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 BAA07g13210 A07 21259374 C T missense_variant MODERATE c.2729G>A|p.Gly910Asp S276
2 BAA07g13210 A07 21259410 T G missense_variant MODERATE c.2693A>C|p.Gln898Pro S181
S203
3 BAA07g13210 A07 21259581 C T missense_variant MODERATE c.2597G>A|p.Arg866Lys S261
4 BAA07g13210 A07 21259796 C T synonymous_variant LOW c.2382G>A|p.Arg794Arg S217
5 BAA07g13210 A07 21260246 G A synonymous_variant LOW c.1932C>T|p.Asn644Asn S271
6 BAA07g13210 A07 21260414 G A synonymous_variant LOW c.1764C>T|p.Phe588Phe S139
7 BAA07g13210 A07 21260453 G A synonymous_variant LOW c.1725C>T|p.Asn575Asn S183
8 BAA07g13210 A07 21260468 G A synonymous_variant LOW c.1710C>T|p.Arg570Arg S171
9 BAA07g13210 A07 21261292 C T missense_variant MODERATE c.965G>A|p.Arg322Lys S292
10 BAA07g13210 A07 21261632 C T missense_variant MODERATE c.625G>A|p.Glu209Lys S159
S243
11 BAA07g13210 A07 21261689 C T missense_variant MODERATE c.568G>A|p.Glu190Lys S35
12 BAA07g13210 A07 21261824 C T missense_variant MODERATE c.433G>A|p.Ala145Thr S32
13 BAA07g13210 A07 21261865 C T missense_variant MODERATE c.392G>A|p.Arg131Lys S103
14 BAA07g13210 A07 21261877 G A missense_variant MODERATE c.380C>T|p.Ser127Phe S219
S72
15 BAA07g13210 A07 21261995 C T missense_variant MODERATE c.262G>A|p.Glu88Lys S121
16 BAA07g13210 A07 21262178 C A missense_variant MODERATE c.79G>T|p.Asp27Tyr S170
17 BAA07g13210 A07 21262207 C T missense_variant MODERATE c.50G>A|p.Gly17Glu S142
18 BAA07g13210 A07 21262420 C T upstream_gene_variant MODIFIER c.-164G>A| S204
19 BAA07g13210 A07 21263018 C T upstream_gene_variant MODIFIER c.-762G>A| S204
20 BAA07g13210 A07 21264150 C T upstream_gene_variant MODIFIER c.-1894G>A| S294
21 BAA07g13210 A07 21264886 G A upstream_gene_variant MODIFIER c.-2630C>T| S246
22 BAA07g13210 A07 21265526 C T upstream_gene_variant MODIFIER c.-3270G>A| S306
S308
23 BAA07g13210 A07 21266059 G A upstream_gene_variant MODIFIER c.-3803C>T| S119