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
126601 BAA10g15310 A10 15713356 C T upstream_gene_variant MODIFIER c.-4051G>A| S113
126602 BAA10g15310 A10 15713464 C T upstream_gene_variant MODIFIER c.-4159G>A| S84
S93
126603 BAA10g15310 A10 15713676 G A upstream_gene_variant MODIFIER c.-4371C>T| S181
126604 BAA10g15310 A10 15713683 C T upstream_gene_variant MODIFIER c.-4378G>A| S150
126605 BAA10g15330 A10 15716105 C T missense_variant MODERATE c.1456G>A|p.Glu486Lys S302
126606 BAA10g15330 A10 15716712 C T synonymous_variant LOW c.849G>A|p.Leu283Leu S246
126607 BAA10g15330 A10 15717243 G A synonymous_variant LOW c.318C>T|p.Asp106Asp S138
126608 BAA10g15330 A10 15717574 G A upstream_gene_variant MODIFIER c.-14C>T| S137
S215
126609 BAA10g15330 A10 15718504 C T upstream_gene_variant MODIFIER c.-944G>A| S54
126610 BAA10g15340 A10 15718906 C T synonymous_variant LOW c.288G>A|p.Thr96Thr S187
126611 BAA10g15340 A10 15719057 C T missense_variant MODERATE c.223G>A|p.Asp75Asn S152
126612 BAA10g15330 A10 15719257 G A upstream_gene_variant MODIFIER c.-1697C>T| S286
126613 BAA10g15330 A10 15719973 C T upstream_gene_variant MODIFIER c.-2413G>A| S202
126614 BAA10g15330 A10 15719987 C T upstream_gene_variant MODIFIER c.-2427G>A| S12
126615 BAA10g15330 A10 15721262 C T upstream_gene_variant MODIFIER c.-3702G>A| S84
S93
126616 BAA10g15360 A10 15722136 T C missense_variant MODERATE c.772A>G|p.Lys258Glu S62
126617 BAA10g15360 A10 15722966 C T missense_variant MODERATE c.346G>A|p.Glu116Lys S259
126618 BAA10g15360 A10 15726116 C T upstream_gene_variant MODIFIER c.-2805G>A| S206
126619 BAA10g15360 A10 15726607 C T upstream_gene_variant MODIFIER c.-3296G>A| S123
126620 BAA10g15360 A10 15726951 G A upstream_gene_variant MODIFIER c.-3640C>T| S35
126621 BAA10g15360 A10 15727220 C T upstream_gene_variant MODIFIER c.-3909G>A| S200
126622 BAA10g15360 A10 15727270 G A upstream_gene_variant MODIFIER c.-3959C>T| S234
126623 BAA10g15380 A10 15730928 C T missense_variant MODERATE c.143G>A|p.Gly48Glu S2
126624 BAA10g15380 A10 15734299 C T upstream_gene_variant MODIFIER c.-3229G>A| S26
126625 BAA10g15390 A10 15739734 G A upstream_gene_variant MODIFIER c.-4142C>T| S32