Variant #0000544555 (NC_000011.9:g.533874T>C, LRRC56(NM_198075.3):c.-4153T>C)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.533874T>C
DNA change (hg38) g.533874T>C
Published as -
ISCN -
DB-ID C11orf35_000002
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_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.182A>G r.(?) p.(Gln61Arg)
C11orf35 NM_173573.2 +?/. - c.*21106A>G r.(=) p.(=)
LRRC56 NM_198075.3 +?/. - c.-4153T>C r.(?) p.(=)