Variant #0001014464 (NC_000008.10:g.94777845A>T, NM_153704.5:c.622A>T (TMEM67))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.94777845A>T
DNA change (hg38) -
Published as TMEM67(NM_153704.5):c.622A>T (p.R208*, p.(Arg208*)), TMEM67(NM_153704.6):c.622A>T (p.R208*)
ISCN -
DB-ID TMEM67_000006 See all 23 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00018 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM67 NM_153704.5 +/. - c.622A>T r.(?) p.(Arg208Ter)


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