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


Gene ID

Results: 1 - 39 of 39 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g08570 A08 7828968 C T downstream_gene_variant MODIFIER c.*3445G>A| S82
S92
2 BAA08g08570 A08 7829046 C T downstream_gene_variant MODIFIER c.*3367G>A| S80
3 BAA08g08570 A08 7829134 G A downstream_gene_variant MODIFIER c.*3279C>T| S62
4 BAA08g08570 A08 7829378 C T downstream_gene_variant MODIFIER c.*3035G>A| S71
5 BAA08g08570 A08 7829470 G A downstream_gene_variant MODIFIER c.*2943C>T| S274
6 BAA08g08570 A08 7830010 C T downstream_gene_variant MODIFIER c.*2403G>A| S255
7 BAA08g08570 A08 7831055 G A downstream_gene_variant MODIFIER c.*1358C>T| S229
8 BAA08g08570 A08 7831331 G A downstream_gene_variant MODIFIER c.*1082C>T| S267
S288
9 BAA08g08570 A08 7832339 G A downstream_gene_variant MODIFIER c.*74C>T| S190
10 BAA08g08570 A08 7832621 C T missense_variant MODERATE c.5864G>A|p.Arg1955Lys S79
S84
11 BAA08g08570 A08 7833300 C T missense_variant MODERATE c.5269G>A|p.Glu1757Lys S44
12 BAA08g08570 A08 7833626 G A missense_variant MODERATE c.4943C>T|p.Thr1648Ile S129
13 BAA08g08570 A08 7833744 G A missense_variant MODERATE c.4825C>T|p.Leu1609Phe S183
14 BAA08g08570 A08 7834519 G A missense_variant MODERATE c.4283C>T|p.Ser1428Phe S72
15 BAA08g08570 A08 7834716 C T synonymous_variant LOW c.4161G>A|p.Glu1387Glu S203
16 BAA08g08570 A08 7835135 C T missense_variant&splice_region_variant MODERATE c.3742G>A|p.Val1248Ile S292
17 BAA08g08570 A08 7835143 G A splice_region_variant&intron_variant LOW c.3742-8C>T| S203
18 BAA08g08570 A08 7835400 C T missense_variant MODERATE c.3605G>A|p.Ser1202Asn S157
S163
19 BAA08g08570 A08 7835720 C T intron_variant MODIFIER c.3534+84G>A| S79
S84
20 BAA08g08570 A08 7836555 C T synonymous_variant LOW c.3078G>A|p.Lys1026Lys S74
21 BAA08g08570 A08 7836929 C T intron_variant MODIFIER c.3042+16G>A| S60
22 BAA08g08570 A08 7837000 G A missense_variant MODERATE c.2987C>T|p.Pro996Leu S275
23 BAA08g08570 A08 7837136 C T missense_variant MODERATE c.2851G>A|p.Glu951Lys S291
24 BAA08g08570 A08 7837945 G A intron_variant MODIFIER c.2262-10C>T| S196
25 BAA08g08570 A08 7838784 G A missense_variant MODERATE c.1516C>T|p.Pro506Ser S37