Variant #0000530204 (NC_000007.13:g.103202327C>T, NM_005045.3:c.5284G>A (RELN))

Chromosome 7
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.103202327C>T
DNA change (hg38) g.103561880C>T
Published as RELN(NM_005045.3):c.5284G>A (p.(Val1762Ile)), RELN(NM_005045.4):c.5284G>A (p.V1762I), RELN(NM_173054.2):c.5284G>A (p.V1762I)
ISCN -
DB-ID RELN_000022 See all 10 reported entries
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) 0.00466 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RELN NM_005045.3 -?/. - c.5284G>A r.(?) p.(Val1762Ile)


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