Variant #0000253358 (NC_000011.9:g.534242A>G, LRRC56(NM_198075.3):c.-3785A>G)

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.534242A>G
DNA change (hg38) g.534242A>G
Published as HRAS(NM_005343.2):c.81T>C (p.H27=), HRAS(NM_176795.4):c.81T>C (p.H27=)
ISCN -
DB-ID HRAS_000017 See all 2 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) 0.3157 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 -/. - c.81T>C r.(?) p.(His27=)
C11orf35 NM_173573.2 -/. - c.*20738T>C r.(=) p.(=)
LRRC56 NM_198075.3 -/. - c.-3785A>G r.(?) p.(=)