Variant #0000003009 (NC_000001.11:g.152409586C>T, CRNN(NM_016190.3):c.*8G>A)

Individual ID 00000749
Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.152409586C>T
Published as -
Reference Iman Salahshourifar et al.(2015)
DB-ID CRNN_000004 See all 4 reported entries
dbSNP ID rs10888486
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
CRNN NM_016190.3 +/. - c.*8G>A - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000843 DNA IHC;PCR;SEQ CRNN 5 Nur Aisyah Athirah