Variant #0000929917 (NC_000011.9:g.533879G>A, NM_198075.3:c.-4148G>A (LRRC56))

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.533879G>A
DNA change (hg38) -
Published as HRAS(NM_005343.4):c.177C>T (p.A59=)
ISCN -
DB-ID C11orf35_000047
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) 0.00012 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 -?/. - c.177C>T r.(?) p.(=)
C11orf35 NM_173573.2 -?/. - c.*21101C>T r.(=) p.(=)
LRRC56 NM_198075.3 -?/. - c.-4148G>A r.(?) p.(=)


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