Product Details

SNP ID

rs7238897

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:57545826 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTAGCTGGAGAAAATTGACAAAAA[A/C]AATAGAAAGTTTGTAAAATGATCAA

Phenotype

MIM: 612386

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

FECH PubMed Links

Additional Information

For this assay, SNP(s) [rs146687823] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

FECH

Gene Name

ferrochelatase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000140.3	6293	UTR 3			NP_000131.2
NM_001012515.2	6293	UTR 3			NP_001012533.1
XM_011525881.1	6293	Intron			XP_011524183.1
XM_011525882.2	6293	Intron			XP_011524184.1
XM_017025614.1	6293	Intron			XP_016881103.1

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