Variant #0000530263 (NC_000007.13:g.103292201G>A, NM_005045.3:c.1799C>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.103292201G>A
DNA change (hg38) g.103651754G>A
Published as RELN(NM_005045.3):c.1799C>T (p.(Ser600Phe)), RELN(NM_005045.4):c.1799C>T (p.S600F), RELN(NM_173054.2):c.1799C>T (p.S600F)
ISCN -
DB-ID RELN_000247 See all 4 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) 0.01068 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 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.1799C>T r.(?) p.(Ser600Phe)


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