Product Details

SNP ID
rs76738785
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:88724997 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTATGTCTTCACAGGGAGGGTGAC[A/G]TAGAAAATTAGAAGAAAAAATTGGT
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 Intron NP_001124477.1
NM_001193347.1 Intron NP_001180276.1
NM_001193348.1 Intron NP_001180277.1
NM_001193349.1 Intron NP_001180278.1
NM_001193350.1 Intron NP_001180279.1
NM_001308002.1 Intron NP_001294931.1
NM_002397.4 Intron NP_002388.2
XM_005248511.2 Intron XP_005248568.1
XM_006714619.2 Intron XP_006714682.1
XM_006714625.3 Intron XP_006714688.1
XM_011543396.2 Intron XP_011541698.1
XM_011543397.2 Intron XP_011541699.1
XM_011543400.1 Intron XP_011541702.1
XM_011543401.1 Intron XP_011541703.1
XM_017009475.1 Intron XP_016864964.1
XM_017009476.1 Intron XP_016864965.1
XM_017009477.1 Intron XP_016864966.1
XM_017009478.1 Intron XP_016864967.1
XM_017009479.1 Intron XP_016864968.1
XM_017009480.1 Intron XP_016864969.1
XM_017009481.1 Intron XP_016864970.1
XM_017009482.1 Intron XP_016864971.1
XM_017009483.1 Intron XP_016864972.1

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