Genomic variant #0000086041

Individual ID 00056050
Chromosome 4
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.15559104C>T
DNA change (hg38) g.15557481C>T
Published as -
ISCN -
DB-ID CC2D2A_000030
Variant remarks -
Reference PubMed: Watson 2016, Journal: Watson 2016
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Christopher Watson




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
CC2D2A NM_001080522.2 +/. 22 c.2803C>T - r.(?) p.(Arg935*)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000056005 DNA SEQ-NG - - - 2 Christopher Watson