Variant #0000243969 (NC_000014.8:g.72742931A>G, NM_000021.3:c.(953A>G) (PSEN1))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.72742931A>G
DNA change (hg38) g.72276223A>G
Published as -
ISCN -
DB-ID PSEN1_000205 See all 6 reported entries
Variant remarks Observed at equal frequencies in patients and unaffected controls.. /r/Point mutation in coding region predicting an amino acid substitution
Reference -
ClinVar ID -
dbSNP ID rs17125721
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +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     
PSEN1 NM_000021.3 -/? 9 c.(953A>G) r.(?) p.(Glu318Gly)


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