Variant #0000964556 (NC_000007.13:g.286470_286503dup, NC_000007.13(NM_020223.3):c.953_956+30dup (FAM20C))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.286470_286503dup
DNA change (hg38) -
Published as FAM20C(NM_020223.3):c.953_956+30dup (p.(Ile320Ter)), FAM20C(NM_020223.4):NULL, FAM20C(NM_020223.4):c.956+5_956+6ins34, FAM20C(NM_020223.4):c.957_95...
ISCN -
DB-ID FAM20C_000027 See all 4 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM20C NM_020223.3 -/. - c.953_956+30dup r.spl? p.?


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