This site uses cookies!

We use cookies for security, analytics and session persistence reasons. Please refer to our Cookie Policy for more information.

Select Cookie Preferences (Hover for info)

Details for AMN1:c.656G>A, p.Cys219Tyr

CHROMOSOME

12

GENOMIC COORDINATES

hg19	hg38
31841988	31689054

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

C

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.656G>A

PROTEIN CHANGE

p.Cys219Tyr

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
None	None	None	None	None	None

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Possibly Damaging	3.48505	Disease causing

DBSNP ID

1 combination linked to AMN1:c.656G>A, p.Cys219Tyr

1 disease linked to AMN1:c.656G>A, p.Cys219Tyr

Kallmann syndrome

Found any issues with the data on this page? Report this entry.