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 BAA02g29230 A02 16700292 C T missense_variant MODERATE c.2368G>A|p.Gly790Ser S276
2 BAA02g29230 A02 16700627 G A synonymous_variant LOW c.2115C>T|p.Ile705Ile S187
3 BAA02g29230 A02 16700685 C T missense_variant MODERATE c.2057G>A|p.Cys686Tyr S40
S49
4 BAA02g29230 A02 16700816 G A intron_variant MODIFIER c.2019-93C>T| S72
S78
5 BAA02g29230 A02 16701202 G A intron_variant MODIFIER c.2019-479C>T| S113
S117
S122
S266
S297
S55
S65
S9
6 BAA02g29230 A02 16701218 C T intron_variant MODIFIER c.2019-495G>A| S299
7 BAA02g29230 A02 16702224 C T intron_variant MODIFIER c.2019-1501G>A| S219
8 BAA02g29230 A02 16702704 C T intron_variant MODIFIER c.2019-1981G>A| S64
9 BAA02g29230 A02 16704835 G A intron_variant MODIFIER c.2018+791C>T| S10
10 BAA02g29230 A02 16704898 C T intron_variant MODIFIER c.2018+728G>A| S182
11 BAA02g29230 A02 16704909 G A intron_variant MODIFIER c.2018+717C>T| S35
12 BAA02g29230 A02 16704960 G A intron_variant MODIFIER c.2018+666C>T| S229
13 BAA02g29230 A02 16706497 C T intron_variant MODIFIER c.1780-303G>A| S203
14 BAA02g29230 A02 16708246 C T missense_variant MODERATE c.1411G>A|p.Asp471Asn S11
15 BAA02g29230 A02 16708394 C T synonymous_variant LOW c.1263G>A|p.Ser421Ser S212
16 BAA02g29230 A02 16708541 C T synonymous_variant LOW c.1116G>A|p.Gln372Gln S308
17 BAA02g29230 A02 16708724 G A synonymous_variant LOW c.933C>T|p.Leu311Leu S256
18 BAA02g29230 A02 16708746 T A missense_variant MODERATE c.911A>T|p.Asp304Val S204
19 BAA02g29230 A02 16709103 G A missense_variant MODERATE c.554C>T|p.Ser185Phe S113
20 BAA02g29230 A02 16709114 C T synonymous_variant LOW c.543G>A|p.Arg181Arg S167
21 BAA02g29230 A02 16710631 C T upstream_gene_variant MODIFIER c.-51G>A| S159
S188
S243
S276
S298
S299
22 BAA02g29230 A02 16710646 C T upstream_gene_variant MODIFIER c.-66G>A| S219
S72
23 BAA02g29230 A02 16710715 C T upstream_gene_variant MODIFIER c.-135G>A| S218
24 BAA02g29230 A02 16710895 C T upstream_gene_variant MODIFIER c.-315G>A| S303
25 BAA02g29230 A02 16711400 C T upstream_gene_variant MODIFIER c.-820G>A| S15