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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g24190 A01 12658976 G A upstream_gene_variant MODIFIER c.-3747G>A| S33
2 BAA01g24190 A01 12659003 G A upstream_gene_variant MODIFIER c.-3720G>A| S190
3 BAA01g24190 A01 12659628 C T upstream_gene_variant MODIFIER c.-3095C>T| S166
4 BAA01g24190 A01 12662831 C T missense_variant MODERATE c.109C>T|p.Pro37Ser S114
5 BAA01g24190 A01 12663239 G A splice_donor_variant&intron_variant HIGH c.318+1G>A| S281
6 BAA01g24190 A01 12663508 G A missense_variant MODERATE c.430G>A|p.Asp144Asn S262
7 BAA01g24190 A01 12663967 C T stop_gained&splice_region_variant HIGH c.691C>T|p.Gln231* S185
8 BAA01g24190 A01 12664603 G A synonymous_variant LOW c.816G>A|p.Lys272Lys S173
9 BAA01g24190 A01 12665570 G A missense_variant MODERATE c.1306G>A|p.Gly436Arg S71
10 BAA01g24190 A01 12665576 G A missense_variant MODERATE c.1312G>A|p.Glu438Lys S159
S243
11 BAA01g24190 A01 12665593 G A synonymous_variant LOW c.1329G>A|p.Glu443Glu S280
12 BAA01g24190 A01 12666177 G A missense_variant MODERATE c.1822G>A|p.Ala608Thr S9
13 BAA01g24190 A01 12666429 C T stop_gained HIGH c.2074C>T|p.Gln692* S164
14 BAA01g24190 A01 12667176 C T intron_variant MODIFIER c.2616-37C>T| S205
15 BAA01g24190 A01 12667609 G A synonymous_variant LOW c.3012G>A|p.Lys1004Lys S56
16 BAA01g24190 A01 12668083 G A synonymous_variant LOW c.3486G>A|p.Lys1162Lys S288
17 BAA01g24190 A01 12669122 C T downstream_gene_variant MODIFIER c.*407C>T| S242
18 BAA01g24190 A01 12669150 C T downstream_gene_variant MODIFIER c.*435C>T| S198
19 BAA01g24190 A01 12669351 G A downstream_gene_variant MODIFIER c.*636G>A| S302
20 BAA01g24190 A01 12669753 C T downstream_gene_variant MODIFIER c.*1038C>T| S200
21 BAA01g24190 A01 12669926 G A downstream_gene_variant MODIFIER c.*1211G>A| S240
22 BAA01g24190 A01 12670614 G A downstream_gene_variant MODIFIER c.*1899G>A| S9
23 BAA01g24190 A01 12671018 C T downstream_gene_variant MODIFIER c.*2303C>T| S205
24 BAA01g24190 A01 12671240 G A downstream_gene_variant MODIFIER c.*2525G>A| S298
25 BAA01g24190 A01 12671340 G A downstream_gene_variant MODIFIER c.*2625G>A| S60