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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g41780 A03 19650927 C T missense_variant MODERATE c.1894G>A|p.Asp632Asn S108
2 BAA03g41780 A03 19651258 C T synonymous_variant LOW c.1563G>A|p.Ser521Ser S42
3 BAA03g41780 A03 19651969 C T intron_variant MODIFIER c.1279-262G>A| S35
4 BAA03g41780 A03 19652115 T A intron_variant MODIFIER c.1279-408A>T| S241
5 BAA03g41780 A03 19652745 C T intron_variant MODIFIER c.1278+299G>A| S32
6 BAA03g41780 A03 19652893 C T intron_variant MODIFIER c.1278+151G>A| S278
7 BAA03g41780 A03 19652998 C T intron_variant MODIFIER c.1278+46G>A| S67
8 BAA03g41780 A03 19653114 G T missense_variant MODERATE c.1208C>A|p.Pro403His S233
9 BAA03g41780 A03 19654528 C T intron_variant MODIFIER c.1100+107G>A| S158
10 BAA03g41780 A03 19654565 G A intron_variant MODIFIER c.1100+70C>T| S168
11 BAA03g41780 A03 19654688 G A synonymous_variant LOW c.1047C>T|p.Tyr349Tyr S197
12 BAA03g41780 A03 19654705 C T missense_variant MODERATE c.1030G>A|p.Val344Met S274
S3
13 BAA03g41780 A03 19655072 C T intron_variant MODIFIER c.752-89G>A| S32
14 BAA03g41780 A03 19655297 G A intron_variant MODIFIER c.752-314C>T| S25
15 BAA03g41780 A03 19656179 C T intron_variant MODIFIER c.752-1196G>A| S179
16 BAA03g41780 A03 19656270 G A intron_variant MODIFIER c.752-1287C>T| S289
S290
17 BAA03g41780 A03 19656500 G A intron_variant MODIFIER c.751+1178C>T| S245
18 BAA03g41780 A03 19656757 C T intron_variant MODIFIER c.751+921G>A| S32
19 BAA03g41780 A03 19656774 G A intron_variant MODIFIER c.751+904C>T| S262
20 BAA03g41780 A03 19657081 G A intron_variant MODIFIER c.751+597C>T| S48
21 BAA03g41780 A03 19657307 C T intron_variant MODIFIER c.751+371G>A| S116
22 BAA03g41780 A03 19657958 G A synonymous_variant LOW c.471C>T|p.Arg157Arg S260
23 BAA03g41780 A03 19658422 G A intron_variant MODIFIER c.394-273C>T| S44
24 BAA03g41780 A03 19658518 G A intron_variant MODIFIER c.394-369C>T| S146
25 BAA03g41780 A03 19658600 G A intron_variant MODIFIER c.394-451C>T| S189