Product Details

SNP ID

rs185990656

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:16067748 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGTGCAAATTCACAGCTCGCCAG[C/T]GCTTAAACACTCTGTAAACTGCAGC

Phenotype

MIM: 613338

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MARCH11 PubMed Links

Gene Details

Gene

MARCH11

Gene Name

membrane associated ring-CH-type finger 11

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102562.1	1145	Missense Mutation	CAC,CGC	H311R	NP_001096032.1

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