Variant #0000345871 (NC_000008.10:g.94784818G>C, NM_153704.5:c.653G>C (TMEM67))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.94784818G>C
DNA change (hg38) g.93772590G>C
Published as TMEM67(NM_153704.5):c.653G>C (p.G218A), TMEM67(NM_153704.6):c.653G>C (p.(Gly218Ala))
ISCN -
DB-ID TMEM67_000073 See all 5 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) 0.00016 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM67 NM_153704.5 ?/. - c.653G>C r.(?) p.(Gly218Ala)


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