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
119401 BAA10g11470 A10 13040003 G A downstream_gene_variant MODIFIER c.*4133C>T| S45
119402 BAA10g11470 A10 13041494 G A downstream_gene_variant MODIFIER c.*2642C>T| S192
119403 BAA10g11460 A10 13043329 C T downstream_gene_variant MODIFIER c.*431C>T| S152
119404 BAA10g11460 A10 13043921 C T downstream_gene_variant MODIFIER c.*1023C>T| S40
S49
119405 BAA10g11470 A10 13044255 C G missense_variant MODERATE c.1654G>C|p.Gly552Arg S4
119406 BAA10g11470 A10 13044636 C T missense_variant MODERATE c.1273G>A|p.Val425Ile S270
119407 BAA10g11470 A10 13045368 C T missense_variant MODERATE c.625G>A|p.Val209Met S56
119408 BAA10g11470 A10 13045398 C T missense_variant MODERATE c.595G>A|p.Gly199Arg S203
119409 BAA10g11470 A10 13045493 G A missense_variant MODERATE c.500C>T|p.Ala167Val S267
119410 BAA10g11470 A10 13047649 C T upstream_gene_variant MODIFIER c.-1657G>A| S165
119411 BAA10g11470 A10 13050839 C T upstream_gene_variant MODIFIER c.-4847G>A| S169
119412 BAA10g11470 A10 13050900 G A upstream_gene_variant MODIFIER c.-4908C>T| S134
119413 BAA10g11480 A10 13052912 C T upstream_gene_variant MODIFIER c.-4437C>T| S167
119414 BAA10g11480 A10 13052988 C T upstream_gene_variant MODIFIER c.-4361C>T| S78
119415 BAA10g11480 A10 13057354 G A synonymous_variant LOW c.6G>A|p.Lys2Lys S234
119416 BAA10g11480 A10 13057542 C T missense_variant MODERATE c.194C>T|p.Ser65Phe S165
119417 BAA10g11480 A10 13057858 G A intron_variant MODIFIER c.287+154G>A| S262
119418 BAA10g11480 A10 13057986 T C intron_variant MODIFIER c.287+282T>C| S171
119419 BAA10g11480 A10 13058279 C T intron_variant MODIFIER c.287+575C>T| S196
119420 BAA10g11480 A10 13058553 G A intron_variant MODIFIER c.288-426G>A| S284
119421 BAA10g11480 A10 13058564 C T intron_variant MODIFIER c.288-415C>T| S86
119422 BAA10g11480 A10 13058741 C T intron_variant MODIFIER c.288-238C>T| S185
119423 BAA10g11480 A10 13058795 G A intron_variant MODIFIER c.288-184G>A| S66
119424 BAA10g11480 A10 13059227 G A intron_variant MODIFIER c.494+42G>A| S50
119425 BAA10g11480 A10 13059641 G A splice_acceptor_variant&intron_variant HIGH c.607-1G>A| S181