Variant #0000568019 (NC_000019.9:g.50143211A>G, NM_021228.2:c.-2295A>G (SCAF1))

Chromosome 19
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.50143211A>G
DNA change (hg38) g.49639954A>G
Published as RRAS(NM_006270.3):c.145T>C (p.(Phe49Leu)), RRAS(NM_006270.5):c.145T>C (p.F49L)
ISCN -
DB-ID RRAS_000001 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) 0.00072 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRAS NM_006270.3 -?/. - c.145T>C r.(?) p.(Phe49Leu)
SCAF1 NM_021228.2 -?/. - c.-2295A>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.