Variant #0000017043 (NC_000001.10:g.46658069G>A, NM_001243766.1:c.1324C>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.46658069G>A
DNA change (hg38) g.46192397G>A
Published as 1465C>T, R442C
ISCN -
DB-ID POMGNT1_000007 See all 14 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 2025-03-13 07:53:52 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +?/. 16 c.1324C>T r.(?) p.(Arg442Cys)
POMGNT1 NM_017739.3 +?/. - c.1324C>T r.(?) p.(Arg442Cys)


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