Variant #0000436607 (NC_000015.9:g.38591632T>A, SPRED1(NM_152594.2):c.91T>A)

Individual ID 00205929
Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.38591632T>A
DNA change (hg38) g.38299431T>A
Published as -
ISCN -
DB-ID SPRED1_000140
Variant remarks Domain: EVH-1
Reference Messiaen UAB, unpublished novel mutation
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Ludwine Messiaen
Database submission license No license selected
Created by Ludwine Messiaen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPRED1 NM_152594.2 ?/? 2 c.91T>A r.91u>a p.Trp31Arg



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000206959 DNA SEQ blood - SPRED1 1 Ludwine Messiaen