Variant #0001032123 (NC_000001.10:g.53676743T>C, NM_000098.2:c.1397T>C (CPT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.53676743T>C
DNA change (hg38) -
Published as CPT2(NM_000098.3):c.1397T>C (p.(Val466Ala))
ISCN -
DB-ID CPT2_000058
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPT2 NM_000098.2 ?/. - c.1397T>C r.(?) p.(Val466Ala)
C1orf123 NM_017887.1 ?/. - c.*3588A>G r.(=) p.(=)


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