Product Details

SNP ID

rs142931346

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:103676919 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCAGCTGTCTTCTTTCCTGAGGAGG[C/T]CCCTCTCATTTTACTTCTCTGCATG

Phenotype

MIM: 300409

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MORF4L2 PubMed Links

Gene Details

Gene

MORF4L2

Gene Name

mortality factor 4 like 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142418.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135890.1
NM_001142419.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135891.1
NM_001142420.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135892.1
NM_001142421.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135893.1
NM_001142422.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135894.1
NM_001142423.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135895.1
NM_001142424.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135896.1
NM_001142425.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135897.1
NM_001142426.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135898.1
NM_001142427.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135899.1
NM_001142428.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135900.1
NM_001142429.1	613	Intron			NP_001135901.1
NM_001142430.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135902.1
NM_001142431.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135903.1
NM_001142432.1	613	Missense Mutation	ACC,GCC	T37A	NP_001135904.1
NM_012286.2	613	Missense Mutation	ACC,GCC	T37A	NP_036418.1

View Full Product Details