Variant #0000017180 (NC_000006.11:g.74072947_74072950del, NM_001017361.2:c.299_302del (KHDC3L))

Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74072947_74072950del
DNA change (hg38) g.73363224_73363227del
Published as -
ISCN -
DB-ID KHDC3L_000004
Variant remarks Mutation found in individual of African-American origin with recurrent molar pregnancies (MoUS70 in Reddy 2013)
Reference PubMed: Reddy et al. 2013
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 2013-03-14 10:16:36 +01:00 (CET)
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.299_302del r.(?) p.Ile100Argfs*2


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