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 BAA08g05400 A08 4041866 G A downstream_gene_variant MODIFIER c.*4633C>T| S32
2 BAA08g05400 A08 4042166 C T downstream_gene_variant MODIFIER c.*4333G>A| S43
3 BAA08g05400 A08 4043806 C T downstream_gene_variant MODIFIER c.*2693G>A| S280
4 BAA08g05400 A08 4044095 C T downstream_gene_variant MODIFIER c.*2404G>A| S162
5 BAA08g05400 A08 4044397 C T downstream_gene_variant MODIFIER c.*2102G>A| S116
S118
S148
S210
S295
S54
6 BAA08g05400 A08 4046275 C T downstream_gene_variant MODIFIER c.*224G>A| S86
7 BAA08g05400 A08 4046301 C T downstream_gene_variant MODIFIER c.*198G>A| S126
8 BAA08g05400 A08 4046502 C T synonymous_variant LOW c.744G>A|p.Gln248Gln S176
9 BAA08g05400 A08 4046603 C T missense_variant MODERATE c.643G>A|p.Val215Ile S296
10 BAA08g05400 A08 4047994 G A intron_variant MODIFIER c.541-1289C>T| S8
11 BAA08g05400 A08 4048806 G A intron_variant MODIFIER c.540+1574C>T| S72
S78
12 BAA08g05400 A08 4048927 G A intron_variant MODIFIER c.540+1453C>T| S125
13 BAA08g05400 A08 4048993 C T intron_variant MODIFIER c.540+1387G>A| S36
14 BAA08g05400 A08 4049020 C T intron_variant MODIFIER c.540+1360G>A| S294
15 BAA08g05400 A08 4049520 G A intron_variant MODIFIER c.540+860C>T| S265
16 BAA08g05400 A08 4049685 C T intron_variant MODIFIER c.540+695G>A| S232
17 BAA08g05400 A08 4051023 G A missense_variant MODERATE c.62C>T|p.Ser21Phe S81
S85
18 BAA08g05400 A08 4051129 C T upstream_gene_variant MODIFIER c.-45G>A| S44
S6
19 BAA08g05400 A08 4051209 C T upstream_gene_variant MODIFIER c.-125G>A| S164
20 BAA08g05400 A08 4051798 G A upstream_gene_variant MODIFIER c.-714C>T| S240
21 BAA08g05400 A08 4051896 G A upstream_gene_variant MODIFIER c.-812C>T| S16
22 BAA08g05400 A08 4051970 G A upstream_gene_variant MODIFIER c.-886C>T| S266
23 BAA08g05400 A08 4052085 G A upstream_gene_variant MODIFIER c.-1001C>T| S5
24 BAA08g05400 A08 4052361 C T upstream_gene_variant MODIFIER c.-1277G>A| S149
25 BAA08g05400 A08 4052373 C T upstream_gene_variant MODIFIER c.-1289G>A| S6