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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