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 BAA09g65350 A09 60243055 G A splice_region_variant&synonymous_variant LOW c.2934C>T|p.Gly978Gly S216
2 BAA09g65350 A09 60243162 C T splice_donor_variant&intron_variant HIGH c.2932+1G>A| S153
S213
3 BAA09g65350 A09 60243888 G A missense_variant MODERATE c.2599C>T|p.Leu867Phe S238
4 BAA09g65350 A09 60246236 G A missense_variant MODERATE c.1814C>T|p.Thr605Ile S127
5 BAA09g65350 A09 60246411 G A missense_variant MODERATE c.1742C>T|p.Thr581Met S181
6 BAA09g65350 A09 60247670 C T intron_variant MODIFIER c.1192-72G>A| S237
7 BAA09g65350 A09 60247811 G A intron_variant MODIFIER c.1191+43C>T| S15
S3
8 BAA09g65350 A09 60247835 C T intron_variant MODIFIER c.1191+19G>A| S133
9 BAA09g65350 A09 60248010 C T intron_variant MODIFIER c.1084-49G>A| S275
10 BAA09g65350 A09 60249241 C T splice_region_variant&synonymous_variant LOW c.777G>A|p.Lys259Lys S176
11 BAA09g65350 A09 60249940 G A missense_variant MODERATE c.587C>T|p.Ala196Val S128
12 BAA09g65350 A09 60250684 G A intron_variant MODIFIER c.394+178C>T| S178
13 BAA09g65350 A09 60250722 G A intron_variant MODIFIER c.394+140C>T| S2
14 BAA09g65350 A09 60251247 C T intron_variant MODIFIER c.274-115G>A| S118
15 BAA09g65350 A09 60251624 C T missense_variant MODERATE c.157G>A|p.Val53Ile S162
16 BAA09g65350 A09 60252930 G A missense_variant MODERATE c.29C>T|p.Ser10Phe S155
S211
17 BAA09g65350 A09 60254539 G A upstream_gene_variant MODIFIER c.-1581C>T| S167
18 BAA09g65350 A09 60254954 C T upstream_gene_variant MODIFIER c.-1996G>A| S107