Variant #0000001417 (NC_000006.11:g.74072970_74072973del, NM_001017361.2:c.322_325del (KHDC3L))

Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74072970_74072973del
DNA change (hg38) g.73363247_73363250del
Published as -
ISCN -
DB-ID KHDC3L_000002
Variant remarks Mutation found in individual of Tunisian origin with recurrent molar pregnancies (family T in Parry 2011)
Reference PubMed: Parry et al. 2011
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rosemary Fisher
Database submission license No license selected
Created by Rosemary Fisher
Date created 2012-07-17 13:57:58 +02:00 (CEST)
Date last edited 2020-06-19 14:59:46 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KHDC3L NM_001017361.2 +/+ 2 c.322_325del r.(?) p.(Asp108Ilefs*30)


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