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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g30960 A10 22753909 G A upstream_gene_variant MODIFIER c.-4904G>A| S178
2 BAA10g30960 A10 22754754 G A upstream_gene_variant MODIFIER c.-4059G>A| S50
3 BAA10g30960 A10 22755878 C T upstream_gene_variant MODIFIER c.-2935C>T| S295
4 BAA10g30960 A10 22758048 G A upstream_gene_variant MODIFIER c.-765G>A| S223
5 BAA10g30960 A10 22759164 G A synonymous_variant LOW c.57G>A|p.Pro19Pro S18
S256
6 BAA10g30960 A10 22759366 C T missense_variant MODERATE c.101C>T|p.Ser34Leu S168
7 BAA10g30960 A10 22759422 C T missense_variant MODERATE c.157C>T|p.Pro53Ser S203
8 BAA10g30960 A10 22759703 C T synonymous_variant LOW c.351C>T|p.Tyr117Tyr S308
9 BAA10g30960 A10 22760028 G A intron_variant MODIFIER c.410-85G>A| S173
10 BAA10g30960 A10 22760085 G A intron_variant MODIFIER c.410-28G>A| S46
11 BAA10g30960 A10 22760150 G A stop_gained HIGH c.447G>A|p.Trp149* S71
12 BAA10g30960 A10 22761628 C T missense_variant MODERATE c.1286C>T|p.Pro429Leu S112
13 BAA10g30960 A10 22761689 G A intron_variant MODIFIER c.1328+19G>A| S174
14 BAA10g30960 A10 22763136 A C missense_variant MODERATE c.1944A>C|p.Glu648Asp S110
S112
S121
S147
S163
S199
S219
S222
S240
S48
S70
S83
S93
15 BAA10g30960 A10 22763789 C T missense_variant MODERATE c.2099C>T|p.Pro700Leu S89
16 BAA10g30960 A10 22766373 G A synonymous_variant LOW c.3048G>A|p.Glu1016Glu S228
17 BAA10g30960 A10 22766956 G A missense_variant MODERATE c.3331G>A|p.Val1111Met S139