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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g01280 A05 750438 C T upstream_gene_variant MODIFIER c.-4621C>T| S171
S205
2 BAA05g01280 A05 750915 G A upstream_gene_variant MODIFIER c.-4144G>A| S245
3 BAA05g01280 A05 751558 G C upstream_gene_variant MODIFIER c.-3501G>C| S192
4 BAA05g01280 A05 752162 C T upstream_gene_variant MODIFIER c.-2897C>T| S19
5 BAA05g01280 A05 754438 C T upstream_gene_variant MODIFIER c.-621C>T| S174
S27
6 BAA05g01280 A05 754906 G A upstream_gene_variant MODIFIER c.-153G>A| S111
7 BAA05g01280 A05 755103 C T synonymous_variant LOW c.45C>T|p.Ile15Ile S167
8 BAA05g01280 A05 755187 C T synonymous_variant LOW c.129C>T|p.Pro43Pro S128
9 BAA05g01280 A05 755264 G A missense_variant MODERATE c.206G>A|p.Arg69His S217
S248
10 BAA05g01280 A05 755620 G A intron_variant MODIFIER c.382+180G>A| S174
S216
S27
S39
11 BAA05g01280 A05 755713 G A intron_variant MODIFIER c.383-131G>A| S16
12 BAA05g01280 A05 756056 G A missense_variant MODERATE c.595G>A|p.Ala199Thr S295
13 BAA05g01280 A05 756276 C G missense_variant MODERATE c.815C>G|p.Ala272Gly S143
14 BAA05g01280 A05 756353 G A missense_variant MODERATE c.892G>A|p.Val298Met S282
15 BAA05g01280 A05 756833 C T missense_variant MODERATE c.1372C>T|p.Pro458Ser S13
16 BAA05g01280 A05 758309 G A missense_variant MODERATE c.2848G>A|p.Ala950Thr S219
S72
17 BAA05g01280 A05 758459 G A intron_variant MODIFIER c.2962+36G>A| S157
S163
18 BAA05g01280 A05 758484 G A intron_variant MODIFIER c.2962+61G>A| S163
19 BAA05g01280 A05 758881 G A missense_variant MODERATE c.3253G>A|p.Glu1085Lys S67
20 BAA05g01280 A05 759653 C T intron_variant MODIFIER c.3642+62C>T| S103
21 BAA05g01280 A05 760735 C T intron_variant MODIFIER c.4326+81C>T| S287
22 BAA05g01280 A05 760903 G A missense_variant MODERATE c.4369G>A|p.Gly1457Ser S56
23 BAA05g01280 A05 760911 G A synonymous_variant LOW c.4377G>A|p.Thr1459Thr S1
S90
24 BAA05g01280 A05 762444 T C synonymous_variant LOW c.5790T>C|p.Asn1930Asn S13
S140
S168
25 BAA05g01280 A05 763289 C T synonymous_variant LOW c.6240C>T|p.Asp2080Asp S13