Unique variants in gene FAM98C

Information The variants shown are described using the NM_174905.3 transcript reference sequence.

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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.875C>A VUS r.(?) p.(Thr292Asn) g.38897674C>A - FAM98C(NM_174905.3):c.875C>A (p.(Thr292Asn)) - FAM98C_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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