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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g38560 A06 25257311 T A missense_variant MODERATE c.3986A>T|p.Asn1329Ile S134
2 BAA06g38560 A06 25257354 C T missense_variant MODERATE c.3943G>A|p.Asp1315Asn S135
3 BAA06g38560 A06 25259565 G A intron_variant MODIFIER c.2668-47C>T| S158
4 BAA06g38560 A06 25259662 G A missense_variant MODERATE c.2657C>T|p.Ala886Val S208
S93
5 BAA06g38560 A06 25259751 C T missense_variant MODERATE c.2568G>A|p.Met856Ile S62
6 BAA06g38560 A06 25259818 C T missense_variant MODERATE c.2501G>A|p.Ser834Asn S124
7 BAA06g38560 A06 25260323 G A stop_gained HIGH c.1996C>T|p.Gln666* S206
S26
8 BAA06g38560 A06 25261427 G A missense_variant MODERATE c.971C>T|p.Ser324Phe S187
9 BAA06g38560 A06 25261503 G A intron_variant MODIFIER c.954+34C>T| S70
10 BAA06g38560 A06 25262095 C T missense_variant MODERATE c.766G>A|p.Ala256Thr S205
11 BAA06g38560 A06 25262447 C T intron_variant MODIFIER c.580-85G>A| S252
12 BAA06g38560 A06 25263019 C T missense_variant MODERATE c.448G>A|p.Glu150Lys S94
13 BAA06g38560 A06 25263598 C A missense_variant MODERATE c.41G>T|p.Gly14Val S13
S140
S168
S219
S279
S64
S72
14 BAA06g38560 A06 25264565 C T upstream_gene_variant MODIFIER c.-927G>A| S153
15 BAA06g38560 A06 25264907 C T upstream_gene_variant MODIFIER c.-1269G>A| S298
16 BAA06g38560 A06 25264966 G A upstream_gene_variant MODIFIER c.-1328C>T| S229
17 BAA06g38560 A06 25266273 G A upstream_gene_variant MODIFIER c.-2635C>T| S138
18 BAA06g38560 A06 25266335 C T upstream_gene_variant MODIFIER c.-2697G>A| S221
19 BAA06g38560 A06 25266339 C T upstream_gene_variant MODIFIER c.-2701G>A| S295
20 BAA06g38560 A06 25266579 C T upstream_gene_variant MODIFIER c.-2941G>A| S296
21 BAA06g38560 A06 25266766 C T upstream_gene_variant MODIFIER c.-3128G>A| S106
22 BAA06g38560 A06 25267383 G A upstream_gene_variant MODIFIER c.-3745C>T| S217