Variant #0000016653 (NC_000008.10:g.94798513C>T, NM_153704.5:c.1351C>T (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.94798513C>T
DNA change (hg38) g.93786285C>T
Published as 1351C>T: R451X
ISCN -
DB-ID TMEM67_000019 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs116647652
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
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 13:02:47 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM67 NM_153704.5 +/. 13 c.1351C>T r.(1351c>u) p.(Arg451*)


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