Product Details

SNP ID
rs200106860
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:15639714 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGATTTTTAAAAATTCCAGAGTTTG[C/G]TCATTTAGAAAGAAGGCATTGTTGA
Phenotype
MIM: 300631
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TMEM27 PubMed Links

Gene Details

Gene
TMEM27
Gene Name
transmembrane protein 27
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020665.5 616 Missense Mutation GAC,GAG D120E NP_065716.1
XM_017029680.1 616 Missense Mutation GAC,GAG D68E XP_016885169.1
XM_017029681.1 616 Intron XP_016885170.1

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