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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g19080 A07 24910961 G A upstream_gene_variant MODIFIER c.-2245G>A| S278
2 BAA07g19080 A07 24913439 G A missense_variant MODERATE c.163G>A|p.Ala55Thr S139
3 BAA07g19080 A07 24914260 C T intron_variant MODIFIER c.372-86C>T| S106
S110
4 BAA07g19080 A07 24915648 C T intron_variant MODIFIER c.732-42C>T| S274
5 BAA07g19080 A07 24915704 G A missense_variant MODERATE c.746G>A|p.Ser249Asn S235
6 BAA07g19080 A07 24917276 C T intron_variant MODIFIER c.941+942C>T| S144
7 BAA07g19080 A07 24917580 C T intron_variant MODIFIER c.941+1246C>T| S162
8 BAA07g19080 A07 24918333 G A intron_variant MODIFIER c.941+1999G>A| S46
9 BAA07g19080 A07 24919083 G A intron_variant MODIFIER c.941+2749G>A| S231
10 BAA07g19080 A07 24919208 G A intron_variant MODIFIER c.941+2874G>A| S174
S265
S27
S39
11 BAA07g19080 A07 24921685 G A intron_variant MODIFIER c.942-1680G>A| S183
12 BAA07g19080 A07 24921891 G A intron_variant MODIFIER c.942-1474G>A| S54
13 BAA07g19080 A07 24921978 C T intron_variant MODIFIER c.942-1387C>T| S173
14 BAA07g19080 A07 24922471 C T intron_variant MODIFIER c.942-894C>T| S218
15 BAA07g19080 A07 24923934 G A synonymous_variant LOW c.1143G>A|p.Arg381Arg S301
16 BAA07g19080 A07 24924539 G A intron_variant MODIFIER c.1210+390G>A| S296
17 BAA07g19080 A07 24925138 C T intron_variant MODIFIER c.1211-244C>T| S281
18 BAA07g19080 A07 24925348 G A intron_variant MODIFIER c.1211-34G>A| S131
19 BAA07g19080 A07 24925759 G A missense_variant MODERATE c.1588G>A|p.Val530Ile S40
S49
20 BAA07g19080 A07 24926112 C T intron_variant MODIFIER c.1793-38C>T| S126
21 BAA07g19080 A07 24926768 A C missense_variant MODERATE c.2126A>C|p.Asn709Thr S164
S17
S178
S259
S297
22 BAA07g19080 A07 24926773 G A missense_variant MODERATE c.2131G>A|p.Glu711Lys S121
23 BAA07g19080 A07 24927140 G A synonymous_variant LOW c.2343G>A|p.Glu781Glu S106
24 BAA07g19080 A07 24927328 C T intron_variant MODIFIER c.2504+27C>T| S148
S30
25 BAA07g19080 A07 24927413 G A missense_variant MODERATE c.2548G>A|p.Glu850Lys S296