Product Details

SNP ID
rs147907707
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:5891681 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGAGGCGTGCTCCTGGGCGCGCCC[C/G]CGGAACTGGAGTTGACACCCCCTGG
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TMEM200C PubMed Links

Gene Details

Gene
TMEM200C
Gene Name
transmembrane protein 200C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080209.1 424 Missense Mutation GCG,GGG A128G NP_001073678.1
XM_005258130.4 424 Missense Mutation GCG,GGG A128G XP_005258187.1
XM_011525729.2 424 Missense Mutation GCG,GGG A128G XP_011524031.1

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