Product Details

SNP ID

rs186353882

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:88722661 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTTGACTGAGGGACTTTCCCTTTC[A/G]TCCGGCGAAGGTCTGGTGAGTCCAA

Phenotype

MIM: 600662

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MEF2C PubMed Links

Gene Details

Gene

MEF2C

Gene Name

myocyte enhancer factor 2C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001131005.2	1480	Silent Mutation			NP_001124477.1
NM_001193347.1	1480	Silent Mutation			NP_001180276.1
NM_001193348.1	1480	Silent Mutation			NP_001180277.1
NM_001193349.1	1480	Silent Mutation			NP_001180278.1
NM_001193350.1	1480	Silent Mutation			NP_001180279.1
NM_001308002.1	1480	Silent Mutation			NP_001294931.1
NM_002397.4	1480	Silent Mutation			NP_002388.2
XM_005248511.2	1480	Silent Mutation			XP_005248568.1
XM_006714619.2	1480	Silent Mutation			XP_006714682.1
XM_006714625.3	1480	Silent Mutation			XP_006714688.1
XM_011543396.2	1480	Silent Mutation			XP_011541698.1
XM_011543397.2	1480	Silent Mutation			XP_011541699.1
XM_011543400.1	1480	Silent Mutation			XP_011541702.1
XM_011543401.1	1480	Silent Mutation			XP_011541703.1
XM_017009475.1	1480	Silent Mutation			XP_016864964.1
XM_017009476.1	1480	Silent Mutation			XP_016864965.1
XM_017009477.1	1480	Silent Mutation			XP_016864966.1
XM_017009478.1	1480	Silent Mutation			XP_016864967.1
XM_017009479.1	1480	Silent Mutation			XP_016864968.1
XM_017009480.1	1480	Silent Mutation			XP_016864969.1
XM_017009481.1	1480	Silent Mutation			XP_016864970.1
XM_017009482.1	1480	Silent Mutation			XP_016864971.1
XM_017009483.1	1480	Silent Mutation			XP_016864972.1

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