Variant #0000544557 (NC_000011.9:g.534288C>G, NM_198075.3:c.-3739C>G (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>G
DNA change (hg38) g.534288C>G
Published as -
ISCN -
DB-ID HRAS_000001 See all 2 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HRAS NM_005343.2 +/. - c.35G>C r.(?) p.(Gly12Ala)
C11orf35 NM_173573.2 +/. - c.*20692G>C r.(=) p.(=)
LRRC56 NM_198075.3 +/. - c.-3739C>G r.(?) p.(=)


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