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 BAA10g17450 A10 16773189 G A upstream_gene_variant MODIFIER c.-2368G>A| S216
2 BAA10g17450 A10 16774462 G A upstream_gene_variant MODIFIER c.-1095G>A| S105
S106
3 BAA10g17450 A10 16774897 G A upstream_gene_variant MODIFIER c.-660G>A| S284
4 BAA10g17450 A10 16775576 G A missense_variant MODERATE c.20G>A|p.Arg7Gln S75
S81
5 BAA10g17450 A10 16780751 C T intron_variant MODIFIER c.654-1454C>T| S110
6 BAA10g17450 A10 16780877 C T intron_variant MODIFIER c.654-1328C>T| S42
7 BAA10g17450 A10 16783059 C T splice_region_variant&intron_variant LOW c.1346+6C>T| S282
8 BAA10g17450 A10 16783120 C T intron_variant MODIFIER c.1347-30C>T| S124
9 BAA10g17450 A10 16784223 C T intron_variant MODIFIER c.1418+1002C>T| S224
10 BAA10g17450 A10 16784403 G A intron_variant MODIFIER c.1419-1013G>A| S223
11 BAA10g17450 A10 16785165 C T intron_variant MODIFIER c.1419-251C>T| S122
12 BAA10g17450 A10 16785787 G A missense_variant MODERATE c.1702G>A|p.Gly568Ser S174
S27
13 BAA10g17450 A10 16785981 G A intron_variant MODIFIER c.1810-9G>A| S132
S215
S89
14 BAA10g17450 A10 16786056 G A missense_variant MODERATE c.1876G>A|p.Asp626Asn S72
S78
15 BAA10g17450 A10 16786761 G A splice_acceptor_variant&intron_variant HIGH c.2003-1G>A| S298
16 BAA10g17450 A10 16790027 C T synonymous_variant LOW c.2433C>T|p.Cys811Cys S143
S171
17 BAA10g17450 A10 16790586 C T synonymous_variant LOW c.2841C>T|p.Phe947Phe S25
18 BAA10g17450 A10 16791008 C T missense_variant MODERATE c.3115C>T|p.Leu1039Phe S45
19 BAA10g17450 A10 16791508 G A synonymous_variant LOW c.3615G>A|p.Lys1205Lys S261