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


Gene ID

Results: 1 - 13 of 13 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g39230 A07 35273862 G A missense_variant MODERATE c.2210C>T|p.Thr737Ile S87
2 BAA07g39230 A07 35275965 C T missense_variant MODERATE c.1066G>A|p.Ala356Thr S8
3 BAA07g39230 A07 35276278 G A missense_variant MODERATE c.851C>T|p.Ser284Leu S171
4 BAA07g39230 A07 35276542 G A splice_region_variant&intron_variant LOW c.744+7C>T| S110
5 BAA07g39230 A07 35276600 C T synonymous_variant LOW c.693G>A|p.Lys231Lys S42
6 BAA07g39230 A07 35276741 C T synonymous_variant LOW c.552G>A|p.Glu184Glu S86
7 BAA07g39230 A07 35277025 G A synonymous_variant LOW c.268C>T|p.Leu90Leu S126
8 BAA07g39230 A07 35277403 C T upstream_gene_variant MODIFIER c.-111G>A| S303
9 BAA07g39230 A07 35277521 C T upstream_gene_variant MODIFIER c.-229G>A| S132
S137
S138
S288
10 BAA07g39230 A07 35278397 G A upstream_gene_variant MODIFIER c.-1105C>T| S136
11 BAA07g39230 A07 35278889 C T upstream_gene_variant MODIFIER c.-1597G>A| S61
12 BAA07g39230 A07 35279479 C T upstream_gene_variant MODIFIER c.-2187G>A| S34
13 BAA07g39230 A07 35281800 G A upstream_gene_variant MODIFIER c.-4508C>T| S136