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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g04430 A09 2616242 C T upstream_gene_variant MODIFIER c.-3571C>T| S255
S264
2 BAA09g04430 A09 2616874 G A upstream_gene_variant MODIFIER c.-2939G>A| S296
3 BAA09g04430 A09 2617143 C T upstream_gene_variant MODIFIER c.-2670C>T| S276
4 BAA09g04430 A09 2617334 C T upstream_gene_variant MODIFIER c.-2479C>T| S292
5 BAA09g04430 A09 2617461 G A upstream_gene_variant MODIFIER c.-2352G>A| S281
6 BAA09g04430 A09 2618389 G A upstream_gene_variant MODIFIER c.-1424G>A| S267
7 BAA09g04430 A09 2618781 G A upstream_gene_variant MODIFIER c.-1032G>A| S45
8 BAA09g04430 A09 2618976 C A upstream_gene_variant MODIFIER c.-837C>A| S298
9 BAA09g04430 A09 2619108 G A upstream_gene_variant MODIFIER c.-705G>A| S201
10 BAA09g04430 A09 2619821 G A synonymous_variant LOW c.9G>A|p.Lys3Lys S127
11 BAA09g04430 A09 2620412 G A missense_variant MODERATE c.532G>A|p.Ala178Thr S139
12 BAA09g04430 A09 2620495 G A stop_gained HIGH c.615G>A|p.Trp205* S236
13 BAA09g04430 A09 2620763 G A missense_variant MODERATE c.883G>A|p.Glu295Lys S32
14 BAA09g04430 A09 2620822 G A synonymous_variant LOW c.942G>A|p.Gln314Gln S226
15 BAA09g04430 A09 2621276 G A missense_variant MODERATE c.1396G>A|p.Glu466Lys S28
16 BAA09g04430 A09 2621529 G A missense_variant MODERATE c.1552G>A|p.Asp518Asn S81
S85
17 BAA09g04430 A09 2622048 G A intron_variant MODIFIER c.1855+216G>A| S130
18 BAA09g04430 A09 2623807 C T downstream_gene_variant MODIFIER c.*391C>T| S186
19 BAA09g04430 A09 2624118 C T downstream_gene_variant MODIFIER c.*702C>T| S107
20 BAA09g04430 A09 2624848 G A downstream_gene_variant MODIFIER c.*1432G>A| S187
21 BAA09g04430 A09 2625005 T A downstream_gene_variant MODIFIER c.*1589T>A| S166
22 BAA09g04430 A09 2626983 G A downstream_gene_variant MODIFIER c.*3567G>A| S218