Variant #0000799406 (NC_000001.10:g.46662482C>A, NM_001243766.1:c.275G>T (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.46662482C>A
DNA change (hg38) -
Published as POMGNT1(NM_001243766.1):c.275G>T (p.G92V)
ISCN -
DB-ID POMGNT1_000178
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.-6617C>A r.(?) p.(=)
POMGNT1 NM_001243766.1 ?/. - c.275G>T r.(?) p.(Gly92Val)
POMGNT1 NM_017739.3 ?/. - c.275G>T r.(?) p.(Gly92Val)


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