Product Details

SNP ID

rs61736594

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:65169932 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGGGGGCCTGTGCCGAATCTCGGC[C/T]TCTGGCCCAGAGAGCCTCCTGGGAG

Phenotype

MIM: 607844

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LEMD3 PubMed Links

Gene Details

Gene

LEMD3

Gene Name

LEM domain containing 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001167614.1	362	Silent Mutation	GCC,GCT	A112A	NP_001161086.1
NM_014319.4	362	Silent Mutation	GCC,GCT	A112A	NP_055134.2

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