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 XRCC1:c.1738C>T, p.Arg580Trp

CHROMOSOME

19

GENOMIC COORDINATES

hg19	hg38
44047814	43543662

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

G

ALTERNATE ALLELE

A

TRANSCRIPT

CDNA CHANGE

c.1738C>T

PROTEIN CHANGE

p.Arg580Trp

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
3.977e-05	0.0	0.0	0.0	0.0	0.0	6.155e-05	0.0001629	6.533e-05

ESP
AA	EA
0.0	0.0001163

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	4.230359	Polymorphism

DBSNP ID

1 combination linked to XRCC1:c.1738C>T, p.Arg580Trp

1 disease linked to XRCC1:c.1738C>T, p.Arg580Trp

Isolated anencephaly

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