Variant #0000999134 (NC_000011.9:g.532662T>C, NM_198075.3:c.-5365T>C (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.532662T>C
DNA change (hg38) -
Published as HRAS(NM_005343.2):c.544A>G (p.(Met182Val))
ISCN -
DB-ID C11orf35_000052
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.544A>G r.(?) p.(Met182Val)
C11orf35 NM_173573.2 ?/. - c.*22318A>G r.(=) p.(=)
LRRC56 NM_198075.3 ?/. - c.-5365T>C r.(?) p.(=)


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