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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g32740 A09 41341382 G A upstream_gene_variant MODIFIER c.-4506G>A| S42
2 BAA09g32740 A09 41341661 C T upstream_gene_variant MODIFIER c.-4227C>T| S275
3 BAA09g32740 A09 41342826 C T upstream_gene_variant MODIFIER c.-3062C>T| S144
4 BAA09g32740 A09 41343512 G A upstream_gene_variant MODIFIER c.-2376G>A| S262
S79
S91
5 BAA09g32740 A09 41343620 C T upstream_gene_variant MODIFIER c.-2268C>T| S55
6 BAA09g32740 A09 41343697 G A upstream_gene_variant MODIFIER c.-2191G>A| S181
7 BAA09g32740 A09 41344384 C T upstream_gene_variant MODIFIER c.-1504C>T| S245
8 BAA09g32740 A09 41344474 C T upstream_gene_variant MODIFIER c.-1414C>T| S109
9 BAA09g32740 A09 41344523 C T upstream_gene_variant MODIFIER c.-1365C>T| S135
10 BAA09g32740 A09 41344572 C T upstream_gene_variant MODIFIER c.-1316C>T| S261
S274
11 BAA09g32740 A09 41344596 C T upstream_gene_variant MODIFIER c.-1292C>T| S202
12 BAA09g32740 A09 41344714 C T upstream_gene_variant MODIFIER c.-1174C>T| S283
13 BAA09g32740 A09 41345109 A G upstream_gene_variant MODIFIER c.-779A>G| S109
14 BAA09g32740 A09 41346763 C T missense_variant MODERATE c.616C>T|p.Leu206Phe S206
S26
15 BAA09g32740 A09 41346833 C T missense_variant MODERATE c.686C>T|p.Pro229Leu S267
16 BAA09g32740 A09 41347021 G A missense_variant MODERATE c.874G>A|p.Ala292Thr S124
17 BAA09g32740 A09 41348168 G A downstream_gene_variant MODIFIER c.*1058G>A| S67