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


Gene ID

Results: 1 - 25 of 25 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g66120 A09 60585609 C T synonymous_variant LOW c.5025G>A|p.Glu1675Glu S192
2 BAA09g66120 A09 60585877 C T missense_variant MODERATE c.4757G>A|p.Arg1586Lys S105
3 BAA09g66120 A09 60585918 G A synonymous_variant LOW c.4716C>T|p.Phe1572Phe S99
4 BAA09g66120 A09 60586938 C T missense_variant MODERATE c.4060G>A|p.Gly1354Arg S207
S215
5 BAA09g66120 A09 60587175 C T missense_variant MODERATE c.3823G>A|p.Glu1275Lys S64
6 BAA09g66120 A09 60587641 C T synonymous_variant LOW c.3357G>A|p.Gln1119Gln S163
7 BAA09g66120 A09 60587685 C T missense_variant MODERATE c.3313G>A|p.Ala1105Thr S117
8 BAA09g66120 A09 60587955 C T missense_variant MODERATE c.3043G>A|p.Glu1015Lys S224
9 BAA09g66120 A09 60588114 C T splice_donor_variant&intron_variant HIGH c.3021+1G>A| S105
10 BAA09g66120 A09 60588276 C T intron_variant MODIFIER c.2960-100G>A| S159
S299
11 BAA09g66120 A09 60588448 C T intron_variant MODIFIER c.2960-272G>A| S278
12 BAA09g66120 A09 60589942 C T synonymous_variant LOW c.2367G>A|p.Val789Val S302
13 BAA09g66120 A09 60590701 C T intron_variant MODIFIER c.1921-47G>A| S20
14 BAA09g66120 A09 60590967 C T intron_variant MODIFIER c.1920+63G>A| S249
15 BAA09g66120 A09 60591450 C T missense_variant MODERATE c.1649G>A|p.Gly550Glu S100
16 BAA09g66120 A09 60591516 C T missense_variant MODERATE c.1583G>A|p.Ser528Asn S256
17 BAA09g66120 A09 60592809 G A synonymous_variant LOW c.1056C>T|p.Asp352Asp S233
18 BAA09g66120 A09 60593793 C T missense_variant MODERATE c.656G>A|p.Arg219His S221
19 BAA09g66120 A09 60593813 C T synonymous_variant LOW c.636G>A|p.Gln212Gln S15
S153
S2
S213
S3
S34
20 BAA09g66120 A09 60594998 C T missense_variant MODERATE c.88G>A|p.Glu30Lys S296
21 BAA09g66120 A09 60595541 C T upstream_gene_variant MODIFIER c.-456G>A| S280
22 BAA09g66120 A09 60596519 G A upstream_gene_variant MODIFIER c.-1434C>T| S167
23 BAA09g66120 A09 60596752 G A upstream_gene_variant MODIFIER c.-1667C>T| S189
24 BAA09g66120 A09 60598397 C T upstream_gene_variant MODIFIER c.-3312G>A| S269
25 BAA09g66120 A09 60598862 G A upstream_gene_variant MODIFIER c.-3777C>T| S11