Details for UNC13D:c.684-1G>A,

CHROMOSOME 17
GENOMIC COORDINATES
hg19hg38
7383665875840577
VARIANT EFFECT splicing
ANNOTATION FLAG automatically_attributed_and_verified
GENE UNC13D
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_199242.2
CDNA CHANGE c.684-1G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.252307Disease causing
DBSNP ID NA
1 combination linked to UNC13D:c.684-1G>A, OLI055
1 disease linked to UNC13D:c.684-1G>A, Primary hemophagocytic lymphohistiocytosis

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