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 BAA04g04330 A04 2712096 G A intron_variant MODIFIER c.2248-135C>T| S165
S261
2 BAA04g04330 A04 2712532 G A intron_variant MODIFIER c.2247+294C>T| S54
3 BAA04g04330 A04 2712567 G A intron_variant MODIFIER c.2247+259C>T| S211
S227
4 BAA04g04330 A04 2713177 C T stop_gained HIGH c.1896G>A|p.Trp632* S246
5 BAA04g04330 A04 2713309 G A intron_variant MODIFIER c.1871-107C>T| S175
S177
6 BAA04g04330 A04 2713346 C T intron_variant MODIFIER c.1871-144G>A| S97
7 BAA04g04330 A04 2713430 C T intron_variant MODIFIER c.1870+199G>A| S115
8 BAA04g04330 A04 2713547 G A intron_variant MODIFIER c.1870+82C>T| S11
9 BAA04g04330 A04 2713638 G A missense_variant MODERATE c.1861C>T|p.Leu621Phe S280
10 BAA04g04330 A04 2713748 G A missense_variant MODERATE c.1751C>T|p.Thr584Ile S99
11 BAA04g04330 A04 2714333 G A missense_variant MODERATE c.1166C>T|p.Ser389Leu S124
12 BAA04g04330 A04 2714385 G A missense_variant MODERATE c.1114C>T|p.Pro372Ser S65
13 BAA04g04330 A04 2714766 C T intron_variant MODIFIER c.1042-309G>A| S165
14 BAA04g04330 A04 2714897 G A intron_variant MODIFIER c.1042-440C>T| S143
15 BAA04g04330 A04 2714932 C T intron_variant MODIFIER c.1042-475G>A| S263
16 BAA04g04330 A04 2715118 G A intron_variant MODIFIER c.1042-661C>T| S144
17 BAA04g04330 A04 2715228 C T intron_variant MODIFIER c.1042-771G>A| S134
18 BAA04g04330 A04 2715361 G A intron_variant MODIFIER c.1041+875C>T| S278
19 BAA04g04330 A04 2715586 G A intron_variant MODIFIER c.1041+650C>T| S108
20 BAA04g04330 A04 2715603 C T intron_variant MODIFIER c.1041+633G>A| S179
21 BAA04g04330 A04 2716265 G A missense_variant MODERATE c.1012C>T|p.Pro338Ser S266
22 BAA04g04330 A04 2716504 C T intron_variant MODIFIER c.976-203G>A| S293
23 BAA04g04330 A04 2716702 A G intron_variant MODIFIER c.976-401T>C| S150
S172
S202
S217
24 BAA04g04330 A04 2716896 C T intron_variant MODIFIER c.975+294G>A| S95
25 BAA04g04330 A04 2717021 C T intron_variant MODIFIER c.975+169G>A| S89