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 International |
Created by |
Johan den Dunnen |
Date created |
2023-10-31 16:41:00 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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