Product Details

SNP ID

rs61732371

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:224379635 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACCCTGAACTTGCAGATGAAGGA[A/G]ACATTCTGAAATTGTCTTCCTGGTA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM124B PubMed Links

Gene Details

Gene

FAM124B

Gene Name

family with sequence similarity 124 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122779.1	1657	Missense Mutation	CTC,TTC	L436F	NP_001116251.1
NM_024785.2	1657	UTR 3			NP_079061.2

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