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
134151 BAA10g20370-BAA10g20380 A10 18362099 C T intergenic_region MODIFIER n.18362099C>T| S168
S219
S72
134152 BAA10g20380 A10 18364215 C T upstream_gene_variant MODIFIER c.-3275C>T| S247
134153 BAA10g20380 A10 18365111 C T upstream_gene_variant MODIFIER c.-2379C>T| S45
134154 BAA10g20380 A10 18369198 C T synonymous_variant LOW c.492C>T|p.Ser164Ser S11
134155 BAA10g20380 A10 18369388 C T missense_variant MODERATE c.682C>T|p.Pro228Ser S8
134156 BAA10g20390 A10 18370474 G A upstream_gene_variant MODIFIER c.-420G>A| S233
134157 BAA10g20380 A10 18371414 C T downstream_gene_variant MODIFIER c.*1706C>T| S107
134158 BAA10g20380 A10 18371487 G A downstream_gene_variant MODIFIER c.*1779G>A| S198
134159 BAA10g20380 A10 18371804 C T downstream_gene_variant MODIFIER c.*2096C>T| S282
134160 BAA10g20380 A10 18371912 G A downstream_gene_variant MODIFIER c.*2204G>A| S303
134161 BAA10g20380 A10 18371997 C T downstream_gene_variant MODIFIER c.*2289C>T| S189
134162 BAA10g20380 A10 18372226 C T downstream_gene_variant MODIFIER c.*2518C>T| S206
S26
134163 BAA10g20380 A10 18372246 T A downstream_gene_variant MODIFIER c.*2538T>A| S204
134164 BAA10g20390 A10 18372986 G A missense_variant MODERATE c.514G>A|p.Asp172Asn S263
134165 BAA10g20390 A10 18373568 C T missense_variant MODERATE c.905C>T|p.Ala302Val S12
134166 BAA10g20390 A10 18373590 C T synonymous_variant LOW c.927C>T|p.Ile309Ile S286
134167 BAA10g20390 A10 18373656 C T synonymous_variant LOW c.993C>T|p.Pro331Pro S183
134168 BAA10g20400 A10 18377628 C T upstream_gene_variant MODIFIER c.-432G>A| S83
S88
134169 BAA10g20400 A10 18378273 C T upstream_gene_variant MODIFIER c.-1077G>A| S169
134170 BAA10g20400 A10 18378792 C T upstream_gene_variant MODIFIER c.-1596G>A| S6
134171 BAA10g20400 A10 18379663 G A upstream_gene_variant MODIFIER c.-2467C>T| S85
134172 BAA10g20400 A10 18379890 G A upstream_gene_variant MODIFIER c.-2694C>T| S159
S243
134173 BAA10g20400 A10 18380310 C T upstream_gene_variant MODIFIER c.-3114G>A| S140
134174 BAA10g20400 A10 18380673 C T upstream_gene_variant MODIFIER c.-3477G>A| S306
S308
134175 BAA10g20400 A10 18381761 C T upstream_gene_variant MODIFIER c.-4565G>A| S221