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 BAA08g07600 A08 6862452 C T missense_variant MODERATE c.5750G>A|p.Arg1917Lys S272
2 BAA08g07600 A08 6863067 C T missense_variant MODERATE c.5135G>A|p.Gly1712Glu S262
3 BAA08g07600 A08 6863148 G A missense_variant MODERATE c.5054C>T|p.Pro1685Leu S103
4 BAA08g07600 A08 6864336 C T synonymous_variant LOW c.4128G>A|p.Gln1376Gln S281
5 BAA08g07600 A08 6864774 C T synonymous_variant LOW c.3777G>A|p.Glu1259Glu S57
6 BAA08g07600 A08 6865018 G A intron_variant MODIFIER c.3567-34C>T| S288
7 BAA08g07600 A08 6865388 C T missense_variant MODERATE c.3250G>A|p.Glu1084Lys S208
8 BAA08g07600 A08 6865394 C T missense_variant MODERATE c.3244G>A|p.Val1082Ile S1
S90
9 BAA08g07600 A08 6865831 G A intron_variant MODIFIER c.2964+14C>T| S148
10 BAA08g07600 A08 6866362 C T synonymous_variant LOW c.2619G>A|p.Arg873Arg S38
11 BAA08g07600 A08 6866574 G A intron_variant MODIFIER c.2497-9C>T| S130
12 BAA08g07600 A08 6867184 G A synonymous_variant LOW c.2130C>T|p.Cys710Cys S69
13 BAA08g07600 A08 6867250 C T synonymous_variant LOW c.2064G>A|p.Leu688Leu S47
14 BAA08g07600 A08 6867482 G A missense_variant MODERATE c.1933C>T|p.His645Tyr S87
15 BAA08g07600 A08 6867490 C T missense_variant MODERATE c.1925G>A|p.Gly642Asp S295
16 BAA08g07600 A08 6867652 C T missense_variant MODERATE c.1853G>A|p.Arg618Lys S113
17 BAA08g07600 A08 6868066 G A missense_variant MODERATE c.1673C>T|p.Ala558Val S33
18 BAA08g07600 A08 6870805 C T upstream_gene_variant MODIFIER c.-13G>A| S276
19 BAA08g07600 A08 6871107 C T upstream_gene_variant MODIFIER c.-315G>A| S252
20 BAA08g07600 A08 6871480 C T upstream_gene_variant MODIFIER c.-688G>A| S17
21 BAA08g07600 A08 6872073 T A upstream_gene_variant MODIFIER c.-1281A>T| S110
22 BAA08g07600 A08 6873050 G A upstream_gene_variant MODIFIER c.-2258C>T| S224
23 BAA08g07600 A08 6873698 G A upstream_gene_variant MODIFIER c.-2906C>T| S48