View genomic variant #0000001016

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.1815999G>A
Published as -
GERP 4.440
Segregation -
DB-ID NDUFS6_000001 See all 2 reported entries
MSCV MSCV_0001016
dbSNP ID rs267606913
Frequency -
Sources ; clinVar; Ensembl;
Reference 19259137
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.
Legend  

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 0000001016 +/+ - 4/4 c.344G>A p.(=) probably_damaging(1) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000006389;
Chromosome 5:1815999..1815999
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 21057
Disease database name and identifier MONDO:MONDO:0032615, MedGen:C4748767, OMIM:618232
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 9
HGVS variant names NC 000005.9:g.1815999G>A
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:CA117913|OMIM:603848.0003
Gene symbol:Gene id. NDUFS6:4726
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 267606913
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