Variant #0001032104 (NC_000001.10:g.46660051_46660052del, NM_001243766.1:c.776_777del (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46660051_46660052del
DNA change (hg38) -
Published as POMGNT1(NM_017739.4):c.776_777del (p.(Thr259Argfs*14))
ISCN -
DB-ID LURAP1_000039
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LURAP1 NM_001013615.2 +?/. - c.-9048_-9047del r.(?) p.(=)
POMGNT1 NM_001243766.1 +?/. - c.776_777del r.(?) p.(Thr259Argfs*14)
POMGNT1 NM_017739.3 +?/. - c.776_777del r.(?) p.(Thr259Argfs*14)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.