Variant #0000924606 (NC_000007.13:g.103123324C>T, NM_005045.3:c.10276G>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.103123324C>T
DNA change (hg38) -
Published as RELN(NM_005045.4):c.10276G>A (p.V3426I)
ISCN -
DB-ID RELN_000344
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) 0.0003 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 2023-04-16 21:50:28 +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.10276G>A r.(?) p.(Val3426Ile)
SLC26A5 NM_198999.2 -?/. - c.-36962G>A r.(?) p.(=)


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