All transcript variants in gene ZNF500

Information The variants shown are described using the NM_021646.1 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.1219C>T likely benign r.(?) p.(Arg407Trp) g.4802601G>A - C16orf71:NM_021646.1:c.1219C>T, NM_139170.2:c.*3885G>A - ZNF500_000002 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.1397C>T likely benign r.(?) p.(Pro466Leu) g.4802423G>A - C16orf71:NM_021646.1:c.1397C>T, NM_139170.2:c.*3707G>A - ZNF500_000001 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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