Variant #0001053747 (NC_000011.9:g.533311_533330del, NM_198075.3:c.-4716_-4697del (LRRC56))

Chromosome 11
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.533311_533330del
DNA change (hg38) -
Published as HRAS(NM_001318054.2):c.169_188del (p.(Ser57Metfs*2))
ISCN -
DB-ID C11orf35_000063
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 -/. - c.450+132_450+151del r.(=) p.(=)
C11orf35 NM_173573.2 -/. - c.*21659_*21678del r.(=) p.(=)
LRRC56 NM_198075.3 -/. - c.-4716_-4697del r.(?) p.(=)


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