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
141701 BAA10g26720 A10 21080536 C T missense_variant MODERATE c.148G>A|p.Ala50Thr S257
141702 BAA10g26730 A10 21081658 G A splice_region_variant&intron_variant LOW c.798+7C>T| S231
141703 BAA10g26720 A10 21081997 G A upstream_gene_variant MODIFIER c.-1314C>T| S179
141704 BAA10g26720 A10 21084869 C T upstream_gene_variant MODIFIER c.-4186G>A| S11
141705 BAA10g26740 A10 21085115 G A stop_gained HIGH c.546G>A|p.Trp182* S158
141706 BAA10g26740 A10 21085603 C T missense_variant MODERATE c.835C>T|p.Arg279Cys S168
141707 BAA10g26730 A10 21085704 C T upstream_gene_variant MODIFIER c.-2067G>A| S296
141708 BAA10g26730 A10 21085814 G A upstream_gene_variant MODIFIER c.-2177C>T| S198
141709 BAA10g26730 A10 21087614 G A upstream_gene_variant MODIFIER c.-3977C>T| S75
141710 BAA10g26750 A10 21087641 G A synonymous_variant LOW c.6G>A|p.Thr2Thr S164
141711 BAA10g26750 A10 21087878 C T synonymous_variant LOW c.243C>T|p.Asn81Asn S308
141712 BAA10g26750 A10 21087974 G A synonymous_variant LOW c.339G>A|p.Leu113Leu S100
141713 BAA10g26750 A10 21087983 G A synonymous_variant LOW c.348G>A|p.Lys116Lys S249
141714 BAA10g26730 A10 21088057 G A upstream_gene_variant MODIFIER c.-4420C>T| S15
S156
S2
S3
S34
S4
S6
141715 BAA10g26760 A10 21088750 C T splice_region_variant&stop_retained_variant LOW c.1568G>A|p.Ter523Ter S103
141716 BAA10g26760 A10 21089152 C T missense_variant MODERATE c.1357G>A|p.Asp453Asn S246
141717 BAA10g26760 A10 21090017 C T stop_gained HIGH c.753G>A|p.Trp251* S5
141718 BAA10g26760 A10 21090575 G A synonymous_variant LOW c.195C>T|p.Ser65Ser S125
141719 BAA10g26760 A10 21090589 C T missense_variant MODERATE c.181G>A|p.Glu61Lys S275
141720 BAA10g26760 A10 21091828 C T upstream_gene_variant MODIFIER c.-1059G>A| S33
141721 BAA10g26760 A10 21091886 G A upstream_gene_variant MODIFIER c.-1117C>T| S144
S240
141722 BAA10g26770 A10 21092643 G A missense_variant MODERATE c.247G>A|p.Val83Met S65
141723 BAA10g26770 A10 21096161 G A missense_variant MODERATE c.2258G>A|p.Arg753Lys S125
141724 BAA10g26780 A10 21096230 C T upstream_gene_variant MODIFIER c.-1594C>T| S2
141725 BAA10g26780 A10 21096266 C T upstream_gene_variant MODIFIER c.-1558C>T| S286