Variant #0000530160 (NC_000007.13:g.103130212_103130217del, NM_005045.3:c.9742_9747del (RELN))

Chromosome 7
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.103130212_103130217del
DNA change (hg38) g.103489765_103489770del
Published as -
ISCN -
DB-ID RELN_000193
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RELN NM_005045.3 ?/. - c.9742_9747del r.(?) p.(Ile3248_Cys3249del)
SLC26A5 NM_198999.2 ?/. - c.-43848_-43843del r.(?) p.(=)


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