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


Gene ID

Results: 1 - 34 of 34 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA03g50940 A03 24697025 C T synonymous_variant LOW c.210C>T|p.Ile70Ile S216
2 BAA03g50940 A03 24697873 G A missense_variant MODERATE c.1058G>A|p.Ser353Asn S48
3 BAA03g50940 A03 24702073 C T missense_variant MODERATE c.2332C>T|p.Leu778Phe S67
4 BAA03g50940 A03 24702275 G A missense_variant MODERATE c.2426G>A|p.Arg809Gln S96
5 BAA03g50940 A03 24702357 C T intron_variant MODIFIER c.2467+41C>T| S79
S84
6 BAA03g50940 A03 24702500 C T synonymous_variant LOW c.2502C>T|p.Arg834Arg S251
7 BAA03g50940 A03 24702747 G A missense_variant MODERATE c.2749G>A|p.Asp917Asn S169
8 BAA03g50940 A03 24702900 C T missense_variant MODERATE c.2902C>T|p.Pro968Ser S163
9 BAA03g50940 A03 24703269 C T intron_variant MODIFIER c.3187+84C>T| S187
10 BAA03g50940 A03 24703997 G A intron_variant MODIFIER c.3187+812G>A| S298
11 BAA03g50940 A03 24704104 C T intron_variant MODIFIER c.3187+919C>T| S301
S304
12 BAA03g50940 A03 24704130 C T intron_variant MODIFIER c.3187+945C>T| S79
S91
13 BAA03g50940 A03 24705223 C T intron_variant MODIFIER c.3188-842C>T| S119
14 BAA03g50940 A03 24705748 C T intron_variant MODIFIER c.3188-317C>T| S158
15 BAA03g50940 A03 24705859 G A intron_variant MODIFIER c.3188-206G>A| S152
16 BAA03g50940 A03 24706371 C T missense_variant MODERATE c.3494C>T|p.Ser1165Phe S184
17 BAA03g50940 A03 24706432 G A intron_variant MODIFIER c.3524+31G>A| S259
18 BAA03g50940 A03 24706856 G A intron_variant MODIFIER c.3525-305G>A| S76
19 BAA03g50940 A03 24706966 G A intron_variant MODIFIER c.3525-195G>A| S302
20 BAA03g50940 A03 24707313 C T splice_region_variant&intron_variant LOW c.3592-8C>T| S23
21 BAA03g50940 A03 24707660 C T intron_variant MODIFIER c.3673+258C>T| S40
S49
22 BAA03g50940 A03 24708089 C T intron_variant MODIFIER c.3673+687C>T| S192
23 BAA03g50940 A03 24708843 C T intron_variant MODIFIER c.3673+1441C>T| S8
24 BAA03g50940 A03 24709621 C T intron_variant MODIFIER c.3674-1130C>T| S172
S217
25 BAA03g50940 A03 24710315 G A intron_variant MODIFIER c.3674-436G>A| S28