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
177301 BAA02g18760 A02 9649384 G A missense_variant MODERATE c.838G>A|p.Asp280Asn S180
177302 BAA02g18770 A02 9650356 C T upstream_gene_variant MODIFIER c.-2975C>T| S308
177303 BAA02g18770 A02 9651028 C T upstream_gene_variant MODIFIER c.-2303C>T| S32
177304 BAA02g18770 A02 9651271 G A upstream_gene_variant MODIFIER c.-2060G>A| S28
177305 BAA02g18770 A02 9651285 G A upstream_gene_variant MODIFIER c.-2046G>A| S197
177306 BAA02g18770 A02 9651895 A G upstream_gene_variant MODIFIER c.-1436A>G| S178
177307 BAA02g18770 A02 9651934 G A upstream_gene_variant MODIFIER c.-1397G>A| S126
177308 BAA02g18770 A02 9652142 G A upstream_gene_variant MODIFIER c.-1189G>A| S41
177309 BAA02g18770 A02 9653286 G A upstream_gene_variant MODIFIER c.-45G>A| S149
177310 BAA02g18770 A02 9653341 C T missense_variant MODERATE c.11C>T|p.Ser4Phe S105
S106
177311 BAA02g18770 A02 9653433 C T synonymous_variant LOW c.103C>T|p.Leu35Leu S283
177312 BAA02g18770 A02 9654306 G A missense_variant MODERATE c.907G>A|p.Glu303Lys S206
S26
177313 BAA02g18770 A02 9654323 G A synonymous_variant LOW c.924G>A|p.Ala308Ala S217
177314 BAA02g18770 A02 9655132 C T missense_variant MODERATE c.1562C>T|p.Ser521Leu S299
177315 BAA02g18770 A02 9655322 G A synonymous_variant LOW c.1668G>A|p.Arg556Arg S279
177316 BAA02g18770 A02 9655608 G A missense_variant MODERATE c.1870G>A|p.Glu624Lys S13
177317 BAA02g18770 A02 9655805 C T synonymous_variant LOW c.2067C>T|p.Asn689Asn S163
177318 BAA02g18770 A02 9656969 C T missense_variant MODERATE c.2863C>T|p.Leu955Phe S194
177319 BAA02g18770 A02 9657117 C T splice_region_variant&intron_variant LOW c.2931-5C>T| S58
177320 BAA02g18770 A02 9657146 G A synonymous_variant LOW c.2955G>A|p.Arg985Arg S70
177321 BAA02g18780 A02 9659418 C T missense_variant MODERATE c.2023G>A|p.Glu675Lys S186
177322 BAA02g18780 A02 9659781 C T missense_variant MODERATE c.1660G>A|p.Ala554Thr S167
177323 BAA02g18780 A02 9660040 C T synonymous_variant LOW c.1401G>A|p.Glu467Glu S308
177324 BAA02g18780 A02 9660171 C T missense_variant MODERATE c.1270G>A|p.Glu424Lys S71
177325 BAA02g18780 A02 9661255 C T synonymous_variant LOW c.543G>A|p.Glu181Glu S200