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 BAA09g48320 A09 52192779 G A upstream_gene_variant MODIFIER c.-4146G>A| S62
2 BAA09g48320 A09 52192903 G A upstream_gene_variant MODIFIER c.-4022G>A| S172
S217
3 BAA09g48320 A09 52193006 G A upstream_gene_variant MODIFIER c.-3919G>A| S289
S290
4 BAA09g48320 A09 52193954 C T upstream_gene_variant MODIFIER c.-2971C>T| S19
5 BAA09g48320 A09 52195947 C T upstream_gene_variant MODIFIER c.-978C>T| S19
6 BAA09g48320 A09 52196952 C T missense_variant MODERATE c.28C>T|p.Pro10Ser S230
7 BAA09g48320 A09 52197126 G A intron_variant MODIFIER c.168+34G>A| S194
8 BAA09g48320 A09 52197421 C T intron_variant MODIFIER c.169-323C>T| S163
9 BAA09g48320 A09 52197833 G A synonymous_variant LOW c.258G>A|p.Leu86Leu S216
S241
S265
10 BAA09g48320 A09 52198228 C T missense_variant MODERATE c.653C>T|p.Ala218Val S204
11 BAA09g48320 A09 52198568 G A intron_variant MODIFIER c.714+279G>A| S143
12 BAA09g48320 A09 52198615 C T intron_variant MODIFIER c.714+326C>T| S50
13 BAA09g48320 A09 52198874 C T intron_variant MODIFIER c.714+585C>T| S199
14 BAA09g48320 A09 52199496 G A intron_variant MODIFIER c.715-998G>A| S166
15 BAA09g48320 A09 52201854 G A missense_variant MODERATE c.1121G>A|p.Arg374Lys S177
16 BAA09g48320 A09 52202004 C T downstream_gene_variant MODIFIER c.*8C>T| S68
17 BAA09g48320 A09 52202657 C T downstream_gene_variant MODIFIER c.*661C>T| S15
S2
S3
18 BAA09g48320 A09 52202917 G A downstream_gene_variant MODIFIER c.*921G>A| S132
S215
19 BAA09g48320 A09 52203910 G A downstream_gene_variant MODIFIER c.*1914G>A| S158
20 BAA09g48320 A09 52205048 C T downstream_gene_variant MODIFIER c.*3052C>T| S115
21 BAA09g48320 A09 52206228 G A downstream_gene_variant MODIFIER c.*4232G>A| S48
22 BAA09g48320 A09 52206234 G A downstream_gene_variant MODIFIER c.*4238G>A| S13