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
69551 BAA01g36390 A01 24390170 G A missense_variant MODERATE c.1823C>T|p.Ala608Val S20
69552 BAA01g36390 A01 24391086 C T missense_variant MODERATE c.1429G>A|p.Gly477Ser S183
S198
69553 BAA01g36390 A01 24391413 C T splice_acceptor_variant&intron_variant HIGH c.1285-1G>A| S32
69554 BAA01g36390 A01 24391543 G T missense_variant MODERATE c.1251C>A|p.Asn417Lys S117
S124
S148
S172
S210
S286
S298
S8
69555 BAA01g36390 A01 24391828 C T missense_variant MODERATE c.1103G>A|p.Arg368Lys S39
69556 BAA01g36390 A01 24391851 C T synonymous_variant LOW c.1080G>A|p.Glu360Glu S120
69557 BAA01g36400 A01 24392208 C T downstream_gene_variant MODIFIER c.*3201G>A| S174
S27
69558 BAA01g36390 A01 24393447 C T missense_variant MODERATE c.322G>A|p.Glu108Lys S264
69559 BAA01g36390 A01 24394043 C T missense_variant MODERATE c.25G>A|p.Glu9Lys S208
69560 BAA01g36400 A01 24395611 G A missense_variant MODERATE c.1577C>T|p.Ala526Val S123
69561 BAA01g36400 A01 24395856 G A synonymous_variant LOW c.1332C>T|p.Leu444Leu S168
69562 BAA01g36400 A01 24396576 C T synonymous_variant LOW c.834G>A|p.Glu278Glu S148
S210
S30
S31
69563 BAA01g36400 A01 24396899 C T synonymous_variant LOW c.588G>A|p.Arg196Arg S289
S290
69564 BAA01g36390 A01 24396977 C T upstream_gene_variant MODIFIER c.-2910G>A| S98
69565 BAA01g36390 A01 24397540 G A upstream_gene_variant MODIFIER c.-3473C>T| S199
69566 BAA01g36400 A01 24398012 G A synonymous_variant LOW c.81C>T|p.Phe27Phe S262
69567 BAA01g36400 A01 24399513 G A upstream_gene_variant MODIFIER c.-1421C>T| S172
S217
69568 BAA01g36400 A01 24399531 C G upstream_gene_variant MODIFIER c.-1439G>C| S132
S137
S215
69569 BAA01g36400 A01 24399666 C T upstream_gene_variant MODIFIER c.-1574G>A| S153
69570 BAA01g36410 A01 24400745 G A missense_variant MODERATE c.224G>A|p.Gly75Glu S1
S90
69571 BAA01g36400 A01 24401490 C T upstream_gene_variant MODIFIER c.-3398G>A| S89
69572 BAA01g36400 A01 24401696 G A upstream_gene_variant MODIFIER c.-3604C>T| S197
S281
69573 BAA01g36400 A01 24401784 C T upstream_gene_variant MODIFIER c.-3692G>A| S288
69574 BAA01g36420 A01 24401858 C T missense_variant MODERATE c.5C>T|p.Ser2Leu S158
69575 BAA01g36420 A01 24401955 G A missense_variant MODERATE c.102G>A|p.Met34Ile S267