Variant #0000911143 (NC_000001.10:g.84670162C>T, NC_000001.10(NM_182948.2):c.906+1674C>T (PRKACB))

Chromosome 1
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.84670162C>T
DNA change (hg38) -
Published as PRKACB(NM_001300915.2):c.784C>T (p.(Gln262*)), PRKACB(NM_182948.4):c.906+1674C>T
ISCN -
DB-ID PRKACB_000005 See all 2 reported entries
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) 5.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKACB NM_182948.2 ?/. - c.906+1674C>T r.(=) p.(=)


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