Variant #0001063062 (NC_000001.10:g.46658049_46658053dup, NM_001243766.1:c.1350_1354dup (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46658049_46658053dup
DNA change (hg38) -
Published as POMGNT1(NM_001243766.1):c.1350_1354dup (p.(Val452AlafsTer59))
ISCN -
DB-ID LURAP1_000042
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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LURAP1 NM_001013615.2 ?/. - c.-11050_-11046dup r.(?) p.(=)
POMGNT1 NM_001243766.1 ?/. - c.1350_1354dup r.(?) p.(Val452Alafs*59)
POMGNT1 NM_017739.3 ?/. - c.1350_1354dup r.(?) p.(Val452Alafs*59)


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