View genomic variant #0000000846

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.206992550C>T
Published as -
GERP 5.630
Segregation -
DB-ID NDUFS1_000008 See all 2 reported entries
MSCV MSCV_0000846
dbSNP ID rs397515447
Frequency -
Sources ; clinVar; Ensembl;
Reference 20382551
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 0000000846 +/+ - 15/18 c.1747G>A p.(Asp583Asn) probably_damaging(1) missense_variant - deleterious(0)
NDUFS1 00000202 NM_001199982.1 0000000846 +/+ - 13/16 c.1522G>A p.(Asp508Asn) probably_damaging(0.999) missense_variant - deleterious(0.01)
NDUFS1 00000203 NM_001199983.1 0000000846 +/+ - 15/18 c.1684G>A p.(Asp562Asn) probably_damaging(1) missense_variant - tolerated(0.13)
NDUFS1 00000206 NM_001199984.1 0000000846 +/+ - 16/19 c.1897G>A p.(Asp633Asn) probably_damaging(1) missense_variant - deleterious(0.01)
NDUFS1 00000205 NM_005006.6 0000000846 +/+ - 16/19 c.1855G>A p.(Asp619Asn) probably_damaging(1) missense_variant - deleterious(0.01)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000043634;
Chromosome 2:206992550..206992550
ClinVar Allele ID 65581
Disease database name and identifier MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 5
HGVS variant names NC 000002.11:g.206992550C>T
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA143869|OMIM:157655.0006
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 397515447
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