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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g56980 A09 56389483 G A missense_variant MODERATE c.520G>A|p.Ala174Thr S110
2 BAA09g56980 A09 56390206 C T synonymous_variant LOW c.1243C>T|p.Leu415Leu S274
3 BAA09g56980 A09 56390367 C T synonymous_variant LOW c.1404C>T|p.Leu468Leu S174
S27
4 BAA09g56980 A09 56391305 G A missense_variant MODERATE c.2254G>A|p.Glu752Lys S249
5 BAA09g56980 A09 56391675 C T missense_variant MODERATE c.2624C>T|p.Ser875Phe S81
S85
6 BAA09g56980 A09 56391941 G A missense_variant MODERATE c.2890G>A|p.Val964Ile S47
7 BAA09g56980 A09 56392649 G A intron_variant MODIFIER c.3323-29G>A| S166
8 BAA09g56980 A09 56393532 C T missense_variant MODERATE c.3926C>T|p.Ser1309Leu S41
9 BAA09g56980 A09 56393870 G A missense_variant MODERATE c.4189G>A|p.Gly1397Ser S263
10 BAA09g56980 A09 56394602 C T intron_variant MODIFIER c.4567+165C>T| S153
S213
11 BAA09g56980 A09 56397249 G A intron_variant MODIFIER c.4567+2812G>A| S23
12 BAA09g56980 A09 56397617 C T intron_variant MODIFIER c.4567+3180C>T| S66
13 BAA09g56980 A09 56398006 C T intron_variant MODIFIER c.4567+3569C>T| S152
14 BAA09g56980 A09 56399576 C T intron_variant MODIFIER c.4568-2715C>T| S265
15 BAA09g56980 A09 56403247 G A missense_variant MODERATE c.4990G>A|p.Glu1664Lys S266
16 BAA09g56980 A09 56403347 C T missense_variant MODERATE c.5090C>T|p.Ser1697Phe S160