Variant #0000520894 (NC_000003.11:g.9986194G>A, NM_015513.4:c.1194G>A (CRELD1))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9986194G>A
DNA change (hg38) g.9944510G>A
Published as CRELD1(NM_015513.4):c.1194G>A (p.A398=), CRELD1(NM_015513.6):c.1194G>A (p.A398=)
ISCN -
DB-ID CRELD1_000020 See all 3 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) 0.00064 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.1194G>A r.(?) p.(Ala398=)
PRRT3 NM_207351.3 -/. - c.*1717C>T r.(=) p.(=)


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