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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g37770 A09 45850114 G C downstream_gene_variant MODIFIER c.*224C>G| S140
S142
S143
S144
S164
S168
S177
S201
S219
S230
S232
S233
S302
S63
S64
S72
2 BAA09g37770 A09 45850316 G A downstream_gene_variant MODIFIER c.*22C>T| S11
3 BAA09g37770 A09 45850904 C T missense_variant MODERATE c.2155G>A|p.Asp719Asn S182
4 BAA09g37770 A09 45851028 C T intron_variant MODIFIER c.2132-101G>A| S247
5 BAA09g37770 A09 45851068 C T intron_variant MODIFIER c.2131+108G>A| S247
6 BAA09g37770 A09 45851252 G T synonymous_variant LOW c.2055C>A|p.Leu685Leu S7
7 BAA09g37770 A09 45851623 C T missense_variant MODERATE c.1684G>A|p.Val562Ile S213
8 BAA09g37770 A09 45852493 G A intron_variant MODIFIER c.1187+31C>T| S265
9 BAA09g37770 A09 45852556 G A synonymous_variant LOW c.1155C>T|p.Val385Val S59
10 BAA09g37770 A09 45853673 C T intron_variant MODIFIER c.871-833G>A| S183
S198
11 BAA09g37770 A09 45853703 A T intron_variant MODIFIER c.871-863T>A| S249
12 BAA09g37770 A09 45853923 G A intron_variant MODIFIER c.871-1083C>T| S216
13 BAA09g37770 A09 45855532 G A intron_variant MODIFIER c.871-2692C>T| S249
14 BAA09g37770 A09 45855821 C T intron_variant MODIFIER c.871-2981G>A| S9
15 BAA09g37770 A09 45855956 A G intron_variant MODIFIER c.871-3116T>C| S100
16 BAA09g37770 A09 45856360 C T intron_variant MODIFIER c.871-3520G>A| S33
17 BAA09g37770 A09 45856872 C T intron_variant MODIFIER c.871-4032G>A| S206
S26
18 BAA09g37770 A09 45858918 C T intron_variant MODIFIER c.870+5124G>A| S241
19 BAA09g37770 A09 45859695 C T intron_variant MODIFIER c.870+4347G>A| S192
20 BAA09g37770 A09 45861179 C T intron_variant MODIFIER c.870+2863G>A| S174
21 BAA09g37770 A09 45862005 C T intron_variant MODIFIER c.870+2037G>A| S86
22 BAA09g37770 A09 45862276 C T intron_variant MODIFIER c.870+1766G>A| S239
23 BAA09g37770 A09 45863605 G A intron_variant MODIFIER c.870+437C>T| S85
24 BAA09g37770 A09 45863854 C T intron_variant MODIFIER c.870+188G>A| S41
25 BAA09g37770 A09 45863898 C T intron_variant MODIFIER c.870+144G>A| S50