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 BAA06g18600 A06 9499979 C T upstream_gene_variant MODIFIER c.-4912C>T| S272
2 BAA06g18600 A06 9505066 C T missense_variant MODERATE c.176C>T|p.Ala59Val S157
3 BAA06g18600 A06 9506545 C T intron_variant MODIFIER c.589-61C>T| S278
4 BAA06g18600 A06 9507290 C T intron_variant MODIFIER c.795+49C>T| S252
5 BAA06g18600 A06 9507646 C T missense_variant MODERATE c.929C>T|p.Ser310Phe S18
6 BAA06g18600 A06 9508193 C T intron_variant MODIFIER c.1177-26C>T| S15
S156
S3
S34
S4
S6
7 BAA06g18600 A06 9509189 C T intron_variant MODIFIER c.1659+107C>T| S183
S198
8 BAA06g18600 A06 9509203 G A intron_variant MODIFIER c.1659+121G>A| S143
9 BAA06g18600 A06 9509647 C T missense_variant MODERATE c.1709C>T|p.Ser570Phe S267
10 BAA06g18600 A06 9509726 G A synonymous_variant LOW c.1788G>A|p.Lys596Lys S33
11 BAA06g18600 A06 9510062 G A missense_variant&splice_region_variant MODERATE c.1997G>A|p.Arg666Lys S125
12 BAA06g18600 A06 9510241 G A missense_variant MODERATE c.2078G>A|p.Ser693Asn S92
13 BAA06g18600 A06 9510280 C T missense_variant MODERATE c.2117C>T|p.Ser706Phe S283
14 BAA06g18600 A06 9510532 C T splice_region_variant&intron_variant LOW c.2173-4C>T| S157
15 BAA06g18600 A06 9510917 G A missense_variant MODERATE c.2465G>A|p.Gly822Glu S265
16 BAA06g18600 A06 9510993 G A intron_variant MODIFIER c.2485-37G>A| S47
17 BAA06g18600 A06 9511057 G A missense_variant MODERATE c.2512G>A|p.Glu838Lys S246
18 BAA06g18600 A06 9512354 C T downstream_gene_variant MODIFIER c.*1127C>T| S162
19 BAA06g18600 A06 9512442 C T downstream_gene_variant MODIFIER c.*1215C>T| S70
20 BAA06g18600 A06 9512604 G A downstream_gene_variant MODIFIER c.*1377G>A| S190
21 BAA06g18600 A06 9512632 G A downstream_gene_variant MODIFIER c.*1405G>A| S278
22 BAA06g18600 A06 9512718 C T downstream_gene_variant MODIFIER c.*1491C>T| S20
23 BAA06g18600 A06 9513471 C T downstream_gene_variant MODIFIER c.*2244C>T| S249