All variants in the CHRNG gene

Information The variants shown are described using the NM_005199.4 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
+/. 10 c.1210C>T r.(?) p.(Gln404*) - pathogenic g.233409251C>T g.232544541C>T - - CHRNG_000068 - - ClinVar-487641 - Uniparental disomy, maternal allele - 0 controls - 0 - Florian Erger
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