Variant #0000944909 (NC_000011.9:g.124793752_124793754delinsAA, NM_152722.4:c.580_582delinsTT (HEPACAM))

Chromosome 11
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.124793752_124793754delinsAA
DNA change (hg38) g.124923856_124923858delinsAA
Published as -
ISCN -
DB-ID HEPACAM_000022 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rogier Min
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-10-31 16:41:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HEPACAM NM_152722.4 +?/. - c.580_582delinsTT r.(?) p.(Leu194PhefsTer61)


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