Variant #0000616015 (NC_000011.9:g.534242A>G, NM_198075.3:c.-3785A>G (LRRC56))

Individual ID 00000037
Chromosome 11
Allele Paternal (inferred)
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.534242A>G
Reference -
DB-ID HRAS_000002 See all 16 reported entries
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) 0.3157 View details
Owner LOVD
Database submission license No license selected
Created by LOVD
Date created 2016-08-24 17:34:05 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
HRAS NM_001130442.1 ./. - c.81T>C 81 r.(?) p.(=) - coding-synonymous -
HRAS NM_005343.2 ./. - c.81T>C 81 r.(?) p.(=) - coding-synonymous -
HRAS NM_176795.3 ./. - c.81T>C 81 r.(?) p.(=) - coding-synonymous -
LRRC56 NM_198075.3 ./. - c.-3785A>G -3785 r.(=) p.(=) - utr-5 -



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Genes screened     

Variants found     

Owner     
0000000049 DNA SEQ-NG - - 59467 LOVD