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     
+?/. - c.420G>A r.(?) p.(Trp140*) ACMG likely pathogenic g.233406153G>A g.232541443G>A - - CHRNG_000084 ACMG grading: PVS1,PM2 - - rs201762781 Germline - - - 0 - Andreas Laner
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