Details for ADGRV1:c.10790A>T,

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
9004142890745611
VARIANT EFFECT None
ANNOTATION FLAG None
GENE ADGRV1
REFERENCE ALLELE A
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.10790A>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging2.531887Polymorphism
DBSNP ID NA
1 combination linked to ADGRV1:c.10790A>T, OLI1319
1 disease linked to ADGRV1:c.10790A>T, Rare genetic deafness

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