Variant #0000505721 (NC_000001.10:g.227071475C>T, NM_000447.2:c.211C>T (PSEN2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.227071475C>T
DNA change (hg38) g.226883774C>T
Published as PSEN2(NM_000447.2):c.211C>T (p.R71W), PSEN2(NM_000447.3):c.211C>T (p.R71W)
ISCN -
DB-ID PSEN2_000021 See all 7 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) 0.00369 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSEN2 NM_000447.2 -?/. - c.211C>T r.(?) p.(Arg71Trp)


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