Variant #0000688199 (NC_000001.10:g.53675848_53675849del, NM_000098.2:c.502_503del (CPT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.53675848_53675849del
DNA change (hg38) -
Published as CPT2(NM_000098.2):c.502_503delGC (p.A168Wfs*16)
ISCN -
DB-ID CPT2_000037
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
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.502_503del r.(?) p.(Ala168TrpfsTer16)
C1orf123 NM_017887.1 +?/. - c.*4482_*4483del r.(=) p.(=)


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