Product Details

SNP ID
rs149666002
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:112862572 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACCATCGCAGAGGGAAGGCGAATC[C/G]CCATAAGTAAGGTAAGCAAGATGGC
Phenotype
MIM: 182175
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SRP19 PubMed Links

Gene Details

Gene
SRP19
Gene Name
signal recognition particle 19
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001204193.1 295 Missense Mutation CCC,GCC P36A NP_001191122.1
NM_001204194.1 295 Missense Mutation CCC,GCC P36A NP_001191123.1
NM_001204196.1 295 Intron NP_001191125.1
NM_001204199.1 295 Missense Mutation CCC,GCC P36A NP_001191128.1
NM_003135.2 295 Missense Mutation CCC,GCC P36A NP_003126.1

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