Variant #0000016953 (NC_000006.11:g.74072455G>T, NM_001017361.2:c.3G>T (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.74072455G>T
DNA change (hg38) g.73362732G>T
Published as -
ISCN -
DB-ID KHDC3L_000001
Variant remarks Mutations found in proband and aunt of Pakistani origin with recurrent molar pregnancies (family L in Parry 2011)
Reference PubMed: Parry et al. 2011
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Rosemary Fisher
Database submission license No license selected
Created by Rosemary Fisher
Date created 2012-12-18 17:30:47 +01:00 (CET)
Date last edited 2019-12-04 12:41:11 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KHDC3L NM_001017361.2 +/+ 1 c.3G>T r.(?) p.Met1Ile


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