Variant #0001050105 (NC_000001.10:g.46657853G>C, NM_001243766.1:c.1456C>G (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.46657853G>C
DNA change (hg38) -
Published as POMGNT1(NM_017739.3):c.1456C>G (p.R486G)
ISCN -
DB-ID POMGNT1_000163 See all 2 reported entries
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2025-11-01 13:22:20 +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.-11246G>C r.(?) p.(=)
POMGNT1 NM_001243766.1 ?/. - c.1456C>G r.(?) p.(Arg486Gly)
POMGNT1 NM_017739.3 ?/. - c.1456C>G r.(?) p.(Arg486Gly)


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