Variant #0001022237 (NC_000001.10:g.54272211C>T, NC_000001.10(NM_018087.4):c.892-21G>A (TMEM48))

Chromosome 1
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.54272211C>T
DNA change (hg38) g.53806538C>T
Published as -
ISCN -
DB-ID TMEM48_000003 See all 5 reported entries
Variant remarks in vitro analysis 293T cells mini-gene exon trapping assay: effect on RNA exon skipping
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Tjakko van Ham
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-11-05 16:15:00 +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     
TMEM48 NM_018087.4 ?/. 8i c.892-21G>A r.[892_984del,=] p.Ala298_Lys328del


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