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
172651 BAA02g16350 A02 7979306 G A upstream_gene_variant MODIFIER c.-4215C>T| S20
172652 BAA02g16370 A02 7979694 C T missense_variant MODERATE c.910G>A|p.Asp304Asn S127
172653 BAA02g16370 A02 7980015 C T synonymous_variant LOW c.738G>A|p.Glu246Glu S275
172654 BAA02g16370 A02 7980387 C T missense_variant MODERATE c.531G>A|p.Met177Ile S15
S3
172655 BAA02g16370 A02 7980572 G A synonymous_variant LOW c.423C>T|p.His141His S180
172656 BAA02g16360 A02 7981308 C T downstream_gene_variant MODIFIER c.*2920C>T| S13
172657 BAA02g16370 A02 7981535 G A missense_variant MODERATE c.137C>T|p.Thr46Ile S229
172658 BAA02g16370 A02 7981555 G A synonymous_variant LOW c.117C>T|p.Phe39Phe S50
172659 BAA02g16370 A02 7982504 G A upstream_gene_variant MODIFIER c.-833C>T| S149
S245
172660 BAA02g16370 A02 7982800 C T upstream_gene_variant MODIFIER c.-1129G>A| S99
172661 BAA02g16370 A02 7983604 G A upstream_gene_variant MODIFIER c.-1933C>T| S279
172662 BAA02g16370 A02 7984448 G A upstream_gene_variant MODIFIER c.-2777C>T| S33
172663 BAA02g16380 A02 7986428 C T missense_variant MODERATE c.1310G>A|p.Gly437Glu S202
172664 BAA02g16380 A02 7986731 G A missense_variant MODERATE c.1007C>T|p.Ser336Phe S269
172665 BAA02g16380 A02 7986745 G A synonymous_variant LOW c.993C>T|p.Leu331Leu S176
172666 BAA02g16380 A02 7987433 G A missense_variant MODERATE c.305C>T|p.Ser102Leu S173
172667 BAA02g16380 A02 7987524 G A synonymous_variant LOW c.214C>T|p.Leu72Leu S74
172668 BAA02g16380 A02 7987798 A G upstream_gene_variant MODIFIER c.-61T>C| S39
172669 BAA02g16380 A02 7988262 C T upstream_gene_variant MODIFIER c.-525G>A| S13
172670 BAA02g16380 A02 7989116 C T upstream_gene_variant MODIFIER c.-1379G>A| S207
172671 BAA02g16390 A02 7990121 C T missense_variant MODERATE c.293G>A|p.Gly98Asp S293
172672 BAA02g16380 A02 7990369 C T upstream_gene_variant MODIFIER c.-2632G>A| S216
172673 BAA02g16390 A02 7990500 C T missense_variant MODERATE c.125G>A|p.Gly42Glu S42
172674 BAA02g16380 A02 7991088 C T upstream_gene_variant MODIFIER c.-3351G>A| S139
172675 BAA02g16380 A02 7991332 G A upstream_gene_variant MODIFIER c.-3595C>T| S251