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
141551 BAA10g26560 A10 21018210 C T downstream_gene_variant MODIFIER c.*1252G>A| S250
141552 BAA10g26550 A10 21018359 G A synonymous_variant LOW c.978G>A|p.Leu326Leu S197
141553 BAA10g26550 A10 21018998 G A downstream_gene_variant MODIFIER c.*417G>A| S32
141554 BAA10g26550 A10 21019616 G A downstream_gene_variant MODIFIER c.*1035G>A| S286
141555 BAA10g26550 A10 21021487 G A downstream_gene_variant MODIFIER c.*2906G>A| S219
141556 BAA10g26560 A10 21022101 G A missense_variant MODERATE c.3724C>T|p.Leu1242Phe S173
141557 BAA10g26550 A10 21022361 C T downstream_gene_variant MODIFIER c.*3780C>T| S259
S93
141558 BAA10g26560 A10 21024560 G A synonymous_variant LOW c.2256C>T|p.Ser752Ser S62
141559 BAA10g26560 A10 21026109 G A missense_variant MODERATE c.707C>T|p.Ser236Phe S81
S85
141560 BAA10g26560 A10 21026267 C T synonymous_variant LOW c.549G>A|p.Glu183Glu S20
141561 BAA10g26560 A10 21026348 C T synonymous_variant LOW c.468G>A|p.Arg156Arg S45
141562 BAA10g26560 A10 21028057 G A upstream_gene_variant MODIFIER c.-1242C>T| S190
141563 BAA10g26560 A10 21029705 G A upstream_gene_variant MODIFIER c.-2890C>T| S273
141564 BAA10g26560 A10 21029732 G A upstream_gene_variant MODIFIER c.-2917C>T| S130
141565 BAA10g26580 A10 21031515 G A synonymous_variant LOW c.919C>T|p.Leu307Leu S261
141566 BAA10g26590 A10 21031913 G A upstream_gene_variant MODIFIER c.-1614G>A| S13
141567 BAA10g26580 A10 21032563 C T missense_variant MODERATE c.244G>A|p.Asp82Asn S238
141568 BAA10g26580 A10 21032695 G A missense_variant MODERATE c.190C>T|p.Leu64Phe S233
141569 BAA10g26590 A10 21035700 C T synonymous_variant LOW c.1083C>T|p.Asp361Asp S281
141570 BAA10g26590 A10 21036268 G A missense_variant MODERATE c.1394G>A|p.Gly465Glu S130
141571 BAA10g26590 A10 21037708 G A synonymous_variant LOW c.2127G>A|p.Gln709Gln S255
141572 BAA10g26590 A10 21038233 C T synonymous_variant LOW c.2298C>T|p.Asp766Asp S291
141573 BAA10g26600 A10 21038451 C T upstream_gene_variant MODIFIER c.-1209C>T| S308
141574 BAA10g26600 A10 21038581 G A upstream_gene_variant MODIFIER c.-1079G>A| S279
141575 BAA10g26590 A10 21039773 C T downstream_gene_variant MODIFIER c.*871C>T| S157
S163