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
77401 BAA01g40880 A01 27068640 T C upstream_gene_variant MODIFIER c.-1088A>G| S298
77402 BAA01g40880 A01 27068895 C T upstream_gene_variant MODIFIER c.-1343G>A| S56
77403 BAA01g40880 A01 27069180 G A upstream_gene_variant MODIFIER c.-1628C>T| S271
77404 BAA01g40880 A01 27069251 G A upstream_gene_variant MODIFIER c.-1699C>T| S283
77405 BAA01g40880 A01 27069480 C T upstream_gene_variant MODIFIER c.-1928G>A| S107
77406 BAA01g40880 A01 27069681 G A upstream_gene_variant MODIFIER c.-2129C>T| S268
77407 BAA01g40880 A01 27071048 C T upstream_gene_variant MODIFIER c.-3496G>A| S203
77408 BAA01g40880 A01 27071074 C T upstream_gene_variant MODIFIER c.-3522G>A| S132
S137
S215
S89
77409 BAA01g40880 A01 27071106 C T upstream_gene_variant MODIFIER c.-3554G>A| S63
77410 BAA01g40880 A01 27071901 C T upstream_gene_variant MODIFIER c.-4349G>A| S302
77411 BAA01g40890 A01 27071963 G A missense_variant MODERATE c.106G>A|p.Asp36Asn S42
77412 BAA01g40890 A01 27073160 G A missense_variant MODERATE c.1009G>A|p.Glu337Lys S187
77413 BAA01g40890 A01 27073330 T C synonymous_variant LOW c.1179T>C|p.Pro393Pro S88
77414 BAA01g40890 A01 27073600 G A missense_variant MODERATE c.1363G>A|p.Glu455Lys S108
77415 BAA01g40890 A01 27073630 C T missense_variant MODERATE c.1393C>T|p.Pro465Ser S136
77416 BAA01g40890 A01 27073719 G A synonymous_variant LOW c.1482G>A|p.Arg494Arg S308
77417 BAA01g40900 A01 27074017 C T upstream_gene_variant MODIFIER c.-1421C>T| S281
77418 BAA01g40890 A01 27074373 G A missense_variant&splice_region_variant MODERATE c.1612G>A|p.Asp538Asn S221
77419 BAA01g40890 A01 27074445 G A missense_variant MODERATE c.1684G>A|p.Glu562Lys S177
77420 BAA01g40910 A01 27077227 G A missense_variant MODERATE c.160C>T|p.Leu54Phe S104
77421 BAA01g40910 A01 27077881 C T upstream_gene_variant MODIFIER c.-495G>A| S162
77422 BAA01g40910 A01 27080023 C T upstream_gene_variant MODIFIER c.-2637G>A| S115
77423 BAA01g40910 A01 27080664 C T upstream_gene_variant MODIFIER c.-3278G>A| S216
77424 BAA01g40910 A01 27080822 G A upstream_gene_variant MODIFIER c.-3436C>T| S108
77425 BAA01g40910 A01 27081301 C T upstream_gene_variant MODIFIER c.-3915G>A| S305