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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g17800 A02 8856718 C T missense_variant MODERATE c.4679G>A|p.Ser1560Asn S179
2 BAA02g17800 A02 8856943 C T missense_variant MODERATE c.4454G>A|p.Gly1485Glu S88
3 BAA02g17800 A02 8857251 G A missense_variant MODERATE c.4325C>T|p.Ala1442Val S87
4 BAA02g17800 A02 8857281 G A missense_variant MODERATE c.4295C>T|p.Pro1432Leu S236
5 BAA02g17800 A02 8858231 C T missense_variant MODERATE c.3542G>A|p.Arg1181Lys S206
S26
6 BAA02g17800 A02 8858266 G A synonymous_variant LOW c.3507C>T|p.Phe1169Phe S236
7 BAA02g17800 A02 8858529 G A missense_variant MODERATE c.3244C>T|p.Pro1082Ser S303
8 BAA02g17800 A02 8858628 G A missense_variant MODERATE c.3145C>T|p.Leu1049Phe S162
9 BAA02g17800 A02 8859196 G A synonymous_variant LOW c.2577C>T|p.Leu859Leu S53
10 BAA02g17800 A02 8859444 C T intron_variant MODIFIER c.2398-69G>A| S302
11 BAA02g17800 A02 8859590 G A intron_variant MODIFIER c.2397+138C>T| S279
12 BAA02g17800 A02 8859662 C T intron_variant MODIFIER c.2397+66G>A| S84
S93
13 BAA02g17800 A02 8859954 G A missense_variant MODERATE c.2171C>T|p.Pro724Leu S116
14 BAA02g17800 A02 8860810 C T synonymous_variant LOW c.1494G>A|p.Leu498Leu S87
15 BAA02g17800 A02 8860960 G A synonymous_variant LOW c.1344C>T|p.His448His S150
16 BAA02g17800 A02 8861562 C T missense_variant MODERATE c.916G>A|p.Asp306Asn S185
S203
S273
17 BAA02g17800 A02 8863063 G A intron_variant MODIFIER c.124+160C>T| S81
S85
18 BAA02g17800 A02 8864906 G A upstream_gene_variant MODIFIER c.-1457C>T| S293
19 BAA02g17800 A02 8865011 T A upstream_gene_variant MODIFIER c.-1562A>T| S211
20 BAA02g17800 A02 8867117 G A upstream_gene_variant MODIFIER c.-3668C>T| S10
S282
21 BAA02g17800 A02 8867643 G A upstream_gene_variant MODIFIER c.-4194C>T| S187
22 BAA02g17800 A02 8868024 C T upstream_gene_variant MODIFIER c.-4575G>A| S186
23 BAA02g17800 A02 8868045 C G upstream_gene_variant MODIFIER c.-4596G>C| S289
S290