View genomic variant #0000000888

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.240964718T>C
Published as -
GERP 3.040
Segregation -
DB-ID NDUFA10_000001 See all 2 reported entries
MSCV MSCV_0000888
dbSNP ID rs387906872
Frequency -
Sources ; clinVar; ensembl;
Reference 21150889
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.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFA10 00000183 NM_004544.3 0000000888 +/+ - 1/4 c.1A>G p.? unknown(0) initiator_codon_variant,NMD_transcript_variant - -
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ClinVar @ MSeqDR

RCVaccession RCV000023345;
Chromosome 2:240964718..240964718
Allele frequencies from ExAC 0.00009
ClinVar Allele ID 39349
Disease database name and identifier MONDO:MONDO:0032626, MedGen:C4748796, OMIM:618243
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 22
HGVS variant names NC 000002.11:g.240964718T>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:CA129185|OMIM:603835.0001
Gene symbol:Gene id. NDUFA10:4705
Molecular consequence SO:0001582|initiator codon variant, SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 387906872
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