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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g21290 A05 13533801 C T upstream_gene_variant MODIFIER c.-4072C>T| S216
2 BAA05g21290 A05 13534171 G A upstream_gene_variant MODIFIER c.-3702G>A| S219
S72
3 BAA05g21290 A05 13534376 G A upstream_gene_variant MODIFIER c.-3497G>A| S55
4 BAA05g21290 A05 13534412 G A upstream_gene_variant MODIFIER c.-3461G>A| S257
5 BAA05g21290 A05 13535071 C T upstream_gene_variant MODIFIER c.-2802C>T| S35
6 BAA05g21290 A05 13535743 C T upstream_gene_variant MODIFIER c.-2130C>T| S100
7 BAA05g21290 A05 13535968 G A upstream_gene_variant MODIFIER c.-1905G>A| S76
8 BAA05g21290 A05 13536264 C T upstream_gene_variant MODIFIER c.-1609C>T| S251
9 BAA05g21290 A05 13536522 C T upstream_gene_variant MODIFIER c.-1351C>T| S203
10 BAA05g21290 A05 13536662 C T upstream_gene_variant MODIFIER c.-1211C>T| S287
11 BAA05g21290 A05 13536729 C T upstream_gene_variant MODIFIER c.-1144C>T| S198
12 BAA05g21290 A05 13537757 G A upstream_gene_variant MODIFIER c.-116G>A| S40
S49
13 BAA05g21290 A05 13537861 G A upstream_gene_variant MODIFIER c.-12G>A| S216
S265
14 BAA05g21290 A05 13537934 C T missense_variant MODERATE c.62C>T|p.Pro21Leu S65
15 BAA05g21290 A05 13538100 G T synonymous_variant LOW c.228G>T|p.Val76Val S23
16 BAA05g21290 A05 13539706 G A intron_variant MODIFIER c.362+1472G>A| S151
S263
17 BAA05g21290 A05 13539731 G A intron_variant MODIFIER c.362+1497G>A| S123
18 BAA05g21290 A05 13540055 G A intron_variant MODIFIER c.363-1252G>A| S308
19 BAA05g21290 A05 13540457 G A intron_variant MODIFIER c.363-850G>A| S265
S51
20 BAA05g21290 A05 13540942 G A intron_variant MODIFIER c.363-365G>A| S4
21 BAA05g21290 A05 13542164 C T intron_variant MODIFIER c.583+637C>T| S207
S234
22 BAA05g21290 A05 13542198 C T intron_variant MODIFIER c.583+671C>T| S47
23 BAA05g21290 A05 13542615 C T intron_variant MODIFIER c.583+1088C>T| S71
24 BAA05g21290 A05 13542837 G A intron_variant MODIFIER c.584-1170G>A| S132
S137
S89
25 BAA05g21290 A05 13542940 C T intron_variant MODIFIER c.584-1067C>T| S63