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
148651 BAA10g32980 A10 23559853 G A upstream_gene_variant MODIFIER c.-2823C>T| S240
148652 BAA10g32990 A10 23560111 C T missense_variant MODERATE c.1127G>A|p.Ser376Asn S169
148653 BAA10g32990 A10 23560238 C T missense_variant MODERATE c.1000G>A|p.Ala334Thr S20
148654 BAA10g32980 A10 23560838 G A upstream_gene_variant MODIFIER c.-3808C>T| S94
148655 BAA10g33000 A10 23562054 G A downstream_gene_variant MODIFIER c.*4658C>T| S125
148656 BAA10g33000 A10 23563735 C T downstream_gene_variant MODIFIER c.*2977G>A| S103
148657 BAA10g32990 A10 23564040 G A upstream_gene_variant MODIFIER c.-190C>T| S240
148658 BAA10g32990 A10 23564339 C T upstream_gene_variant MODIFIER c.-489G>A| S119
148659 BAA10g32990 A10 23566494 G A upstream_gene_variant MODIFIER c.-2644C>T| S203
148660 BAA10g33000 A10 23567597 G A synonymous_variant LOW c.510C>T|p.Leu170Leu S113
148661 BAA10g33000 A10 23567741 C T synonymous_variant LOW c.366G>A|p.Pro122Pro S18
148662 BAA10g33000 A10 23567820 G A missense_variant MODERATE c.287C>T|p.Ser96Phe S178
148663 BAA10g33010 A10 23569548 G A missense_variant MODERATE c.2843C>T|p.Thr948Ile S264
148664 BAA10g33000 A10 23570082 C T upstream_gene_variant MODIFIER c.-1196G>A| S260
148665 BAA10g33010 A10 23571337 G A missense_variant MODERATE c.2021C>T|p.Ala674Val S164
148666 BAA10g33000 A10 23571939 G A upstream_gene_variant MODIFIER c.-3053C>T| S231
148667 BAA10g33010 A10 23572101 G A splice_region_variant&intron_variant LOW c.1845-7C>T| S181
148668 BAA10g33010 A10 23572525 G A synonymous_variant LOW c.1686C>T|p.Asn562Asn S217
S248
148669 BAA10g33010 A10 23574163 G A synonymous_variant LOW c.1029C>T|p.Val343Val S132
S137
S215
S89
148670 BAA10g33010 A10 23574201 G A intron_variant MODIFIER c.1026-35C>T| S84
S93
148671 BAA10g33010 A10 23574258 C T intron_variant MODIFIER c.1026-92G>A| S279
148672 BAA10g33010 A10 23574342 C T intron_variant MODIFIER c.1025+140G>A| S153
S213
148673 BAA10g33010 A10 23574396 C T intron_variant MODIFIER c.1025+86G>A| S110
148674 BAA10g33010 A10 23574452 G A intron_variant MODIFIER c.1025+30C>T| S286
148675 BAA10g33010 A10 23575031 G A synonymous_variant LOW c.645C>T|p.Val215Val S284