Variant #0000617800 (NC_000019.9:g.50143203C>T, NM_021228.2:c.-2303C>T (SCAF1))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.50143203C>T
DNA change (hg38) g.49639946C>T
Published as RRAS(NM_006270.4):c.153G>A (p.Q51=)
ISCN -
DB-ID RRAS_000009
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 10:45:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RRAS NM_006270.3 ?/. - c.153G>A r.(?) p.(Gln51=)
SCAF1 NM_021228.2 ?/. - c.-2303C>T r.(?) p.(=)


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