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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g41460 A06 26964947 C T upstream_gene_variant MODIFIER c.-4336C>T| S117
2 BAA06g41460 A06 26965514 C T upstream_gene_variant MODIFIER c.-3769C>T| S295
3 BAA06g41460 A06 26966072 G A upstream_gene_variant MODIFIER c.-3211G>A| S118
4 BAA06g41460 A06 26966870 C T upstream_gene_variant MODIFIER c.-2413C>T| S177
5 BAA06g41460 A06 26967339 C T upstream_gene_variant MODIFIER c.-1944C>T| S78
6 BAA06g41460 A06 26967468 C T upstream_gene_variant MODIFIER c.-1815C>T| S106
7 BAA06g41460 A06 26968582 C T upstream_gene_variant MODIFIER c.-701C>T| S203
8 BAA06g41460 A06 26968598 C T upstream_gene_variant MODIFIER c.-685C>T| S157
9 BAA06g41460 A06 26968609 C T upstream_gene_variant MODIFIER c.-674C>T| S286
10 BAA06g41460 A06 26969402 C T synonymous_variant LOW c.51C>T|p.Gly17Gly S301
S304
11 BAA06g41460 A06 26969770 C T synonymous_variant LOW c.261C>T|p.Val87Val S46
12 BAA06g41460 A06 26970061 G A synonymous_variant LOW c.552G>A|p.Lys184Lys S251
13 BAA06g41460 A06 26970096 C T missense_variant MODERATE c.587C>T|p.Ser196Phe S5
14 BAA06g41460 A06 26970241 C T synonymous_variant LOW c.732C>T|p.Asn244Asn S172
S217
15 BAA06g41460 A06 26971780 C T downstream_gene_variant MODIFIER c.*756C>T| S301
S304
16 BAA06g41460 A06 26972557 G A downstream_gene_variant MODIFIER c.*1533G>A| S292