Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 27 of 27 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g13290 A05 6876148 C T upstream_gene_variant MODIFIER c.-4250C>T| S281
2 BAA05g13290 A05 6876977 C T upstream_gene_variant MODIFIER c.-3421C>T| S259
3 BAA05g13290 A05 6878043 C T upstream_gene_variant MODIFIER c.-2355C>T| S127
4 BAA05g13290 A05 6879937 C T upstream_gene_variant MODIFIER c.-461C>T| S174
S27
5 BAA05g13290 A05 6880092 G A upstream_gene_variant MODIFIER c.-306G>A| S282
6 BAA05g13290 A05 6880926 C T stop_gained HIGH c.352C>T|p.Gln118* S206
S26
7 BAA05g13290 A05 6881068 T C intron_variant MODIFIER c.423-21T>C| S7
8 BAA05g13290 A05 6881598 G A splice_donor_variant&intron_variant HIGH c.744+1G>A| S79
S91
9 BAA05g13290 A05 6881679 G A missense_variant MODERATE c.748G>A|p.Asp250Asn S95
10 BAA05g13290 A05 6881988 C T intron_variant MODIFIER c.929+23C>T| S17
11 BAA05g13290 A05 6882703 C T intron_variant MODIFIER c.1194+37C>T| S188
12 BAA05g13290 A05 6882800 G A stop_gained HIGH c.1239G>A|p.Trp413* S41
13 BAA05g13290 A05 6882877 C T intron_variant MODIFIER c.1272-32C>T| S132
S137
S215
S89
14 BAA05g13290 A05 6882916 C T missense_variant MODERATE c.1279C>T|p.Arg427Trp S95
15 BAA05g13290 A05 6883904 C T missense_variant MODERATE c.1840C>T|p.Pro614Ser S9
16 BAA05g13290 A05 6885161 G A intron_variant MODIFIER c.2412+50G>A| S172
S217
17 BAA05g13290 A05 6885169 C T intron_variant MODIFIER c.2413-53C>T| S193
S35
18 BAA05g13290 A05 6885247 C T missense_variant MODERATE c.2438C>T|p.Ala813Val S82
S92
19 BAA05g13290 A05 6885339 C T intron_variant MODIFIER c.2507+23C>T| S286
20 BAA05g13290 A05 6885497 G A missense_variant MODERATE c.2584G>A|p.Ala862Thr S173
21 BAA05g13290 A05 6885893 C T missense_variant MODERATE c.2816C>T|p.Thr939Met S198
22 BAA05g13290 A05 6885948 G A synonymous_variant LOW c.2871G>A|p.Glu957Glu S150
23 BAA05g13290 A05 6886211 C T splice_region_variant&synonymous_variant LOW c.2976C>T|p.Ser992Ser S113
24 BAA05g13290 A05 6886561 C T synonymous_variant LOW c.3231C>T|p.Pro1077Pro S188
25 BAA05g13290 A05 6886933 C T splice_region_variant&intron_variant LOW c.3368-3C>T| S204