Product Details

SNP ID

rs4778627

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:78879934 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CGAATTGAAGCTATTGAAACAAATT[A/G]AACTGTTGTGGTTATTTTGGTTTTC

Phenotype

MIM: 607303

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

MORF4L1 PubMed Links

Additional Information

For this assay, SNP(s) [rs150086538] are located under a primer 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

MORF4L1

Gene Name

mortality factor 4 like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001265603.1		Intron			NP_001252532.1
NM_001265604.1		Intron			NP_001252533.1
NM_001265605.1		Intron			NP_001252534.1
NM_006791.3		Intron			NP_006782.1
NM_206839.2		Intron			NP_996670.1
XM_017021872.1		Intron			XP_016877361.1

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