Variant #0000894221 (NC_000017.10:g.66596772_66596774dup, NM_017565.3:c.43_45dup (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.66596772_66596774dup
DNA change (hg38) -
Published as FAM20A(NM_017565.4):c.43_45dup (p.(Leu15dup)), FAM20A(NM_017565.4):c.43_45dupCTG (p.L15dup)
ISCN -
DB-ID FAM20A_000040 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM20A NM_017565.3 -?/. - c.43_45dup r.(?) p.(Leu15dup)


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