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 BAA06g26770 A06 18388712 C T upstream_gene_variant MODIFIER c.-4659C>T| S303
2 BAA06g26770 A06 18388791 C T upstream_gene_variant MODIFIER c.-4580C>T| S151
S263
3 BAA06g26770 A06 18388898 C T upstream_gene_variant MODIFIER c.-4473C>T| S298
4 BAA06g26770 A06 18389571 G A upstream_gene_variant MODIFIER c.-3800G>A| S76
5 BAA06g26770 A06 18389776 C T upstream_gene_variant MODIFIER c.-3595C>T| S298
6 BAA06g26770 A06 18390197 G A upstream_gene_variant MODIFIER c.-3174G>A| S123
7 BAA06g26770 A06 18391068 G A upstream_gene_variant MODIFIER c.-2303G>A| S136
8 BAA06g26770 A06 18391861 C T upstream_gene_variant MODIFIER c.-1510C>T| S283
9 BAA06g26770 A06 18392080 G A upstream_gene_variant MODIFIER c.-1291G>A| S264
10 BAA06g26770 A06 18393051 C T upstream_gene_variant MODIFIER c.-320C>T| S6
11 BAA06g26770 A06 18395354 C T missense_variant MODERATE c.1772C>T|p.Ala591Val S14
12 BAA06g26770 A06 18395802 C T synonymous_variant LOW c.2220C>T|p.Phe740Phe S57
13 BAA06g26770 A06 18396583 C T intron_variant MODIFIER c.2452-384C>T| S278
14 BAA06g26770 A06 18396877 C T intron_variant MODIFIER c.2452-90C>T| S267
15 BAA06g26770 A06 18397603 G A intron_variant MODIFIER c.2592+496G>A| S184
16 BAA06g26770 A06 18398245 C T intron_variant MODIFIER c.2593-136C>T| S45
17 BAA06g26770 A06 18398925 G A missense_variant MODERATE c.3137G>A|p.Arg1046His S61
18 BAA06g26770 A06 18400304 G A missense_variant MODERATE c.3962G>A|p.Gly1321Asp S209
19 BAA06g26770 A06 18400310 C T missense_variant MODERATE c.3968C>T|p.Pro1323Leu S84
S93
20 BAA06g26770 A06 18400915 G A missense_variant MODERATE c.4573G>A|p.Asp1525Asn S219
S72
21 BAA06g26770 A06 18405427 G A downstream_gene_variant MODIFIER c.*2005G>A| S265
22 BAA06g26770 A06 18405500 C T downstream_gene_variant MODIFIER c.*2078C>T| S79
S84
23 BAA06g26770 A06 18405501 G A downstream_gene_variant MODIFIER c.*2079G>A| S224
24 BAA06g26770 A06 18405504 G A downstream_gene_variant MODIFIER c.*2082G>A| S162
25 BAA06g26770 A06 18405957 C T downstream_gene_variant MODIFIER c.*2535C>T| S172
S217