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
147501 BAA10g31840 A10 23117830 G A missense_variant&splice_region_variant MODERATE c.928G>A|p.Glu310Lys S249
147502 BAA10g31840 A10 23118618 C T missense_variant MODERATE c.1373C>T|p.Thr458Ile S78
S83
147503 BAA10g31850 A10 23119266 C T missense_variant MODERATE c.2228G>A|p.Arg743Lys S211
S227
147504 BAA10g31850 A10 23119936 C T synonymous_variant LOW c.1737G>A|p.Thr579Thr S262
147505 BAA10g31850 A10 23120630 C T missense_variant MODERATE c.1043G>A|p.Arg348Lys S229
147506 BAA10g31850 A10 23121540 C T missense_variant MODERATE c.683G>A|p.Gly228Glu S176
147507 BAA10g31850 A10 23121595 G A missense_variant MODERATE c.628C>T|p.Pro210Ser S265
147508 BAA10g31850 A10 23122151 G A missense_variant MODERATE c.304C>T|p.Leu102Phe S216
147509 BAA10g31850 A10 23122246 G A missense_variant MODERATE c.280C>T|p.Pro94Ser S65
147510 BAA10g31850 A10 23122343 G A synonymous_variant LOW c.183C>T|p.Asp61Asp S240
147511 BAA10g31850 A10 23122430 G A synonymous_variant LOW c.96C>T|p.His32His S84
S93
147512 BAA10g31860 A10 23123768 C T missense_variant MODERATE c.628C>T|p.Leu210Phe S18
147513 BAA10g31860 A10 23124071 G A synonymous_variant LOW c.843G>A|p.Gln281Gln S212
147514 BAA10g31860 A10 23124182 G A missense_variant MODERATE c.883G>A|p.Ala295Thr S233
147515 BAA10g31860 A10 23124266 G A missense_variant MODERATE c.967G>A|p.Val323Ile S273
147516 BAA10g31850 A10 23124393 C T upstream_gene_variant MODIFIER c.-1868G>A| S203
147517 BAA10g31870 A10 23125332 C T missense_variant MODERATE c.202C>T|p.Pro68Ser S11
147518 BAA10g31870 A10 23125351 C T missense_variant MODERATE c.221C>T|p.Ser74Phe S210
147519 BAA10g31870 A10 23125612 C T missense_variant MODERATE c.482C>T|p.Pro161Leu S225
147520 BAA10g31870 A10 23125773 C T missense_variant MODERATE c.643C>T|p.Pro215Ser S84
147521 BAA10g31870 A10 23126447 C T missense_variant MODERATE c.1252C>T|p.Arg418Cys S169
147522 BAA10g31890 A10 23128539 G A upstream_gene_variant MODIFIER c.-4897G>A| S259
147523 BAA10g31890 A10 23128872 C T upstream_gene_variant MODIFIER c.-4564C>T| S277
147524 BAA10g31870 A10 23129868 C T splice_region_variant&intron_variant LOW c.2194-6C>T| S234
147525 BAA10g31880 A10 23131359 C T synonymous_variant LOW c.1068G>A|p.Ser356Ser S280