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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g36570 A06 24242455 C T downstream_gene_variant MODIFIER c.*2036G>A| S293
2 BAA06g36570 A06 24242860 C T downstream_gene_variant MODIFIER c.*1631G>A| S234
3 BAA06g36570 A06 24243127 G A downstream_gene_variant MODIFIER c.*1364C>T| S133
4 BAA06g36570 A06 24244737 C T synonymous_variant LOW c.2619G>A|p.Lys873Lys S144
S148
S30
S31
5 BAA06g36570 A06 24245303 C T missense_variant MODERATE c.2053G>A|p.Asp685Asn S221
6 BAA06g36570 A06 24249070 G A intron_variant MODIFIER c.1172-2886C>T| S197
7 BAA06g36570 A06 24249776 G A intron_variant MODIFIER c.1172-3592C>T| S19
8 BAA06g36570 A06 24249931 C T intron_variant MODIFIER c.1172-3747G>A| S291
9 BAA06g36570 A06 24250050 C T intron_variant MODIFIER c.1172-3866G>A| S153
10 BAA06g36570 A06 24250873 G A intron_variant MODIFIER c.1171+4001C>T| S162
11 BAA06g36570 A06 24251558 C T intron_variant MODIFIER c.1171+3316G>A| S293
12 BAA06g36570 A06 24254626 C T intron_variant MODIFIER c.1171+248G>A| S6
13 BAA06g36570 A06 24255079 G A intron_variant MODIFIER c.1024+37C>T| S201
14 BAA06g36570 A06 24255242 C T missense_variant MODERATE c.898G>A|p.Asp300Asn S177
15 BAA06g36570 A06 24255622 G A missense_variant MODERATE c.518C>T|p.Ser173Phe S103
16 BAA06g36570 A06 24255771 C T synonymous_variant LOW c.369G>A|p.Lys123Lys S74
17 BAA06g36570 A06 24256527 G A upstream_gene_variant MODIFIER c.-183C>T| S192
18 BAA06g36570 A06 24258048 C T upstream_gene_variant MODIFIER c.-1704G>A| S37
19 BAA06g36570 A06 24260393 C T upstream_gene_variant MODIFIER c.-4049G>A| S144
20 BAA06g36570 A06 24260802 G A upstream_gene_variant MODIFIER c.-4458C>T| S93
21 BAA06g36570 A06 24260812 G A upstream_gene_variant MODIFIER c.-4468C>T| S44