Variant #0001003619 (NC_000017.10:g.66538952T>C, NC_000017.10(NM_017565.3):c.813-2A>G (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.66538952T>C
DNA change (hg38) -
Published as PRKAR1A(NM_001276290.1):c.974-8273T>C (p.?)
ISCN -
DB-ID FAM20A_000002 See all 2 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) 1.0E-5 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 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     
PRKAR1A NM_002734.4 ?/. - c.*12362T>C r.(=) p.(=)
FAM20A NM_017565.3 ?/. - c.813-2A>G r.spl? p.?


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