All transcript variants in gene RXFP2

Information The variants shown are described using the NM_130806.3 transcript reference sequence.

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Effect     

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     
-?/. - c.1594C>G likely benign r.(?) p.(Arg532Gly) g.32367033C>G - RXFP2(NM_001166058.1):c.1522C>G (p.(Arg508Gly)) - RXFP2_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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