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


Gene ID

Results: 1 - 40 of 40 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g18660 A05 10751551 C T upstream_gene_variant MODIFIER c.-50C>T| S57
2 BAA05g18660 A05 10751753 C T synonymous_variant LOW c.153C>T|p.Phe51Phe S174
3 BAA05g18660 A05 10751774 G A synonymous_variant LOW c.174G>A|p.Leu58Leu S109
4 BAA05g18660 A05 10751791 G A missense_variant MODERATE c.191G>A|p.Gly64Glu S178
5 BAA05g18660 A05 10752062 G A synonymous_variant LOW c.462G>A|p.Arg154Arg S296
6 BAA05g18660 A05 10752701 G A intron_variant MODIFIER c.1022+25G>A| S134
7 BAA05g18660 A05 10752930 G A splice_region_variant&intron_variant LOW c.1188+5G>A| S178
8 BAA05g18660 A05 10753162 G A intron_variant MODIFIER c.1188+237G>A| S152
9 BAA05g18660 A05 10753841 G A intron_variant MODIFIER c.1188+916G>A| S39
10 BAA05g18660 A05 10754937 G A intron_variant MODIFIER c.1188+2012G>A| S266
11 BAA05g18660 A05 10755433 C T intron_variant MODIFIER c.1188+2508C>T| S8
12 BAA05g18660 A05 10755702 C T intron_variant MODIFIER c.1188+2777C>T| S216
13 BAA05g18660 A05 10755845 C T intron_variant MODIFIER c.1188+2920C>T| S103
14 BAA05g18660 A05 10755936 G A intron_variant MODIFIER c.1188+3011G>A| S185
S273
15 BAA05g18660 A05 10756736 C T intron_variant MODIFIER c.1189-3216C>T| S140
16 BAA05g18660 A05 10756755 G A intron_variant MODIFIER c.1189-3197G>A| S192
17 BAA05g18660 A05 10756921 C T intron_variant MODIFIER c.1189-3031C>T| S251
18 BAA05g18660 A05 10756976 C T intron_variant MODIFIER c.1189-2976C>T| S83
S88
19 BAA05g18660 A05 10757150 G A intron_variant MODIFIER c.1189-2802G>A| S3
20 BAA05g18660 A05 10757530 G A intron_variant MODIFIER c.1189-2422G>A| S257
21 BAA05g18660 A05 10757719 C T intron_variant MODIFIER c.1189-2233C>T| S280
22 BAA05g18660 A05 10757866 G A intron_variant MODIFIER c.1189-2086G>A| S212
23 BAA05g18660 A05 10759800 C T intron_variant MODIFIER c.1189-152C>T| S281
24 BAA05g18660 A05 10759931 G A intron_variant MODIFIER c.1189-21G>A| S129
25 BAA05g18660 A05 10763742 C T splice_region_variant&intron_variant LOW c.3111-8C>T| S119