Variant #0000277779 (NC_000011.9:g.533311G>C, LRRC56(NM_198075.3):c.-4716G>C)

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.533311G>C
DNA change (hg38) g.533311G>C
Published as HRAS(NM_176795.4):c.498C>G (p.P166=)
ISCN -
DB-ID HRAS_000004
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) 6.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 -?/. - c.450+142C>G r.(=) p.(=)
C11orf35 NM_173573.2 -?/. - c.*21669C>G r.(=) p.(=)
LRRC56 NM_198075.3 -?/. - c.-4716G>C r.(?) p.(=)