Variant #0000320701 (NC_000001.10:g.27877964_27877975del, NM_001029882.2:c.659_670del (AHDC1))

Chromosome 1
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.27877964_27877975del
DNA change (hg38) g.27551453_27551464del
Published as AHDC1(NM_001029882.2):c.659_670del (p.(Ala220_Thr223del))
ISCN -
DB-ID AHDC1_000014
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AHDC1 NM_001029882.2 ?/. - c.659_670del r.(?) p.(Ala220_Thr223del)


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