Details for NSMF:c.1165-14_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.1165-14_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.1165-14_22del, OLI389
1 disease linked to NSMF:c.1165-14_22del, Kallmann syndrome
Found any issues with the data on this page? Report this entry.