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 BAA06g38770 A06 25388364 C T missense_variant MODERATE c.5014G>A|p.Gly1672Arg S242
2 BAA06g38770 A06 25389024 G A missense_variant MODERATE c.4417C>T|p.Leu1473Phe S136
3 BAA06g38770 A06 25390069 C T synonymous_variant LOW c.3582G>A|p.Val1194Val S100
4 BAA06g38770 A06 25390094 C T missense_variant MODERATE c.3557G>A|p.Gly1186Asp S86
5 BAA06g38770 A06 25390245 C T missense_variant MODERATE c.3406G>A|p.Gly1136Arg S221
S296
6 BAA06g38770 A06 25390651 C T intron_variant MODIFIER c.3061-61G>A| S189
7 BAA06g38770 A06 25391383 C T missense_variant MODERATE c.2737G>A|p.Gly913Ser S179
8 BAA06g38770 A06 25392286 G A intron_variant MODIFIER c.2272-36C>T| S164
9 BAA06g38770 A06 25392437 G A missense_variant MODERATE c.2210C>T|p.Pro737Leu S39
10 BAA06g38770 A06 25393687 G A missense_variant MODERATE c.1712C>T|p.Thr571Ile S210
S225
11 BAA06g38770 A06 25393783 C T intron_variant MODIFIER c.1639-23G>A| S45
12 BAA06g38770 A06 25393902 G A missense_variant MODERATE c.1607C>T|p.Ser536Phe S67
13 BAA06g38770 A06 25394354 G A synonymous_variant LOW c.1272C>T|p.Leu424Leu S133
S172
S217
14 BAA06g38770 A06 25396474 C T upstream_gene_variant MODIFIER c.-384G>A| S35
15 BAA06g38770 A06 25399113 G A upstream_gene_variant MODIFIER c.-3023C>T| S240
16 BAA06g38770 A06 25399447 C T upstream_gene_variant MODIFIER c.-3357G>A| S236
17 BAA06g38770 A06 25400167 C T upstream_gene_variant MODIFIER c.-4077G>A| S5