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


Gene ID

Results: 1 - 36 of 36 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g16780 A09 9868035 G A downstream_gene_variant MODIFIER c.*3226C>T| S249
2 BAA09g16780 A09 9868278 C T downstream_gene_variant MODIFIER c.*2983G>A| S303
3 BAA09g16780 A09 9868898 C T downstream_gene_variant MODIFIER c.*2363G>A| S143
4 BAA09g16780 A09 9869449 G A downstream_gene_variant MODIFIER c.*1812C>T| S148
S210
5 BAA09g16780 A09 9869550 G A downstream_gene_variant MODIFIER c.*1711C>T| S233
6 BAA09g16780 A09 9870320 C T downstream_gene_variant MODIFIER c.*941G>A| S138
7 BAA09g16780 A09 9871349 C T splice_region_variant&intron_variant LOW c.3481-8G>A| S84
S93
8 BAA09g16780 A09 9871398 C T intron_variant MODIFIER c.3481-57G>A| S68
9 BAA09g16780 A09 9872413 G A missense_variant MODERATE c.3010C>T|p.Arg1004Trp S55
10 BAA09g16780 A09 9872414 C T synonymous_variant LOW c.3009G>A|p.Ala1003Ala S281
11 BAA09g16780 A09 9873999 G A synonymous_variant LOW c.2758C>T|p.Leu920Leu S61
12 BAA09g16780 A09 9875538 C T intron_variant MODIFIER c.2500+12G>A| S177
13 BAA09g16780 A09 9875638 C G synonymous_variant LOW c.2412G>C|p.Ala804Ala S62
14 BAA09g16780 A09 9876096 C T missense_variant MODERATE c.2215G>A|p.Glu739Lys S174
S27
15 BAA09g16780 A09 9876108 C T missense_variant MODERATE c.2203G>A|p.Asp735Asn S174
S27
16 BAA09g16780 A09 9878346 G A intron_variant MODIFIER c.1632+73C>T| S163
17 BAA09g16780 A09 9878430 C T missense_variant MODERATE c.1621G>A|p.Glu541Lys S43
18 BAA09g16780 A09 9878504 G A missense_variant&splice_region_variant MODERATE c.1547C>T|p.Ser516Phe S73
19 BAA09g16780 A09 9879904 C T intron_variant MODIFIER c.1345+95G>A| S62
20 BAA09g16780 A09 9882262 T A intron_variant MODIFIER c.568-398A>T| S50
21 BAA09g16780 A09 9883554 C T intron_variant MODIFIER c.568-1690G>A| S263
22 BAA09g16780 A09 9884833 G A intron_variant MODIFIER c.568-2969C>T| S40
S49
23 BAA09g16780 A09 9886278 A C intron_variant MODIFIER c.567+1994T>G| S32
24 BAA09g16780 A09 9887159 C T intron_variant MODIFIER c.567+1113G>A| S204
25 BAA09g16780 A09 9887195 G A intron_variant MODIFIER c.567+1077C>T| S190