Variant #0000655040 (NC_000003.11:g.9985640T>A, NC_000003.11(NM_015513.4):c.1049-409T>A (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.9985640T>A
DNA change (hg38) g.9943956T>A
Published as CRELD1(NM_001031717.4):c.1103T>A (p.L368*)
ISCN -
DB-ID CRELD1_000039
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.1049-409T>A r.(=) p.(=)
PRRT3 NM_207351.3 ?/. - c.*2271A>T r.(=) p.(=)


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