Variant #0000321833 (NC_000011.9:g.532661A>G, LRRC56(NM_198075.3):c.-5366A>G)

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.532661A>G
DNA change (hg38) g.532661A>G
Published as HRAS(NM_001130442.1):c.545T>C (p.(Met182Thr))
ISCN -
DB-ID C11orf35_000001
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) 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.545T>C r.(?) p.(Met182Thr)
C11orf35 NM_173573.2 -?/. - c.*22319T>C r.(=) p.(=)
LRRC56 NM_198075.3 -?/. - c.-5366A>G r.(?) p.(=)