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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g16220 A04 20697401 G A upstream_gene_variant MODIFIER c.-4241G>A| S36
2 BAA04g16220 A04 20697477 C T upstream_gene_variant MODIFIER c.-4165C>T| S192
3 BAA04g16220 A04 20697979 C T upstream_gene_variant MODIFIER c.-3663C>T| S84
S93
4 BAA04g16220 A04 20698601 G T upstream_gene_variant MODIFIER c.-3041G>T| S11
5 BAA04g16220 A04 20699727 G A upstream_gene_variant MODIFIER c.-1915G>A| S283
6 BAA04g16220 A04 20700272 G A upstream_gene_variant MODIFIER c.-1370G>A| S165
7 BAA04g16220 A04 20701879 C T intron_variant MODIFIER c.72+166C>T| S92
8 BAA04g16220 A04 20702368 C T missense_variant MODERATE c.172C>T|p.Pro58Ser S73
9 BAA04g16220 A04 20702432 C T missense_variant MODERATE c.236C>T|p.Ala79Val S270
10 BAA04g16220 A04 20702807 G A missense_variant MODERATE c.611G>A|p.Arg204His S259
11 BAA04g16220 A04 20702878 G A missense_variant MODERATE c.682G>A|p.Glu228Lys S137
12 BAA04g16220 A04 20703155 C T missense_variant MODERATE c.959C>T|p.Ala320Val S10
13 BAA04g16220 A04 20703719 C T missense_variant MODERATE c.1523C>T|p.Ser508Phe S117
14 BAA04g16220 A04 20707124 C T synonymous_variant LOW c.4774C>T|p.Leu1592Leu S210
15 BAA04g16220 A04 20707762 G A synonymous_variant LOW c.5412G>A|p.Gln1804Gln S288
16 BAA04g16220 A04 20707821 C T missense_variant MODERATE c.5471C>T|p.Ala1824Val S264
17 BAA04g16220 A04 20708299 C T synonymous_variant LOW c.5851C>T|p.Leu1951Leu S228
18 BAA04g16220 A04 20708973 G A missense_variant&splice_region_variant MODERATE c.6335G>A|p.Ser2112Asn S186
19 BAA04g16220 A04 20709033 G A missense_variant MODERATE c.6395G>A|p.Gly2132Asp S33
20 BAA04g16220 A04 20711848 G A downstream_gene_variant MODIFIER c.*2739G>A| S288
21 BAA04g16220 A04 20712343 C T downstream_gene_variant MODIFIER c.*3234C>T| S264
22 BAA04g16220 A04 20712834 G A downstream_gene_variant MODIFIER c.*3725G>A| S120
23 BAA04g16220 A04 20713906 A C downstream_gene_variant MODIFIER c.*4797A>C| S260