Variant #0001052559 (NC_000007.13:g.618916C>T, NM_017802.3:c.-147442C>T (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.618916C>T
DNA change (hg38) -
Published as PRKAR1B(NM_001164760.2):c.868G>A (p.(Asp290Asn))
ISCN -
DB-ID chr7_007321
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKAR1B NM_001164758.1 ?/. - c.868G>A r.(?) p.(Asp290Asn)
HEATR2 NM_017802.3 ?/. - c.-147442C>T r.(?) p.(=)


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