Variant #0000658478 (NC_000019.9:g.11666091_11666092del, NM_001111035.1:c.*19752_*19753del (ACP5))

Chromosome 19
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.11666091_11666092del
DNA change (hg38) g.11555276_11555277del
Published as ELOF1(NM_001363675.2):c.-11-29_-11-28delTT
ISCN -
DB-ID CNN1_000002 See all 2 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +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     
ACP5 NM_001111035.1 -/. - c.*19752_*19753del r.(=) p.(=)
CNN1 NM_001299.4 -/. - c.*5481_*5482del r.(=) p.(=)
ELOF1 NM_032377.3 -/. - c.-18-893_-18-892del r.(=) p.(=)


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