Product Details

SNP ID

rs138329092

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:77196958 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTTTGCCTATTGCGTAGTAGTCA[C/G]AGCAATCTTTATATATTAGATGTTG

Phenotype

MIM: 605351

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

CCDC146 PubMed Links

Gene Details

Gene

CCDC146

Gene Name

coiled-coil domain containing 146

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020879.2	681	Intron			NP_065930.2

Gene

FGL2

Gene Name

fibrinogen like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006682.2	681	Missense Mutation	TCT,TGT	S214C	NP_006673.1

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