Details for FBN2:c.7357T>A, p.Cys2453Ser

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
127613686128277994
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE FBN2
REFERENCE ALLELE A
ALTERNATE ALLELE T
TRANSCRIPT NM_001999.3
CDNA CHANGE c.7357T>A
PROTEIN CHANGE p.Cys2453Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.081465Disease causing
DBSNP ID NA
1 combination linked to FBN2:c.7357T>A, p.Cys2453Ser OLI291
1 disease linked to FBN2:c.7357T>A, p.Cys2453Ser Adolescent idiopathic scoliosis

Found any issues with the data on this page? Report this entry.