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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g12700 A01 5997894 G A missense_variant MODERATE c.3218C>T|p.Ser1073Phe S79
S91
2 BAA01g12700 A01 5998173 C T missense_variant MODERATE c.3113G>A|p.Gly1038Glu S210
S225
3 BAA01g12700 A01 5999205 G A synonymous_variant LOW c.2721C>T|p.Pro907Pro S247
4 BAA01g12700 A01 5999963 C T missense_variant MODERATE c.2491G>A|p.Gly831Ser S132
S137
S215
5 BAA01g12700 A01 6000362 G A missense_variant MODERATE c.2251C>T|p.Pro751Ser S302
S84
S93
6 BAA01g12700 A01 6000405 G A synonymous_variant LOW c.2208C>T|p.Ile736Ile S193
7 BAA01g12700 A01 6000778 G A intron_variant MODIFIER c.1954-44C>T| S122
8 BAA01g12700 A01 6001492 G A intron_variant MODIFIER c.1814+34C>T| S195
9 BAA01g12700 A01 6002155 C T missense_variant MODERATE c.1364G>A|p.Ser455Asn S48
10 BAA01g12700 A01 6002250 G A intron_variant MODIFIER c.1329+35C>T| S40
S49
11 BAA01g12700 A01 6002807 G A intron_variant MODIFIER c.1122+12C>T| S229
12 BAA01g12700 A01 6003773 G A missense_variant MODERATE c.587C>T|p.Pro196Leu S247
13 BAA01g12700 A01 6003774 G A missense_variant MODERATE c.586C>T|p.Pro196Ser S236
14 BAA01g12700 A01 6003781 C T stop_gained HIGH c.579G>A|p.Trp193* S76
15 BAA01g12700 A01 6003942 A G synonymous_variant LOW c.528T>C|p.Asp176Asp S127
16 BAA01g12700 A01 6005258 G A upstream_gene_variant MODIFIER c.-479C>T| S273
17 BAA01g12700 A01 6007650 T C upstream_gene_variant MODIFIER c.-2871A>G| S249
18 BAA01g12700 A01 6008743 G A upstream_gene_variant MODIFIER c.-3964C>T| S168
19 BAA01g12700 A01 6009254 C T upstream_gene_variant MODIFIER c.-4475G>A| S53