Variant #0000393501 (NC_000023.10:g.68749709C>T, FAM155B(NM_015686.2):c.1329C>T)

Individual ID 00172759
Chromosome X
Allele Parent #1
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.68749709C>T
DNA change (hg38) g.69529866C>T
Published as T443T
ISCN -
DB-ID FAM155B_000012
Variant remarks found once, nonrecurrent change
Reference PubMed: Tarpey 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/208 cases
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.00047 View details
Owner Lucy Raymond
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM155B NM_015686.2 ?/. - c.1329C>T r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000173642 DNA SEQ - - WWC3 1 Lucy Raymond