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


Gene ID

Results: 1 - 29 of 29 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g38920 A06 25480993 C T intron_variant MODIFIER c.1123-71G>A| S202
2 BAA06g38920 A06 25481439 G A synonymous_variant LOW c.1107C>T|p.Phe369Phe S11
3 BAA06g38920 A06 25481678 C T missense_variant MODERATE c.868G>A|p.Asp290Asn S34
4 BAA06g38920 A06 25482299 G A intron_variant MODIFIER c.507+15C>T| S173
5 BAA06g38920 A06 25484993 G T intron_variant MODIFIER c.284-2456C>A| S270
6 BAA06g38920 A06 25485675 G A intron_variant MODIFIER c.284-3138C>T| S59
7 BAA06g38920 A06 25486084 G A intron_variant MODIFIER c.284-3547C>T| S216
8 BAA06g38920 A06 25486197 G A intron_variant MODIFIER c.284-3660C>T| S136
9 BAA06g38920 A06 25486211 C T intron_variant MODIFIER c.284-3674G>A| S165
10 BAA06g38920 A06 25486864 G A intron_variant MODIFIER c.284-4327C>T| S151
11 BAA06g38920 A06 25487877 G A intron_variant MODIFIER c.284-5340C>T| S263
12 BAA06g38920 A06 25488286 C T intron_variant MODIFIER c.284-5749G>A| S174
S27
13 BAA06g38920 A06 25489826 G A intron_variant MODIFIER c.284-7289C>T| S187
14 BAA06g38920 A06 25490953 C T intron_variant MODIFIER c.284-8416G>A| S155
S211
15 BAA06g38920 A06 25493001 C T intron_variant MODIFIER c.284-10464G>A| S95
16 BAA06g38920 A06 25494150 T G intron_variant MODIFIER c.283+10409A>C| S150
17 BAA06g38920 A06 25501052 C T intron_variant MODIFIER c.283+3507G>A| S172
18 BAA06g38920 A06 25501153 C T intron_variant MODIFIER c.283+3406G>A| S165
19 BAA06g38920 A06 25501283 G A intron_variant MODIFIER c.283+3276C>T| S287
20 BAA06g38920 A06 25501868 G A intron_variant MODIFIER c.283+2691C>T| S140
21 BAA06g38920 A06 25504678 C T missense_variant MODERATE c.164G>A|p.Gly55Glu S286
22 BAA06g38920 A06 25505469 C T upstream_gene_variant MODIFIER c.-628G>A| S111
23 BAA06g38920 A06 25505910 G A upstream_gene_variant MODIFIER c.-1069C>T| S1
S89
S90
24 BAA06g38920 A06 25506301 C T upstream_gene_variant MODIFIER c.-1460G>A| S171
25 BAA06g38920 A06 25506996 G A upstream_gene_variant MODIFIER c.-2155C>T| S105