Variant #0000655039 (NC_000003.11:g.9982571C>T, NM_015513.4:c.498C>T (CRELD1))

Chromosome 3
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.9982571C>T
DNA change (hg38) g.9940887C>T
Published as CRELD1(NM_015513.4):c.498C>T (p.Y166=)
ISCN -
DB-ID CRELD1_000038
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) 0.00038 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-06-12 11:25:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRELD1 NM_015513.4 -?/. - c.498C>T r.(?) p.(Tyr166=)
PRRT3 NM_207351.3 -?/. - c.*5340G>A r.(=) p.(=)


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