View genomic variant #0000000345

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.68549350G>A
Published as -
GERP 5.340
Segregation -
DB-ID CPT1A_000006 See all 2 reported entries
MSCV MSCV_0000345
dbSNP ID rs80356790
Frequency -
Sources ; clinvar; ensembl;
Reference 12189492;14517221;20301700
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     
CPT1A 00000660 NM_001031847.2 0000000345 +/+ - 11/19 c.1241C>T p.(Ala414Val) probably_damaging(0.984) missense_variant - deleterious(0)
CPT1A 00000662 NM_001876.3 0000000345 +/+ - 11/19 c.1241C>T p.(Ala414Val) probably_damaging(0.984) missense_variant - deleterious(0)
CPT1A 00000664 XM_005273762.1 0000000345 +/+ - 11/19 c.1337C>T p.(Ala446Val) - missense_variant - -
CPT1A 00000661 XM_005273763.1 0000000345 +/+ - 11/19 c.1337C>T p.(Ala446Val) - missense_variant - -
CPT1A 00000663 XM_005273764.1 0000000345 +/+ - 11/19 c.1241C>T p.(Ala414Val) probably_damaging(0.984) missense_variant - deleterious(0)
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000009632;
Chromosome 11:68549350..68549350
ClinVar Allele ID 24104
Disease database name and identifier MONDO:MONDO:0009705, MedGen:C1829703, OMIM:255120, Orphanet:156
ClinVar preferred disease name Carnitine palmitoyl transferase 1A deficiency
HGVS variant names NC 000011.9:g.68549350G>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:CA340854|OMIM:600528.0004|UniProtKB:P50416#VAR 020553
Gene symbol:Gene id. CPT1A:1374|LOC126861244:126861244
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 80356790
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