Product Details

SNP ID: rs11247115
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:99582399 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GATTTCCTTTCCCAGGCCAGACTGT[C/G]CTGTCCTTGAAAACTGGATTCCTTC
Phenotype: MIM: 600660
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: MEF2A PubMed Links

Gene Details

Transcript Accession	SNP Type	Protein ID
NM_001130926.2	Intron	NP_001124398.1
NM_001130927.2	Intron	NP_001124399.1
NM_001130928.2	Intron	NP_001124400.1
NM_001171894.2	Intron	NP_001165365.1
NM_001319206.1	Intron	NP_001306135.1
NM_005587.3	Intron	NP_005578.2
XM_005254914.2	Intron	XP_005254971.1
XM_005254915.2	Intron	XP_005254972.1
XM_005254916.3	Intron	XP_005254973.1
XM_011521571.2	Intron	XP_011519873.1
XM_011521572.2	Intron	XP_011519874.1
XM_011521573.2	Intron	XP_011519875.1
XM_011521576.2	Intron	XP_011519878.1
XM_011521577.2	Intron	XP_011519879.1
XM_011521578.2	Intron	XP_011519880.1
XM_011521579.2	Intron	XP_011519881.1
XM_011521581.2	Intron	XP_011519883.1
XM_011521582.2	Intron	XP_011519884.1
XM_011521583.2	Intron	XP_011519885.1
XM_011521585.2	Intron	XP_011519887.1
XM_011521586.2	Intron	XP_011519888.1
XM_011521587.2	Intron	XP_011519889.1
XM_011521590.2	Intron	XP_011519892.1
XM_017022190.1	Intron	XP_016877679.1
XM_017022191.1	Intron	XP_016877680.1
XM_017022192.1	Intron	XP_016877681.1
XM_017022193.1	Intron	XP_016877682.1
XM_017022194.1	Intron	XP_016877683.1
XM_017022195.1	Intron	XP_016877684.1
XM_017022196.1	Intron	XP_016877685.1
XM_017022197.1	Intron	XP_016877686.1
XM_017022198.1	Intron	XP_016877687.1
XM_017022199.1	Intron	XP_016877688.1
XM_017022200.1	Intron	XP_016877689.1
XM_017022201.1	Intron	XP_016877690.1
XM_017022202.1	Intron	XP_016877691.1
XM_017022203.1	Intron	XP_016877692.1
XM_017022204.1	Intron	XP_016877693.1