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
171851 BAA02g15840 A02 7711112 G A splice_region_variant&synonymous_variant LOW c.1200G>A|p.Glu400Glu S146
171852 BAA02g15840 A02 7711240 G A missense_variant MODERATE c.1226G>A|p.Arg409His S126
171853 BAA02g15840 A02 7711667 C T missense_variant MODERATE c.1442C>T|p.Thr481Ile S139
171854 BAA02g15840 A02 7711946 G A missense_variant MODERATE c.1582G>A|p.Gly528Arg S308
171855 BAA02g15840 A02 7713061 C T synonymous_variant LOW c.2250C>T|p.Ile750Ile S40
S49
171856 BAA02g15850 A02 7714444 C T missense_variant MODERATE c.253G>A|p.Gly85Arg S262
171857 BAA02g15850 A02 7714769 C T missense_variant MODERATE c.73G>A|p.Glu25Lys S299
171858 BAA02g15850 A02 7715090 G A upstream_gene_variant MODIFIER c.-249C>T| S48
171859 BAA02g15860 A02 7716128 C T missense_variant MODERATE c.67C>T|p.Leu23Phe S244
171860 BAA02g15860 A02 7716678 G A missense_variant MODERATE c.617G>A|p.Ser206Asn S295
171861 BAA02g15860 A02 7716785 C T missense_variant MODERATE c.724C>T|p.Leu242Phe S165
171862 BAA02g15860 A02 7717137 C T missense_variant MODERATE c.1076C>T|p.Ser359Phe S299
171863 BAA02g15850 A02 7718768 G A upstream_gene_variant MODIFIER c.-3927C>T| S296
171864 BAA02g15850 A02 7718979 C T upstream_gene_variant MODIFIER c.-4138G>A| S42
171865 BAA02g15850 A02 7719012 C T upstream_gene_variant MODIFIER c.-4171G>A| S51
171866 BAA02g15850 A02 7719129 G A upstream_gene_variant MODIFIER c.-4288C>T| S133
171867 BAA02g15870 A02 7721057 C T upstream_gene_variant MODIFIER c.-1801C>T| S103
171868 BAA02g15870 A02 7721142 G A upstream_gene_variant MODIFIER c.-1716G>A| S125
171869 BAA02g15870 A02 7721893 C T upstream_gene_variant MODIFIER c.-965C>T| S15
S2
S3
S34
S4
S6
171870 BAA02g15870 A02 7723231 C T synonymous_variant LOW c.258C>T|p.Phe86Phe S88
171871 BAA02g15870 A02 7723699 G A synonymous_variant LOW c.642G>A|p.Lys214Lys S56
171872 BAA02g15870 A02 7724023 C T synonymous_variant LOW c.898C>T|p.Leu300Leu S209
171873 BAA02g15870 A02 7724361 C T missense_variant MODERATE c.1151C>T|p.Ser384Phe S75
S81
171874 BAA02g15870 A02 7724508 G A synonymous_variant LOW c.1224G>A|p.Arg408Arg S193
171875 BAA02g15870 A02 7724547 G A synonymous_variant LOW c.1263G>A|p.Gln421Gln S298