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
92601 BAA10g02290 A10 1087276 G A synonymous_variant LOW c.801C>T|p.Asp267Asp S58
92602 BAA10g02290 A10 1087337 G A missense_variant MODERATE c.740C>T|p.Pro247Leu S20
92603 BAA10g02290 A10 1087743 G A missense_variant MODERATE c.502C>T|p.Pro168Ser S121
92604 BAA10g02280 A10 1089622 G A upstream_gene_variant MODIFIER c.-3334C>T| S55
92605 BAA10g02280 A10 1089950 C T upstream_gene_variant MODIFIER c.-3662G>A| S25
92606 BAA10g02280 A10 1090246 G A upstream_gene_variant MODIFIER c.-3958C>T| S69
92607 BAA10g02300 A10 1090650 G A missense_variant MODERATE c.187G>A|p.Ala63Thr S71
92608 BAA10g02290 A10 1091319 G A upstream_gene_variant MODIFIER c.-2994C>T| S33
92609 BAA10g02290 A10 1092140 C T upstream_gene_variant MODIFIER c.-3815G>A| S40
S49
92610 BAA10g02290 A10 1092656 C T upstream_gene_variant MODIFIER c.-4331G>A| S122
92611 BAA10g02290 A10 1092753 G A upstream_gene_variant MODIFIER c.-4428C>T| S151
S263
92612 BAA10g02290 A10 1092783 G A upstream_gene_variant MODIFIER c.-4458C>T| S250
92613 BAA10g02290 A10 1093166 C T upstream_gene_variant MODIFIER c.-4841G>A| S190
92614 BAA10g02310 A10 1093313 C T splice_region_variant&intron_variant LOW c.93+7C>T| S221
92615 BAA10g02330 A10 1094763 C T upstream_gene_variant MODIFIER c.-4091C>T| S191
92616 BAA10g02330 A10 1095910 G A upstream_gene_variant MODIFIER c.-2944G>A| S230
92617 BAA10g02320 A10 1096906 G A missense_variant MODERATE c.127C>T|p.Leu43Phe S157
S163
92618 BAA10g02320 A10 1097185 C T missense_variant MODERATE c.11G>A|p.Gly4Glu S265
92619 BAA10g02320 A10 1097404 G A upstream_gene_variant MODIFIER c.-209C>T| S65
92620 BAA10g02330 A10 1099060 C T synonymous_variant LOW c.76C>T|p.Leu26Leu S299
92621 BAA10g02330 A10 1099298 C T missense_variant MODERATE c.218C>T|p.Pro73Leu S11
92622 BAA10g02330 A10 1100135 G A missense_variant MODERATE c.749G>A|p.Arg250Lys S208
92623 BAA10g02330 A10 1100517 G A missense_variant MODERATE c.1057G>A|p.Asp353Asn S295
92624 BAA10g02320 A10 1101566 G A upstream_gene_variant MODIFIER c.-4371C>T| S70
92625 BAA10g02340 A10 1101742 G A missense_variant MODERATE c.149G>A|p.Arg50Lys S262