Variant #0000016652 (NC_000008.10:g.94798498G>C, NM_153704.5:c.1336G>C (TMEM67))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.94798498G>C
DNA change (hg38) g.93786270G>C
Published as -
ISCN -
DB-ID TMEM67_000018 See all 2 reported entries
Variant remarks -
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 2023-11-28 22:12:32 +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 +?/. 14 c.1336G>C r.(1336g>c) p.(Asp446His)


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