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SNP ID

rs148633922

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:157162488 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAAAGACGATCATCTCCGTCTTCT[C/T]GGATGTCATAGTGCCACTGATCATC

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM71B PubMed Links

Gene Details

Gene

FAM71B

Gene Name

family with sequence similarity 71 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_130899.2	1877	Missense Mutation	AAG,GAG	K593E	NP_570969.2

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