Variant #0000526272 (NC_000005.9:g.88057041G>A, MEF2C(NM_002397.4):c.363C>T)

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.88057041G>A
DNA change (hg38) g.88761224G>A
Published as MEF2C(NM_002397.4):c.363C>T (p.N121=)
ISCN -
DB-ID MEF2C_000027
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEF2C NM_002397.4 -?/. - c.363C>T r.(?) p.(Asn121=)