Details for PITX2:c.698C>T, p.Ser233Leu

CHROMOSOME 4
GENOMIC COORDINATES
hg19hg38
111539399110618243
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE PITX2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_153427.2
CDNA CHANGE c.698C>T
PROTEIN CHANGE p.Ser233Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.471665Disease causing
DBSNP ID NA
1 combination linked to PITX2:c.698C>T, p.Ser233Leu OLI253
1 disease linked to PITX2:c.698C>T, p.Ser233Leu Axenfeld-Rieger syndrome

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