Product Details

SNP ID

rs77743549

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:30752287 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGAAGTTTAACTTGGAATGTCTCC[A/C]CAAGACCTTCGGCCCTGGTGAGCAG

Phenotype

MIM: 604854

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

INMT PubMed Links

Gene Details

Gene

INMT

Gene Name

indolethylamine N-methyltransferase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199219.1	153	Missense Mutation	CAC,CCC	H46P	NP_001186148.1
NM_006774.4	153	Missense Mutation	CAC,CCC	H46P	NP_006765.4

Gene

INMT-FAM188B

Gene Name

INMT-FAM188B readthrough (NMD candidate)

There are no transcripts associated with this gene.

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