Variant #0001046667 (NC_000017.10:g.66511679A>G, NM_017565.3:c.*21939T>C (FAM20A))

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.66511679A>G
DNA change (hg38) -
Published as PRKAR1A(NM_002734.5):c.139A>G (p.M47V)
ISCN -
DB-ID FAM20A_000064
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +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.*95075A>G r.(=) p.(=)
PRKAR1A NM_002734.4 ?/. - c.139A>G r.(?) p.(Met47Val)
ARSG NM_014960.4 ?/. - c.*95075A>G r.(=) p.(=)
FAM20A NM_017565.3 ?/. - c.*21939T>C r.(=) p.(=)
WIPI1 NM_017983.5 ?/. - c.-58117T>C r.(?) p.(=)


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