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
141151 BAA10g26170 A10 20866772 C T stop_gained HIGH c.874C>T|p.Gln292* S204
141152 BAA10g26170 A10 20866897 C T synonymous_variant LOW c.999C>T|p.Phe333Phe S98
141153 BAA10g26170 A10 20866901 G A missense_variant MODERATE c.1003G>A|p.Asp335Asn S63
141154 BAA10g26170 A10 20866995 G A missense_variant MODERATE c.1097G>A|p.Gly366Glu S136
141155 BAA10g26170 A10 20867094 G A missense_variant MODERATE c.1196G>A|p.Arg399His S192
141156 BAA10g26170 A10 20867334 C T missense_variant MODERATE c.1436C>T|p.Ser479Phe S20
141157 BAA10g26170 A10 20867689 C T synonymous_variant LOW c.1791C>T|p.Phe597Phe S203
141158 BAA10g26160 A10 20867861 C T upstream_gene_variant MODIFIER c.-3431G>A| S115
141159 BAA10g26160 A10 20868362 G A upstream_gene_variant MODIFIER c.-3932C>T| S252
141160 BAA10g26160 A10 20869158 G A upstream_gene_variant MODIFIER c.-4728C>T| S7
141161 BAA10g26170 A10 20869949 C T downstream_gene_variant MODIFIER c.*2122C>T| S13
141162 BAA10g26170 A10 20872005 C T downstream_gene_variant MODIFIER c.*4178C>T| S39
141163 BAA10g26190 A10 20872511 C T splice_acceptor_variant&intron_variant HIGH c.2221-1G>A| S302
141164 BAA10g26180 A10 20874127 G A downstream_gene_variant MODIFIER c.*4205G>A| S208
S219
141165 BAA10g26190 A10 20876230 G A missense_variant MODERATE c.118C>T|p.Leu40Phe S284
141166 BAA10g26200 A10 20878154 G A synonymous_variant LOW c.1243C>T|p.Leu415Leu S109
141167 BAA10g26190 A10 20878656 G A upstream_gene_variant MODIFIER c.-2309C>T| S57
141168 BAA10g26200 A10 20879141 C T missense_variant MODERATE c.547G>A|p.Glu183Lys S308
141169 BAA10g26200 A10 20879679 G A splice_region_variant&intron_variant LOW c.200-4C>T| S278
141170 BAA10g26200 A10 20879807 G A missense_variant MODERATE c.145C>T|p.Leu49Phe S288
141171 BAA10g26200 A10 20879848 G A missense_variant MODERATE c.104C>T|p.Ser35Leu S263
141172 BAA10g26210 A10 20881347 C T synonymous_variant LOW c.495G>A|p.Pro165Pro S292
141173 BAA10g26210 A10 20881580 C T missense_variant MODERATE c.262G>A|p.Gly88Arg S148
S210
S30
S31
141174 BAA10g26210 A10 20881662 C T stop_gained HIGH c.180G>A|p.Trp60* S18
141175 BAA10g26200 A10 20882419 C T upstream_gene_variant MODIFIER c.-2468G>A| S199