View genomic variant #0000015244

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.12057358T>G
Published as -
GERP -
Segregation -
DB-ID MFN2_000041
MSCV MSCV_0015244
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 0000015244 ./. - - c.479T>G - r.(?) p.(Val160Gly) - - - -
MFN2 00000004 NM_014874.3 0000015244 ./. - - c.479T>G - r.(?) p.(Val160Gly) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV001056342;
Chromosome 1:12057358..12057358
ClinVar Allele ID 822627
Disease database name and identifier MONDO:MONDO:0018993, MedGen:C0270914, Orphanet:ORPHA64746
ClinVar preferred disease name Charcot-Marie-Tooth disease, type 2
HGVS variant names NC 000001.10:g.12057358T>C
ClinVar review status criteria provided, single submitter
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 879253861
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000235092;
Chromosome 1:12057358..12057358
ClinVar Allele ID 244147
Disease database name and identifier MONDO:MONDO:0012231, MedGen:C4721887, OMIM:609260, Orphanet:ORPHA99947
ClinVar preferred disease name Charcot-Marie-Tooth disease, type 2A2A
HGVS variant names NC 000001.10:g.12057358T>G
ClinVar review status criteria provided, single submitter
Clinical Significance 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 879253861
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