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 TNIK:c.1660C>A, p.Pro554Thr

CHROMOSOME

3

GENOMIC COORDINATES

hg19	hg38
170846529	171128740

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed_and_verified

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1660C>A

PROTEIN CHANGE

p.Pro554Thr

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	3.545827	None

DBSNP ID

1 combination linked to TNIK:c.1660C>A, p.Pro554Thr

1 disease linked to TNIK:c.1660C>A, p.Pro554Thr

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