geneid | 391059 |
---|---|
ensemblid | ENSG00000156869.14 |
hgncid | 27622 |
symbol | FRRS1 |
name | ferric chelate reductase 1 |
refseq_nuc | NM_001361041.2 |
refseq_prot | NP_001347970.1 |
ensembl_nuc | ENST00000646001.2 |
ensembl_prot | ENSP00000496583.2 |
mane_status | MANE Select |
chr | chr1 |
start | 99703970 |
end | 99766635 |
strand | - |
ver | v1.2 |
region | chr1:99703970-99766635 |
region5000 | chr1:99698970-99771635 |
regionname0 | FRRS1_chr1_99703970_99766635 |
regionname5000 | FRRS1_chr1_99698970_99771635 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 592 | 256 | 52 | 54 | 106 | 4 | 38 | 78 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002 | 0/0 | 592 | 56 | 32 | 6 | 16 | 0 | 2 | 14 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0003 | 0/0 | 592 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0004 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0005 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1779 | 126 | 7 | 27 | 72 | 2 | 17 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0002 | 0/1 | 1779 | 115 | 41 | 25 | 33 | 2 | 13 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0003 | 0/0 | 1779 | 54 | 31 | 6 | 16 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0004 | 0/0 | 1779 | 15 | 4 | 2 | 1 | 0 | 8 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0005 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0006 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0007 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0008 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0009 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
c0010 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5193 | 15 | 0 | 2 | 11 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0002 | 0/0 | 5185 | 10 | 5 | 1 | 4 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0003 | 0/0 | 5190 | 8 | 1 | 0 | 7 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0004 | 0/0 | 5194 | 7 | 7 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0005 | 0/0 | 5194 | 7 | 1 | 3 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0006 | 0/0 | 5192 | 7 | 7 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0007 | 0/0 | 5188 | 7 | 0 | 4 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0008 | 0/0 | 5183 | 7 | 1 | 1 | 4 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0009 | 0/0 | 5183 | 6 | 0 | 1 | 3 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0010 | 0/0 | 5193 | 5 | 4 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0011 | 0/0 | 5190 | 5 | 0 | 0 | 5 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0012 | 0/0 | 5191 | 5 | 0 | 0 | 5 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0013 | 0/0 | 5185 | 4 | 1 | 1 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0014 | 0/0 | 5190 | 4 | 0 | 4 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0015 | 0/0 | 5184 | 4 | 3 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0016 | 0/0 | 5182 | 4 | 0 | 0 | 3 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0017 | 0/1 | 5184 | 4 | 0 | 1 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0018 | 0/0 | 5193 | 4 | 0 | 3 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0019 | 0/0 | 5192 | 4 | 0 | 0 | 1 | 0 | 3 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0020 | 0/0 | 5190 | 4 | 1 | 1 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0021 | 0/0 | 5190 | 4 | 1 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0022 | 0/0 | 5193 | 4 | 0 | 1 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0023 | 0/0 | 5190 | 4 | 0 | 0 | 3 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0024 | 0/0 | 5189 | 3 | 0 | 0 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0025 | 0/0 | 5191 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0026 | 0/0 | 5193 | 3 | 1 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0027 | 0/0 | 5184 | 3 | 0 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0028 | 0/0 | 5190 | 3 | 0 | 2 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0029 | 0/0 | 5192 | 3 | 0 | 2 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0030 | 0/0 | 5193 | 3 | 0 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0031 | 0/0 | 5191 | 3 | 0 | 0 | 2 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0032 | 0/0 | 5194 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0033 | 0/0 | 5192 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0034 | 0/0 | 5186 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0035 | 0/0 | 5194 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0036 | 0/0 | 5195 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0037 | 0/0 | 5195 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0038 | 0/0 | 5195 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0039 | 0/0 | 5193 | 2 | 0 | 0 | 0 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0040 | 0/0 | 5190 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0041 | 0/0 | 5188 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0042 | 0/0 | 5185 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0043 | 0/0 | 5178 | 2 | 0 | 2 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0044 | 0/0 | 5182 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0045 | 0/0 | 5183 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0046 | 0/0 | 5184 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0047 | 0/0 | 5193 | 2 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0048 | 0/0 | 5193 | 2 | 0 | 0 | 1 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0049 | 0/0 | 5196 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0050 | 0/0 | 5193 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0051 | 0/0 | 5195 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0052 | 0/0 | 5191 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0053 | 0/0 | 5195 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0054 | 0/0 | 5193 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0055 | 0/0 | 5188 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0056 | 0/0 | 5191 | 2 | 0 | 0 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0057 | 0/0 | 5190 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0058 | 0/0 | 5189 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0059 | 0/0 | 5191 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0060 | 0/0 | 5194 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0061 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0062 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0063 | 0/0 | 5192 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0064 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0065 | 0/0 | 5189 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0066 | 0/0 | 5189 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0067 | 0/0 | 5192 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0068 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0069 | 0/0 | 5189 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0070 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0071 | 0/0 | 5186 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0072 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0073 | 0/0 | 5208 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0074 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0075 | 0/0 | 5206 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0076 | 0/0 | 5204 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0077 | 0/0 | 5206 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0078 | 0/0 | 5207 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0079 | 0/0 | 5208 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0080 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0081 | 0/0 | 5206 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0082 | 0/0 | 5192 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0083 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0084 | 0/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0085 | 0/0 | 5207 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0086 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0087 | 0/0 | 5195 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0088 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0089 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0090 | 0/0 | 5194 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0091 | 0/0 | 5194 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0092 | 0/0 | 5192 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0093 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0094 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0095 | 0/0 | 5194 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0096 | 0/0 | 5206 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0097 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0098 | 0/0 | 5192 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0099 | 0/0 | 5182 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0100 | 0/0 | 5183 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0101 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0102 | 0/0 | 5189 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0103 | 0/0 | 5189 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0104 | 0/0 | 5194 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0105 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0106 | 0/0 | 5193 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0107 | 0/0 | 5183 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0108 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0109 | 0/0 | 5185 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0110 | 0/0 | 5188 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0111 | 0/0 | 5188 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0112 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0113 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0114 | 0/0 | 5182 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0115 | 0/0 | 5183 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0116 | 0/0 | 5183 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0117 | 0/0 | 5183 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0118 | 0/0 | 5185 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0119 | 0/0 | 5185 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0120 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0121 | 0/0 | 5177 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0122 | 0/0 | 5178 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0123 | 0/0 | 5182 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0124 | 0/0 | 5185 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0125 | 0/0 | 5182 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0126 | 0/0 | 5183 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0127 | 0/0 | 5185 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0128 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0129 | 0/0 | 5167 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0130 | 0/0 | 5188 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0131 | 0/0 | 5183 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0132 | 0/0 | 5209 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0133 | 0/0 | 5195 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0134 | 0/0 | 5196 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0135 | 0/0 | 5194 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0136 | 0/0 | 5194 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0137 | 0/0 | 5196 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0138 | 0/0 | 5196 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0139 | 1/0 | 5193 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0140 | 0/0 | 5194 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0141 | 0/0 | 5194 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0142 | 0/0 | 5195 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0143 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0144 | 0/0 | 5198 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0145 | 0/0 | 5195 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0146 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0147 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0148 | 0/0 | 5188 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0149 | 0/0 | 5189 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0150 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0151 | 0/0 | 5191 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0152 | 0/0 | 5192 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0153 | 0/0 | 5192 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0154 | 0/0 | 5194 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0155 | 0/0 | 5195 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0156 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0157 | 0/0 | 5194 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0158 | 0/0 | 5188 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0159 | 0/0 | 5189 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0160 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0161 | 0/0 | 5192 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0162 | 0/0 | 5183 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0163 | 0/0 | 5193 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0164 | 0/0 | 5182 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0165 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
t0166 | 0/0 | 5184 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0005 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1779 | 126 | 7 | 27 | 72 | 2 | 17 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002 | 0/1 | 1779 | 115 | 41 | 25 | 33 | 2 | 13 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004 | 0/0 | 1779 | 15 | 4 | 2 | 1 | 0 | 8 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003 | 0/0 | 1779 | 54 | 31 | 6 | 16 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0007 | 0/0 | 1779 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0008 | 0/0 | 1779 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0003c0005 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0003c0006 | 0/0 | 1779 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0004c0010 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0005c0009 | 0/0 | 1779 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6971 | 15 | 0 | 2 | 11 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0003 | 0/0 | 6968 | 8 | 1 | 0 | 7 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0011 | 0/0 | 6968 | 5 | 0 | 0 | 5 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0012 | 0/0 | 6969 | 5 | 0 | 0 | 5 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0018 | 0/0 | 6971 | 4 | 0 | 3 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0019 | 0/0 | 6970 | 4 | 0 | 0 | 1 | 0 | 3 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0020 | 0/0 | 6968 | 4 | 1 | 1 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0021 | 0/0 | 6968 | 4 | 1 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0022 | 0/0 | 6971 | 4 | 0 | 1 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0023 | 0/0 | 6968 | 4 | 0 | 0 | 3 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0028 | 0/0 | 6968 | 3 | 0 | 2 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0029 | 0/0 | 6970 | 3 | 0 | 2 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0030 | 0/0 | 6971 | 3 | 0 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0031 | 0/0 | 6969 | 3 | 0 | 0 | 2 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0047 | 0/0 | 6971 | 2 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0048 | 0/0 | 6971 | 2 | 0 | 0 | 1 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0049 | 0/0 | 6974 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0050 | 0/0 | 6971 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0051 | 0/0 | 6973 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0052 | 0/0 | 6969 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0053 | 0/0 | 6973 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0054 | 0/0 | 6971 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0055 | 0/0 | 6966 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0056 | 0/0 | 6969 | 2 | 0 | 0 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0057 | 0/0 | 6968 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0132 | 0/0 | 6987 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0133 | 0/0 | 6973 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0134 | 0/0 | 6974 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0135 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0136 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0137 | 0/0 | 6974 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0138 | 0/0 | 6974 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0139 | 1/0 | 6971 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0140 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0141 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0142 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0143 | 0/0 | 6973 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0144 | 0/0 | 6976 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0145 | 0/0 | 6973 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0146 | 0/0 | 6968 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0147 | 0/0 | 6973 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0148 | 0/0 | 6966 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0149 | 0/0 | 6967 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0150 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0151 | 0/0 | 6969 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0152 | 0/0 | 6970 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0153 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0154 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0155 | 0/0 | 6973 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0156 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0157 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0158 | 0/0 | 6966 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0159 | 0/0 | 6967 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0160 | 0/0 | 6968 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0161 | 0/0 | 6970 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0162 | 0/0 | 6961 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0163 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0164 | 0/0 | 6960 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0165 | 0/0 | 6962 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0001t0166 | 0/0 | 6962 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0006 | 0/0 | 6970 | 4 | 4 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0007 | 0/0 | 6966 | 7 | 0 | 4 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0008 | 0/0 | 6961 | 7 | 1 | 1 | 4 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0009 | 0/0 | 6961 | 6 | 0 | 1 | 3 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0010 | 0/0 | 6971 | 5 | 4 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0014 | 0/0 | 6968 | 4 | 0 | 4 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0015 | 0/0 | 6962 | 4 | 3 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0016 | 0/0 | 6960 | 4 | 0 | 0 | 3 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0017 | 0/1 | 6962 | 4 | 0 | 1 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0026 | 0/0 | 6971 | 3 | 1 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0027 | 0/0 | 6962 | 3 | 0 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0038 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0040 | 0/0 | 6968 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0041 | 0/0 | 6966 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0042 | 0/0 | 6963 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0043 | 0/0 | 6956 | 2 | 0 | 2 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0044 | 0/0 | 6960 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0045 | 0/0 | 6961 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0046 | 0/0 | 6962 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0081 | 0/0 | 6984 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0082 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0083 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0085 | 0/0 | 6985 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0086 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0087 | 0/0 | 6973 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0088 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0089 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0090 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0091 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0092 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0093 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0094 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0095 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0096 | 0/0 | 6984 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0097 | 0/0 | 6968 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0098 | 0/0 | 6970 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0099 | 0/0 | 6960 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0100 | 0/0 | 6961 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0101 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0102 | 0/0 | 6967 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0103 | 0/0 | 6967 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0104 | 0/0 | 6972 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0105 | 0/0 | 6968 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0106 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0107 | 0/0 | 6961 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0108 | 0/0 | 6962 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0109 | 0/0 | 6963 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0110 | 0/0 | 6966 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0111 | 0/0 | 6966 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0112 | 0/0 | 6968 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0113 | 0/0 | 6952 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0114 | 0/0 | 6960 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0115 | 0/0 | 6961 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0116 | 0/0 | 6961 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0117 | 0/0 | 6961 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0118 | 0/0 | 6963 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0119 | 0/0 | 6963 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0120 | 0/0 | 6952 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0121 | 0/0 | 6955 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0122 | 0/0 | 6956 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0123 | 0/0 | 6960 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0124 | 0/0 | 6963 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0125 | 0/0 | 6960 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0126 | 0/0 | 6961 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0127 | 0/0 | 6963 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0128 | 0/0 | 6962 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0129 | 0/0 | 6945 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0002t0130 | 0/0 | 6966 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0006 | 0/0 | 6970 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0038 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0039 | 0/0 | 6971 | 2 | 0 | 0 | 0 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0073 | 0/0 | 6986 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0074 | 0/0 | 6991 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0075 | 0/0 | 6984 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0076 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0077 | 0/0 | 6984 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0078 | 0/0 | 6985 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0079 | 0/0 | 6986 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0080 | 0/0 | 6991 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0001c0004t0084 | 0/0 | 6971 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0002 | 0/0 | 6963 | 9 | 5 | 1 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0004 | 0/0 | 6972 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0005 | 0/0 | 6972 | 7 | 1 | 3 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0013 | 0/0 | 6963 | 4 | 1 | 1 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0024 | 0/0 | 6967 | 3 | 0 | 0 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0025 | 0/0 | 6969 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0032 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0033 | 0/0 | 6970 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0034 | 0/0 | 6964 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0035 | 0/0 | 6972 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0036 | 0/0 | 6973 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0037 | 0/0 | 6973 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0058 | 0/0 | 6967 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0059 | 0/0 | 6969 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0060 | 0/0 | 6972 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0061 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0062 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0063 | 0/0 | 6970 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0064 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0065 | 0/0 | 6967 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0066 | 0/0 | 6967 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0067 | 0/0 | 6970 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0068 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0069 | 0/0 | 6967 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0070 | 0/0 | 6973 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0003t0071 | 0/0 | 6964 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0007t0072 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0002c0008t0131 | 0/0 | 6961 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0003c0005t0004 | 0/0 | 6972 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0003c0006t0004 | 0/0 | 6972 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0004c0010t0032 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
a0005c0009t0002 | 0/0 | 6963 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | copy fasta | chr1 | 99698970 | 99771635 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0011g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0012g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0012g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0012g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0018g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0018g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0018g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0018g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0019g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0019g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0019g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0019g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0020g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0020g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0020g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0021g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0021g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0021g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0021g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0022g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0022g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0022g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0022g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0023g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0023g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0023g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0028g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0028g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0028g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0029g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0029g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0029g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0030g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0030g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0030g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0031g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0031g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0031g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0047g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0047g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0048g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0048g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0049g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0049g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0050g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0050g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0051g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0051g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0052g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0052g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0053g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0053g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0054g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0054g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0055g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0055g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0056g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0056g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0057g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0057g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0132g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0133g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0134g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0135g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0136g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0137g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0138g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0139g0210 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0140g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0141g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0142g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0143g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0144g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0145g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0146g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0147g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0148g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0149g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0150g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0151g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0152g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0153g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0154g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0155g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0156g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0157g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0158g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0159g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0160g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0161g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0162g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0163g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0164g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0165g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0001t0166g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0007g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0008g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0008g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0009g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0009g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0010g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0010g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0014g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0014g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0014g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0015g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0015g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0016g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0016g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0016g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0017g0005 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0017g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0017g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0026g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0026g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0026g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0027g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0027g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0027g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0038g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0040g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0041g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0041g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0042g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0042g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0043g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0043g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0044g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0045g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0045g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0046g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0046g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0081g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0082g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0083g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0085g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0086g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0087g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0088g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0089g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0090g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0091g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0092g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0093g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0094g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0095g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0096g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0097g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0098g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0099g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0100g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0101g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0102g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0103g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0104g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0105g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0106g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0107g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0108g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0109g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0110g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0111g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0112g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0113g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0114g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0115g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0116g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0117g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0118g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0119g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0120g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0121g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0122g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0123g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0124g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0125g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0126g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0127g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0128g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0129g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0002t0130g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0038g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0039g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0039g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0073g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0074g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0075g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0076g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0077g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0078g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0079g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0080g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0001c0004t0084g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0013g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0013g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0013g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0024g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0024g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0024g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0025g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0025g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0032g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0033g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0033g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0034g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0034g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0035g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0035g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0036g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0036g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0037g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0037g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0058g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0059g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0060g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0061g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0062g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0063g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0064g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0065g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0066g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0067g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0068g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0069g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0070g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0003t0071g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0007t0072g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0002c0008t0131g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0003c0005t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0003c0005t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0003c0006t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0003c0006t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0004c0010t0032g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
a0005c0009t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0057 | g0216 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00408 | hp2 | a0001 | c0001 | t0056 | g0173 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00423 | hp1 | a0001 | c0001 | t0052 | g0190 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00423 | hp2 | a0001 | c0002 | t0042 | g0083 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00609 | hp2 | a0001 | c0001 | t0052 | g0199 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00621 | hp1 | a0001 | c0002 | t0008 | g0056 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00621 | hp2 | a0001 | c0002 | t0009 | g0088 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00639 | hp1 | a0001 | c0001 | t0152 | g0180 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00639 | hp2 | a0001 | c0002 | t0007 | g0071 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00642 | hp1 | a0001 | c0001 | t0136 | g0196 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00642 | hp2 | a0001 | c0001 | t0047 | g0177 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00673 | hp1 | a0001 | c0002 | t0009 | g0068 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00673 | hp2 | a0002 | c0003 | t0024 | g0259 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00735 | hp1 | a0002 | c0003 | t0013 | g0015 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00735 | hp2 | a0002 | c0003 | t0005 | g0299 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00738 | hp1 | a0001 | c0002 | t0046 | g0069 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00738 | hp2 | a0001 | c0001 | t0030 | g0169 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00741 | hp1 | a0001 | c0002 | t0043 | g0064 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG00741 | hp2 | a0001 | c0001 | t0021 | g0133 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01069 | hp1 | a0002 | c0003 | t0035 | g0063 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01069 | hp2 | a0001 | c0001 | t0028 | g0158 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01074 | hp1 | a0002 | c0003 | t0005 | g0271 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01081 | hp1 | a0001 | c0004 | t0077 | g0024 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01081 | hp2 | a0001 | c0001 | t0145 | g0132 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01106 | hp1 | a0001 | c0002 | t0027 | g0240 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01106 | hp2 | a0001 | c0001 | t0021 | g0129 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01109 | hp1 | a0001 | c0001 | t0135 | g0130 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01109 | hp2 | a0002 | c0003 | t0002 | g0289 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01167 | hp1 | a0001 | c0001 | t0020 | g0120 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01167 | hp2 | a0001 | c0002 | t0087 | g0117 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01192 | hp1 | a0001 | c0004 | t0078 | g0025 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01192 | hp2 | a0001 | c0002 | t0014 | g0256 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01255 | hp1 | a0001 | c0001 | t0029 | g0135 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01255 | hp2 | a0001 | c0002 | t0014 | g0261 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01256 | hp1 | a0001 | c0001 | t0030 | g0168 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01256 | hp2 | a0001 | c0002 | t0095 | g0237 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01257 | hp1 | a0001 | c0002 | t0027 | g0243 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01257 | hp2 | a0001 | c0001 | t0018 | g0128 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01261 | hp1 | a0001 | c0002 | t0027 | g0241 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01261 | hp2 | a0001 | c0002 | t0007 | g0075 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01346 | hp1 | a0001 | c0002 | t0009 | g0060 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01346 | hp2 | a0001 | c0001 | t0134 | g0142 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01361 | hp1 | a0001 | c0002 | t0043 | g0065 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01361 | hp2 | a0001 | c0001 | t0161 | g0157 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01433 | hp1 | a0001 | c0001 | t0151 | g0148 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01433 | hp2 | a0001 | c0001 | t0140 | g0167 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01496 | hp2 | a0001 | c0001 | t0029 | g0149 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0119 | EUR | IBS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01515 | hp2 | a0001 | c0002 | t0116 | g0067 | EUR | IBS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01884 | hp1 | a0001 | c0004 | t0006 | g0034 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01884 | hp2 | a0001 | c0002 | t0085 | g0278 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01891 | hp1 | a0002 | c0003 | t0033 | g0290 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0251 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01928 | hp1 | a0001 | c0002 | t0014 | g0012 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01928 | hp2 | a0001 | c0002 | t0045 | g0044 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01934 | hp1 | a0001 | c0001 | t0030 | g0207 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01934 | hp2 | a0001 | c0002 | t0103 | g0263 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01943 | hp1 | a0001 | c0002 | t0041 | g0076 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01943 | hp2 | a0001 | c0001 | t0018 | g0140 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01978 | hp1 | a0002 | c0003 | t0005 | g0270 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01978 | hp2 | a0001 | c0001 | t0028 | g0202 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01981 | hp1 | a0001 | c0002 | t0111 | g0257 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01981 | hp2 | a0001 | c0001 | t0022 | g0166 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01993 | hp1 | a0001 | c0002 | t0091 | g0255 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01993 | hp2 | a0001 | c0002 | t0007 | g0080 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02015 | hp1 | a0001 | c0001 | t0020 | g0185 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02027 | hp1 | a0001 | c0002 | t0009 | g0066 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02027 | hp2 | a0001 | c0001 | t0149 | g0232 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02055 | hp1 | a0001 | c0002 | t0122 | g0100 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02055 | hp2 | a0001 | c0002 | t0101 | g0050 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02056 | hp1 | a0001 | c0001 | t0055 | g0188 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02056 | hp2 | a0001 | c0001 | t0012 | g0221 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02080 | hp1 | a0002 | c0003 | t0066 | g0254 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02080 | hp2 | a0001 | c0001 | t0137 | g0212 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02132 | hp1 | a0001 | c0001 | t0023 | g0010 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02132 | hp2 | a0001 | c0002 | t0008 | g0003 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02135 | hp1 | a0001 | c0001 | t0053 | g0152 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02135 | hp2 | a0001 | c0002 | t0041 | g0085 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02145 | hp1 | a0002 | c0003 | t0061 | g0110 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02145 | hp2 | a0001 | c0002 | t0098 | g0280 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02148 | hp1 | a0001 | c0002 | t0017 | g0061 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02148 | hp2 | a0001 | c0002 | t0097 | g0253 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02155 | hp1 | a0001 | c0001 | t0011 | g0011 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02165 | hp1 | a0001 | c0001 | t0023 | g0010 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02165 | hp2 | a0001 | c0001 | t0147 | g0121 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02257 | hp1 | a0001 | c0002 | t0044 | g0014 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02257 | hp2 | a0002 | c0003 | t0037 | g0091 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02258 | hp1 | a0002 | c0003 | t0036 | g0286 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02258 | hp2 | a0001 | c0002 | t0015 | g0052 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02280 | hp1 | a0001 | c0001 | t0049 | g0208 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02280 | hp2 | a0002 | c0003 | t0036 | g0285 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02293 | hp1 | a0001 | c0001 | t0018 | g0139 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02293 | hp2 | a0001 | c0002 | t0014 | g0012 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02300 | hp1 | a0001 | c0002 | t0007 | g0242 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02300 | hp2 | a0001 | c0001 | t0164 | g0151 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02451 | hp1 | a0001 | c0002 | t0121 | g0099 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02451 | hp2 | a0003 | c0005 | t0004 | g0037 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02572 | hp1 | a0002 | c0003 | t0005 | g0266 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02572 | hp2 | a0001 | c0002 | t0107 | g0113 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02602 | hp1 | a0001 | c0001 | t0019 | g0187 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02602 | hp2 | a0001 | c0001 | t0019 | g0160 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02622 | hp1 | a0002 | c0003 | t0004 | g0103 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02622 | hp2 | a0001 | c0002 | t0010 | g0001 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02630 | hp1 | a0001 | c0001 | t0020 | g0205 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02630 | hp2 | a0001 | c0002 | t0008 | g0090 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02647 | hp1 | a0001 | c0002 | t0114 | g0279 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02647 | hp2 | a0001 | c0002 | t0042 | g0049 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02683 | hp1 | a0001 | c0004 | t0039 | g0026 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02683 | hp2 | a0001 | c0002 | t0008 | g0039 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02698 | hp1 | a0001 | c0001 | t0023 | g0193 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02698 | hp2 | a0001 | c0002 | t0119 | g0017 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02717 | hp1 | a0002 | c0003 | t0002 | g0252 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02717 | hp2 | a0001 | c0002 | t0115 | g0112 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02735 | hp1 | a0001 | c0002 | t0017 | g0005 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02735 | hp2 | a0001 | c0001 | t0132 | g0136 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02738 | hp1 | a0001 | c0001 | t0056 | g0209 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02738 | hp2 | a0001 | c0002 | t0109 | g0247 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02809 | hp1 | a0002 | c0003 | t0068 | g0096 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02809 | hp2 | a0002 | c0003 | t0004 | g0008 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02886 | hp1 | a0002 | c0003 | t0062 | g0095 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02886 | hp2 | a0001 | c0001 | t0142 | g0172 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02895 | hp1 | a0002 | c0003 | t0059 | g0297 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02895 | hp2 | a0001 | c0002 | t0010 | g0001 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02896 | hp1 | a0002 | c0003 | t0025 | g0007 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02896 | hp2 | a0002 | c0003 | t0034 | g0287 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0042 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02897 | hp2 | a0002 | c0003 | t0025 | g0007 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02922 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02922 | hp2 | a0001 | c0004 | t0006 | g0035 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02965 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02965 | hp2 | a0001 | c0002 | t0006 | g0109 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02970 | hp1 | a0002 | c0003 | t0025 | g0104 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02970 | hp2 | a0003 | c0006 | t0004 | g0115 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0108 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02976 | hp2 | a0003 | c0005 | t0004 | g0036 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03017 | hp2 | a0001 | c0001 | t0144 | g0144 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03041 | hp1 | a0001 | c0002 | t0113 | g0265 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03041 | hp2 | a0003 | c0006 | t0004 | g0114 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03098 | hp1 | a0002 | c0003 | t0071 | g0292 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03098 | hp2 | a0001 | c0002 | t0089 | g0093 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03130 | hp1 | a0001 | c0001 | t0049 | g0195 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03130 | hp2 | a0001 | c0002 | t0026 | g0282 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03195 | hp1 | a0001 | c0002 | t0126 | g0269 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03195 | hp2 | a0002 | c0003 | t0060 | g0111 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03209 | hp1 | a0001 | c0002 | t0110 | g0276 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03209 | hp2 | a0001 | c0002 | t0006 | g0009 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03225 | hp1 | a0001 | c0002 | t0120 | g0301 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03225 | hp2 | a0001 | c0002 | t0010 | g0001 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03239 | hp1 | a0001 | c0001 | t0166 | g0137 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03239 | hp2 | a0001 | c0001 | t0138 | g0098 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03453 | hp1 | a0001 | c0002 | t0088 | g0284 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03453 | hp2 | a0002 | c0003 | t0067 | g0107 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03486 | hp1 | a0001 | c0002 | t0038 | g0062 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03486 | hp2 | a0001 | c0002 | t0083 | g0268 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03490 | hp1 | a0001 | c0002 | t0010 | g0040 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03490 | hp2 | a0001 | c0001 | t0019 | g0165 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03491 | hp1 | a0001 | c0004 | t0074 | g0030 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03491 | hp2 | a0001 | c0002 | t0009 | g0086 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03516 | hp1 | a0002 | c0003 | t0064 | g0239 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03516 | hp2 | a0001 | c0004 | t0006 | g0033 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03540 | hp1 | a0002 | c0007 | t0072 | g0038 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03540 | hp2 | a0001 | c0002 | t0015 | g0058 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03579 | hp1 | a0002 | c0003 | t0004 | g0008 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03579 | hp2 | a0002 | c0003 | t0034 | g0288 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03669 | hp1 | a0001 | c0002 | t0125 | g0047 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03669 | hp2 | a0002 | c0008 | t0131 | g0178 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03688 | hp1 | a0001 | c0001 | t0047 | g0145 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03688 | hp2 | a0001 | c0001 | t0018 | g0143 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03704 | hp1 | a0002 | c0003 | t0013 | g0262 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03704 | hp2 | a0001 | c0001 | t0146 | g0156 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03710 | hp1 | a0001 | c0004 | t0079 | g0028 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03710 | hp2 | a0001 | c0002 | t0016 | g0004 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03927 | hp1 | a0001 | c0001 | t0031 | g0127 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03927 | hp2 | a0001 | c0002 | t0081 | g0116 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04115 | hp2 | a0001 | c0004 | t0076 | g0032 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04184 | hp1 | a0001 | c0004 | t0084 | g0018 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04184 | hp2 | a0001 | c0002 | t0124 | g0246 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04199 | hp1 | a0001 | c0002 | t0015 | g0081 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04199 | hp2 | a0001 | c0002 | t0112 | g0244 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04204 | hp1 | a0001 | c0001 | t0133 | g0141 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04204 | hp2 | a0001 | c0004 | t0073 | g0027 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04228 | hp1 | a0001 | c0004 | t0080 | g0029 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG04228 | hp2 | a0001 | c0001 | t0160 | g0186 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18522 | hp1 | a0002 | c0003 | t0033 | g0236 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18522 | hp2 | a0001 | c0002 | t0099 | g0106 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18612 | hp1 | a0001 | c0001 | t0011 | g0211 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18612 | hp2 | a0001 | c0002 | t0040 | g0006 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18906 | hp1 | a0001 | c0002 | t0108 | g0283 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18906 | hp2 | a0001 | c0002 | t0006 | g0009 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18942 | hp1 | a0001 | c0002 | t0026 | g0048 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18942 | hp2 | a0001 | c0001 | t0048 | g0191 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18944 | hp1 | a0001 | c0001 | t0057 | g0224 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18944 | hp2 | a0001 | c0002 | t0008 | g0057 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18947 | hp1 | a0002 | c0003 | t0070 | g0294 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18947 | hp2 | a0001 | c0002 | t0092 | g0059 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18948 | hp1 | a0002 | c0003 | t0013 | g0238 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18948 | hp2 | a0001 | c0002 | t0040 | g0006 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18951 | hp1 | a0001 | c0002 | t0117 | g0045 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18952 | hp1 | a0001 | c0002 | t0082 | g0077 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18952 | hp2 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18953 | hp1 | a0001 | c0002 | t0093 | g0072 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18953 | hp2 | a0001 | c0001 | t0053 | g0171 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18959 | hp1 | a0001 | c0001 | t0154 | g0150 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18959 | hp2 | a0001 | c0002 | t0127 | g0043 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18962 | hp1 | a0002 | c0003 | t0024 | g0275 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18962 | hp2 | a0001 | c0001 | t0148 | g0197 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18964 | hp1 | a0001 | c0001 | t0156 | g0220 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18964 | hp2 | a0001 | c0002 | t0007 | g0078 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18967 | hp1 | a0001 | c0001 | t0019 | g0162 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18967 | hp2 | a0004 | c0010 | t0032 | g0272 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18968 | hp1 | a0001 | c0002 | t0045 | g0054 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18968 | hp2 | a0001 | c0001 | t0165 | g0175 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18970 | hp1 | a0001 | c0001 | t0022 | g0181 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18970 | hp2 | a0002 | c0003 | t0002 | g0264 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18974 | hp1 | a0001 | c0002 | t0007 | g0046 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18975 | hp1 | a0001 | c0001 | t0157 | g0235 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18975 | hp2 | a0001 | c0001 | t0055 | g0227 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18978 | hp1 | a0002 | c0003 | t0037 | g0296 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18978 | hp2 | a0001 | c0002 | t0016 | g0070 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18980 | hp1 | a0002 | c0003 | t0005 | g0274 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18980 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18982 | hp2 | a0002 | c0003 | t0024 | g0249 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18983 | hp1 | a0001 | c0001 | t0028 | g0192 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18983 | hp2 | a0002 | c0003 | t0035 | g0293 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18984 | hp1 | a0002 | c0003 | t0002 | g0273 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18984 | hp2 | a0001 | c0001 | t0163 | g0182 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18986 | hp1 | a0001 | c0001 | t0162 | g0183 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18986 | hp2 | a0001 | c0001 | t0011 | g0213 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18987 | hp2 | a0001 | c0004 | t0075 | g0031 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18993 | hp1 | a0002 | c0003 | t0002 | g0248 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18993 | hp2 | a0001 | c0001 | t0050 | g0154 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18998 | hp1 | a0002 | c0003 | t0005 | g0250 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18998 | hp2 | a0001 | c0001 | t0020 | g0194 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19000 | hp1 | a0002 | c0003 | t0032 | g0298 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19000 | hp2 | a0001 | c0002 | t0128 | g0089 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19002 | hp1 | a0001 | c0001 | t0023 | g0170 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19002 | hp2 | a0001 | c0002 | t0102 | g0020 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19003 | hp1 | a0001 | c0001 | t0054 | g0124 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19003 | hp2 | a0001 | c0001 | t0022 | g0164 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19004 | hp1 | a0001 | c0001 | t0011 | g0217 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19004 | hp2 | a0002 | c0003 | t0058 | g0260 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19005 | hp1 | a0001 | c0001 | t0155 | g0155 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19005 | hp2 | a0001 | c0001 | t0012 | g0219 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19007 | hp1 | a0001 | c0001 | t0153 | g0146 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19007 | hp2 | a0001 | c0002 | t0017 | g0094 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19010 | hp1 | a0001 | c0001 | t0143 | g0122 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19010 | hp2 | a0001 | c0001 | t0051 | g0200 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19030 | hp1 | a0001 | c0002 | t0118 | g0245 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19030 | hp2 | a0001 | c0002 | t0104 | g0051 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19043 | hp1 | a0001 | c0002 | t0123 | g0118 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19043 | hp2 | a0002 | c0003 | t0069 | g0102 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19057 | hp1 | a0001 | c0001 | t0150 | g0097 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19057 | hp2 | a0001 | c0001 | t0031 | g0163 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19062 | hp1 | a0001 | c0001 | t0012 | g0123 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19062 | hp2 | a0001 | c0001 | t0022 | g0161 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19063 | hp1 | a0001 | c0001 | t0054 | g0233 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19063 | hp2 | a0001 | c0002 | t0026 | g0079 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19066 | hp1 | a0001 | c0002 | t0086 | g0074 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19068 | hp1 | a0005 | c0009 | t0002 | g0258 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19070 | hp1 | a0001 | c0002 | t0046 | g0055 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19070 | hp2 | a0001 | c0001 | t0031 | g0125 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19072 | hp1 | a0001 | c0002 | t0129 | g0021 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19072 | hp2 | a0001 | c0001 | t0050 | g0153 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19079 | hp1 | a0001 | c0001 | t0159 | g0226 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19079 | hp2 | a0001 | c0002 | t0007 | g0073 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19080 | hp2 | a0002 | c0003 | t0005 | g0295 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19082 | hp1 | a0001 | c0002 | t0090 | g0092 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19082 | hp2 | a0001 | c0001 | t0141 | g0225 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19083 | hp1 | a0001 | c0001 | t0012 | g0215 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19083 | hp2 | a0001 | c0002 | t0008 | g0082 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19089 | hp1 | a0001 | c0001 | t0158 | g0201 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19089 | hp2 | a0001 | c0002 | t0130 | g0019 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19091 | hp1 | a0001 | c0002 | t0016 | g0004 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19240 | hp1 | a0002 | c0003 | t0063 | g0291 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA19240 | hp2 | a0002 | c0003 | t0065 | g0101 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA20752 | hp1 | a0001 | c0001 | t0048 | g0198 | EUR | TSI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA20752 | hp2 | a0001 | c0002 | t0100 | g0041 | EUR | TSI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA20905 | hp1 | a0001 | c0002 | t0009 | g0087 | SAS | GIH | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA20905 | hp2 | a0001 | c0004 | t0039 | g0023 | SAS | GIH | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01123 | hp1 | a0001 | c0002 | t0008 | g0003 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG01123 | hp2 | a0001 | c0001 | t0021 | g0131 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02109 | hp1 | a0002 | c0003 | t0013 | g0015 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02109 | hp2 | a0001 | c0002 | t0094 | g0300 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02486 | hp1 | a0001 | c0002 | t0096 | g0281 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02486 | hp2 | a0001 | c0002 | t0105 | g0022 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02559 | hp1 | a0001 | c0001 | t0051 | g0204 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG02559 | hp2 | a0001 | c0002 | t0015 | g0053 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03471 | hp1 | a0001 | c0004 | t0038 | g0016 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
HG03471 | hp2 | a0001 | c0002 | t0044 | g0014 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18955 | hp1 | a0001 | c0002 | t0016 | g0084 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0228 | AFR | USA | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA20300 | hp2 | a0001 | c0002 | t0106 | g0277 | AFR | USA | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA21309 | hp1 | a0002 | c0003 | t0002 | g0267 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
NA21309 | hp2 | a0001 | c0001 | t0021 | g0231 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0017 | g0005 | REF | REF | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0139 | g0210 | REF | REF | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99709114
|
C | T | 4 | a0002a0003a0004others(1): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
missense_variant | MODERATE | c.1693G>A | p.Ala565Thr | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1827/6971 | 1693/1779 | 565/592 | chr1 | 99709114 | ||
chr1:99710875
|
C | T | 1 | a0005 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1555G>A | p.Gly519Arg | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/17 | 1689/6971 | 1555/1779 | 519/592 | chr1 | 99710875 | ||
chr1:99712143
|
G | A | 1 | a0003 | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.1442C>T | p.Thr481Ile | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/17 | 1576/6971 | 1442/1779 | 481/592 | chr1 | 99712143 | ||
chr1:99740911
|
T | G | 1 | a0004 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.458A>C | p.Tyr153Ser | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/17 | 592/6971 | 458/1779 | 153/592 | chr1 | 99740911 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99738092
|
C | T | 8 | a0001c0002a0001c0004a0002c0003others(5): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
synonymous_variant | LOW | c.753G>A | p.Gln251Gln | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/17 | 887/6971 | 753/1779 | 251/592 | chr1 | 99738092 | ||
chr1:99738137
|
G | A | 8 | a0001c0002a0001c0004a0002c0003others(5): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
synonymous_variant | LOW | c.708C>T | p.Ser236Ser | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/17 | 842/6971 | 708/1779 | 236/592 | chr1 | 99738137 | ||
chr1:99742262
|
C | G | 3 | a0001c0004a0002c0007a0003c0005 | 18 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
synonymous_variant | LOW | c.345G>C | p.Val115Val | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/17 | 479/6971 | 345/1779 | 115/592 | chr1 | 99742262 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99704004
|
T | C | 1 | a0001c0002t0105 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5024A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 5024 | chr1 | 99704004 | |||||
chr1:99704546
|
T | C | 17 | a0001c0002t0088a0002c0003t0002a0002c0003t0005others(14): Show | 40 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4482A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 4482 | chr1 | 99704546 | |||||
chr1:99704946
|
T | C | 80 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(77): Show | 141 | HG00408.hp1 HG00642.hp1 HG00673.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*4082A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 4082 | chr1 | 99704946 | |||||
chr1:99705017
|
C | T | 1 | a0002c0003t0063 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4011G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 4011 | chr1 | 99705017 | |||||
chr1:99705083
|
G | A | 6 | a0001c0002t0085a0001c0002t0089a0001c0002t0094others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3945C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3945 | chr1 | 99705083 | |||||
chr1:99705424
|
C | T | 2 | a0001c0001t0135a0001c0001t0145 | 2 | HG01081.hp2 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3604G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3604 | chr1 | 99705424 | |||||
chr1:99705695
|
T | A | 2 | a0001c0002t0121a0001c0002t0122 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3333A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3333 | chr1 | 99705695 | |||||
chr1:99705854
|
A | G | 45 | a0001c0001t0133a0001c0001t0134a0001c0001t0144others(42): Show | 75 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3174T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3174 | chr1 | 99705854 | |||||
chr1:99706170
|
T | C | 4 | a0001c0002t0085a0001c0002t0089a0001c0002t0094others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2858A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2858 | chr1 | 99706170 | |||||
chr1:99706212
|
T | A | 4 | a0001c0002t0085a0001c0002t0089a0001c0002t0094others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2816A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2816 | chr1 | 99706212 | |||||
chr1:99706223
|
C | CA | 25 | a0001c0002t0085a0001c0002t0089a0001c0002t0094others(22): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | |||||
chr1:99706223
|
C | CAA | 12 | a0001c0002t0088a0002c0003t0033a0002c0003t0034others(9): Show | 16 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | |||||
chr1:99706223
|
C | CAAA | 5 | a0001c0001t0133a0001c0001t0134a0001c0002t0081others(2): Show | 5 | HG01167.hp2 HG01346.hp2 HG03927.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | |||||
chr1:99706223
|
C | CAAAA | 3 | a0001c0001t0144a0001c0002t0101a0001c0002t0104 | 3 | HG02055.hp2 HG03017.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insTTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | |||||
chr1:99706224
|
C | A | 45 | a0001c0001t0133a0001c0001t0134a0001c0001t0144others(42): Show | 75 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2804G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706224 | |||||
chr1:99706269
|
G | A | 1 | a0001c0002t0106 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2759C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2759 | chr1 | 99706269 | |||||
chr1:99706408
|
CA | C | 39 | a0001c0001t0133a0001c0001t0134a0001c0001t0144others(36): Show | 69 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2619delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2619 | chr1 | 99706408 | |||||
chr1:99706542
|
G | A | 1 | a0001c0002t0105 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2486C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2486 | chr1 | 99706542 | |||||
chr1:99706750
|
C | T | 1 | a0001c0002t0088 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2278G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2278 | chr1 | 99706750 | |||||
chr1:99706891
|
C | CA | 44 | a0001c0001t0142a0001c0001t0156a0001c0002t0085others(41): Show | 74 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2136dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2136 | chr1 | 99706891 | |||||
chr1:99706891
|
CA | C | 7 | a0001c0001t0150a0001c0002t0006a0001c0002t0038others(4): Show | 12 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2136delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2136 | chr1 | 99706891 | |||||
chr1:99706944
|
A | G | 2 | a0001c0002t0081a0001c0002t0087 | 2 | HG01167.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2084 | chr1 | 99706944 | |||||
chr1:99707196
|
G | C | 1 | a0001c0001t0050 | 2 | NA18993.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1832 | chr1 | 99707196 | |||||
chr1:99707345
|
G | A | 18 | a0001c0001t0166a0001c0002t0008a0001c0002t0009others(15): Show | 46 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1683C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1683 | chr1 | 99707345 | |||||
chr1:99707678
|
T | C | 1 | a0001c0002t0116 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1350A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1350 | chr1 | 99707678 | |||||
chr1:99707742
|
C | T | 2 | a0001c0002t0113a0001c0002t0120 | 2 | HG03041.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1286G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1286 | chr1 | 99707742 | |||||
chr1:99707973
|
G | A | 32 | a0002c0003t0002a0002c0003t0004a0002c0003t0005others(29): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1055 | chr1 | 99707973 | |||||
chr1:99708174
|
T | C | 12 | a0001c0001t0018a0001c0001t0021a0001c0001t0029others(9): Show | 20 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*854A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 854 | chr1 | 99708174 | |||||
chr1:99708368
|
G | A | 1 | a0001c0002t0112 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 660 | chr1 | 99708368 | |||||
chr1:99708375
|
A | G | 32 | a0002c0003t0002a0002c0003t0004a0002c0003t0005others(29): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*653T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 653 | chr1 | 99708375 | |||||
chr1:99708441
|
A | T | 2 | a0001c0002t0081a0001c0002t0087 | 2 | HG01167.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 587 | chr1 | 99708441 | |||||
chr1:99708461
|
G | T | 1 | a0002c0003t0071 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 567 | chr1 | 99708461 | |||||
chr1:99708530
|
A | G | 171 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(168): Show | 317 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*498T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 498 | chr1 | 99708530 | |||||
chr1:99708549
|
G | A | 1 | a0001c0004t0084 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 479 | chr1 | 99708549 | |||||
chr1:99708597
|
C | CA | 8 | a0001c0001t0140a0001c0001t0141a0001c0001t0142others(5): Show | 8 | HG01256.hp2 HG01433.hp2 HG01993.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*430dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 430 | chr1 | 99708597 | |||||
chr1:99708597
|
C | CAA | 7 | a0001c0001t0051a0001c0001t0053a0001c0001t0143others(4): Show | 9 | HG01081.hp2 HG02135.hp1 HG02165.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*429_*430dupTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 430 | chr1 | 99708597 | |||||
chr1:99708597
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0096 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420_*430dupTTTTTT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 430 | chr1 | 99708597 | |||||
chr1:99708597
|
CAAA | C | 7 | a0001c0001t0028a0001c0002t0086a0002c0003t0025others(4): Show | 12 | HG01069.hp2 HG01891.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*428_*430delTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 428 | chr1 | 99708597 | |||||
chr1:99708597
|
CAAAAA | C | 5 | a0002c0003t0024a0002c0003t0058a0002c0003t0065others(2): Show | 7 | HG00673.hp2 HG02080.hp1 NA18962.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*426_*430delTTTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 426 | chr1 | 99708597 | |||||
chr1:99708597
|
CAAAAAAA others(2): Show |
C | 2 | a0002c0003t0013a0002c0003t0034 | 6 | HG00735.hp1 HG02109.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*430delTTTTTT others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 422 | chr1 | 99708597 | |||||
chr1:99708616
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0113 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*411delATATAT others(13): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708616 | |||||
chr1:99708618
|
AAAAAAAA others(2): Show |
A | 3 | a0002c0003t0002a0002c0003t0071a0005c0009t0002 | 11 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*401_*409delATTTTT others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708618 | |||||
chr1:99708618
|
AAAAAAAA others(4): Show |
A | 1 | a0002c0008t0131 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399_*409delATATTT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708618 | |||||
chr1:99708618
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0120 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*409delATATAT others(13): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708618 | |||||
chr1:99708619
|
A | T | 1 | a0002c0007t0072 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 409 | chr1 | 99708619 | |||||
chr1:99708620
|
AAAAAAAT others(4): Show |
A | 1 | a0001c0002t0099 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397_*407delATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708620 | |||||
chr1:99708620
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0002t0043 | 2 | HG00741.hp1 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*407delATATAT others(9): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708620 | |||||
chr1:99708620
|
AAAAAAAT others(10): Show |
A | 1 | a0001c0002t0121 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*407delATATAT others(11): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708620 | |||||
chr1:99708621
|
A | T | 8 | a0002c0003t0032a0002c0003t0058a0002c0003t0059others(5): Show | 8 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*407T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 407 | chr1 | 99708621 | |||||
chr1:99708621
|
AAAAAATA others(3): Show |
A | 1 | a0001c0002t0100 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397_*406delATATAT others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708621 | |||||
chr1:99708621
|
AAAAAATA others(9): Show |
A | 1 | a0001c0002t0122 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*406delATATAT others(10): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708621 | |||||
chr1:99708623
|
A | T | 13 | a0001c0001t0047a0002c0003t0024a0002c0003t0032others(10): Show | 17 | HG00642.hp2 HG00673.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*405T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 405 | chr1 | 99708623 | |||||
chr1:99708623
|
AAAATATA others(3): Show |
A | 1 | a0001c0002t0107 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395_*404delATATAT others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 395 | chr1 | 99708623 | |||||
chr1:99708623
|
AAAATATA others(19): Show |
A | 1 | a0001c0002t0129 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379_*404delATATAT others(20): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 379 | chr1 | 99708623 | |||||
chr1:99708624
|
AAATAT | A | 2 | a0001c0001t0148a0001c0002t0007 | 8 | HG00639.hp2 HG01261.hp2 HG01993.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*403delATATT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708624 | |||||
chr1:99708624
|
AAATATAT others(4): Show |
A | 1 | a0001c0002t0114 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*403delATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708624 | |||||
chr1:99708625
|
A | AAAAAAAA others(13): Show |
1 | a0001c0004t0080 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAA others(5): Show |
1 | a0001c0002t0085 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATTTTT others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAA others(9): Show |
1 | a0001c0001t0132 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(10): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAA others(13): Show |
1 | a0001c0004t0074 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAA others(8): Show |
1 | a0001c0004t0079 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(9): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAA others(7): Show |
1 | a0001c0004t0078 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(8): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAT others(4): Show |
1 | a0001c0002t0081 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAAAAT others(6): Show |
1 | a0001c0004t0077 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAATAT others(4): Show |
1 | a0001c0004t0076 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAATAT others(6): Show |
1 | a0001c0004t0075 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAAATAT others(8): Show |
1 | a0001c0004t0073 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(9): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AAAT | 5 | a0001c0001t0049a0001c0001t0137a0001c0001t0138others(2): Show | 6 | HG02080.hp2 HG02280.hp1 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*402_*403insATT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | AT | 3 | a0001c0001t0134a0001c0001t0135a0001c0001t0136 | 3 | HG00642.hp1 HG01109.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*402_*403insA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | |||||
chr1:99708625
|
A | T | 26 | a0001c0001t0047a0001c0001t0048a0001c0001t0133others(23): Show | 36 | HG00642.hp2 HG00673.hp2 HG01069.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*403T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 403 | chr1 | 99708625 | |||||
chr1:99708625
|
AAT | A | 7 | a0001c0001t0012a0001c0001t0031a0001c0001t0052others(4): Show | 15 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*401_*402delAT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708625 | |||||
chr1:99708625
|
AATAT | A | 7 | a0001c0001t0149a0001c0001t0156a0001c0001t0159others(4): Show | 7 | HG01934.hp2 HG02027.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*402delATAT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708625 | |||||
chr1:99708625
|
AATATATA others(1): Show |
A | 7 | a0001c0002t0042a0001c0002t0108a0001c0002t0109others(4): Show | 8 | HG00423.hp2 HG02647.hp2 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*395_*402delATATAT others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 395 | chr1 | 99708625 | |||||
chr1:99708625
|
AATATATA others(3): Show |
A | 7 | a0001c0001t0162a0001c0002t0008a0001c0002t0009others(4): Show | 19 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*402delATATAT others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708625 | |||||
chr1:99708626
|
AT | A | 7 | a0001c0001t0019a0001c0001t0029a0001c0001t0152others(4): Show | 12 | HG00639.hp1 HG01255.hp1 HG01361.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*401delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708626 | |||||
chr1:99708626
|
ATAT | A | 10 | a0001c0001t0003a0001c0001t0011a0001c0001t0020others(7): Show | 35 | HG00408.hp1 HG00741.hp2 HG01106.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*401delATA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708626 | |||||
chr1:99708626
|
ATATAT | A | 8 | a0001c0001t0055a0001c0001t0158a0001c0002t0041others(5): Show | 10 | HG01943.hp1 HG01981.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*397_*401delATATA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708626 | |||||
chr1:99708626
|
ATATATAT others(2): Show |
A | 8 | a0001c0001t0165a0001c0001t0166a0001c0002t0015others(5): Show | 17 | HG00738.hp1 HG01106.hp1 HG01257.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*401delATATAT others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708626 | |||||
chr1:99708626
|
ATATATAT others(4): Show |
A | 5 | a0001c0001t0164a0001c0002t0016a0001c0002t0044others(2): Show | 9 | HG02257.hp1 HG02300.hp2 HG03471.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*391_*401delATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708626 | |||||
chr1:99708627
|
T | A | 12 | a0001c0001t0022a0001c0001t0030a0001c0001t0053others(9): Show | 19 | HG00738.hp2 HG01256.hp1 HG01256.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*401A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708627 | |||||
chr1:99708629
|
T | A | 14 | a0001c0001t0012a0001c0001t0022a0001c0001t0031others(11): Show | 25 | HG00408.hp2 HG00639.hp1 HG01361.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*399A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708629 | |||||
chr1:99708631
|
T | A | 15 | a0001c0001t0003a0001c0001t0012a0001c0001t0023others(12): Show | 34 | HG00408.hp1 HG00408.hp2 HG01192.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708631 | |||||
chr1:99708633
|
T | A | 9 | a0001c0001t0057a0001c0001t0158a0001c0001t0159others(6): Show | 10 | HG00408.hp1 HG01361.hp2 HG01981.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*395A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 395 | chr1 | 99708633 | |||||
chr1:99708635
|
T | A | 5 | a0001c0001t0163a0001c0002t0118a0001c0002t0119others(2): Show | 5 | HG02698.hp2 HG04184.hp2 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708635 | |||||
chr1:99708637
|
T | A | 12 | a0001c0001t0163a0001c0001t0165a0001c0001t0166others(9): Show | 24 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*391A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708637 | |||||
chr1:99708639
|
T | A | 7 | a0001c0002t0044a0001c0002t0045a0001c0002t0046others(4): Show | 10 | HG00738.hp1 HG01928.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 389 | chr1 | 99708639 | |||||
chr1:99708641
|
T | A | 1 | a0001c0002t0128 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 387 | chr1 | 99708641 | |||||
chr1:99708654
|
A | G | 31 | a0002c0003t0002a0002c0003t0004a0002c0003t0005others(28): Show | 61 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*374T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 374 | chr1 | 99708654 | |||||
chr1:99708662
|
A | C | 32 | a0002c0003t0002a0002c0003t0004a0002c0003t0005others(29): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*366T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 366 | chr1 | 99708662 | |||||
chr1:99708899
|
T | C | 1 | a0001c0002t0130 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 129 | chr1 | 99708899 | |||||
chr1:99748931
|
C | T | 111 | a0001c0002t0006a0001c0002t0007a0001c0002t0008others(108): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 2/17 | 163 | chr1 | 99748931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:99709316
|
T | A | 1 | a0001c0001t0021g0133 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1625-57A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709316 | ||||||
chr1:99709320
|
T | A | 68 | a0001c0002t0081g0116a0001c0002t0085g0278a0001c0002t0087g0117others(65): Show | 72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1625-61A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709320 | ||||||
chr1:99709321
|
A | T | 1 | a0001c0002t0042g0049 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1625-62T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709321 | ||||||
chr1:99709685
|
C | T | 4 | a0002c0003t0004g0008a0002c0003t0004g0103a0002c0003t0065g0101others(1): Show | 5 | HG02622.hp1 HG02809.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1625-426G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709685 | ||||||
chr1:99709686
|
A | G | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1625-427T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709686 | ||||||
chr1:99709739
|
G | A | 1 | a0002c0003t0037g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1625-480C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709739 | ||||||
chr1:99709817
|
A | C | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1625-558T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709817 | ||||||
chr1:99709992
|
A | C | 1 | a0001c0002t0015g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1625-733T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709992 | ||||||
chr1:99710065
|
G | A | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+741C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710065 | ||||||
chr1:99710091
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0206a0001c0001t0050g0153others(4): Show | 9 | HG02135.hp1 NA18954.hp2 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1624+715C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710091 | ||||||
chr1:99710099
|
C | G | 1 | a0001c0001t0003g0222 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1624+707G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710099 | ||||||
chr1:99710142
|
G | T | 31 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(28): Show | 33 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1624+664C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710142 | ||||||
chr1:99710202
|
A | G | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+604T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710202 | ||||||
chr1:99710208
|
G | A | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+598C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710208 | ||||||
chr1:99710210
|
C | A | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+596G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710210 | ||||||
chr1:99710353
|
T | TCTGG | 63 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(60): Show | 67 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1624+449_1624+452d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710353 | ||||||
chr1:99710507
|
A | C | 1 | a0001c0002t0109g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1624+299T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710507 | ||||||
chr1:99710528
|
C | A | 58 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(55): Show | 62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+278G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710528 | ||||||
chr1:99710689
|
A | G | 3 | a0001c0001t0020g0185a0001c0001t0052g0190a0001c0001t0160g0186 | 3 | HG00423.hp1 HG02015.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1624+117T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710689 | ||||||
chr1:99710735
|
G | A | 1 | a0002c0003t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1624+71C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710735 | ||||||
chr1:99710760
|
T | G | 2 | a0001c0002t0085g0278a0001c0002t0105g0022 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1624+46A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710760 | ||||||
chr1:99711015
|
T | C | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1481-66A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711015 | ||||||
chr1:99711278
|
C | T | 2 | a0001c0001t0133g0141a0001c0001t0134g0142 | 2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1481-329G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711278 | ||||||
chr1:99711279
|
G | T | 1 | a0001c0001t0021g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1481-330C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711279 | ||||||
chr1:99711341
|
A | G | 1 | a0002c0003t0013g0015 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1481-392T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711341 | ||||||
chr1:99711586
|
C | G | 1 | a0001c0002t0086g0074 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1480+519G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711586 | ||||||
chr1:99711717
|
A | C | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1480+388T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711717 | ||||||
chr1:99711970
|
G | A | 31 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(28): Show | 33 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1480+135C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711970 | ||||||
chr1:99712099
|
T | C | 2 | a0001c0002t0085g0278a0001c0002t0105g0022 | 2 | HG01884.hp2 HG02486.hp2 |
splice_region_variant&intron_variant | LOW | c.1480+6A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99712099 | ||||||
chr1:99712397
|
A | G | 1 | a0002c0003t0005g0270 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1421+21T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 13/16 | chr1 | 99712397 | ||||||
chr1:99712399
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1421+19T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 13/16 | chr1 | 99712399 | ||||||
chr1:99712413
|
A | G | 1 | a0001c0002t0007g0073 | 1 | NA19079.hp2 | splice_region_variant&intron_variant | LOW | c.1421+5T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 13/16 | chr1 | 99712413 | ||||||
chr1:99712728
|
T | C | 1 | a0002c0003t0035g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1324-213A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99712728 | ||||||
chr1:99712885
|
C | T | 1 | a0002c0003t0034g0287 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1324-370G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99712885 | ||||||
chr1:99712998
|
G | GGGACTAG others(558): Show |
49 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(46): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1324-484_1324-483i others(567): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99712998 | ||||||
chr1:99713152
|
A | C | 49 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(46): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1324-637T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713152 | ||||||
chr1:99713266
|
T | C | 6 | a0001c0001t0001g0159a0001c0001t0019g0160a0001c0001t0019g0165others(3): Show | 6 | HG00738.hp2 HG01256.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-751A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713266 | ||||||
chr1:99713343
|
G | T | 3 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281 | 3 | HG02109.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1324-828C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713343 | ||||||
chr1:99713494
|
G | A | 49 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(46): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1324-979C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713494 | ||||||
chr1:99713565
|
A | G | 2 | a0002c0003t0060g0111a0002c0003t0061g0110 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1324-1050T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713565 | ||||||
chr1:99713743
|
T | C | 158 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0055g0188others(155): Show | 169 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(166): Show |
intron_variant | MODIFIER | c.1324-1228A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713743 | ||||||
chr1:99713934
|
C | T | 1 | a0001c0001t0147g0121 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1324-1419G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713934 | ||||||
chr1:99714060
|
A | G | 1 | a0002c0003t0035g0063 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1323+1526T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714060 | ||||||
chr1:99714112
|
C | T | 2 | a0001c0002t0113g0265a0001c0002t0120g0301 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1323+1474G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714112 | ||||||
chr1:99714185
|
CT | C | 6 | a0001c0001t0050g0154a0001c0002t0026g0079a0001c0002t0129g0021others(3): Show | 6 | HG02145.hp1 HG03195.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+1400delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714185 | ||||||
chr1:99714247
|
G | A | 1 | a0001c0001t0163g0182 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1323+1339C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714247 | ||||||
chr1:99714329
|
G | A | 2 | a0001c0004t0006g0033a0001c0004t0006g0034 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1323+1257C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714329 | ||||||
chr1:99714393
|
A | G | 3 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281 | 3 | HG02109.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1323+1193T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714393 | ||||||
chr1:99714478
|
G | A | 14 | a0002c0003t0033g0236a0002c0003t0033g0290a0002c0003t0034g0287others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1323+1108C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714478 | ||||||
chr1:99714536
|
C | T | 52 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(49): Show | 54 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1323+1050G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714536 | ||||||
chr1:99714970
|
T | C | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1323+616A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714970 | ||||||
chr1:99715108
|
C | T | 1 | a0002c0003t0059g0297 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1323+478G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715108 | ||||||
chr1:99715127
|
G | A | 4 | a0001c0002t0099g0106a0001c0002t0107g0113a0001c0002t0114g0279others(1): Show | 4 | HG02572.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+459C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715127 | ||||||
chr1:99715198
|
G | T | 1 | a0001c0001t0003g0126 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1323+388C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715198 | ||||||
chr1:99715489
|
C | T | 2 | a0001c0001t0021g0131a0001c0001t0136g0196 | 2 | HG00642.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1323+97G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715489 | ||||||
chr1:99715537
|
T | C | 2 | a0001c0002t0009g0088a0001c0002t0127g0043 | 2 | HG00621.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1323+49A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715537 | ||||||
chr1:99715823
|
A | C | 2 | a0001c0001t0047g0177a0001c0001t0048g0198 | 2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1237-151T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715823 | ||||||
chr1:99715824
|
GA | G | 7 | a0001c0002t0089g0093a0001c0002t0096g0281a0002c0003t0033g0236others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237-153delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715824 | ||||||
chr1:99715870
|
T | C | 52 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(49): Show | 54 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1237-198A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715870 | ||||||
chr1:99715916
|
T | C | 158 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0055g0188others(155): Show | 169 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(166): Show |
intron_variant | MODIFIER | c.1237-244A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715916 | ||||||
chr1:99716218
|
A | G | 4 | a0003c0005t0004g0036a0003c0005t0004g0037a0003c0006t0004g0114others(1): Show | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-546T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716218 | ||||||
chr1:99716264
|
A | C | 1 | a0001c0001t0018g0139 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1237-592T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716264 | ||||||
chr1:99716275
|
G | A | 1 | a0001c0004t0006g0033 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1237-603C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716275 | ||||||
chr1:99716277
|
T | G | 1 | a0001c0001t0162g0183 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1237-605A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716277 | ||||||
chr1:99716320
|
A | T | 1 | a0002c0003t0070g0294 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1237-648T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716320 | ||||||
chr1:99716341
|
G | A | 152 | a0001c0001t0001g0134a0001c0001t0132g0136a0001c0001t0162g0183others(149): Show | 163 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(160): Show |
intron_variant | MODIFIER | c.1237-669C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716341 | ||||||
chr1:99716414
|
T | C | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1237-742A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716414 | ||||||
chr1:99716474
|
G | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1237-802C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716474 | ||||||
chr1:99716503
|
G | A | 49 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(46): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1237-831C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716503 | ||||||
chr1:99716895
|
T | G | 156 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0055g0188others(153): Show | 167 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(164): Show |
intron_variant | MODIFIER | c.1236+515A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716895 | ||||||
chr1:99716923
|
T | C | 1 | a0001c0004t0006g0033 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1236+487A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716923 | ||||||
chr1:99716927
|
G | A | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1236+483C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716927 | ||||||
chr1:99717023
|
T | C | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1236+387A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717023 | ||||||
chr1:99717144
|
C | G | 1 | a0001c0001t0142g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1236+266G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717144 | ||||||
chr1:99717279
|
G | A | 1 | a0001c0002t0009g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1236+131C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717279 | ||||||
chr1:99717328
|
C | T | 120 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0132g0136others(117): Show | 130 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.1236+82G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717328 | ||||||
chr1:99717794
|
T | C | 1 | a0001c0002t0081g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1121-269A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99717794 | ||||||
chr1:99717801
|
C | A | 12 | a0001c0001t0001g0134a0001c0001t0162g0183a0001c0001t0163g0182others(9): Show | 12 | HG01074.hp2 HG01106.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121-276G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99717801 | ||||||
chr1:99718047
|
C | T | 2 | a0001c0004t0006g0033a0001c0004t0006g0034 | 2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1121-522G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718047 | ||||||
chr1:99718096
|
G | A | 1 | a0001c0002t0120g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1121-571C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718096 | ||||||
chr1:99718188
|
T | A | 1 | a0002c0003t0058g0260 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1121-663A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718188 | ||||||
chr1:99718338
|
G | C | 21 | a0001c0001t0132g0136a0001c0002t0038g0062a0001c0002t0044g0014others(18): Show | 22 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1121-813C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718338 | ||||||
chr1:99718428
|
A | T | 1 | a0001c0004t0075g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1121-903T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718428 | ||||||
chr1:99718456
|
G | A | 2 | a0001c0002t0101g0050a0001c0002t0104g0051 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1121-931C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718456 | ||||||
chr1:99718474
|
G | A | 2 | a0001c0002t0101g0050a0001c0002t0104g0051 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1121-949C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718474 | ||||||
chr1:99718612
|
A | G | 1 | a0001c0001t0056g0209 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1120+922T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718612 | ||||||
chr1:99718788
|
T | C | 2 | a0001c0002t0010g0001a0001c0002t0010g0042 | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+746A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718788 | ||||||
chr1:99718902
|
T | G | 49 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(46): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1120+632A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718902 | ||||||
chr1:99718987
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1120+547T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718987 | ||||||
chr1:99719044
|
T | C | 3 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109 | 4 | HG02965.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+490A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719044 | ||||||
chr1:99719070
|
CA | C | 56 | a0001c0002t0085g0278a0001c0002t0089g0093a0001c0002t0094g0300others(53): Show | 58 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.1120+463delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719070 | ||||||
chr1:99719070
|
CAA | C | 118 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0132g0136others(115): Show | 128 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.1120+462_1120+463d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719070 | ||||||
chr1:99719122
|
G | T | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1120+412C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719122 | ||||||
chr1:99719349
|
C | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1120+185G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719349 | ||||||
chr1:99719407
|
C | CA | 114 | a0001c0001t0001g0134a0001c0001t0049g0208a0001c0001t0055g0227others(111): Show | 124 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.1120+126dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719407 | ||||||
chr1:99719407
|
C | CAA | 54 | a0001c0002t0015g0052a0001c0002t0026g0079a0001c0002t0089g0093others(51): Show | 56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1120+125_1120+126d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719407 | ||||||
chr1:99719407
|
CA | C | 9 | a0001c0001t0003g0126a0001c0001t0012g0123a0001c0001t0020g0194others(6): Show | 9 | HG01256.hp2 NA18998.hp2 NA19003.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120+126delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719407 | ||||||
chr1:99719726
|
G | T | 118 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0132g0136others(115): Show | 128 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.1007-79C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719726 | ||||||
chr1:99719853
|
T | C | 1 | a0001c0001t0020g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1007-206A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719853 | ||||||
chr1:99719864
|
G | C | 2 | a0001c0002t0101g0050a0001c0002t0104g0051 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1007-217C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719864 | ||||||
chr1:99719893
|
G | C | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1007-246C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719893 | ||||||
chr1:99719902
|
T | C | 2 | a0001c0001t0047g0177a0001c0001t0048g0198 | 2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1007-255A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719902 | ||||||
chr1:99720199
|
A | T | 1 | a0002c0003t0037g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1007-552T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720199 | ||||||
chr1:99720350
|
T | C | 2 | a0001c0002t0113g0265a0001c0002t0120g0301 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1007-703A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720350 | ||||||
chr1:99720370
|
G | A | 54 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(51): Show | 56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1007-723C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720370 | ||||||
chr1:99720420
|
G | A | 8 | a0002c0003t0004g0008a0002c0003t0004g0103a0002c0003t0025g0007others(5): Show | 10 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007-773C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720420 | ||||||
chr1:99720834
|
A | AAC | 10 | a0001c0001t0001g0159a0001c0001t0001g0179a0001c0001t0001g0206others(7): Show | 10 | HG00642.hp2 HG01256.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1007-1189_1007-118 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AAC | A | 46 | a0001c0001t0001g0184a0001c0001t0001g0189a0001c0001t0003g0218others(43): Show | 47 | HG00423.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1007-1189_1007-118 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AACAC | A | 22 | a0001c0001t0001g0134a0001c0001t0003g0126a0001c0001t0012g0123others(19): Show | 22 | HG01074.hp2 HG01106.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1007-1191_1007-118 others(8): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AACACAC | A | 66 | a0001c0001t0001g0230a0001c0001t0031g0125a0001c0001t0031g0127others(63): Show | 71 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007-1193_1007-118 others(10): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AACACACA others(1): Show |
A | 11 | a0001c0001t0140g0167a0001c0001t0154g0150a0001c0002t0008g0082others(8): Show | 11 | HG01109.hp2 HG01433.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-1195_1007-118 others(12): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AACACACA others(3): Show |
A | 73 | a0001c0001t0055g0227a0001c0001t0166g0137a0001c0002t0006g0009others(70): Show | 80 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.1007-1197_1007-118 others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AACACACA others(5): Show |
A | 11 | a0001c0002t0015g0052a0001c0002t0015g0053a0001c0002t0094g0300others(8): Show | 11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-1199_1007-118 others(16): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720834
|
AACACACA others(7): Show |
A | 1 | a0001c0002t0007g0242 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1007-1201_1007-118 others(18): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | ||||||
chr1:99720984
|
A | G | 21 | a0001c0001t0132g0136a0001c0002t0038g0062a0001c0002t0044g0014others(18): Show | 22 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1007-1337T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720984 | ||||||
chr1:99720987
|
C | T | 1 | a0001c0001t0003g0138 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1007-1340G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720987 | ||||||
chr1:99721129
|
C | G | 116 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0132g0136others(113): Show | 126 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.1007-1482G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721129 | ||||||
chr1:99721242
|
G | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1007-1595C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721242 | ||||||
chr1:99721349
|
T | G | 1 | a0001c0002t0043g0065 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1007-1702A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721349 | ||||||
chr1:99721364
|
G | A | 7 | a0001c0001t0132g0136a0001c0004t0074g0030a0001c0004t0076g0032others(4): Show | 7 | HG01081.hp1 HG01192.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1717C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721364 | ||||||
chr1:99721475
|
T | C | 31 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(28): Show | 33 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1007-1828A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721475 | ||||||
chr1:99721796
|
G | A | 119 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0132g0136others(116): Show | 129 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1007-2149C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721796 | ||||||
chr1:99721872
|
T | C | 289 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0134others(286): Show | 306 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(303): Show |
intron_variant | MODIFIER | c.1007-2225A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721872 | ||||||
chr1:99721908
|
T | C | 1 | a0002c0003t0013g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1007-2261A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721908 | ||||||
chr1:99722329
|
T | A | 1 | a0001c0002t0009g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1007-2682A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722329 | ||||||
chr1:99722388
|
T | G | 2 | a0001c0001t0030g0168a0001c0001t0030g0169 | 2 | HG00738.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1007-2741A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722388 | ||||||
chr1:99722435
|
G | A | 3 | a0001c0001t0057g0224a0001c0001t0141g0225a0001c0001t0159g0226 | 3 | NA18944.hp1 NA19079.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1007-2788C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722435 | ||||||
chr1:99722452
|
A | G | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1007-2805T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722452 | ||||||
chr1:99722458
|
A | T | 4 | a0002c0003t0034g0287a0002c0003t0034g0288a0002c0003t0036g0285others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-2811T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722458 | ||||||
chr1:99722475
|
A | G | 1 | a0002c0003t0067g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1007-2828T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722475 | ||||||
chr1:99722567
|
C | A | 54 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(51): Show | 56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1007-2920G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722567 | ||||||
chr1:99722611
|
A | G | 1 | a0001c0001t0055g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1007-2964T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722611 | ||||||
chr1:99722760
|
C | T | 84 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(81): Show | 91 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1007-3113G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722760 | ||||||
chr1:99722905
|
A | T | 5 | a0002c0003t0005g0295a0002c0003t0032g0298a0002c0003t0035g0293others(2): Show | 5 | NA18947.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-3258T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722905 | ||||||
chr1:99723015
|
G | A | 8 | a0001c0001t0018g0139a0001c0001t0018g0140a0001c0001t0018g0143others(5): Show | 8 | HG01346.hp2 HG01943.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007-3368C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723015 | ||||||
chr1:99723116
|
A | C | 5 | a0001c0001t0003g0126a0001c0001t0012g0123a0001c0001t0031g0125others(2): Show | 5 | NA19003.hp1 NA19010.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-3469T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723116 | ||||||
chr1:99723378
|
A | C | 1 | a0002c0003t0002g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1007-3731T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723378 | ||||||
chr1:99723574
|
A | G | 2 | a0001c0001t0001g0176a0001c0001t0051g0200 | 2 | NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1007-3927T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723574 | ||||||
chr1:99723658
|
G | A | 1 | a0001c0002t0017g0094 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1007-4011C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723658 | ||||||
chr1:99723664
|
C | T | 2 | a0001c0002t0089g0093a0001c0002t0096g0281 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1007-4017G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723664 | ||||||
chr1:99723785
|
G | A | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1007-4138C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723785 | ||||||
chr1:99724244
|
A | C | 1 | a0001c0001t0052g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1006+4249T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724244 | ||||||
chr1:99724431
|
C | G | 49 | a0002c0003t0002g0013a0002c0003t0002g0248a0002c0003t0002g0251others(46): Show | 51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1006+4062G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724431 | ||||||
chr1:99724454
|
A | G | 3 | a0001c0001t0001g0184a0001c0002t0085g0278a0001c0002t0105g0022 | 3 | HG01496.hp1 HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1006+4039T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724454 | ||||||
chr1:99724541
|
G | A | 116 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0132g0136others(113): Show | 126 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.1006+3952C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724541 | ||||||
chr1:99724677
|
T | C | 1 | a0001c0004t0080g0029 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+3816A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724677 | ||||||
chr1:99724735
|
A | G | 2 | a0002c0003t0036g0285a0002c0003t0036g0286 | 2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1006+3758T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724735 | ||||||
chr1:99725128
|
G | A | 1 | a0002c0003t0002g0267 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1006+3365C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725128 | ||||||
chr1:99725274
|
G | A | 86 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(83): Show | 93 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.1006+3219C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725274 | ||||||
chr1:99725287
|
C | A | 54 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(51): Show | 56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1006+3206G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725287 | ||||||
chr1:99725532
|
G | A | 2 | a0002c0003t0034g0287a0002c0003t0034g0288 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1006+2961C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725532 | ||||||
chr1:99725673
|
G | A | 1 | a0001c0002t0087g0117 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1006+2820C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725673 | ||||||
chr1:99725737
|
G | A | 2 | a0001c0002t0085g0278a0001c0002t0105g0022 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1006+2756C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725737 | ||||||
chr1:99726335
|
C | T | 72 | a0001c0001t0055g0227a0001c0001t0166g0137a0001c0002t0006g0009others(69): Show | 79 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1006+2158G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99726335 | ||||||
chr1:99726714
|
C | T | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1006+1779G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99726714 | ||||||
chr1:99727064
|
T | G | 2 | a0001c0001t0003g0234a0001c0001t0156g0220 | 2 | NA18747.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1006+1429A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727064 | ||||||
chr1:99727438
|
C | T | 9 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+1055G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727438 | ||||||
chr1:99727472
|
C | T | 1 | a0002c0003t0071g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006+1021G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727472 | ||||||
chr1:99727948
|
T | A | 1 | a0002c0003t0067g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1006+545A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727948 | ||||||
chr1:99728012
|
C | T | 1 | a0002c0003t0037g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1006+481G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728012 | ||||||
chr1:99728044
|
C | T | 4 | a0001c0001t0020g0120a0001c0001t0028g0158a0001c0001t0146g0156others(1): Show | 4 | HG01069.hp2 HG01167.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+449G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728044 | ||||||
chr1:99728266
|
AT | A | 14 | a0002c0003t0033g0236a0002c0003t0033g0290a0002c0003t0034g0287others(11): Show | 14 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006+226delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728266 | ||||||
chr1:99728282
|
G | A | 4 | a0002c0003t0034g0287a0002c0003t0034g0288a0002c0003t0036g0285others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+211C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728282 | ||||||
chr1:99728404
|
C | A | 1 | a0001c0001t0166g0137 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1006+89G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728404 | ||||||
chr1:99728415
|
G | C | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1006+78C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728415 | ||||||
chr1:99728644
|
C | CAA | 3 | a0001c0001t0001g0179a0001c0001t0030g0207a0001c0001t0152g0180 | 3 | HG00639.hp1 HG01934.hp1 HG04115.hp1 |
splice_region_variant&intron_variant | LOW | c.859-6_859-5dupTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99728644 | ||||||
chr1:99728749
|
C | G | 183 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(180): Show | 196 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(193): Show |
intron_variant | MODIFIER | c.859-109G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99728749 | ||||||
chr1:99729056
|
G | T | 1 | a0001c0002t0114g0279 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.859-416C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729056 | ||||||
chr1:99729075
|
T | G | 2 | a0001c0001t0162g0183a0001c0001t0163g0182 | 2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.859-435A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729075 | ||||||
chr1:99729082
|
A | G | 1 | a0001c0001t0012g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.859-442T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729082 | ||||||
chr1:99729174
|
CAAA | C | 3 | a0001c0002t0089g0093a0001c0002t0094g0300a0001c0002t0096g0281 | 3 | HG02109.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.858+473_858+475del others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729174 | ||||||
chr1:99729290
|
C | T | 3 | a0001c0001t0049g0195a0001c0001t0049g0208a0001c0001t0142g0172 | 3 | HG02280.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.858+360G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729290 | ||||||
chr1:99729322
|
C | CCT | 183 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(180): Show | 196 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(193): Show |
intron_variant | MODIFIER | c.858+326_858+327dup others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729322 | ||||||
chr1:99729338
|
G | A | 71 | a0001c0001t0055g0227a0001c0001t0166g0137a0001c0002t0006g0009others(68): Show | 78 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.858+312C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729338 | ||||||
chr1:99729340
|
CTGTA | C | 71 | a0001c0001t0055g0227a0001c0001t0166g0137a0001c0002t0006g0009others(68): Show | 78 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.858+306_858+309del others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729340 | ||||||
chr1:99729347
|
C | CT | 71 | a0001c0001t0055g0227a0001c0001t0166g0137a0001c0002t0006g0009others(68): Show | 78 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.858+302dupA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729347 | ||||||
chr1:99729406
|
G | A | 183 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(180): Show | 196 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(193): Show |
intron_variant | MODIFIER | c.858+244C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729406 | ||||||
chr1:99729458
|
C | T | 183 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(180): Show | 196 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(193): Show |
intron_variant | MODIFIER | c.858+192G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729458 | ||||||
chr1:99729461
|
C | G | 183 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(180): Show | 196 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(193): Show |
intron_variant | MODIFIER | c.858+189G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729461 | ||||||
chr1:99729921
|
A | G | 183 | a0001c0001t0001g0134a0001c0001t0055g0227a0001c0001t0162g0183others(180): Show | 196 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(193): Show |
intron_variant | MODIFIER | c.760-173T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99729921 | ||||||
chr1:99730029
|
G | A | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.760-281C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730029 | ||||||
chr1:99730260
|
C | T | 182 | a0001c0001t0001g0134a0001c0001t0162g0183a0001c0001t0163g0182others(179): Show | 195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.760-512G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730260 | ||||||
chr1:99730561
|
A | T | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.760-813T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730561 | ||||||
chr1:99730563
|
A | T | 179 | a0001c0001t0001g0134a0001c0001t0166g0137a0001c0002t0006g0009others(176): Show | 192 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(189): Show |
intron_variant | MODIFIER | c.760-815T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730563 | ||||||
chr1:99730585
|
G | A | 1 | a0001c0001t0031g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.760-837C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730585 | ||||||
chr1:99730593
|
C | T | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.760-845G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730593 | ||||||
chr1:99730595
|
A | C | 1 | a0002c0003t0067g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-847T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730595 | ||||||
chr1:99730613
|
G | A | 2 | a0001c0001t0001g0147a0001c0002t0124g0246 | 2 | HG02155.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.760-865C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730613 | ||||||
chr1:99730634
|
A | G | 14 | a0001c0002t0007g0071a0001c0002t0007g0073a0001c0002t0007g0075others(11): Show | 15 | HG00621.hp2 HG00639.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-886T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730634 | ||||||
chr1:99730643
|
A | G | 1 | a0002c0003t0002g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.760-895T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730643 | ||||||
chr1:99730652
|
G | A | 171 | a0001c0001t0001g0134a0001c0002t0006g0009a0001c0002t0006g0108others(168): Show | 184 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(181): Show |
intron_variant | MODIFIER | c.760-904C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730652 | ||||||
chr1:99730664
|
C | G | 2 | a0001c0001t0003g0138a0001c0002t0014g0256 | 2 | HG01192.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.760-916G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730664 | ||||||
chr1:99730683
|
T | A | 1 | a0001c0002t0110g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.760-935A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730683 | ||||||
chr1:99730683
|
T | C | 5 | a0001c0002t0009g0066a0001c0002t0010g0001a0001c0002t0010g0042others(2): Show | 7 | HG02027.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-935A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730683 | ||||||
chr1:99730695
|
G | A | 1 | a0001c0002t0014g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.760-947C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730695 | ||||||
chr1:99730728
|
A | G | 1 | a0001c0004t0039g0026 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.760-980T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730728 | ||||||
chr1:99730760
|
A | G | 1 | a0002c0003t0005g0299 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.760-1012T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730760 | ||||||
chr1:99730824
|
G | A | 62 | a0001c0001t0001g0134a0001c0001t0020g0205a0001c0002t0007g0242others(59): Show | 64 | HG00673.hp2 HG01074.hp1 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.760-1076C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730824 | ||||||
chr1:99730866
|
C | CA | 162 | a0001c0001t0001g0134a0001c0001t0003g0228a0001c0001t0020g0205others(159): Show | 174 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(171): Show |
intron_variant | MODIFIER | c.760-1119dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730866 | ||||||
chr1:99730866
|
C | CAA | 18 | a0001c0002t0016g0070a0001c0002t0026g0079a0001c0002t0026g0282others(15): Show | 18 | HG01081.hp1 HG01192.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.760-1120_760-1119d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730866 | ||||||
chr1:99730866
|
CA | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0206a0001c0001t0050g0153others(5): Show | 10 | HG02135.hp1 NA18954.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-1119delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730866 | ||||||
chr1:99731054
|
C | T | 111 | a0001c0001t0001g0134a0001c0002t0006g0009a0001c0002t0006g0108others(108): Show | 118 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(115): Show |
intron_variant | MODIFIER | c.760-1306G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731054 | ||||||
chr1:99731105
|
A | G | 84 | a0001c0001t0001g0105a0001c0001t0001g0147a0001c0001t0001g0174others(81): Show | 86 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.760-1357T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731105 | ||||||
chr1:99731241
|
A | G | 1 | a0001c0001t0138g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.760-1493T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731241 | ||||||
chr1:99731295
|
A | G | 1 | a0001c0002t0046g0055 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.760-1547T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731295 | ||||||
chr1:99731434
|
T | G | 1 | a0002c0003t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.760-1686A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731434 | ||||||
chr1:99731503
|
T | C | 59 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(56): Show | 61 | HG00673.hp2 HG01074.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.760-1755A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731503 | ||||||
chr1:99731922
|
A | G | 1 | a0001c0002t0007g0071 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.760-2174T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731922 | ||||||
chr1:99731935
|
A | C | 1 | a0001c0002t0027g0241 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.760-2187T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731935 | ||||||
chr1:99732010
|
T | C | 2 | a0002c0003t0033g0290a0002c0003t0059g0297 | 2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.760-2262A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732010 | ||||||
chr1:99732048
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-2300A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732048 | ||||||
chr1:99732067
|
G | C | 3 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100 | 3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.760-2319C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732067 | ||||||
chr1:99732207
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-2459G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732207 | ||||||
chr1:99732268
|
C | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-2520G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732268 | ||||||
chr1:99732503
|
T | C | 99 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(96): Show | 105 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.760-2755A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732503 | ||||||
chr1:99732542
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-2794G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732542 | ||||||
chr1:99732600
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-2852T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732600 | ||||||
chr1:99732707
|
T | C | 9 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(6): Show | 10 | HG02145.hp1 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-2959A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732707 | ||||||
chr1:99732741
|
T | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-2993A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732741 | ||||||
chr1:99732831
|
T | C | 8 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(5): Show | 9 | HG02145.hp1 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-3083A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732831 | ||||||
chr1:99732843
|
A | G | 99 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(96): Show | 105 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.760-3095T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732843 | ||||||
chr1:99732844
|
AT | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0134others(102): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.760-3097delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732844 | ||||||
chr1:99732844
|
ATTT | A | 65 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(62): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.760-3099_760-3097d others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732844 | ||||||
chr1:99732844
|
ATTTT | A | 112 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(109): Show | 119 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.760-3100_760-3097d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732844 | ||||||
chr1:99732871
|
T | A | 1 | a0001c0002t0123g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.760-3123A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732871 | ||||||
chr1:99732954
|
C | T | 1 | a0002c0003t0067g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-3206G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732954 | ||||||
chr1:99733000
|
C | T | 1 | a0001c0001t0030g0207 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.760-3252G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733000 | ||||||
chr1:99733045
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-3297C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733045 | ||||||
chr1:99733151
|
G | A | 1 | a0001c0001t0049g0208 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.760-3403C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733151 | ||||||
chr1:99733243
|
C | T | 67 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(64): Show | 70 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.760-3495G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733243 | ||||||
chr1:99733249
|
A | C | 1 | a0002c0003t0035g0293 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.760-3501T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733249 | ||||||
chr1:99733333
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-3585G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733333 | ||||||
chr1:99733546
|
C | T | 2 | a0001c0002t0045g0054a0001c0002t0128g0089 | 2 | NA18968.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.760-3798G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733546 | ||||||
chr1:99733579
|
G | A | 1 | a0002c0003t0002g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.760-3831C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733579 | ||||||
chr1:99733583
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-3835C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733583 | ||||||
chr1:99733644
|
C | A | 1 | a0002c0003t0013g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.760-3896G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733644 | ||||||
chr1:99733646
|
A | G | 1 | a0002c0003t0005g0250 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.760-3898T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733646 | ||||||
chr1:99733675
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-3927T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733675 | ||||||
chr1:99733694
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-3946T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733694 | ||||||
chr1:99733888
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-4140G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733888 | ||||||
chr1:99734011
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+4075G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734011 | ||||||
chr1:99734012
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+4074T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734012 | ||||||
chr1:99734279
|
G | A | 1 | a0001c0002t0123g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.759+3807C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734279 | ||||||
chr1:99734504
|
GT | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+3581delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734504 | ||||||
chr1:99734506
|
G | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+3580C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734506 | ||||||
chr1:99734539
|
G | A | 1 | a0001c0002t0008g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.759+3547C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734539 | ||||||
chr1:99734628
|
C | T | 67 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(64): Show | 73 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.759+3458G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734628 | ||||||
chr1:99734723
|
A | G | 12 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(9): Show | 13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+3363T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734723 | ||||||
chr1:99734730
|
G | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+3356C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734730 | ||||||
chr1:99734823
|
G | C | 12 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(9): Show | 13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+3263C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734823 | ||||||
chr1:99734885
|
T | A | 2 | a0001c0004t0074g0030a0001c0004t0080g0029 | 2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.759+3201A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734885 | ||||||
chr1:99734992
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+3094C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734992 | ||||||
chr1:99735053
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+3033T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735053 | ||||||
chr1:99735124
|
G | A | 5 | a0002c0003t0033g0236a0002c0003t0033g0290a0002c0003t0059g0297others(2): Show | 5 | HG01891.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+2962C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735124 | ||||||
chr1:99735169
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+2917T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735169 | ||||||
chr1:99735176
|
G | T | 1 | a0001c0002t0027g0240 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.759+2910C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735176 | ||||||
chr1:99735397
|
T | C | 1 | a0001c0002t0090g0092 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.759+2689A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735397 | ||||||
chr1:99735456
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0203 | 2 | HG02015.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.759+2630C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735456 | ||||||
chr1:99735565
|
G | C | 1 | a0001c0002t0127g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759+2521C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735565 | ||||||
chr1:99735581
|
C | T | 5 | a0002c0003t0033g0236a0002c0003t0033g0290a0002c0003t0059g0297others(2): Show | 5 | HG01891.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+2505G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735581 | ||||||
chr1:99735688
|
G | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+2398C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735688 | ||||||
chr1:99735736
|
T | C | 4 | a0002c0003t0034g0287a0002c0003t0034g0288a0002c0003t0036g0285others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.759+2350A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735736 | ||||||
chr1:99735764
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+2322G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735764 | ||||||
chr1:99735814
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+2272G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735814 | ||||||
chr1:99735868
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+2218G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735868 | ||||||
chr1:99735894
|
G | A | 8 | a0001c0002t0105g0022a0002c0003t0004g0008a0002c0003t0004g0103others(5): Show | 11 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.759+2192C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735894 | ||||||
chr1:99736052
|
T | C | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.759+2034A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736052 | ||||||
chr1:99736104
|
A | G | 1 | a0001c0002t0115g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.759+1982T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736104 | ||||||
chr1:99736346
|
A | T | 27 | a0001c0001t0001g0105a0001c0001t0001g0147a0001c0001t0001g0174others(24): Show | 28 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.759+1740T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736346 | ||||||
chr1:99736422
|
G | A | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.759+1664C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736422 | ||||||
chr1:99736527
|
C | A | 1 | a0001c0001t0030g0207 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.759+1559G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736527 | ||||||
chr1:99736553
|
A | G | 289 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0134others(286): Show | 306 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(303): Show |
intron_variant | MODIFIER | c.759+1533T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736553 | ||||||
chr1:99736560
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1526T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736560 | ||||||
chr1:99736561
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1525A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736561 | ||||||
chr1:99736577
|
C | A | 1 | a0002c0003t0013g0015 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.759+1509G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736577 | ||||||
chr1:99736629
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1457T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736629 | ||||||
chr1:99736631
|
A | G | 21 | a0001c0002t0007g0080a0001c0002t0009g0068a0001c0002t0015g0053others(18): Show | 21 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+1455T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736631 | ||||||
chr1:99736632
|
G | A | 21 | a0001c0002t0007g0080a0001c0002t0009g0068a0001c0002t0015g0053others(18): Show | 21 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+1454C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736632 | ||||||
chr1:99736632
|
GT | G | 157 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(154): Show | 170 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(167): Show |
intron_variant | MODIFIER | c.759+1453delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736632 | ||||||
chr1:99736633
|
T | G | 21 | a0001c0002t0007g0080a0001c0002t0009g0068a0001c0002t0015g0053others(18): Show | 21 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+1453A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736633 | ||||||
chr1:99736667
|
T | C | 65 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(62): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.759+1419A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736667 | ||||||
chr1:99736676
|
C | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1410G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736676 | ||||||
chr1:99736719
|
T | C | 96 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(93): Show | 102 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.759+1367A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736719 | ||||||
chr1:99736719
|
T | G | 4 | a0001c0001t0001g0174a0001c0001t0001g0203a0001c0001t0023g0010others(1): Show | 5 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+1367A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736719 | ||||||
chr1:99736759
|
TAA | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1325_759+1326d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736759 | ||||||
chr1:99736772
|
T | TAATAA | 177 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(174): Show | 190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1309_759+1313d others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736772 | ||||||
chr1:99736790
|
T | A | 1 | a0002c0003t0033g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1296A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736790 | ||||||
chr1:99736792
|
A | T | 1 | a0002c0003t0033g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1294T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736792 | ||||||
chr1:99736795
|
T | A | 1 | a0002c0003t0033g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1291A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736795 | ||||||
chr1:99736796
|
A | T | 1 | a0002c0003t0033g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1290T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736796 | ||||||
chr1:99736810
|
A | AT | 177 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(174): Show | 190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1275dupA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736810 | ||||||
chr1:99736812
|
A | C | 67 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(64): Show | 73 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.759+1274T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736812 | ||||||
chr1:99736813
|
A | T | 1 | a0002c0003t0033g0290 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1273T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736813 | ||||||
chr1:99736820
|
G | C | 18 | a0001c0004t0006g0033a0001c0004t0006g0034a0001c0004t0006g0035others(15): Show | 18 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.759+1266C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736820 | ||||||
chr1:99736833
|
T | TA | 111 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(108): Show | 118 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(115): Show |
intron_variant | MODIFIER | c.759+1252dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736833 | ||||||
chr1:99736872
|
C | A | 1 | a0001c0001t0021g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.759+1214G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736872 | ||||||
chr1:99736906
|
A | T | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.759+1180T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736906 | ||||||
chr1:99737032
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1054G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737032 | ||||||
chr1:99737034
|
T | C | 1 | a0001c0004t0074g0030 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.759+1052A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737034 | ||||||
chr1:99737045
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1041T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737045 | ||||||
chr1:99737046
|
C | CCCTT | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+1039_759+1040i others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737046 | ||||||
chr1:99737068
|
T | C | 1 | a0001c0002t0099g0106 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.759+1018A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737068 | ||||||
chr1:99737124
|
T | C | 1 | a0001c0001t0165g0175 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.759+962A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737124 | ||||||
chr1:99737167
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+919C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737167 | ||||||
chr1:99737273
|
T | TA | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+812dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737273 | ||||||
chr1:99737287
|
C | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+799G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737287 | ||||||
chr1:99737344
|
T | C | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.759+742A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737344 | ||||||
chr1:99737549
|
C | T | 12 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(9): Show | 13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+537G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737549 | ||||||
chr1:99737726
|
T | C | 1 | a0002c0003t0002g0264 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.759+360A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737726 | ||||||
chr1:99737782
|
G | A | 6 | a0002c0003t0004g0008a0002c0003t0004g0103a0002c0003t0025g0007others(3): Show | 8 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.759+304C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737782 | ||||||
chr1:99737868
|
G | T | 2 | a0001c0002t0010g0001a0001c0002t0010g0042 | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+218C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737868 | ||||||
chr1:99737876
|
G | A | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.759+210C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737876 | ||||||
chr1:99737888
|
G | C | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.759+198C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737888 | ||||||
chr1:99737899
|
C | T | 2 | a0001c0002t0015g0052a0001c0002t0015g0053 | 2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.759+187G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737899 | ||||||
chr1:99737937
|
T | G | 1 | a0002c0003t0036g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.759+149A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737937 | ||||||
chr1:99737945
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+141G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737945 | ||||||
chr1:99737971
|
G | A | 1 | a0001c0002t0123g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.759+115C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737971 | ||||||
chr1:99738015
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+71T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99738015 | ||||||
chr1:99738041
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.759+45C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99738041 | ||||||
chr1:99738346
|
C | T | 29 | a0001c0002t0081g0116a0001c0002t0087g0117a0001c0002t0105g0022others(26): Show | 32 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.577-78G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738346 | ||||||
chr1:99738443
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-175C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738443 | ||||||
chr1:99738533
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-265C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738533 | ||||||
chr1:99738577
|
A | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-309T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738577 | ||||||
chr1:99738746
|
T | C | 70 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(67): Show | 73 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.577-478A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738746 | ||||||
chr1:99738812
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-544G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738812 | ||||||
chr1:99738877
|
C | T | 1 | a0001c0001t0003g0222 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.577-609G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738877 | ||||||
chr1:99738892
|
C | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-624G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738892 | ||||||
chr1:99738896
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-628G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738896 | ||||||
chr1:99738925
|
T | C | 1 | a0001c0001t0011g0011 | 2 | HG02155.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.577-657A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738925 | ||||||
chr1:99739090
|
G | T | 2 | a0001c0001t0052g0199a0001c0001t0056g0173 | 2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.577-822C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739090 | ||||||
chr1:99739221
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-953C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739221 | ||||||
chr1:99739261
|
C | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.577-993G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739261 | ||||||
chr1:99739294
|
A | C | 2 | a0001c0001t0001g0176a0001c0001t0051g0200 | 2 | NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.577-1026T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739294 | ||||||
chr1:99739491
|
G | T | 1 | a0001c0001t0029g0135 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.577-1223C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739491 | ||||||
chr1:99739533
|
G | A | 9 | a0001c0002t0007g0242a0001c0002t0027g0240a0001c0002t0027g0241others(6): Show | 9 | HG01106.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.576+1260C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739533 | ||||||
chr1:99739546
|
G | T | 2 | a0002c0003t0025g0007a0002c0003t0025g0104 | 3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.576+1247C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739546 | ||||||
chr1:99739740
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.576+1053T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739740 | ||||||
chr1:99739852
|
T | C | 1 | a0001c0001t0001g0206 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.576+941A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739852 | ||||||
chr1:99739880
|
G | GT | 119 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0134others(116): Show | 123 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.576+912dupA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739880 | ||||||
chr1:99739896
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.576+897T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739896 | ||||||
chr1:99739993
|
G | A | 31 | a0001c0001t0003g0126a0001c0001t0003g0214a0001c0001t0003g0218others(28): Show | 32 | HG00408.hp1 HG02027.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.576+800C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739993 | ||||||
chr1:99740032
|
A | G | 18 | a0001c0002t0014g0012a0001c0002t0014g0256a0001c0002t0014g0261others(15): Show | 19 | HG00673.hp2 HG01192.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.576+761T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740032 | ||||||
chr1:99740194
|
A | C | 1 | a0001c0002t0115g0112 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.576+599T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740194 | ||||||
chr1:99740218
|
GA | G | 68 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(65): Show | 75 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.576+574delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740218 | ||||||
chr1:99740596
|
T | G | 1 | a0001c0001t0023g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.576+197A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740596 | ||||||
chr1:99740729
|
C | T | 1 | a0001c0002t0105g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.576+64G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740729 | ||||||
chr1:99740736
|
G | A | 1 | a0001c0001t0003g0222 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.576+57C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740736 | ||||||
chr1:99741065
|
A | G | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.429-125T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741065 | ||||||
chr1:99741108
|
C | T | 1 | a0001c0001t0166g0137 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.429-168G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741108 | ||||||
chr1:99741109
|
G | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.429-169C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741109 | ||||||
chr1:99741245
|
T | C | 76 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(73): Show | 81 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(78): Show |
intron_variant | MODIFIER | c.429-305A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741245 | ||||||
chr1:99741267
|
T | C | 8 | a0001c0001t0018g0139a0001c0001t0018g0140a0001c0001t0018g0143others(5): Show | 8 | HG01346.hp2 HG01943.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-327A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741267 | ||||||
chr1:99741324
|
C | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.429-384G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741324 | ||||||
chr1:99741340
|
C | A | 67 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(64): Show | 70 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.429-400G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741340 | ||||||
chr1:99741424
|
T | C | 1 | a0001c0002t0120g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.429-484A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741424 | ||||||
chr1:99741602
|
A | C | 2 | a0001c0002t0105g0022a0002c0003t0013g0015 | 3 | HG00735.hp1 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.428+577T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741602 | ||||||
chr1:99741641
|
C | T | 1 | a0001c0002t0007g0046 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.428+538G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741641 | ||||||
chr1:99741651
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.428+528A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741651 | ||||||
chr1:99741745
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.428+434T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741745 | ||||||
chr1:99741771
|
C | T | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.428+408G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741771 | ||||||
chr1:99741939
|
A | G | 1 | a0001c0001t0021g0129 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.428+240T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741939 | ||||||
chr1:99742553
|
A | G | 2 | a0002c0003t0060g0111a0002c0003t0061g0110 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.334-280T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742553 | ||||||
chr1:99742598
|
T | C | 1 | a0001c0001t0151g0148 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.334-325A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742598 | ||||||
chr1:99742719
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-446G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742719 | ||||||
chr1:99742755
|
T | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-482A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742755 | ||||||
chr1:99742759
|
C | T | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-486G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742759 | ||||||
chr1:99742783
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-510T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742783 | ||||||
chr1:99742808
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-535A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742808 | ||||||
chr1:99742872
|
T | C | 85 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0001g0147others(82): Show | 87 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.334-599A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742872 | ||||||
chr1:99743174
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-901T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743174 | ||||||
chr1:99743195
|
G | A | 1 | a0001c0001t0048g0198 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-922C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743195 | ||||||
chr1:99743384
|
T | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-1111A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743384 | ||||||
chr1:99743388
|
T | C | 2 | a0002c0003t0002g0273a0002c0003t0005g0274 | 2 | NA18980.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.334-1115A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743388 | ||||||
chr1:99743400
|
G | A | 1 | a0001c0004t0075g0031 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.334-1127C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743400 | ||||||
chr1:99743645
|
A | C | 1 | a0001c0002t0097g0253 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.334-1372T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743645 | ||||||
chr1:99743708
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-1435A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743708 | ||||||
chr1:99743747
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-1474C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743747 | ||||||
chr1:99743825
|
G | A | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.334-1552C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743825 | ||||||
chr1:99743924
|
G | A | 2 | a0001c0001t0052g0199a0001c0001t0056g0173 | 2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.334-1651C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743924 | ||||||
chr1:99744059
|
G | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-1786C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744059 | ||||||
chr1:99744064
|
T | TAAAA | 81 | a0001c0002t0006g0109a0001c0002t0007g0046a0001c0002t0007g0071others(78): Show | 86 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.334-1795_334-1792d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744064 | ||||||
chr1:99744064
|
T | TAAAAA | 17 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0017g0005others(14): Show | 19 | HG01167.hp2 HG02145.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.334-1796_334-1792d others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744064 | ||||||
chr1:99744075
|
A | AAAAAG | 5 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(2): Show | 6 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1803_334-1802i others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744075 | ||||||
chr1:99744075
|
A | AAAAG | 66 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(63): Show | 69 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.334-1806_334-1803d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744075 | ||||||
chr1:99744153
|
G | A | 1 | a0001c0001t0020g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.334-1880C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744153 | ||||||
chr1:99744164
|
T | C | 5 | a0002c0003t0005g0295a0002c0003t0032g0298a0002c0003t0035g0293others(2): Show | 5 | NA18947.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1891A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744164 | ||||||
chr1:99744213
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-1940C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744213 | ||||||
chr1:99744403
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2130T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744403 | ||||||
chr1:99744424
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2151A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744424 | ||||||
chr1:99744452
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2179T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744452 | ||||||
chr1:99744510
|
G | C | 23 | a0001c0002t0081g0116a0001c0002t0087g0117a0001c0002t0105g0022others(20): Show | 24 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.334-2237C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744510 | ||||||
chr1:99744553
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2280T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744553 | ||||||
chr1:99744578
|
G | A | 23 | a0001c0002t0081g0116a0001c0002t0087g0117a0001c0002t0105g0022others(20): Show | 24 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.334-2305C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744578 | ||||||
chr1:99744599
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2326A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744599 | ||||||
chr1:99744707
|
AC | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2435delG | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744707 | ||||||
chr1:99744709
|
C | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2436G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744709 | ||||||
chr1:99744723
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.334-2450G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744723 | ||||||
chr1:99744865
|
G | A | 1 | a0002c0003t0024g0275 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.333+2429C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744865 | ||||||
chr1:99744969
|
CA | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0134others(104): Show | 110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.333+2324delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | ||||||
chr1:99744969
|
CAA | C | 7 | a0001c0001t0001g0174a0001c0001t0011g0211a0001c0001t0018g0128others(4): Show | 7 | HG01255.hp1 HG01257.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+2323_333+2324d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | ||||||
chr1:99744969
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0004t0076g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.333+2315_333+2324d others(12): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | ||||||
chr1:99744969
|
CAAAAAAA others(4): Show |
C | 11 | a0001c0002t0130g0019a0001c0004t0039g0023a0001c0004t0039g0026others(8): Show | 11 | HG01081.hp1 HG01192.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.333+2314_333+2324d others(13): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | ||||||
chr1:99744969
|
CAAAAAAA others(5): Show |
C | 166 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(163): Show | 179 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.333+2313_333+2324d others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | ||||||
chr1:99744969
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0011g0011 | 2 | HG02155.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.333+2312_333+2324d others(15): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | ||||||
chr1:99745259
|
A | G | 65 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(62): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.333+2035T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745259 | ||||||
chr1:99745279
|
G | C | 1 | a0002c0003t0067g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.333+2015C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745279 | ||||||
chr1:99745323
|
T | G | 1 | a0001c0001t0053g0171 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.333+1971A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745323 | ||||||
chr1:99745366
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+1928G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745366 | ||||||
chr1:99745407
|
G | A | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.333+1887C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745407 | ||||||
chr1:99745416
|
G | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+1878C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745416 | ||||||
chr1:99745428
|
A | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+1866T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745428 | ||||||
chr1:99745449
|
C | T | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.333+1845G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745449 | ||||||
chr1:99745482
|
G | C | 65 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(62): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.333+1812C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745482 | ||||||
chr1:99745548
|
G | T | 17 | a0001c0004t0006g0034a0001c0004t0006g0035a0001c0004t0038g0016others(14): Show | 17 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.333+1746C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745548 | ||||||
chr1:99745561
|
A | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+1733T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745561 | ||||||
chr1:99745607
|
C | T | 1 | a0002c0003t0002g0252 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.333+1687G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745607 | ||||||
chr1:99745683
|
C | CTAAATAA others(5): Show |
176 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(173): Show | 189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.333+1610_333+1611i others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745683 | ||||||
chr1:99745683
|
C | CTAAATAA others(9): Show |
1 | a0001c0004t0006g0034 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333+1610_333+1611i others(18): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745683 | ||||||
chr1:99745755
|
T | C | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.333+1539A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745755 | ||||||
chr1:99745763
|
C | T | 2 | a0001c0004t0077g0024a0001c0004t0078g0025 | 2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.333+1531G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745763 | ||||||
chr1:99745888
|
C | A | 4 | a0002c0003t0034g0287a0002c0003t0034g0288a0002c0003t0036g0285others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+1406G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745888 | ||||||
chr1:99745888
|
C | G | 174 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(171): Show | 187 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(184): Show |
intron_variant | MODIFIER | c.333+1406G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745888 | ||||||
chr1:99746003
|
G | GTAC | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+1290_333+1291i others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746003 | ||||||
chr1:99746004
|
C | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+1290G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746004 | ||||||
chr1:99746044
|
A | G | 4 | a0001c0002t0008g0090a0001c0002t0042g0049a0001c0002t0101g0050others(1): Show | 4 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+1250T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746044 | ||||||
chr1:99746171
|
A | G | 1 | a0001c0001t0056g0173 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.333+1123T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746171 | ||||||
chr1:99746285
|
T | C | 17 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(14): Show | 18 | HG00639.hp2 HG01261.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.333+1009A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746285 | ||||||
chr1:99746319
|
T | C | 2 | a0001c0002t0026g0282a0001c0002t0096g0281 | 2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.333+975A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746319 | ||||||
chr1:99746482
|
A | G | 1 | a0001c0001t0003g0228 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.333+812T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746482 | ||||||
chr1:99746556
|
G | C | 1 | a0001c0001t0153g0146 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.333+738C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746556 | ||||||
chr1:99746884
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+410G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746884 | ||||||
chr1:99746989
|
A | G | 1 | a0001c0002t0026g0048 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.333+305T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746989 | ||||||
chr1:99746997
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+297G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746997 | ||||||
chr1:99747016
|
T | C | 1 | a0001c0001t0003g0228 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.333+278A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747016 | ||||||
chr1:99747069
|
C | T | 1 | a0001c0001t0142g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333+225G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747069 | ||||||
chr1:99747106
|
AAC | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.333+186_333+187del others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747106 | ||||||
chr1:99747237
|
G | T | 12 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(9): Show | 13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.333+57C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747237 | ||||||
chr1:99747492
|
G | C | 1 | a0001c0004t0006g0035 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197-62C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747492 | ||||||
chr1:99747557
|
T | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.197-127A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747557 | ||||||
chr1:99747559
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.197-129A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747559 | ||||||
chr1:99747595
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.197-165A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747595 | ||||||
chr1:99747743
|
C | T | 1 | a0001c0002t0125g0047 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.197-313G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747743 | ||||||
chr1:99747752
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.197-322A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747752 | ||||||
chr1:99747910
|
G | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.197-480C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747910 | ||||||
chr1:99748167
|
T | TAA | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.196+405_196+406ins others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748167 | ||||||
chr1:99748351
|
AG | A | 68 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(65): Show | 72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.196+221delC | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748351 | ||||||
chr1:99748382
|
C | T | 1 | a0001c0002t0007g0046 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+191G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748382 | ||||||
chr1:99748408
|
T | C | 1 | a0002c0003t0025g0104 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.196+165A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748408 | ||||||
chr1:99748835
|
T | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-1+62A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 2/16 | chr1 | 99748835 | ||||||
chr1:99748863
|
T | C | 1 | a0001c0001t0051g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+34A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 2/16 | chr1 | 99748863 | ||||||
chr1:99749022
|
G | A | 64 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(61): Show | 70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105-21C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749022 | ||||||
chr1:99749078
|
C | T | 57 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(54): Show | 60 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.-105-77G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749078 | ||||||
chr1:99749122
|
G | A | 1 | a0001c0002t0124g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-105-121C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749122 | ||||||
chr1:99749138
|
T | G | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-137A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749138 | ||||||
chr1:99749169
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-168C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749169 | ||||||
chr1:99749221
|
G | C | 65 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(62): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.-105-220C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749221 | ||||||
chr1:99749280
|
C | T | 1 | a0001c0001t0164g0151 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-105-279G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749280 | ||||||
chr1:99749434
|
G | A | 1 | a0001c0002t0119g0017 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-105-433C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749434 | ||||||
chr1:99749442
|
T | C | 67 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(64): Show | 73 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.-105-441A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749442 | ||||||
chr1:99749453
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-452C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749453 | ||||||
chr1:99749718
|
G | A | 1 | a0001c0002t0127g0043 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-105-717C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749718 | ||||||
chr1:99749779
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-778T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749779 | ||||||
chr1:99749914
|
T | A | 1 | a0001c0002t0009g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-105-913A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749914 | ||||||
chr1:99750051
|
G | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-1050C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750051 | ||||||
chr1:99750064
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-1063G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750064 | ||||||
chr1:99750113
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-1112A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750113 | ||||||
chr1:99750163
|
G | T | 1 | a0002c0003t0002g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-105-1162C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750163 | ||||||
chr1:99750293
|
G | C | 2 | a0002c0003t0034g0287a0002c0003t0034g0288 | 2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-105-1292C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750293 | ||||||
chr1:99750325
|
A | C | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-105-1324T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750325 | ||||||
chr1:99750392
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-1391A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750392 | ||||||
chr1:99750425
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-1424A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750425 | ||||||
chr1:99750490
|
T | A | 1 | a0001c0002t0015g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-105-1489A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750490 | ||||||
chr1:99750677
|
G | GA | 169 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(166): Show | 180 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(177): Show |
intron_variant | MODIFIER | c.-105-1677dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750677 | ||||||
chr1:99750677
|
G | GAA | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-1678_-105-167 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750677 | ||||||
chr1:99750752
|
G | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-1751C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750752 | ||||||
chr1:99750773
|
G | T | 1 | a0001c0001t0142g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-105-1772C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750773 | ||||||
chr1:99750949
|
A | C | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-105-1948T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750949 | ||||||
chr1:99751039
|
C | G | 11 | a0001c0004t0039g0023a0001c0004t0039g0026a0001c0004t0073g0027others(8): Show | 11 | HG01081.hp1 HG01192.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-2038G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751039 | ||||||
chr1:99751130
|
C | A | 1 | a0001c0001t0020g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-105-2129G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751130 | ||||||
chr1:99751201
|
T | TA | 7 | a0001c0001t0003g0228a0001c0001t0012g0223a0001c0001t0055g0227others(4): Show | 7 | NA18944.hp1 NA18952.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105-2201dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751201 | ||||||
chr1:99751557
|
T | C | 1 | a0001c0001t0051g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-105-2556A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751557 | ||||||
chr1:99751712
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-2711C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751712 | ||||||
chr1:99751847
|
A | G | 1 | a0001c0001t0154g0150 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-105-2846T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751847 | ||||||
chr1:99751920
|
T | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-2919A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751920 | ||||||
chr1:99752027
|
C | T | 1 | a0001c0002t0120g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-105-3026G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752027 | ||||||
chr1:99752116
|
T | G | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-105-3115A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752116 | ||||||
chr1:99752127
|
C | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-3126G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752127 | ||||||
chr1:99752332
|
G | A | 21 | a0001c0002t0081g0116a0001c0002t0087g0117a0001c0002t0105g0022others(18): Show | 21 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-105-3331C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752332 | ||||||
chr1:99752632
|
C | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0159a0001c0001t0001g0206others(22): Show | 27 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-105-3631G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752632 | ||||||
chr1:99752691
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-3690T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752691 | ||||||
chr1:99752694
|
T | C | 4 | a0001c0002t0008g0082a0001c0002t0016g0084a0001c0002t0041g0085others(1): Show | 4 | HG00423.hp2 HG02135.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105-3693A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752694 | ||||||
chr1:99752709
|
A | T | 43 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(40): Show | 46 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-105-3708T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752709 | ||||||
chr1:99752863
|
A | G | 1 | a0002c0003t0037g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-105-3862T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752863 | ||||||
chr1:99752872
|
T | C | 1 | a0001c0001t0020g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-105-3871A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752872 | ||||||
chr1:99752904
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-3903T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752904 | ||||||
chr1:99752967
|
C | A | 1 | a0001c0002t0009g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-105-3966G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752967 | ||||||
chr1:99753231
|
A | AG | 175 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(172): Show | 188 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(185): Show |
intron_variant | MODIFIER | c.-105-4231_-105-423 others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753231 | ||||||
chr1:99753232
|
A | G | 1 | a0001c0002t0130g0019 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-105-4231T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753232 | ||||||
chr1:99753255
|
T | C | 1 | a0001c0001t0029g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-105-4254A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753255 | ||||||
chr1:99753403
|
T | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-4402A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753403 | ||||||
chr1:99753420
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-4419C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753420 | ||||||
chr1:99753454
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-4453G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753454 | ||||||
chr1:99753471
|
A | G | 1 | a0001c0002t0117g0045 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-105-4470T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753471 | ||||||
chr1:99753490
|
G | A | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-105-4489C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753490 | ||||||
chr1:99753539
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-4538C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753539 | ||||||
chr1:99753603
|
T | TA | 18 | a0001c0002t0007g0242a0001c0002t0026g0282a0001c0002t0027g0240others(15): Show | 18 | HG01106.hp1 HG01256.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-105-4603dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753603 | ||||||
chr1:99753609
|
A | G | 22 | a0001c0002t0081g0116a0001c0002t0087g0117a0001c0002t0105g0022others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-105-4608T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753609 | ||||||
chr1:99753639
|
G | C | 1 | a0001c0002t0105g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-4638C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753639 | ||||||
chr1:99753816
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-4815C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753816 | ||||||
chr1:99753874
|
T | C | 1 | a0002c0003t0068g0096 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-105-4873A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753874 | ||||||
chr1:99753879
|
T | C | 166 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(163): Show | 178 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(175): Show |
intron_variant | MODIFIER | c.-105-4878A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753879 | ||||||
chr1:99754120
|
G | A | 1 | a0001c0002t0105g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-5119C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754120 | ||||||
chr1:99754374
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-5373C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754374 | ||||||
chr1:99754495
|
G | C | 4 | a0001c0002t0088g0284a0001c0002t0106g0277a0001c0002t0108g0283others(1): Show | 4 | HG03209.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105-5494C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754495 | ||||||
chr1:99754507
|
A | AAG | 11 | a0001c0001t0001g0134a0001c0001t0018g0128a0001c0001t0021g0129others(8): Show | 11 | HG00741.hp2 HG01074.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105-5508_-105-550 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754507 | ||||||
chr1:99754507
|
A | G | 7 | a0001c0002t0094g0300a0002c0003t0004g0008a0002c0003t0004g0103others(4): Show | 9 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105-5506T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754507 | ||||||
chr1:99754507
|
AAG | A | 169 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(166): Show | 180 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(177): Show |
intron_variant | MODIFIER | c.-105-5508_-105-550 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754507 | ||||||
chr1:99754509
|
G | A | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-5508C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754509 | ||||||
chr1:99754641
|
G | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-5640C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754641 | ||||||
chr1:99754840
|
C | T | 1 | a0001c0002t0085g0278 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-105-5839G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754840 | ||||||
chr1:99754869
|
T | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-5868A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754869 | ||||||
chr1:99754904
|
G | A | 179 | a0001c0001t0001g0206a0001c0002t0006g0009a0001c0002t0006g0108others(176): Show | 192 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(189): Show |
intron_variant | MODIFIER | c.-105-5903C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754904 | ||||||
chr1:99754966
|
G | C | 1 | a0001c0002t0009g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-105-5965C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754966 | ||||||
chr1:99755044
|
T | C | 1 | a0002c0003t0002g0289 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-105-6043A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755044 | ||||||
chr1:99755077
|
T | A | 177 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(174): Show | 190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-6076A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755077 | ||||||
chr1:99755080
|
T | A | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-6079A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755080 | ||||||
chr1:99755191
|
C | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-6190G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755191 | ||||||
chr1:99755191
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-105-6190G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755191 | ||||||
chr1:99755263
|
T | TA | 172 | a0001c0002t0006g0009a0001c0002t0006g0109a0001c0002t0007g0046others(169): Show | 185 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(182): Show |
intron_variant | MODIFIER | c.-105-6263dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755263 | ||||||
chr1:99755264
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-105-6263T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755264 | ||||||
chr1:99755282
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-6281G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755282 | ||||||
chr1:99755335
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-6334T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755335 | ||||||
chr1:99755407
|
C | T | 1 | a0001c0002t0106g0277 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-105-6406G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755407 | ||||||
chr1:99755408
|
G | A | 1 | a0001c0002t0009g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-105-6407C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755408 | ||||||
chr1:99755457
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-6456C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755457 | ||||||
chr1:99755622
|
G | A | 1 | a0001c0002t0120g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-105-6621C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755622 | ||||||
chr1:99755754
|
G | A | 1 | a0001c0001t0030g0207 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-105-6753C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755754 | ||||||
chr1:99755808
|
A | G | 1 | a0001c0002t0110g0276 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105-6807T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755808 | ||||||
chr1:99755844
|
C | T | 1 | a0002c0003t0002g0248 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-105-6843G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755844 | ||||||
chr1:99755845
|
C | T | 1 | a0002c0003t0002g0248 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-105-6844G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755845 | ||||||
chr1:99755930
|
T | A | 1 | a0001c0001t0049g0208 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-105-6929A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755930 | ||||||
chr1:99756047
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7046T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756047 | ||||||
chr1:99756064
|
G | A | 18 | a0001c0004t0006g0033a0001c0004t0006g0034a0001c0004t0006g0035others(15): Show | 18 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-105-7063C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756064 | ||||||
chr1:99756332
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7331G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756332 | ||||||
chr1:99756372
|
C | T | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-7371G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756372 | ||||||
chr1:99756450
|
CA | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7450delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756450 | ||||||
chr1:99756543
|
T | A | 68 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(65): Show | 72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.-105-7542A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756543 | ||||||
chr1:99756547
|
A | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7546T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756547 | ||||||
chr1:99756663
|
A | T | 39 | a0001c0002t0014g0012a0001c0002t0014g0256a0001c0002t0014g0261others(36): Show | 42 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-105-7662T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756663 | ||||||
chr1:99756684
|
G | A | 8 | a0001c0002t0121g0099a0001c0002t0122g0100a0002c0003t0004g0008others(5): Show | 10 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-105-7683C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756684 | ||||||
chr1:99756691
|
T | C | 1 | a0001c0002t0105g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-7690A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756691 | ||||||
chr1:99756731
|
A | G | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7730T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756731 | ||||||
chr1:99756748
|
T | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7747A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756748 | ||||||
chr1:99756847
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-7846A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756847 | ||||||
chr1:99756923
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-105-7922T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756923 | ||||||
chr1:99757080
|
CT | C | 36 | a0001c0001t0003g0126a0001c0001t0003g0229a0001c0001t0056g0209others(33): Show | 40 | HG00735.hp1 HG01167.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-105-8080delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757080 | ||||||
chr1:99757097
|
A | T | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-8096T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757097 | ||||||
chr1:99757272
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-8271A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757272 | ||||||
chr1:99757297
|
T | A | 11 | a0002c0003t0013g0015a0002c0003t0033g0236a0002c0003t0033g0290others(8): Show | 12 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-105-8296A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757297 | ||||||
chr1:99757501
|
C | T | 1 | a0001c0004t0039g0023 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-105-8500G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757501 | ||||||
chr1:99757527
|
A | G | 1 | a0001c0002t0105g0022 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-8526T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757527 | ||||||
chr1:99757598
|
G | A | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-8597C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757598 | ||||||
chr1:99757937
|
G | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-106+8670C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757937 | ||||||
chr1:99757948
|
AG | A | 14 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(11): Show | 15 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-106+8658delC | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757948 | ||||||
chr1:99757949
|
GGA | G | 164 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(161): Show | 176 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(173): Show |
intron_variant | MODIFIER | c.-106+8656_-106+865 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757949 | ||||||
chr1:99757950
|
GA | G | 54 | a0001c0001t0001g0134a0001c0001t0003g0126a0001c0001t0003g0138others(51): Show | 55 | HG00408.hp1 HG00741.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-106+8656delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757950 | ||||||
chr1:99757976
|
A | G | 300 | a0001c0001t0001g0002a0001c0001t0001g0105a0001c0001t0001g0134others(297): Show | 317 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(314): Show |
intron_variant | MODIFIER | c.-106+8631T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757976 | ||||||
chr1:99758063
|
G | C | 22 | a0001c0002t0081g0116a0001c0002t0087g0117a0001c0002t0105g0022others(19): Show | 22 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-106+8544C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758063 | ||||||
chr1:99758446
|
G | A | 5 | a0002c0003t0033g0236a0002c0003t0033g0290a0002c0003t0059g0297others(2): Show | 5 | HG01891.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106+8161C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758446 | ||||||
chr1:99758542
|
G | A | 1 | a0001c0002t0008g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106+8065C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758542 | ||||||
chr1:99758570
|
C | T | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-106+8037G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758570 | ||||||
chr1:99758579
|
C | T | 99 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(96): Show | 106 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.-106+8028G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758579 | ||||||
chr1:99758609
|
CAT | C | 176 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(173): Show | 189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.-106+7996_-106+799 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758609 | ||||||
chr1:99758663
|
T | C | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-106+7944A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758663 | ||||||
chr1:99758716
|
TGGGCAAA others(16): Show |
T | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7868_-106+789 others(27): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758716 | ||||||
chr1:99758740
|
T | C | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7867A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758740 | ||||||
chr1:99758827
|
C | G | 177 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(174): Show | 190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-106+7780G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758827 | ||||||
chr1:99758843
|
C | T | 176 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(173): Show | 189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.-106+7764G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758843 | ||||||
chr1:99758848
|
G | A | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7759C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758848 | ||||||
chr1:99758850
|
G | A | 1 | a0002c0003t0037g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-106+7757C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758850 | ||||||
chr1:99758894
|
G | C | 32 | a0001c0001t0001g0230a0001c0001t0003g0126a0001c0001t0003g0214others(29): Show | 33 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.-106+7713C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758894 | ||||||
chr1:99758927
|
C | T | 9 | a0001c0002t0007g0242a0001c0002t0027g0240a0001c0002t0027g0241others(6): Show | 9 | HG01106.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-106+7680G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758927 | ||||||
chr1:99759006
|
C | G | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7601G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759006 | ||||||
chr1:99759050
|
C | G | 89 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(86): Show | 95 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.-106+7557G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759050 | ||||||
chr1:99759055
|
C | T | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-106+7552G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759055 | ||||||
chr1:99759056
|
G | C | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7551C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759056 | ||||||
chr1:99759080
|
A | G | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7527T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759080 | ||||||
chr1:99759095
|
C | T | 2 | a0002c0003t0065g0101a0002c0003t0069g0102 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-106+7512G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759095 | ||||||
chr1:99759391
|
T | C | 1 | a0002c0003t0071g0292 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-106+7216A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759391 | ||||||
chr1:99759583
|
A | G | 9 | a0001c0002t0094g0300a0001c0002t0121g0099a0001c0002t0122g0100others(6): Show | 11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-106+7024T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759583 | ||||||
chr1:99759628
|
A | G | 1 | a0002c0003t0013g0238 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-106+6979T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759628 | ||||||
chr1:99759687
|
T | C | 2 | a0003c0005t0004g0036a0003c0005t0004g0037 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-106+6920A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759687 | ||||||
chr1:99759761
|
C | T | 164 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(161): Show | 176 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(173): Show |
intron_variant | MODIFIER | c.-106+6846G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759761 | ||||||
chr1:99760041
|
C | T | 6 | a0002c0003t0004g0008a0002c0003t0004g0103a0002c0003t0025g0007others(3): Show | 8 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-106+6566G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760041 | ||||||
chr1:99760149
|
T | C | 2 | a0001c0002t0081g0116a0001c0002t0087g0117 | 2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-106+6458A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760149 | ||||||
chr1:99760258
|
T | C | 8 | a0001c0002t0121g0099a0001c0002t0122g0100a0002c0003t0004g0008others(5): Show | 10 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106+6349A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760258 | ||||||
chr1:99760319
|
G | A | 1 | a0001c0002t0123g0118 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-106+6288C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760319 | ||||||
chr1:99760532
|
A | T | 2 | a0001c0002t0010g0040a0001c0002t0100g0041 | 2 | HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-106+6075T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760532 | ||||||
chr1:99760698
|
G | A | 5 | a0002c0003t0005g0295a0002c0003t0032g0298a0002c0003t0035g0293others(2): Show | 5 | NA18947.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-106+5909C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760698 | ||||||
chr1:99760709
|
G | A | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+5898C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760709 | ||||||
chr1:99761178
|
G | A | 6 | a0002c0003t0004g0008a0002c0003t0004g0103a0002c0003t0025g0007others(3): Show | 8 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-106+5429C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761178 | ||||||
chr1:99761191
|
A | G | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-106+5416T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761191 | ||||||
chr1:99761215
|
G | A | 1 | a0001c0001t0021g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-106+5392C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761215 | ||||||
chr1:99761367
|
A | G | 1 | a0001c0002t0089g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-106+5240T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761367 | ||||||
chr1:99761538
|
C | A | 1 | a0001c0001t0138g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-106+5069G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761538 | ||||||
chr1:99761788
|
TA | T | 87 | a0001c0001t0031g0127a0001c0002t0007g0046a0001c0002t0007g0071others(84): Show | 93 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.-106+4818delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761788 | ||||||
chr1:99761877
|
A | G | 1 | a0001c0002t0099g0106 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-106+4730T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761877 | ||||||
chr1:99761896
|
T | C | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+4711A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761896 | ||||||
chr1:99762401
|
C | T | 1 | a0001c0002t0008g0039 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-106+4206G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762401 | ||||||
chr1:99762476
|
T | C | 1 | a0001c0002t0090g0092 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-106+4131A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762476 | ||||||
chr1:99762479
|
C | CTT | 64 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(61): Show | 70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-106+4126_-106+412 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762479 | ||||||
chr1:99762513
|
A | G | 1 | a0001c0002t0095g0237 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-106+4094T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762513 | ||||||
chr1:99762711
|
A | C | 5 | a0001c0001t0003g0126a0001c0001t0012g0123a0001c0001t0031g0125others(2): Show | 5 | NA19003.hp1 NA19010.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106+3896T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762711 | ||||||
chr1:99762890
|
T | C | 1 | a0001c0002t0017g0094 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-106+3717A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762890 | ||||||
chr1:99762951
|
T | C | 4 | a0001c0001t0003g0234a0001c0001t0054g0233a0001c0001t0149g0232others(1): Show | 4 | HG02027.hp2 NA18747.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106+3656A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762951 | ||||||
chr1:99763250
|
C | T | 1 | a0002c0003t0033g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-106+3357G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763250 | ||||||
chr1:99763357
|
A | G | 2 | a0001c0002t0121g0099a0001c0002t0122g0100 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-106+3250T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763357 | ||||||
chr1:99763736
|
T | C | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+2871A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763736 | ||||||
chr1:99763817
|
G | A | 65 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(62): Show | 71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.-106+2790C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763817 | ||||||
chr1:99763859
|
A | G | 1 | a0001c0001t0147g0121 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-106+2748T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763859 | ||||||
chr1:99763868
|
C | CA | 83 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(80): Show | 89 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.-106+2738dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763868 | ||||||
chr1:99763868
|
CA | C | 91 | a0001c0001t0020g0120a0001c0001t0029g0119a0001c0002t0006g0009others(88): Show | 98 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.-106+2738delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763868 | ||||||
chr1:99764066
|
T | A | 1 | a0002c0003t0005g0299 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-106+2541A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764066 | ||||||
chr1:99764321
|
G | C | 1 | a0001c0002t0089g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-106+2286C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764321 | ||||||
chr1:99764482
|
A | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-106+2125T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764482 | ||||||
chr1:99764555
|
C | T | 178 | a0001c0002t0006g0009a0001c0002t0006g0108a0001c0002t0006g0109others(175): Show | 191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-106+2052G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764555 | ||||||
chr1:99764582
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-106+2025G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764582 | ||||||
chr1:99764641
|
C | T | 77 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(74): Show | 83 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.-106+1966G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764641 | ||||||
chr1:99765123
|
A | G | 1 | a0001c0002t0119g0017 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-106+1484T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765123 | ||||||
chr1:99765140
|
A | C | 1 | a0001c0004t0038g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-106+1467T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765140 | ||||||
chr1:99765285
|
C | T | 1 | a0001c0001t0138g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-106+1322G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765285 | ||||||
chr1:99765311
|
T | C | 68 | a0001c0002t0007g0242a0001c0002t0014g0012a0001c0002t0014g0256others(65): Show | 72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.-106+1296A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765311 | ||||||
chr1:99765511
|
G | C | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+1096C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765511 | ||||||
chr1:99765662
|
G | A | 1 | a0001c0002t0120g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-106+945C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765662 | ||||||
chr1:99765844
|
G | T | 1 | a0001c0001t0150g0097 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-106+763C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765844 | ||||||
chr1:99766138
|
G | A | 1 | a0001c0002t0017g0094 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-106+469C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766138 | ||||||
chr1:99766143
|
G | A | 1 | a0001c0002t0094g0300 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-106+464C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766143 | ||||||
chr1:99766437
|
T | A | 2 | a0002c0003t0062g0095a0002c0003t0068g0096 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+170A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766437 | ||||||
chr1:99766518
|
A | G | 87 | a0001c0002t0007g0046a0001c0002t0007g0071a0001c0002t0007g0073others(84): Show | 93 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.-106+89T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766518 | ||||||
chr1:99766564
|
T | C | 1 | a0001c0002t0120g0301 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-106+43A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766564 |