Variant #0000064953 (NC_000018.9:g.2700919A>G, NC_000018.9(NM_015295.2):c.1647+3A>G (SMCHD1))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (!)
DNA change (genomic) (Relative to hg19 / GRCh37) g.2700919A>G
DNA change (hg38) g.2700921A>G
Published as -
ISCN -
DB-ID SMCHD1_000004 See all 2 reported entries
Variant remarks -
Reference Winder, US
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Tom Winder
Database submission license No license selected
Created by Tom Winder
Date created 2014-06-27 18:57:10 +02:00 (CEST)
Date last edited 2020-07-14 16:22:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
SMCHD1 NM_015295.2 +?/. 13i c.1647+3A>G - r.spl? p.?



Screenings

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