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
5601 BAA01g04610 A01 2047054 G A downstream_gene_variant MODIFIER c.*762C>T| S146
5602 BAA01g04610 A01 2047429 G A downstream_gene_variant MODIFIER c.*387C>T| S289
S290
5603 BAA01g04610 A01 2048672 G A splice_region_variant&intron_variant LOW c.588+7C>T| S250
5604 BAA01g04610 A01 2049035 C T splice_region_variant&intron_variant LOW c.402+8G>A| S25
5605 BAA01g04610 A01 2051783 G A upstream_gene_variant MODIFIER c.-1940C>T| S289
S290
5606 BAA01g04610 A01 2052937 C T upstream_gene_variant MODIFIER c.-3094G>A| S111
5607 BAA01g04620 A01 2053343 C T synonymous_variant LOW c.1188G>A|p.Gln396Gln S125
5608 BAA01g04620 A01 2055563 C T upstream_gene_variant MODIFIER c.-147G>A| S206
S26
5609 BAA01g04630 A01 2056649 C T missense_variant MODERATE c.355G>A|p.Glu119Lys S158
5610 BAA01g04620 A01 2057408 C T upstream_gene_variant MODIFIER c.-1992G>A| S270
5611 BAA01g04620 A01 2057411 C T upstream_gene_variant MODIFIER c.-1995G>A| S51
5612 BAA01g04640 A01 2057858 C T synonymous_variant LOW c.234G>A|p.Pro78Pro S7
5613 BAA01g04640 A01 2057991 C T missense_variant MODERATE c.176G>A|p.Arg59Lys S236
5614 BAA01g04650 A01 2059159 C T splice_donor_variant&intron_variant HIGH c.162+1G>A| S36
5615 BAA01g04620 A01 2059448 T A upstream_gene_variant MODIFIER c.-4032A>T| S276
5616 BAA01g04650 A01 2059626 G A synonymous_variant LOW c.9C>T|p.Phe3Phe S136
5617 BAA01g04630 A01 2061307 C T upstream_gene_variant MODIFIER c.-4220G>A| S79
S84
5618 BAA01g04630 A01 2061920 C T upstream_gene_variant MODIFIER c.-4833G>A| S240
5619 BAA01g04650 A01 2064162 C T upstream_gene_variant MODIFIER c.-4528G>A| S111
5620 BAA01g04660 A01 2064958 C T upstream_gene_variant MODIFIER c.-3216C>T| S18
5621 BAA01g04660 A01 2066153 C T upstream_gene_variant MODIFIER c.-2021C>T| S235
S236
S260
5622 BAA01g04660 A01 2066409 G A upstream_gene_variant MODIFIER c.-1765G>A| S234
5623 BAA01g04660 A01 2066703 C T upstream_gene_variant MODIFIER c.-1471C>T| S117
5624 BAA01g04660 A01 2066829 G A upstream_gene_variant MODIFIER c.-1345G>A| S295
5625 BAA01g04660 A01 2067050 G A upstream_gene_variant MODIFIER c.-1124G>A| S13