All variants in the CHCHD10 gene

Information The variants shown are described using the NM_213720.1 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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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.261+11A>G r.(=) p.(=) - benign g.24109550T>C g.23767363T>C CHCHD10(NM_001301339.2):c.261+11A>G - CHCHD10_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_AMC
-/. - c.261+11A>G r.(=) p.(=) - benign g.24109550T>C g.23767363T>C CHCHD10(NM_001301339.2):c.261+11A>G - CHCHD10_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_VUmc
-/. - c.261+11A>G r.(=) p.(=) - benign g.24109550T>C g.23767363T>C CHCHD10(NM_001301339.2):c.261+11A>G - CHCHD10_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
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