Genomic variant #0000016464

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.15572069T>C
DNA change (hg38) g.15570446T>C
Published as W1182R
ISCN -
DB-ID CC2D2A_000022 See all 2 reported entries
Variant remarks 1 British MKS6 family (com-het)
Reference PubMed: Otto et al. 2011
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency 33/4111 CON het
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Anne Polvi




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
CC2D2A NM_001080522.2 +?/+? 31 c.3544T>C - r.(3544u>c) p.(Trp1182Arg)