Genomic variant #0000251317

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79202486A>G
DNA change (hg38) -
Published as FRAS1(NM_025074.6):c.1072-66A>G
ISCN -
DB-ID FRAS1_000286
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.27895 View details
Owner VKGL-NL




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
FRAS1 NM_025074.6 -/. - c.1072-66A>G benign r.(=) p.(=)