Variant #0000297641 (NC_000007.13:g.103629727G>A, NM_005045.3:c.77C>T (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.103629727G>A
DNA change (hg38) g.103989280G>A
Published as RELN(NM_005045.3):c.77C>T (p.A26V), RELN(NM_005045.4):c.77C>T (p.A26V)
ISCN -
DB-ID RELN_000161 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) 0.00033 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RELN NM_005045.3 ?/. - c.77C>T r.(?) p.(Ala26Val)


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