Variant #0000860914 (NC_000007.13:g.80302110del, NM_001001547.2:c.1150del (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.80302110del
DNA change (hg38) -
Published as CD36(NM_001001547.3):c.1150delG (p.A384Qfs*19), CD36(NM_001001548.2):c.1150delG (p.A384Qfs*19)
ISCN -
DB-ID CD36_000008 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) 0.00039 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +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     
CD36 NM_001001547.2 +/. - c.1150del r.(?) p.(Ala384GlnfsTer19)


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