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SNP ID

rs75449619

Assay Type

Functionally tested

NCBI dbSNP Submissions

13

Location

Chr.1:203641535 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGCCCCTAAATAAGAGGGCATGC[A/G]AGTTGTCCCAGAATCTGTGGATTCA

Phenotype

MIM: 108732

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

ATP2B4 PubMed Links

Gene Details

Gene

ATP2B4

Gene Name

ATPase plasma membrane Ca2+ transporting 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001396.2		Intron			NP_001001396.1
NM_001684.4		Intron			NP_001675.3

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