Product Details

SNP ID
rs199961375
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:93754939 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATGGCGACGCGCGGTGGGGCTGGG[A/G]TGGCAATGGCGGTTTGGTCCCTCTT
Phenotype
MIM: 609884
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TMEM67 PubMed Links

Gene Details

Gene
TMEM67
Gene Name
transmembrane protein 67
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142301.1 23 Intron NP_001135773.1
NM_153704.5 23 Missense Mutation ATG,GTG M9V NP_714915.3
XM_006716686.3 23 UTR 5 XP_006716749.1
XM_011517363.2 23 Missense Mutation ATG,GTG M9V XP_011515665.1

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