Variant #0000548244 (NC_000012.11:g.49319208_49319225del, NM_033124.4:c.*3982_*3999del (CCDC65))

Chromosome 12
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.49319208_49319225del
DNA change (hg38) g.48925425_48925442del
Published as FKBP11(NM_001143781.1):c.-777_-760del (p.(=))
ISCN -
DB-ID CCDC65_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKBP11 NM_016594.2 ?/. - c.-11_7del r.? p.?
CCDC65 NM_033124.4 ?/. - c.*3982_*3999del r.(=) p.(=)


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