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
129401 BAA10g17280 A10 16712852 C T missense_variant MODERATE c.1140G>A|p.Met380Ile S190
129402 BAA10g17280 A10 16713577 C T missense_variant MODERATE c.415G>A|p.Glu139Lys S246
129403 BAA10g17290 A10 16715019 G A missense_variant MODERATE c.751C>T|p.His251Tyr S122
129404 BAA10g17280 A10 16717574 G A upstream_gene_variant MODIFIER c.-3583C>T| S276
129405 BAA10g17300 A10 16717944 C T missense_variant MODERATE c.1087G>A|p.Glu363Lys S281
129406 BAA10g17280 A10 16718635 G A upstream_gene_variant MODIFIER c.-4644C>T| S17
129407 BAA10g17280 A10 16718637 G A upstream_gene_variant MODIFIER c.-4646C>T| S126
129408 BAA10g17280 A10 16718667 C T upstream_gene_variant MODIFIER c.-4676G>A| S47
129409 BAA10g17290 A10 16719430 G A upstream_gene_variant MODIFIER c.-3661C>T| S186
129410 BAA10g17290 A10 16719665 G A upstream_gene_variant MODIFIER c.-3896C>T| S180
129411 BAA10g17290 A10 16720599 G A upstream_gene_variant MODIFIER c.-4830C>T| S112
129412 BAA10g17290 A10 16720645 C T upstream_gene_variant MODIFIER c.-4876G>A| S189
129413 BAA10g17290 A10 16720671 C T upstream_gene_variant MODIFIER c.-4902G>A| S47
129414 BAA10g17310 A10 16721945 C T stop_gained HIGH c.1511G>A|p.Trp504* S117
129415 BAA10g17310 A10 16722391 G A synonymous_variant LOW c.1065C>T|p.Asn355Asn S295
129416 BAA10g17310 A10 16722633 G A stop_gained HIGH c.823C>T|p.Gln275* S298
129417 BAA10g17310 A10 16722696 T C missense_variant MODERATE c.760A>G|p.Thr254Ala S133
S265
S286
S91
129418 BAA10g17310 A10 16723193 G A missense_variant MODERATE c.263C>T|p.Thr88Ile S94
129419 BAA10g17320 A10 16723632 G A missense_variant MODERATE c.175G>A|p.Asp59Asn S128
129420 BAA10g17320 A10 16725137 G A missense_variant MODERATE c.829G>A|p.Glu277Lys S292
129421 BAA10g17330 A10 16726219 G A missense_variant MODERATE c.562G>A|p.Ala188Thr S112
129422 BAA10g17330 A10 16726276 G A missense_variant MODERATE c.619G>A|p.Asp207Asn S64
129423 BAA10g17310 A10 16727657 C T upstream_gene_variant MODIFIER c.-4202G>A| S283
129424 BAA10g17340 A10 16727941 C T synonymous_variant LOW c.180C>T|p.Tyr60Tyr S193
129425 BAA10g17340 A10 16728212 G A missense_variant MODERATE c.451G>A|p.Val151Met S273