Variant #0000340235 (NC_000011.9:g.533546G>A, LRRC56(NM_198075.3):c.-4481G>A)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.533546G>A
DNA change (hg38) g.533546G>A
Published as HRAS(NM_001318054.1):c.38C>T (p.T13I), HRAS(NM_176795.4):c.357C>T (p.D119=)
ISCN -
DB-ID HRAS_000008 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00103 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 -?/. - c.357C>T r.(?) p.(Asp119=)
C11orf35 NM_173573.2 -?/. - c.*21434C>T r.(=) p.(=)
LRRC56 NM_198075.3 -?/. - c.-4481G>A r.(?) p.(=)