Product Details

SNP ID

rs11728800

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:15473372 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGTATTACGAATGGTCAGAGAAGAG[C/T]TCTCTGATAATAAAATTTCAGCTGA

Phenotype

MIM: 612013

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CC2D2A PubMed Links

Gene Details

Gene

CC2D2A

Gene Name

coiled-coil and C2 domain containing 2A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080522.2		Intron			NP_001073991.2
NM_001164720.1		Intron			NP_001158192.1
NM_020785.2		Intron			NP_065836.2
XM_005248177.1		Intron			XP_005248234.1
XM_011513872.2		Intron			XP_011512174.1
XM_011513874.2		Intron			XP_011512176.1
XM_017008482.1		Intron			XP_016863971.1

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