Details for NSMF:c.1159-14_22del,

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
NoneNone
VARIANT EFFECT unknown
ANNOTATION FLAG not_found_in_databases
GENE NSMF
REFERENCE ALLELE None
ALTERNATE ALLELE None
TRANSCRIPT N.A.
CDNA CHANGE c.1159-14_22del
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNoneNoneNone
DBSNP ID NA
1 combination linked to NSMF:c.1159-14_22del, OLI408
1 disease linked to NSMF:c.1159-14_22del, Kallmann syndrome
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