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
97351 BAA10g05260 A10 2718179 G A upstream_gene_variant MODIFIER c.-132C>T| S265
97352 BAA10g05260 A10 2718617 G A upstream_gene_variant MODIFIER c.-570C>T| S45
97353 BAA10g05260 A10 2718639 G A upstream_gene_variant MODIFIER c.-592C>T| S86
97354 BAA10g05280 A10 2723395 G A upstream_gene_variant MODIFIER c.-777C>T| S5
97355 BAA10g05290 A10 2723579 G A synonymous_variant LOW c.132G>A|p.Arg44Arg S20
97356 BAA10g05310 A10 2729304 G A missense_variant MODERATE c.166C>T|p.Leu56Phe S133
97357 BAA10g05320 A10 2730886 G A missense_variant MODERATE c.541C>T|p.Pro181Ser S78
97358 BAA10g05310 A10 2733459 G A upstream_gene_variant MODIFIER c.-3990C>T| S184
97359 BAA10g05330 A10 2735016 G A missense_variant MODERATE c.706G>A|p.Ala236Thr S207
97360 BAA10g05330 A10 2736045 C T synonymous_variant LOW c.1144C>T|p.Leu382Leu S162
97361 BAA10g05340 A10 2738720 C T upstream_gene_variant MODIFIER c.-2032G>A| S206
S26
97362 BAA10g05340 A10 2739142 C T upstream_gene_variant MODIFIER c.-2454G>A| S128
97363 BAA10g05340 A10 2739509 G A upstream_gene_variant MODIFIER c.-2821C>T| S251
97364 BAA10g05350 A10 2740254 G A synonymous_variant LOW c.204G>A|p.Glu68Glu S13
97365 BAA10g05350 A10 2740963 C T missense_variant MODERATE c.490C>T|p.Pro164Ser S132
S137
S215
S89
97366 BAA10g05350 A10 2741425 G A missense_variant MODERATE c.763G>A|p.Val255Ile S292
97367 BAA10g05350 A10 2741813 G A intron_variant MODIFIER c.959+11G>A| S268
97368 BAA10g05350 A10 2744370 G A intron_variant MODIFIER c.2074-40G>A| S198
97369 BAA10g05350 A10 2744569 G A splice_acceptor_variant&intron_variant HIGH c.2156-1G>A| S9
97370 BAA10g05350 A10 2745128 G A missense_variant MODERATE c.2401G>A|p.Glu801Lys S167
97371 BAA10g05350 A10 2745312 G A splice_acceptor_variant&intron_variant HIGH c.2493-1G>A| S150
97372 BAA10g05350 A10 2745738 C T intron_variant MODIFIER c.2739-20C>T| S60
97373 BAA10g05350 A10 2746736 G A missense_variant MODERATE c.3268G>A|p.Glu1090Lys S33
97374 BAA10g05350 A10 2747559 G A splice_acceptor_variant&intron_variant HIGH c.3702-1G>A| S7
97375 BAA10g05350 A10 2749042 C T synonymous_variant LOW c.4558C>T|p.Leu1520Leu S270