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SNP ID

rs137944304

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:34943919 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGAAGCTGGAAGACGCACGGGCTC[G/T]TTGTGAGGGCCAGGAGATGACAACC

Phenotype

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM47B PubMed Links

Gene Details

Gene

FAM47B

Gene Name

family with sequence similarity 47 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152631.2		Intron			NP_689844.2

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