Variant #0000017040 (NC_000001.10:g.46658200C>G, NM_001243766.1:c.1274G>C (POMGNT1))

Chromosome 1
Allele Both (homozygous)
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.46658200C>G
DNA change (hg38) g.46192528C>G
Published as -
ISCN -
DB-ID POMGNT1_000012 See all 6 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) 0 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 2022-03-08 19:38:46 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +?/. 15 c.1274G>C r.(?) p.(Trp425Ser)
POMGNT1 NM_017739.3 +?/. - c.1274G>C r.(?) p.(Trp425Ser)


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