Variant #0000861902 (NC_000010.10:g.32832301A>T, NM_024688.2:c.-24823A>T (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.32832301A>T
DNA change (hg38) -
Published as CCDC7(NM_001321115.1):c.1067A>T (p.E356V)
ISCN -
DB-ID C10orf68_000003
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf68 NM_024688.2 ?/. - c.-24823A>T r.(?) p.(=)
CCDC7 NM_145023.4 ?/. - c.1067A>T r.(?) p.(Glu356Val)


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