Details for MYO7A:c.6051+9C>T,

CHROMOSOME 11
GENOMIC COORDINATES
hg19hg38
7691985777208812
VARIANT EFFECT unknown
ANNOTATION FLAG manually_attributed
GENE MYO7A
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_000260.5
CDNA CHANGE c.6051+9C>T
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone0.54307Polymorphism
DBSNP ID rs747742075
1 combination linked to MYO7A:c.6051+9C>T, OLI348
1 disease linked to MYO7A:c.6051+9C>T, 46,XY disorder of sex development

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