Variant #0000922212 (NC_000010.10:g.101824970G>A, NM_001308.2:c.734C>T (CPN1))

Chromosome 10
Allele Parent #2
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.101824970G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CPN1_000010 See all 3 reported entries
Variant remarks -
Reference Journal: Vincent 2024
ClinVar ID -
dbSNP ID rs371070915
Origin CLASSIFICATION record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 8.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-03-31 11:22:01 +02:00 (CEST)
Date last edited 2024-02-12 08:42:58 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPN1 NM_001308.2 +?/+? 4 c.734C>T r.(?) p.(Thr245Met)


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