Variant #0000570846 (NC_000021.8:g.46702264C>T, NM_133635.4:c.638G>A (POFUT2))

Chromosome 21
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.46702264C>T
DNA change (hg38) g.45282349C>T
Published as POFUT2(NM_015227.5):c.638G>A (p.R213Q), POFUT2(NM_133635.4):c.638G>A (p.(Arg213Gln))
ISCN -
DB-ID POFUT2_000002 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) 0.00053 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POFUT2 NM_133635.4 ?/. - c.638G>A r.(?) p.(Arg213Gln)


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