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
29651 BAA01g20890 A01 10292059 C T missense_variant MODERATE c.431G>A|p.Cys144Tyr S275
29652 BAA01g20890 A01 10292372 G A missense_variant MODERATE c.118C>T|p.Leu40Phe S263
29653 BAA01g20890 A01 10292399 C T missense_variant MODERATE c.91G>A|p.Asp31Asn S95
29654 BAA01g20880 A01 10292513 G A upstream_gene_variant MODIFIER c.-4259C>T| S301
S304
29655 BAA01g20880 A01 10293066 C T upstream_gene_variant MODIFIER c.-4812G>A| S176
29656 BAA01g20880 A01 10293243 T A upstream_gene_variant MODIFIER c.-4989A>T| S38
29657 BAA01g20890 A01 10293818 C T upstream_gene_variant MODIFIER c.-1329G>A| S146
29658 BAA01g20890 A01 10295163 G A upstream_gene_variant MODIFIER c.-2674C>T| S268
29659 BAA01g20890 A01 10295307 G A upstream_gene_variant MODIFIER c.-2818C>T| S229
29660 BAA01g20900 A01 10295522 G A synonymous_variant LOW c.165G>A|p.Ser55Ser S58
29661 BAA01g20900 A01 10295707 G A missense_variant MODERATE c.350G>A|p.Cys117Tyr S162
29662 BAA01g20890 A01 10295954 G A upstream_gene_variant MODIFIER c.-3465C>T| S149
29663 BAA01g20900 A01 10295973 C T splice_region_variant&intron_variant LOW c.388-3C>T| S247
29664 BAA01g20890 A01 10296362 C T upstream_gene_variant MODIFIER c.-3873G>A| S69
29665 BAA01g20890 A01 10296397 G A upstream_gene_variant MODIFIER c.-3908C>T| S294
29666 BAA01g20900 A01 10296431 C T splice_region_variant&intron_variant LOW c.487-7C>T| S177
29667 BAA01g20890 A01 10296796 G A upstream_gene_variant MODIFIER c.-4307C>T| S207
29668 BAA01g20900 A01 10297448 G A missense_variant MODERATE c.919G>A|p.Ala307Thr S126
29669 BAA01g20910 A01 10298064 G A missense_variant MODERATE c.40G>A|p.Asp14Asn S49
29670 BAA01g20910 A01 10298204 G A synonymous_variant LOW c.180G>A|p.Ala60Ala S34
29671 BAA01g20910 A01 10298431 C T missense_variant MODERATE c.407C>T|p.Pro136Leu S167
29672 BAA01g20900 A01 10299364 C T downstream_gene_variant MODIFIER c.*1812C>T| S203
29673 BAA01g20900 A01 10299601 C T downstream_gene_variant MODIFIER c.*2049C>T| S270
29674 BAA01g20920 A01 10299700 G A missense_variant MODERATE c.1297C>T|p.Pro433Ser S68
S81
S85
29675 BAA01g20920 A01 10299851 G A synonymous_variant LOW c.1146C>T|p.Leu382Leu S94