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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g21390 A05 13646798 G A upstream_gene_variant MODIFIER c.-4732G>A| S158
2 BAA05g21390 A05 13647815 G A upstream_gene_variant MODIFIER c.-3715G>A| S179
3 BAA05g21390 A05 13648196 G A upstream_gene_variant MODIFIER c.-3334G>A| S161
4 BAA05g21390 A05 13648559 G A upstream_gene_variant MODIFIER c.-2971G>A| S37
5 BAA05g21390 A05 13648877 C T upstream_gene_variant MODIFIER c.-2653C>T| S27
6 BAA05g21390 A05 13648932 G A upstream_gene_variant MODIFIER c.-2598G>A| S265
7 BAA05g21390 A05 13649562 C T upstream_gene_variant MODIFIER c.-1968C>T| S99
8 BAA05g21390 A05 13649709 G A upstream_gene_variant MODIFIER c.-1821G>A| S264
9 BAA05g21390 A05 13649943 G A upstream_gene_variant MODIFIER c.-1587G>A| S257
10 BAA05g21390 A05 13650395 C T upstream_gene_variant MODIFIER c.-1135C>T| S54
11 BAA05g21390 A05 13650847 T A upstream_gene_variant MODIFIER c.-683T>A| S217
S248
12 BAA05g21390 A05 13651577 C T synonymous_variant LOW c.48C>T|p.Phe16Phe S5
13 BAA05g21390 A05 13651587 G A missense_variant MODERATE c.58G>A|p.Ala20Thr S62
14 BAA05g21390 A05 13652283 C T intron_variant MODIFIER c.527+227C>T| S206
S26
15 BAA05g21390 A05 13652315 G A intron_variant MODIFIER c.527+259G>A| S114
16 BAA05g21390 A05 13652462 G A intron_variant MODIFIER c.527+406G>A| S168
17 BAA05g21390 A05 13652492 G A intron_variant MODIFIER c.527+436G>A| S97
18 BAA05g21390 A05 13653020 C T intron_variant MODIFIER c.527+964C>T| S202
19 BAA05g21390 A05 13653133 G A intron_variant MODIFIER c.528-924G>A| S80
20 BAA05g21390 A05 13653938 C T intron_variant MODIFIER c.528-119C>T| S169
21 BAA05g21390 A05 13654064 G A missense_variant MODERATE c.535G>A|p.Glu179Lys S249
22 BAA05g21390 A05 13654243 C T synonymous_variant LOW c.714C>T|p.Leu238Leu S174
23 BAA05g21390 A05 13654414 C T synonymous_variant LOW c.885C>T|p.Asn295Asn S229
24 BAA05g21390 A05 13655048 C T missense_variant MODERATE c.1129C>T|p.Leu377Phe S17
25 BAA05g21390 A05 13655533 C T downstream_gene_variant MODIFIER c.*414C>T| S295