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


Gene ID

Results: 1 - 41 of 41 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g69900 A09 62192364 C T upstream_gene_variant MODIFIER c.-4597C>T| S36
2 BAA09g69900 A09 62194918 C T upstream_gene_variant MODIFIER c.-2043C>T| S120
3 BAA09g69900 A09 62197847 C T missense_variant MODERATE c.887C>T|p.Pro296Leu S83
S88
4 BAA09g69900 A09 62197880 G A missense_variant MODERATE c.920G>A|p.Ser307Asn S200
5 BAA09g69900 A09 62198050 C T missense_variant MODERATE c.998C>T|p.Thr333Ile S256
6 BAA09g69900 A09 62198243 G A synonymous_variant LOW c.1191G>A|p.Lys397Lys S148
S210
S30
S31
7 BAA09g69900 A09 62198267 C T synonymous_variant LOW c.1215C>T|p.Val405Val S204
8 BAA09g69900 A09 62198696 C T splice_region_variant&intron_variant LOW c.1638+6C>T| S66
9 BAA09g69900 A09 62198891 G A missense_variant MODERATE c.1660G>A|p.Glu554Lys S155
S211
10 BAA09g69900 A09 62199559 C T synonymous_variant LOW c.2328C>T|p.Asn776Asn S224
11 BAA09g69900 A09 62199837 G A missense_variant MODERATE c.2456G>A|p.Arg819Lys S260
12 BAA09g69900 A09 62200862 C T intron_variant MODIFIER c.2684+797C>T| S236
13 BAA09g69900 A09 62201122 G A intron_variant MODIFIER c.2684+1057G>A| S156
S4
S6
14 BAA09g69900 A09 62201736 C T intron_variant MODIFIER c.2684+1671C>T| S156
15 BAA09g69900 A09 62201966 C T intron_variant MODIFIER c.2684+1901C>T| S11
16 BAA09g69900 A09 62202154 C T intron_variant MODIFIER c.2684+2089C>T| S113
17 BAA09g69900 A09 62202582 C T intron_variant MODIFIER c.2685-1796C>T| S58
18 BAA09g69900 A09 62204495 C T synonymous_variant LOW c.2802C>T|p.Ala934Ala S78
S83
19 BAA09g69900 A09 62204545 C T missense_variant MODERATE c.2852C>T|p.Ser951Leu S78
S83
20 BAA09g69900 A09 62207074 C T missense_variant MODERATE c.4538C>T|p.Ser1513Leu S221
21 BAA09g69900 A09 62207635 G A missense_variant MODERATE c.4925G>A|p.Arg1642His S38
22 BAA09g69900 A09 62208658 G A missense_variant MODERATE c.5380G>A|p.Asp1794Asn S268
23 BAA09g69900 A09 62208682 C T missense_variant MODERATE c.5404C>T|p.Pro1802Ser S224
24 BAA09g69900 A09 62208920 G A intron_variant MODIFIER c.5548+15G>A| S159
S299
25 BAA09g69900 A09 62210021 C T missense_variant MODERATE c.6106C>T|p.Pro2036Ser S152