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


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g33110 A10 23637304 C T missense_variant MODERATE c.4234G>A|p.Glu1412Lys S156
2 BAA10g33110 A10 23637915 C T missense_variant MODERATE c.3623G>A|p.Ser1208Asn S108
3 BAA10g33110 A10 23638184 C T synonymous_variant LOW c.3354G>A|p.Gln1118Gln S204
4 BAA10g33110 A10 23638555 C T synonymous_variant LOW c.3066G>A|p.Gly1022Gly S105
5 BAA10g33110 A10 23639081 C T missense_variant MODERATE c.2540G>A|p.Gly847Glu S255
6 BAA10g33110 A10 23640134 G A missense_variant MODERATE c.1870C>T|p.Arg624Cys S249
7 BAA10g33110 A10 23640385 C T missense_variant MODERATE c.1706G>A|p.Gly569Glu S80
8 BAA10g33110 A10 23641333 C T missense_variant MODERATE c.1090G>A|p.Glu364Lys S25
9 BAA10g33110 A10 23641563 G A missense_variant MODERATE c.937C>T|p.Leu313Phe S226
10 BAA10g33110 A10 23642238 C T missense_variant MODERATE c.523G>A|p.Glu175Lys S292
11 BAA10g33110 A10 23642725 G A intron_variant MODIFIER c.221-97C>T| S68
12 BAA10g33110 A10 23642812 G A intron_variant MODIFIER c.221-184C>T| S37
13 BAA10g33110 A10 23643235 C T intron_variant MODIFIER c.220+108G>A| S82
S92
14 BAA10g33110 A10 23643387 C T missense_variant MODERATE c.176G>A|p.Gly59Glu S44
15 BAA10g33110 A10 23645541 G A upstream_gene_variant MODIFIER c.-1979C>T| S171
16 BAA10g33110 A10 23647699 G A upstream_gene_variant MODIFIER c.-4137C>T| S71