Unique variants in gene FAM86B2

Information The variants shown are described using the NM_001137610.1 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.650_653del VUS r.(?) p.(Asp217Alafs*4) g.12286233_12286236del - FAM86B2(NM_001137610.1):c.650_653delACAG (p.D217Afs*4) - FAM86B2_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-?/. 1 - c.854G>A likely benign r.(?) p.(Arg285His) g.12285204C>T - FAM86B2(NM_001137610.1):c.854G>A (p.(Arg285His)) - FAM86B2_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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