Details for CA2:c.232+1G>A,

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
8637769985465470
VARIANT EFFECT splicing
ANNOTATION FLAG manually_attributed
GENE CA2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000067.3
CDNA CHANGE c.232+1G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00020.00.00140.00.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
4.026e-060.02.921e-050.00.00.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone5.869853Disease causing
DBSNP ID rs573750741
1 combination linked to CA2:c.232+1G>A, OLI264
1 disease linked to CA2:c.232+1G>A, Osteopetrosis,Mental retardation,Short stature,Spastic paraparesis

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