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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g03760 A07 3070021 G A downstream_gene_variant MODIFIER c.*3713C>T| S45
2 BAA07g03760 A07 3070879 G A downstream_gene_variant MODIFIER c.*2855C>T| S159
S243
S299
3 BAA07g03760 A07 3070937 C T downstream_gene_variant MODIFIER c.*2797G>A| S191
4 BAA07g03760 A07 3071052 C T downstream_gene_variant MODIFIER c.*2682G>A| S174
S216
5 BAA07g03760 A07 3071555 C T downstream_gene_variant MODIFIER c.*2179G>A| S221
6 BAA07g03760 A07 3071801 C T downstream_gene_variant MODIFIER c.*1933G>A| S218
7 BAA07g03760 A07 3072173 G A downstream_gene_variant MODIFIER c.*1561C>T| S44
8 BAA07g03760 A07 3072867 G A downstream_gene_variant MODIFIER c.*867C>T| S201
9 BAA07g03760 A07 3073932 C T missense_variant MODERATE c.2581G>A|p.Gly861Ser S167
10 BAA07g03760 A07 3073945 G A synonymous_variant LOW c.2568C>T|p.Ser856Ser S208
S219
11 BAA07g03760 A07 3074108 C T missense_variant MODERATE c.2486G>A|p.Gly829Asp S149
S267
12 BAA07g03760 A07 3074240 C T missense_variant MODERATE c.2437G>A|p.Asp813Asn S121
13 BAA07g03760 A07 3074410 G A synonymous_variant LOW c.2358C>T|p.Leu786Leu S46
14 BAA07g03760 A07 3074429 G A missense_variant MODERATE c.2339C>T|p.Ala780Val S92
15 BAA07g03760 A07 3075852 C T intron_variant MODIFIER c.1782+45G>A| S13
16 BAA07g03760 A07 3076195 C T splice_region_variant&synonymous_variant LOW c.1602G>A|p.Arg534Arg S250
17 BAA07g03760 A07 3076494 C T synonymous_variant LOW c.1482G>A|p.Arg494Arg S97
18 BAA07g03760 A07 3076503 C T synonymous_variant LOW c.1473G>A|p.Ser491Ser S79
S84
19 BAA07g03760 A07 3076612 C T intron_variant MODIFIER c.1398+35G>A| S302
20 BAA07g03760 A07 3076854 G A missense_variant MODERATE c.1279C>T|p.Leu427Phe S280
21 BAA07g03760 A07 3077366 C T missense_variant MODERATE c.1004G>A|p.Arg335Lys S196
22 BAA07g03760 A07 3078768 C T missense_variant MODERATE c.425G>A|p.Ser142Asn S18
23 BAA07g03760 A07 3078787 G A missense_variant MODERATE c.406C>T|p.Leu136Phe S264
24 BAA07g03760 A07 3079561 G A missense_variant MODERATE c.89C>T|p.Ala30Val S84
25 BAA07g03760 A07 3080283 G T upstream_gene_variant MODIFIER c.-634C>A| S233
S252
S262
S281
S54
S85