Variant #0000307084 (NC_000003.11:g.49397668T>A, NM_001664.2:c.556A>T (RHOA))

Chromosome 3
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.49397668T>A
DNA change (hg38) g.49360235T>A
Published as RHOA(NM_001664.3):c.556A>T (p.K186*)
ISCN -
DB-ID RHOA_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-15 09:57:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPX1 NM_000581.2 ?/. - c.-1957A>T r.(?) p.(=)
RHOA NM_001664.2 ?/. - c.556A>T r.(?) p.(Lys186Ter)


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