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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g04570 A08 3308387 C T intron_variant MODIFIER c.36+4401C>T| S205
2 BAA08g04570 A08 3309737 G A intron_variant MODIFIER c.36+5751G>A| S237
3 BAA08g04570 A08 3316413 C T intron_variant MODIFIER c.36+12427C>T| S15
S3
4 BAA08g04570 A08 3316696 G A intron_variant MODIFIER c.36+12710G>A| S65
5 BAA08g04570 A08 3322829 C T intron_variant MODIFIER c.37-7497C>T| S71
6 BAA08g04570 A08 3323989 G A intron_variant MODIFIER c.37-6337G>A| S204
7 BAA08g04570 A08 3324175 C T intron_variant MODIFIER c.37-6151C>T| S132
S137
S89
8 BAA08g04570 A08 3324272 G A intron_variant MODIFIER c.37-6054G>A| S178
9 BAA08g04570 A08 3325088 C T intron_variant MODIFIER c.37-5238C>T| S176
10 BAA08g04570 A08 3325478 G A intron_variant MODIFIER c.37-4848G>A| S107
11 BAA08g04570 A08 3326622 C T intron_variant MODIFIER c.37-3704C>T| S174
S216
S241
12 BAA08g04570 A08 3327509 G A intron_variant MODIFIER c.37-2817G>A| S179
13 BAA08g04570 A08 3329015 C T intron_variant MODIFIER c.37-1311C>T| S247
14 BAA08g04570 A08 3329704 G A intron_variant MODIFIER c.37-622G>A| S58
15 BAA08g04570 A08 3329999 C T intron_variant MODIFIER c.37-327C>T| S213
16 BAA08g04570 A08 3333889 C T missense_variant MODERATE c.844C>T|p.Pro282Ser S250
17 BAA08g04570 A08 3333930 C T synonymous_variant LOW c.885C>T|p.Ile295Ile S164
18 BAA08g04570 A08 3334060 G A missense_variant&splice_region_variant MODERATE c.1015G>A|p.Asp339Asn S95
19 BAA08g04570 A08 3334198 C T missense_variant MODERATE c.1064C>T|p.Ala355Val S34
20 BAA08g04570 A08 3334238 C T synonymous_variant LOW c.1104C>T|p.Ser368Ser S48
21 BAA08g04570 A08 3334343 G A splice_acceptor_variant&intron_variant HIGH c.1123-1G>A| S37
22 BAA08g04570 A08 3334870 G A downstream_gene_variant MODIFIER c.*19G>A| S187