Product Details

SNP ID

rs140413541

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:224379731 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAAGGACACTGTTGTTTTTGGAGG[C/T]AGCCACCCCCAAGGAAGAGGCTGGC

Phenotype

Polymorphism

C/T, 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	1561	Missense Mutation	ACC,GCC	T404A	NP_001116251.1
NM_024785.2	1561	UTR 3			NP_079061.2

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