Variant #0000039759 (NC_000001.10:g.46660273C>G, NM_001243766.1:c.703G>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.46660273C>G
DNA change (hg38) g.46194601C>G
Published as -
ISCN -
DB-ID POMGNT1_000154 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 2014-07-26 20:27:20 +02:00 (CEST)
Date last edited 2022-03-08 20:35:39 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMGNT1 NM_001243766.1 +?/. 8 c.703G>C r.(?) p.(Gly235Arg)
POMGNT1 NM_017739.3 +?/. - c.703G>C r.(?) p.(Gly235Arg)


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