Variant #0001005945 (NC_000022.10:g.21989092G>T, NM_152612.2:c.740G>T (CCDC116))

Chromosome 22
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.21989092G>T
DNA change (hg38) -
Published as CCDC116(NM_152612.2):c.740G>T (p.(Gly247Val))
ISCN -
DB-ID CCDC116_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) 0.00128 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 2024-08-28 13:16:32 +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     
YDJC NM_001017964.1 -?/. - c.-4789C>A r.(?) p.(=)
SDF2L1 NM_022044.2 -?/. - c.-7534G>T r.(?) p.(=)
CCDC116 NM_152612.2 -?/. - c.740G>T r.(?) p.(Gly247Val)


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