View genomic variant #0000000083

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.161183463T>C
Published as -
GERP 5.530
Segregation -
DB-ID NDUFS2_000003 See all 2 reported entries
MSCV MSCV_0000083
dbSNP ID rs121434429
Frequency -
Sources ; clinVar; Ensembl;
Reference 11220739
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS2 00000209 NM_001166159.1 0000000083 +/+ - 12/13 c.1237T>C p.(Ser413Pro) probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS2 00000208 NM_004550.4 0000000083 +/+ - 12/13 c.1237T>C p.? probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS2 00000207 XM_005245208.1 0000000083 +/+ - 12/13 c.1237T>C p.(Ser413Pro) probably_damaging(0.998) missense_variant - deleterious(0)
NDUFS2 00000210 XM_005245209.1 0000000083 +/+ - 11/13 c.943T>C p.(Ser315Pro) - missense_variant - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000007103; RCV000199278;
Chromosome 1:161183463..161183463
ClinVar Allele ID 21750
Disease database name and identifier MONDO:MONDO:0032611, MedGen:C4748759, OMIM:618228|MedGen:CN517202
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 6|not provided
HGVS variant names NC 000001.10:g.161183463T>C
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA118443|OMIM:602985.0003|UniProtKB:O75306#VAR 019537
Gene symbol:Gene id. NDUFS2:4720
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 121434429
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