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


Gene ID

Results: 1 - 23 of 23 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g05640 A06 3173769 G A missense_variant MODERATE c.6250C>T|p.Pro2084Ser S244
2 BAA06g05640 A06 3174163 C T missense_variant MODERATE c.5923G>A|p.Glu1975Lys S156
3 BAA06g05640 A06 3175235 C T missense_variant MODERATE c.5090G>A|p.Gly1697Glu S175
4 BAA06g05640 A06 3175565 T C missense_variant MODERATE c.4901A>G|p.Asp1634Gly S260
5 BAA06g05640 A06 3176079 G A synonymous_variant LOW c.4491C>T|p.Pro1497Pro S291
6 BAA06g05640 A06 3176088 C T synonymous_variant LOW c.4482G>A|p.Lys1494Lys S301
S304
7 BAA06g05640 A06 3176513 C T missense_variant MODERATE c.4057G>A|p.Glu1353Lys S269
8 BAA06g05640 A06 3176648 C T missense_variant MODERATE c.3922G>A|p.Glu1308Lys S223
9 BAA06g05640 A06 3177114 G A intron_variant MODIFIER c.3520-64C>T| S246
10 BAA06g05640 A06 3177655 C T intron_variant MODIFIER c.3414+223G>A| S279
11 BAA06g05640 A06 3179139 G A intron_variant MODIFIER c.2302-68C>T| S244
12 BAA06g05640 A06 3180030 C T synonymous_variant LOW c.1995G>A|p.Glu665Glu S162
13 BAA06g05640 A06 3180907 C T missense_variant MODERATE c.1360G>A|p.Asp454Asn S1
S90
14 BAA06g05640 A06 3181018 C T missense_variant MODERATE c.1249G>A|p.Asp417Asn S34
15 BAA06g05640 A06 3183627 G A upstream_gene_variant MODIFIER c.-1361C>T| S181
16 BAA06g05640 A06 3184228 C T upstream_gene_variant MODIFIER c.-1962G>A| S301
S304
17 BAA06g05640 A06 3185268 C T upstream_gene_variant MODIFIER c.-3002G>A| S37
18 BAA06g05640 A06 3185714 G A upstream_gene_variant MODIFIER c.-3448C>T| S244
19 BAA06g05640 A06 3186189 G A upstream_gene_variant MODIFIER c.-3923C>T| S113
20 BAA06g05640 A06 3186327 G A upstream_gene_variant MODIFIER c.-4061C>T| S297
21 BAA06g05640 A06 3186481 G A upstream_gene_variant MODIFIER c.-4215C>T| S280
22 BAA06g05640 A06 3186859 C T upstream_gene_variant MODIFIER c.-4593G>A| S183
S198
23 BAA06g05640 A06 3187229 C T upstream_gene_variant MODIFIER c.-4963G>A| S98