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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g24660 A05 29671226 C T upstream_gene_variant MODIFIER c.-3972C>T| S84
S93
2 BAA05g24660 A05 29671531 C T upstream_gene_variant MODIFIER c.-3667C>T| S188
3 BAA05g24660 A05 29671733 G A upstream_gene_variant MODIFIER c.-3465G>A| S270
4 BAA05g24660 A05 29672099 G A upstream_gene_variant MODIFIER c.-3099G>A| S46
5 BAA05g24660 A05 29672556 G A upstream_gene_variant MODIFIER c.-2642G>A| S257
6 BAA05g24660 A05 29673099 G A upstream_gene_variant MODIFIER c.-2099G>A| S203
S292
7 BAA05g24660 A05 29673163 G A upstream_gene_variant MODIFIER c.-2035G>A| S59
8 BAA05g24660 A05 29675018 G A upstream_gene_variant MODIFIER c.-180G>A| S298
9 BAA05g24660 A05 29675156 C T upstream_gene_variant MODIFIER c.-42C>T| S63
10 BAA05g24660 A05 29675184 G A upstream_gene_variant MODIFIER c.-14G>A| S225
S73
11 BAA05g24660 A05 29675223 G A missense_variant MODERATE c.26G>A|p.Gly9Glu S124
12 BAA05g24660 A05 29675324 C T missense_variant MODERATE c.50C>T|p.Ala17Val S162
13 BAA05g24660 A05 29675538 G A synonymous_variant LOW c.264G>A|p.Gly88Gly S152
14 BAA05g24660 A05 29675682 G A synonymous_variant LOW c.408G>A|p.Ala136Ala S231
15 BAA05g24660 A05 29675773 G A missense_variant MODERATE c.499G>A|p.Asp167Asn S11
16 BAA05g24660 A05 29676888 G A synonymous_variant LOW c.1263G>A|p.Lys421Lys S230
17 BAA05g24660 A05 29677219 G A missense_variant MODERATE c.1594G>A|p.Glu532Lys S219
18 BAA05g24660 A05 29677230 C T synonymous_variant LOW c.1605C>T|p.Ser535Ser S195
19 BAA05g24660 A05 29677493 C T synonymous_variant LOW c.1797C>T|p.Gly599Gly S202
20 BAA05g24660 A05 29677496 G A synonymous_variant LOW c.1800G>A|p.Lys600Lys S296
21 BAA05g24660 A05 29677534 G A missense_variant MODERATE c.1838G>A|p.Gly613Glu S118
22 BAA05g24660 A05 29679073 C T missense_variant MODERATE c.2744C>T|p.Ala915Val S280
23 BAA05g24660 A05 29679322 G A missense_variant MODERATE c.2993G>A|p.Gly998Glu S110
24 BAA05g24660 A05 29679324 G A missense_variant MODERATE c.2995G>A|p.Glu999Lys S301
S304
25 BAA05g24660 A05 29680125 G A downstream_gene_variant MODIFIER c.*787G>A| S283