Variant #0000536634 (NC_000009.11:g.134398416dup, NM_007171.3:c.2167dup (POMT1))

Chromosome 9
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.134398416dup
DNA change (hg38) g.131523029dup
Published as POMT1(NM_001077365.2):c.2101dup (p.(Asp701GlyfsTer8)), POMT1(NM_001136113.1):c.2101dupG (p.D701Gfs*8), POMT1(NM_001136113.2):c.2101dupG (p.D701Gfs*8)
ISCN -
DB-ID POMT1_000013 See all 26 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.2167dup r.(?) p.(Asp723GlyfsTer8)
UCK1 NM_031432.2 ?/. - c.*2014dup r.(?) p.(=)


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