Variant #0001042133 (NC_000017.10:g.66519090G>A, NM_017565.3:c.*14528C>T (FAM20A))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66519090G>A
DNA change (hg38) -
Published as PRKAR1A(NM_002734.5):c.348+23G>A
ISCN -
DB-ID FAM20A_000059
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) 0.00036 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 2025-05-05 21:14:00 +02:00 (CEST)
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.*102486G>A r.(=) p.(=)
PRKAR1A NM_002734.4 -?/. - c.348+23G>A r.(=) p.(=)
ARSG NM_014960.4 -?/. - c.*102486G>A r.(=) p.(=)
FAM20A NM_017565.3 -?/. - c.*14528C>T r.(=) p.(=)
WIPI1 NM_017983.5 -?/. - c.-65528C>T r.(?) p.(=)


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