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


Gene ID

Results: 1 - 30 of 30 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA10g01800 A10 858844 G A missense_variant MODERATE c.8132C>T|p.Ser2711Phe S168
2 BAA10g01800 A10 859222 C T missense_variant MODERATE c.7754G>A|p.Arg2585His S244
3 BAA10g01800 A10 859235 G A missense_variant MODERATE c.7741C>T|p.Leu2581Phe S295
4 BAA10g01800 A10 859619 C T missense_variant MODERATE c.7357G>A|p.Val2453Ile S241
S39
5 BAA10g01800 A10 859632 G A synonymous_variant LOW c.7344C>T|p.Asn2448Asn S64
6 BAA10g01800 A10 859759 C T missense_variant MODERATE c.7217G>A|p.Cys2406Tyr S122
7 BAA10g01800 A10 860093 C T missense_variant MODERATE c.6883G>A|p.Asp2295Asn S275
8 BAA10g01800 A10 860557 G A missense_variant MODERATE c.6419C>T|p.Ser2140Leu S107
9 BAA10g01800 A10 861185 C T intron_variant MODIFIER c.5817-26G>A| S287
10 BAA10g01800 A10 861345 G A missense_variant MODERATE c.5797C>T|p.Leu1933Phe S219
11 BAA10g01800 A10 862227 G A missense_variant MODERATE c.4915C>T|p.Pro1639Ser S230
12 BAA10g01800 A10 862853 G A missense_variant MODERATE c.4289C>T|p.Ser1430Phe S76
13 BAA10g01800 A10 863035 C T intron_variant MODIFIER c.4165+36G>A| S114
14 BAA10g01800 A10 863085 G A missense_variant MODERATE c.4151C>T|p.Ala1384Val S251
15 BAA10g01800 A10 863117 G A synonymous_variant LOW c.4119C>T|p.Leu1373Leu S148
S210
S30
16 BAA10g01800 A10 863179 G A missense_variant MODERATE c.4057C>T|p.Leu1353Phe S83
S88
17 BAA10g01800 A10 863260 C T missense_variant MODERATE c.3976G>A|p.Asp1326Asn S270
18 BAA10g01800 A10 863633 G A synonymous_variant LOW c.3603C>T|p.Phe1201Phe S151
S263
19 BAA10g01800 A10 865338 C T synonymous_variant LOW c.2232G>A|p.Thr744Thr S117
20 BAA10g01800 A10 866653 C T missense_variant MODERATE c.1063G>A|p.Glu355Lys S157
21 BAA10g01800 A10 867720 G A synonymous_variant LOW c.591C>T|p.Leu197Leu S120
22 BAA10g01800 A10 868976 C T missense_variant MODERATE c.166G>A|p.Asp56Asn S60
23 BAA10g01800 A10 868997 C T missense_variant MODERATE c.145G>A|p.Ala49Thr S23
24 BAA10g01800 A10 869574 C T upstream_gene_variant MODIFIER c.-433G>A| S67
25 BAA10g01800 A10 870064 C T upstream_gene_variant MODIFIER c.-923G>A| S31