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 BAA09g08230 A09 4595814 C T missense_variant MODERATE c.2843G>A|p.Arg948Lys S54
2 BAA09g08230 A09 4595911 C T intron_variant MODIFIER c.2803-57G>A| S87
3 BAA09g08230 A09 4596498 G A intron_variant MODIFIER c.2566-287C>T| S33
4 BAA09g08230 A09 4597470 C T intron_variant MODIFIER c.2565+908G>A| S257
5 BAA09g08230 A09 4597982 G A intron_variant MODIFIER c.2565+396C>T| S295
6 BAA09g08230 A09 4598216 G A intron_variant MODIFIER c.2565+162C>T| S60
7 BAA09g08230 A09 4598256 G A intron_variant MODIFIER c.2565+122C>T| S178
8 BAA09g08230 A09 4598665 G A intron_variant MODIFIER c.2347-69C>T| S130
9 BAA09g08230 A09 4598821 C T intron_variant MODIFIER c.2347-225G>A| S272
10 BAA09g08230 A09 4599288 C T intron_variant MODIFIER c.2346+15G>A| S287
11 BAA09g08230 A09 4599315 G A synonymous_variant LOW c.2334C>T|p.Leu778Leu S80
12 BAA09g08230 A09 4599350 G A missense_variant MODERATE c.2299C>T|p.Leu767Phe S7
13 BAA09g08230 A09 4599885 G A synonymous_variant LOW c.1899C>T|p.Pro633Pro S98
14 BAA09g08230 A09 4600272 C T synonymous_variant LOW c.1512G>A|p.Gln504Gln S56
15 BAA09g08230 A09 4600900 G A intron_variant MODIFIER c.1285+161C>T| S187
16 BAA09g08230 A09 4601024 G A intron_variant MODIFIER c.1285+37C>T| S163
17 BAA09g08230 A09 4601280 C T missense_variant MODERATE c.1066G>A|p.Val356Met S186
18 BAA09g08230 A09 4601347 C T synonymous_variant LOW c.999G>A|p.Lys333Lys S282
19 BAA09g08230 A09 4601416 G A synonymous_variant LOW c.930C>T|p.Arg310Arg S14
S216
20 BAA09g08230 A09 4602814 C T upstream_gene_variant MODIFIER c.-469G>A| S173
21 BAA09g08230 A09 4603609 C T upstream_gene_variant MODIFIER c.-1264G>A| S130
22 BAA09g08230 A09 4604128 C T upstream_gene_variant MODIFIER c.-1783G>A| S270
23 BAA09g08230 A09 4605366 G A upstream_gene_variant MODIFIER c.-3021C>T| S72