Variant #0000299083 (NC_000007.13:g.590184C>A, NM_017802.3:c.-176174C>A (HEATR2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.590184C>A
DNA change (hg38) g.550547C>A
Published as PRKAR1B(NM_001164761.2):c.1029G>T (p.G343=)
ISCN -
DB-ID PRKAR1B_000003
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) 4.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKAR1B NM_001164758.1 -?/. - c.1029G>T r.(?) p.(Gly343=)
HEATR2 NM_017802.3 -?/. - c.-176174C>A r.(?) p.(=)


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