Product Details

SNP ID
rs199668837
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:230843509 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGGTCTCTCACGTTCGGTGCTCA[C/T]GTTGGGAAGAGGACGCTGCTCCTGA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C1orf198 PubMed Links

Gene Details

Gene
C1orf198
Gene Name
chromosome 1 open reading frame 198
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136494.1 874 Missense Mutation ATG,GTG M220V NP_001129966.1
NM_001136495.1 874 Missense Mutation ATG,GTG M128V NP_001129967.1
NM_032800.2 874 Missense Mutation ATG,GTG M258V NP_116189.1
XM_017002599.1 874 Missense Mutation ATG,GTG M128V XP_016858088.1

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