Product Details

SNP ID

rs202208768

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:41909810 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTAGATGAAGATTTTCCTGAAGACT[C/G]TTCTTCACAGAAAGTAAAAGAGCTG

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C5orf51 PubMed Links

Gene Details

Gene

C5orf51

Gene Name

chromosome 5 open reading frame 51

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_175921.5	425	Missense Mutation	TCT,TGT	S91C	NP_787117.3
XM_005248289.4	425	Missense Mutation	TCT,TGT	S91C	XP_005248346.1
XM_011514032.2	425	Missense Mutation	TCT,TGT	S18C	XP_011512334.1

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