Product Details

SNP ID

rs10081966

Assay Type

Functionally tested

NCBI dbSNP Submissions

40

Location

Chr.1:161303870 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAATGAAGGCAGATTGATTTTTTTT[A/T]AAAGACATTGAAGACACCCCTCAAA

Phenotype

MIM: 159440

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

MPZ PubMed Links

Gene Details

Gene

MPZ

Gene Name

myelin protein zero

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000530.7	1181	Intron			NP_000521.2
NM_001315491.1	1181	Intron			NP_001302420.1
XM_017001321.1	1181	UTR 3			XP_016856810.1

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