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


Gene ID

Results: 1 - 60 of 60 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g05940 A08 4595469 G A upstream_gene_variant MODIFIER c.-4441G>A| S239
S33
2 BAA08g05940 A08 4595484 C T upstream_gene_variant MODIFIER c.-4426C>T| S172
3 BAA08g05940 A08 4595547 G A upstream_gene_variant MODIFIER c.-4363G>A| S249
4 BAA08g05940 A08 4595679 C T upstream_gene_variant MODIFIER c.-4231C>T| S303
5 BAA08g05940 A08 4598537 C T upstream_gene_variant MODIFIER c.-1373C>T| S233
6 BAA08g05940 A08 4598896 G A upstream_gene_variant MODIFIER c.-1014G>A| S109
7 BAA08g05940 A08 4600466 C T intron_variant MODIFIER c.208-228C>T| S223
8 BAA08g05940 A08 4600858 C T missense_variant&splice_region_variant MODERATE c.278C>T|p.Ala93Val S67
9 BAA08g05940 A08 4601883 G A missense_variant MODERATE c.838G>A|p.Gly280Arg S119
10 BAA08g05940 A08 4601945 C T synonymous_variant LOW c.900C>T|p.Arg300Arg S180
11 BAA08g05940 A08 4602476 C T intron_variant MODIFIER c.1216-36C>T| S209
12 BAA08g05940 A08 4603363 G A intron_variant MODIFIER c.1438+629G>A| S5
13 BAA08g05940 A08 4603750 C T intron_variant MODIFIER c.1438+1016C>T| S226
14 BAA08g05940 A08 4603816 C T intron_variant MODIFIER c.1438+1082C>T| S120
15 BAA08g05940 A08 4604399 G A intron_variant MODIFIER c.1438+1665G>A| S11
16 BAA08g05940 A08 4604568 C T intron_variant MODIFIER c.1438+1834C>T| S191
17 BAA08g05940 A08 4606006 C T intron_variant MODIFIER c.1439-3116C>T| S28
18 BAA08g05940 A08 4606309 C T intron_variant MODIFIER c.1439-2813C>T| S144
19 BAA08g05940 A08 4606356 C T intron_variant MODIFIER c.1439-2766C>T| S96
20 BAA08g05940 A08 4607440 C T intron_variant MODIFIER c.1439-1682C>T| S178
21 BAA08g05940 A08 4609459 G A synonymous_variant LOW c.1776G>A|p.Lys592Lys S262
22 BAA08g05940 A08 4609705 G A missense_variant MODERATE c.1978G>A|p.Asp660Asn S108
23 BAA08g05940 A08 4609903 G A missense_variant MODERATE c.2176G>A|p.Glu726Lys S181
24 BAA08g05940 A08 4609958 C T missense_variant MODERATE c.2231C>T|p.Ala744Val S50
25 BAA08g05940 A08 4610037 C T intron_variant MODIFIER c.2289+21C>T| S6