Variant #0000532707 (NC_000007.13:g.80292323_80292326dup, NM_001001547.2:c.447_450dup (CD36))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.80292323_80292326dup
DNA change (hg38) g.80663007_80663010dup
Published as CD36(NM_001001548.2):c.447_450dupTCAA (p.N151Sfs*14)
ISCN -
DB-ID CD36_000013
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 09:58:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD36 NM_001001547.2 +/. - c.447_450dup r.(?) p.(Asn151SerfsTer14)


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