View genomic variant #0000023515

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.129267300T>C
Published as -
GERP -
Segregation -
DB-ID AIFM1_000005
MSCV MSCV_0023515
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
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     
AIFM1 00000028 NM_001130846.2 0000023515 ./. - - c.380A>G p.(Gln127Arg) - - - -
AIFM1 00000027 NM_001130847.3 0000023515 ./. - - c.*664A>G p.(=) - - - -
AIFM1 00000026 NM_004208.3 0000023515 ./. - - c.1436A>G p.(Gln479Arg) - - - -
AIFM1 00000025 NM_145812.2 0000023515 ./. - - c.1424A>G p.(Gln475Arg) - - - -
AIFM1 00000024 NM_145813.2 0000023515 ./. - - c.575A>G p.(Gln192Arg) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000408758;
Chromosome X:129267300..129267300
ClinVar Allele ID 354190
Disease database name and identifier MONDO:MONDO:0010437, MedGen:C3151753, OMIM:300816, Orphanet:238329
ClinVar preferred disease name Severe X-linked mitochondrial encephalomyopathy
HGVS variant names NC 000023.10:g.129267300T>C
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:CA10654936
Gene symbol:Gene id. AIFM1:9131|RAB33A:9363
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 1057516211
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