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 (#0000174)
Patient ID	AKU_VIL_20
Disease	AKU
Reference	Vilboux et al. (2009), Slovakia (Slovak Republic):Bratislava
Remarks	Compound heterozygous
# Reported	1
Geographic origin	USA
Patient/Affected_per_Family	1
Families Patients	1
Submitter	Andrea Zatkova

Variant data
Allele	Parent #2
Reported pathogenicity	Pathogenic
Concluded pathogenicity	Pathogenic
DB-ID	AKU_00037
Exon	06
DNA change	c.413_434+35del
RNA change	r.(?)
Protein	p.(Gly115Metfs*33)
Original description	G115fs (?), c.413_434+35del57
Links	rs762629587
Variant remarks	deletion/exon skipping/frameshift?
Predicted Mutation Effect**	-
Reference	Vilboux et al. (2009)
Mutation HOT-SPOT	-
Allele code	AKU_VIL_20a
Type	deletion
Re-site	-
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_00037

c.413_434+35del

r.(?)

p.(Gly115Metfs*33)

G115fs (?), c.413_434+35del57

rs762629587

deletion/exon skipping/frameshift?

Vilboux et al. (2009)

AKU_VIL_20a

deletion

DNA

SEQ

exon

+/+

Parent #1

AKU_00097

c.1102A>G

r.(?)

p.(Met368Val)

M368V

rs120074173

missense

Hexamer disruption

de Bernabe et al. (1998)

AKU_VIL_20b

substitution

(+)BtsIMutI, HpyCH4III, Tsp45I, TspRI

DNA

SEQ

exon

HGD mutation database

homogentisate 1,2-dioxygenase (HGD)