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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g10320 A05 5232867 G A upstream_gene_variant MODIFIER c.-4651G>A| S144
2 BAA05g10320 A05 5234125 G A upstream_gene_variant MODIFIER c.-3393G>A| S38
3 BAA05g10320 A05 5235446 G A upstream_gene_variant MODIFIER c.-2072G>A| S66
4 BAA05g10320 A05 5235466 C T upstream_gene_variant MODIFIER c.-2052C>T| S13
5 BAA05g10320 A05 5235467 T G upstream_gene_variant MODIFIER c.-2051T>G| S119
6 BAA05g10320 A05 5235610 G C upstream_gene_variant MODIFIER c.-1908G>C| S135
S152
S68
7 BAA05g10320 A05 5236996 G A upstream_gene_variant MODIFIER c.-522G>A| S173
8 BAA05g10320 A05 5237447 C T upstream_gene_variant MODIFIER c.-71C>T| S207
9 BAA05g10320 A05 5237660 C T missense_variant MODERATE c.143C>T|p.Ser48Phe S295
10 BAA05g10320 A05 5237757 G A synonymous_variant LOW c.240G>A|p.Glu80Glu S299
11 BAA05g10320 A05 5237845 G A missense_variant MODERATE c.328G>A|p.Ala110Thr S67
12 BAA05g10320 A05 5238087 G A missense_variant MODERATE c.475G>A|p.Glu159Lys S4
13 BAA05g10320 A05 5239779 C T intron_variant MODIFIER c.1053+107C>T| S111
14 BAA05g10320 A05 5240032 G A intron_variant MODIFIER c.1098+31G>A| S187
S188
S276
S298
15 BAA05g10320 A05 5240561 C T intron_variant MODIFIER c.1374+35C>T| S273
16 BAA05g10320 A05 5240680 C T intron_variant MODIFIER c.1375-35C>T| S250
17 BAA05g10320 A05 5240748 G A missense_variant MODERATE c.1408G>A|p.Glu470Lys S148
S210
18 BAA05g10320 A05 5242776 C T missense_variant MODERATE c.2276C>T|p.Ala759Val S36
19 BAA05g10320 A05 5242812 G A missense_variant MODERATE c.2312G>A|p.Gly771Asp S262
20 BAA05g10320 A05 5243833 G A missense_variant MODERATE c.3047G>A|p.Arg1016Lys S79
S91
21 BAA05g10320 A05 5244262 C T missense_variant MODERATE c.3476C>T|p.Ala1159Val S157
22 BAA05g10320 A05 5244387 G A missense_variant MODERATE c.3601G>A|p.Glu1201Lys S308
23 BAA05g10320 A05 5244569 C T stop_gained HIGH c.3718C>T|p.Gln1240* S57
24 BAA05g10320 A05 5244664 C T synonymous_variant LOW c.3813C>T|p.Ser1271Ser S188
25 BAA05g10320 A05 5244741 C T missense_variant MODERATE c.3890C>T|p.Ser1297Phe S98