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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g07540 A02 3237552 C T missense_variant MODERATE c.4711G>A|p.Val1571Met S15
S3
2 BAA02g07540 A02 3238517 G A synonymous_variant LOW c.3970C>T|p.Leu1324Leu S59
3 BAA02g07540 A02 3238693 C T intron_variant MODIFIER c.3844-50G>A| S171
4 BAA02g07540 A02 3238939 G A missense_variant MODERATE c.3764C>T|p.Ser1255Leu S133
5 BAA02g07540 A02 3241730 T C intron_variant MODIFIER c.2630+191A>G| S157
S166
S167
S236
S262
S263
6 BAA02g07540 A02 3241985 G A missense_variant MODERATE c.2566C>T|p.Leu856Phe S296
7 BAA02g07540 A02 3242563 C T intron_variant MODIFIER c.2249-171G>A| S192
8 BAA02g07540 A02 3244034 C T intron_variant MODIFIER c.1670-262G>A| S250
9 BAA02g07540 A02 3244604 C T intron_variant MODIFIER c.1669+107G>A| S32
10 BAA02g07540 A02 3244643 C T intron_variant MODIFIER c.1669+68G>A| S56
11 BAA02g07540 A02 3244879 G A missense_variant MODERATE c.1501C>T|p.Pro501Ser S125
12 BAA02g07540 A02 3244947 G A missense_variant MODERATE c.1433C>T|p.Ala478Val S23
13 BAA02g07540 A02 3244984 G A missense_variant MODERATE c.1396C>T|p.Pro466Ser S59
14 BAA02g07540 A02 3245687 G A missense_variant MODERATE c.911C>T|p.Ser304Phe S205
15 BAA02g07540 A02 3246937 C T missense_variant MODERATE c.371G>A|p.Gly124Glu S277
16 BAA02g07540 A02 3249000 C T upstream_gene_variant MODIFIER c.-1250G>A| S152
17 BAA02g07540 A02 3249233 G A upstream_gene_variant MODIFIER c.-1483C>T| S197
18 BAA02g07540 A02 3251072 G A upstream_gene_variant MODIFIER c.-3322C>T| S190
19 BAA02g07540 A02 3251327 G A upstream_gene_variant MODIFIER c.-3577C>T| S136
20 BAA02g07540 A02 3252503 G A upstream_gene_variant MODIFIER c.-4753C>T| S139