Unique variants in gene RFX2

Information The variants shown are described using the NM_000635.3 transcript reference sequence.

1 entry on 1 page. Showing entry 1.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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     
?/. 1 - c.589A>G VUS r.(?) p.(Asn197Asp) g.6026182T>C - rfx2(NM_134433,NM_000635):c.589A>G (p.Asn197Asp) - RFX2_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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