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


Gene ID

Results: 1 - 20 of 20 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g42950 A09 49171660 G A missense_variant MODERATE c.2941C>T|p.Leu981Phe S298
2 BAA09g42950 A09 49171680 C T missense_variant MODERATE c.2921G>A|p.Arg974Lys S36
3 BAA09g42950 A09 49173180 C T intron_variant MODIFIER c.2019+15G>A| S159
S243
S299
4 BAA09g42950 A09 49173221 C T missense_variant MODERATE c.1993G>A|p.Glu665Lys S125
5 BAA09g42950 A09 49173809 C T intron_variant MODIFIER c.1635+33G>A| S303
6 BAA09g42950 A09 49173991 G A intron_variant MODIFIER c.1539+33C>T| S46
7 BAA09g42950 A09 49174681 C T missense_variant MODERATE c.1152G>A|p.Met384Ile S260
8 BAA09g42950 A09 49174893 G A missense_variant MODERATE c.1049C>T|p.Ala350Val S17
9 BAA09g42950 A09 49174999 G A intron_variant MODIFIER c.1021+9C>T| S81
S85
10 BAA09g42950 A09 49175430 C T missense_variant MODERATE c.856G>A|p.Glu286Lys S15
S156
S2
S3
S4
11 BAA09g42950 A09 49176691 C T intron_variant MODIFIER c.136-57G>A| S30
S31
12 BAA09g42950 A09 49176780 G A intron_variant MODIFIER c.136-146C>T| S91
13 BAA09g42950 A09 49176906 C T intron_variant MODIFIER c.135+44G>A| S251
14 BAA09g42950 A09 49176992 C T synonymous_variant LOW c.93G>A|p.Gln31Gln S115
15 BAA09g42950 A09 49177470 G A upstream_gene_variant MODIFIER c.-386C>T| S204
16 BAA09g42950 A09 49178260 G A upstream_gene_variant MODIFIER c.-1176C>T| S150
17 BAA09g42950 A09 49179083 C T upstream_gene_variant MODIFIER c.-1999G>A| S229
18 BAA09g42950 A09 49179533 C T upstream_gene_variant MODIFIER c.-2449G>A| S302
19 BAA09g42950 A09 49180456 T A upstream_gene_variant MODIFIER c.-3372A>T| S28
20 BAA09g42950 A09 49182048 G A upstream_gene_variant MODIFIER c.-4964C>T| S48