Product Details

SNP ID

rs4895353

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:118842057 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTCTTACATGCGGCCAAATATCATT[A/C]CTAACTATAATACACACTCTCACAT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

DTWD2 PubMed Links

Gene Details

Gene

DTWD2

Gene Name

DTW domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001308081.1		Intron			NP_001295010.1
NM_173666.3		Intron			NP_775937.1
XM_011543338.2		Intron			XP_011541640.2
XM_011543340.2		Intron			XP_011541642.1

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