Variant #0001003618 (NC_000017.10:g.66520205T>C, NM_017565.3:c.*13413A>G (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.66520205T>C
DNA change (hg38) -
Published as PRKAR1A(NM_001369389.1):c.489T>C (p.T163=)
ISCN -
DB-ID FAM20A_000055
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) 0.0002 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:16:32 +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.*103601T>C r.(=) p.(=)
PRKAR1A NM_002734.4 -?/. - c.489T>C r.(?) p.(=)
ARSG NM_014960.4 -?/. - c.*103601T>C r.(=) p.(=)
FAM20A NM_017565.3 -?/. - c.*13413A>G r.(=) p.(=)
WIPI1 NM_017983.5 -?/. - c.-66643A>G r.(?) p.(=)


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