Full data view for gene ZCCHC8

Information The variants shown are described using the NM_017612.3 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.75G>A r.(?) p.(Lys25=) Unknown - likely benign g.122985313C>T g.122500766C>T ZCCHC8(NM_017612.4):c.75G>A (p.K25=) - ZCCHC8_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.470G>A r.(?) p.(Cys157Tyr) Unknown - likely benign g.122973964C>T g.122489417C>T ZCCHC8(NM_017612.4):c.470G>A (p.C157Y) - ZCCHC8_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.1777G>T r.(?) p.(Ala593Ser) Unknown - likely benign g.122958391C>A g.122473844C>A ZCCHC8(NM_017612.4):c.1777G>T (p.A593S) - ZCCHC8_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-?/. - c.2064A>G r.(?) p.(Ile688Met) Unknown - likely benign g.122958104T>C g.122473557T>C ZCCHC8(NM_017612.3):c.2064A>G (p.(Ile688Met)) - ZCCHC8_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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