Variant #0000717118 (NC_000001.10:g.207940495_207940500del, NM_002389.4:c.811_816del (CD46))

Chromosome 1
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.207940495_207940500del
DNA change (hg38) -
Published as CD46(NM_002389.4):c.811_816delGACAGT (p.D271_S272del), CD46(NM_172351.2):c.811_816delGACAGT (p.(Asp271_Ser272del))
ISCN -
DB-ID CD46_000037 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) 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD46 NM_002389.4 ?/. - c.811_816del r.(?) p.(Asp271_Ser272del)


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