Product Details

SNP ID

hCV88646506

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:53484291 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATTAGCCTATGAGGGAAAGTGTA[A/T]CAGTAGGTATTCTGGATTGAGGAAG

Phenotype

MIM: 136470

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FST PubMed Links

Gene Details

Gene

FST

Gene Name

follistatin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006350.3	1077	Missense Mutation	AAC,ATC	N240I	NP_006341.1
NM_013409.2	1077	Missense Mutation	AAC,ATC	N240I	NP_037541.1

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