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


Gene ID

Results: 1 - 19 of 19 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA08g25790 A08 18478058 A G intron_variant MODIFIER c.427-31A>G| S74
2 BAA08g25790 A08 18479016 G A missense_variant MODERATE c.748G>A|p.Glu250Lys S259
3 BAA08g25790 A08 18479226 C T intron_variant MODIFIER c.830+128C>T| S262
4 BAA08g25790 A08 18479835 C T intron_variant MODIFIER c.906+81C>T| S209
5 BAA08g25790 A08 18479880 C T intron_variant MODIFIER c.906+126C>T| S295
6 BAA08g25790 A08 18481012 C T intron_variant MODIFIER c.1380+21C>T| S90
7 BAA08g25790 A08 18481047 C T intron_variant MODIFIER c.1381-20C>T| S81
S85
8 BAA08g25790 A08 18481261 T G missense_variant MODERATE c.1575T>G|p.His525Gln S193
S288
9 BAA08g25790 A08 18482044 C T intron_variant MODIFIER c.1872+217C>T| S284
10 BAA08g25790 A08 18482324 C T splice_region_variant&synonymous_variant LOW c.1875C>T|p.Leu625Leu S299
11 BAA08g25790 A08 18483432 C T intron_variant MODIFIER c.2226+231C>T| S51
12 BAA08g25790 A08 18483876 G A intron_variant MODIFIER c.2330+88G>A| S86
13 BAA08g25790 A08 18484000 C T intron_variant MODIFIER c.2331-71C>T| S249
14 BAA08g25790 A08 18484178 C T missense_variant MODERATE c.2438C>T|p.Thr813Ile S213
15 BAA08g25790 A08 18484823 C T missense_variant MODERATE c.2699C>T|p.Thr900Ile S156
16 BAA08g25790 A08 18485466 C T intron_variant MODIFIER c.3286-46C>T| S135
17 BAA08g25790 A08 18486800 C T missense_variant MODERATE c.3755C>T|p.Ser1252Phe S144
18 BAA08g25790 A08 18488448 G A synonymous_variant LOW c.4896G>A|p.Pro1632Pro S301
S304
19 BAA08g25790 A08 18494144 G A downstream_gene_variant MODIFIER c.*4977G>A| S84
S93