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


Gene ID

Results: 1 - 24 of 24 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g19910 A05 12101601 C T missense_variant MODERATE c.3878G>A|p.Arg1293Lys S89
2 BAA05g19910 A05 12104176 G A intron_variant MODIFIER c.2329-15C>T| S274
3 BAA05g19910 A05 12104866 G A synonymous_variant LOW c.2031C>T|p.Asn677Asn S134
4 BAA05g19910 A05 12106307 G A synonymous_variant LOW c.1440C>T|p.Ile480Ile S308
5 BAA05g19910 A05 12106420 C T missense_variant MODERATE c.1327G>A|p.Val443Met S2
6 BAA05g19910 A05 12107255 G A missense_variant MODERATE c.722C>T|p.Ser241Phe S4
7 BAA05g19910 A05 12107603 G A intron_variant MODIFIER c.718-344C>T| S157
S163
8 BAA05g19910 A05 12107836 G A intron_variant MODIFIER c.718-577C>T| S289
9 BAA05g19910 A05 12108108 G A intron_variant MODIFIER c.718-849C>T| S6
10 BAA05g19910 A05 12108271 C T intron_variant MODIFIER c.718-1012G>A| S72
S78
11 BAA05g19910 A05 12108329 C T intron_variant MODIFIER c.718-1070G>A| S201
12 BAA05g19910 A05 12108860 C G intron_variant MODIFIER c.718-1601G>C| S53
13 BAA05g19910 A05 12109071 C T intron_variant MODIFIER c.718-1812G>A| S45
14 BAA05g19910 A05 12113992 C T intron_variant MODIFIER c.156+255G>A| S184
15 BAA05g19910 A05 12114015 G A intron_variant MODIFIER c.156+232C>T| S296
16 BAA05g19910 A05 12114538 G A upstream_gene_variant MODIFIER c.-136C>T| S292
17 BAA05g19910 A05 12114984 G A upstream_gene_variant MODIFIER c.-582C>T| S272
18 BAA05g19910 A05 12115424 G A upstream_gene_variant MODIFIER c.-1022C>T| S272
19 BAA05g19910 A05 12115955 C T upstream_gene_variant MODIFIER c.-1553G>A| S202
20 BAA05g19910 A05 12117395 G A upstream_gene_variant MODIFIER c.-2993C>T| S204
21 BAA05g19910 A05 12117474 G A upstream_gene_variant MODIFIER c.-3072C>T| S203
22 BAA05g19910 A05 12117517 C T upstream_gene_variant MODIFIER c.-3115G>A| S162
23 BAA05g19910 A05 12118758 G A upstream_gene_variant MODIFIER c.-4356C>T| S192
24 BAA05g19910 A05 12119057 G A upstream_gene_variant MODIFIER c.-4655C>T| S204