Product Details

SNP ID
rs150069873
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:124314026 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAAGAAAATTAAAGGAAACATTCC[C/T]AGAATGCAGCCAATAGTCACCCCAA
Phenotype
MIM: 616609
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM65 PubMed Links

Gene Details

Gene
TMEM65
Gene Name
transmembrane protein 65
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_194291.2 259 Silent Mutation CTA,CTG L219L NP_919267.2
XM_011516847.2 259 Silent Mutation CTA,CTG L219L XP_011515149.1
XM_017013104.1 259 Silent Mutation CTA,CTG L81L XP_016868593.1
XM_017013105.1 259 Intron XP_016868594.1

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