Details for OPTN:c.626+1G>T,

CHROMOSOME 10
GENOMIC COORDINATES
hg19hg38
1315834113116341
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE OPTN
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_021980.4
CDNA CHANGE c.626+1G>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone4.754235Disease causing
DBSNP ID NA
1 combination linked to OPTN:c.626+1G>T, OLI774
1 disease linked to OPTN:c.626+1G>T, Amyotrophic lateral sclerosis

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