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 BAA09g62940 A09 59105218 G A downstream_gene_variant MODIFIER c.*30C>T| S243
2 BAA09g62940 A09 59106046 G A intron_variant MODIFIER c.2095-306C>T| S189
3 BAA09g62940 A09 59106048 C T intron_variant MODIFIER c.2095-308G>A| S20
4 BAA09g62940 A09 59106131 G A intron_variant MODIFIER c.2095-391C>T| S25
5 BAA09g62940 A09 59106916 G A intron_variant MODIFIER c.2094+259C>T| S79
S91
6 BAA09g62940 A09 59107191 G A missense_variant MODERATE c.2078C>T|p.Ser693Phe S81
S85
7 BAA09g62940 A09 59107435 C T missense_variant MODERATE c.1834G>A|p.Asp612Asn S17
8 BAA09g62940 A09 59107501 C T missense_variant MODERATE c.1768G>A|p.Gly590Arg S273
9 BAA09g62940 A09 59107676 G A missense_variant MODERATE c.1676C>T|p.Ser559Phe S73
10 BAA09g62940 A09 59107760 C T missense_variant MODERATE c.1592G>A|p.Arg531His S17
11 BAA09g62940 A09 59109526 G A stop_gained HIGH c.1198C>T|p.Gln400* S265
12 BAA09g62940 A09 59110560 C T missense_variant MODERATE c.392G>A|p.Arg131Lys S51
13 BAA09g62940 A09 59110697 C T synonymous_variant LOW c.255G>A|p.Thr85Thr S192
14 BAA09g62940 A09 59113300 G A upstream_gene_variant MODIFIER c.-2349C>T| S291
15 BAA09g62940 A09 59113391 C T upstream_gene_variant MODIFIER c.-2440G>A| S209
16 BAA09g62940 A09 59113903 C T upstream_gene_variant MODIFIER c.-2952G>A| S100