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
86901 BAA01g46200 A01 30855709 C T upstream_gene_variant MODIFIER c.-3187G>A| S98
86902 BAA01g46200 A01 30855996 C T upstream_gene_variant MODIFIER c.-3474G>A| S266
86903 BAA01g46210 A01 30856988 G A missense_variant MODERATE c.326C>T|p.Pro109Leu S144
86904 BAA01g46210 A01 30857130 C T missense_variant MODERATE c.184G>A|p.Asp62Asn S256
86905 BAA01g46210 A01 30858163 G A upstream_gene_variant MODIFIER c.-761C>T| S172
S217
86906 BAA01g46210 A01 30858528 C T upstream_gene_variant MODIFIER c.-1126G>A| S94
86907 BAA01g46210 A01 30858663 G A upstream_gene_variant MODIFIER c.-1261C>T| S189
86908 BAA01g46220 A01 30858783 C T missense_variant MODERATE c.64C>T|p.Leu22Phe S282
86909 BAA01g46210 A01 30859852 G A upstream_gene_variant MODIFIER c.-2450C>T| S202
86910 BAA01g46210 A01 30860062 C T upstream_gene_variant MODIFIER c.-2660G>A| S282
86911 BAA01g46210 A01 30860079 C T upstream_gene_variant MODIFIER c.-2677G>A| S165
86912 BAA01g46220 A01 30860257 C T missense_variant MODERATE c.302C>T|p.Thr101Ile S206
S26
86913 BAA01g46230 A01 30861425 C T missense_variant MODERATE c.37C>T|p.Leu13Phe S174
86914 BAA01g46210 A01 30861486 C T upstream_gene_variant MODIFIER c.-4084G>A| S261
86915 BAA01g46230 A01 30861716 C T missense_variant MODERATE c.77C>T|p.Ser26Leu S303
86916 BAA01g46240 A01 30862727 C T upstream_gene_variant MODIFIER c.-2520C>T| S128
86917 BAA01g46240 A01 30863363 G A upstream_gene_variant MODIFIER c.-1884G>A| S48
86918 BAA01g46230 A01 30864237 C T synonymous_variant LOW c.1326C>T|p.Val442Val S216
86919 BAA01g46230 A01 30864502 G A missense_variant MODERATE c.1411G>A|p.Gly471Arg S172
86920 BAA01g46220 A01 30865509 G A downstream_gene_variant MODIFIER c.*4975G>A| S79
S91
86921 BAA01g46230 A01 30865716 G A downstream_gene_variant MODIFIER c.*1113G>A| S185
86922 BAA01g46230 A01 30865975 C T downstream_gene_variant MODIFIER c.*1372C>T| S37
86923 BAA01g46240 A01 30866429 G A splice_region_variant&intron_variant LOW c.227-4G>A| S143
86924 BAA01g46250 A01 30867092 G A stop_gained HIGH c.1762C>T|p.Gln588* S308
86925 BAA01g46230 A01 30868407 C T downstream_gene_variant MODIFIER c.*3804C>T| S134