Unique variants in gene ZNF638

Information The variants shown are described using the NM_014497.4 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Reported     

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     
-?/. 1 - c.737A>G likely benign r.(?) p.(Gln246Arg) g.71576821A>G - ZNF638(NM_001252612.1):c.737A>G (p.Q246R) - ZNF638_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.2194A>T VUS r.(?) p.(Ile732Phe) g.71597064A>T - ZNF638(NM_001252612.1):c.2194A>T (p.I732F) - ZNF638_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.4397G>C VUS r.(?) p.(Gly1466Ala) g.71651041G>C - ZNF638(NM_001252612.1):c.4397G>C (p.G1466A) - ZNF638_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.4925T>A VUS r.(?) p.(Leu1642His) g.71653924T>A - ZNF638(NM_001252612.1):c.4925T>A (p.L1642H) - ZNF638_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.4928T>C VUS r.(?) p.(Phe1643Ser) g.71653927T>C - ZNF638(NM_001014972.2):c.4928T>C (p.(Phe1643Ser)) - ZNF638_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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