Product Details

SNP ID

rs202099108

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:108884451 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACCTGAAACAGCATTGCAAGGCAAC[C/T]GAGGCTCCAAAGTCTCTGATGAGTG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C7orf66 PubMed Links

Gene Details

Gene

C7orf66

Gene Name

chromosome 7 open reading frame 66

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001024607.2	137	Missense Mutation	AGT,GGT	S28G	NP_001019778.1

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