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


Gene ID

Results: 1 - 30 of 30 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA04g29390 A04 28482643 G A upstream_gene_variant MODIFIER c.-3883G>A| S179
2 BAA04g29390 A04 28482918 G A upstream_gene_variant MODIFIER c.-3608G>A| S262
3 BAA04g29390 A04 28484738 A T upstream_gene_variant MODIFIER c.-1788A>T| S158
4 BAA04g29390 A04 28485200 G A upstream_gene_variant MODIFIER c.-1326G>A| S144
5 BAA04g29390 A04 28485512 G A upstream_gene_variant MODIFIER c.-1014G>A| S281
6 BAA04g29390 A04 28486150 A T upstream_gene_variant MODIFIER c.-376A>T| S282
7 BAA04g29390 A04 28486226 G A upstream_gene_variant MODIFIER c.-300G>A| S242
8 BAA04g29390 A04 28486280 C T upstream_gene_variant MODIFIER c.-246C>T| S32
9 BAA04g29390 A04 28487079 C T missense_variant MODERATE c.554C>T|p.Ser185Phe S148
S210
10 BAA04g29390 A04 28487091 C T missense_variant MODERATE c.566C>T|p.Pro189Leu S240
11 BAA04g29390 A04 28487268 G A missense_variant MODERATE c.743G>A|p.Gly248Glu S277
12 BAA04g29390 A04 28488009 C T missense_variant MODERATE c.1484C>T|p.Ser495Phe S2
13 BAA04g29390 A04 28488086 C T missense_variant MODERATE c.1561C>T|p.Pro521Ser S62
14 BAA04g29390 A04 28488247 C T synonymous_variant LOW c.1722C>T|p.Pro574Pro S200
15 BAA04g29390 A04 28488377 G A missense_variant MODERATE c.1852G>A|p.Val618Ile S198
16 BAA04g29390 A04 28488588 G A missense_variant MODERATE c.1906G>A|p.Asp636Asn S39
17 BAA04g29390 A04 28488819 C T missense_variant MODERATE c.2137C>T|p.Leu713Phe S6
18 BAA04g29390 A04 28488875 G A stop_gained HIGH c.2193G>A|p.Trp731* S218
S268
S269
19 BAA04g29390 A04 28489019 C T synonymous_variant LOW c.2337C>T|p.Leu779Leu S117
20 BAA04g29390 A04 28489217 C T synonymous_variant LOW c.2535C>T|p.Tyr845Tyr S81
S85
21 BAA04g29390 A04 28489752 C T synonymous_variant LOW c.2938C>T|p.Leu980Leu S303
22 BAA04g29390 A04 28490021 T G intron_variant MODIFIER c.3111+96T>G| S129
S153
S162
S201
S233
S266
S291
S57
S58
S98
23 BAA04g29390 A04 28490386 C A intron_variant MODIFIER c.3112-224C>A| S26
24 BAA04g29390 A04 28490442 C T intron_variant MODIFIER c.3112-168C>T| S135
25 BAA04g29390 A04 28490930 C T intron_variant MODIFIER c.3225+207C>T| S283