Variant #0000999136 (NC_000011.9:g.534288C>T, NM_198075.3:c.-3739C>T (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.534288C>T
DNA change (hg38) -
Published as HRAS(NM_176795.3):c.35G>A (p.(Gly12Asp)), HRAS(NM_176795.5):c.35G>A (p.G12D)
ISCN -
DB-ID HRAS_000012 See all 4 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.35G>A r.(?) p.(Gly12Asp)
C11orf35 NM_173573.2 +/. - c.*20692G>A r.(=) p.(=)
LRRC56 NM_198075.3 +/. - c.-3739C>T r.(?) p.(=)


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