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


Gene ID

Results: 1 - 35 of 35 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g08850 A06 4497270 G A upstream_gene_variant MODIFIER c.-1292G>A| S9
2 BAA06g08850 A06 4497865 C T upstream_gene_variant MODIFIER c.-697C>T| S158
3 BAA06g08850 A06 4498900 G A synonymous_variant LOW c.339G>A|p.Ala113Ala S48
4 BAA06g08850 A06 4499081 G A missense_variant MODERATE c.520G>A|p.Glu174Lys S151
S263
5 BAA06g08850 A06 4499097 C T missense_variant MODERATE c.536C>T|p.Thr179Ile S263
6 BAA06g08850 A06 4500182 G A intron_variant MODIFIER c.591-938G>A| S180
7 BAA06g08850 A06 4500335 G A intron_variant MODIFIER c.591-785G>A| S165
8 BAA06g08850 A06 4501943 C T intron_variant MODIFIER c.1036+378C>T| S36
9 BAA06g08850 A06 4502929 G A intron_variant MODIFIER c.1037-620G>A| S42
10 BAA06g08850 A06 4503080 C T intron_variant MODIFIER c.1037-469C>T| S263
11 BAA06g08850 A06 4503142 G A intron_variant MODIFIER c.1037-407G>A| S84
S93
12 BAA06g08850 A06 4503249 A T intron_variant MODIFIER c.1037-300A>T| S38
13 BAA06g08850 A06 4503291 G A intron_variant MODIFIER c.1037-258G>A| S58
14 BAA06g08850 A06 4503384 C T intron_variant MODIFIER c.1037-165C>T| S130
S255
15 BAA06g08850 A06 4504313 C T stop_gained HIGH c.1348C>T|p.Gln450* S178
16 BAA06g08850 A06 4504474 G A synonymous_variant LOW c.1509G>A|p.Glu503Glu S218
17 BAA06g08850 A06 4505214 C T intron_variant MODIFIER c.1875+374C>T| S266
18 BAA06g08850 A06 4506383 G A intron_variant MODIFIER c.1876-1096G>A| S249
19 BAA06g08850 A06 4506471 G T intron_variant MODIFIER c.1876-1008G>T| S1
S90
20 BAA06g08850 A06 4506530 C T intron_variant MODIFIER c.1876-949C>T| S175
S177
21 BAA06g08850 A06 4507888 C T missense_variant MODERATE c.2285C>T|p.Ser762Leu S38
22 BAA06g08850 A06 4507927 G A missense_variant MODERATE c.2324G>A|p.Arg775Gln S280
23 BAA06g08850 A06 4509511 G A intron_variant MODIFIER c.3825+83G>A| S209
24 BAA06g08850 A06 4510115 G A missense_variant MODERATE c.3928G>A|p.Gly1310Ser S179
25 BAA06g08850 A06 4510277 G A intron_variant MODIFIER c.3992+98G>A| S33