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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g20640 A06 10960036 C T upstream_gene_variant MODIFIER c.-3304C>T| S155
S211
2 BAA06g20640 A06 10961349 C T upstream_gene_variant MODIFIER c.-1991C>T| S112
3 BAA06g20640 A06 10961384 C G upstream_gene_variant MODIFIER c.-1956C>G| S156
4 BAA06g20640 A06 10962202 C T upstream_gene_variant MODIFIER c.-1138C>T| S282
5 BAA06g20640 A06 10962973 G A upstream_gene_variant MODIFIER c.-367G>A| S71
6 BAA06g20640 A06 10963150 C T upstream_gene_variant MODIFIER c.-190C>T| S18
7 BAA06g20640 A06 10963243 C T upstream_gene_variant MODIFIER c.-97C>T| S112
8 BAA06g20640 A06 10963575 C T missense_variant MODERATE c.236C>T|p.Thr79Ile S208
9 BAA06g20640 A06 10963623 G A splice_region_variant&intron_variant LOW c.244-4G>A| S64
10 BAA06g20640 A06 10963640 G A missense_variant MODERATE c.257G>A|p.Arg86Lys S233
11 BAA06g20640 A06 10964301 G A synonymous_variant LOW c.708G>A|p.Lys236Lys S72
S78
12 BAA06g20640 A06 10964302 G A missense_variant MODERATE c.709G>A|p.Glu237Lys S284
13 BAA06g20640 A06 10965794 C T intron_variant MODIFIER c.817-781C>T| S301
S304
14 BAA06g20640 A06 10966391 C T intron_variant MODIFIER c.817-184C>T| S282
15 BAA06g20640 A06 10967434 C T intron_variant MODIFIER c.1106+505C>T| S251
16 BAA06g20640 A06 10968152 G A intron_variant MODIFIER c.1107-77G>A| S270
17 BAA06g20640 A06 10968632 G A downstream_gene_variant MODIFIER c.*301G>A| S144
18 BAA06g20640 A06 10969423 C T downstream_gene_variant MODIFIER c.*1092C>T| S266
19 BAA06g20640 A06 10969771 G A downstream_gene_variant MODIFIER c.*1440G>A| S136
20 BAA06g20640 A06 10971559 G A downstream_gene_variant MODIFIER c.*3228G>A| S77
S82
21 BAA06g20640 A06 10972559 C T downstream_gene_variant MODIFIER c.*4228C>T| S136
22 BAA06g20640 A06 10973115 G A downstream_gene_variant MODIFIER c.*4784G>A| S177