Product Details

SNP ID
rs141681332
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:56911265 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGCTCTTCCACTGCAGAAGAGGG[A/C]GATTTCTCCAAGGGCCCCATTCGCT
Phenotype
MIM: 600571
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
REST PubMed Links

Gene Details

Gene
REST
Gene Name
RE1 silencing transcription factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001193508.1 935 Silent Mutation GGA,GGC G209G NP_001180437.1
NM_005612.4 935 Silent Mutation GGA,GGC G209G NP_005603.3
XM_011534401.2 935 Silent Mutation GGA,GGC G209G XP_011532703.1
XM_017008527.1 935 Silent Mutation GGA,GGC G209G XP_016864016.1

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