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


Gene ID

Results: 1 - 42 of 42 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g00520 A01 244399 G A upstream_gene_variant MODIFIER c.-1008G>A| S108
2 BAA01g00520 A01 244962 G A upstream_gene_variant MODIFIER c.-445G>A| S165
3 BAA01g00520 A01 245454 G A synonymous_variant LOW c.48G>A|p.Lys16Lys S15
S3
4 BAA01g00520 A01 245628 C T intron_variant MODIFIER c.173-33C>T| S276
5 BAA01g00520 A01 245747 G A missense_variant MODERATE c.259G>A|p.Val87Met S13
6 BAA01g00520 A01 245762 C T missense_variant MODERATE c.274C>T|p.Pro92Ser S4
7 BAA01g00520 A01 246053 C T missense_variant MODERATE c.565C>T|p.Pro189Ser S155
S211
8 BAA01g00520 A01 246251 G A missense_variant MODERATE c.763G>A|p.Glu255Lys S242
9 BAA01g00520 A01 246345 G A missense_variant MODERATE c.857G>A|p.Gly286Asp S234
10 BAA01g00520 A01 247300 G A synonymous_variant LOW c.1812G>A|p.Thr604Thr S274
11 BAA01g00520 A01 249881 C T missense_variant MODERATE c.2698C>T|p.Leu900Phe S282
12 BAA01g00520 A01 250010 G A missense_variant MODERATE c.2827G>A|p.Val943Ile S136
13 BAA01g00520 A01 250111 C T synonymous_variant LOW c.2928C>T|p.Leu976Leu S46
14 BAA01g00520 A01 250717 C T synonymous_variant LOW c.3358C>T|p.Leu1120Leu S236
15 BAA01g00520 A01 250880 G A missense_variant MODERATE c.3521G>A|p.Arg1174Lys S37
16 BAA01g00520 A01 251098 G A intron_variant MODIFIER c.3534+205G>A| S78
17 BAA01g00520 A01 251224 C T intron_variant MODIFIER c.3535-166C>T| S171
18 BAA01g00520 A01 251321 C T intron_variant MODIFIER c.3535-69C>T| S58
19 BAA01g00520 A01 251780 C T missense_variant MODERATE c.3925C>T|p.Leu1309Phe S38
20 BAA01g00520 A01 251783 C T synonymous_variant LOW c.3928C>T|p.Leu1310Leu S75
S81
21 BAA01g00520 A01 252089 C T intron_variant MODIFIER c.4176+58C>T| S158
22 BAA01g00520 A01 252356 C T missense_variant MODERATE c.4376C>T|p.Thr1459Ile S68
23 BAA01g00520 A01 252435 G A synonymous_variant LOW c.4455G>A|p.Gln1485Gln S96
24 BAA01g00520 A01 252535 C T synonymous_variant LOW c.4555C>T|p.Leu1519Leu S11
25 BAA01g00520 A01 253300 G A intron_variant MODIFIER c.4875+21G>A| S165