Variant #0000994441 (NC_000004.11:g.79173606C>T, NM_025074.6:c.370C>T (FRAS1))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79173606C>T
DNA change (hg38) -
Published as FRAS1(NM_025074.6):c.370C>T (p.(Arg124*)), FRAS1(NM_025074.7):c.370C>T (p.R124*)
ISCN -
DB-ID FRAS1_000025 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FRAS1 NM_025074.6 +/. - c.370C>T r.(?) p.(Arg124Ter)


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