Details for ANOS1:c.1062+4A>C,

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
85385368570495
VARIANT EFFECT None
ANNOTATION FLAG None
GENE ANOS1
REFERENCE ALLELE T
ALTERNATE ALLELE G
TRANSCRIPT NM_000216
CDNA CHANGE c.1062+4A>C
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone1.62829None
DBSNP ID NA
1 combination linked to ANOS1:c.1062+4A>C, OLI1106
1 disease linked to ANOS1:c.1062+4A>C, Kallmann syndrome

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