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
96501 BAA10g04700 A10 2411260 G A upstream_gene_variant MODIFIER c.-2684G>A| S72
S78
96502 BAA10g04700 A10 2412312 G A upstream_gene_variant MODIFIER c.-1632G>A| S57
96503 BAA10g04690 A10 2412534 C T synonymous_variant LOW c.477G>A|p.Glu159Glu S193
96504 BAA10g04690 A10 2412596 G A missense_variant MODERATE c.415C>T|p.Pro139Ser S66
96505 BAA10g04690 A10 2412601 C T missense_variant MODERATE c.410G>A|p.Gly137Glu S47
96506 BAA10g04690 A10 2412810 G A synonymous_variant LOW c.279C>T|p.Ile93Ile S295
96507 BAA10g04690 A10 2412927 G A synonymous_variant LOW c.162C>T|p.Tyr54Tyr S229
96508 BAA10g04690 A10 2413012 C T missense_variant MODERATE c.77G>A|p.Gly26Glu S237
96509 BAA10g04690 A10 2413470 G A upstream_gene_variant MODIFIER c.-382C>T| S184
96510 BAA10g04690 A10 2413671 G A upstream_gene_variant MODIFIER c.-583C>T| S136
96511 BAA10g04690 A10 2413697 G A upstream_gene_variant MODIFIER c.-609C>T| S158
96512 BAA10g04690 A10 2413714 C T upstream_gene_variant MODIFIER c.-626G>A| S275
96513 BAA10g04700 A10 2414011 C T missense_variant MODERATE c.68C>T|p.Ala23Val S91
96514 BAA10g04700 A10 2414334 G A missense_variant MODERATE c.391G>A|p.Gly131Ser S219
96515 BAA10g04690 A10 2415298 G A upstream_gene_variant MODIFIER c.-2210C>T| S192
96516 BAA10g04710 A10 2416467 G A missense_variant MODERATE c.281C>T|p.Pro94Leu S157
S163
96517 BAA10g04710 A10 2416553 G A synonymous_variant LOW c.195C>T|p.Asp65Asp S13
96518 BAA10g04690 A10 2417113 C T upstream_gene_variant MODIFIER c.-4025G>A| S246
96519 BAA10g04710 A10 2418204 C T upstream_gene_variant MODIFIER c.-1457G>A| S226
96520 BAA10g04720 A10 2421101 G A stop_gained HIGH c.723G>A|p.Trp241* S174
S216
S241
S39
96521 BAA10g04710 A10 2421139 C T upstream_gene_variant MODIFIER c.-4392G>A| S294
96522 BAA10g04720 A10 2421736 G A missense_variant MODERATE c.1012G>A|p.Gly338Arg S216
96523 BAA10g04720 A10 2422092 G A splice_region_variant&intron_variant LOW c.1200+5G>A| S293
96524 BAA10g04720 A10 2422372 C T missense_variant MODERATE c.1315C>T|p.Pro439Ser S143
96525 BAA10g04720 A10 2422433 G A missense_variant MODERATE c.1376G>A|p.Gly459Glu S242