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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g20440 A06 10830240 C T downstream_gene_variant MODIFIER c.*4377G>A| S17
2 BAA06g20440 A06 10833360 C T downstream_gene_variant MODIFIER c.*1257G>A| S179
3 BAA06g20440 A06 10833653 T A downstream_gene_variant MODIFIER c.*964A>T| S128
S197
S308
4 BAA06g20440 A06 10834313 C T downstream_gene_variant MODIFIER c.*304G>A| S171
5 BAA06g20440 A06 10835598 C T synonymous_variant LOW c.4083G>A|p.Val1361Val S278
6 BAA06g20440 A06 10835775 C T missense_variant&splice_region_variant MODERATE c.4000G>A|p.Glu1334Lys S183
S198
7 BAA06g20440 A06 10836205 C T missense_variant MODERATE c.3673G>A|p.Glu1225Lys S121
8 BAA06g20440 A06 10836300 G A intron_variant MODIFIER c.3608-30C>T| S292
9 BAA06g20440 A06 10839164 C T missense_variant MODERATE c.1709G>A|p.Gly570Glu S244
10 BAA06g20440 A06 10839655 C T synonymous_variant LOW c.1218G>A|p.Gln406Gln S281
11 BAA06g20440 A06 10839859 C T synonymous_variant LOW c.1014G>A|p.Lys338Lys S132
S137
S215
S89
12 BAA06g20440 A06 10840036 G A synonymous_variant LOW c.837C>T|p.Ser279Ser S275
13 BAA06g20440 A06 10840363 C T synonymous_variant LOW c.510G>A|p.Glu170Glu S126
S255
S59
14 BAA06g20440 A06 10840429 C T synonymous_variant LOW c.444G>A|p.Gln148Gln S239
15 BAA06g20440 A06 10840974 G A upstream_gene_variant MODIFIER c.-102C>T| S302
16 BAA06g20440 A06 10842417 G A upstream_gene_variant MODIFIER c.-1545C>T| S233
17 BAA06g20440 A06 10844533 G A upstream_gene_variant MODIFIER c.-3661C>T| S110
18 BAA06g20440 A06 10844536 C T upstream_gene_variant MODIFIER c.-3664G>A| S46
19 BAA06g20440 A06 10845203 G A upstream_gene_variant MODIFIER c.-4331C>T| S234
S255
20 BAA06g20440 A06 10845784 G A upstream_gene_variant MODIFIER c.-4912C>T| S50