Product Details

SNP ID

rs4646408

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:17507897 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGCATGGCTGATGTCCTCTGGAGG[C/T]GGCTTATGCGTCCCCCAGAGCCCTG

Phenotype

MIM: 602391

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PEMT PubMed Links

Gene Details

Gene

PEMT

Gene Name

phosphatidylethanolamine N-methyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001267551.1		Intron			NP_001254480.1
NM_001267552.1		Intron			NP_001254481.1
NM_007169.2		Intron			NP_009100.2
NM_148172.2		Intron			NP_680477.1
NM_148173.1		Intron			NP_680478.1
XM_006721418.3		Intron			XP_006721481.2
XM_017024016.1		Intron			XP_016879505.1

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