View genomic variant #0000019125

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.44161337_44161339del
Published as -
GERP -
Segregation -
DB-ID LRPPRC_000094
MSCV MSCV_0019125
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
LRPPRC 00000168 NM_133259.3 0000019125 ./. - - c.2726_2728del p.(Lys909del) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000202395;
Chromosome 2:44161337..44161339
ClinVar Allele ID 214819
Disease database name and identifier MONDO:MONDO:0009069, MedGen:C1857355, OMIM:220111, Orphanet:70472
ClinVar preferred disease name Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type
HGVS variant names NC 000002.11:g.44161338CTT[1]
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type Microsatellite
Sequence Ontology for variant type SO:0000289
Variant clinical sources reported ClinGen:CA279903|OMIM:607544.0005
Gene symbol:Gene id. LRPPRC:10128
Molecular consequence SO:0001822|inframe deletion
Allele origin
dbSNP ID 863225445
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None