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
16951 BAA01g12770 A01 6042664 G A missense_variant MODERATE c.1076C>T|p.Ser359Phe S297
16952 BAA01g12770 A01 6043465 G A missense_variant MODERATE c.356C>T|p.Thr119Ile S109
16953 BAA01g12770 A01 6043467 T A synonymous_variant LOW c.354A>T|p.Ala118Ala S109
16954 BAA01g12770 A01 6043480 C T missense_variant MODERATE c.341G>A|p.Ser114Asn S62
16955 BAA01g12760 A01 6044092 C T upstream_gene_variant MODIFIER c.-3700G>A| S260
16956 BAA01g12760 A01 6044325 C T upstream_gene_variant MODIFIER c.-3933G>A| S289
S290
16957 BAA01g12780 A01 6046074 C T missense_variant MODERATE c.2018G>A|p.Gly673Glu S90
16958 BAA01g12780 A01 6046248 G A missense_variant MODERATE c.1844C>T|p.Thr615Ile S191
16959 BAA01g12780 A01 6046285 T G missense_variant MODERATE c.1807A>C|p.Lys603Gln S263
16960 BAA01g12780 A01 6047080 G A missense_variant MODERATE c.1106C>T|p.Ala369Val S114
16961 BAA01g12780 A01 6047248 C T splice_acceptor_variant&intron_variant HIGH c.939-1G>A| S260
16962 BAA01g12780 A01 6047410 G A synonymous_variant LOW c.861C>T|p.Ile287Ile S181
16963 BAA01g12780 A01 6047926 C T missense_variant MODERATE c.418G>A|p.Asp140Asn S128
16964 BAA01g12780 A01 6050802 C T upstream_gene_variant MODIFIER c.-2215G>A| S144
16965 BAA01g12780 A01 6050892 C T upstream_gene_variant MODIFIER c.-2305G>A| S277
16966 BAA01g12780 A01 6051036 C T upstream_gene_variant MODIFIER c.-2449G>A| S128
16967 BAA01g12790 A01 6051382 G A missense_variant MODERATE c.211G>A|p.Ala71Thr S174
16968 BAA01g12790 A01 6051707 G A missense_variant MODERATE c.536G>A|p.Gly179Glu S34
16969 BAA01g12790 A01 6052056 C T synonymous_variant LOW c.885C>T|p.Tyr295Tyr S305
16970 BAA01g12790 A01 6052705 C T stop_gained HIGH c.1444C>T|p.Gln482* S148
S210
S30
S31
16971 BAA01g12790 A01 6052868 C T missense_variant MODERATE c.1607C>T|p.Ser536Phe S260
16972 BAA01g12790 A01 6053002 C T synonymous_variant LOW c.1741C>T|p.Leu581Leu S128
16973 BAA01g12790 A01 6053346 C T synonymous_variant LOW c.2085C>T|p.Gly695Gly S100
16974 BAA01g12790 A01 6053506 G A missense_variant MODERATE c.2245G>A|p.Glu749Lys S292
16975 BAA01g12790 A01 6053785 G A missense_variant MODERATE c.2524G>A|p.Asp842Asn S262