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 LAMA5:c.3728C>T, p.Pro1243Leu

CHROMOSOME

20

GENOMIC COORDINATES

hg19	hg38
60905923	62330867

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.3728C>T

PROTEIN CHANGE

p.Pro1243Leu

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
4.139e-05	0.0	8.598e-05	0.0	9.079e-05	0.0	5.372e-05	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Benign	2.586118	Disease causing

DBSNP ID

2 combinations linked to LAMA5:c.3728C>T, p.Pro1243Leu

1 disease linked to LAMA5:c.3728C>T, p.Pro1243Leu

Benign familial hematuria

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