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 BAA01g37470 A01 25001024 G A upstream_gene_variant MODIFIER c.-4271G>A| S86
2 BAA01g37470 A01 25001452 C T upstream_gene_variant MODIFIER c.-3843C>T| S74
3 BAA01g37470 A01 25001567 C T upstream_gene_variant MODIFIER c.-3728C>T| S104
S52
4 BAA01g37470 A01 25005442 G A missense_variant MODERATE c.70G>A|p.Ala24Thr S209
5 BAA01g37470 A01 25005804 G A splice_acceptor_variant&intron_variant HIGH c.205-1G>A| S95
6 BAA01g37470 A01 25006610 C T missense_variant MODERATE c.1010C>T|p.Ser337Leu S59
7 BAA01g37470 A01 25007273 C T intron_variant MODIFIER c.1032+641C>T| S46
8 BAA01g37470 A01 25008614 C T intron_variant MODIFIER c.1033-1243C>T| S203
9 BAA01g37470 A01 25008800 C T intron_variant MODIFIER c.1033-1057C>T| S77
10 BAA01g37470 A01 25008918 C T intron_variant MODIFIER c.1033-939C>T| S230
11 BAA01g37470 A01 25009578 T A intron_variant MODIFIER c.1033-279T>A| S210
12 BAA01g37470 A01 25009861 G A missense_variant MODERATE c.1037G>A|p.Arg346Lys S263
13 BAA01g37470 A01 25009862 G A synonymous_variant LOW c.1038G>A|p.Arg346Arg S283
14 BAA01g37470 A01 25009988 G A intron_variant MODIFIER c.1152+12G>A|
15 BAA01g37470 A01 25010038 G A intron_variant MODIFIER c.1152+62G>A| S97
16 BAA01g37470 A01 25010115 C A intron_variant MODIFIER c.1152+139C>A| S94
17 BAA01g37470 A01 25010275 C T intron_variant MODIFIER c.1152+299C>T| S97
18 BAA01g37470 A01 25010848 G A intron_variant MODIFIER c.1152+872G>A| S287
19 BAA01g37470 A01 25010980 G A intron_variant MODIFIER c.1152+1004G>A| S290
20 BAA01g37470 A01 25011305 C T intron_variant MODIFIER c.1152+1329C>T| S10
21 BAA01g37470 A01 25011385 C T intron_variant MODIFIER c.1152+1409C>T| S228
22 BAA01g37470 A01 25012927 C T intron_variant MODIFIER c.1153-2367C>T| S249
23 BAA01g37470 A01 25013639 G A intron_variant MODIFIER c.1153-1655G>A| S6
24 BAA01g37470 A01 25014144 C T intron_variant MODIFIER c.1153-1150C>T| S293
25 BAA01g37470 A01 25015463 C T intron_variant MODIFIER c.1297+25C>T| S17