Product Details

SNP ID

rs2298729

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:104470865 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGGTAAATATTTGTCCTGATGGGA[C/T]GGCCTTAAGAACCCTGACTGTGATA

Phenotype

MIM: 611645

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CXXC4 PubMed Links

Gene Details

Gene

CXXC4

Gene Name

CXXC finger protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025212.3	3161	UTR 3			NP_079488.2
XM_011532284.2	3161	UTR 3			XP_011530586.1
XM_017008652.1	3161	UTR 3			XP_016864141.1

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