Product Details

SNP ID

rs79015645

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:119157856 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACTTCACCCTCGGAATCGCCACC[G/T]ACCCCGGCCCCGCCGCCCACCACCC

Phenotype

MIM: 614330

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

C1QL2 PubMed Links

Gene Details

Gene

C1QL2

Gene Name

complement C1q like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_182528.3	1040	Silent Mutation	GTA,GTC	V138V	NP_872334.2

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