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
7001 BAA01g05730 A01 2555467 G A upstream_gene_variant MODIFIER c.-1015C>T| S172
S217
7002 BAA01g05730 A01 2555827 C T upstream_gene_variant MODIFIER c.-1375G>A| S134
7003 BAA01g05730 A01 2556552 C T upstream_gene_variant MODIFIER c.-2100G>A| S225
S73
7004 BAA01g05740 A01 2557364 G A synonymous_variant LOW c.5538C>T|p.Leu1846Leu S6
7005 BAA01g05740 A01 2557485 G A missense_variant MODERATE c.5417C>T|p.Thr1806Ile S23
7006 BAA01g05740 A01 2557540 G A missense_variant MODERATE c.5362C>T|p.Pro1788Ser S13
7007 BAA01g05740 A01 2558171 C T stop_gained HIGH c.4952G>A|p.Trp1651* S18
7008 BAA01g05730 A01 2558248 C T upstream_gene_variant MODIFIER c.-3796G>A| S71
7009 BAA01g05740 A01 2559109 G A missense_variant MODERATE c.4160C>T|p.Pro1387Leu S146
7010 BAA01g05740 A01 2559906 G A synonymous_variant LOW c.3600C>T|p.Asn1200Asn S201
7011 BAA01g05740 A01 2560007 C T missense_variant MODERATE c.3499G>A|p.Ala1167Thr S171
7012 BAA01g05740 A01 2560065 C T splice_acceptor_variant&intron_variant HIGH c.3442-1G>A| S206
S26
7013 BAA01g05740 A01 2560092 G A intron_variant MODIFIER c.3442-28C>T| S279
7014 BAA01g05740 A01 2560808 C T missense_variant MODERATE c.3058G>A|p.Glu1020Lys S267
7015 BAA01g05740 A01 2560858 G A missense_variant MODERATE c.3008C>T|p.Thr1003Ile S183
S198
7016 BAA01g05740 A01 2561806 C T missense_variant MODERATE c.2371G>A|p.Asp791Asn S112
7017 BAA01g05740 A01 2563477 G A synonymous_variant LOW c.1578C>T|p.Tyr526Tyr S144
7018 BAA01g05760 A01 2563744 G A upstream_gene_variant MODIFIER c.-4894G>A| S37
7019 BAA01g05740 A01 2565573 C T missense_variant MODERATE c.194G>A|p.Ser65Asn S51
7020 BAA01g05740 A01 2565649 C T missense_variant MODERATE c.118G>A|p.Glu40Lys S130
7021 BAA01g05740 A01 2566194 G A missense_variant MODERATE c.17C>T|p.Ser6Phe S142
7022 BAA01g05770 A01 2572302 G A missense_variant MODERATE c.1081G>A|p.Gly361Arg S235
7023 BAA01g05750 A01 2572459 G A upstream_gene_variant MODIFIER c.-4271C>T| S169
7024 BAA01g05770 A01 2572618 C T synonymous_variant LOW c.1335C>T|p.His445His S36
7025 BAA01g05770 A01 2572783 C T synonymous_variant LOW c.1425C>T|p.Leu475Leu S67