Variant #0000976024 (NC_000003.11:g.9984830A>C, NM_015513.4:c.887A>C (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.9984830A>C
DNA change (hg38) -
Published as CRELD1(NM_001077415.3):c.887A>C (p.(Tyr296Ser))
ISCN -
DB-ID CRELD1_000042
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CRELD1 NM_015513.4 ?/. - c.887A>C r.(?) p.(Tyr296Ser)
PRRT3 NM_207351.3 ?/. - c.*3081T>G r.(=) p.(=)


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