All transcript variants in gene FAM133A

Information The variants shown are described using the NM_173698.2 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.-1395_-1390del r.(?) p.(=) - VUS g.92928123_92928128del - NAP1L3(NM_004538.5):c.190_195del (p.(Ser64_Ser65del)) - NAP1L3_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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