Product Details

SNP ID

rs150094545

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:16680005 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGAGCAGTCGAACTGTCCCGGC[A/G]CCACCCCATCGCGTCCTGGCTGTGC

Phenotype

MIM: 611235

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TMEM38A PubMed Links

Gene Details

Gene

TMEM38A

Gene Name

transmembrane protein 38A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_024074.2	237	Missense Mutation	CAC,CGC	H49R	NP_076979.1

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