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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18370 A10 17208249 C T upstream_gene_variant MODIFIER c.-4756C>T| S48
2 BAA10g18370 A10 17208933 C T upstream_gene_variant MODIFIER c.-4072C>T| S116
3 BAA10g18370 A10 17209040 G A upstream_gene_variant MODIFIER c.-3965G>A| S181
4 BAA10g18370 A10 17211059 C T upstream_gene_variant MODIFIER c.-1946C>T| S225
S73
5 BAA10g18370 A10 17211375 C T upstream_gene_variant MODIFIER c.-1630C>T| S45
6 BAA10g18370 A10 17211505 C T upstream_gene_variant MODIFIER c.-1500C>T| S87
7 BAA10g18370 A10 17211507 C T upstream_gene_variant MODIFIER c.-1498C>T| S275
8 BAA10g18370 A10 17211562 C A upstream_gene_variant MODIFIER c.-1443C>A| S259
9 BAA10g18370 A10 17211813 G A upstream_gene_variant MODIFIER c.-1192G>A| S219
S72
10 BAA10g18370 A10 17212126 G A upstream_gene_variant MODIFIER c.-879G>A| S131
11 BAA10g18370 A10 17213351 C T synonymous_variant LOW c.144C>T|p.Leu48Leu S183
12 BAA10g18370 A10 17213430 C T missense_variant MODERATE c.223C>T|p.Pro75Ser S260
13 BAA10g18370 A10 17213582 G A synonymous_variant LOW c.375G>A|p.Lys125Lys S278
14 BAA10g18370 A10 17214495 G T synonymous_variant LOW c.1053G>T|p.Leu351Leu S222
S227
S75
15 BAA10g18370 A10 17214775 G A missense_variant MODERATE c.1163G>A|p.Arg388Lys S109
16 BAA10g18370 A10 17219673 C T downstream_gene_variant MODIFIER c.*4526C>T| S61
17 BAA10g18370 A10 17219863 C T downstream_gene_variant MODIFIER c.*4716C>T| S202