Unique variants in gene CUL9

Information The variants shown are described using the NM_015089.2 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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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     
?/., -?/. 2 - c.845G>A likely benign r.(?) p.(G282E) g.43153787G>A - CUL9:NM_003131.2:c.*6859G>A, NM_015089.2:c.845G>A - CUL9_000001 VKGL data sharing initiative Nederland; correct HGVS to be checked - - rs61743561 Germline, CLASSIFICATION record yes - - - - Xiang Jiao, VKGL-NL_Leiden
?/. 1 - c.2871_2873del - r.(?) p.(Gly958del) g.43166414_43166416del - - - CUL9_000004 - - - rs141674093 Germline yes - - - - Xiang Jiao
?/. 1 - c.3511G>A VUS r.(?) p.(Glu1171Lys) g.43168436G>A - CUL9:c.3511G>A (E1171K) - CUL9_000002 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
-?/. 1 - c.7166G>A likely benign - - g.43191017G>A - CUL9:NM_006443.2:c.*2454C>T, NM_015089.2:c.7166G>A, … - CUL9_000003 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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