Product Details

SNP ID
rs149217026
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:66609494 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTTTGCTATCTCCATCACGGCCAT[C/T]GCCAAGTACTCGGATGGGGCTTCCA
Phenotype
MIM: 607886 MIM: 607887
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CMTM3 PubMed Links

Gene Details

Gene
CMTM3
Gene Name
CKLF like MARVEL transmembrane domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144601.3 713 Silent Mutation ATC,ATT I121I NP_653202.1
NM_181553.2 713 Silent Mutation ATC,ATT I121I NP_853531.1
XM_006721131.1 713 Silent Mutation ATC,ATT I121I XP_006721194.1
XM_011522861.1 713 Intron XP_011521163.1
Gene
CMTM4
Gene Name
CKLF like MARVEL transmembrane domain containing 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_178818.2 713 Intron NP_848933.1
NM_181521.2 713 Intron NP_852662.1
XM_011522882.1 713 Intron XP_011521184.1
XM_017022954.1 713 Intron XP_016878443.1

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