Product Details

SNP ID

rs104894611

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:56594327 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCAGCACTATCTCCACATCCGCC[C/G]GGCACCCAGCGACAACCTGCCCCTG

Phenotype

MIM: 602991

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

NOG PubMed Links

Gene Details

Gene

NOG

Gene Name

noggin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005450.4	629	Missense Mutation	CCG,CGG	P35R	NP_005441.1

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