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
148751 BAA10g33060 A10 23591337 C T upstream_gene_variant MODIFIER c.-4444C>T| S142
148752 BAA10g33060 A10 23591848 C T upstream_gene_variant MODIFIER c.-3933C>T| S140
148753 BAA10g33060 A10 23592133 G A upstream_gene_variant MODIFIER c.-3648G>A| S240
148754 BAA10g33060 A10 23592242 C T upstream_gene_variant MODIFIER c.-3539C>T| S224
148755 BAA10g33060 A10 23592258 C T upstream_gene_variant MODIFIER c.-3523C>T| S283
148756 BAA10g33050 A10 23594588 C T missense_variant MODERATE c.233G>A|p.Arg78Lys S13
148757 BAA10g33050 A10 23594661 G A missense_variant MODERATE c.160C>T|p.Leu54Phe S128
148758 BAA10g33050 A10 23595002 G A upstream_gene_variant MODIFIER c.-182C>T| S181
148759 BAA10g33050 A10 23595389 G A upstream_gene_variant MODIFIER c.-569C>T| S289
S290
148760 BAA10g33050 A10 23597382 C T upstream_gene_variant MODIFIER c.-2562G>A| S75
S81
148761 BAA10g33060 A10 23598511 C T missense_variant MODERATE c.268C>T|p.Leu90Phe S296
148762 BAA10g33060 A10 23599504 C T stop_gained HIGH c.1261C>T|p.Gln421* S218
148763 BAA10g33060 A10 23599525 C T missense_variant MODERATE c.1282C>T|p.Pro428Ser S148
S210
S30
S31
148764 BAA10g33060 A10 23600584 G A missense_variant MODERATE c.2255G>A|p.Gly752Glu S183
S198
148765 BAA10g33060 A10 23600740 G A missense_variant MODERATE c.2411G>A|p.Gly804Glu S237
148766 BAA10g33060 A10 23600842 G A missense_variant MODERATE c.2513G>A|p.Arg838Lys S274
148767 BAA10g33060 A10 23601082 C T missense_variant MODERATE c.2753C>T|p.Ser918Phe S186
148768 BAA10g33060 A10 23601372 C T stop_gained HIGH c.3043C>T|p.Arg1015* S230
148769 BAA10g33060 A10 23602293 C T intron_variant MODIFIER c.3182+782C>T| S83
S88
148770 BAA10g33060 A10 23602586 G A intron_variant MODIFIER c.3183-618G>A| S59
148771 BAA10g33060 A10 23603102 G A intron_variant MODIFIER c.3183-102G>A| S158
148772 BAA10g33060 A10 23606862 G A intron_variant MODIFIER c.3661+3180G>A| S262
148773 BAA10g33060 A10 23608324 C T intron_variant MODIFIER c.3661+4642C>T| S292
148774 BAA10g33060 A10 23608682 C T intron_variant MODIFIER c.3661+5000C>T| S87
148775 BAA10g33060 A10 23608871 C T intron_variant MODIFIER c.3661+5189C>T| S177