Variant #0000717836 (NC_000002.11:g.131098577C>A, NM_032357.2:c.334G>T (CCDC115))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.131098577C>A
DNA change (hg38) -
Published as CCDC115(NM_001321118.1):c.319G>T (p.E107*)
ISCN -
DB-ID CCDC115_000007
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC115 NM_032357.2 +/. - c.334G>T r.(?) p.(Glu112*)
IMP4 NM_033416.1 +/. - c.-1929C>A r.(?) p.(=)


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