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Details for LAMA2:c.379A>G, p.Thr127Ala

CHROMOSOME

6

GENOMIC COORDINATES

hg19	hg38
129381024	129059879

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

A

ALTERNATE ALLELE

G

TRANSCRIPT

N.A.

CDNA CHANGE

c.379A>G

PROTEIN CHANGE

p.Thr127Ala

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
5.0	0.0	0.0	0.0	0.0	0.0	5.0	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Possibly Damaging	3.618027	Disease causing

DBSNP ID

1 combination linked to LAMA2:c.379A>G, p.Thr127Ala

1 disease linked to LAMA2:c.379A>G, p.Thr127Ala

Congenital nephrotic syndrome

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