Variant #0000001416 (NC_000006.11:g.74072453A>G, NM_001017361.2:c.1A>G (KHDC3L))

Chromosome 6
Allele Parent #1
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.74072453A>G
DNA change (hg38) g.73362730A>G
Published as -
ISCN -
DB-ID KHDC3L_000003
Variant remarks One of two mutations found in two sisters of Iranian origin with recurrent molar pregnancies (case B in Fallahian 2013)
Reference PubMed: Parry et al. 2011, PubMed: Fallahian et al. 2013
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
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 13:45:37 +02:00 (CEST)
Date last edited 2019-12-04 12:41:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KHDC3L NM_001017361.2 +/+ 1 c.1A>G r.(?) p.Met1Val


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