Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g18900 A10 17515219 G A upstream_gene_variant MODIFIER c.-3505G>A| S293
2 BAA10g18900 A10 17516344 G A upstream_gene_variant MODIFIER c.-2380G>A| S289
S290
3 BAA10g18900 A10 17516425 G A upstream_gene_variant MODIFIER c.-2299G>A| S32
4 BAA10g18900 A10 17516460 C T upstream_gene_variant MODIFIER c.-2264C>T| S269
5 BAA10g18900 A10 17516648 G A upstream_gene_variant MODIFIER c.-2076G>A| S59
6 BAA10g18900 A10 17516766 G A upstream_gene_variant MODIFIER c.-1958G>A| S69
7 BAA10g18900 A10 17516769 C T upstream_gene_variant MODIFIER c.-1955C>T| S48
8 BAA10g18900 A10 17517376 C T upstream_gene_variant MODIFIER c.-1348C>T| S183
9 BAA10g18900 A10 17518152 C T upstream_gene_variant MODIFIER c.-572C>T| S144
10 BAA10g18900 A10 17518737 G A missense_variant MODERATE c.14G>A|p.Arg5Lys S209
11 BAA10g18900 A10 17519963 G A synonymous_variant LOW c.315G>A|p.Leu105Leu S151
S263
12 BAA10g18900 A10 17520444 C T synonymous_variant LOW c.504C>T|p.Arg168Arg S87
13 BAA10g18900 A10 17521366 C T intron_variant MODIFIER c.919-117C>T| S208
S93
14 BAA10g18900 A10 17521714 G A intron_variant MODIFIER c.1021-13G>A| S299
15 BAA10g18900 A10 17522491 C T splice_region_variant&intron_variant LOW c.1201-8C>T| S40
16 BAA10g18900 A10 17522502 C T missense_variant MODERATE c.1204C>T|p.Leu402Phe S30
S31
17 BAA10g18900 A10 17522567 G A synonymous_variant LOW c.1269G>A|p.Lys423Lys S82
18 BAA10g18900 A10 17522604 C T intron_variant MODIFIER c.1289+17C>T| S186
19 BAA10g18900 A10 17523910 G A missense_variant MODERATE c.1916G>A|p.Gly639Glu S252
20 BAA10g18900 A10 17524105 G A missense_variant&splice_region_variant MODERATE c.1945G>A|p.Glu649Lys S132
S137
S215
21 BAA10g18900 A10 17524915 G A missense_variant MODERATE c.2282G>A|p.Arg761Lys S39
22 BAA10g18900 A10 17524940 C T synonymous_variant LOW c.2307C>T|p.Leu769Leu S177
23 BAA10g18900 A10 17525331 C T intron_variant MODIFIER c.2512-9C>T| S110
24 BAA10g18900 A10 17525479 C T intron_variant MODIFIER c.2637+14C>T| S124
25 BAA10g18900 A10 17526071 G A missense_variant MODERATE c.2848G>A|p.Gly950Arg S109