Variant #0000889983 (NC_000011.9:g.534286C>G, NM_198075.3:c.-3741C>G (LRRC56))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.534286C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID C11orf35_000043
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 +/. - c.37G>C r.(?) p.(Gly13Arg)
C11orf35 NM_173573.2 +/. - c.*20694G>C r.(=) p.(=)
LRRC56 NM_198075.3 +/. - c.-3741C>G r.(?) p.(=)


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