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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
115901 BAA10g10030 A10 11824178 C T upstream_gene_variant MODIFIER c.-574G>A| S132
S137
S215
115902 BAA10g10030 A10 11825530 G A upstream_gene_variant MODIFIER c.-1926C>T| S148
S30
S31
115903 BAA10g10030 A10 11828076 G A upstream_gene_variant MODIFIER c.-4472C>T| S112
115904 BAA10g10030 A10 11828179 G A upstream_gene_variant MODIFIER c.-4575C>T| S18
115905 BAA10g10040 A10 11829069 G A upstream_gene_variant MODIFIER c.-46G>A| S176
115906 BAA10g10040 A10 11829133 C T missense_variant MODERATE c.19C>T|p.Leu7Phe S20
115907 BAA10g10040 A10 11829375 G A stop_gained HIGH c.261G>A|p.Trp87* S292
115908 BAA10g10040 A10 11830497 C T synonymous_variant LOW c.1383C>T|p.Leu461Leu S197
115909 BAA10g10040 A10 11830532 C T missense_variant MODERATE c.1418C>T|p.Ala473Val S206
S26
115910 BAA10g10040 A10 11830779 G A synonymous_variant LOW c.1665G>A|p.Gly555Gly S202
115911 BAA10g10050 A10 11831416 G A upstream_gene_variant MODIFIER c.-1363G>A| S306
S308
115912 BAA10g10050 A10 11833795 G A synonymous_variant LOW c.642G>A|p.Gln214Gln S139
115913 BAA10g10040 A10 11834243 C T downstream_gene_variant MODIFIER c.*3269C>T| S38
115914 BAA10g10050 A10 11835802 G A missense_variant MODERATE c.1240G>A|p.Ala414Thr S245
115915 BAA10g10050 A10 11836620 C T intron_variant MODIFIER c.1600+240C>T| S308
115916 BAA10g10050 A10 11837608 G A intron_variant MODIFIER c.1872+161G>A| S148
S210
S30
S31
115917 BAA10g10050 A10 11837870 C T missense_variant MODERATE c.1900C>T|p.Leu634Phe S268
115918 BAA10g10050 A10 11838363 G A missense_variant MODERATE c.2125G>A|p.Ala709Thr S226
115919 BAA10g10050 A10 11838872 G A intron_variant MODIFIER c.2340+218G>A| S245
115920 BAA10g10050 A10 11839976 C T intron_variant MODIFIER c.2730-87C>T| S34
115921 BAA10g10050 A10 11840435 G A intron_variant MODIFIER c.2958+144G>A| S129
115922 BAA10g10050 A10 11840526 C T intron_variant MODIFIER c.2958+235C>T| S308
115923 BAA10g10050 A10 11840599 C T intron_variant MODIFIER c.2959-175C>T| S20
115924 BAA10g10050 A10 11840946 G A intron_variant MODIFIER c.3087+44G>A| S202
115925 BAA10g10050 A10 11841173 C T intron_variant MODIFIER c.3216+36C>T| S56