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


Gene ID

Results: 1 - 21 of 21 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g32750 A10 23425212 C T missense_variant MODERATE c.6800G>A|p.Arg2267Lys S54
2 BAA10g32750 A10 23426018 G A missense_variant MODERATE c.6254C>T|p.Pro2085Leu S162
3 BAA10g32750 A10 23426738 C T splice_region_variant&synonymous_variant LOW c.5952G>A|p.Glu1984Glu S308
4 BAA10g32750 A10 23428896 G A synonymous_variant LOW c.4350C>T|p.Ile1450Ile S271
5 BAA10g32750 A10 23429092 C T missense_variant MODERATE c.4154G>A|p.Gly1385Asp S142
6 BAA10g32750 A10 23429662 G A missense_variant MODERATE c.3584C>T|p.Pro1195Leu S16
7 BAA10g32750 A10 23430992 G A synonymous_variant LOW c.2254C>T|p.Leu752Leu S249
8 BAA10g32750 A10 23431405 C T missense_variant MODERATE c.1841G>A|p.Arg614Lys S16
S217
S56
9 BAA10g32750 A10 23434405 G A intron_variant MODIFIER c.1359-2133C>T| S125
10 BAA10g32750 A10 23434660 G A intron_variant MODIFIER c.1359-2388C>T| S62
11 BAA10g32750 A10 23435808 C T intron_variant MODIFIER c.1359-3536G>A| S142
12 BAA10g32750 A10 23437236 C T intron_variant MODIFIER c.1359-4964G>A| S168
13 BAA10g32750 A10 23437833 G A intron_variant MODIFIER c.1358+5380C>T| S35
14 BAA10g32750 A10 23439389 C T intron_variant MODIFIER c.1358+3824G>A| S84
15 BAA10g32750 A10 23439428 G A intron_variant MODIFIER c.1358+3785C>T| S9
16 BAA10g32750 A10 23444371 C T synonymous_variant LOW c.840G>A|p.Gln280Gln S177
17 BAA10g32750 A10 23444598 G A synonymous_variant LOW c.723C>T|p.Cys241Cys S271
18 BAA10g32750 A10 23444602 C T missense_variant MODERATE c.719G>A|p.Gly240Glu S206
S246
S26
19 BAA10g32750 A10 23444955 C T missense_variant MODERATE c.454G>A|p.Glu152Lys S121
20 BAA10g32750 A10 23446419 C T upstream_gene_variant MODIFIER c.-1011G>A| S218
21 BAA10g32750 A10 23449578 C T upstream_gene_variant MODIFIER c.-4170G>A| S103