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 BAA06g05850 A06 3268970 C T missense_variant MODERATE c.262C>T|p.Pro88Ser S271
2 BAA06g05850 A06 3272438 G A missense_variant MODERATE c.1574G>A|p.Arg525Gln S64
3 BAA06g05850 A06 3272613 C T splice_region_variant&intron_variant LOW c.1621-4C>T| S295
S78
4 BAA06g05850 A06 3273187 C T missense_variant MODERATE c.1777C>T|p.Leu593Phe S157
5 BAA06g05850 A06 3274349 C T intron_variant MODIFIER c.2385-42C>T| S17
6 BAA06g05850 A06 3274971 G A missense_variant MODERATE c.2713G>A|p.Asp905Asn S295
7 BAA06g05850 A06 3275704 C T intron_variant MODIFIER c.2872-80C>T| S132
S137
S89
8 BAA06g05850 A06 3275865 C T missense_variant MODERATE c.2953C>T|p.Leu985Phe S130
9 BAA06g05850 A06 3276693 G A intron_variant MODIFIER c.3387+26G>A| S151
S263
10 BAA06g05850 A06 3276743 C T missense_variant MODERATE c.3392C>T|p.Ala1131Val S202
11 BAA06g05850 A06 3276769 C T missense_variant MODERATE c.3418C>T|p.Pro1140Ser S79
S84
12 BAA06g05850 A06 3276826 C T synonymous_variant LOW c.3475C>T|p.Leu1159Leu S176
13 BAA06g05850 A06 3276863 C T missense_variant MODERATE c.3512C>T|p.Ser1171Leu S173
14 BAA06g05850 A06 3277367 G A missense_variant MODERATE c.3863G>A|p.Arg1288Lys S218
15 BAA06g05850 A06 3278699 C T missense_variant MODERATE c.4469C>T|p.Ala1490Val S2
16 BAA06g05850 A06 3278796 G A intron_variant MODIFIER c.4545+21G>A| S153
17 BAA06g05850 A06 3279237 C T missense_variant MODERATE c.4628C>T|p.Pro1543Leu S209
18 BAA06g05850 A06 3279309 C T missense_variant MODERATE c.4700C>T|p.Pro1567Leu S70
19 BAA06g05850 A06 3280429 G A missense_variant MODERATE c.5189G>A|p.Ser1730Asn S108
20 BAA06g05850 A06 3280638 T A splice_region_variant&intron_variant LOW c.5328-8T>A| S279
21 BAA06g05850 A06 3280699 G A splice_region_variant&intron_variant LOW c.5376+5G>A| S110
22 BAA06g05850 A06 3281939 G A missense_variant MODERATE c.5746G>A|p.Asp1916Asn S244