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 BAA10g08430 A10 10231490 C T upstream_gene_variant MODIFIER c.-1648C>T| S86
2 BAA10g08430 A10 10231899 G A upstream_gene_variant MODIFIER c.-1239G>A| S230
3 BAA10g08430 A10 10232569 G A upstream_gene_variant MODIFIER c.-569G>A| S100
4 BAA10g08430 A10 10232648 C T upstream_gene_variant MODIFIER c.-490C>T| S70
5 BAA10g08430 A10 10233137 G A upstream_gene_variant MODIFIER c.-1G>A| S161
6 BAA10g08430 A10 10233436 G A splice_region_variant&intron_variant LOW c.209+6G>A| S157
S163
7 BAA10g08430 A10 10233646 C T intron_variant MODIFIER c.282-26C>T| S235
8 BAA10g08430 A10 10233706 C T missense_variant MODERATE c.316C>T|p.Leu106Phe S131
9 BAA10g08430 A10 10234106 C T intron_variant MODIFIER c.356+360C>T| S155
10 BAA10g08430 A10 10234516 C T intron_variant MODIFIER c.357-210C>T| S268
11 BAA10g08430 A10 10234787 C T missense_variant MODERATE c.418C>T|p.Leu140Phe S167
12 BAA10g08430 A10 10234818 C T intron_variant MODIFIER c.428+21C>T| S233
13 BAA10g08430 A10 10234831 C T intron_variant MODIFIER c.428+34C>T| S46
14 BAA10g08430 A10 10235049 G A synonymous_variant LOW c.588G>A|p.Lys196Lys S32
15 BAA10g08430 A10 10235460 C T missense_variant MODERATE c.760C>T|p.Leu254Phe S166
16 BAA10g08430 A10 10235835 C T synonymous_variant LOW c.930C>T|p.Ile310Ile S269
17 BAA10g08430 A10 10236018 C T splice_region_variant&intron_variant LOW c.1028+7C>T| S122
18 BAA10g08430 A10 10237085 C T stop_gained HIGH c.1045C>T|p.Arg349* S167
19 BAA10g08430 A10 10237331 G A missense_variant MODERATE c.1199G>A|p.Gly400Glu S88
20 BAA10g08430 A10 10237494 G A synonymous_variant LOW c.1362G>A|p.Gly454Gly S15
S3
21 BAA10g08430 A10 10237538 C T missense_variant MODERATE c.1406C>T|p.Thr469Ile S189
22 BAA10g08430 A10 10238403 G A missense_variant MODERATE c.2023G>A|p.Glu675Lys S25