All variants in the CXorf30 gene

Information The variants shown are described using the NM_001098843.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.1801A>G r.(?) p.(Met601Val) - benign g.36403020A>G g.36384905A>G CFAP47(NM_001304548.1):c.9463A>G (p.M3155V), CXorf30(NM_001098843.4):c.1801A>G (p.(Met601Val)) - CXorf30_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
?/. - c.1801A>G r.(?) p.(Met601Val) - VUS g.36403020A>G g.36384905A>G CFAP47(NM_001304548.1):c.9463A>G (p.M3155V), CXorf30(NM_001098843.4):c.1801A>G (p.(Met601Val)) - CXorf30_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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