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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g07820 A10 4840151 G A upstream_gene_variant MODIFIER c.-4971G>A| S281
2 BAA10g07820 A10 4840473 G A upstream_gene_variant MODIFIER c.-4649G>A| S247
3 BAA10g07820 A10 4840960 C T upstream_gene_variant MODIFIER c.-4162C>T| S38
4 BAA10g07820 A10 4841137 C T upstream_gene_variant MODIFIER c.-3985C>T| S2
5 BAA10g07820 A10 4841314 C T upstream_gene_variant MODIFIER c.-3808C>T| S202
6 BAA10g07820 A10 4841448 G A upstream_gene_variant MODIFIER c.-3674G>A| S45
7 BAA10g07820 A10 4841461 T A upstream_gene_variant MODIFIER c.-3661T>A| S35
8 BAA10g07820 A10 4841462 C T upstream_gene_variant MODIFIER c.-3660C>T| S155
S211
9 BAA10g07820 A10 4842028 G A upstream_gene_variant MODIFIER c.-3094G>A| S48
10 BAA10g07820 A10 4842035 C T upstream_gene_variant MODIFIER c.-3087C>T| S210
S225
11 BAA10g07820 A10 4845319 C T synonymous_variant LOW c.198C>T|p.Thr66Thr S297
12 BAA10g07820 A10 4846650 C T intron_variant MODIFIER c.462+1067C>T| S183
13 BAA10g07820 A10 4847763 C T intron_variant MODIFIER c.463-86C>T| S124
14 BAA10g07820 A10 4847797 C T intron_variant MODIFIER c.463-52C>T| S305
15 BAA10g07820 A10 4848632 C T missense_variant MODERATE c.794C>T|p.Ser265Phe S259
16 BAA10g07820 A10 4851328 G A downstream_gene_variant MODIFIER c.*1340G>A| S25
17 BAA10g07820 A10 4851556 G A downstream_gene_variant MODIFIER c.*1568G>A| S291
18 BAA10g07820 A10 4852061 C T downstream_gene_variant MODIFIER c.*2073C>T| S40
S49
19 BAA10g07820 A10 4852445 G A downstream_gene_variant MODIFIER c.*2457G>A| S53
20 BAA10g07820 A10 4853310 C T downstream_gene_variant MODIFIER c.*3322C>T| S294