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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g14920 A10 15480580 G A downstream_gene_variant MODIFIER c.*2579C>T| S18
2 BAA10g14920 A10 15481366 G A downstream_gene_variant MODIFIER c.*1793C>T| S209
3 BAA10g14920 A10 15481521 G A downstream_gene_variant MODIFIER c.*1638C>T| S208
4 BAA10g14920 A10 15481588 G A downstream_gene_variant MODIFIER c.*1571C>T| S250
5 BAA10g14920 A10 15481766 G A downstream_gene_variant MODIFIER c.*1393C>T| S245
6 BAA10g14920 A10 15482647 G A downstream_gene_variant MODIFIER c.*512C>T| S18
7 BAA10g14920 A10 15482869 G A downstream_gene_variant MODIFIER c.*290C>T| S138
8 BAA10g14920 A10 15483295 G A intron_variant MODIFIER c.3211+40C>T| S176
9 BAA10g14920 A10 15483308 G A intron_variant MODIFIER c.3211+27C>T| S120
10 BAA10g14920 A10 15483579 G A synonymous_variant LOW c.3063C>T|p.Asn1021Asn S65
11 BAA10g14920 A10 15483902 G A intron_variant MODIFIER c.2904+25C>T| S132
S137
S215
12 BAA10g14920 A10 15484759 G A intron_variant MODIFIER c.2484+17C>T| S144
13 BAA10g14920 A10 15484858 G A missense_variant MODERATE c.2402C>T|p.Ala801Val S283
14 BAA10g14920 A10 15484951 C T intron_variant MODIFIER c.2385+14G>A| S84
S93
15 BAA10g14920 A10 15485966 G A intron_variant MODIFIER c.1875+45C>T| S62
16 BAA10g14920 A10 15486223 C T intron_variant MODIFIER c.1764+24G>A| S259
17 BAA10g14920 A10 15486372 C T intron_variant MODIFIER c.1666-27G>A| S180
18 BAA10g14920 A10 15487245 G A splice_region_variant&intron_variant LOW c.1291-3C>T| S3
19 BAA10g14920 A10 15489538 C T synonymous_variant LOW c.174G>A|p.Arg58Arg S104
S52
20 BAA10g14920 A10 15490198 G A upstream_gene_variant MODIFIER c.-387C>T| S71
21 BAA10g14920 A10 15490773 G A upstream_gene_variant MODIFIER c.-962C>T| S110
22 BAA10g14920 A10 15491536 G A upstream_gene_variant MODIFIER c.-1725C>T| S36
23 BAA10g14920 A10 15492550 C T upstream_gene_variant MODIFIER c.-2739G>A| S10
24 BAA10g14920 A10 15494277 G A upstream_gene_variant MODIFIER c.-4466C>T| S167