Product Details

SNP ID
rs143666543
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:59990806 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATGAGATTGTAGTTGTGAATGAGG[C/T]GTCTGGCTCGTTCCTTCTCCAGAAC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C1orf87 PubMed Links

Gene Details

Gene
C1orf87
Gene Name
chromosome 1 open reading frame 87
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152377.2 1426 Missense Mutation CAC,CGC H503R NP_689590.1
XM_017000307.1 1426 Missense Mutation CAC,CGC H455R XP_016855796.1
XM_017000308.1 1426 Intron XP_016855797.1

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