All transcript 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     

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.737A>G r.(?) p.(Gln246Arg) - likely benign g.71576821A>G g.71349691A>G ZNF638(NM_001252612.1):c.737A>G (p.Q246R) - ZNF638_000005 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. - c.2194A>T r.(?) p.(Ile732Phe) - VUS g.71597064A>T g.71369934A>T ZNF638(NM_001252612.1):c.2194A>T (p.I732F) - ZNF638_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. - c.4397G>C r.(?) p.(Gly1466Ala) - VUS g.71651041G>C g.71423911G>C ZNF638(NM_001252612.1):c.4397G>C (p.G1466A) - ZNF638_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. - c.4925T>A r.(?) p.(Leu1642His) - VUS g.71653924T>A g.71426794T>A ZNF638(NM_001252612.1):c.4925T>A (p.L1642H) - ZNF638_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
?/. - c.4928T>C r.(?) p.(Phe1643Ser) - VUS g.71653927T>C g.71426797T>C ZNF638(NM_001014972.2):c.4928T>C (p.(Phe1643Ser)) - ZNF638_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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