Variant #0000301209 (NC_000017.10:g.66518940G>A, NM_017565.3:c.*14678C>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.66518940G>A
DNA change (hg38) g.68522799G>A
Published as PRKAR1A(NM_001369389.1):c.221G>A (p.R74H), PRKAR1A(NM_002734.5):c.221G>A (p.R74H), PRKAR1A(NM_212471.2):c.221G>A (p.R74H)
ISCN -
DB-ID PRKAR1A_000025 See all 3 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) 0.00039 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 -?/. - c.*102336G>A r.(=) p.(=)
PRKAR1A NM_002734.4 -?/. - c.221G>A r.(?) p.(Arg74His)
ARSG NM_014960.4 -?/. - c.*102336G>A r.(=) p.(=)
FAM20A NM_017565.3 -?/. - c.*14678C>T r.(=) p.(=)
WIPI1 NM_017983.5 -?/. - c.-65378C>T r.(?) p.(=)


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