Variant #0000520890 (NC_000003.11:g.9985774A>G, NC_000003.11(NM_015513.4):c.1049-275A>G (CRELD1))

Chromosome 3
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.9985774A>G
DNA change (hg38) g.9944090A>G
Published as CRELD1(NM_001031717.3):c.1237A>G (p.I413V)
ISCN -
DB-ID CRELD1_000017
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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRELD1 NM_015513.4 ?/. - c.1049-275A>G r.(=) p.(=)
PRRT3 NM_207351.3 ?/. - c.*2137T>C r.(=) p.(=)


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