Product Details

SNP ID

hCV27852471

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:45230771 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGGCTGGGGCTATGGGGAGAGGG[C/G]CACCGCCATACTGCCCATGGAGCCA

Phenotype

MIM: 604656

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FMNL1 PubMed Links

Gene Details

Gene

FMNL1

Gene Name

formin like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005892.3		Intron			NP_005883.2

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