Variant #0000281131 (NC_000003.11:g.49394834G>A, NM_001664.2:c.*2808C>T (RHOA))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49394834G>A
DNA change (hg38) g.49357401G>A
Published as GPX1(NM_000581.4):c.599C>T (p.P200L)
ISCN -
DB-ID GPX1_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) 0.28072 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.599C>T r.(?) p.?
RHOA NM_001664.2 -/. - c.*2808C>T r.(=) p.(=)


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