View genomic variant #0000015261

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.12062126A>G
Published as -
GERP -
Segregation -
DB-ID MFN2_000013
MSCV MSCV_0015261
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

2 entries on 1 page. Showing entries 1 - 2.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MFN2 00000005 NM_001127660.1 0000015261 ./. - - c.1126A>G - r.(?) p.(Met376Val) - - - -
MFN2 00000004 NM_014874.3 0000015261 ./. - - c.1126A>G - r.(?) p.(Met376Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000790031;
Chromosome 1:12062126..12062126
ClinVar Allele ID 624938
Disease database name and identifier MONDO:MONDO:0015626, MedGen:C0007959, OMIM:PS118220, Orphanet:ORPHA166, SNOMED CT:50548001
ClinVar preferred disease name Charcot-Marie-Tooth disease
HGVS variant names NC 000001.10:g.12062126A>C
ClinVar review status no assertion criteria provided
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MFN2:9927
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 863224967
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000793093; RCV001542541; RCV001552650; RCV002051828;
Chromosome 1:12062126..12062126
ClinVar Allele ID 213790
Disease database name and identifier MONDO:MONDO:0012231, MedGen:C4721887, OMIM:609260, Orphanet:ORPHA99947|MONDO:MONDO:0018993, MedGen:C0270914, Orphanet:ORPHA64746|MONDO:MONDO:0019551, MedGen:C0393807, Orphanet:ORPHA90120, SNOMED CT:128203003|MedGen:CN517202
ClinVar preferred disease name Charcot-Marie-Tooth disease, type 2A2A|Charcot-Marie-Tooth disease, type 2|Hereditary motor and sensory neuropathy with optic atrophy|not provided
HGVS variant names NC 000001.10:g.12062126A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MFN2:9927
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 863224967
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