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
177501 BAA02g18850 A02 9708290 G A stop_gained HIGH c.718C>T|p.Gln240* S281
S282
177502 BAA02g18840 A02 9708992 G A downstream_gene_variant MODIFIER c.*4478G>A| S191
177503 BAA02g18850 A02 9709353 C T synonymous_variant LOW c.45G>A|p.Gln15Gln S34
177504 BAA02g18850 A02 9709577 C T upstream_gene_variant MODIFIER c.-84G>A| S58
177505 BAA02g18850 A02 9710522 G A upstream_gene_variant MODIFIER c.-1029C>T| S291
177506 BAA02g18850 A02 9710562 C T upstream_gene_variant MODIFIER c.-1069G>A| S94
177507 BAA02g18850 A02 9710714 A G upstream_gene_variant MODIFIER c.-1221T>C| S282
177508 BAA02g18850 A02 9711024 G A upstream_gene_variant MODIFIER c.-1531C>T| S257
177509 BAA02g18850 A02 9711064 A T upstream_gene_variant MODIFIER c.-1571T>A| S218
S232
S243
S244
S42
177510 BAA02g18860 A02 9716140 G A downstream_gene_variant MODIFIER c.*1695C>T| S184
177511 BAA02g18860 A02 9717899 G A missense_variant MODERATE c.1301C>T|p.Pro434Leu S247
177512 BAA02g18860 A02 9719513 G A synonymous_variant LOW c.750C>T|p.Tyr250Tyr S272
177513 BAA02g18860 A02 9721187 C T missense_variant MODERATE c.40G>A|p.Asp14Asn S32
177514 BAA02g18860 A02 9721678 C T upstream_gene_variant MODIFIER c.-452G>A| S255
177515 BAA02g18860 A02 9724444 G A upstream_gene_variant MODIFIER c.-3218C>T| S202
177516 BAA02g18870 A02 9727135 C T synonymous_variant LOW c.705G>A|p.Arg235Arg S233
177517 BAA02g18870 A02 9727405 G A intron_variant MODIFIER c.574-48C>T| S235
177518 BAA02g18870 A02 9727946 C T missense_variant MODERATE c.284G>A|p.Gly95Glu S79
S84
177519 BAA02g18870 A02 9728810 G A upstream_gene_variant MODIFIER c.-517C>T| S306
S308
177520 BAA02g18870 A02 9729218 C T upstream_gene_variant MODIFIER c.-925G>A| S1
S90
177521 BAA02g18870 A02 9730051 C T upstream_gene_variant MODIFIER c.-1758G>A| S104
S52
177522 BAA02g18870 A02 9730533 G A upstream_gene_variant MODIFIER c.-2240C>T| S276
177523 BAA02g18870 A02 9731031 C T upstream_gene_variant MODIFIER c.-2738G>A| S250
177524 BAA02g18880 A02 9734237 G A missense_variant MODERATE c.748G>A|p.Ala250Thr S19
177525 BAA02g18880 A02 9734339 G A missense_variant MODERATE c.850G>A|p.Gly284Arg S155
S211