Variant #0000017049 (NC_000001.10:g.46652588_46657586del, NM_001243766.1:c.1539+184_*38{0} (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.46652588_46657586del
DNA change (hg38) g.46186916_46191914del
Published as -
ISCN -
DB-ID POMGNT1_000113 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2013-01-31 14:09:45 +01:00 (CET)
Date last edited 2025-03-14 20:01:46 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +/. 17i_23_ c.1539+184_*38{0} r.? p.?
POMGNT1 NM_017739.3 +/. 17i_22_ c.1539+184_*589{0} r.? p.?


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