Variant #0000297258 (NC_000001.10:g.46656145C>T, NM_001243766.1:c.1649G>A (POMGNT1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.46656145C>T
DNA change (hg38) g.46190473C>T
Published as POMGNT1(NM_001243766.2):c.1649G>A (p.S550N)
ISCN -
DB-ID POMGNT1_000003 See all 5 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LURAP1 NM_001013615.2 +/. - c.-12954C>T r.(?) p.(=)
POMGNT1 NM_001243766.1 +/. - c.1649G>A r.(?) p.(Ser550Asn)
TSPAN1 NM_005727.3 +/. - c.*4940C>T r.(=) p.(=)
POMGNT1 NM_017739.3 +/. - c.1649G>A r.(?) p.(Ser550Asn)


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