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
71501 BAA01g37460 A01 25002618 C T upstream_gene_variant MODIFIER c.-608G>A| S82
71502 BAA01g37460 A01 25003171 G A upstream_gene_variant MODIFIER c.-1161C>T| S278
71503 BAA01g37460 A01 25004324 C T upstream_gene_variant MODIFIER c.-2314G>A| S12
71504 BAA01g37460 A01 25005201 G A upstream_gene_variant MODIFIER c.-3191C>T| S265
71505 BAA01g37470 A01 25005442 G A missense_variant MODERATE c.70G>A|p.Ala24Thr S209
71506 BAA01g37460 A01 25005626 G A upstream_gene_variant MODIFIER c.-3616C>T| S221
71507 BAA01g37470 A01 25005804 G A splice_acceptor_variant&intron_variant HIGH c.205-1G>A| S95
71508 BAA01g37470 A01 25006610 C T missense_variant MODERATE c.1010C>T|p.Ser337Leu S59
71509 BAA01g37470 A01 25007273 C T intron_variant MODIFIER c.1032+641C>T| S46
71510 BAA01g37470 A01 25008614 C T intron_variant MODIFIER c.1033-1243C>T| S203
71511 BAA01g37470 A01 25008800 C T intron_variant MODIFIER c.1033-1057C>T| S77
71512 BAA01g37470 A01 25008918 C T intron_variant MODIFIER c.1033-939C>T| S230
71513 BAA01g37470 A01 25009578 T A intron_variant MODIFIER c.1033-279T>A| S210
71514 BAA01g37470 A01 25009861 G A missense_variant MODERATE c.1037G>A|p.Arg346Lys S263
71515 BAA01g37470 A01 25009862 G A synonymous_variant LOW c.1038G>A|p.Arg346Arg S283
71516 BAA01g37470 A01 25009988 G A intron_variant MODIFIER c.1152+12G>A|
71517 BAA01g37470 A01 25010038 G A intron_variant MODIFIER c.1152+62G>A| S97
71518 BAA01g37470 A01 25010115 C A intron_variant MODIFIER c.1152+139C>A| S94
71519 BAA01g37470 A01 25010275 C T intron_variant MODIFIER c.1152+299C>T| S97
71520 BAA01g37470 A01 25010848 G A intron_variant MODIFIER c.1152+872G>A| S287
71521 BAA01g37470 A01 25010980 G A intron_variant MODIFIER c.1152+1004G>A| S290
71522 BAA01g37470 A01 25011305 C T intron_variant MODIFIER c.1152+1329C>T| S10
71523 BAA01g37470 A01 25011385 C T intron_variant MODIFIER c.1152+1409C>T| S228
71524 BAA01g37470 A01 25012927 C T intron_variant MODIFIER c.1153-2367C>T| S249
71525 BAA01g37470 A01 25013639 G A intron_variant MODIFIER c.1153-1655G>A| S6