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
132201 BAA10g19160 A10 17690190 C T downstream_gene_variant MODIFIER c.*4395C>T| S199
132202 BAA10g19190 A10 17690406 C T synonymous_variant LOW c.4392G>A|p.Pro1464Pro S191
132203 BAA10g19190 A10 17690454 G A synonymous_variant LOW c.4344C>T|p.Phe1448Phe S288
132204 BAA10g19190 A10 17690624 C T missense_variant MODERATE c.4174G>A|p.Val1392Ile S86
132205 BAA10g19190 A10 17690792 C T missense_variant MODERATE c.4006G>A|p.Val1336Met S277
132206 BAA10g19190 A10 17691445 C T missense_variant MODERATE c.3353G>A|p.Arg1118Lys S177
132207 BAA10g19190 A10 17691643 G A missense_variant MODERATE c.3155C>T|p.Thr1052Ile S75
S81
132208 BAA10g19190 A10 17694632 G A synonymous_variant LOW c.166C>T|p.Leu56Leu S160
132209 BAA10g19190 A10 17694767 C T missense_variant MODERATE c.31G>A|p.Asp11Asn S18
132210 BAA10g19190 A10 17694901 G A upstream_gene_variant MODIFIER c.-104C>T| S158
132211 BAA10g19190 A10 17694917 G A upstream_gene_variant MODIFIER c.-120C>T| S195
132212 BAA10g19190 A10 17695265 G A upstream_gene_variant MODIFIER c.-468C>T| S197
132213 BAA10g19190 A10 17696358 C T upstream_gene_variant MODIFIER c.-1561G>A| S52
132214 BAA10g19190 A10 17696452 G A upstream_gene_variant MODIFIER c.-1655C>T| S295
132215 BAA10g19220 A10 17701429 C T upstream_gene_variant MODIFIER c.-2081C>T| S224
132216 BAA10g19220 A10 17701700 G A upstream_gene_variant MODIFIER c.-1810G>A| S63
132217 BAA10g19220 A10 17701933 C T upstream_gene_variant MODIFIER c.-1577C>T| S187
132218 BAA10g19220 A10 17702062 G A upstream_gene_variant MODIFIER c.-1448G>A| S111
S117
132219 BAA10g19220 A10 17702328 G A upstream_gene_variant MODIFIER c.-1182G>A| S198
132220 BAA10g19220 A10 17702560 G A upstream_gene_variant MODIFIER c.-950G>A| S212
132221 BAA10g19220 A10 17703341 C T upstream_gene_variant MODIFIER c.-169C>T| S262
132222 BAA10g19220 A10 17704394 G A missense_variant MODERATE c.523G>A|p.Asp175Asn S50
132223 BAA10g19220 A10 17704453 C T splice_region_variant&synonymous_variant LOW c.582C>T|p.Ala194Ala S242
132224 BAA10g19220 A10 17705004 G A missense_variant MODERATE c.707G>A|p.Gly236Glu S28
132225 BAA10g19220 A10 17705418 G A missense_variant MODERATE c.1121G>A|p.Gly374Asp S112
S97