Variant #0000808233 (NC_000017.10:g.66520112G>A, NC_000017.10(NM_002734.4):c.441-45G>A (PRKAR1A))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66520112G>A
DNA change (hg38) -
Published as PRKAR1A(NM_212471.2):c.441-45G>A
ISCN -
DB-ID FAM20A_000032
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) 0.00487 View details
Owner VKGL-NL_NKI
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_NKI
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -/. - c.*103508G>A r.(=) p.(=)
PRKAR1A NM_002734.4 -/. - c.441-45G>A r.(=) p.(=)
ARSG NM_014960.4 -/. - c.*103508G>A r.(=) p.(=)
FAM20A NM_017565.3 -/. - c.*13506C>T r.(=) p.(=)
WIPI1 NM_017983.5 -/. - c.-66550C>T r.(?) p.(=)


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