Variant #0000306947 (NC_000007.13:g.103292176G>A, NM_005045.3:c.1824C>T (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.103292176G>A
DNA change (hg38) g.103651729G>A
Published as RELN(NM_005045.3):c.1824C>T (p.C608=), RELN(NM_005045.4):c.1824C>T (p.C608=)
ISCN -
DB-ID RELN_000134 See all 2 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) 0.00111 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.1824C>T r.(?) p.(Cys608=)


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