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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g19130 A05 11180870 C T upstream_gene_variant MODIFIER c.-3083C>T| S67
2 BAA05g19130 A05 11181228 C T upstream_gene_variant MODIFIER c.-2725C>T| S255
3 BAA05g19130 A05 11182856 C T upstream_gene_variant MODIFIER c.-1097C>T| S172
4 BAA05g19130 A05 11184012 G A synonymous_variant LOW c.60G>A|p.Thr20Thr S294
5 BAA05g19130 A05 11184156 G A synonymous_variant LOW c.204G>A|p.Leu68Leu S294
6 BAA05g19130 A05 11184265 G A missense_variant MODERATE c.313G>A|p.Glu105Lys S180
7 BAA05g19130 A05 11184854 C T missense_variant MODERATE c.902C>T|p.Thr301Ile S292
8 BAA05g19130 A05 11185011 C T missense_variant&splice_region_variant MODERATE c.916C>T|p.Leu306Phe S202
9 BAA05g19130 A05 11185084 C T missense_variant MODERATE c.989C>T|p.Ala330Val S28
10 BAA05g19130 A05 11185417 C T synonymous_variant LOW c.1191C>T|p.Thr397Thr S9
11 BAA05g19130 A05 11185542 C T missense_variant MODERATE c.1316C>T|p.Ser439Phe S216
12 BAA05g19130 A05 11185566 C T missense_variant MODERATE c.1340C>T|p.Ser447Phe S236
13 BAA05g19130 A05 11185672 C T synonymous_variant LOW c.1446C>T|p.Thr482Thr S143
14 BAA05g19130 A05 11185731 C T missense_variant MODERATE c.1505C>T|p.Ala502Val S185
15 BAA05g19130 A05 11185886 G A missense_variant MODERATE c.1660G>A|p.Glu554Lys S308
16 BAA05g19130 A05 11187251 G A missense_variant MODERATE c.2230G>A|p.Asp744Asn S252
17 BAA05g19130 A05 11187267 G A missense_variant MODERATE c.2246G>A|p.Arg749Lys S6
18 BAA05g19130 A05 11187571 G A synonymous_variant LOW c.2295G>A|p.Glu765Glu S56
19 BAA05g19130 A05 11187574 G A synonymous_variant LOW c.2298G>A|p.Arg766Arg S292