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
38201 BAA01g24670 A01 13142720 G A upstream_gene_variant MODIFIER c.-4189C>T| S23
38202 BAA01g24670 A01 13143236 G A upstream_gene_variant MODIFIER c.-4705C>T| S239
38203 BAA01g24670 A01 13143281 G A upstream_gene_variant MODIFIER c.-4750C>T| S172
S294
38204 BAA01g24670 A01 13143312 G A upstream_gene_variant MODIFIER c.-4781C>T| S7
38205 BAA01g24690 A01 13152143 C T upstream_gene_variant MODIFIER c.-141C>T| S64
38206 BAA01g24690 A01 13152293 C T missense_variant MODERATE c.10C>T|p.Leu4Phe S155
38207 BAA01g24690 A01 13152692 C T missense_variant MODERATE c.320C>T|p.Ser107Leu S241
S27
S39
38208 BAA01g24690 A01 13153118 G A synonymous_variant LOW c.681G>A|p.Lys227Lys S173
38209 BAA01g24690 A01 13153462 G A missense_variant MODERATE c.1025G>A|p.Arg342Lys S245
38210 BAA01g24690 A01 13154411 G A synonymous_variant LOW c.1974G>A|p.Leu658Leu S71
38211 BAA01g24690 A01 13155949 C T intron_variant MODIFIER c.2715+266C>T| S192
38212 BAA01g24690 A01 13156217 G A intron_variant MODIFIER c.2716-45G>A| S91
38213 BAA01g24690 A01 13156258 C T splice_region_variant&intron_variant LOW c.2716-4C>T| S117
38214 BAA01g24690 A01 13156477 G A synonymous_variant LOW c.2931G>A|p.Glu977Glu S17
38215 BAA01g24690 A01 13156736 C T stop_gained HIGH c.3190C>T|p.Arg1064* S150
38216 BAA01g24690 A01 13157352 C T synonymous_variant LOW c.3723C>T|p.Val1241Val S77
S82
38217 BAA01g24690 A01 13157988 C T intron_variant MODIFIER c.4207-35C>T| S242
38218 BAA01g24690 A01 13158948 C T synonymous_variant LOW c.4902C>T|p.Thr1634Thr S51
38219 BAA01g24690 A01 13159435 G A splice_acceptor_variant&intron_variant HIGH c.5206-1G>A| S165
38220 BAA01g24690 A01 13161145 C T synonymous_variant LOW c.6078C>T|p.Ile2026Ile S273
38221 BAA01g24690 A01 13162313 G A missense_variant MODERATE c.6950G>A|p.Arg2317His S296
38222 BAA01g24700 A01 13162374 C T downstream_gene_variant MODIFIER c.*4287G>A| S163
38223 BAA01g24690 A01 13163652 G A synonymous_variant LOW c.7872G>A|p.Gln2624Gln S155
S211
38224 BAA01g24710 A01 13164296 C T upstream_gene_variant MODIFIER c.-3274C>T| S208
S93
38225 BAA01g24690 A01 13164357 C T missense_variant MODERATE c.8198C>T|p.Ala2733Val S159
S243