Variant #0001066868 (NC_000017.10:g.66521052G>A, NC_000017.10(NM_002734.4):c.503-1G>A (PRKAR1A))

Chromosome 17
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.66521052G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr17_011058
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 +?/. - c.*104448G>A r.(=) p.(=)
PRKAR1A NM_002734.4 +?/. - c.503-1G>A r.spl? p.?
ARSG NM_014960.4 +?/. - c.*104448G>A r.(=) p.(=)
FAM20A NM_017565.3 +?/. - c.*12566C>T r.(=) p.(=)
WIPI1 NM_017983.5 +?/. - c.-67490C>T r.(?) p.(=)


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