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
158601 BAA02g06170 A02 2621357 G A missense_variant MODERATE c.802G>A|p.Glu268Lys S189
158602 BAA02g06170 A02 2621455 G A synonymous_variant LOW c.900G>A|p.Arg300Arg S202
158603 BAA02g06180 A02 2622375 G A upstream_gene_variant MODIFIER c.-229G>A| S188
158604 BAA02g06180 A02 2623053 C T synonymous_variant LOW c.450C>T|p.Leu150Leu S180
158605 BAA02g06190 A02 2623655 G A upstream_gene_variant MODIFIER c.-148G>A| S136
158606 BAA02g06190 A02 2624141 G A synonymous_variant LOW c.339G>A|p.Glu113Glu S67
158607 BAA02g06190 A02 2624417 G A stop_gained HIGH c.615G>A|p.Trp205* S96
158608 BAA02g06190 A02 2625733 G A missense_variant MODERATE c.1931G>A|p.Gly644Glu S161
158609 BAA02g06190 A02 2625819 G A missense_variant MODERATE c.2017G>A|p.Glu673Lys S48
158610 BAA02g06190 A02 2625953 G A synonymous_variant LOW c.2151G>A|p.Gly717Gly S143
158611 BAA02g06200 A02 2627169 A T upstream_gene_variant MODIFIER c.-225A>T| S38
158612 BAA02g06200 A02 2627377 C T upstream_gene_variant MODIFIER c.-17C>T| S65
158613 BAA02g06210 A02 2628961 G A missense_variant MODERATE c.265G>A|p.Glu89Lys S5
158614 BAA02g06210 A02 2629061 C T missense_variant MODERATE c.365C>T|p.Ser122Leu S47
158615 BAA02g06210 A02 2629101 G A stop_gained HIGH c.405G>A|p.Trp135* S237
158616 BAA02g06210 A02 2630248 G A missense_variant MODERATE c.1552G>A|p.Glu518Lys S48
158617 BAA02g06220 A02 2631170 C T missense_variant MODERATE c.3767G>A|p.Gly1256Glu S226
158618 BAA02g06190 A02 2631256 C T downstream_gene_variant MODIFIER c.*4984C>T| S18
158619 BAA02g06220 A02 2631874 C T missense_variant MODERATE c.3403G>A|p.Glu1135Lys S278
158620 BAA02g06220 A02 2632523 G A missense_variant MODERATE c.2915C>T|p.Ser972Phe S266
158621 BAA02g06220 A02 2633282 C T synonymous_variant LOW c.2259G>A|p.Lys753Lys S116
158622 BAA02g06210 A02 2634428 G A downstream_gene_variant MODIFIER c.*3935G>A| S95
158623 BAA02g06220 A02 2634866 C T synonymous_variant LOW c.1224G>A|p.Glu408Glu S278
158624 BAA02g06220 A02 2635686 G A missense_variant MODERATE c.736C>T|p.Arg246Cys S223
158625 BAA02g06220 A02 2636126 G T splice_region_variant&intron_variant LOW c.466-8C>A| S131
S196
S28
S49