View genomic variant #0000019369

Chromosome 2
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.207009730A>C
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000032
MSCV MSCV_0019369
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

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS1 00000204 NM_001199981.1 0000019369 ./. - - c.650T>G p.(Val217Gly) - - - -
NDUFS1 00000202 NM_001199982.1 0000019369 ./. - - c.425T>G p.(Val142Gly) - - - -
NDUFS1 00000203 NM_001199983.1 0000019369 ./. - - c.587T>G p.(Val196Gly) - - - -
NDUFS1 00000206 NM_001199984.1 0000019369 ./. - - c.800T>G p.(Val267Gly) - - - -
NDUFS1 00000205 NM_005006.6 0000019369 ./. - - c.758T>G p.(Val253Gly) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000170569;
Chromosome 2:207009730..207009730
ClinVar Allele ID 188274
Disease database name and identifier MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550
ClinVar preferred disease name Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
HGVS variant names NC 000002.11:g.207009730A>C
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA274773
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 786205666
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