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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g12990 A07 21081206 C T upstream_gene_variant MODIFIER c.-4298C>T| S292
2 BAA07g12990 A07 21081633 C T upstream_gene_variant MODIFIER c.-3871C>T| S165
3 BAA07g12990 A07 21081637 G A upstream_gene_variant MODIFIER c.-3867G>A| S139
4 BAA07g12990 A07 21082323 G A upstream_gene_variant MODIFIER c.-3181G>A| S98
5 BAA07g12990 A07 21082338 G A upstream_gene_variant MODIFIER c.-3166G>A| S298
6 BAA07g12990 A07 21082780 A G upstream_gene_variant MODIFIER c.-2724A>G| S267
7 BAA07g12990 A07 21084015 G A upstream_gene_variant MODIFIER c.-1489G>A| S79
S91
8 BAA07g12990 A07 21084093 C T upstream_gene_variant MODIFIER c.-1411C>T| S265
9 BAA07g12990 A07 21084959 C T upstream_gene_variant MODIFIER c.-545C>T| S162
10 BAA07g12990 A07 21084993 A T upstream_gene_variant MODIFIER c.-511A>T| S185
11 BAA07g12990 A07 21085560 G A synonymous_variant LOW c.57G>A|p.Lys19Lys S13
12 BAA07g12990 A07 21086242 G A intron_variant MODIFIER c.535+27G>A| S219
S72
13 BAA07g12990 A07 21087750 C T intron_variant MODIFIER c.819+831C>T| S58
14 BAA07g12990 A07 21087757 C T intron_variant MODIFIER c.819+838C>T| S274
15 BAA07g12990 A07 21090010 C T intron_variant MODIFIER c.820-783C>T| S42
16 BAA07g12990 A07 21090680 G A intron_variant MODIFIER c.820-113G>A| S219
S72
17 BAA07g12990 A07 21090700 G A intron_variant MODIFIER c.820-93G>A| S238
18 BAA07g12990 A07 21090838 G A missense_variant MODERATE c.865G>A|p.Asp289Asn S228
19 BAA07g12990 A07 21090938 C T missense_variant MODERATE c.965C>T|p.Pro322Leu S132
S137
S215
20 BAA07g12990 A07 21091090 C T intron_variant MODIFIER c.1030+87C>T| S250
21 BAA07g12990 A07 21091585 G A missense_variant MODERATE c.1186G>A|p.Gly396Ser S104
S105
22 BAA07g12990 A07 21091822 G A synonymous_variant LOW c.1338G>A|p.Leu446Leu S280
23 BAA07g12990 A07 21092123 G T stop_gained HIGH c.1639G>T|p.Glu547* S218
24 BAA07g12990 A07 21092225 C T missense_variant MODERATE c.1741C>T|p.Pro581Ser S20
25 BAA07g12990 A07 21092253 G A missense_variant MODERATE c.1769G>A|p.Arg590Lys S209