Genomic variant #0000439828

Individual ID 00208600
Chromosome 6
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.41903798C>A
DNA change (hg38) g.41936060C>A
Published as -
ISCN -
DB-ID CCND3_000001
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs33966734
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.01015 View details
Owner Xiang Jiao
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCND3 NM_001760.3 ?/. - c.759G>T r.(?) p.(Glu253Asp)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000209649 DNA SEQ-NG-I Blood - - 12 Xiang Jiao