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

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