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
148501 BAA10g32820 A10 23474176 G A upstream_gene_variant MODIFIER c.-4711C>T| S191
148502 BAA10g32830 A10 23474439 G A missense_variant MODERATE c.848G>A|p.Ser283Asn S180
148503 BAA10g32830 A10 23475490 G A intron_variant MODIFIER c.1423-15G>A| S202
148504 BAA10g32830 A10 23475634 C T missense_variant MODERATE c.1552C>T|p.Leu518Phe S73
S91
148505 BAA10g32830 A10 23476130 G A missense_variant MODERATE c.1930G>A|p.Glu644Lys S249
148506 BAA10g32830 A10 23476332 G A missense_variant MODERATE c.2132G>A|p.Ser711Asn S219
S72
148507 BAA10g32840 A10 23477393 C T upstream_gene_variant MODIFIER c.-4387C>T| S48
148508 BAA10g32840 A10 23478973 G A upstream_gene_variant MODIFIER c.-2807G>A| S241
148509 BAA10g32840 A10 23479055 C T upstream_gene_variant MODIFIER c.-2725C>T| S2
148510 BAA10g32840 A10 23481955 G A missense_variant MODERATE c.176G>A|p.Arg59His S256
148511 BAA10g32840 A10 23482079 G A synonymous_variant LOW c.300G>A|p.Gln100Gln S159
S243
148512 BAA10g32830 A10 23482601 C T downstream_gene_variant MODIFIER c.*4635C>T| S28
148513 BAA10g32830 A10 23482946 G T downstream_gene_variant MODIFIER c.*4980G>T| S5
148514 BAA10g32850 A10 23486152 C T synonymous_variant LOW c.2169G>A|p.Leu723Leu S152
148515 BAA10g32850 A10 23487104 G A synonymous_variant LOW c.1398C>T|p.Leu466Leu S50
148516 BAA10g32850 A10 23487177 G A missense_variant MODERATE c.1325C>T|p.Thr442Ile S276
148517 BAA10g32860 A10 23487323 C T downstream_gene_variant MODIFIER c.*4827G>A| S80
148518 BAA10g32850 A10 23487987 C T missense_variant MODERATE c.928G>A|p.Gly310Arg S242
148519 BAA10g32850 A10 23488501 C T synonymous_variant LOW c.414G>A|p.Gly138Gly S36
148520 BAA10g32850 A10 23488573 C T synonymous_variant LOW c.342G>A|p.Glu114Glu S67
148521 BAA10g32850 A10 23488601 G A missense_variant MODERATE c.314C>T|p.Ser105Phe S197
148522 BAA10g32850 A10 23488863 G A missense_variant MODERATE c.52C>T|p.Arg18Cys S262
148523 BAA10g32850 A10 23489370 C T upstream_gene_variant MODIFIER c.-456G>A| S177
148524 BAA10g32850 A10 23489700 C T upstream_gene_variant MODIFIER c.-786G>A| S67
148525 BAA10g32850 A10 23490911 G A upstream_gene_variant MODIFIER c.-1997C>T| S289
S290
S77
S82