Variant #0000913625 (NC_000011.9:g.534285C>A, NM_198075.3:c.-3742C>A (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.534285C>A
DNA change (hg38) -
Published as HRAS(NM_005343.2):c.38G>T (p.(Gly13Val)), HRAS(NM_176795.5):c.38G>T (p.G13V)
ISCN -
DB-ID HRAS_000020 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 +/. - c.38G>T r.(?) p.(Gly13Val)
C11orf35 NM_173573.2 +/. - c.*20695G>T r.(=) p.(=)
LRRC56 NM_198075.3 +/. - c.-3742C>A r.(?) p.(=)


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