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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g10140 A04 16359806 G C downstream_gene_variant MODIFIER c.*3593C>G| S174
S27
2 BAA04g10140 A04 16361038 C T downstream_gene_variant MODIFIER c.*2361G>A| S159
S299
3 BAA04g10140 A04 16361204 G A downstream_gene_variant MODIFIER c.*2195C>T| S259
4 BAA04g10140 A04 16361233 G A downstream_gene_variant MODIFIER c.*2166C>T| S12
5 BAA04g10140 A04 16361315 G A downstream_gene_variant MODIFIER c.*2084C>T| S153
S213
6 BAA04g10140 A04 16361415 C T downstream_gene_variant MODIFIER c.*1984G>A| S60
7 BAA04g10140 A04 16361682 C T downstream_gene_variant MODIFIER c.*1717G>A| S98
8 BAA04g10140 A04 16362485 C T downstream_gene_variant MODIFIER c.*914G>A| S291
9 BAA04g10140 A04 16362538 C T downstream_gene_variant MODIFIER c.*861G>A| S140
10 BAA04g10140 A04 16362834 G A downstream_gene_variant MODIFIER c.*565C>T| S153
S213
11 BAA04g10140 A04 16363030 C T downstream_gene_variant MODIFIER c.*369G>A| S243
12 BAA04g10140 A04 16363134 G A downstream_gene_variant MODIFIER c.*265C>T| S74
13 BAA04g10140 A04 16363523 G A missense_variant MODERATE c.1349C>T|p.Thr450Ile S126
14 BAA04g10140 A04 16363627 C T intron_variant MODIFIER c.1278-33G>A| S155
S211
15 BAA04g10140 A04 16364215 G A intron_variant MODIFIER c.1065+26C>T| S62
16 BAA04g10140 A04 16364226 G A intron_variant MODIFIER c.1065+15C>T| S58
17 BAA04g10140 A04 16365359 C T missense_variant MODERATE c.571G>A|p.Gly191Arg S65
18 BAA04g10140 A04 16367363 C T upstream_gene_variant MODIFIER c.-291G>A| S242
19 BAA04g10140 A04 16368051 C T upstream_gene_variant MODIFIER c.-979G>A| S117
20 BAA04g10140 A04 16370995 G A upstream_gene_variant MODIFIER c.-3923C>T| S183
S198
21 BAA04g10140 A04 16371000 C T upstream_gene_variant MODIFIER c.-3928G>A| S267
22 BAA04g10140 A04 16371892 C T upstream_gene_variant MODIFIER c.-4820G>A| S182