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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g01510 A07 1108524 G A upstream_gene_variant MODIFIER c.-3120G>A| S112
2 BAA07g01510 A07 1108571 C T upstream_gene_variant MODIFIER c.-3073C>T| S136
3 BAA07g01510 A07 1109922 C T upstream_gene_variant MODIFIER c.-1722C>T| S150
4 BAA07g01510 A07 1111315 C T upstream_gene_variant MODIFIER c.-329C>T| S23
5 BAA07g01510 A07 1112910 G A missense_variant MODERATE c.684G>A|p.Met228Ile S15
6 BAA07g01510 A07 1113015 G A synonymous_variant LOW c.789G>A|p.Thr263Thr S225
S73
7 BAA07g01510 A07 1113843 G A missense_variant MODERATE c.1043G>A|p.Arg348Lys S50
8 BAA07g01510 A07 1114073 G A splice_region_variant&synonymous_variant LOW c.1098G>A|p.Lys366Lys S175
9 BAA07g01510 A07 1114331 G A synonymous_variant LOW c.1356G>A|p.Gln452Gln S111
10 BAA07g01510 A07 1114349 C T synonymous_variant LOW c.1374C>T|p.Ser458Ser S155
S211
11 BAA07g01510 A07 1114657 G A missense_variant MODERATE c.1682G>A|p.Gly561Asp S193
12 BAA07g01510 A07 1116786 C T missense_variant MODERATE c.2738C>T|p.Ala913Val S120
13 BAA07g01510 A07 1117612 C T missense_variant MODERATE c.3364C>T|p.Pro1122Ser S152
14 BAA07g01510 A07 1118138 C T downstream_gene_variant MODIFIER c.*293C>T| S133
S202