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


Gene ID

Results: 1 - 31 of 31 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g07340 A10 4200935 G A missense_variant&splice_region_variant MODERATE c.2759C>T|p.Ala920Val S198
2 BAA10g07340 A10 4201971 C T missense_variant MODERATE c.2227G>A|p.Asp743Asn S116
3 BAA10g07340 A10 4202172 C T missense_variant MODERATE c.2108G>A|p.Arg703Lys S44
4 BAA10g07340 A10 4203351 C T synonymous_variant LOW c.1377G>A|p.Glu459Glu S235
5 BAA10g07340 A10 4203561 G A synonymous_variant LOW c.1323C>T|p.Pro441Pro S251
6 BAA10g07340 A10 4203779 C T missense_variant MODERATE c.1207G>A|p.Gly403Arg S35
7 BAA10g07340 A10 4203824 C T missense_variant MODERATE c.1162G>A|p.Gly388Arg S188
8 BAA10g07340 A10 4205458 C T intron_variant MODIFIER c.1149+663G>A| S84
S93
9 BAA10g07340 A10 4205678 G A intron_variant MODIFIER c.1149+443C>T| S161
10 BAA10g07340 A10 4206144 G A synonymous_variant LOW c.1126C>T|p.Leu376Leu S18
11 BAA10g07340 A10 4207277 G A intron_variant MODIFIER c.1014-1021C>T| S129
12 BAA10g07340 A10 4208379 G A intron_variant MODIFIER c.1014-2123C>T| S125
13 BAA10g07340 A10 4210557 C T intron_variant MODIFIER c.1013+3888G>A| S35
14 BAA10g07340 A10 4211177 G A intron_variant MODIFIER c.1013+3268C>T| S57
15 BAA10g07340 A10 4213866 G A intron_variant MODIFIER c.1013+579C>T| S295
16 BAA10g07340 A10 4213987 C T intron_variant MODIFIER c.1013+458G>A| S199
17 BAA10g07340 A10 4214495 G A synonymous_variant LOW c.963C>T|p.Leu321Leu S13
S140
S219
S278
S64
S72
18 BAA10g07340 A10 4214533 C T missense_variant MODERATE c.925G>A|p.Glu309Lys S132
S137
S215
19 BAA10g07340 A10 4215139 T C missense_variant MODERATE c.613A>G|p.Thr205Ala S53
20 BAA10g07340 A10 4215345 G A missense_variant MODERATE c.479C>T|p.Pro160Leu S36
21 BAA10g07340 A10 4216086 G A missense_variant MODERATE c.49C>T|p.Pro17Ser S286
22 BAA10g07340 A10 4216919 C T upstream_gene_variant MODIFIER c.-785G>A| S205
23 BAA10g07340 A10 4217451 C T upstream_gene_variant MODIFIER c.-1317G>A| S177
24 BAA10g07340 A10 4217895 G A upstream_gene_variant MODIFIER c.-1761C>T| S33
25 BAA10g07340 A10 4217991 C T upstream_gene_variant MODIFIER c.-1857G>A| S51