LOVD - Variant listings for MLYCD

About this overview [Show]

Patient data (#0000535)
Patient ID MILJA
Disease Developmental Delay, Acidosis, Hypoglycaemia,
Reference/Submitter Haan EA, et al (1986) Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect. Eur J Pediatr 144:567-70., :Edinburgh
Template DNA
Technique Direct Sequencing
Remarks DNA Type: Genomic;Mutation Segregates with Phenotype: Yes;Expression Analysis Confirms Phenotype : Yes;Normal Individuals Tested: 71-80; Sample Origin: Cell Line
# Reported 1
Population -
Gender Male
Sequence Inheritance -
Phenotype Inheritance -
Second PCR Yes
CIS No
Conserved residue n/a
Related Phenotype -
Unrelated  Phenotype -
Submitter Patrick Wrightman

Variant data
Allele Unknown
Reported pathogenicity Unknown
Concluded pathogenicity Unknown
Exon 01
Legacy DNA ID c.473delG
DNA change c.473delG
RNA change r.?
Protein change -
RNA information RNA Frame Change: Frameshift ;RNA Splice Change: n/a;RNA Transcription Change: T2; RNA Sequence Change: Deletion
Protein information Premature Termination
DB-ID MLYCD_00002
Location Exon
Base number 473
5' Sequence Context GCTGC
Original Sequence G
Variant Sequence -
3' Sequence Context GGCCG
Type Deletion
Domain n/a
Detection Method Direct Sequencing
RE Site -
Frequency -

1 entry in MLYCD

Path. Allele
Exon Descending
Ascending
Legacy DNA ID Descending
Ascending
DNA change Descending
Ascending
RNA change Descending
Ascending
Protein change Descending
Ascending
RNA information Descending
Ascending
Protein information Descending
Ascending
DB-ID Descending
Ascending
Location Descending
Ascending
Base number Descending
Ascending
5' Sequence Context Descending
Ascending
Original Sequence Descending
Ascending
Variant Sequence Descending
Ascending
3' Sequence Context Descending
Ascending
Type Descending
Ascending
Domain Descending
Ascending
Detection Method Descending
Ascending
RE Site Descending
Ascending
Frequency Descending
Ascending
?/? Unknown 01 c.473delG c.473delG r.? - RNA Frame Change: Frameshift ;RNA Splice Change: n/a;RNA Transcription Change: T2; RNA Sequence Change: Deletion Premature Termination MLYCD_00002 Exon 473 GCTGC G - GGCCG Deletion n/a Direct Sequencing - -