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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g05390 A07 4767321 C T downstream_gene_variant MODIFIER c.*4825G>A| S27
2 BAA07g05390 A07 4772357 C T missense_variant MODERATE c.1595G>A|p.Arg532Lys S200
3 BAA07g05390 A07 4772390 G A missense_variant MODERATE c.1562C>T|p.Pro521Leu S107
4 BAA07g05390 A07 4773921 G A intron_variant MODIFIER c.1333+651C>T| S275
5 BAA07g05390 A07 4774659 C T missense_variant MODERATE c.1246G>A|p.Val416Ile S41
6 BAA07g05390 A07 4774790 C T missense_variant MODERATE c.1227G>A|p.Met409Ile S138
7 BAA07g05390 A07 4774939 G A intron_variant MODIFIER c.1091-13C>T| S142
8 BAA07g05390 A07 4775240 G A intron_variant MODIFIER c.978-11C>T| S87
9 BAA07g05390 A07 4775251 T G intron_variant MODIFIER c.978-22A>C| S1
S90
10 BAA07g05390 A07 4775588 G A missense_variant MODERATE c.898C>T|p.Pro300Ser S129
11 BAA07g05390 A07 4776405 G A stop_gained HIGH c.301C>T|p.Gln101* S166
12 BAA07g05390 A07 4776960 C T intron_variant MODIFIER c.87-341G>A| S302
13 BAA07g05390 A07 4777139 G A intron_variant MODIFIER c.87-520C>T| S175
14 BAA07g05390 A07 4777991 G A intron_variant MODIFIER c.86+95C>T| S177
15 BAA07g05390 A07 4778038 C T intron_variant MODIFIER c.86+48G>A| S53
16 BAA07g05390 A07 4781778 C T upstream_gene_variant MODIFIER c.-3607G>A| S167
17 BAA07g05390 A07 4781921 G T upstream_gene_variant MODIFIER c.-3750C>A| S68
18 BAA07g05390 A07 4782030 C T upstream_gene_variant MODIFIER c.-3859G>A| S128
19 BAA07g05390 A07 4782089 C T upstream_gene_variant MODIFIER c.-3918G>A| S267
20 BAA07g05390 A07 4782452 G A upstream_gene_variant MODIFIER c.-4281C>T| S183
21 BAA07g05390 A07 4782841 C T upstream_gene_variant MODIFIER c.-4670G>A| S167
22 BAA07g05390 A07 4783125 G A upstream_gene_variant MODIFIER c.-4954C>T| S51