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


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g35870 A09 44177656 C T downstream_gene_variant MODIFIER c.*1268G>A| S298
2 BAA09g35870 A09 44177919 C T downstream_gene_variant MODIFIER c.*1005G>A| S8
3 BAA09g35870 A09 44179462 C T missense_variant MODERATE c.4421G>A|p.Gly1474Glu S143
4 BAA09g35870 A09 44180698 C T missense_variant MODERATE c.3587G>A|p.Ser1196Asn S202
5 BAA09g35870 A09 44180824 G A missense_variant MODERATE c.3461C>T|p.Ala1154Val S150
6 BAA09g35870 A09 44180865 G A synonymous_variant LOW c.3420C>T|p.Ile1140Ile S189
7 BAA09g35870 A09 44181811 C T intron_variant MODIFIER c.2714+9G>A| S159
S243
S299
8 BAA09g35870 A09 44181904 G A missense_variant MODERATE c.2630C>T|p.Ser877Leu S176
9 BAA09g35870 A09 44182067 C T missense_variant MODERATE c.2467G>A|p.Glu823Lys S80
10 BAA09g35870 A09 44183352 G A intron_variant MODIFIER c.1738-75C>T| S166
11 BAA09g35870 A09 44183906 G A missense_variant MODERATE c.1505C>T|p.Ser502Phe S176
12 BAA09g35870 A09 44184548 G A intron_variant MODIFIER c.1234-122C>T| S123
13 BAA09g35870 A09 44184649 G A intron_variant MODIFIER c.1233+83C>T| S200
14 BAA09g35870 A09 44184657 C T intron_variant MODIFIER c.1233+75G>A| S159
S243
S299
15 BAA09g35870 A09 44185157 C T intron_variant MODIFIER c.1051-112G>A| S171
16 BAA09g35870 A09 44185473 C T intron_variant MODIFIER c.985-49G>A| S64
17 BAA09g35870 A09 44185543 C T intron_variant MODIFIER c.984+99G>A| S242
18 BAA09g35870 A09 44186405 G A intron_variant MODIFIER c.707-14C>T| S130
19 BAA09g35870 A09 44186905 C T intron_variant MODIFIER c.550-21G>A| S92
20 BAA09g35870 A09 44187011 C T splice_region_variant&synonymous_variant LOW c.549G>A|p.Gln183Gln S245
21 BAA09g35870 A09 44187148 C T missense_variant MODERATE c.506G>A|p.Gly169Asp S23
22 BAA09g35870 A09 44188647 C T upstream_gene_variant MODIFIER c.-890G>A| S104
S52
23 BAA09g35870 A09 44188691 C T upstream_gene_variant MODIFIER c.-934G>A| S157
S163
24 BAA09g35870 A09 44189114 C T upstream_gene_variant MODIFIER c.-1357G>A| S208
S219
25 BAA09g35870 A09 44189443 G A upstream_gene_variant MODIFIER c.-1686C>T| S10