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


Gene ID

Results: 1 - 29 of 29 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g41880 A01 27849057 G A upstream_gene_variant MODIFIER c.-4983G>A| S212
2 BAA01g41880 A01 27849186 G A upstream_gene_variant MODIFIER c.-4854G>A| S152
S207
3 BAA01g41880 A01 27849229 C T upstream_gene_variant MODIFIER c.-4811C>T| S73
4 BAA01g41880 A01 27849669 C T upstream_gene_variant MODIFIER c.-4371C>T| S303
5 BAA01g41880 A01 27849861 A G upstream_gene_variant MODIFIER c.-4179A>G| S108
6 BAA01g41880 A01 27849886 G A upstream_gene_variant MODIFIER c.-4154G>A| S271
7 BAA01g41880 A01 27853323 C T upstream_gene_variant MODIFIER c.-717C>T| S23
8 BAA01g41880 A01 27853597 C T upstream_gene_variant MODIFIER c.-443C>T| S171
9 BAA01g41880 A01 27853966 C T upstream_gene_variant MODIFIER c.-74C>T| S63
10 BAA01g41880 A01 27854182 G A intron_variant MODIFIER c.45+98G>A| S217
S248
11 BAA01g41880 A01 27855247 C T intron_variant MODIFIER c.340-30C>T| S221
12 BAA01g41880 A01 27855713 G A synonymous_variant LOW c.600G>A|p.Arg200Arg S238
13 BAA01g41880 A01 27855967 C T intron_variant MODIFIER c.754+18C>T| S181
S289
S290
14 BAA01g41880 A01 27856349 C T missense_variant MODERATE c.971C>T|p.Ser324Phe S305
15 BAA01g41880 A01 27856569 G A missense_variant MODERATE c.1103G>A|p.Gly368Glu S262
16 BAA01g41880 A01 27856853 C T intron_variant MODIFIER c.1245+10C>T| S256
17 BAA01g41880 A01 27856971 C T missense_variant MODERATE c.1271C>T|p.Thr424Ile S288
18 BAA01g41880 A01 27856995 G A missense_variant MODERATE c.1295G>A|p.Gly432Glu S229
19 BAA01g41880 A01 27857161 C T intron_variant MODIFIER c.1443+18C>T| S64
20 BAA01g41880 A01 27857533 G A intron_variant MODIFIER c.1620+45G>A| S152
21 BAA01g41880 A01 27857542 G A intron_variant MODIFIER c.1620+54G>A| S199
22 BAA01g41880 A01 27859592 G A intron_variant MODIFIER c.2877-16G>A| S138
23 BAA01g41880 A01 27859631 G A missense_variant MODERATE c.2900G>A|p.Gly967Asp S271
24 BAA01g41880 A01 27859930 C T missense_variant MODERATE c.3199C>T|p.Pro1067Ser S110
S81
S85
25 BAA01g41880 A01 27859940 G A missense_variant MODERATE c.3209G>A|p.Gly1070Glu S197