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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g26450 A06 18098092 C T downstream_gene_variant MODIFIER c.*4853G>A| S34
2 BAA06g26450 A06 18098444 C T downstream_gene_variant MODIFIER c.*4501G>A| S15
S3
3 BAA06g26450 A06 18098586 C T downstream_gene_variant MODIFIER c.*4359G>A| S289
S290
4 BAA06g26450 A06 18099048 C T downstream_gene_variant MODIFIER c.*3897G>A| S124
5 BAA06g26450 A06 18099064 C T downstream_gene_variant MODIFIER c.*3881G>A| S205
6 BAA06g26450 A06 18099235 G A downstream_gene_variant MODIFIER c.*3710C>T| S180
7 BAA06g26450 A06 18100352 G A downstream_gene_variant MODIFIER c.*2593C>T| S180
S183
S198
S248
8 BAA06g26450 A06 18100614 C T downstream_gene_variant MODIFIER c.*2331G>A| S18
9 BAA06g26450 A06 18100628 C T downstream_gene_variant MODIFIER c.*2317G>A| S187
10 BAA06g26450 A06 18100927 G A downstream_gene_variant MODIFIER c.*2018C>T| S89
11 BAA06g26450 A06 18101146 G A downstream_gene_variant MODIFIER c.*1799C>T| S246
12 BAA06g26450 A06 18102441 C T downstream_gene_variant MODIFIER c.*504G>A| S135
13 BAA06g26450 A06 18102451 G A downstream_gene_variant MODIFIER c.*494C>T| S144
14 BAA06g26450 A06 18103696 C T missense_variant MODERATE c.1439G>A|p.Gly480Glu S187
15 BAA06g26450 A06 18108612 G A upstream_gene_variant MODIFIER c.-606C>T| S122
16 BAA06g26450 A06 18110076 C T upstream_gene_variant MODIFIER c.-2070G>A| S134
17 BAA06g26450 A06 18110825 G A upstream_gene_variant MODIFIER c.-2819C>T| S131
18 BAA06g26450 A06 18110894 C T upstream_gene_variant MODIFIER c.-2888G>A| S221
19 BAA06g26450 A06 18110952 G A upstream_gene_variant MODIFIER c.-2946C>T| S48
20 BAA06g26450 A06 18111378 C T upstream_gene_variant MODIFIER c.-3372G>A| S172
21 BAA06g26450 A06 18111927 C T upstream_gene_variant MODIFIER c.-3921G>A| S150
22 BAA06g26450 A06 18112919 G A upstream_gene_variant MODIFIER c.-4913C>T| S188
23 BAA06g26450 A06 18112972 G A upstream_gene_variant MODIFIER c.-4966C>T| S136