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


Gene ID

Results: 1 - 26 of 26 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g23430 A05 28082746 G A downstream_gene_variant MODIFIER c.*4027C>T| S62
2 BAA05g23430 A05 28082850 C T downstream_gene_variant MODIFIER c.*3923G>A| S100
3 BAA05g23430 A05 28082899 C T downstream_gene_variant MODIFIER c.*3874G>A| S170
4 BAA05g23430 A05 28083557 G A downstream_gene_variant MODIFIER c.*3216C>T| S190
5 BAA05g23430 A05 28083705 A T downstream_gene_variant MODIFIER c.*3068T>A| S48
6 BAA05g23430 A05 28087782 C T intron_variant MODIFIER c.782-616G>A| S177
7 BAA05g23430 A05 28088403 C T intron_variant MODIFIER c.782-1237G>A| S37
8 BAA05g23430 A05 28088949 G A intron_variant MODIFIER c.781+1710C>T| S129
9 BAA05g23430 A05 28089138 C T intron_variant MODIFIER c.781+1521G>A| S169
10 BAA05g23430 A05 28089396 C T intron_variant MODIFIER c.781+1263G>A| S17
11 BAA05g23430 A05 28089608 C T intron_variant MODIFIER c.781+1051G>A| S192
12 BAA05g23430 A05 28090646 G A intron_variant MODIFIER c.781+13C>T| S144
13 BAA05g23430 A05 28090945 C T intron_variant MODIFIER c.535-40G>A| S241
14 BAA05g23430 A05 28091026 C T intron_variant MODIFIER c.535-121G>A| S192
15 BAA05g23430 A05 28091436 C T missense_variant MODERATE c.469G>A|p.Asp157Asn S206
S26
16 BAA05g23430 A05 28091499 G A synonymous_variant LOW c.406C>T|p.Leu136Leu S54
17 BAA05g23430 A05 28091850 C T intron_variant MODIFIER c.113-58G>A| S294
18 BAA05g23430 A05 28092000 C T intron_variant MODIFIER c.113-208G>A| S192
19 BAA05g23430 A05 28092268 C T intron_variant MODIFIER c.112+266G>A| S232
20 BAA05g23430 A05 28092648 G A upstream_gene_variant MODIFIER c.-3C>T| S265
21 BAA05g23430 A05 28092692 C T upstream_gene_variant MODIFIER c.-47G>A| S245
22 BAA05g23430 A05 28093191 G A upstream_gene_variant MODIFIER c.-546C>T| S122
S280
23 BAA05g23430 A05 28093199 G A upstream_gene_variant MODIFIER c.-554C>T| S197
24 BAA05g23430 A05 28093304 G A upstream_gene_variant MODIFIER c.-659C>T| S134
25 BAA05g23430 A05 28093743 C T upstream_gene_variant MODIFIER c.-1098G>A| S202