Variant #0000722314 (NC_000009.11:g.134381562del, NM_007171.3:c.184del (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.134381562del
DNA change (hg38) -
Published as POMT1(NM_001077365.2):c.184del (p.(Asp62Metfs*18)), POMT1(NM_007171.4):c.184delG (p.D62Mfs*18)
ISCN -
DB-ID UCK1_000030 See all 2 reported entries
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.184del r.(?) p.(Asp62Metfs*18)
UCK1 NM_031432.2 +/. - c.*18866del r.(?) p.(=)


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