Variant #0000681721 (NC_000021.8:g.42540264C>T, NM_182832.2:c.*10839G>A (PLAC4))

Chromosome 21
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.42540264C>T
DNA change (hg38) -
Published as BACE2(NM_138991.2):c.74C>T (p.A25V)
ISCN -
DB-ID BACE2_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BACE2 NM_012105.3 -?/. - c.74C>T r.(?) p.(Ala25Val)
PLAC4 NM_182832.2 -?/. - c.*10839G>A r.(=) p.(=)


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