Variant #0000016637 (NC_000008.10:g.94768004del, NC_000008.10(NM_153704.5):c.224-2del (TMEM67))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.94768004del
DNA change (hg38) g.93755776del
Published as IVS1-2delA
ISCN -
DB-ID TMEM67_000003 See all 2 reported entries
Variant remarks RNA skips exon 2
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-12-04 16:18:31 +01:00 (CET)
Date last edited 2023-11-29 12:56:19 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM67 NM_153704.5 +/. 1i c.224-2del r.224_312del p.Gly75Glufs*15


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