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 BAA02g18690 A02 9578681 G A downstream_gene_variant MODIFIER c.*99C>T| S177
2 BAA02g18690 A02 9579854 G A missense_variant MODERATE c.15248C>T|p.Ala5083Val S159
S243
3 BAA02g18690 A02 9579936 C T missense_variant MODERATE c.15166G>A|p.Gly5056Arg S183
S198
4 BAA02g18690 A02 9580184 C T missense_variant MODERATE c.14918G>A|p.Arg4973Lys S242
5 BAA02g18690 A02 9580217 G A missense_variant MODERATE c.14885C>T|p.Pro4962Leu S293
6 BAA02g18690 A02 9580851 C T missense_variant MODERATE c.14251G>A|p.Asp4751Asn S308
7 BAA02g18690 A02 9582646 C T missense_variant MODERATE c.12844G>A|p.Asp4282Asn S94
8 BAA02g18690 A02 9584200 C T missense_variant MODERATE c.11845G>A|p.Asp3949Asn S124
9 BAA02g18690 A02 9585323 G A missense_variant MODERATE c.11299C>T|p.Leu3767Phe S36
10 BAA02g18690 A02 9585561 G A missense_variant MODERATE c.11159C>T|p.Pro3720Leu S265
11 BAA02g18690 A02 9585861 G A intron_variant MODIFIER c.10987-9C>T| S187
12 BAA02g18690 A02 9588124 G A intron_variant MODIFIER c.9554-14C>T| S256
13 BAA02g18690 A02 9588768 C T intron_variant MODIFIER c.9198-24G>A| S18
14 BAA02g18690 A02 9589628 C T missense_variant MODERATE c.8807G>A|p.Ser2936Asn S71
15 BAA02g18690 A02 9591057 G A synonymous_variant LOW c.8100C>T|p.Ser2700Ser S202
16 BAA02g18690 A02 9591270 G A synonymous_variant LOW c.7887C>T|p.Leu2629Leu S205
17 BAA02g18690 A02 9591680 C T missense_variant MODERATE c.7477G>A|p.Glu2493Lys S216
S241
S265
S39
18 BAA02g18690 A02 9591696 C T synonymous_variant LOW c.7461G>A|p.Gln2487Gln S255
19 BAA02g18690 A02 9592307 C T missense_variant MODERATE c.6850G>A|p.Val2284Met S88
20 BAA02g18690 A02 9592367 G A intron_variant MODIFIER c.6826-36C>T| S43
21 BAA02g18690 A02 9592410 G A missense_variant&splice_region_variant MODERATE c.6824C>T|p.Thr2275Met S17
22 BAA02g18690 A02 9592764 G A missense_variant MODERATE c.6470C>T|p.Ser2157Phe S125
23 BAA02g18690 A02 9592812 G A missense_variant MODERATE c.6422C>T|p.Ala2141Val S150
24 BAA02g18690 A02 9593057 C T synonymous_variant LOW c.6177G>A|p.Glu2059Glu S216
25 BAA02g18690 A02 9593935 G A missense_variant MODERATE c.5387C>T|p.Ser1796Phe S86
S98