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


Gene ID

Results: 1 - 29 of 29 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g34280 A06 23060236 G A upstream_gene_variant MODIFIER c.-706G>A| S50
2 BAA06g34280 A06 23060934 G A upstream_gene_variant MODIFIER c.-8G>A| S11
3 BAA06g34280 A06 23061930 C T missense_variant MODERATE c.989C>T|p.Pro330Leu S200
4 BAA06g34280 A06 23062323 C T missense_variant MODERATE c.1382C>T|p.Ser461Phe S178
5 BAA06g34280 A06 23062539 C T missense_variant MODERATE c.1598C>T|p.Ser533Phe S221
6 BAA06g34280 A06 23063120 C T missense_variant MODERATE c.2179C>T|p.Leu727Phe S18
7 BAA06g34280 A06 23063242 G A synonymous_variant LOW c.2301G>A|p.Glu767Glu S298
8 BAA06g34280 A06 23064055 G A intron_variant MODIFIER c.2880+162G>A| S32
9 BAA06g34280 A06 23064277 C T intron_variant MODIFIER c.2880+384C>T| S259
10 BAA06g34280 A06 23064501 C T intron_variant MODIFIER c.2880+608C>T| S46
11 BAA06g34280 A06 23065050 C T intron_variant MODIFIER c.2880+1157C>T| S178
12 BAA06g34280 A06 23065285 C T intron_variant MODIFIER c.2880+1392C>T| S83
13 BAA06g34280 A06 23065303 C T intron_variant MODIFIER c.2880+1410C>T| S283
14 BAA06g34280 A06 23065317 C T intron_variant MODIFIER c.2880+1424C>T| S6
15 BAA06g34280 A06 23066284 T A intron_variant MODIFIER c.2880+2391T>A| S155
S211
16 BAA06g34280 A06 23067771 C T intron_variant MODIFIER c.2880+3878C>T| S296
17 BAA06g34280 A06 23067882 G A intron_variant MODIFIER c.2880+3989G>A| S219
S72
18 BAA06g34280 A06 23068455 G A intron_variant MODIFIER c.2880+4562G>A| S123
19 BAA06g34280 A06 23068476 G A intron_variant MODIFIER c.2880+4583G>A| S204
20 BAA06g34280 A06 23070047 A C intron_variant MODIFIER c.2881-5671A>C| S236
21 BAA06g34280 A06 23071531 G A intron_variant MODIFIER c.2881-4187G>A| S12
22 BAA06g34280 A06 23071923 G A intron_variant MODIFIER c.2881-3795G>A| S169
23 BAA06g34280 A06 23072209 G A intron_variant MODIFIER c.2881-3509G>A| S263
24 BAA06g34280 A06 23072718 C T intron_variant MODIFIER c.2881-3000C>T| S132
S137
S215
25 BAA06g34280 A06 23072870 C T intron_variant MODIFIER c.2881-2848C>T| S1
S161
S228
S90