Variant #0000540132 (NC_000010.10:g.61552768_61552773dup, NM_005436.4:c.1332_1337dup (CCDC6))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61552768_61552773dup
DNA change (hg38) g.59793010_59793015dup
Published as CCDC6(NM_005436.4):c.1332_1337dupACCTCC (p.P447_P448dup)
ISCN -
DB-ID CCDC6_000006
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC6 NM_005436.4 -/. - c.1332_1337dup r.(?) p.(Pro447_Pro448dup)


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