Details for EML1:

CHROMOSOME 14
GENOMIC COORDINATES
hg19hg38
10038056499914227
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE EML1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00040.00.00290.00.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00038570.00.0026020.00.00.02.638e-050.00065150.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.055394Polymorphism
DBSNP ID NA
1 combination linked to EML1: OLI490
1 disease linked to EML1: Rare pervasive developmental disorder

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