View genomic variant #0000021295

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.1815950T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS6_000008
MSCV MSCV_0021295
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.11856 View details
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     
NDUFS6 00000214 NM_004553.4 0000021295 ./. - - c.310-15T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000287086; RCV001513342; RCV001543892;
Chromosome 5:1815950..1815950
Allele frequencies from ESP 0.11856
Allele frequencies from ExAC 0.05446
Allele frequencies from TGP 0.11921
ClinVar Allele ID 303479
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0032615, MedGen:C4748767, OMIM:618232|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010
ClinVar preferred disease name not provided|Mitochondrial complex 1 deficiency, nuclear type 9|Mitochondrial complex I deficiency, nuclear type 1
HGVS variant names NC 000005.9:g.1815950T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA3187709
Gene symbol:Gene id. NDUFS6:4726
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 10058270
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