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


Gene ID

Results: 1 - 32 of 32 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g19240 A09 11685327 G A upstream_gene_variant MODIFIER c.-2043G>A| S201
2 BAA09g19240 A09 11685334 C T upstream_gene_variant MODIFIER c.-2036C>T| S148
3 BAA09g19240 A09 11686776 C T upstream_gene_variant MODIFIER c.-594C>T| S211
S227
4 BAA09g19240 A09 11687339 G A upstream_gene_variant MODIFIER c.-31G>A| S1
5 BAA09g19240 A09 11687766 C T intron_variant MODIFIER c.183+90C>T| S143
6 BAA09g19240 A09 11688048 G A intron_variant MODIFIER c.184-138G>A| S229
7 BAA09g19240 A09 11688130 G A intron_variant MODIFIER c.184-56G>A| S245
8 BAA09g19240 A09 11688438 G A missense_variant MODERATE c.436G>A|p.Asp146Asn S226
9 BAA09g19240 A09 11688748 C T missense_variant MODERATE c.638C>T|p.Ser213Phe S168
10 BAA09g19240 A09 11688861 G A intron_variant MODIFIER c.713+38G>A| S208
11 BAA09g19240 A09 11689173 C T missense_variant MODERATE c.925C>T|p.Pro309Ser S305
12 BAA09g19240 A09 11690437 G A missense_variant MODERATE c.1531G>A|p.Asp511Asn S81
13 BAA09g19240 A09 11690596 G A missense_variant MODERATE c.1690G>A|p.Val564Met S301
S304
14 BAA09g19240 A09 11690905 C T missense_variant MODERATE c.1999C>T|p.Arg667Cys S96
15 BAA09g19240 A09 11691076 C T missense_variant MODERATE c.2170C>T|p.Pro724Ser S62
16 BAA09g19240 A09 11691363 G A synonymous_variant LOW c.2457G>A|p.Lys819Lys S42
17 BAA09g19240 A09 11691777 G A synonymous_variant LOW c.2871G>A|p.Lys957Lys S28
18 BAA09g19240 A09 11691964 C T missense_variant MODERATE c.3058C>T|p.Pro1020Ser S87
19 BAA09g19240 A09 11692009 C T missense_variant MODERATE c.3103C>T|p.Leu1035Phe S263
20 BAA09g19240 A09 11692724 G A synonymous_variant LOW c.3642G>A|p.Lys1214Lys S25
S264
S293
21 BAA09g19240 A09 11692748 C T synonymous_variant LOW c.3666C>T|p.His1222His S263
22 BAA09g19240 A09 11694523 G A intron_variant MODIFIER c.5360-59G>A| S20
23 BAA09g19240 A09 11694575 G A splice_region_variant&intron_variant LOW c.5360-7G>A| S251
24 BAA09g19240 A09 11694671 G A missense_variant MODERATE c.5449G>A|p.Asp1817Asn S183
S198
25 BAA09g19240 A09 11695474 C T synonymous_variant LOW c.5902C>T|p.Leu1968Leu S9