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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g17890 A07 24044845 G A upstream_gene_variant MODIFIER c.-2972G>A| S171
2 BAA07g17890 A07 24045335 C T upstream_gene_variant MODIFIER c.-2482C>T| S149
3 BAA07g17890 A07 24045631 G A upstream_gene_variant MODIFIER c.-2186G>A| S271
4 BAA07g17890 A07 24046122 G A upstream_gene_variant MODIFIER c.-1695G>A| S25
5 BAA07g17890 A07 24046488 G T upstream_gene_variant MODIFIER c.-1329G>T| S212
6 BAA07g17890 A07 24047605 C T upstream_gene_variant MODIFIER c.-212C>T| S247
7 BAA07g17890 A07 24047797 C T upstream_gene_variant MODIFIER c.-20C>T| S249
8 BAA07g17890 A07 24047918 C T synonymous_variant LOW c.102C>T|p.Gly34Gly S267
9 BAA07g17890 A07 24048112 C T missense_variant MODERATE c.296C>T|p.Thr99Met S34
10 BAA07g17890 A07 24048213 C T stop_gained HIGH c.397C>T|p.Gln133* S36
11 BAA07g17890 A07 24048735 G A missense_variant MODERATE c.670G>A|p.Ala224Thr S183
12 BAA07g17890 A07 24049569 C T splice_region_variant&intron_variant LOW c.1134-3C>T| S305
13 BAA07g17890 A07 24049840 G A synonymous_variant LOW c.1293G>A|p.Gln431Gln S80
14 BAA07g17890 A07 24050299 C T synonymous_variant LOW c.1557C>T|p.Asn519Asn S275
15 BAA07g17890 A07 24050477 G A missense_variant MODERATE c.1630G>A|p.Asp544Asn S73
16 BAA07g17890 A07 24050958 G A synonymous_variant LOW c.1941G>A|p.Lys647Lys S218
S267
S268
S269
17 BAA07g17890 A07 24050971 G A splice_donor_variant&intron_variant HIGH c.1953+1G>A| S218
S267
S268
S269
18 BAA07g17890 A07 24051209 C T intron_variant MODIFIER c.2091+15C>T| S287
19 BAA07g17890 A07 24051325 G A missense_variant MODERATE c.2135G>A|p.Gly712Glu S182
20 BAA07g17890 A07 24051965 C T synonymous_variant LOW c.2529C>T|p.Pro843Pro S14
S224