Product Details

SNP ID
rs13027
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:15230089 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TACTCATTATAGTAATAATAGCAGC[C/T]TAGCTAGGTACAAAAGCAGTTATAA
Phenotype
MIM: 601097
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PMP22 PubMed Links

Gene Details

Gene
PMP22
Gene Name
peripheral myelin protein 22
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000304.3 1510 UTR 3 NP_000295.1
NM_001281455.1 1510 UTR 3 NP_001268384.1
NM_001281456.1 1510 UTR 3 NP_001268385.1
NM_153321.2 1510 UTR 3 NP_696996.1
NM_153322.2 1510 UTR 3 NP_696997.1
XM_017024775.1 1510 Intron XP_016880264.1
XM_017024776.1 1510 Intron XP_016880265.1

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