Variant #0000017957 (NC_000001.10:g.46659545C>T, NM_001243766.1:c.932G>A (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46659545C>T
DNA change (hg38) g.46193873C>T
Published as 1073G>A (R311Q)
ISCN -
DB-ID POMGNT1_000008 See all 11 reported entries
Variant remarks variants c.794G>A (Arg265His) and c.932G>A (Arg311Gln) segregate together
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-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 2013-04-22 14:03:10 +02:00 (CEST)
Date last edited 2022-03-08 20:39:46 +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 -?/. 10 c.932G>A r.(?) p.(Arg311Gln)
POMGNT1 NM_017739.3 -?/. - c.932G>A r.(?) p.(Arg311Gln)


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