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Details for COL4A5:c.1960G>T, p.Asp654Tyr

CHROMOSOME

X

GENOMIC COORDINATES

hg19	hg38
107844634	108601404

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

T

TRANSCRIPT

CDNA CHANGE

c.1960G>T

PROTEIN CHANGE

p.Asp654Tyr

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	4.067553	Disease causing

DBSNP ID

2 combinations linked to COL4A5:c.1960G>T, p.Asp654Tyr

1 disease linked to COL4A5:c.1960G>T, p.Asp654Tyr

Benign familial hematuria

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