Product Details

SNP ID
rs201412775
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:55720872 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCACCGCGGTGACCACGATGCCGG[C/T]GATGAAGACAACCACAGCAAAGGGG
Phenotype
MIM: 616334
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM100 PubMed Links

Gene Details

Gene
TMEM100
Gene Name
transmembrane protein 100
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099640.1 2365 Missense Mutation ACC,GCC T67A NP_001093110.1
NM_018286.2 2365 Missense Mutation ACC,GCC T67A NP_060756.2
XM_017024814.1 2365 Missense Mutation ACC,GCC T67A XP_016880303.1
XM_017024815.1 2365 Missense Mutation ACC,GCC T67A XP_016880304.1
XM_017024816.1 2365 Missense Mutation ACC,GCC T67A XP_016880305.1

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