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
118501 BAA10g10970 A10 12731318 C T missense_variant MODERATE c.691G>A|p.Val231Ile S46
118502 BAA10g10970 A10 12731386 G A missense_variant MODERATE c.623C>T|p.Ser208Phe S36
118503 BAA10g10970 A10 12731826 G A synonymous_variant LOW c.183C>T|p.Phe61Phe S296
118504 BAA10g10970 A10 12733231 C T upstream_gene_variant MODIFIER c.-1223G>A| S19
118505 BAA10g10970 A10 12733633 C T upstream_gene_variant MODIFIER c.-1625G>A| S305
118506 BAA10g10970 A10 12733990 C T upstream_gene_variant MODIFIER c.-1982G>A| S249
118507 BAA10g10970 A10 12734757 G A upstream_gene_variant MODIFIER c.-2749C>T| S181
118508 BAA10g10970 A10 12736443 C T upstream_gene_variant MODIFIER c.-4435G>A| S177
118509 BAA10g10970 A10 12736598 C T upstream_gene_variant MODIFIER c.-4590G>A| S204
118510 BAA10g10980 A10 12737141 G A upstream_gene_variant MODIFIER c.-2647C>T| S67
118511 BAA10g10980 A10 12737772 C T upstream_gene_variant MODIFIER c.-3278G>A| S277
118512 BAA10g10980 A10 12737851 G A upstream_gene_variant MODIFIER c.-3357C>T| S157
S163
118513 BAA10g10980 A10 12738381 C T upstream_gene_variant MODIFIER c.-3887G>A| S40
S49
118514 BAA10g10990 A10 12739804 G A upstream_gene_variant MODIFIER c.-4058G>A| S276
118515 BAA10g10990 A10 12739986 C A upstream_gene_variant MODIFIER c.-3876C>A| S59
118516 BAA10g10990 A10 12740682 G A upstream_gene_variant MODIFIER c.-3180G>A| S291
118517 BAA10g10990 A10 12740962 C A upstream_gene_variant MODIFIER c.-2900C>A| S239
118518 BAA10g10990 A10 12741932 G A upstream_gene_variant MODIFIER c.-1930G>A| S198
118519 BAA10g10990 A10 12743071 G A upstream_gene_variant MODIFIER c.-791G>A| S216
118520 BAA10g10990 A10 12743293 G A upstream_gene_variant MODIFIER c.-569G>A| S50
118521 BAA10g10990 A10 12743754 G A upstream_gene_variant MODIFIER c.-108G>A| S184
118522 BAA10g10990 A10 12744569 G A downstream_gene_variant MODIFIER c.*363G>A| S202
118523 BAA10g10990 A10 12745194 C T downstream_gene_variant MODIFIER c.*988C>T| S48
118524 BAA10g10990 A10 12745328 C T downstream_gene_variant MODIFIER c.*1122C>T| S206
S26
118525 BAA10g10990 A10 12745362 G A downstream_gene_variant MODIFIER c.*1156G>A| S286