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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g19430 A06 10036520 G A upstream_gene_variant MODIFIER c.-4818G>A| S229
2 BAA06g19430 A06 10036811 G A upstream_gene_variant MODIFIER c.-4527G>A| S15
S3
3 BAA06g19430 A06 10037410 G A upstream_gene_variant MODIFIER c.-3928G>A| S259
4 BAA06g19430 A06 10037426 G A upstream_gene_variant MODIFIER c.-3912G>A| S136
5 BAA06g19430 A06 10038031 C T upstream_gene_variant MODIFIER c.-3307C>T| S269
6 BAA06g19430 A06 10039025 C T upstream_gene_variant MODIFIER c.-2313C>T| S60
7 BAA06g19430 A06 10039216 G A upstream_gene_variant MODIFIER c.-2122G>A| S280
8 BAA06g19430 A06 10039221 G A upstream_gene_variant MODIFIER c.-2117G>A| S138
9 BAA06g19430 A06 10040294 C T upstream_gene_variant MODIFIER c.-1044C>T| S293
10 BAA06g19430 A06 10041439 G A stop_gained HIGH c.102G>A|p.Trp34* S122
11 BAA06g19430 A06 10042236 G A missense_variant MODERATE c.322G>A|p.Ala108Thr S59
12 BAA06g19430 A06 10042432 G A synonymous_variant LOW c.435G>A|p.Leu145Leu S201
13 BAA06g19430 A06 10042710 G A synonymous_variant LOW c.579G>A|p.Leu193Leu S72
14 BAA06g19430 A06 10042791 C T synonymous_variant LOW c.660C>T|p.Leu220Leu S163
15 BAA06g19430 A06 10043388 C T missense_variant MODERATE c.862C>T|p.Arg288Cys S18
16 BAA06g19430 A06 10044092 G A synonymous_variant LOW c.1287G>A|p.Leu429Leu S163
17 BAA06g19430 A06 10044455 C T missense_variant MODERATE c.1580C>T|p.Ser527Phe S112
18 BAA06g19430 A06 10044633 G A synonymous_variant LOW c.1758G>A|p.Lys586Lys S197
19 BAA06g19430 A06 10044775 G A missense_variant MODERATE c.1900G>A|p.Val634Ile S283
20 BAA06g19430 A06 10045053 C T synonymous_variant LOW c.2178C>T|p.Asn726Asn S126
21 BAA06g19430 A06 10045322 C T missense_variant MODERATE c.2372C>T|p.Ala791Val S283
22 BAA06g19430 A06 10047490 G A downstream_gene_variant MODIFIER c.*2128G>A| S181
23 BAA06g19430 A06 10049601 G A downstream_gene_variant MODIFIER c.*4239G>A| S129
24 BAA06g19430 A06 10049631 C T downstream_gene_variant MODIFIER c.*4269C>T| S189
25 BAA06g19430 A06 10050210 G A downstream_gene_variant MODIFIER c.*4848G>A| S144