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
24551 BAA01g17780 A01 8644211 C T downstream_gene_variant MODIFIER c.*1600G>A| S88
24552 BAA01g17780 A01 8644928 C T downstream_gene_variant MODIFIER c.*883G>A| S179
24553 BAA01g17780 A01 8644963 G A downstream_gene_variant MODIFIER c.*848C>T| S195
24554 BAA01g17780 A01 8644970 G A downstream_gene_variant MODIFIER c.*841C>T| S262
24555 BAA01g17770 A01 8645511 C T missense_variant MODERATE c.1507C>T|p.Pro503Ser S302
24556 BAA01g17780 A01 8646609 C T missense_variant MODERATE c.721G>A|p.Ala241Thr S40
S49
24557 BAA01g17790 A01 8647129 G A upstream_gene_variant MODIFIER c.-4671G>A| S274
24558 BAA01g17780 A01 8647237 G A missense_variant MODERATE c.490C>T|p.Leu164Phe S178
24559 BAA01g17780 A01 8647352 C T synonymous_variant LOW c.375G>A|p.Lys125Lys S88
24560 BAA01g17780 A01 8647364 G A synonymous_variant LOW c.363C>T|p.Ile121Ile S94
24561 BAA01g17780 A01 8647511 C T missense_variant MODERATE c.292G>A|p.Gly98Arg S51
24562 BAA01g17780 A01 8648668 G A upstream_gene_variant MODIFIER c.-866C>T| S84
S93
24563 BAA01g17780 A01 8649663 C T upstream_gene_variant MODIFIER c.-1861G>A| S255
24564 BAA01g17780 A01 8651533 G A upstream_gene_variant MODIFIER c.-3731C>T| S172
S217
24565 BAA01g17790 A01 8652796 C T missense_variant MODERATE c.913C>T|p.Leu305Phe S192
24566 BAA01g17790 A01 8652952 C T missense_variant MODERATE c.1069C>T|p.Pro357Ser S282
24567 BAA01g17790 A01 8653347 G A synonymous_variant LOW c.1389G>A|p.Arg463Arg S105
S106
24568 BAA01g17790 A01 8655589 C T downstream_gene_variant MODIFIER c.*652C>T| S20
24569 BAA01g17790 A01 8657437 G A downstream_gene_variant MODIFIER c.*2500G>A| S58
24570 BAA01g17800 A01 8657727 C T splice_acceptor_variant&intron_variant HIGH c.2371-1G>A| S89
24571 BAA01g17800 A01 8657807 G A splice_region_variant&intron_variant LOW c.2370+8C>T| S37
24572 BAA01g17800 A01 8657837 C T missense_variant MODERATE c.2348G>A|p.Arg783Lys S139
24573 BAA01g17800 A01 8658164 C T missense_variant MODERATE c.2119G>A|p.Asp707Asn S265
24574 BAA01g17800 A01 8658552 C T missense_variant MODERATE c.1942G>A|p.Val648Ile S9
24575 BAA01g17800 A01 8658656 G A splice_region_variant&intron_variant LOW c.1846-8C>T| S129