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
4551 BAA01g03660 A01 1661726 G A upstream_gene_variant MODIFIER c.-4674G>A| S209
S86
4552 BAA01g03660 A01 1663078 G A upstream_gene_variant MODIFIER c.-3322G>A| S146
4553 BAA01g03660 A01 1663220 G A upstream_gene_variant MODIFIER c.-3180G>A| S242
4554 BAA01g03660 A01 1663651 G A upstream_gene_variant MODIFIER c.-2749G>A| S6
4555 BAA01g03660 A01 1664987 G A upstream_gene_variant MODIFIER c.-1413G>A| S123
4556 BAA01g03660 A01 1665183 C T upstream_gene_variant MODIFIER c.-1217C>T| S16
4557 BAA01g03660 A01 1667032 G A missense_variant MODERATE c.353G>A|p.Arg118Lys S84
S93
4558 BAA01g03660 A01 1667370 G A missense_variant MODERATE c.691G>A|p.Gly231Arg S289
S290
4559 BAA01g03660 A01 1667586 G A downstream_gene_variant MODIFIER c.*40G>A| S209
4560 BAA01g03660 A01 1667904 C T downstream_gene_variant MODIFIER c.*358C>T| S158
4561 BAA01g03660 A01 1668938 A C downstream_gene_variant MODIFIER c.*1392A>C| S32
4562 BAA01g03660 A01 1668941 C T downstream_gene_variant MODIFIER c.*1395C>T| S166
4563 BAA01g03660 A01 1669287 G A downstream_gene_variant MODIFIER c.*1741G>A| S165
4564 BAA01g03670 A01 1671067 G A upstream_gene_variant MODIFIER c.-932C>T| S173
4565 BAA01g03670 A01 1671883 C T upstream_gene_variant MODIFIER c.-1748G>A| S35
4566 BAA01g03680 A01 1673627 G A missense_variant MODERATE c.526C>T|p.His176Tyr S250
4567 BAA01g03680 A01 1673754 G A synonymous_variant LOW c.474C>T|p.Asn158Asn S175
4568 BAA01g03670 A01 1674186 G A upstream_gene_variant MODIFIER c.-4051C>T| S303
4569 BAA01g03670 A01 1674693 C T upstream_gene_variant MODIFIER c.-4558G>A| S278
4570 BAA01g03680 A01 1676146 C T upstream_gene_variant MODIFIER c.-1085G>A| S282
4571 BAA01g03690 A01 1680747 G A synonymous_variant LOW c.522G>A|p.Ser174Ser S247
4572 BAA01g03690 A01 1680850 G A missense_variant MODERATE c.625G>A|p.Glu209Lys S190
4573 BAA01g03690 A01 1681073 C T missense_variant MODERATE c.848C>T|p.Ala283Val S218
4574 BAA01g03690 A01 1681340 C T missense_variant MODERATE c.1115C>T|p.Thr372Met S189
4575 BAA01g03700 A01 1681722 G A downstream_gene_variant MODIFIER c.*1531C>T| S110