Variant #0000544556 (NC_000011.9:g.534286C>A, LRRC56(NM_198075.3):c.-3741C>A)

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.534286C>A
DNA change (hg38) g.534286C>A
Published as HRAS(NM_001130442.1):c.37G>T (p.(Gly13Cys))
ISCN -
DB-ID HRAS_000011 See all 4 reported entries
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) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 +/. - c.37G>T r.(?) p.(Gly13Cys)
C11orf35 NM_173573.2 +/. - c.*20694G>T r.(=) p.(=)
LRRC56 NM_198075.3 +/. - c.-3741C>A r.(?) p.(=)