Variant #0000717553 (NC_000001.10:g.53676278A>G, NM_000098.2:c.932A>G (CPT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.53676278A>G
DNA change (hg38) -
Published as CPT2(NM_000098.3):c.932A>G (p.N311S)
ISCN -
DB-ID CPT2_000043 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00032 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT2 NM_000098.2 -?/. - c.932A>G r.(?) p.(Asn311Ser)
C1orf123 NM_017887.1 -?/. - c.*4053T>C r.(=) p.(=)


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