All variants in the CXorf30 gene

Information The variants shown are described using the NM_001098843.4 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.364C>G r.(?) p.(Gln122Glu) - VUS g.36322019C>G g.36303904C>G CFAP47(NM_001304548.1):c.8026C>G (p.Q2676E) - CXorf59_000022 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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