Variant #0000862592 (NC_000011.9:g.58919627_58919630del, NM_001312909.1:c.486_489del (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.58919627_58919630del
DNA change (hg38) -
Published as FAM111A(NM_001142519.1):c.483_486del (p.(Lys163Argfs*87))
ISCN -
DB-ID FAM111A_000013
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM111A NM_001312909.1 ?/. - c.486_489del r.(?) p.(Lys163Argfs*87)
FAM111A NM_022074.3 ?/. - c.486_489del r.(?) p.(Lys163Argfs*87)


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