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 BAA08g09720 A08 8818637 C T downstream_gene_variant MODIFIER c.*4411G>A| S173
2 BAA08g09720 A08 8818681 G A downstream_gene_variant MODIFIER c.*4367C>T| S136
S188
3 BAA08g09720 A08 8820569 C T downstream_gene_variant MODIFIER c.*2479G>A| S256
4 BAA08g09720 A08 8820769 C T downstream_gene_variant MODIFIER c.*2279G>A| S104
S52
5 BAA08g09720 A08 8821207 G A downstream_gene_variant MODIFIER c.*1841C>T| S107
6 BAA08g09720 A08 8821260 G A downstream_gene_variant MODIFIER c.*1788C>T| S8
7 BAA08g09720 A08 8821354 C T downstream_gene_variant MODIFIER c.*1694G>A| S17
8 BAA08g09720 A08 8822539 C T downstream_gene_variant MODIFIER c.*509G>A| S170
9 BAA08g09720 A08 8823044 G A downstream_gene_variant MODIFIER c.*4C>T| S151
10 BAA08g09720 A08 8823197 G A missense_variant MODERATE c.1003C>T|p.Pro335Ser S224
11 BAA08g09720 A08 8823236 C T missense_variant MODERATE c.964G>A|p.Asp322Asn S173
12 BAA08g09720 A08 8823361 G A intron_variant MODIFIER c.942-103C>T| S139
13 BAA08g09720 A08 8823624 G A intron_variant MODIFIER c.942-366C>T| S115
14 BAA08g09720 A08 8823709 C T intron_variant MODIFIER c.942-451G>A| S262
15 BAA08g09720 A08 8823984 G A intron_variant MODIFIER c.942-726C>T| S108
16 BAA08g09720 A08 8828114 G A splice_region_variant&intron_variant LOW c.396+7C>T| S146
17 BAA08g09720 A08 8829385 G A upstream_gene_variant MODIFIER c.-676C>T| S128
18 BAA08g09720 A08 8830563 C T upstream_gene_variant MODIFIER c.-1854G>A| S237
19 BAA08g09720 A08 8831507 C T upstream_gene_variant MODIFIER c.-2798G>A| S268
20 BAA08g09720 A08 8832293 C T upstream_gene_variant MODIFIER c.-3584G>A| S152
S185
21 BAA08g09720 A08 8832476 G A upstream_gene_variant MODIFIER c.-3767C>T| S65
22 BAA08g09720 A08 8832677 C T upstream_gene_variant MODIFIER c.-3968G>A| S52