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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g27030 A01 15340843 C T upstream_gene_variant MODIFIER c.-4485C>T| S252
2 BAA01g27030 A01 15340881 C T upstream_gene_variant MODIFIER c.-4447C>T| S231
3 BAA01g27030 A01 15340903 G A upstream_gene_variant MODIFIER c.-4425G>A| S122
4 BAA01g27030 A01 15342811 G A upstream_gene_variant MODIFIER c.-2517G>A| S249
5 BAA01g27030 A01 15344890 G A upstream_gene_variant MODIFIER c.-438G>A| S156
S213
6 BAA01g27030 A01 15344898 G A upstream_gene_variant MODIFIER c.-430G>A| S265
7 BAA01g27030 A01 15345278 G A upstream_gene_variant MODIFIER c.-50G>A| S274
8 BAA01g27030 A01 15345541 C T missense_variant MODERATE c.214C>T|p.Leu72Phe S130
9 BAA01g27030 A01 15346070 C T intron_variant MODIFIER c.622+12C>T| S295
10 BAA01g27030 A01 15347025 G A missense_variant MODERATE c.688G>A|p.Glu230Lys S74
11 BAA01g27030 A01 15350780 G A missense_variant MODERATE c.1544G>A|p.Ser515Asn S121
12 BAA01g27030 A01 15350802 G A intron_variant MODIFIER c.1554+12G>A| S84
S93
13 BAA01g27030 A01 15350906 C T intron_variant MODIFIER c.1555-61C>T| S143
14 BAA01g27030 A01 15351003 C T missense_variant MODERATE c.1591C>T|p.Pro531Ser S38
15 BAA01g27030 A01 15351059 C T synonymous_variant LOW c.1647C>T|p.Val549Val S208
16 BAA01g27030 A01 15351135 C T missense_variant MODERATE c.1723C>T|p.Arg575Trp S11
17 BAA01g27030 A01 15351296 C T synonymous_variant LOW c.1794C>T|p.Arg598Arg S255
18 BAA01g27030 A01 15351488 C T downstream_gene_variant MODIFIER c.*117C>T| S256
19 BAA01g27030 A01 15351505 G A downstream_gene_variant MODIFIER c.*134G>A| S235
20 BAA01g27030 A01 15353265 G A downstream_gene_variant MODIFIER c.*1894G>A| S172
S217
21 BAA01g27030 A01 15355415 G A downstream_gene_variant MODIFIER c.*4044G>A| S144
22 BAA01g27030 A01 15355499 G A downstream_gene_variant MODIFIER c.*4128G>A| S286
23 BAA01g27030 A01 15355520 G A downstream_gene_variant MODIFIER c.*4149G>A| S58
24 BAA01g27030 A01 15355573 G A downstream_gene_variant MODIFIER c.*4202G>A| S291