Variants - Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified using a quantitative integrated evaluation

Variant data
Allele	Unknown
Reported pathogenicity	No known pathogenicity
Concluded pathogenicity	Unknown
Exon	25
DNA change	c.9292T>C
BIC DNA change	9520T>C
Protein change	p.Y3098H
Posterior P	0.00001
IARC Class	1 - Not pathogenic or of no clinical significance
Key Observational Reference	Easton DF et al., Am J Hum Genet, 81: 873-883, 2007.
Prior P reference	Tavtigian et al., Human Mutation 29: 1342-1354, 2008.
Missense analysis Prior P	0.03
Splicing prior P	0.01
Other Prior P	0.00
Combined prior P	0.03
Segregation LR	5.012
Pathology LR	-
Sum Family LR	0.00035
Co-occurrence LR	0.195
case-control LR	-
Product of LRs	0.00034
Comments	-

1 entry in BRCA2

Path.

Allele

Exon

DNA change

BIC DNA change

Protein change

Posterior P

IARC Class

Key Observational Reference

Prior P reference

Missense analysis Prior P

Splicing prior P

Other Prior P

Combined prior P

Segregation LR

Pathology LR

Sum Family LR

Co-occurrence LR

case-control LR

Product of LRs

Comments

-/?

Unknown

9520T>C

p.Y3098H

0.00001

1 - Not pathogenic or of no clinical significance

Easton DF et al., Am J Hum Genet, 81: 873-883, 2007.

Tavtigian et al., Human Mutation 29: 1342-1354, 2008.

0.03

0.01

0.00

0.03

5.012

0.00035

0.195

0.00034

Database of BRCA1 and BRCA2 sequence variants that have been clinically reclassified using a quantitative integrated evaluation