Variant #0000848765 (NC_000001.10:g.53676924T>C, NM_000098.2:c.1578T>C (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.53676924T>C
DNA change (hg38) -
Published as CPT2(NM_000098.2):c.1578T>C (p.G526=), CPT2(NM_000098.3):c.1578T>C (p.G526=)
ISCN -
DB-ID CPT2_000041 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) 0.00432 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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.1578T>C r.(?) p.(Gly526=)
C1orf123 NM_017887.1 -?/. - c.*3407A>G r.(=) p.(=)


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