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
103301 BAA10g07710 A10 4693659 C T stop_gained HIGH c.192G>A|p.Trp64* S242
103302 BAA10g07710 A10 4693693 C T missense_variant MODERATE c.158G>A|p.Arg53Lys S235
103303 BAA10g07720 A10 4693877 C T downstream_gene_variant MODIFIER c.*1328G>A| S224
103304 BAA10g07710 A10 4694489 C T upstream_gene_variant MODIFIER c.-381G>A| S174
S27
103305 BAA10g07710 A10 4694588 G A upstream_gene_variant MODIFIER c.-480C>T| S241
103306 BAA10g07710 A10 4694878 C T upstream_gene_variant MODIFIER c.-770G>A| S79
S91
103307 BAA10g07720 A10 4697271 G A missense_variant MODERATE c.575C>T|p.Ala192Val S120
103308 BAA10g07720 A10 4697299 G A synonymous_variant LOW c.547C>T|p.Leu183Leu S45
103309 BAA10g07710 A10 4698941 G A upstream_gene_variant MODIFIER c.-4833C>T| S105
S106
103310 BAA10g07710 A10 4699078 C T upstream_gene_variant MODIFIER c.-4970G>A| S88
103311 BAA10g07720 A10 4699193 C T upstream_gene_variant MODIFIER c.-1262G>A| S206
S26
103312 BAA10g07720 A10 4699685 C T upstream_gene_variant MODIFIER c.-1754G>A| S281
103313 BAA10g07720 A10 4701287 A T upstream_gene_variant MODIFIER c.-3356T>A| S198
103314 BAA10g07730 A10 4702144 G A missense_variant MODERATE c.508G>A|p.Asp170Asn S268
103315 BAA10g07730 A10 4702243 G A missense_variant MODERATE c.607G>A|p.Ala203Thr S192
103316 BAA10g07720 A10 4702582 C T upstream_gene_variant MODIFIER c.-4651G>A| S161
103317 BAA10g07730 A10 4702675 C T missense_variant MODERATE c.919C>T|p.Leu307Phe S97
103318 BAA10g07730 A10 4703258 G A missense_variant MODERATE c.1502G>A|p.Ser501Asn S78
103319 BAA10g07730 A10 4704440 C T missense_variant MODERATE c.2246C>T|p.Pro749Leu S165
103320 BAA10g07730 A10 4704722 G A missense_variant MODERATE c.2528G>A|p.Gly843Glu S19
103321 BAA10g07730 A10 4704774 G A synonymous_variant LOW c.2580G>A|p.Ala860Ala S164
103322 BAA10g07730 A10 4704846 G A synonymous_variant LOW c.2652G>A|p.Lys884Lys S68
103323 BAA10g07740 A10 4706200 G A missense_variant MODERATE c.454G>A|p.Glu152Lys S125
103324 BAA10g07730 A10 4706380 C T downstream_gene_variant MODIFIER c.*1522C>T| S155
S211
103325 BAA10g07730 A10 4706778 G A downstream_gene_variant MODIFIER c.*1920G>A| S292