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 BAA01g22910 A01 11635067 G A missense_variant&splice_region_variant MODERATE c.6679C>T|p.Arg2227Trp S245
2 BAA01g22910 A01 11635093 G A missense_variant MODERATE c.6653C>T|p.Ala2218Val S288
3 BAA01g22910 A01 11637793 G A synonymous_variant LOW c.5331C>T|p.Leu1777Leu S202
4 BAA01g22910 A01 11639301 C T missense_variant MODERATE c.4273G>A|p.Glu1425Lys S305
5 BAA01g22910 A01 11639681 G A missense_variant MODERATE c.3893C>T|p.Ser1298Phe S108
6 BAA01g22910 A01 11640149 C T missense_variant MODERATE c.3505G>A|p.Glu1169Lys S95
7 BAA01g22910 A01 11640303 G A intron_variant MODIFIER c.3457+100C>T| S94
8 BAA01g22910 A01 11640315 C T intron_variant MODIFIER c.3457+88G>A| S201
9 BAA01g22910 A01 11640629 G A synonymous_variant LOW c.3231C>T|p.Val1077Val S172
S217
10 BAA01g22910 A01 11641659 C T intron_variant MODIFIER c.2330-129G>A| S167
11 BAA01g22910 A01 11642207 C T missense_variant MODERATE c.2215G>A|p.Ala739Thr S51
12 BAA01g22910 A01 11642299 G A missense_variant MODERATE c.2123C>T|p.Ala708Val S293
13 BAA01g22910 A01 11642877 C T synonymous_variant LOW c.1545G>A|p.Gln515Gln S55
14 BAA01g22910 A01 11643016 G A missense_variant MODERATE c.1406C>T|p.Pro469Leu S212
15 BAA01g22910 A01 11643777 C T synonymous_variant LOW c.645G>A|p.Lys215Lys S53
16 BAA01g22910 A01 11643924 C T synonymous_variant LOW c.498G>A|p.Glu166Glu S170
17 BAA01g22910 A01 11644799 C T upstream_gene_variant MODIFIER c.-378G>A| S69
18 BAA01g22910 A01 11647089 C T upstream_gene_variant MODIFIER c.-2668G>A| S242
19 BAA01g22910 A01 11647478 C T upstream_gene_variant MODIFIER c.-3057G>A| S142
20 BAA01g22910 A01 11647608 C T upstream_gene_variant MODIFIER c.-3187G>A| S140
21 BAA01g22910 A01 11647747 C T upstream_gene_variant MODIFIER c.-3326G>A| S166
22 BAA01g22910 A01 11647840 G A upstream_gene_variant MODIFIER c.-3419C>T| S94
23 BAA01g22910 A01 11647984 C T upstream_gene_variant MODIFIER c.-3563G>A| S211
S227
24 BAA01g22910 A01 11648589 C T upstream_gene_variant MODIFIER c.-4168G>A| S198