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


Gene ID

Results: 1 - 22 of 22 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA06g00210 A06 170364 G A upstream_gene_variant MODIFIER c.-4276G>A| S286
2 BAA06g00210 A06 176093 C T missense_variant MODERATE c.1079C>T|p.Ser360Phe S109
3 BAA06g00210 A06 176564 C T missense_variant MODERATE c.1550C>T|p.Thr517Ile S150
4 BAA06g00210 A06 176809 G A missense_variant MODERATE c.1795G>A|p.Asp599Asn S67
5 BAA06g00210 A06 176836 C T missense_variant MODERATE c.1822C>T|p.Leu608Phe S255
6 BAA06g00210 A06 177566 G A missense_variant MODERATE c.2552G>A|p.Gly851Glu S72
S78
7 BAA06g00210 A06 177918 G A synonymous_variant LOW c.2904G>A|p.Arg968Arg S35
8 BAA06g00210 A06 178323 C T synonymous_variant LOW c.3309C>T|p.Val1103Val S82
S92
9 BAA06g00210 A06 179071 C T synonymous_variant LOW c.4057C>T|p.Leu1353Leu S219
S72
10 BAA06g00210 A06 179821 C T missense_variant MODERATE c.4807C>T|p.Leu1603Phe S185
11 BAA06g00210 A06 179875 G A missense_variant MODERATE c.4861G>A|p.Val1621Ile S100
12 BAA06g00210 A06 180666 C T synonymous_variant LOW c.5652C>T|p.Val1884Val S279
13 BAA06g00210 A06 180948 C T synonymous_variant LOW c.5934C>T|p.Leu1978Leu S269
14 BAA06g00210 A06 181531 G A missense_variant MODERATE c.6517G>A|p.Gly2173Ser S262
15 BAA06g00210 A06 181656 G A synonymous_variant LOW c.6642G>A|p.Gly2214Gly S182
16 BAA06g00210 A06 181784 G A missense_variant MODERATE c.6770G>A|p.Gly2257Asp S71
17 BAA06g00210 A06 182426 G A missense_variant MODERATE c.7412G>A|p.Gly2471Glu S265
18 BAA06g00210 A06 182672 C T missense_variant MODERATE c.7658C>T|p.Thr2553Ile S5
19 BAA06g00210 A06 182734 C T missense_variant MODERATE c.7720C>T|p.Pro2574Ser S23
20 BAA06g00210 A06 185010 C T missense_variant MODERATE c.9461C>T|p.Pro3154Leu S4
21 BAA06g00210 A06 186112 G A missense_variant&splice_region_variant MODERATE c.10387G>A|p.Glu3463Lys S90
22 BAA06g00210 A06 186547 C T missense_variant MODERATE c.10658C>T|p.Ala3553Val S261