Variant #0000974280 (NC_000002.11:g.131098505G>C, NM_032357.2:c.406C>G (CCDC115))

Chromosome 2
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.131098505G>C
DNA change (hg38) -
Published as CCDC115(NM_032357.4):c.406C>G (p.(Gln136Glu))
ISCN -
DB-ID CCDC115_000009
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) 0.00027 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 2024-04-19 20:20:39 +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     
CCDC115 NM_032357.2 ?/. - c.406C>G r.(?) p.(Gln136Glu)
IMP4 NM_033416.1 ?/. - c.-2001G>C r.(?) p.(=)


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