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


Gene ID

Results: 1 - 28 of 28 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g12760 A05 6569121 C T upstream_gene_variant MODIFIER c.-3677C>T| S121
2 BAA05g12760 A05 6569792 C T upstream_gene_variant MODIFIER c.-3006C>T| S181
3 BAA05g12760 A05 6570152 C T upstream_gene_variant MODIFIER c.-2646C>T| S95
4 BAA05g12760 A05 6571741 G A upstream_gene_variant MODIFIER c.-1057G>A| S212
5 BAA05g12760 A05 6571941 G A upstream_gene_variant MODIFIER c.-857G>A| S34
6 BAA05g12760 A05 6571998 G A upstream_gene_variant MODIFIER c.-800G>A| S79
S91
7 BAA05g12760 A05 6572966 C T missense_variant MODERATE c.91C>T|p.Arg31Trp S114
8 BAA05g12760 A05 6572992 T A synonymous_variant LOW c.117T>A|p.Pro39Pro S26
9 BAA05g12760 A05 6573257 G A missense_variant MODERATE c.382G>A|p.Gly128Ser S160
10 BAA05g12760 A05 6573687 C T missense_variant MODERATE c.812C>T|p.Ala271Val S277
11 BAA05g12760 A05 6573717 C T missense_variant MODERATE c.842C>T|p.Pro281Leu S169
12 BAA05g12760 A05 6573740 G A missense_variant MODERATE c.865G>A|p.Gly289Ser S278
13 BAA05g12760 A05 6573837 C T missense_variant MODERATE c.962C>T|p.Pro321Leu S271
14 BAA05g12760 A05 6574279 C T synonymous_variant LOW c.1134C>T|p.Leu378Leu S87
15 BAA05g12760 A05 6574680 G A missense_variant MODERATE c.1535G>A|p.Gly512Glu S107
16 BAA05g12760 A05 6574751 G A missense_variant MODERATE c.1606G>A|p.Asp536Asn S173
17 BAA05g12760 A05 6574838 G A missense_variant MODERATE c.1693G>A|p.Gly565Arg S37
18 BAA05g12760 A05 6575237 G A splice_acceptor_variant&intron_variant HIGH c.1981-1G>A| S178
19 BAA05g12760 A05 6575915 G A synonymous_variant LOW c.2286G>A|p.Arg762Arg S112
20 BAA05g12760 A05 6576050 G A synonymous_variant LOW c.2421G>A|p.Ser807Ser S57
21 BAA05g12760 A05 6576239 C T stop_gained&splice_region_variant HIGH c.2518C>T|p.Gln840* S84
S93
22 BAA05g12760 A05 6576722 C T missense_variant MODERATE c.2933C>T|p.Ser978Leu S152
23 BAA05g12760 A05 6576844 C T missense_variant MODERATE c.3055C>T|p.Pro1019Ser S195
24 BAA05g12760 A05 6576885 G A missense_variant MODERATE c.3096G>A|p.Met1032Ile S276
25 BAA05g12760 A05 6576981 G A downstream_gene_variant MODIFIER c.*24G>A| S109