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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
147051 BAA10g31450 A10 22948843 G A upstream_gene_variant MODIFIER c.-3441C>T| S202
147052 BAA10g31450 A10 22949474 C T upstream_gene_variant MODIFIER c.-4072G>A| S157
S163
147053 BAA10g31450 A10 22949572 C T upstream_gene_variant MODIFIER c.-4170G>A| S234
147054 BAA10g31470 A10 22952880 C T upstream_gene_variant MODIFIER c.-4026C>T| S204
147055 BAA10g31470 A10 22955334 C T upstream_gene_variant MODIFIER c.-1572C>T| S295
147056 BAA10g31470 A10 22955762 C T upstream_gene_variant MODIFIER c.-1144C>T| S244
147057 BAA10g31470 A10 22956008 G A upstream_gene_variant MODIFIER c.-898G>A| S226
147058 BAA10g31470 A10 22956964 G A missense_variant MODERATE c.59G>A|p.Arg20Lys S262
147059 BAA10g31470 A10 22957560 G A missense_variant MODERATE c.655G>A|p.Glu219Lys S122
147060 BAA10g31470 A10 22958887 C T downstream_gene_variant MODIFIER c.*1274C>T| S150
147061 BAA10g31480 A10 22961421 G A upstream_gene_variant MODIFIER c.-4653G>A| S137
S215
147062 BAA10g31480 A10 22963554 G A upstream_gene_variant MODIFIER c.-2520G>A| S184
147063 BAA10g31480 A10 22964043 G A upstream_gene_variant MODIFIER c.-2031G>A| S122
147064 BAA10g31480 A10 22964054 G A upstream_gene_variant MODIFIER c.-2020G>A| S68
147065 BAA10g31480 A10 22964349 C T upstream_gene_variant MODIFIER c.-1725C>T| S11
147066 BAA10g31480 A10 22966354 G A missense_variant MODERATE c.157G>A|p.Asp53Asn S9
147067 BAA10g31480 A10 22967566 G A downstream_gene_variant MODIFIER c.*159G>A| S165
147068 BAA10g31480 A10 22967626 G A downstream_gene_variant MODIFIER c.*219G>A| S249
147069 BAA10g31490 A10 22967688 C T missense_variant MODERATE c.2042G>A|p.Arg681Lys S13
147070 BAA10g31490 A10 22967777 G A synonymous_variant LOW c.1953C>T|p.Leu651Leu S228
147071 BAA10g31490 A10 22968298 C T missense_variant MODERATE c.1689G>A|p.Met563Ile S244
147072 BAA10g31490 A10 22968305 C T missense_variant MODERATE c.1682G>A|p.Gly561Glu S146
147073 BAA10g31490 A10 22969865 C T missense_variant MODERATE c.848G>A|p.Gly283Glu S305
147074 BAA10g31490 A10 22969883 C T missense_variant MODERATE c.830G>A|p.Cys277Tyr S295
147075 BAA10g31490 A10 22970112 C T synonymous_variant LOW c.696G>A|p.Glu232Glu S242