Variant #0000016636 (NC_000008.10:g.94767303A>G, NM_153704.5:c.161A>G (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.94767303A>G |
DNA change (hg38) |
g.93755075A>G |
Published as |
- |
ISCN |
- |
DB-ID |
TMEM67_000002 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 |
No license selected |
Created by |
Anne Polvi |
Date created |
2012-12-04 16:18:31 +01:00 (CET) |
Date last edited |
2023-11-27 23:52:15 +01:00 (CET) |

Variant on transcripts
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