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 BAA02g34070 A02 29204355 C T upstream_gene_variant MODIFIER c.-2947C>T| S240
2 BAA02g34070 A02 29204462 G A upstream_gene_variant MODIFIER c.-2840G>A| S34
3 BAA02g34070 A02 29205244 C T upstream_gene_variant MODIFIER c.-2058C>T| S246
4 BAA02g34070 A02 29205308 G A upstream_gene_variant MODIFIER c.-1994G>A| S125
5 BAA02g34070 A02 29205738 G A upstream_gene_variant MODIFIER c.-1564G>A| S306
S308
6 BAA02g34070 A02 29206953 G A upstream_gene_variant MODIFIER c.-349G>A| S228
7 BAA02g34070 A02 29207057 G A upstream_gene_variant MODIFIER c.-245G>A| S71
8 BAA02g34070 A02 29207068 G A upstream_gene_variant MODIFIER c.-234G>A| S111
9 BAA02g34070 A02 29211475 G A missense_variant MODERATE c.425G>A|p.Arg142Lys S272
10 BAA02g34070 A02 29211540 G A missense_variant MODERATE c.490G>A|p.Gly164Arg S95
11 BAA02g34070 A02 29211722 C T intron_variant MODIFIER c.533+56C>T| S37
12 BAA02g34070 A02 29212822 C T intron_variant MODIFIER c.534-505C>T| S79
S84
13 BAA02g34070 A02 29213160 C T intron_variant MODIFIER c.534-167C>T| S15
S156
S3
S34
14 BAA02g34070 A02 29213243 A C intron_variant MODIFIER c.534-84A>C| S51
S77
15 BAA02g34070 A02 29215198 G A missense_variant MODERATE c.1217G>A|p.Gly406Glu S268
16 BAA02g34070 A02 29215946 G A splice_region_variant&intron_variant LOW c.1959+6G>A| S187
17 BAA02g34070 A02 29216119 C T splice_region_variant&intron_variant LOW c.1960-5C>T| S212
18 BAA02g34070 A02 29216557 G A missense_variant MODERATE c.2231G>A|p.Gly744Asp S224
19 BAA02g34070 A02 29216596 G A missense_variant MODERATE c.2270G>A|p.Ser757Asn S279