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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
170151 BAA02g14950 A02 7109940 C T upstream_gene_variant MODIFIER c.-2686C>T| S135
170152 BAA02g14940 A02 7110568 C T missense_variant MODERATE c.190G>A|p.Val64Met S65
170153 BAA02g14940 A02 7110768 G A upstream_gene_variant MODIFIER c.-11C>T| S291
170154 BAA02g14940 A02 7112246 C T upstream_gene_variant MODIFIER c.-1489G>A| S121
170155 BAA02g14940 A02 7112376 C T upstream_gene_variant MODIFIER c.-1619G>A| S277
170156 BAA02g14940 A02 7112615 C T upstream_gene_variant MODIFIER c.-1858G>A| S131
170157 BAA02g14950 A02 7112676 C T synonymous_variant LOW c.51C>T|p.Arg17Arg S25
170158 BAA02g14950 A02 7112688 C T splice_region_variant&synonymous_variant LOW c.63C>T|p.Ala21Ala S249
170159 BAA02g14940 A02 7112787 C T upstream_gene_variant MODIFIER c.-2030G>A| S201
170160 BAA02g14950 A02 7113270 G A synonymous_variant LOW c.156G>A|p.Arg52Arg S157
S166
S257
S263
170161 BAA02g14940 A02 7113851 C T upstream_gene_variant MODIFIER c.-3094G>A| S206
S26
170162 BAA02g14950 A02 7115231 C T synonymous_variant LOW c.1057C>T|p.Leu353Leu S78
S83
170163 BAA02g14950 A02 7115291 G A missense_variant MODERATE c.1117G>A|p.Glu373Lys S95
170164 BAA02g14950 A02 7116107 C T missense_variant MODERATE c.1334C>T|p.Thr445Ile S273
170165 BAA02g14950 A02 7116578 G A synonymous_variant LOW c.1638G>A|p.Arg546Arg S297
170166 BAA02g14950 A02 7116818 C T synonymous_variant LOW c.1767C>T|p.Val589Val S152
170167 BAA02g14950 A02 7117773 C T synonymous_variant LOW c.2506C>T|p.Leu836Leu S281
170168 BAA02g14950 A02 7118036 G A stop_gained HIGH c.2769G>A|p.Trp923* S111
170169 BAA02g14950 A02 7118577 C T missense_variant MODERATE c.3061C>T|p.Leu1021Phe S33
170170 BAA02g14950 A02 7119006 G A synonymous_variant LOW c.3375G>A|p.Val1125Val S305
170171 BAA02g14950 A02 7119007 C T missense_variant MODERATE c.3376C>T|p.Leu1126Phe S189
170172 BAA02g14950 A02 7119119 G A missense_variant MODERATE c.3488G>A|p.Ser1163Asn S203
170173 BAA02g14950 A02 7119372 G A splice_donor_variant&intron_variant HIGH c.3601+1G>A| S153
S213
170174 BAA02g14950 A02 7121592 G A downstream_gene_variant MODIFIER c.*1952G>A| S132
S215
170175 BAA02g14960 A02 7122705 G A synonymous_variant LOW c.321C>T|p.Val107Val S111