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


Gene ID

Results: 1 - 29 of 29 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g20000 A05 12170135 C T upstream_gene_variant MODIFIER c.-4746C>T| S175
2 BAA05g20000 A05 12175194 G A splice_acceptor_variant&intron_variant HIGH c.166-1G>A| S179
3 BAA05g20000 A05 12177867 C T intron_variant MODIFIER c.1716+65C>T| S17
4 BAA05g20000 A05 12178553 C T intron_variant MODIFIER c.1870-255C>T| S295
5 BAA05g20000 A05 12178599 G A intron_variant MODIFIER c.1870-209G>A| S125
6 BAA05g20000 A05 12178962 G A intron_variant MODIFIER c.1991+33G>A| S75
S76
S81
7 BAA05g20000 A05 12179627 G A missense_variant MODERATE c.2266G>A|p.Ala756Thr S124
8 BAA05g20000 A05 12179790 C T intron_variant MODIFIER c.2318+111C>T| S255
9 BAA05g20000 A05 12180174 C T intron_variant MODIFIER c.2319-161C>T| S203
10 BAA05g20000 A05 12180234 C T intron_variant MODIFIER c.2319-101C>T| S205
11 BAA05g20000 A05 12181349 G A synonymous_variant LOW c.2898G>A|p.Leu966Leu S107
12 BAA05g20000 A05 12182715 G A synonymous_variant LOW c.3384G>A|p.Lys1128Lys S173
13 BAA05g20000 A05 12183282 C T intron_variant MODIFIER c.3567+239C>T| S53
14 BAA05g20000 A05 12183375 C T intron_variant MODIFIER c.3568-213C>T| S157
S163
15 BAA05g20000 A05 12183517 G A intron_variant MODIFIER c.3568-71G>A| S66
16 BAA05g20000 A05 12184703 G A intron_variant MODIFIER c.4081-15G>A| S104
S52
17 BAA05g20000 A05 12184757 G A missense_variant MODERATE c.4120G>A|p.Asp1374Asn S60
18 BAA05g20000 A05 12185051 G A intron_variant MODIFIER c.4240+64G>A| S218
19 BAA05g20000 A05 12185588 C T missense_variant MODERATE c.4325C>T|p.Ser1442Phe S28
20 BAA05g20000 A05 12185642 G A intron_variant MODIFIER c.4350+29G>A| S308
21 BAA05g20000 A05 12186267 C T intron_variant MODIFIER c.4591-124C>T| S133
S172
S217
22 BAA05g20000 A05 12186815 G A intron_variant MODIFIER c.4770+101G>A| S94
23 BAA05g20000 A05 12188554 C T missense_variant MODERATE c.5513C>T|p.Thr1838Ile S270
24 BAA05g20000 A05 12189048 C T intron_variant MODIFIER c.5737-24C>T| S36
25 BAA05g20000 A05 12190411 G A missense_variant MODERATE c.6379G>A|p.Asp2127Asn S148