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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g46720 A02 37886462 C T splice_region_variant&intron_variant LOW c.3273+6G>A| S179
2 BAA02g46720 A02 37886520 G A missense_variant MODERATE c.3221C>T|p.Pro1074Leu S1
S90
3 BAA02g46720 A02 37887111 G A missense_variant MODERATE c.2992C>T|p.Leu998Phe S50
4 BAA02g46720 A02 37887159 G A missense_variant MODERATE c.2944C>T|p.Leu982Phe S113
5 BAA02g46720 A02 37887564 C T splice_region_variant&intron_variant LOW c.2862+7G>A| S255
6 BAA02g46720 A02 37889871 C T missense_variant MODERATE c.1861G>A|p.Asp621Asn S122
7 BAA02g46720 A02 37891688 C T missense_variant MODERATE c.907G>A|p.Gly303Arg S53
8 BAA02g46720 A02 37891707 C T synonymous_variant LOW c.888G>A|p.Lys296Lys S263
9 BAA02g46720 A02 37891723 G A missense_variant MODERATE c.872C>T|p.Ser291Phe S132
S137
S215
10 BAA02g46720 A02 37891987 C T missense_variant MODERATE c.608G>A|p.Ser203Asn S13
11 BAA02g46720 A02 37892121 C T synonymous_variant LOW c.474G>A|p.Gln158Gln S303
12 BAA02g46720 A02 37892811 G A upstream_gene_variant MODIFIER c.-217C>T| S136
13 BAA02g46720 A02 37895222 C T upstream_gene_variant MODIFIER c.-2628G>A| S289
S290
14 BAA02g46720 A02 37895342 C T upstream_gene_variant MODIFIER c.-2748G>A| S129
15 BAA02g46720 A02 37895451 G A upstream_gene_variant MODIFIER c.-2857C>T| S30
16 BAA02g46720 A02 37895682 C T upstream_gene_variant MODIFIER c.-3088G>A| S198
S52
17 BAA02g46720 A02 37895716 G A upstream_gene_variant MODIFIER c.-3122C>T| S28
18 BAA02g46720 A02 37895754 C T upstream_gene_variant MODIFIER c.-3160G>A| S231
19 BAA02g46720 A02 37896306 C T upstream_gene_variant MODIFIER c.-3712G>A| S299
20 BAA02g46720 A02 37896396 C T upstream_gene_variant MODIFIER c.-3802G>A| S234
21 BAA02g46720 A02 37896557 G A upstream_gene_variant MODIFIER c.-3963C>T| S10
22 BAA02g46720 A02 37897414 G A upstream_gene_variant MODIFIER c.-4820C>T| S57
23 BAA02g46720 A02 37897467 C T upstream_gene_variant MODIFIER c.-4873G>A| S144