Variant #0000611916 (NC_000009.11:g.134395539del, NM_007171.3:c.1723del (POMT1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.134395539del
DNA change (hg38) g.131520152del
Published as POMT1(NM_001353198.2):c.1561delC (p.L521Wfs*23)
ISCN -
DB-ID UCK1_000024
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 +/. - c.1723del r.(?) p.(Leu575TrpfsTer23)
UCK1 NM_031432.2 +/. - c.*4890del r.(?) p.(=)


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