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
129451 BAA10g17340 A10 16728353 C T missense_variant MODERATE c.592C>T|p.Leu198Phe S199
129452 BAA10g17350 A10 16728614 C T upstream_gene_variant MODIFIER c.-961C>T| S247
129453 BAA10g17350 A10 16728739 C T upstream_gene_variant MODIFIER c.-836C>T| S229
129454 BAA10g17350 A10 16730088 G A synonymous_variant LOW c.483G>A|p.Gly161Gly S293
129455 BAA10g17350 A10 16730320 G A missense_variant MODERATE c.715G>A|p.Val239Met S75
S81
129456 BAA10g17360 A10 16731463 C T upstream_gene_variant MODIFIER c.-1325C>T| S202
129457 BAA10g17360 A10 16732033 C T upstream_gene_variant MODIFIER c.-755C>T| S197
129458 BAA10g17360 A10 16732287 G A upstream_gene_variant MODIFIER c.-501G>A| S180
129459 BAA10g17360 A10 16733419 C T missense_variant MODERATE c.632C>T|p.Ala211Val S84
S93
129460 BAA10g17360 A10 16733552 G A synonymous_variant LOW c.765G>A|p.Gln255Gln S57
129461 BAA10g17370 A10 16735302 G A synonymous_variant LOW c.156G>A|p.Glu52Glu S263
129462 BAA10g17370 A10 16735397 G A missense_variant MODERATE c.251G>A|p.Gly84Glu S186
129463 BAA10g17370 A10 16735413 G A synonymous_variant LOW c.267G>A|p.Arg89Arg S221
129464 BAA10g17370 A10 16735473 C T synonymous_variant LOW c.327C>T|p.Asn109Asn S54
129465 BAA10g17370 A10 16735659 C T synonymous_variant LOW c.513C>T|p.Ile171Ile S47
129466 BAA10g17380 A10 16737100 C T missense_variant MODERATE c.71G>A|p.Gly24Glu S8
129467 BAA10g17380 A10 16737598 G A upstream_gene_variant MODIFIER c.-428C>T| S69
129468 BAA10g17390 A10 16740622 C T synonymous_variant LOW c.372C>T|p.Pro124Pro S199
129469 BAA10g17390 A10 16741032 G A missense_variant MODERATE c.656G>A|p.Gly219Glu S255
129470 BAA10g17400 A10 16748601 G A missense_variant&splice_region_variant MODERATE c.761G>A|p.Gly254Glu S167
129471 BAA10g17400 A10 16748933 C T synonymous_variant LOW c.1008C>T|p.Phe336Phe S14
S224
129472 BAA10g17410 A10 16750606 A T upstream_gene_variant MODIFIER c.-835A>T| S206
129473 BAA10g17410 A10 16751429 C T upstream_gene_variant MODIFIER c.-12C>T| S123
129474 BAA10g17420 A10 16751856 G A missense_variant MODERATE c.31G>A|p.Gly11Ser S166
129475 BAA10g17400 A10 16752554 G A downstream_gene_variant MODIFIER c.*2459G>A| S181