Variant #0000949718 (NC_000011.9:g.532724C>T, NM_198075.3:c.-5303C>T (LRRC56))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.532724C>T
DNA change (hg38) -
Published as HRAS(NM_005343.4):c.482G>A (p.R161H)
ISCN -
DB-ID C11orf35_000048
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) 2.0E-5 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 2023-11-27 17:35:39 +01:00 (CET)
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.482G>A r.(?) p.(Arg161His)
C11orf35 NM_173573.2 ?/. - c.*22256G>A r.(=) p.(=)
LRRC56 NM_198075.3 ?/. - c.-5303C>T r.(?) p.(=)


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