Variant #0000562864 (NC_000017.10:g.66526546C>T, NM_017565.3:c.*7072G>A (FAM20A))

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.66526546C>T
DNA change (hg38) g.68530405C>T
Published as PRKAR1A(NM_001276289.1):c.1102C>T (p.(Arg368Ter))
ISCN -
DB-ID PRKAR1A_000010 See all 21 reported entries
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 2019-07-18 18:22:55 +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.*109942C>T r.(=) p.(=)
PRKAR1A NM_002734.4 +?/. - c.1102C>T r.(?) p.(Arg368Ter)
ARSG NM_014960.4 +?/. - c.*109942C>T r.(=) p.(=)
FAM20A NM_017565.3 +?/. - c.*7072G>A r.(=) p.(=)
WIPI1 NM_017983.5 +?/. - c.-72984G>A r.(?) p.(=)


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