Variant #0000678760 (NC_000010.10:g.104176651G>A, NM_001270965.1:c.145C>T (PSD))

Chromosome 10
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.104176651G>A
DNA change (hg38) -
Published as PSD(NM_001270965.1):c.145C>T (p.R49*)
ISCN -
DB-ID FBXL15_000017
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSD NM_001270965.1 ?/. - c.145C>T r.(?) p.(Arg49Ter)
FBXL15 NM_024326.3 ?/. - c.-4236G>A r.(?) p.(=)


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