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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g31460 A07 31319292 G A splice_region_variant&intron_variant LOW c.771+6G>A| S51
2 BAA07g31460 A07 31322087 C T intron_variant MODIFIER c.1360-371C>T| S265
3 BAA07g31460 A07 31322119 C T intron_variant MODIFIER c.1360-339C>T| S136
4 BAA07g31460 A07 31322192 C T intron_variant MODIFIER c.1360-266C>T| S192
5 BAA07g31460 A07 31322374 C T intron_variant MODIFIER c.1360-84C>T| S296
6 BAA07g31460 A07 31322685 C T intron_variant MODIFIER c.1526+61C>T| S161
7 BAA07g31460 A07 31322717 A T intron_variant MODIFIER c.1526+93A>T| S158
8 BAA07g31460 A07 31323279 C T intron_variant MODIFIER c.1526+655C>T| S292
9 BAA07g31460 A07 31323430 C T intron_variant MODIFIER c.1526+806C>T| S179
10 BAA07g31460 A07 31323477 G A intron_variant MODIFIER c.1526+853G>A| S223
11 BAA07g31460 A07 31323617 G A intron_variant MODIFIER c.1526+993G>A| S6
12 BAA07g31460 A07 31323635 G A intron_variant MODIFIER c.1526+1011G>A| S53
13 BAA07g31460 A07 31324070 G A intron_variant MODIFIER c.1527-1235G>A| S183
S198
14 BAA07g31460 A07 31325513 C T stop_gained HIGH c.1648C>T|p.Gln550* S292
15 BAA07g31460 A07 31327267 C T intron_variant MODIFIER c.2768-11C>T| S197
16 BAA07g31460 A07 31327960 C T missense_variant MODERATE c.3362C>T|p.Thr1121Ile S262
17 BAA07g31460 A07 31328202 G A missense_variant MODERATE c.3604G>A|p.Ala1202Thr S142
18 BAA07g31460 A07 31329878 G A synonymous_variant LOW c.4365G>A|p.Glu1455Glu S298