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
65501 BAA01g34260 A01 22954181 G A upstream_gene_variant MODIFIER c.-1817G>A| S252
65502 BAA01g34260 A01 22956385 G A missense_variant MODERATE c.388G>A|p.Gly130Arg S79
S91
65503 BAA01g34260 A01 22956711 G A intron_variant MODIFIER c.546+168G>A| S110
65504 BAA01g34260 A01 22956856 G A intron_variant MODIFIER c.546+313G>A| S45
65505 BAA01g34260 A01 22957096 C T intron_variant MODIFIER c.547-446C>T| S208
S219
65506 BAA01g34260 A01 22957837 C T missense_variant MODERATE c.842C>T|p.Ser281Leu S39
65507 BAA01g34260 A01 22958394 G A intron_variant MODIFIER c.1018+381G>A| S257
65508 BAA01g34260 A01 22958463 C T intron_variant MODIFIER c.1018+450C>T| S115
65509 BAA01g34260 A01 22958595 C T intron_variant MODIFIER c.1018+582C>T| S146
65510 BAA01g34260 A01 22958799 C T intron_variant MODIFIER c.1018+786C>T| S28
65511 BAA01g34260 A01 22958963 G A intron_variant MODIFIER c.1018+950G>A| S105
S106
65512 BAA01g34260 A01 22959302 A C intron_variant MODIFIER c.1018+1289A>C| S15
S156
S3
S38
65513 BAA01g34260 A01 22959375 C T intron_variant MODIFIER c.1018+1362C>T| S270
65514 BAA01g34260 A01 22960636 C T intron_variant MODIFIER c.1019-1135C>T| S161
65515 BAA01g34260 A01 22961002 C T intron_variant MODIFIER c.1019-769C>T| S23
65516 BAA01g34260 A01 22961529 C T intron_variant MODIFIER c.1019-242C>T| S247
65517 BAA01g34260 A01 22962084 G A synonymous_variant LOW c.1332G>A|p.Gly444Gly S188
65518 BAA01g34260 A01 22962854 G A missense_variant MODERATE c.2102G>A|p.Gly701Glu S202
65519 BAA01g34260 A01 22965025 C T synonymous_variant LOW c.3885C>T|p.Pro1295Pro S56
65520 BAA01g34260 A01 22965498 G A missense_variant MODERATE c.4211G>A|p.Gly1404Glu S274
65521 BAA01g34260 A01 22966513 C T intron_variant MODIFIER c.4976-32C>T| S50
65522 BAA01g34260 A01 22966784 G T missense_variant&splice_region_variant MODERATE c.5215G>T|p.Gly1739Cys S16
65523 BAA01g34260 A01 22967050 C T downstream_gene_variant MODIFIER c.*49C>T| S305
65524 BAA01g34260 A01 22967113 A T downstream_gene_variant MODIFIER c.*112A>T| S279
65525 BAA01g34260 A01 22967351 G A downstream_gene_variant MODIFIER c.*350G>A| S291