1184_409-1174d others(13): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691738 | ||||||
chr20:35691738
|
CA | C | 23 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0108others(20): Show | 28 | HG00738.hp2 HG01167.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.409-1174delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691738 | ||||||
chr20:35691832
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.409-1267G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691832 | ||||||
chr20:35691880
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.409-1315G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35691880 | ||||||
chr20:35692020
|
T | TA | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-1456dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692020 | ||||||
chr20:35692142
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.409-1577G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692142 | ||||||
chr20:35692194
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.409-1629T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692194 | ||||||
chr20:35692387
|
A | T | 35 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(32): Show | 38 | HG00099.hp2 HG00639.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.409-1822T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692387 | ||||||
chr20:35692391
|
T | A | 3 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0076 | 3 | NA18950.hp1 NA18972.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.409-1826A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692391 | ||||||
chr20:35692399
|
TA | T | 30 | a0001c0001t0002g0048a0001c0001t0002g0073a0001c0001t0003g0010others(27): Show | 33 | HG01069.hp1 HG01074.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.409-1835delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692399 | ||||||
chr20:35692401
|
A | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.409-1836T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692401 | ||||||
chr20:35692431
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.409-1866C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692431 | ||||||
chr20:35692432
|
G | A | 11 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.409-1867C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692432 | ||||||
chr20:35692525
|
A | AC | 12 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0029others(9): Show | 13 | HG01109.hp2 HG01261.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-1961dupG | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692525 | ||||||
chr20:35692526
|
C | CCA | 3 | a0001c0001t0001g0030a0001c0001t0001g0092a0001c0001t0001g0093 | 3 | HG01361.hp2 HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.409-1962_409-1961i others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692526 | ||||||
chr20:35692527
|
T | A | 15 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0029others(12): Show | 16 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.409-1962A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692527 | ||||||
chr20:35692527
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0032 | 2 | HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.409-1962A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692527 | ||||||
chr20:35692527
|
T | TA | 35 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0022others(32): Show | 39 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.409-1963dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692527 | ||||||
chr20:35692527
|
TA | T | 40 | a0001c0001t0001g0037a0001c0001t0001g0096a0001c0001t0001g0108others(37): Show | 45 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.409-1963delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692527 | ||||||
chr20:35692527
|
TAA | T | 6 | a0001c0001t0001g0166a0001c0001t0002g0046a0001c0001t0002g0047others(3): Show | 6 | HG02040.hp1 HG02698.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.409-1964_409-1963d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692527 | ||||||
chr20:35692527
|
TAAA | T | 22 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(19): Show | 25 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.409-1965_409-1963d others(5): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692527 | ||||||
chr20:35692996
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.409-2431G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35692996 | ||||||
chr20:35693004
|
G | GA | 50 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0211others(47): Show | 57 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.409-2440dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693004 | ||||||
chr20:35693055
|
TGGGGTCC others(15): Show |
T | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2512_409-2491d others(24): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693055 | ||||||
chr20:35693087
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2522T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693087 | ||||||
chr20:35693094
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2529A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693094 | ||||||
chr20:35693098
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2533A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693098 | ||||||
chr20:35693101
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2536A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693101 | ||||||
chr20:35693108
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2543C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693108 | ||||||
chr20:35693123
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2558C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693123 | ||||||
chr20:35693136
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2571A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693136 | ||||||
chr20:35693180
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2615C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693180 | ||||||
chr20:35693216
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2651A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693216 | ||||||
chr20:35693221
|
G | T | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2656C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693221 | ||||||
chr20:35693227
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2662G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693227 | ||||||
chr20:35693247
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.409-2682G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693247 | ||||||
chr20:35693690
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.408+2687C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693690 | ||||||
chr20:35693692
|
G | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+2685C>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693692 | ||||||
chr20:35693725
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.408+2652A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693725 | ||||||
chr20:35693971
|
T | A | 28 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(25): Show | 31 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.408+2406A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35693971 | ||||||
chr20:35694018
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.408+2359G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694018 | ||||||
chr20:35694131
|
A | G | 94 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0035others(91): Show | 104 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.408+2246T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694131 | ||||||
chr20:35694143
|
C | CT | 14 | a0001c0001t0001g0083a0001c0001t0001g0096a0001c0001t0001g0097others(11): Show | 14 | HG01081.hp2 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+2233dupA | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694143 | ||||||
chr20:35694143
|
CTT | C | 26 | a0001c0001t0003g0010a0001c0001t0003g0021a0001c0001t0003g0181others(23): Show | 29 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(26): Show |
intron_variant | MODIFIER | c.408+2232_408+2233d others(4): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694143 | ||||||
chr20:35694411
|
C | G | 1 | a0001c0001t0003g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.408+1966G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694411 | ||||||
chr20:35694465
|
AT | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168 | 3 | HG02698.hp2 HG03491.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.408+1911delA | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694465 | ||||||
chr20:35694694
|
T | C | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.408+1683A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694694 | ||||||
chr20:35694714
|
C | T | 1 | a0001c0001t0008g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.408+1663G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35694714 | ||||||
chr20:35695207
|
C | A | 1 | a0001c0001t0003g0207 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.408+1170G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35695207 | ||||||
chr20:35695280
|
C | T | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.408+1097G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35695280 | ||||||
chr20:35695346
|
C | G | 1 | a0001c0001t0003g0187 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.408+1031G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35695346 | ||||||
chr20:35695704
|
A | G | 46 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(43): Show | 50 | HG01074.hp2 HG01109.hp2 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.408+673T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35695704 | ||||||
chr20:35695764
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.408+613C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35695764 | ||||||
chr20:35695845
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.408+532A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35695845 | ||||||
chr20:35696033
|
T | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 18 | HG01109.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.408+344A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35696033 | ||||||
chr20:35696123
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.408+254C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 4/12 | chr20 | 35696123 | ||||||
chr20:35696631
|
C | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-171G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696631 | ||||||
chr20:35696675
|
T | TA | 41 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(38): Show | 46 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.325-216dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696675 | ||||||
chr20:35696696
|
T | C | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.325-236A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696696 | ||||||
chr20:35696767
|
G | A | 39 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.325-307C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696767 | ||||||
chr20:35696872
|
T | G | 1 | a0001c0001t0001g0170 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.325-412A>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696872 | ||||||
chr20:35696963
|
G | A | 13 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(10): Show | 15 | HG00423.hp1 HG00544.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.325-503C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696963 | ||||||
chr20:35696991
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.325-531T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35696991 | ||||||
chr20:35697012
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.325-552T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697012 | ||||||
chr20:35697055
|
G | A | 10 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(7): Show | 11 | HG00738.hp2 HG01167.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.325-595C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697055 | ||||||
chr20:35697302
|
T | TA | 13 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(10): Show | 16 | HG01109.hp2 HG01261.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.324+381dupT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697302 | ||||||
chr20:35697302
|
T | TAAA | 24 | a0001c0001t0003g0021a0001c0001t0003g0181a0001c0001t0003g0182others(21): Show | 25 | HG01074.hp2 HG01515.hp1 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.324+379_324+381dup others(3): Show |
NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697302 | ||||||
chr20:35697302
|
TA | T | 17 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0083others(14): Show | 19 | HG00423.hp1 HG00544.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.324+381delT | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697302 | ||||||
chr20:35697372
|
A | G | 2 | a0001c0001t0003g0181a0001c0001t0003g0182 | 2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.324+312T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697372 | ||||||
chr20:35697427
|
G | A | 9 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.324+257C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697427 | ||||||
chr20:35697520
|
C | T | 113 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0023others(110): Show | 124 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.324+164G>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697520 | ||||||
chr20:35697600
|
T | A | 40 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(37): Show | 43 | HG00099.hp2 HG00639.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.324+84A>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697600 | ||||||
chr20:35697680
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG00673.hp2 | splice_region_variant&intron_variant | LOW | c.324+4A>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 3/12 | chr20 | 35697680 | ||||||
chr20:35697871
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.208-71G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/12 | chr20 | 35697871 | ||||||
chr20:35697960
|
C | G | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0210others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.208-160G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/12 | chr20 | 35697960 | ||||||
chr20:35698131
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.208-331C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/12 | chr20 | 35698131 | ||||||
chr20:35698329
|
G | T | 39 | a0001c0001t0002g0006a0001c0001t0002g0013a0001c0001t0002g0014others(36): Show | 44 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.207+152C>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/12 | chr20 | 35698329 | ||||||
chr20:35698357
|
G | A | 12 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0210others(9): Show | 14 | HG00423.hp1 HG00544.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.207+124C>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/12 | chr20 | 35698357 | ||||||
chr20:35698393
|
A | T | 13 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0038others(10): Show | 13 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.207+88T>A | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 2/12 | chr20 | 35698393 | ||||||
chr20:35698688
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0033a0001c0001t0001g0034 | 6 | HG01261.hp1 HG02293.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-98T>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 1/12 | chr20 | 35698688 | ||||||
chr20:35698734
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.98-144T>G | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 1/12 | chr20 | 35698734 | ||||||
chr20:35698867
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.98-277G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 1/12 | chr20 | 35698867 | ||||||
chr20:35698875
|
C | A | 1 | a0001c0001t0002g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.98-285G>T | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 1/12 | chr20 | 35698875 | ||||||
chr20:35698944
|
TTG | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 8 | HG01109.hp2 HG01261.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+246_97+247delCA | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 1/12 | chr20 | 35698944 | ||||||
chr20:35698974
|
C | G | 2 | a0001c0001t0005g0025a0001c0001t0005g0026 | 2 | HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.97+218G>C | NFS1 | ENSG00000244005.13 | transcript | ENST00000374092.9 | protein_coding | 1/12 | chr20 | 35698974 |