Variant #0000805982 (NC_000012.11:g.94072701C>A, NM_003805.3:c.151C>A (CRADD))

Chromosome 12
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.94072701C>A
DNA change (hg38) -
Published as CRADD(NM_001320099.1):c.151C>A (p.L51I), CRADD(NM_003805.5):c.151C>A (p.L51I)
ISCN -
DB-ID CRADD_000001 See all 2 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) 0.00126 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 2021-09-17 14:40:49 +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     
CRADD NM_003805.3 -?/. - c.151C>A r.(?) p.(Leu51Ile)


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