Product Details

SNP ID

rs76609278

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:108915795 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGCAGCACCTACCTGGGCGATGAA[C/T]GGAGTGATGAGAGCACCCACTCTTG

Phenotype

MIM: 611699

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SVOP PubMed Links

Gene Details

Gene

SVOP

Gene Name

SV2 related protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018711.4	1800	Silent Mutation	CCA,CCG	P476P	NP_061181.1

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