Variant #0000017065 (NC_000001.10:g.46655129C>A, NC_000001.10(NM_001243766.1):c.1869+27G>T (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.46655129C>A
DNA change (hg38) g.46189457C>A
Published as -
ISCN -
DB-ID POMGNT1_000024 See all 7 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) 8.0E-5 View details
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 2025-03-15 12:20:58 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +?/. 21i c.1869+27G>T r.spl p.?
POMGNT1 NM_017739.3 +?/. 21i c.1895+1G>T r.spl p.?


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