Product Details

SNP ID
rs149495867
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:37637062 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTCTGACTTGAATGGACACACTCT[A/C]TTTCCTACCTGTAACCCCAGTGTGT
Phenotype
MIM: 603651
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
TRPC4 PubMed Links

Gene Details

Gene
TRPC4
Gene Name
transient receptor potential cation channel subfamily C member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135955.1 3571 Missense Mutation AAG,AAT K841N NP_001129427.1
NM_001135956.1 3571 Missense Mutation AAG,AAT K776N NP_001129428.1
NM_001135957.1 3571 Missense Mutation AAG,AAT K784N NP_001129429.1
NM_001135958.1 3571 Missense Mutation AAG,AAT K752N NP_001129430.1
NM_003306.1 3571 Missense Mutation AAG,AAT K930N NP_003297.1
NM_016179.2 3571 Missense Mutation AAG,AAT K925N NP_057263.1
XM_011535206.1 3571 Missense Mutation AAG,AAT K510N XP_011533508.1
XM_017020723.1 3571 Missense Mutation AAG,AAT K510N XP_016876212.1
XM_017020724.1 3571 Missense Mutation AAG,AAT K505N XP_016876213.1

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