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 BAA01g26360 A01 14671323 C T missense_variant MODERATE c.2644G>A|p.Gly882Ser S25
2 BAA01g26360 A01 14671660 C T missense_variant MODERATE c.2588G>A|p.Ser863Asn S295
3 BAA01g26360 A01 14672279 G A synonymous_variant LOW c.2256C>T|p.Asn752Asn S96
4 BAA01g26360 A01 14672724 C T missense_variant MODERATE c.2039G>A|p.Arg680Lys S273
5 BAA01g26360 A01 14672754 C T missense_variant MODERATE c.2009G>A|p.Arg670Lys S4
6 BAA01g26360 A01 14673723 G A intron_variant MODIFIER c.1614+205C>T| S275
7 BAA01g26360 A01 14673743 C T intron_variant MODIFIER c.1614+185G>A| S25
S264
8 BAA01g26360 A01 14675360 G A missense_variant MODERATE c.1448C>T|p.Ser483Phe S105
S106
9 BAA01g26360 A01 14675414 C T missense_variant MODERATE c.1394G>A|p.Gly465Glu S35
10 BAA01g26360 A01 14675451 C T missense_variant MODERATE c.1357G>A|p.Val453Ile S44
11 BAA01g26360 A01 14675601 C T missense_variant MODERATE c.1207G>A|p.Glu403Lys S269
12 BAA01g26360 A01 14675820 C T missense_variant MODERATE c.988G>A|p.Glu330Lys S125
13 BAA01g26360 A01 14676682 C T synonymous_variant LOW c.408G>A|p.Glu136Glu S251
14 BAA01g26360 A01 14676861 G A stop_gained HIGH c.229C>T|p.Gln77* S308
15 BAA01g26360 A01 14676960 C T missense_variant MODERATE c.130G>A|p.Asp44Asn S159
S243
16 BAA01g26360 A01 14677301 G A upstream_gene_variant MODIFIER c.-212C>T| S83
S88
17 BAA01g26360 A01 14677411 C T upstream_gene_variant MODIFIER c.-322G>A| S54
18 BAA01g26360 A01 14677711 G A upstream_gene_variant MODIFIER c.-622C>T| S238
19 BAA01g26360 A01 14677946 G A upstream_gene_variant MODIFIER c.-857C>T| S245
20 BAA01g26360 A01 14679133 G A upstream_gene_variant MODIFIER c.-2044C>T| S71
21 BAA01g26360 A01 14680811 C T upstream_gene_variant MODIFIER c.-3722G>A| S153
22 BAA01g26360 A01 14681078 C T upstream_gene_variant MODIFIER c.-3989G>A| S260
23 BAA01g26360 A01 14681973 C T upstream_gene_variant MODIFIER c.-4884G>A| S198