All variants in the NUP107 gene

Information The variants shown are described using the NM_020401.2 transcript reference sequence.

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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.*4304T>G r.(=) p.(=) - likely benign g.69140546T>G g.68746766T>G SLC35E3(NM_018656.2):c.389T>G (p.(Ile130Ser)) - NUP107_000015 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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