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


Gene ID

Results: 1 - 55 of 55 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g16610 A02 8130134 C T missense_variant MODERATE c.5938G>A|p.Asp1980Asn S112
2 BAA02g16610 A02 8132817 G A intron_variant MODIFIER c.5368-2113C>T| S269
3 BAA02g16610 A02 8133262 G A intron_variant MODIFIER c.5368-2558C>T| S184
4 BAA02g16610 A02 8134255 C T intron_variant MODIFIER c.5368-3551G>A| S255
5 BAA02g16610 A02 8134372 C T intron_variant MODIFIER c.5368-3668G>A| S63
6 BAA02g16610 A02 8134756 C T intron_variant MODIFIER c.5368-4052G>A| S252
7 BAA02g16610 A02 8135354 G A intron_variant MODIFIER c.5368-4650C>T| S213
8 BAA02g16610 A02 8135471 G A intron_variant MODIFIER c.5368-4767C>T| S193
9 BAA02g16610 A02 8135768 C T intron_variant MODIFIER c.5368-5064G>A| S206
S26
10 BAA02g16610 A02 8136637 C T intron_variant MODIFIER c.5368-5933G>A| S270
11 BAA02g16610 A02 8138193 C T intron_variant MODIFIER c.5367+6257G>A| S39
12 BAA02g16610 A02 8138519 C A intron_variant MODIFIER c.5367+5931G>T| S61
13 BAA02g16610 A02 8138792 G A intron_variant MODIFIER c.5367+5658C>T| S280
14 BAA02g16610 A02 8139325 C T intron_variant MODIFIER c.5367+5125G>A| S193
15 BAA02g16610 A02 8139988 C T intron_variant MODIFIER c.5367+4462G>A| S203
16 BAA02g16610 A02 8140426 C T intron_variant MODIFIER c.5367+4024G>A| S5
17 BAA02g16610 A02 8140819 G A intron_variant MODIFIER c.5367+3631C>T| S279
18 BAA02g16610 A02 8141724 G A intron_variant MODIFIER c.5367+2726C>T| S69
19 BAA02g16610 A02 8143347 G A intron_variant MODIFIER c.5367+1103C>T| S41
20 BAA02g16610 A02 8144263 A T intron_variant MODIFIER c.5367+187T>A| S274
21 BAA02g16610 A02 8144831 C T synonymous_variant LOW c.4986G>A|p.Arg1662Arg S202
22 BAA02g16610 A02 8145946 C T intron_variant MODIFIER c.4019-148G>A| S208
S219
23 BAA02g16610 A02 8146613 G A intron_variant MODIFIER c.4019-815C>T| S62
24 BAA02g16610 A02 8148170 G A intron_variant MODIFIER c.4019-2372C>T| S13
S168
S279
S64
25 BAA02g16610 A02 8148368 G A intron_variant MODIFIER c.4019-2570C>T| S139