Variant #0001056155 (NC_000017.10:g.66519038_66519044del, NM_002734.4:c.319_325del (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.66519038_66519044del
DNA change (hg38) -
Published as PRKAR1A(NM_002734.5):c.319_325del (p.(Glu107Metfs*20))
ISCN -
DB-ID FAM20A_000065
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.*102434_*102440del r.(=) p.(=)
PRKAR1A NM_002734.4 +?/. - c.319_325del r.(?) p.(Glu107Metfs*20)
ARSG NM_014960.4 +?/. - c.*102434_*102440del r.(=) p.(=)
FAM20A NM_017565.3 +?/. - c.*14575_*14581del r.(=) p.(=)
WIPI1 NM_017983.5 +?/. - c.-65481_-65475del r.(?) p.(=)


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