Variant #0000801714 (NC_000004.11:g.79188491G>A, NM_025074.6:c.886G>A (FRAS1))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.79188491G>A
DNA change (hg38) -
Published as FRAS1(NM_001166133.1):c.886G>A (p.(Glu296Lys)), FRAS1(NM_025074.7):c.886G>A (p.E296K)
ISCN -
DB-ID FRAS1_000043 See all 4 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) 0.00096 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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.886G>A r.(?) p.(Glu296Lys)


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