Details for BRWD3:c.592-3T>C,

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
7999975580744256
VARIANT EFFECT splicing
ANNOTATION FLAG automatically_attributed_and_verified
GENE BRWD3
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_153252.4
CDNA CHANGE c.592-3T>C
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone0.664471Disease causing
DBSNP ID rs1602384989
1 combination linked to BRWD3:c.592-3T>C, OLI798
1 disease linked to BRWD3:c.592-3T>C, Arthrogryposis syndrome

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