Variant #0000853030 (NC_000011.9:g.533506G>A, NM_198075.3:c.-4521G>A (LRRC56))

Chromosome 11
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.533506G>A
DNA change (hg38) -
Published as HRAS(NM_176795.4):c.397C>T (p.L133F)
ISCN -
DB-ID C11orf35_000040
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 ?/. - c.397C>T r.(?) p.(Leu133Phe)
C11orf35 NM_173573.2 ?/. - c.*21474C>T r.(=) p.(=)
LRRC56 NM_198075.3 ?/. - c.-4521G>A r.(?) p.(=)


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