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


Gene ID

Results: 1 - 37 of 37 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g33580 A09 42123567 C T upstream_gene_variant MODIFIER c.-4540C>T| S248
S77
2 BAA09g33580 A09 42123593 C T upstream_gene_variant MODIFIER c.-4514C>T| S237
3 BAA09g33580 A09 42124187 C T upstream_gene_variant MODIFIER c.-3920C>T| S246
4 BAA09g33580 A09 42125196 A T upstream_gene_variant MODIFIER c.-2911A>T| S132
S137
S89
5 BAA09g33580 A09 42126520 G A upstream_gene_variant MODIFIER c.-1587G>A| S200
6 BAA09g33580 A09 42128115 G A synonymous_variant LOW c.9G>A|p.Glu3Glu S230
7 BAA09g33580 A09 42128578 G A missense_variant MODERATE c.379G>A|p.Gly127Arg S233
8 BAA09g33580 A09 42128693 G A intron_variant MODIFIER c.453+41G>A| S190
S210
9 BAA09g33580 A09 42129130 C T intron_variant MODIFIER c.454-117C>T| S198
10 BAA09g33580 A09 42129658 G A missense_variant MODERATE c.865G>A|p.Val289Ile S270
11 BAA09g33580 A09 42130001 C T missense_variant MODERATE c.1106C>T|p.Ser369Phe S83
S88
12 BAA09g33580 A09 42130010 C T missense_variant MODERATE c.1115C>T|p.Ser372Phe S30
S31
13 BAA09g33580 A09 42130381 G A missense_variant MODERATE c.1486G>A|p.Glu496Lys S73
S91
14 BAA09g33580 A09 42130547 C T missense_variant MODERATE c.1652C>T|p.Ala551Val S33
15 BAA09g33580 A09 42130793 C T missense_variant MODERATE c.1898C>T|p.Pro633Leu S60
16 BAA09g33580 A09 42130833 G A stop_gained HIGH c.1938G>A|p.Trp646* S190
17 BAA09g33580 A09 42131317 G A missense_variant MODERATE c.2422G>A|p.Ala808Thr S173
18 BAA09g33580 A09 42132425 C T intron_variant MODIFIER c.2635+895C>T| S140
19 BAA09g33580 A09 42132490 G A intron_variant MODIFIER c.2635+960G>A| S199
20 BAA09g33580 A09 42132656 C T intron_variant MODIFIER c.2636-1095C>T| S245
21 BAA09g33580 A09 42132658 C T intron_variant MODIFIER c.2636-1093C>T| S144
22 BAA09g33580 A09 42132701 C T intron_variant MODIFIER c.2636-1050C>T| S56
23 BAA09g33580 A09 42132905 C T intron_variant MODIFIER c.2636-846C>T| S202
24 BAA09g33580 A09 42133006 C T intron_variant MODIFIER c.2636-745C>T| S67
25 BAA09g33580 A09 42133075 G A intron_variant MODIFIER c.2636-676G>A| S263