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
198351 BAA02g29720 A02 17048092 G T missense_variant MODERATE c.244C>A|p.Gln82Lys S244
198352 BAA02g29720 A02 17048109 G A missense_variant MODERATE c.227C>T|p.Ser76Phe S294
198353 BAA02g29720 A02 17049019 C T missense_variant MODERATE c.40G>A|p.Ala14Thr S283
198354 BAA02g29720 A02 17049455 C T upstream_gene_variant MODIFIER c.-397G>A| S289
S290
198355 BAA02g29720 A02 17049481 C T upstream_gene_variant MODIFIER c.-423G>A| S1
198356 BAA02g29720 A02 17050017 G A upstream_gene_variant MODIFIER c.-959C>T| S89
198357 BAA02g29720 A02 17050121 G A upstream_gene_variant MODIFIER c.-1063C>T| S43
198358 BAA02g29720 A02 17050158 C T upstream_gene_variant MODIFIER c.-1100G>A| S15
S156
S168
S3
S34
198359 BAA02g29720 A02 17050168 G A upstream_gene_variant MODIFIER c.-1110C>T| S37
198360 BAA02g29720 A02 17050810 C T upstream_gene_variant MODIFIER c.-1752G>A| S176
198361 BAA02g29720 A02 17052356 C T upstream_gene_variant MODIFIER c.-3298G>A| S164
198362 BAA02g29720 A02 17052512 C T upstream_gene_variant MODIFIER c.-3454G>A| S174
198363 BAA02g29720 A02 17052806 C T upstream_gene_variant MODIFIER c.-3748G>A| S282
198364 BAA02g29720 A02 17052988 C T upstream_gene_variant MODIFIER c.-3930G>A| S224
198365 BAA02g29720 A02 17053023 G A upstream_gene_variant MODIFIER c.-3965C>T| S251
198366 BAA02g29720 A02 17053301 C A upstream_gene_variant MODIFIER c.-4243G>T| S40
S49
198367 BAA02g29720 A02 17053433 G A upstream_gene_variant MODIFIER c.-4375C>T| S13
198368 BAA02g29720 A02 17053779 G A upstream_gene_variant MODIFIER c.-4721C>T| S10
198369 BAA02g29730 A02 17054872 C T downstream_gene_variant MODIFIER c.*2751C>T| S135
198370 BAA02g29730 A02 17056432 C T downstream_gene_variant MODIFIER c.*4311C>T| S257
198371 BAA02g29740 A02 17060213 C A stop_gained HIGH c.1240G>T|p.Glu414* S14
198372 BAA02g29740 A02 17060265 C T splice_acceptor_variant&intron_variant HIGH c.1189-1G>A| S76
198373 BAA02g29740 A02 17060982 C T missense_variant MODERATE c.622G>A|p.Asp208Asn S92
198374 BAA02g29740 A02 17061071 G A missense_variant MODERATE c.533C>T|p.Ser178Phe S17
S95
198375 BAA02g29740 A02 17062511 G A upstream_gene_variant MODIFIER c.-908C>T| S259