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
1351 BAA01g01090 A01 462967 G A synonymous_variant LOW c.837C>T|p.Asp279Asp S51
1352 BAA01g01090 A01 463266 C T missense_variant MODERATE c.538G>A|p.Glu180Lys S128
1353 BAA01g01090 A01 463989 G A missense_variant MODERATE c.55C>T|p.Pro19Ser S10
1354 BAA01g01090 A01 464688 G A upstream_gene_variant MODIFIER c.-645C>T| S186
1355 BAA01g01090 A01 465730 C T upstream_gene_variant MODIFIER c.-1687G>A| S244
1356 BAA01g01090 A01 466819 G A upstream_gene_variant MODIFIER c.-2776C>T| S162
1357 BAA01g01090 A01 467764 C T upstream_gene_variant MODIFIER c.-3721G>A| S270
1358 BAA01g01090 A01 469035 G A upstream_gene_variant MODIFIER c.-4992C>T| S232
1359 BAA01g01120 A01 469783 G A missense_variant MODERATE c.220C>T|p.Pro74Ser S262
1360 BAA01g01100 A01 470783 G A upstream_gene_variant MODIFIER c.-4063C>T| S98
1361 BAA01g01120 A01 473099 G A upstream_gene_variant MODIFIER c.-3097C>T| S247
1362 BAA01g01120 A01 474157 G A upstream_gene_variant MODIFIER c.-4155C>T| S123
1363 BAA01g01120 A01 474480 C T upstream_gene_variant MODIFIER c.-4478G>A| S97
1364 BAA01g01140 A01 476530 C T synonymous_variant LOW c.990C>T|p.Ser330Ser S48
1365 BAA01g01140 A01 476549 C T missense_variant MODERATE c.1009C>T|p.Leu337Phe S241
1366 BAA01g01140 A01 477643 C T synonymous_variant LOW c.1431C>T|p.Ser477Ser S192
1367 BAA01g01140 A01 477957 G A missense_variant MODERATE c.1745G>A|p.Gly582Glu S60
1368 BAA01g01160 A01 478532 C T upstream_gene_variant MODIFIER c.-3844C>T| S20
1369 BAA01g01160 A01 479255 G A upstream_gene_variant MODIFIER c.-3121G>A| S297
1370 BAA01g01150 A01 479803 G A synonymous_variant LOW c.342C>T|p.Gly114Gly S6
1371 BAA01g01150 A01 480351 G A upstream_gene_variant MODIFIER c.-207C>T| S13
1372 BAA01g01150 A01 482256 C T upstream_gene_variant MODIFIER c.-2112G>A| S18
1373 BAA01g01160 A01 482395 C T missense_variant MODERATE c.20C>T|p.Ala7Val S164
1374 BAA01g01160 A01 483210 G A missense_variant MODERATE c.305G>A|p.Arg102Gln S156
1375 BAA01g01160 A01 483430 C T synonymous_variant LOW c.333C>T|p.Asn111Asn S4