Variants - HGD mutation database - Leiden Open Variation Database

About this overview [Show]
This detailed view shows all details of the selected patient, including all variants reported in this patient. At the bottom of the page, all variants reported in this patient are listed, with the one you are looking at in bold. The link to the UCSC Genome Browser will show the browser zoomed in to the location of the selected variant.

Patient data (#0000118)
Patient ID	AKU_FEL_1
Disease	AKU
Reference	Felbor et al. (1999), Slovakia (Slovak Republic):Bratislava
Remarks	Homozygot
# Reported	1
Geographic origin	Germany
Patient/Affected_per_Family	1
Families Patients	1
Submitter	Andrea Zatkova

Variant data
Allele	Parent #2
Reported pathogenicity	Pathogenic
Concluded pathogenicity	Probably pathogenic
DB-ID	AKU_00006
Exon	02
DNA change	c.74T>C
RNA change	r.(?)
Protein	p.(Leu25Pro)
Original description	L25P
Links	-
Variant remarks	missense
Predicted Mutation Effect**	Protomer destabilisation, Hexamer disruption
Reference	Felbor et al. (1999)
Mutation HOT-SPOT	CCC triplet
Allele code	AKU_FEL_1b
Type	substitution
Re-site	(+)FauI, AciI
Frequency	-
Template	DNA
Technique	SEQ
Location	exon

2 entries in HGD

Path.

Allele

DB-ID

Exon

DNA change

RNA change

Protein

Original description

Links

Variant remarks

Predicted Mutation Effect**

Reference

Mutation HOT-SPOT

Allele code

Type

Re-site

Frequency

Template

Technique

Location

+/+?

Parent #2

AKU_00006

c.74T>C

r.(?)

p.(Leu25Pro)

L25P

missense

Protomer destabilisation, Hexamer disruption

Felbor et al. (1999)

CCC triplet

AKU_FEL_1b

substitution

(+)FauI, AciI

DNA

SEQ

exon

+/+?

Parent #1

AKU_00006

c.74T>C

r.(?)

p.(Leu25Pro)

L25P

missense

Protomer destabilisation, Hexamer disruption

Felbor et al. (1999)

CCC triplet

AKU_FEL_1a

substitution

(+)FauI, AciI

DNA

SEQ

exon

HGD mutation database

homogentisate 1,2-dioxygenase (HGD)