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


Gene ID

Results: 1 - 43 of 43 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g06440 A01 2864050 G A synonymous_variant LOW c.4152C>T|p.Asn1384Asn S294
2 BAA01g06440 A01 2864827 C T synonymous_variant LOW c.3756G>A|p.Lys1252Lys S218
3 BAA01g06440 A01 2865186 C T intron_variant MODIFIER c.3519-31G>A| S68
4 BAA01g06440 A01 2865648 G A intron_variant MODIFIER c.3285+22C>T| S251
5 BAA01g06440 A01 2865690 G A stop_gained HIGH c.3265C>T|p.Arg1089* S298
6 BAA01g06440 A01 2865799 G A intron_variant MODIFIER c.3219-63C>T| S284
7 BAA01g06440 A01 2865925 G A intron_variant MODIFIER c.3218+12C>T| S57
8 BAA01g06440 A01 2866119 G A intron_variant MODIFIER c.3049-13C>T| S116
9 BAA01g06440 A01 2866204 C T intron_variant MODIFIER c.3048+11G>A| S130
10 BAA01g06440 A01 2866733 G A missense_variant MODERATE c.2716C>T|p.Leu906Phe S28
11 BAA01g06440 A01 2866872 G A missense_variant MODERATE c.2665C>T|p.Leu889Phe S142
12 BAA01g06440 A01 2868383 C T intron_variant MODIFIER c.1981+28G>A| S148
S210
S30
S31
13 BAA01g06440 A01 2868966 C T intron_variant MODIFIER c.1604+50G>A| S132
S137
S215
S89
14 BAA01g06440 A01 2869128 G A missense_variant MODERATE c.1492C>T|p.Arg498Cys S219
15 BAA01g06440 A01 2869438 G A intron_variant MODIFIER c.1447-265C>T| S199
16 BAA01g06440 A01 2869721 C T intron_variant MODIFIER c.1447-548G>A| S130
17 BAA01g06440 A01 2870728 C T intron_variant MODIFIER c.1446+1023G>A| S100
18 BAA01g06440 A01 2871134 C T intron_variant MODIFIER c.1446+617G>A| S153
S213
19 BAA01g06440 A01 2871151 G A intron_variant MODIFIER c.1446+600C>T| S129
20 BAA01g06440 A01 2871295 G A intron_variant MODIFIER c.1446+456C>T| S209
21 BAA01g06440 A01 2871342 C T intron_variant MODIFIER c.1446+409G>A| S36
22 BAA01g06440 A01 2871453 C T intron_variant MODIFIER c.1446+298G>A| S255
23 BAA01g06440 A01 2871496 G A intron_variant MODIFIER c.1446+255C>T| S23
24 BAA01g06440 A01 2871540 A T intron_variant MODIFIER c.1446+211T>A| S98
25 BAA01g06440 A01 2871603 C T intron_variant MODIFIER c.1446+148G>A| S46