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
90951 BAA10g00940 A10 450609 C T downstream_gene_variant MODIFIER c.*1992C>T| S244
90952 BAA10g00940 A10 450672 C T downstream_gene_variant MODIFIER c.*2055C>T| S294
90953 BAA10g00950 A10 454905 G A upstream_gene_variant MODIFIER c.-3415C>T| S211
90954 BAA10g00950 A10 455072 C T upstream_gene_variant MODIFIER c.-3582G>A| S202
90955 BAA10g00960 A10 456700 G A upstream_gene_variant MODIFIER c.-2604G>A| S153
S213
90956 BAA10g00970 A10 460695 C T downstream_gene_variant MODIFIER c.*4378G>A| S308
90957 BAA10g00960 A10 460830 C T downstream_gene_variant MODIFIER c.*114C>T| S15
S156
S3
S34
90958 BAA10g00960 A10 461867 G A downstream_gene_variant MODIFIER c.*1151G>A| S67
90959 BAA10g00960 A10 462416 C T downstream_gene_variant MODIFIER c.*1700C>T| S98
90960 BAA10g00960 A10 462827 G A downstream_gene_variant MODIFIER c.*2111G>A| S129
90961 BAA10g00960 A10 463759 C T downstream_gene_variant MODIFIER c.*3043C>T| S135
90962 BAA10g00960 A10 464270 G A downstream_gene_variant MODIFIER c.*3554G>A| S59
90963 BAA10g00960 A10 464582 C T downstream_gene_variant MODIFIER c.*3866C>T| S294
90964 BAA10g00960 A10 464717 C T downstream_gene_variant MODIFIER c.*4001C>T| S139
90965 BAA10g00960 A10 464721 G A downstream_gene_variant MODIFIER c.*4005G>A| S153
S213
90966 BAA10g00970 A10 465111 G A synonymous_variant LOW c.1099C>T|p.Leu367Leu S18
90967 BAA10g00970 A10 465755 C T missense_variant MODERATE c.634G>A|p.Asp212Asn S238
90968 BAA10g00970 A10 466354 C T missense_variant MODERATE c.199G>A|p.Gly67Ser S281
90969 BAA10g00970 A10 466864 C T upstream_gene_variant MODIFIER c.-245G>A| S67
90970 BAA10g00970 A10 468911 G A upstream_gene_variant MODIFIER c.-2292C>T| S100
90971 BAA10g00970 A10 469666 G A upstream_gene_variant MODIFIER c.-3047C>T| S80
90972 BAA10g00980 A10 470442 C T missense_variant MODERATE c.426G>A|p.Met142Ile S74
90973 BAA10g00980 A10 470589 C T synonymous_variant LOW c.390G>A|p.Glu130Glu S152
90974 BAA10g00980 A10 470894 G A missense_variant&splice_region_variant MODERATE c.157C>T|p.Arg53Trp S96
90975 BAA10g00980 A10 471020 G A missense_variant MODERATE c.31C>T|p.Pro11Ser S295