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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g10170 A06 5108621 C T intron_variant MODIFIER c.1380-2221G>A| S28
2 BAA06g10170 A06 5111716 G A missense_variant MODERATE c.1354C>T|p.Pro452Ser S122
3 BAA06g10170 A06 5112993 C T intron_variant MODIFIER c.906-829G>A| S195
4 BAA06g10170 A06 5113484 C T intron_variant MODIFIER c.906-1320G>A| S74
5 BAA06g10170 A06 5113701 G A intron_variant MODIFIER c.906-1537C>T| S41
6 BAA06g10170 A06 5113971 G A intron_variant MODIFIER c.906-1807C>T| S12
7 BAA06g10170 A06 5114321 C T intron_variant MODIFIER c.906-2157G>A| S162
8 BAA06g10170 A06 5114667 C T intron_variant MODIFIER c.906-2503G>A| S262
9 BAA06g10170 A06 5115009 C T intron_variant MODIFIER c.906-2845G>A| S215
10 BAA06g10170 A06 5115569 G A intron_variant MODIFIER c.906-3405C>T| S15
S3
11 BAA06g10170 A06 5115748 G A intron_variant MODIFIER c.906-3584C>T| S208
S219
12 BAA06g10170 A06 5115857 G A intron_variant MODIFIER c.906-3693C>T| S173
13 BAA06g10170 A06 5116225 C T intron_variant MODIFIER c.905+3732G>A| S171
14 BAA06g10170 A06 5116787 C T intron_variant MODIFIER c.905+3170G>A| S148
15 BAA06g10170 A06 5116934 C T intron_variant MODIFIER c.905+3023G>A| S262
16 BAA06g10170 A06 5117154 C T intron_variant MODIFIER c.905+2803G>A| S162
17 BAA06g10170 A06 5117841 C T intron_variant MODIFIER c.905+2116G>A| S176
18 BAA06g10170 A06 5119178 C T intron_variant MODIFIER c.905+779G>A| S177
19 BAA06g10170 A06 5120360 C T missense_variant MODERATE c.502G>A|p.Gly168Ser S260
20 BAA06g10170 A06 5121812 G A upstream_gene_variant MODIFIER c.-581C>T| S54
21 BAA06g10170 A06 5122991 G A upstream_gene_variant MODIFIER c.-1760C>T| S173
22 BAA06g10170 A06 5123000 C T upstream_gene_variant MODIFIER c.-1769G>A| S51
23 BAA06g10170 A06 5124967 C T upstream_gene_variant MODIFIER c.-3736G>A| S16
24 BAA06g10170 A06 5125798 C T upstream_gene_variant MODIFIER c.-4567G>A| S200
25 BAA06g10170 A06 5125878 C T upstream_gene_variant MODIFIER c.-4647G>A| S60