Variant #0000544657 (NC_000011.9:g.58920304_58920307del, NM_001312909.1:c.1163_1166del (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.58920304_58920307del
DNA change (hg38) g.59152831_59152834del
Published as FAM111A(NM_001142519.1):c.1163_1166del (p.(Asp388Alafs*7))
ISCN -
DB-ID FAM111A_000005
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 2019-07-18 18:22:55 +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.1163_1166del r.(?) p.(Asp388AlafsTer7)
FAM111A NM_022074.3 ?/. - c.1163_1166del r.(?) p.(Asp388AlafsTer7)


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