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Details for COL4A3:c.4826G>A, p.Arg1609Gln

CHROMOSOME

2

GENOMIC COORDINATES

hg19	hg38
228175562	227310846

VARIANT EFFECT

None

ANNOTATION FLAG

None

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

N.A.

CDNA CHANGE

c.4826G>A

PROTEIN CHANGE

p.Arg1609Gln

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
1.203e-05	0.0	2.897e-05	0.0	5.563e-05	0.0	8.838e-06	0.0	0.0

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.390255	Disease causing

DBSNP ID

1 combination linked to COL4A3:c.4826G>A, p.Arg1609Gln

1 disease linked to COL4A3:c.4826G>A, p.Arg1609Gln

Alport syndrome

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