Variant #0001007194 (NC_000011.9:g.61160035G>T, NM_001173990.2:c.-69G>T (TMEM216))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.61160035G>T
DNA change (hg38) g.61392563G>T
Published as -
ISCN -
DB-ID TMEM216_000026 See all 46 reported entries
Variant remarks luciferase reporter gene assay showed reduced promotor activity
Reference PubMed: Malka 2024
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-09-10 16:32:58 +02:00 (CEST)
Date last edited 2024-09-10 16:35:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM216 NM_001173990.2 +/. _1 c.-69G>T r.=|red p.=|red


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