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
131651 BAA10g18860 A10 17508832 G A missense_variant MODERATE c.290C>T|p.Ser97Phe S176
131652 BAA10g18860 A10 17508902 C T missense_variant MODERATE c.220G>A|p.Glu74Lys S140
131653 BAA10g18860 A10 17511173 G A upstream_gene_variant MODIFIER c.-2052C>T| S144
131654 BAA10g18860 A10 17512277 C T upstream_gene_variant MODIFIER c.-3156G>A| S274
131655 BAA10g18880 A10 17512863 C T missense_variant MODERATE c.223C>T|p.Arg75Trp S231
131656 BAA10g18860 A10 17513748 C T upstream_gene_variant MODIFIER c.-4627G>A| S249
131657 BAA10g18890 A10 17514347 G A missense_variant MODERATE c.505G>A|p.Val169Met S79
S84
131658 BAA10g18890 A10 17514595 C T synonymous_variant LOW c.753C>T|p.Asp251Asp S64
131659 BAA10g18890 A10 17515040 G A missense_variant MODERATE c.1198G>A|p.Ala400Thr S138
131660 BAA10g18900 A10 17515219 G A upstream_gene_variant MODIFIER c.-3505G>A| S293
131661 BAA10g18900 A10 17516344 G A upstream_gene_variant MODIFIER c.-2380G>A| S289
S290
131662 BAA10g18900 A10 17516425 G A upstream_gene_variant MODIFIER c.-2299G>A| S32
131663 BAA10g18900 A10 17516460 C T upstream_gene_variant MODIFIER c.-2264C>T| S269
131664 BAA10g18900 A10 17516648 G A upstream_gene_variant MODIFIER c.-2076G>A| S59
131665 BAA10g18900 A10 17516766 G A upstream_gene_variant MODIFIER c.-1958G>A| S69
131666 BAA10g18900 A10 17516769 C T upstream_gene_variant MODIFIER c.-1955C>T| S48
131667 BAA10g18900 A10 17517376 C T upstream_gene_variant MODIFIER c.-1348C>T| S183
131668 BAA10g18900 A10 17518152 C T upstream_gene_variant MODIFIER c.-572C>T| S144
131669 BAA10g18900 A10 17518737 G A missense_variant MODERATE c.14G>A|p.Arg5Lys S209
131670 BAA10g18900 A10 17519963 G A synonymous_variant LOW c.315G>A|p.Leu105Leu S151
S263
131671 BAA10g18900 A10 17520444 C T synonymous_variant LOW c.504C>T|p.Arg168Arg S87
131672 BAA10g18900 A10 17521366 C T intron_variant MODIFIER c.919-117C>T| S208
S93
131673 BAA10g18900 A10 17521714 G A intron_variant MODIFIER c.1021-13G>A| S299
131674 BAA10g18900 A10 17522491 C T splice_region_variant&intron_variant LOW c.1201-8C>T| S40
131675 BAA10g18900 A10 17522502 C T missense_variant MODERATE c.1204C>T|p.Leu402Phe S30
S31