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
79601 BAA01g41880 A01 27855247 C T intron_variant MODIFIER c.340-30C>T| S221
79602 BAA01g41880 A01 27855713 G A synonymous_variant LOW c.600G>A|p.Arg200Arg S238
79603 BAA01g41880 A01 27855967 C T intron_variant MODIFIER c.754+18C>T| S181
S289
S290
79604 BAA01g41880 A01 27856349 C T missense_variant MODERATE c.971C>T|p.Ser324Phe S305
79605 BAA01g41880 A01 27856569 G A missense_variant MODERATE c.1103G>A|p.Gly368Glu S262
79606 BAA01g41880 A01 27856853 C T intron_variant MODIFIER c.1245+10C>T| S256
79607 BAA01g41880 A01 27856971 C T missense_variant MODERATE c.1271C>T|p.Thr424Ile S288
79608 BAA01g41880 A01 27856995 G A missense_variant MODERATE c.1295G>A|p.Gly432Glu S229
79609 BAA01g41880 A01 27857161 C T intron_variant MODIFIER c.1443+18C>T| S64
79610 BAA01g41880 A01 27857533 G A intron_variant MODIFIER c.1620+45G>A| S152
79611 BAA01g41880 A01 27857542 G A intron_variant MODIFIER c.1620+54G>A| S199
79612 BAA01g41880 A01 27859592 G A intron_variant MODIFIER c.2877-16G>A| S138
79613 BAA01g41880 A01 27859631 G A missense_variant MODERATE c.2900G>A|p.Gly967Asp S271
79614 BAA01g41880 A01 27859930 C T missense_variant MODERATE c.3199C>T|p.Pro1067Ser S110
S81
S85
79615 BAA01g41880 A01 27859940 G A missense_variant MODERATE c.3209G>A|p.Gly1070Glu S197
79616 BAA01g41880 A01 27860726 G A synonymous_variant LOW c.3906G>A|p.Glu1302Glu S299
79617 BAA01g41880 A01 27860928 C T stop_gained HIGH c.4108C>T|p.Gln1370* S239
79618 BAA01g41880 A01 27861190 G A splice_region_variant&intron_variant LOW c.4365+5G>A| S177
79619 BAA01g41890 A01 27861231 G A upstream_gene_variant MODIFIER c.-3485G>A| S172
S217
79620 BAA01g41890 A01 27861955 C T upstream_gene_variant MODIFIER c.-2761C>T| S8
79621 BAA01g41880 A01 27862337 G A missense_variant MODERATE c.5065G>A|p.Gly1689Arg S139
79622 BAA01g41890 A01 27862470 G A upstream_gene_variant MODIFIER c.-2246G>A| S208
S219
79623 BAA01g41890 A01 27863367 C T upstream_gene_variant MODIFIER c.-1349C>T| S42
79624 BAA01g41890 A01 27863573 G A upstream_gene_variant MODIFIER c.-1143G>A| S308
79625 BAA01g41890 A01 27864843 G A missense_variant MODERATE c.128G>A|p.Gly43Glu S117