Variant #0000860575 (NC_000007.13:g.103138569G>A, NM_005045.3:c.8798C>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.103138569G>A
DNA change (hg38) -
Published as RELN(NM_005045.3):c.8798C>T (p.T2933I), RELN(NM_005045.4):c.8798C>T (p.T2933I)
ISCN -
DB-ID RELN_000326 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) 0.00021 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RELN NM_005045.3 ?/. - c.8798C>T r.(?) p.(Thr2933Ile)
SLC26A5 NM_198999.2 ?/. - c.-52207C>T r.(?) p.(=)


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