Variant #0001037892 (NC_000010.10:g.32974964T>G, NM_024688.2:c.110T>G (C10orf68))

Chromosome 10
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.32974964T>G
DNA change (hg38) -
Published as CCDC7(NM_001321115.2):c.2189T>G (p.(Leu730*))
ISCN -
DB-ID C10orf68_000005
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
C10orf68 NM_024688.2 ?/. - c.110T>G r.(?) p.(Leu37*)
CCDC7 NM_145023.4 ?/. - c.*111601T>G r.(=) p.(=)


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