Product Details

SNP ID

rs45613932

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:406105 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTAACAGCAGGAAAGGCCATAGCC[A/G]GGTCCCCCCAGCTGCCTCCTGGGCT

Phenotype

MIM: 610336

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C2CD4C PubMed Links

Gene Details

Gene

C2CD4C

Gene Name

C2 calcium dependent domain containing 4C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136263.1	1873	UTR 3			NP_001129735.1
XM_011527694.1	1873	UTR 3			XP_011525996.1

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