Variant #0000548238 (NC_000012.11:g.49308242G>A, NM_033124.4:c.356G>A (CCDC65))

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.49308242G>A
DNA change (hg38) g.48914459G>A
Published as CCDC65(NM_033124.4):c.356G>A (p.(Ser119Asn))
ISCN -
DB-ID CCDC65_000002
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKBP11 NM_016594.2 -?/. - c.*7525C>T r.(=) p.(=)
CCDC65 NM_033124.4 -?/. - c.356G>A r.(?) p.(Ser119Asn)


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