Variant #0001066869 (NC_000017.10:g.66533742C>T, NM_002734.4:c.*7152C>T (PRKAR1A))

Chromosome 17
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.66533742C>T
DNA change (hg38) -
Published as FAM20A(NM_017565.4):c.1502G>A (p.(Arg501Lys))
ISCN -
DB-ID chr17_011059
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*117138C>T r.(=) p.(=)
PRKAR1A NM_002734.4 ?/. - c.*7152C>T r.(=) p.(=)
ARSG NM_014960.4 ?/. - c.*117138C>T r.(=) p.(=)
FAM20A NM_017565.3 ?/. - c.1502G>A r.(?) p.(Arg501Lys)
WIPI1 NM_017983.5 ?/. - c.-80180G>A r.(?) p.(=)


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