Variant #0000505725 (NC_000001.10:g.227076719G>C, NM_000447.2:c.756G>C (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.227076719G>C
DNA change (hg38) g.226889018G>C
Published as PSEN2(NM_000447.2):c.756G>C (p.A252=), PSEN2(NM_000447.3):c.756G>C (p.A252=)
ISCN -
DB-ID PSEN2_000062 See all 3 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) 0.00554 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSEN2 NM_000447.2 -?/. - c.756G>C r.(?) p.(Ala252=)


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