Product Details

SNP ID
rs17855423
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:112861386 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGAGACTCTTGTGAAGATGGCTTGC[A/G]CTGCCGCGCGGTCCCCGGCCGACCA
Phenotype
MIM: 182175
Polymorphism
A/G, Transition 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_001204193.1 199 Missense Mutation ACT,GCT T4A NP_001191122.1
NM_001204194.1 199 Missense Mutation ACT,GCT T4A NP_001191123.1
NM_001204196.1 199 Missense Mutation ACT,GCT T4A NP_001191125.1
NM_001204199.1 199 Missense Mutation ACT,GCT T4A NP_001191128.1
NM_003135.2 199 Missense Mutation ACT,GCT T4A NP_003126.1

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