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 BAA06g22260 A06 12089420 C T upstream_gene_variant MODIFIER c.-4477C>T| S205
2 BAA06g22260 A06 12090533 C T upstream_gene_variant MODIFIER c.-3364C>T| S163
3 BAA06g22260 A06 12091347 G A upstream_gene_variant MODIFIER c.-2550G>A| S235
4 BAA06g22260 A06 12091740 C T upstream_gene_variant MODIFIER c.-2157C>T| S203
5 BAA06g22260 A06 12091789 C T upstream_gene_variant MODIFIER c.-2108C>T| S2
6 BAA06g22260 A06 12092899 C T upstream_gene_variant MODIFIER c.-998C>T| S135
7 BAA06g22260 A06 12094907 G A splice_region_variant&intron_variant LOW c.505-4G>A| S267
8 BAA06g22260 A06 12095046 C T missense_variant MODERATE c.640C>T|p.His214Tyr S118
9 BAA06g22260 A06 12095514 G A intron_variant MODIFIER c.802+306G>A| S193
10 BAA06g22260 A06 12097118 G A intron_variant MODIFIER c.803-1330G>A| S237
11 BAA06g22260 A06 12097412 C T intron_variant MODIFIER c.803-1036C>T| S150
12 BAA06g22260 A06 12097491 G A intron_variant MODIFIER c.803-957G>A| S283
13 BAA06g22260 A06 12097758 G A intron_variant MODIFIER c.803-690G>A| S280
14 BAA06g22260 A06 12098105 G A intron_variant MODIFIER c.803-343G>A| S13
15 BAA06g22260 A06 12098295 G A intron_variant MODIFIER c.803-153G>A| S3
16 BAA06g22260 A06 12098548 C T synonymous_variant LOW c.903C>T|p.Leu301Leu S112
17 BAA06g22260 A06 12098658 C T missense_variant MODERATE c.1013C>T|p.Ser338Leu S269
18 BAA06g22260 A06 12099009 G A intron_variant MODIFIER c.1031-276G>A| S213
19 BAA06g22260 A06 12099310 G A synonymous_variant LOW c.1056G>A|p.Arg352Arg S216
20 BAA06g22260 A06 12099444 C T intron_variant MODIFIER c.1152+38C>T| S308
21 BAA06g22260 A06 12099479 C T intron_variant MODIFIER c.1152+73C>T| S135
22 BAA06g22260 A06 12101424 C T downstream_gene_variant MODIFIER c.*1126C>T| S201
23 BAA06g22260 A06 12101883 C T downstream_gene_variant MODIFIER c.*1585C>T| S167
24 BAA06g22260 A06 12101910 G T downstream_gene_variant MODIFIER c.*1612G>T| S138