Variant #0001026032 (NC_000011.9:g.58920855_58920857del, NM_001312909.1:c.1714_1716del (FAM111A))

Chromosome 11
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.58920855_58920857del
DNA change (hg38) -
Published as FAM111A(NM_022074.4):c.1714_1716delATT (p.I572del)
ISCN -
DB-ID FAM111A_000024
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM111A NM_001312909.1 ?/. - c.1714_1716del r.(?) p.(Ile572del)
FAM111A NM_022074.3 ?/. - c.1714_1716del r.(?) p.(Ile572del)


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