Variant #0000017038 (NC_000001.10:g.46660031C>T, NM_001243766.1:c.794G>A (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.46660031C>T
DNA change (hg38) g.46194359C>T
Published as 935G>A (R265H)
ISCN -
DB-ID POMGNT1_000019 See all 10 reported entries
Variant remarks variants c.794G>A (Arg265His) and c.932G>A (Arg311Gln) segregate together, it is unclear which one is (or if both are) causative
Reference -
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-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 2022-03-08 20:36:51 +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 +?/. 9 c.794G>A r.(?) p.(Arg265His)
POMGNT1 NM_017739.3 +?/. - c.794G>A r.(?) p.(Arg265His)


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