Variant #0001042135 (NC_000017.10:g.66538124_66538127del, NC_000017.10(NM_017565.3):c.1109+3_1109+6del (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.66538124_66538127del
DNA change (hg38) -
Published as FAM20A(NM_017565.4):c.1109+3_1109+6del
ISCN -
DB-ID FAM20A_000061
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKAR1A NM_002734.4 ?/. - c.*11534_*11537del r.(=) p.(=)
FAM20A NM_017565.3 ?/. - c.1109+3_1109+6del r.(?) p.(Glu369Glyfs*12)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.