Variant #0001036536 (NC_000007.13:g.794212_794223del, NC_000007.13(NM_017802.3):c.1025-14_1025-3del (HEATR2))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.794212_794223del
DNA change (hg38) -
Published as DNAAF5(NM_017802.4):c.1025-14_1025-3del
ISCN -
DB-ID HEATR2_000056
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
PRKAR1B NM_001164758.1 ?/. - c.-27015_-27004del r.(?) p.(=)
HEATR2 NM_017802.3 ?/. - c.1025-14_1025-3del r.spl? p.?


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