Details for ADGRV1:c.3022+2T>G,

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
8994191090646093
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE ADGRV1
REFERENCE ALLELE T
ALTERNATE ALLELE G
TRANSCRIPT ENST00000405460.9
CDNA CHANGE c.3022+2T>G
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone4.504437Disease causing
DBSNP ID NA
1 combination linked to ADGRV1:c.3022+2T>G, OLI254
1 disease linked to ADGRV1:c.3022+2T>G, Non-syndromic genetic deafness

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