Variant #0001027168 (NC_000019.9:g.11666090_11666092del, NM_001111035.1:c.*19751_*19753del (ACP5))

Chromosome 19
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.11666090_11666092del
DNA change (hg38) -
Published as ELOF1(NM_001363675.4):c.-74-30_-74-28delTTT
ISCN -
DB-ID CNN1_000003
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACP5 NM_001111035.1 -?/. - c.*19751_*19753del r.(=) p.(=)
CNN1 NM_001299.4 -?/. - c.*5480_*5482del r.(=) p.(=)
ELOF1 NM_032377.3 -?/. - c.-18-894_-18-892del r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.