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
1301 BAA01g01030 A01 443268 C T synonymous_variant LOW c.1557G>A|p.Gly519Gly S64
1302 BAA01g01030 A01 443454 C T synonymous_variant LOW c.1371G>A|p.Thr457Thr S265
1303 BAA01g01030 A01 444097 G A missense_variant MODERATE c.728C>T|p.Ser243Phe S221
1304 BAA01g01040 A01 446678 G A synonymous_variant LOW c.372C>T|p.Asp124Asp S103
1305 BAA01g01040 A01 446696 C G synonymous_variant LOW c.354G>C|p.Val118Val S110
S121
S16
S185
S212
S266
S36
1306 BAA01g01040 A01 446711 A G synonymous_variant LOW c.339T>C|p.Ile113Ile S110
S147
S16
S185
S212
S266
S36
1307 BAA01g01040 A01 446946 C T synonymous_variant LOW c.192G>A|p.Arg64Arg S158
1308 BAA01g01050 A01 448342 G A synonymous_variant LOW c.162G>A|p.Pro54Pro S10
1309 BAA01g01030 A01 448648 G A upstream_gene_variant MODIFIER c.-3824C>T| S224
1310 BAA01g01070 A01 450635 G A missense_variant MODERATE c.1345C>T|p.Leu449Phe S177
1311 BAA01g01070 A01 451075 C T missense_variant MODERATE c.1076G>A|p.Ser359Asn S203
1312 BAA01g01070 A01 451736 G A missense_variant MODERATE c.641C>T|p.Ala214Val S161
1313 BAA01g01070 A01 452031 C T synonymous_variant LOW c.423G>A|p.Arg141Arg S284
1314 BAA01g01070 A01 452289 G A synonymous_variant LOW c.165C>T|p.His55His S293
1315 BAA01g01070 A01 454700 C T upstream_gene_variant MODIFIER c.-2247G>A| S262
1316 BAA01g01080 A01 456486 G A synonymous_variant LOW c.1071G>A|p.Glu357Glu S303
1317 BAA01g01080 A01 456572 C T missense_variant MODERATE c.1157C>T|p.Ser386Phe S252
1318 BAA01g01080 A01 457690 C T downstream_gene_variant MODIFIER c.*1072C>T| S18
1319 BAA01g01080 A01 458746 G A downstream_gene_variant MODIFIER c.*2128G>A| S217
1320 BAA01g01080 A01 459649 G A downstream_gene_variant MODIFIER c.*3031G>A| S105
S106
1321 BAA01g01080 A01 461426 C T downstream_gene_variant MODIFIER c.*4808C>T| S46
1322 BAA01g01080 A01 461564 G A downstream_gene_variant MODIFIER c.*4946G>A| S10
1323 BAA01g01090 A01 462489 C T downstream_gene_variant MODIFIER c.*427G>A| S107
1324 BAA01g01090 A01 462588 A T downstream_gene_variant MODIFIER c.*328T>A| S287
1325 BAA01g01090 A01 462722 C T downstream_gene_variant MODIFIER c.*194G>A| S70