Variant #0001037246 (NC_000009.11:g.134386835C>T, NM_007171.3:c.1033C>T (POMT1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.134386835C>T
DNA change (hg38) -
Published as POMT1(NM_001077365.2):c.967C>T (p.(Gln323*))
ISCN -
DB-ID UCK1_000043
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 +?/. - c.1033C>T r.(?) p.(Gln345*)
UCK1 NM_031432.2 +?/. - c.*13592G>A r.(=) p.(=)


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