Variant #0000289183 (NC_000011.9:g.534332G>A, LRRC56(NM_198075.3):c.-3695G>A)

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.534332G>A
DNA change (hg38) g.534332G>A
Published as HRAS(NM_005343.2):c.-10C>T, HRAS(NM_176795.4):c.-10C>T, HRAS(NM_176795.5):c.-10C>T
ISCN -
DB-ID HRAS_000018 See all 3 reported entries
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) 0.04401 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 -/. - c.-10C>T r.(?) p.(=)
C11orf35 NM_173573.2 -/. - c.*20648C>T r.(=) p.(=)
LRRC56 NM_198075.3 -/. - c.-3695G>A r.(?) p.(=)