Product Details

SNP ID
rs201550964
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:44353732 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTCAGCCCTGAGGAAAGCTGGCT[C/G]GGAGCAGGAGGAGGGCTTTGAGGGG
Phenotype
MIM: 603749
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TRPM2 PubMed Links

Gene Details

Gene
TRPM2
Gene Name
transient receptor potential cation channel subfamily M member 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320350.1 537 Missense Mutation TCG,TGG S11W NP_001307279.1
NM_001320351.1 537 Missense Mutation TCG,TGG S11W NP_001307280.1
NM_001320352.1 537 Intron NP_001307281.1
NM_003307.3 537 Missense Mutation TCG,TGG S11W NP_003298.1
XM_005261171.3 537 Missense Mutation TCG,TGG S11W XP_005261228.1
XM_011529736.2 537 Missense Mutation TCG,TGG S11W XP_011528038.1
XM_017028456.1 537 Missense Mutation TCG,TGG S11W XP_016883945.1
XM_017028457.1 537 Missense Mutation TCG,TGG S11W XP_016883946.1

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