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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g04190 A06 2329095 G A upstream_gene_variant MODIFIER c.-987G>A| S62
2 BAA06g04190 A06 2329920 C T upstream_gene_variant MODIFIER c.-162C>T| S63
3 BAA06g04190 A06 2330320 C T missense_variant MODERATE c.239C>T|p.Ala80Val S80
4 BAA06g04190 A06 2331035 G A missense_variant MODERATE c.350G>A|p.Gly117Glu S157
S163
5 BAA06g04190 A06 2331337 G A missense_variant MODERATE c.575G>A|p.Gly192Glu S272
6 BAA06g04190 A06 2331678 G A missense_variant MODERATE c.916G>A|p.Ala306Thr S152
7 BAA06g04190 A06 2332596 C T missense_variant MODERATE c.1208C>T|p.Ser403Leu S167
8 BAA06g04190 A06 2332653 G A missense_variant MODERATE c.1265G>A|p.Gly422Asp S44
9 BAA06g04190 A06 2332655 C T missense_variant MODERATE c.1267C>T|p.Pro423Ser S193
10 BAA06g04190 A06 2333042 C T splice_region_variant&intron_variant LOW c.1513-4C>T| S25
11 BAA06g04190 A06 2333081 G A synonymous_variant LOW c.1548G>A|p.Gln516Gln S219
S72
12 BAA06g04190 A06 2333187 C T missense_variant MODERATE c.1654C>T|p.Pro552Ser S185
13 BAA06g04190 A06 2333299 C T intron_variant MODIFIER c.1717-31C>T| S48
14 BAA06g04190 A06 2333583 G A downstream_gene_variant MODIFIER c.*8G>A| S71
15 BAA06g04190 A06 2334197 G A downstream_gene_variant MODIFIER c.*622G>A| S169
16 BAA06g04190 A06 2334489 A C downstream_gene_variant MODIFIER c.*914A>C| S131
S245
S56
17 BAA06g04190 A06 2334971 G A downstream_gene_variant MODIFIER c.*1396G>A| S38