Genomic variant #0000116246

Individual ID 00072656
Chromosome 1
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Probably affects function
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.241669362C>A
DNA change (hg38) g.241506062C>A
Published as Gly239Val, G239V
ISCN -
DB-ID FH_000054 See all 3 reported entries
Variant remarks UK, not found in 300 chrom
Reference PubMed: Tomlinson, PubMed: Alam
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 Jean-Pierre Bayley
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
FH NM_000143.3 ?/+? 6 c.845G>T r.(?) p.(Gly282Val) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000072813 DNA SEQ;SSCA;CSGE - - FH 1 Jean-Pierre Bayley