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
23501 BAA01g17060 A01 8278598 A G upstream_gene_variant MODIFIER c.-3084A>G| S255
23502 BAA01g17060 A01 8282179 A G intron_variant MODIFIER c.416+82A>G| S61
23503 BAA01g17070 A01 8282553 G A downstream_gene_variant MODIFIER c.*4918C>T| S175
23504 BAA01g17060 A01 8282648 C T missense_variant MODERATE c.472C>T|p.Pro158Ser S8
23505 BAA01g17070 A01 8282883 C T downstream_gene_variant MODIFIER c.*4588G>A| S38
23506 BAA01g17060 A01 8283501 G A synonymous_variant LOW c.798G>A|p.Glu266Glu S116
23507 BAA01g17060 A01 8286507 G A downstream_gene_variant MODIFIER c.*2757G>A| S23
23508 BAA01g17060 A01 8287014 G A downstream_gene_variant MODIFIER c.*3264G>A| S263
23509 BAA01g17070 A01 8287854 G A synonymous_variant LOW c.916C>T|p.Leu306Leu S70
23510 BAA01g17070 A01 8287865 G A missense_variant MODERATE c.905C>T|p.Ser302Phe S139
23511 BAA01g17070 A01 8287929 G A missense_variant MODERATE c.841C>T|p.Pro281Ser S174
S216
S241
S27
S39
23512 BAA01g17070 A01 8287959 G A missense_variant MODERATE c.811C>T|p.Leu271Phe S188
23513 BAA01g17070 A01 8287998 G A missense_variant MODERATE c.772C>T|p.Leu258Phe S124
23514 BAA01g17070 A01 8288015 G A missense_variant MODERATE c.755C>T|p.Ser252Phe S110
23515 BAA01g17070 A01 8288564 C T missense_variant MODERATE c.288G>A|p.Met96Ile S164
23516 BAA01g17070 A01 8290553 C T upstream_gene_variant MODIFIER c.-1702G>A| S213
23517 BAA01g17090 A01 8295179 G A missense_variant MODERATE c.248C>T|p.Pro83Leu S190
23518 BAA01g17080 A01 8295646 C T upstream_gene_variant MODIFIER c.-2328G>A| S25
23519 BAA01g17080 A01 8295685 G T upstream_gene_variant MODIFIER c.-2367C>A| S262
23520 BAA01g17080 A01 8296050 G A upstream_gene_variant MODIFIER c.-2732C>T| S172
23521 BAA01g17080 A01 8296250 C T upstream_gene_variant MODIFIER c.-2932G>A| S242
23522 BAA01g17080 A01 8296960 G A upstream_gene_variant MODIFIER c.-3642C>T| S175
23523 BAA01g17080 A01 8297854 G A upstream_gene_variant MODIFIER c.-4536C>T| S201
23524 BAA01g17080 A01 8298044 G A upstream_gene_variant MODIFIER c.-4726C>T| S40
S49
23525 BAA01g17090 A01 8299724 G T upstream_gene_variant MODIFIER c.-4298C>A| S195