Product Details

SNP ID
rs144844733
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:118841087 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAGCTTGAAGAGGGCGAAGCAAAG[C/T]CTGTCAAGAGAAAAAAGACACTAAA
Phenotype
Polymorphism
C/T, Transition 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 2214 Missense Mutation NP_001295010.1
NM_173666.3 2214 Missense Mutation NP_775937.1
XM_011543338.2 2214 Missense Mutation XP_011541640.2
XM_011543340.2 2214 Missense Mutation XP_011541642.1

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