Product Details

SNP ID
rs146930609
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:71685390 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCACTGAATCCCAAAAATATGGTA[C/T]TCCCTAAAAAAAAAAAAAAAAAAGA
Phenotype
MIM: 605835
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM2 PubMed Links

Gene Details

Gene
TMEM2
Gene Name
transmembrane protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001135820.1 4310 Missense Mutation AAT,AGT N1257S NP_001129292.1
NM_013390.2 4310 Missense Mutation AAT,AGT N1320S NP_037522.1
XM_005251869.4 4310 Missense Mutation AAT,AGT N1320S XP_005251926.1

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